ID stringlengths 13 17 | question stringlengths 88 1.13k | answer stringlengths 6 156 | reference_sequence stringlengths 4.1k 4.1k | variant_sequence stringlengths 4.1k 4.1k |
|---|---|---|---|---|
Task1_train_47400 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CCTGTAGTCCCAGCTAACCTGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGACTGGGCGACAGAGTAAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAGAGCTGGCACCAGAAATCTTCTTAAGGAGGATACTGTTATTGATAAATGACTTGAGTTAGGAAAGGAGACCTGAGGGATAAAGAGTCAGAGTCAAGGGTAGGATGGCTAAATTTCTCTGCGTTGTAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCAGGAATCTGGAGGTGAGGA... | CCTGTAGTCCCAGCTAACCTGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGACTGGGCGACAGAGTAAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAGAGCTGGCACCAGAAATCTTCTTAAGGAGGATACTGTTATTGATAAATGACTTGAGTTAGGAAAGGAGACCTGAGGGATAAAGAGTCAGAGTCAAGGGTAGGATGGCTAAATTTCTCTGCGTTGTAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCAGGAATCTGGAGGTGAGGA... |
Task1_train_47401 | This mutation on Chromosome 19 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CAGACATTGTGTGAACTGGACTAACTCAGTTGAAGCAAGACTTAGAGCCACAGGTAAAAACACGGGCCCTGGGGGCCCTCCCTTGTGGAGAGGATAATCTGTTTCCCAAAATTTATTATATAAAAGATTAGGCATCAGGTAGATCTCAAGGAAATGAGGGGTCTTCAGCTGACATCTCGATAACTTTATATTTTTACTGAGTTGTTGACCGATAAAGGCTGAGGACTTTATATAAAGTATCTTCTTTTTTTTTTTTTCTGAGCCGGAGTCTCTCTCTGTCACCCAGGCTGGAGTGTAGTGGCGTTTTCTTGGCTCACTAC... | CAGACATTGTGTGAACTGGACTAACTCAGTTGAAGCAAGACTTAGAGCCACAGGTAAAAACACGGGCCCTGGGGGCCCTCCCTTGTGGAGAGGATAATCTGTTTCCCAAAATTTATTATATAAAAGATTAGGCATCAGGTAGATCTCAAGGAAATGAGGGGTCTTCAGCTGACATCTCGATAACTTTATATTTTTACTGAGTTGTTGACCGATAAAGGCTGAGGACTTTATATAAAGTATCTTCTTTTTTTTTTTTTCTGAGCCGGAGTCTCTCTCTGTCACCCAGGCTGGAGTGTAGTGGCGTTTTCTTGGCTCACTAC... |
Task1_train_47402 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTGGAAACTTTCTCCAGGCACTAAGCTGGGGCAATCATAAGGCTCATCTCATTGTTTCCTTTCTGTCATGGAAAGCTGTCCTAAGCCCTTTACTTCTCAATGTCTGATGAAGTTCATTCATATATTTTGTGCATCTTTTTTAGATATTTAAGGCAGGAGATTATATACATTAGACATTTACTGTAAAAGAAAAAGGGACTGTTTGGGTTGGCTATGAAAAAGTTAGTCAATATCCAGGTGCATTATGTCATATGCATTCCGTACTCATAATGAAGTATGTTAGTTTCTTTTCCCCCCTTTTTTAGAGTCAGAGTCTTATT... | CTGGAAACTTTCTCCAGGCACTAAGCTGGGGCAATCATAAGGCTCATCTCATTGTTTCCTTTCTGTCATGGAAAGCTGTCCTAAGCCCTTTACTTCTCAATGTCTGATGAAGTTCATTCATATATTTTGTGCATCTTTTTTAGATATTTAAGGCAGGAGATTATATACATTAGACATTTACTGTAAAAGAAAAAGGGACTGTTTGGGTTGGCTATGAAAAAGTTAGTCAATATCCAGGTGCATTATGTCATATGCATTCCGTACTCATAATGAAGTATGTTAGTTTCTTTTCCCCCCTTTTTTAGAGTCAGAGTCTTATT... |
Task1_train_47403 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTTTCTCCAGGCACTAAGCTGGGGCAATCATAAGGCTCATCTCATTGTTTCCTTTCTGTCATGGAAAGCTGTCCTAAGCCCTTTACTTCTCAATGTCTGATGAAGTTCATTCATATATTTTGTGCATCTTTTTTAGATATTTAAGGCAGGAGATTATATACATTAGACATTTACTGTAAAAGAAAAAGGGACTGTTTGGGTTGGCTATGAAAAAGTTAGTCAATATCCAGGTGCATTATGTCATATGCATTCCGTACTCATAATGAAGTATGTTAGTTTCTTTTCCCCCCTTTTTTAGAGTCAGAGTCTTATTCTGTCAC... | CTTTCTCCAGGCACTAAGCTGGGGCAATCATAAGGCTCATCTCATTGTTTCCTTTCTGTCATGGAAAGCTGTCCTAAGCCCTTTACTTCTCAATGTCTGATGAAGTTCATTCATATATTTTGTGCATCTTTTTTAGATATTTAAGGCAGGAGATTATATACATTAGACATTTACTGTAAAAGAAAAAGGGACTGTTTGGGTTGGCTATGAAAAAGTTAGTCAATATCCAGGTGCATTATGTCATATGCATTCCGTACTCATAATGAAGTATGTTAGTTTCTTTTCCCCCCTTTTTTAGAGTCAGAGTCTTATTCTGTCAC... |
Task1_train_47404 | Assess the clinical impact of this variant found on Chromosome 19. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GTTTCCTTTCTGTCATGGAAAGCTGTCCTAAGCCCTTTACTTCTCAATGTCTGATGAAGTTCATTCATATATTTTGTGCATCTTTTTTAGATATTTAAGGCAGGAGATTATATACATTAGACATTTACTGTAAAAGAAAAAGGGACTGTTTGGGTTGGCTATGAAAAAGTTAGTCAATATCCAGGTGCATTATGTCATATGCATTCCGTACTCATAATGAAGTATGTTAGTTTCTTTTCCCCCCTTTTTTAGAGTCAGAGTCTTATTCTGTCACCCACGCTGTAGTGCAGTGGCATGATCATAGCTCACTGCAGTCACTG... | GTTTCCTTTCTGTCATGGAAAGCTGTCCTAAGCCCTTTACTTCTCAATGTCTGATGAAGTTCATTCATATATTTTGTGCATCTTTTTTAGATATTTAAGGCAGGAGATTATATACATTAGACATTTACTGTAAAAGAAAAAGGGACTGTTTGGGTTGGCTATGAAAAAGTTAGTCAATATCCAGGTGCATTATGTCATATGCATTCCGTACTCATAATGAAGTATGTTAGTTTCTTTTCCCCCCTTTTTTAGAGTCAGAGTCTTATTCTGTCACCCACGCTGTAGTGCAGTGGCATGATCATAGCTCACTGCAGTCACTG... |
Task1_train_47405 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTTACTTCTCAATGTCTGATGAAGTTCATTCATATATTTTGTGCATCTTTTTTAGATATTTAAGGCAGGAGATTATATACATTAGACATTTACTGTAAAAGAAAAAGGGACTGTTTGGGTTGGCTATGAAAAAGTTAGTCAATATCCAGGTGCATTATGTCATATGCATTCCGTACTCATAATGAAGTATGTTAGTTTCTTTTCCCCCCTTTTTTAGAGTCAGAGTCTTATTCTGTCACCCACGCTGTAGTGCAGTGGCATGATCATAGCTCACTGCAGTCACTGCAGCCTAGAACTCCTGGACTCAAGCAATCATCTTG... | TTTACTTCTCAATGTCTGATGAAGTTCATTCATATATTTTGTGCATCTTTTTTAGATATTTAAGGCAGGAGATTATATACATTAGACATTTACTGTAAAAGAAAAAGGGACTGTTTGGGTTGGCTATGAAAAAGTTAGTCAATATCCAGGTGCATTATGTCATATGCATTCCGTACTCATAATGAAGTATGTTAGTTTCTTTTCCCCCCTTTTTTAGAGTCAGAGTCTTATTCTGTCACCCACGCTGTAGTGCAGTGGCATGATCATAGCTCACTGCAGTCACTGCAGCCTAGAACTCCTGGACTCAAGCAATCATCTTG... |
Task1_train_47406 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTATTCTGTCACCCACGCTGTAGTGCAGTGGCATGATCATAGCTCACTGCAGTCACTGCAGCCTAGAACTCCTGGACTCAAGCAATCATCTTGCCTCAGCCTCCCAAGTAGCTGGGACTATAGGCACACACCACCATGTCCAGCTATTATTATTTTTTTTTTTTTTTGTAGAGGTAGTCTCGCTATGTTGCCCAGGGTGGTCTCAAACTTGCGGGCTCAAGTGATCTTCCTGCCTTGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGCCACTGTGCCTGGCCAGGTAGGTTAATTTATATAATTTCAGAATAGATACA... | TTATTCTGTCACCCACGCTGTAGTGCAGTGGCATGATCATAGCTCACTGCAGTCACTGCAGCCTAGAACTCCTGGACTCAAGCAATCATCTTGCCTCAGCCTCCCAAGTAGCTGGGACTATAGGCACACACCACCATGTCCAGCTATTATTATTTTTTTTTTTTTTTGTAGAGGTAGTCTCGCTATGTTGCCCAGGGTGGTCTCAAACTTGCGGGCTCAAGTGATCTTCCTGCCTTGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGCCACTGTGCCTGGCCAGGTAGGTTAATTTATATAATTTCAGAATAGATACA... |
Task1_train_47407 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GGACTCAAGCAATCATCTTGCCTCAGCCTCCCAAGTAGCTGGGACTATAGGCACACACCACCATGTCCAGCTATTATTATTTTTTTTTTTTTTTGTAGAGGTAGTCTCGCTATGTTGCCCAGGGTGGTCTCAAACTTGCGGGCTCAAGTGATCTTCCTGCCTTGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGCCACTGTGCCTGGCCAGGTAGGTTAATTTATATAATTTCAGAATAGATACAAATTTACGTTTAGCAACATTTCAAGCACCATAAATCTCATGTTCTTTTTGGACATTTAGGAGTTATTTTCCAG... | GGACTCAAGCAATCATCTTGCCTCAGCCTCCCAAGTAGCTGGGACTATAGGCACACACCACCATGTCCAGCTATTATTATTTTTTTTTTTTTTTGTAGAGGTAGTCTCGCTATGTTGCCCAGGGTGGTCTCAAACTTGCGGGCTCAAGTGATCTTCCTGCCTTGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGCCACTGTGCCTGGCCAGGTAGGTTAATTTATATAATTTCAGAATAGATACAAATTTACGTTTAGCAACATTTCAAGCACCATAAATCTCATGTTCTTTTTGGACATTTAGGAGTTATTTTCCAG... |
Task1_train_47408 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ACAATCATAGCATAAGATTCTCTGATTATAGAATAAAATCTTAACATACTTGCCTCATAATAAGATAGGGAGATTATCCTGGCTTATCTGGGTTTTCACAGTGTAATCACAAGGGTCCTCAAACATGGAAGAGGGAGACAGAACACTCAAGTGTTTGAGTGATGTAAGACTGATTGGCCATTGCTGGTTTTGAAAGGAGGCCCCAAACCACAGAATTTGGGCAGCTTCTAGAAGCTGGAAGGGCAAAGAAAGACGCTCCCCTAGAGCCTCCAAAAAGAAAAGCAGCCCTGTCAACAGCTTGATGTAGCCCCGTGAGATGC... | ACAATCATAGCATAAGATTCTCTGATTATAGAATAAAATCTTAACATACTTGCCTCATAATAAGATAGGGAGATTATCCTGGCTTATCTGGGTTTTCACAGTGTAATCACAAGGGTCCTCAAACATGGAAGAGGGAGACAGAACACTCAAGTGTTTGAGTGATGTAAGACTGATTGGCCATTGCTGGTTTTGAAAGGAGGCCCCAAACCACAGAATTTGGGCAGCTTCTAGAAGCTGGAAGGGCAAAGAAAGACGCTCCCCTAGAGCCTCCAAAAAGAAAAGCAGCCCTGTCAACAGCTTGATGTAGCCCCGTGAGATGC... |
Task1_train_47409 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TGAAGTTCAAAACTTGTGAATAACCAATTGGCCATGCTCTTAATTTAGAAGGTAGTCCTCATCCTAACCCTGTGGTTTGTCTTATTGTTGGCATAAGCACCATTCAGAATAGTTTGAATGATCTATTTTCTTTACCTGAAACTATTTCCTTTATCTAGGAACCGTGGATGATGGCAGTGGGAAACAAAGCAAAATTGCAAGCCAGCATTTTTAAAAAGCTGGATTATATGCATGTAGCTATTTTACCCTCCAGCAGCTGTAGTTAAAAAATGCATATGCCTATATCAGTTGAAAGAGACATACAATATAAGATCAAATTG... | TGAAGTTCAAAACTTGTGAATAACCAATTGGCCATGCTCTTAATTTAGAAGGTAGTCCTCATCCTAACCCTGTGGTTTGTCTTATTGTTGGCATAAGCACCATTCAGAATAGTTTGAATGATCTATTTTCTTTACCTGAAACTATTTCCTTTATCTAGGAACCGTGGATGATGGCAGTGGGAAACAAAGCAAAATTGCAAGCCAGCATTTTTAAAAAGCTGGATTATATGCATGTAGCTATTTTACCCTCCAGCAGCTGTAGTTAAAAAATGCATATGCCTATATCAGTTGAAAGAGACATACAATATAAGATCAAATTG... |
Task1_train_47410 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGTTACTTAGTGGCCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCATTTGGGAGGCCGAAGTGGGTGAATCACGAGGTCAGGAGTTTGAGACCAGCCTGGCAAACATGGTGAAAGTCCATCTCTACTACAAATACAAAAAATTAGCTGGGCGTGGTGGCAGGCACCTGTAATCCCAGCTACTCGGGAGGCTAAGGCAGGAGAATCGCTTGATCCCGGGAGGCAAAGTTTGCAGTGAGCTGAGTTCGTGCCACTGCATTCCATCCTGGGCGACAGAGCAAGGCTCCATCTCAAAAAAAAGGTTACCTAGTAACCCAGGAT... | AGTTACTTAGTGGCCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCATTTGGGAGGCCGAAGTGGGTGAATCACGAGGTCAGGAGTTTGAGACCAGCCTGGCAAACATGGTGAAAGTCCATCTCTACTACAAATACAAAAAATTAGCTGGGCGTGGTGGCAGGCACCTGTAATCCCAGCTACTCGGGAGGCTAAGGCAGGAGAATCGCTTGATCCCGGGAGGCAAAGTTTGCAGTGAGCTGAGTTCGTGCCACTGCATTCCATCCTGGGCGACAGAGCAAGGCTCCATCTCAAAAAAAAGGTTACCTAGTAACCCAGGAT... |
Task1_train_47411 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTACAATCCCGGCTCACAGCCAAAGTATTTTTTGTTGTTTTTTTTTTGTTTTTTGGGGACGGAGTCTCACTCTGTAGCCCAGGCTGGAGTGCAGTGACATGATCCCGGCTCACTGCAACCTCCACCTCCTGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCACCACCGCACCCAGCTAATTCTGTATATTTAGTAGAGACGGCGTTTCACCATGTTAGCCAGGCTGATCTCGAACTCCCGACCTCAGGTGATCTG... | AGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTACAATCCCGGCTCACAGCCAAAGTATTTTTTGTTGTTTTTTTTTTGTTTTTTGGGGACGGAGTCTCACTCTGTAGCCCAGGCTGGAGTGCAGTGACATGATCCCGGCTCACTGCAACCTCCACCTCCTGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCACCACCGCACCCAGCTAATTCTGTATATTTAGTAGAGACGGCGTTTCACCATGTTAGCCAGGCTGATCTCGAACTCCCGACCTCAGGTGATCTG... |
Task1_train_47412 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | CGTGGTGGCTCACGCCTGTAATCCCAGCACTTCAGGAGGCTGAGGCGGGTGGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCCAAGATGATGAAACCCCGTCACTACTAAAAATACAAAAATTAGCCAGGCGCAGTGGCAGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAAGCAGGAGAATCACTTGAACCCCGGAGGCAGAGGGTGCAGCAAGCCAAGATCGTGCCACTGCACTCTAGCCTGGTCAACAGAGCAAGACTACATCTCAAAACAAAACAATACAAAACAAAAAAAATACTGACAGCATCAAGTGG... | CGTGGTGGCTCACGCCTGTAATCCCAGCACTTCAGGAGGCTGAGGCGGGTGGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCCAAGATGATGAAACCCCGTCACTACTAAAAATACAAAAATTAGCCAGGCGCAGTGGCAGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAAGCAGGAGAATCACTTGAACCCCGGAGGCAGAGGGTGCAGCAAGCCAAGATCGTGCCACTGCACTCTAGCCTGGTCAACAGAGCAAGACTACATCTCAAAACAAAACAATACAAAACAAAAAAAATACTGACAGCATCAAGTGG... |
Task1_train_47413 | This mutation on Chromosome 19 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TTATTTCAAAATAAAAACTTACAAAAACATCTTATTTATATTAATTTCATAACACCTGATGTTACTTATAAACTTAAACATATTCAAGTATGGTCAATTACACTTATGAACTGAATATACTGTATCCAGTTTCATTCTGAAGTACTTTAGTTATTCTGAAATAACACAAACTTAGAACCAAAGAAATGCAGGAGCTAATCATATAATAAAATGAGGCAGGCATAAAATACTCCGGTATTATATACAATATTAAATTTTAGTTCGTGATTAGAGGAAGTCACAATTTAAAATGTATAAAATCAGTGACAAGGCAACTAGGA... | TTATTTCAAAATAAAAACTTACAAAAACATCTTATTTATATTAATTTCATAACACCTGATGTTACTTATAAACTTAAACATATTCAAGTATGGTCAATTACACTTATGAACTGAATATACTGTATCCAGTTTCATTCTGAAGTACTTTAGTTATTCTGAAATAACACAAACTTAGAACCAAAGAAATGCAGGAGCTAATCATATAATAAAATGAGGCAGGCATAAAATACTCCGGTATTATATACAATATTAAATTTTAGTTCGTGATTAGAGGAAGTCACAATTTAAAATGTATAAAATCAGTGACAAGGCAACTAGGA... |
Task1_train_47414 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TATCTTCCCACCAAAGGCTTTTATAGTCTGCCACATTCATAGGATTTTTCTCAGTATACAATTTTTAGACATAATGTCCTAAAATATTTTCTCAAATGTTTTGTACATGTTTTCTCTGACACAAAACATGAAGTAACTGATCACTAAATAAACAACCATGTAGTCTGCATTCATGAAATTACTCTTCTTTGCAGATATCTTAAGGGCCTACATCTGGCAAGAGGCTTTCCCAAAATGACTACCTGTGAATTCTCCTGTGTTTAACAAGGATAGACAAGTGCGCAAAAGCTTTCCCACAATCACTACATCCATAGGGCCTC... | TATCTTCCCACCAAAGGCTTTTATAGTCTGCCACATTCATAGGATTTTTCTCAGTATACAATTTTTAGACATAATGTCCTAAAATATTTTCTCAAATGTTTTGTACATGTTTTCTCTGACACAAAACATGAAGTAACTGATCACTAAATAAACAACCATGTAGTCTGCATTCATGAAATTACTCTTCTTTGCAGATATCTTAAGGGCCTACATCTGGCAAGAGGCTTTCCCAAAATGACTACCTGTGAATTCTCCTGTGTTTAACAAGGATAGACAAGTGCGCAAAAGCTTTCCCACAATCACTACATCCATAGGGCCTC... |
Task1_train_47415 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | ACAACAGCAAAAACAAAACAAAACCAAAAAACTCTTATCACTCATGAAATTCTAAGCGTTTTAGGAGCTCTATGCCAGGAACCAGGAACAAAGACCAAATGTATTTCTCATTATACCACAATTTTACACAACAGTAAAAATAAACAGTAATGAGACAGTATATTATGGAATCATTGGCAAGGCAACTAGAAATGAGGATTAAGGTATCCTGACTGAAAATGCACACCAGGTGTATTAGCTGATGTTTAAGGTTATACTTATTAAGAAAAAGCACTCAAATATTCATCATTTTCACCACATTTCATGCCTTCATGAGCTGT... | ACAACAGCAAAAACAAAACAAAACCAAAAAACTCTTATCACTCATGAAATTCTAAGCGTTTTAGGAGCTCTATGCCAGGAACCAGGAACAAAGACCAAATGTATTTCTCATTATACCACAATTTTACACAACAGTAAAAATAAACAGTAATGAGACAGTATATTATGGAATCATTGGCAAGGCAACTAGAAATGAGGATTAAGGTATCCTGACTGAAAATGCACACCAGGTGTATTAGCTGATGTTTAAGGTTATACTTATTAAGAAAAAGCACTCAAATATTCATCATTTTCACCACATTTCATGCCTTCATGAGCTGT... |
Task1_train_47416 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AAATCCTGCCATCAATACTGTCACCTTAAAGTTATTTTCCAGTGTAAACTTTGACACTCACTGAGGTCATATTTCTGAGTAAAGACTTTGTCATGGTCATCATGTTTCTATCAACAATAAGCTCACTTACGTTGAAATCTATGATGAAACCTGATAATAAAGTCTATCTTTCCACAGAAGACTTTTCTTAGTCTTTGTATTCACAGAATTTATCTCTGTATACTTTTCAGACATATGAGCAGAAATTATTGCTCAAAACATCTCCACATTAATATAGTTTATTCAACGTATTTTCATTGACAGAAAATATGAGGTAAAAG... | AAATCCTGCCATCAATACTGTCACCTTAAAGTTATTTTCCAGTGTAAACTTTGACACTCACTGAGGTCATATTTCTGAGTAAAGACTTTGTCATGGTCATCATGTTTCTATCAACAATAAGCTCACTTACGTTGAAATCTATGATGAAACCTGATAATAAAGTCTATCTTTCCACAGAAGACTTTTCTTAGTCTTTGTATTCACAGAATTTATCTCTGTATACTTTTCAGACATATGAGCAGAAATTATTGCTCAAAACATCTCCACATTAATATAGTTTATTCAACGTATTTTCATTGACAGAAAATATGAGGTAAAAG... |
Task1_train_47417 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CTGTATGCGTTCTTTGATGTACATTGAGTACTGACTTTGTGGTGAAGGCTTTTCCACATTCATTGCACTCATAAGGTTTCTCTCCTGTGTGAATTCTCTGATGGGTAATGAGGCCATATTTGTGTGAATAGGATTTTCCGCACTCGGTACATACAAAGGGAGTCTTTCCTGTATGACATCTCTCATGTTGTATGAGGCATATTTTCTGGCTGAAGGCTTTACCACATTCATTGCATTCATAGGGTTTTTCTCCTGTATGAGTTCGCTGATGTATAATAAGAGTGCGCTTTGTGGTGAAGCCTTTACCACATTCATTGCAT... | CTGTATGCGTTCTTTGATGTACATTGAGTACTGACTTTGTGGTGAAGGCTTTTCCACATTCATTGCACTCATAAGGTTTCTCTCCTGTGTGAATTCTCTGATGGGTAATGAGGCCATATTTGTGTGAATAGGATTTTCCGCACTCGGTACATACAAAGGGAGTCTTTCCTGTATGACATCTCTCATGTTGTATGAGGCATATTTTCTGGCTGAAGGCTTTACCACATTCATTGCATTCATAGGGTTTTTCTCCTGTATGAGTTCGCTGATGTATAATAAGAGTGCGCTTTGTGGTGAAGCCTTTACCACATTCATTGCAT... |
Task1_train_47418 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | ACATTTATAAGGTTTCTCTCCAGTATGCATCATCTGATGATTAAGCAGAATTGAACGTACTCTAAAGGCTTTGCCACACTCATTACATTTGTAAGGTTTCTCTCCAGTATGAATACTCCAATGACGTGCGAGGCCTGAGCGATAACGGAAGACCTTGCCACATTCATTACATTTGTAAGGTTTCTCTCCAGTATGAATTCTCCGATGCCTTGCCAGGGTTGTAGTGGAGTTAAAGACTTTCCCACATTCAATACATTTGTATGGCATCTCTCCAGTATGTCTTCTCTGATGGTACACCAGACTTGTTTTATGACTAAAAG... | ACATTTATAAGGTTTCTCTCCAGTATGCATCATCTGATGATTAAGCAGAATTGAACGTACTCTAAAGGCTTTGCCACACTCATTACATTTGTAAGGTTTCTCTCCAGTATGAATACTCCAATGACGTGCGAGGCCTGAGCGATAACGGAAGACCTTGCCACATTCATTACATTTGTAAGGTTTCTCTCCAGTATGAATTCTCCGATGCCTTGCCAGGGTTGTAGTGGAGTTAAAGACTTTCCCACATTCAATACATTTGTATGGCATCTCTCCAGTATGTCTTCTCTGATGGTACACCAGACTTGTTTTATGACTAAAAG... |
Task1_train_47419 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CATCCACATCGCTGCAATGGACATGATCTCATTCCTTTCTATGGCTGCATAGTATCCCATGGTGTATATGTACCACATTTTCTTTATTCAGTCTATCACTGATAAGCATTTGGGTTGATTCCAGGTCTTTGAACATTTCATTTTTTAAAACCATTTATTTGGAAGGTTGTCTCTAGTATGAATACTCTTTCCATTTTGATGTTCGGGTAAAAACCTTAGCATGCACATTACATTTCTGTGGTTCCTCTCAAAGATGTATATTCTGATGCCTAGTGAGTTCCAATGCCTGGGGAAAGCCTCTGACACATACATTTATATGA... | CATCCACATCGCTGCAATGGACATGATCTCATTCCTTTCTATGGCTGCATAGTATCCCATGGTGTATATGTACCACATTTTCTTTATTCAGTCTATCACTGATAAGCATTTGGGTTGATTCCAGGTCTTTGAACATTTCATTTTTTAAAACCATTTATTTGGAAGGTTGTCTCTAGTATGAATACTCTTTCCATTTTGATGTTCGGGTAAAAACCTTAGCATGCACATTACATTTCTGTGGTTCCTCTCAAAGATGTATATTCTGATGCCTAGTGAGTTCCAATGCCTGGGGAAAGCCTCTGACACATACATTTATATGA... |
Task1_train_47420 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | GAGGGAAAACAACCGCCCAAAGGCTTTGCCACATTCAATACATTTGTATCTTTTCTCTCCAGTGTGGATTCTCTGGTGACTTACAAGATGTGAACTATGCCTGAATACCTTGCCACATTCATCACATTTATATGGTTTCTTTCCTGCATGAATTATCTGATGTGCAGTGAGGTTTGAGCTCCGTTTAAAGGTTTTGCCACACTCATTACATTTGTAAGGTCTGTCTCCAGTATGAACAGTCTGATGAAGTCTAAGATGGACACGCTGACTAAAGGAATTCCCACACTGATTGCATTTGTAAGGTTTCTCTCCGGTATGAA... | GAGGGAAAACAACCGCCCAAAGGCTTTGCCACATTCAATACATTTGTATCTTTTCTCTCCAGTGTGGATTCTCTGGTGACTTACAAGATGTGAACTATGCCTGAATACCTTGCCACATTCATCACATTTATATGGTTTCTTTCCTGCATGAATTATCTGATGTGCAGTGAGGTTTGAGCTCCGTTTAAAGGTTTTGCCACACTCATTACATTTGTAAGGTCTGTCTCCAGTATGAACAGTCTGATGAAGTCTAAGATGGACACGCTGACTAAAGGAATTCCCACACTGATTGCATTTGTAAGGTTTCTCTCCGGTATGAA... |
Task1_train_47421 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | TGCCTGGGGAAAGTCTCTGGCACATACGTGTAGATTTCCTATCAGTATAAACTCCCTTCTGTCCAGTAGGGATTGAACTCTGGTAAAGGTTTTGCCACACTCTTTTCATTTGTAAAGCATCTCTGCACTATGAATTATCTATAGATCCACAAGTTTTGATCTTTGAATAGAATTCTTGCCACACATACTGCATTTCAGTAATTTCTCTCCAATATGTATATTCTTTTTTTTTTTTTTTTTTTTTTTGGAGACAAAGTCTTGCTCTGTCGCTCAGGCTGGAGTGCAGTGGTGTGATTTTGGCTCACTGCAACCTCCACCTC... | TGCCTGGGGAAAGTCTCTGGCACATACGTGTAGATTTCCTATCAGTATAAACTCCCTTCTGTCCAGTAGGGATTGAACTCTGGTAAAGGTTTTGCCACACTCTTTTCATTTGTAAAGCATCTCTGCACTATGAATTATCTATAGATCCACAAGTTTTGATCTTTGAATAGAATTCTTGCCACACATACTGCATTTCAGTAATTTCTCTCCAATATGTATATTCTTTTTTTTTTTTTTTTTTTTTTTGGAGACAAAGTCTTGCTCTGTCGCTCAGGCTGGAGTGCAGTGGTGTGATTTTGGCTCACTGCAACCTCCACCTC... |
Task1_train_47422 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | GGATTCTGAATCGAAATAATGGATGTGCACCCAGTCAGTAATCAATGAAAGAGAGTTAATAAGCACAAGTGGGTACCACTGCATTTAAATGATATAAGACCAGAGAGTCAAGAAAGACCTGGATCCCGGAAGAGCTCAATTAAAAAAAAAAAAAGAAAGAAAGAAAGAATCCAAGTGGGCTTTTCCCCCCTAATTATAAAGGAAAAGCCTTCATTCTTTCAATATTGAGTATGATGTTACCTTTCGGCTTTTTATATATGGACTCTATTATGTTAAGTAAGTTCCTCGTATTCCTAGTGTGTTGAGTGTTTTTCTTTCTT... | GGATTCTGAATCGAAATAATGGATGTGCACCCAGTCAGTAATCAATGAAAGAGAGTTAATAAGCACAAGTGGGTACCACTGCATTTAAATGATATAAGACCAGAGAGTCAAGAAAGACCTGGATCCCGGAAGAGCTCAATTAAAAAAAAAAAAAGAAAGAAAGAAAGAATCCAAGTGGGCTTTTCCCCCCTAATTATAAAGGAAAAGCCTTCATTCTTTCAATATTGAGTATGATGTTACCTTTCGGCTTTTTATATATGGACTCTATTATGTTAAGTAAGTTCCTCGTATTCCTAGTGTGTTGAGTGTTTTTCTTTCTT... |
Task1_train_47423 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTTTTTTTTTTTGAGATGGAGTCCTGTTCTGTCGCCCAGGCTGGAGTACAGTGGTGTGATCTCGGCTCACTGCAACTTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGTGAGCACATGCCACCATGTCCAGCTAATTTTTTGAATTTTAGTAGAGACGGGGCTTCACCTTGTTGCCCAGGCTGGTCGCGAACTCCTGAGCTCAGGCAATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTAAGCCACCGTGCCTGGTCGTGTTCATTTTTTTCTTTATTGAGAT... | CTTTTTTTTTTTGAGATGGAGTCCTGTTCTGTCGCCCAGGCTGGAGTACAGTGGTGTGATCTCGGCTCACTGCAACTTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGTGAGCACATGCCACCATGTCCAGCTAATTTTTTGAATTTTAGTAGAGACGGGGCTTCACCTTGTTGCCCAGGCTGGTCGCGAACTCCTGAGCTCAGGCAATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTAAGCCACCGTGCCTGGTCGTGTTCATTTTTTTCTTTATTGAGAT... |
Task1_train_47424 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GAGAGCATCCGAAAAATGTATTAGCGTTTATTTGCTTTTCTTCTCTGTTTTTTGTTTTTGGTCTTTGTAGCTGATACTGTGTTTTTTTTTTTTTTTTTTTTTTTTAAATTAGAGTCTTGCTCTGTAGCCCAGGCTGGAGTGTAATGGCTCCATCTTGGCTCACTGCAATCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCACAGCCTCCTGAGTAGCTGGGATTACAGGTGCATGCCCCCATGTCCATCTAATTTTTGTATTTTTAGTAGAGACAGGCTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGACCT... | GAGAGCATCCGAAAAATGTATTAGCGTTTATTTGCTTTTCTTCTCTGTTTTTTGTTTTTGGTCTTTGTAGCTGATACTGTGTTTTTTTTTTTTTTTTTTTTTTTTAAATTAGAGTCTTGCTCTGTAGCCCAGGCTGGAGTGTAATGGCTCCATCTTGGCTCACTGCAATCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCACAGCCTCCTGAGTAGCTGGGATTACAGGTGCATGCCCCCATGTCCATCTAATTTTTGTATTTTTAGTAGAGACAGGCTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGACCT... |
Task1_train_47425 | This variant is found on Chromosome 19. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TGCTTTGATCCCCTTCTCATCTCCTCTGGTGTATGTTTGTAGATTTTCCTCTTGTGGTTAAGATTGAAGTTACATAAAACATTGTAACAATAAAACATTATTTTAAAATGTCAACAGCTTAACCTTGATTAGGTACCGAAAGCATTACATTATAGCTGTGCTATTTGTTATTGTGCTAGAAGTTCCTTCTATATATGTAATATTCCCATTAACACATTTTAGTGCTTTTTAAATAATTTTGCCTTTGAAATGCTAGGAAAGAAAAGCCAAATTACAAATGAAAAGTACAATAATGCATGATTTTTTTGTTTTCTTTTTTA... | TGCTTTGATCCCCTTCTCATCTCCTCTGGTGTATGTTTGTAGATTTTCCTCTTGTGGTTAAGATTGAAGTTACATAAAACATTGTAACAATAAAACATTATTTTAAAATGTCAACAGCTTAACCTTGATTAGGTACCGAAAGCATTACATTATAGCTGTGCTATTTGTTATTGTGCTAGAAGTTCCTTCTATATATGTAATATTCCCATTAACACATTTTAGTGCTTTTTAAATAATTTTGCCTTTGAAATGCTAGGAAAGAAAAGCCAAATTACAAATGAAAAGTACAATAATGCATGATTTTTTTGTTTTCTTTTTTA... |
Task1_train_47426 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCTATTGTTTTTATCAAAGGCGCATCATCAGTTTATATACGTCTTATATCTTTTAACAGTTGAAATTACATCTTATATATTTTCATGACCTTAAAATTGTTCTACACTGTTATGATAGTGAGTCTATGGCTGTAAGGATAGTAACCTGTTATGGGGATACATGTGCGACAGTTTCTTGATTTTAATCCCGGAACTTATTTTAACTATACTCAGTTAGGTCATTGTCTGTCAATTTACTTTTGATGCTGATCTGTTATTGTTTGATGTTTTTTTTTTTCTTTTTCTGAGATGGAGTCTCTCTTTGTCACCCAGGCTGGAGT... | TCTATTGTTTTTATCAAAGGCGCATCATCAGTTTATATACGTCTTATATCTTTTAACAGTTGAAATTACATCTTATATATTTTCATGACCTTAAAATTGTTCTACACTGTTATGATAGTGAGTCTATGGCTGTAAGGATAGTAACCTGTTATGGGGATACATGTGCGACAGTTTCTTGATTTTAATCCCGGAACTTATTTTAACTATACTCAGTTAGGTCATTGTCTGTCAATTTACTTTTGATGCTGATCTGTTATTGTTTGATGTTTTTTTTTTTCTTTTTCTGAGATGGAGTCTCTCTTTGTCACCCAGGCTGGAGT... |
Task1_train_47427 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | CAGTGGCCATCTAATAGTTTTCTATGATGCCTTTCTGATATTATGTATCTGGAATTAGAGTCAGATCCCACAGGCAAAGGGCTGAGTTCCCAAACACGTCCCCTACCTCAGCAACCAATCACAAGTAGCAGGTTGTCACCTTTCCTTCTTACCAACCAGCTACAGGTTGGGGTTCCCTCAAGCCCCTTCTTGGGGTTGATTACTTTGCTAGGGTGGCCCACAGAACTCAGTAAAACACTTTCTTAGGTTCACTGCCTCACGCTGAAGGATGTTTTGAAGGATACAGATGAAGAGCCGGATGAGGAGATTCACAGGGGGAG... | CAGTGGCCATCTAATAGTTTTCTATGATGCCTTTCTGATATTATGTATCTGGAATTAGAGTCAGATCCCACAGGCAAAGGGCTGAGTTCCCAAACACGTCCCCTACCTCAGCAACCAATCACAAGTAGCAGGTTGTCACCTTTCCTTCTTACCAACCAGCTACAGGTTGGGGTTCCCTCAAGCCCCTTCTTGGGGTTGATTACTTTGCTAGGGTGGCCCACAGAACTCAGTAAAACACTTTCTTAGGTTCACTGCCTCACGCTGAAGGATGTTTTGAAGGATACAGATGAAGAGCCGGATGAGGAGATTCACAGGGGGAG... |
Task1_train_47428 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ATATAGTGCTTTTTAAATGATTTTGTCTTTTAATTACTAGGAAAGAATTATGGGAGGCTGAGGCAGGTGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCTGACATGGCGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGGGGTAACGCATGCCTATAATCCCAGCTACTACTTGGGAGGCTGAGGTGGGAGAATTGTTTGAGCTTGGGAGGGGGAGGTTGCAGTGGGCCAAGATCACGCCACTGCACTCTAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAAAAACAAACAAAAACCATTAAA... | ATATAGTGCTTTTTAAATGATTTTGTCTTTTAATTACTAGGAAAGAATTATGGGAGGCTGAGGCAGGTGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCTGACATGGCGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGGGGTAACGCATGCCTATAATCCCAGCTACTACTTGGGAGGCTGAGGTGGGAGAATTGTTTGAGCTTGGGAGGGGGAGGTTGCAGTGGGCCAAGATCACGCCACTGCACTCTAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAAAAACAAACAAAAACCATTAAA... |
Task1_train_47429 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | TAGCCAGGTGGGGTAACGCATGCCTATAATCCCAGCTACTACTTGGGAGGCTGAGGTGGGAGAATTGTTTGAGCTTGGGAGGGGGAGGTTGCAGTGGGCCAAGATCACGCCACTGCACTCTAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAAAAACAAACAAAAACCATTAAAAGTCAAGTTACAAAAGAAAAGAGTAATAATAAATATCTCTATATTTGATTATTTACTGACCTTTAATGGTGAACTTTCTATTTTCATTGAGGTTAAAGATACTATTTAGAGACCTTTTATTTTATATTGAAGGAGTCCCTTTAGC... | TAGCCAGGTGGGGTAACGCATGCCTATAATCCCAGCTACTACTTGGGAGGCTGAGGTGGGAGAATTGTTTGAGCTTGGGAGGGGGAGGTTGCAGTGGGCCAAGATCACGCCACTGCACTCTAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAAAAACAAACAAAAACCATTAAAAGTCAAGTTACAAAAGAAAAGAGTAATAATAAATATCTCTATATTTGATTATTTACTGACCTTTAATGGTGAACTTTCTATTTTCATTGAGGTTAAAGATACTATTTAGAGACCTTTTATTTTATATTGAAGGAGTCCCTTTAGC... |
Task1_train_47430 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AATGTACTAGGGTTGGTTTTCTTCATCATTTTTTCTTTTTGCTCTTTGGAGCTGATTCTTTTGAATAACATATCTTTCAATTTGCTCATTGTTTTCTGTTCCTTTTGCAGTCTGCTGTTGAATCCCTTAGTGAAATATTACTTCAGTTATCATATTTAAGCTCCAGAATTTCTGTTCTTTTGGTTTTAGTAGTTTCTCCTGTGATTGGTATTCTTTTTCTTTTCATGTAATGTTTGCCTGATTTTATTTAGTTATCTGTCTCTGTTATCTTTTTTAGCTCATTAAGCATCTTAAGGCAGTTGCTTTAAATACCTGTCAAG... | AATGTACTAGGGTTGGTTTTCTTCATCATTTTTTCTTTTTGCTCTTTGGAGCTGATTCTTTTGAATAACATATCTTTCAATTTGCTCATTGTTTTCTGTTCCTTTTGCAGTCTGCTGTTGAATCCCTTAGTGAAATATTACTTCAGTTATCATATTTAAGCTCCAGAATTTCTGTTCTTTTGGTTTTAGTAGTTTCTCCTGTGATTGGTATTCTTTTTCTTTTCATGTAATGTTTGCCTGATTTTATTTAGTTATCTGTCTCTGTTATCTTTTTTAGCTCATTAAGCATCTTAAGGCAGTTGCTTTAAATACCTGTCAAG... |
Task1_train_47431 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTCCTTCATAATCGGAGTCAGTCACTCCTGGGACTACAGTGATGCCTTGCAAGTTAAGGCGGCCTTTGCCTAAAATTAGTTCCATGTATCCTCTTGGTAAAGGTCCTCAAATGCCAGTGGGAATTTTGATAGGTTTGTCTCCACCAACTACTGTTATTTCTCTTGACTGGGAGATCTAATCCTGCACTTCCTGGTGTTCCTGGGGTGAGGGAATCAATGTTTCTCTTGGGACCCATCCCTGAAATGGGCTTGTGGTCTGGACTGAGAATGCCCTGATTGTTTGAGGGGCCCGGGTCCAGGCCACCTTCTCATTTCCCAGC... | CTCCTTCATAATCGGAGTCAGTCACTCCTGGGACTACAGTGATGCCTTGCAAGTTAAGGCGGCCTTTGCCTAAAATTAGTTCCATGTATCCTCTTGGTAAAGGTCCTCAAATGCCAGTGGGAATTTTGATAGGTTTGTCTCCACCAACTACTGTTATTTCTCTTGACTGGGAGATCTAATCCTGCACTTCCTGGTGTTCCTGGGGTGAGGGAATCAATGTTTCTCTTGGGACCCATCCCTGAAATGGGCTTGTGGTCTGGACTGAGAATGCCCTGATTGTTTGAGGGGCCCGGGTCCAGGCCACCTTCTCATTTCCCAGC... |
Task1_train_47432 | Located on Chromosome 19, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGGTGAGACTCTATCTCTACAAAACATACAAAAATTAGCTGGGCATAGTGGTGTGAGCCTGTAGTCCCAGCTACTCGGGAGGCTTAAGAGGATCACTTGAGCCTGGGAGGCAGAGGTTGCAGTGGGTGGATATCACACCCCTGCACTCCAGTCTGGGAAACAGTAAGATCCTATCTCAAAAAAAAAAAAAAAAAAAAAAAAGAAAGAAAGCACTGTAGACATTGTCATCTCTGAAGACACTACTTGTATCTCAGGTAGATACTAAATGTCACTTGATGTGTCAAAAATAAAACCTAACATTTCTTTCTCTTTTTGGGGGG... | TGGTGAGACTCTATCTCTACAAAACATACAAAAATTAGCTGGGCATAGTGGTGTGAGCCTGTAGTCCCAGCTACTCGGGAGGCTTAAGAGGATCACTTGAGCCTGGGAGGCAGAGGTTGCAGTGGGTGGATATCACACCCCTGCACTCCAGTCTGGGAAACAGTAAGATCCTATCTCAAAAAAAAAAAAAAAAAAAAAAAAGAAAGAAAGCACTGTAGACATTGTCATCTCTGAAGACACTACTTGTATCTCAGGTAGATACTAAATGTCACTTGATGTGTCAAAAATAAAACCTAACATTTCTTTCTCTTTTTGGGGGG... |
Task1_train_47433 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | GCCTGTAGTCCCAGCTACTCGGGAGGCTTAAGAGGATCACTTGAGCCTGGGAGGCAGAGGTTGCAGTGGGTGGATATCACACCCCTGCACTCCAGTCTGGGAAACAGTAAGATCCTATCTCAAAAAAAAAAAAAAAAAAAAAAAAGAAAGAAAGCACTGTAGACATTGTCATCTCTGAAGACACTACTTGTATCTCAGGTAGATACTAAATGTCACTTGATGTGTCAAAAATAAAACCTAACATTTCTTTCTCTTTTTGGGGGGGGGAGGGGACGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTC... | GCCTGTAGTCCCAGCTACTCGGGAGGCTTAAGAGGATCACTTGAGCCTGGGAGGCAGAGGTTGCAGTGGGTGGATATCACACCCCTGCACTCCAGTCTGGGAAACAGTAAGATCCTATCTCAAAAAAAAAAAAAAAAAAAAAAAAGAAAGAAAGCACTGTAGACATTGTCATCTCTGAAGACACTACTTGTATCTCAGGTAGATACTAAATGTCACTTGATGTGTCAAAAATAAAACCTAACATTTCTTTCTCTTTTTGGGGGGGGGAGGGGACGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTC... |
Task1_train_47434 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | GCACCCGCCACCACACCCGGCTGATGTTTTGGTGTTCTTAGTAGAGATGCAGTTTCCCCATGTTGGCCAGCCTGTTCTCGAACTCCTGACCTCGTGCTCCACTTGCCTCAGCCTCCCAAGGTGCTGGGATTACAGGTTGTGAGTCGTCGTGCCCAGCCGTTAGTCAGTTCTTATTCCTTATAATGCTGTGTATTTTCTTGACCTCATACATCAGAAGGTAGTGATCTTAACATGTATTTCAGTTCTTATATTGTGTGCTGGTGGTTAAGTAGATGTTGTGGCTTTTTTCTTAAGAGGGAATTGTTTAGAATTCTGCAGGC... | GCACCCGCCACCACACCCGGCTGATGTTTTGGTGTTCTTAGTAGAGATGCAGTTTCCCCATGTTGGCCAGCCTGTTCTCGAACTCCTGACCTCGTGCTCCACTTGCCTCAGCCTCCCAAGGTGCTGGGATTACAGGTTGTGAGTCGTCGTGCCCAGCCGTTAGTCAGTTCTTATTCCTTATAATGCTGTGTATTTTCTTGACCTCATACATCAGAAGGTAGTGATCTTAACATGTATTTCAGTTCTTATATTGTGTGCTGGTGGTTAAGTAGATGTTGTGGCTTTTTTCTTAAGAGGGAATTGTTTAGAATTCTGCAGGC... |
Task1_train_47435 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | ACATATGGCTTTTCGGTATGTGGTATGCAATATAACTGACACACTGCACTCGTTAATGTCACAAAGTGCCACCAGGTGCAGTGGCTCACACCTGTGATCCCAGAAATTTGGGAGGTCAAGGGGGGTGGATTACTTAAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCACATCTCTACTAAAAACACAAAAATTAGCCAGGTGTAGTGGTGTGTGCCTGTAATCCCAGGTACTCAGGAGGTTGAGGAAGGAGAATCACTTCAACCCAGCAGGCAGAGGTTGCAGTGAGCTGAGATTACACCATGACGCTC... | ACATATGGCTTTTCGGTATGTGGTATGCAATATAACTGACACACTGCACTCGTTAATGTCACAAAGTGCCACCAGGTGCAGTGGCTCACACCTGTGATCCCAGAAATTTGGGAGGTCAAGGGGGGTGGATTACTTAAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCACATCTCTACTAAAAACACAAAAATTAGCCAGGTGTAGTGGTGTGTGCCTGTAATCCCAGGTACTCAGGAGGTTGAGGAAGGAGAATCACTTCAACCCAGCAGGCAGAGGTTGCAGTGAGCTGAGATTACACCATGACGCTC... |
Task1_train_47436 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GAGAAACCTTACAAGTGTAATGAATGTGGCAAGGCTTTTAATCAACAATCACACCTTTCACGCCATCAAAGACTTCATACTGGAGTGAAACCTTACAAATGTAAGATTTGTGAGAAGGCTTTTGCGTGTCATTCCTATCTGGCAAACCATACTAGAATTCATAGTGGAGAGAAAACATACAAGTGTAATGAGTGTGGTAAGGCTTTTAATCATCAATCAAGCCTTGCACGTCATCATATACTTCATACTGGAGAGAAACCTTACAAATGTGAAGAATGTGACAAAGTTTTCAGTCAGAAATCAACCCTTGAGAGACATAA... | GAGAAACCTTACAAGTGTAATGAATGTGGCAAGGCTTTTAATCAACAATCACACCTTTCACGCCATCAAAGACTTCATACTGGAGTGAAACCTTACAAATGTAAGATTTGTGAGAAGGCTTTTGCGTGTCATTCCTATCTGGCAAACCATACTAGAATTCATAGTGGAGAGAAAACATACAAGTGTAATGAGTGTGGTAAGGCTTTTAATCATCAATCAAGCCTTGCACGTCATCATATACTTCATACTGGAGAGAAACCTTACAAATGTGAAGAATGTGACAAAGTTTTCAGTCAGAAATCAACCCTTGAGAGACATAA... |
Task1_train_47437 | With a mutation on Chromosome 19, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CAGGCCCCGCCCACCTTCTCGTTGGCTCCACCCAGGCCTGGCTTTAGTCCTGTGCGCACACATCCGCGCAGACCAGGAAGCGGATCCCGTGGAGTGAAGGTCGCACCGCGGCGGTGAGTTTTGCTCTGTGTTGTATTAAGTCTGCACTCCCCATATCCCCGGCACTTCCGTACCTGGGACGTGGGGTCACCACAGACCTGTAAATTCTCGCCCATCTTCCTTCAACCAGAGCAAATGCAGACGTTCCCCTGGGAATCCGGAAGTCGCTTCCTTTTGTGTTTAAAGTCGCCCTGAGGCTGTTCCCGTCTCCAGTCTTTCTG... | CAGGCCCCGCCCACCTTCTCGTTGGCTCCACCCAGGCCTGGCTTTAGTCCTGTGCGCACACATCCGCGCAGACCAGGAAGCGGATCCCGTGGAGTGAAGGTCGCACCGCGGCGGTGAGTTTTGCTCTGTGTTGTATTAAGTCTGCACTCCCCATATCCCCGGCACTTCCGTACCTGGGACGTGGGGTCACCACAGACCTGTAAATTCTCGCCCATCTTCCTTCAACCAGAGCAAATGCAGACGTTCCCCTGGGAATCCGGAAGTCGCTTCCTTTTGTGTTTAAAGTCGCCCTGAGGCTGTTCCCGTCTCCAGTCTTTCTG... |
Task1_train_47438 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | ACCGAGCCCGGCCTACTCACCACCACCTTTACCTCCCGGTTTTAAGCGATTGTCCTGCCTCGGCCTTCCTGAGTAGCTGGAATTACAGGCAAGTGCCACAACATCTAGATAATTTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGATGGTCTCGAACTCCCGACATCAGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACTCAGCCTCCCTGTTTTGAAGGTAACTAGCTGTGTCTTTGTACATCTGCATTTTATAAATGTTACTGTAATTTTCTTGTGAG... | ACCGAGCCCGGCCTACTCACCACCACCTTTACCTCCCGGTTTTAAGCGATTGTCCTGCCTCGGCCTTCCTGAGTAGCTGGAATTACAGGCAAGTGCCACAACATCTAGATAATTTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGATGGTCTCGAACTCCCGACATCAGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACTCAGCCTCCCTGTTTTGAAGGTAACTAGCTGTGTCTTTGTACATCTGCATTTTATAAATGTTACTGTAATTTTCTTGTGAG... |
Task1_train_47439 | A variant affecting Chromosome 19 has been observed. Determine if it's benign or associated with disease. | Benign | GGGATTACAGGTACCCACCACCGTGCCCAGCTAATGTTTTTGTATTTTTAGTAGATATGGGGTTGCACCATGTTGGCCAGGCTGGTGTCGAACTTCTGACCTCATGATTCACCTGCCTCAGACCCCCAAAGTGCTGGGATTACAGGCATGTGCCACCGTGCCCGGACATTAGTCAATTCTTATTCCTTATAGTGCTGTGTATAGTTTTGACCTCATACATCAGAAAGTAGTGACCTTAACATGTATTTCAATTCTTATGTTGTGTACTAGTGGTAAGTACAAGTTGTGGCTTTTTTCTTAATAGGGAATTGTTTACAATT... | GGGATTACAGGTACCCACCACCGTGCCCAGCTAATGTTTTTGTATTTTTAGTAGATATGGGGTTGCACCATGTTGGCCAGGCTGGTGTCGAACTTCTGACCTCATGATTCACCTGCCTCAGACCCCCAAAGTGCTGGGATTACAGGCATGTGCCACCGTGCCCGGACATTAGTCAATTCTTATTCCTTATAGTGCTGTGTATAGTTTTGACCTCATACATCAGAAAGTAGTGACCTTAACATGTATTTCAATTCTTATGTTGTGTACTAGTGGTAAGTACAAGTTGTGGCTTTTTTCTTAATAGGGAATTGTTTACAATT... |
Task1_train_47440 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGCACTCTGGGAGGCTGAGGCGGGCGGATCACGAGGTCAGGAGATCAAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACATAAAATTAGCCGGACATGGTGGCGGGCACCTGTAATCGCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCCGGGAGGTAGAGCTTGCAGTGAGCCGAGATCTCGCCACTGCACCCCAGTCTGGGCAACAGAGTGAGACTCCATCTCAAAAACAATAACCAAAAAAAGAGAATTAGACTTCCTGTGAGCTCTCAGATGGATTATAGTTTGTGAATAAT... | AGCACTCTGGGAGGCTGAGGCGGGCGGATCACGAGGTCAGGAGATCAAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACATAAAATTAGCCGGACATGGTGGCGGGCACCTGTAATCGCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCCGGGAGGTAGAGCTTGCAGTGAGCCGAGATCTCGCCACTGCACCCCAGTCTGGGCAACAGAGTGAGACTCCATCTCAAAAACAATAACCAAAAAAAGAGAATTAGACTTCCTGTGAGCTCTCAGATGGATTATAGTTTGTGAATAAT... |
Task1_train_47441 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCTCAATCTCTTGACTTCATGATCCACCTGCCTCGGTCTCCCAAAGTTCTGGGATTACAGGCATGAGTCACTGGGTCCGGCCCTCCACTATGAATTTTTAATGAACCCTGAGGATGCATCTTAGATTAGTAACCTTTCCAGATTCACTACATTTGCCTGGTTTTTATTGAGTGGATCTCTCACGACAAAATCATGAATATTACACTGAAAGGCTTATTACATTATCTTTGTGTAGTTACTCTCCAGTATAAACCCTGTGATGTTCCGGTTTTGATGCCTGGGTAAAAGCTTAAGCATGCACGTTACATTTGTATGGTTTC... | TCTCAATCTCTTGACTTCATGATCCACCTGCCTCGGTCTCCCAAAGTTCTGGGATTACAGGCATGAGTCACTGGGTCCGGCCCTCCACTATGAATTTTTAATGAACCCTGAGGATGCATCTTAGATTAGTAACCTTTCCAGATTCACTACATTTGCCTGGTTTTTATTGAGTGGATCTCTCACGACAAAATCATGAATATTACACTGAAAGGCTTATTACATTATCTTTGTGTAGTTACTCTCCAGTATAAACCCTGTGATGTTCCGGTTTTGATGCCTGGGTAAAAGCTTAAGCATGCACGTTACATTTGTATGGTTTC... |
Task1_train_47442 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGGCGCATACCTGTAATTCCAGCAACTTCTGAGGCTGAGGCGGGAGAATCGCTTGAACCCGGGAGGCGGAGGTGGTGGTGAGCCGAGATTGTGCCACTGCACTCCAGCCTGGGCAACAAGAGCAAAAACTCCATCTCGGAAAAAGAAAAAAAAGAATGAGATCATGTCCTTTGTAGGGACATGGATGGAGCTGGAAGCCATCGTTCTCAGCAAACTAACACAGGAACAGAAAACCAAACACCGCATGTTCTCACTCATAAGTGGGAGTTGAACGATTAGAACACATGGTCACAGGGAGGGAAGCAACATAGAGCAGGGCC... | TGGCGCATACCTGTAATTCCAGCAACTTCTGAGGCTGAGGCGGGAGAATCGCTTGAACCCGGGAGGCGGAGGTGGTGGTGAGCCGAGATTGTGCCACTGCACTCCAGCCTGGGCAACAAGAGCAAAAACTCCATCTCGGAAAAAGAAAAAAAAGAATGAGATCATGTCCTTTGTAGGGACATGGATGGAGCTGGAAGCCATCGTTCTCAGCAAACTAACACAGGAACAGAAAACCAAACACCGCATGTTCTCACTCATAAGTGGGAGTTGAACGATTAGAACACATGGTCACAGGGAGGGAAGCAACATAGAGCAGGGCC... |
Task1_train_47443 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TATACTCATTTCATTGGGAACGGTTATCTCAAAAATGAATTTTCTGATGTTCTGCATGGAGTGATCTTGGACTGAAGACCTTGCCACACTGATGACATTTGTAAGATTTCTGTCCAGTATAGATTCTCTGATGTCTAATGACGTGTGAACGTGAAGCAAAGGCTTTGCCACAATCATCACACTTGTGAGGTTTCTCTCCTGTATAAATTCTCCTATGTTTTGCATAGGATGAAGCTTGACTGAAGACCTTGGCACAGTCATGACATTTGTAAGGTTTCTCTCCAGTATGAGTTCACCGATGACCTGCAATATGTGAACGA... | TATACTCATTTCATTGGGAACGGTTATCTCAAAAATGAATTTTCTGATGTTCTGCATGGAGTGATCTTGGACTGAAGACCTTGCCACACTGATGACATTTGTAAGATTTCTGTCCAGTATAGATTCTCTGATGTCTAATGACGTGTGAACGTGAAGCAAAGGCTTTGCCACAATCATCACACTTGTGAGGTTTCTCTCCTGTATAAATTCTCCTATGTTTTGCATAGGATGAAGCTTGACTGAAGACCTTGGCACAGTCATGACATTTGTAAGGTTTCTCTCCAGTATGAGTTCACCGATGACCTGCAATATGTGAACGA... |
Task1_train_47444 | A genomic variant on Chromosome 19 is under review. What is the biological outcome — benign or pathogenic? | Benign | ATACTCATTTCATTGGGAACGGTTATCTCAAAAATGAATTTTCTGATGTTCTGCATGGAGTGATCTTGGACTGAAGACCTTGCCACACTGATGACATTTGTAAGATTTCTGTCCAGTATAGATTCTCTGATGTCTAATGACGTGTGAACGTGAAGCAAAGGCTTTGCCACAATCATCACACTTGTGAGGTTTCTCTCCTGTATAAATTCTCCTATGTTTTGCATAGGATGAAGCTTGACTGAAGACCTTGGCACAGTCATGACATTTGTAAGGTTTCTCTCCAGTATGAGTTCACCGATGACCTGCAATATGTGAACGAT... | ATACTCATTTCATTGGGAACGGTTATCTCAAAAATGAATTTTCTGATGTTCTGCATGGAGTGATCTTGGACTGAAGACCTTGCCACACTGATGACATTTGTAAGATTTCTGTCCAGTATAGATTCTCTGATGTCTAATGACGTGTGAACGTGAAGCAAAGGCTTTGCCACAATCATCACACTTGTGAGGTTTCTCTCCTGTATAAATTCTCCTATGTTTTGCATAGGATGAAGCTTGACTGAAGACCTTGGCACAGTCATGACATTTGTAAGGTTTCTCTCCAGTATGAGTTCACCGATGACCTGCAATATGTGAACGAT... |
Task1_train_47445 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | CAGATATCTGTAGTAATGCAGGCATGTGGAGAGGCAGCCACTATGGCACTCCTTATACAAGGAAAAATCTCAAAGGATCCACATGTTGTCATTCAGCCAATTTCCAAAGCAGATGTCAAAGAGCAAGCTAGCCATGTTTACTAACTTGACAACATGTAAATTTTCGCAACTAGCAGGATCAAATATCAAAGTAAAATATTTACTAAAACACAAAGAAGAAAACAACAGACGCTGGGGTCTACTTGAGGGTAGAGAGTGGGAGGAAGGAGAAGACTAGAAAAAATAGCTATTGGGGGCTGGGCACAGTGGCTTACACCTGT... | CAGATATCTGTAGTAATGCAGGCATGTGGAGAGGCAGCCACTATGGCACTCCTTATACAAGGAAAAATCTCAAAGGATCCACATGTTGTCATTCAGCCAATTTCCAAAGCAGATGTCAAAGAGCAAGCTAGCCATGTTTACTAACTTGACAACATGTAAATTTTCGCAACTAGCAGGATCAAATATCAAAGTAAAATATTTACTAAAACACAAAGAAGAAAACAACAGACGCTGGGGTCTACTTGAGGGTAGAGAGTGGGAGGAAGGAGAAGACTAGAAAAAATAGCTATTGGGGGCTGGGCACAGTGGCTTACACCTGT... |
Task1_train_47446 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | AATGTTAAGTCAACACAAACTCAAGTCAATGCTGGACTGACTCTAGTGTCAATTAATGCTTGATGGTTTGCTATACTCACTGCATTGGGAACAGTTATCTCAAAAATGAATTTTCTGATGTTCTGCAAGGAGTGACCTCGGACTCAAGACCTTGCCACACTTCTGACATTTGTAAGATTTCTGTCCAGTAGGGATTCTCTGATGTCTAATGAGGTGTGAACATGAAGTAAAGGCTTTGCCACAATCATCACACATGTGAGGTTTCTCTCCTGTATGAATTCTCCTATGTTTTGCATAGGATGAAGCTTGACTGAAGACCT... | AATGTTAAGTCAACACAAACTCAAGTCAATGCTGGACTGACTCTAGTGTCAATTAATGCTTGATGGTTTGCTATACTCACTGCATTGGGAACAGTTATCTCAAAAATGAATTTTCTGATGTTCTGCAAGGAGTGACCTCGGACTCAAGACCTTGCCACACTTCTGACATTTGTAAGATTTCTGTCCAGTAGGGATTCTCTGATGTCTAATGAGGTGTGAACATGAAGTAAAGGCTTTGCCACAATCATCACACATGTGAGGTTTCTCTCCTGTATGAATTCTCCTATGTTTTGCATAGGATGAAGCTTGACTGAAGACCT... |
Task1_train_47447 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTCATGCACACACATCACATCACGGCGTTACCCACGTGGTGGCCCACCTCTAATCCAAGCTACTGGAGAGGCTGAGGCAACAGAATCACTGTAATCTGGGAGTCAGAGGCTACAGTGAAACAAAATCACCCCACTGCACTCCTGCCTGGACAACAGAGACTCAACTCAAAACAAATTAAAAAATAAAGTAAAATCAATGATGTAAGAAAGCATCCTGTACCACTGATGCCTATCTCCACTTTCCACTCCATCCCAAGTCATTAAAAGTGCAGAGTTTGGCTAAGCGTGGTGGCTCAGGCCTGTAATCCCAGCACTATGGG... | TTCATGCACACACATCACATCACGGCGTTACCCACGTGGTGGCCCACCTCTAATCCAAGCTACTGGAGAGGCTGAGGCAACAGAATCACTGTAATCTGGGAGTCAGAGGCTACAGTGAAACAAAATCACCCCACTGCACTCCTGCCTGGACAACAGAGACTCAACTCAAAACAAATTAAAAAATAAAGTAAAATCAATGATGTAAGAAAGCATCCTGTACCACTGATGCCTATCTCCACTTTCCACTCCATCCCAAGTCATTAAAAGTGCAGAGTTTGGCTAAGCGTGGTGGCTCAGGCCTGTAATCCCAGCACTATGGG... |
Task1_train_47448 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | GCTTGATGGCTTGCTATACTAATGGCATTTGAAACAACTGTCTCCAAAAGGAATTGTCTGATGGTCTGCAAGGAGTGATCTCGGACTGAAGACCTTACCACACTGATGACATTTGTAAGATTTCTGTCCAGCATGGATTCTCTGATGTCTATTGAGGTGTGAATGTGAAGTAAACGCTTTGCCACAATCATCACACTTGTGAGTTTCTCTCCTGTATGAATCCTCCTATGTTTTGCATAGGATGAAACTTGACTGAAGACCTTGCCACAATCATGACATTTATAAGGTTTCTCTCCAGCATGAGTTCGATGATGAATAGC... | GCTTGATGGCTTGCTATACTAATGGCATTTGAAACAACTGTCTCCAAAAGGAATTGTCTGATGGTCTGCAAGGAGTGATCTCGGACTGAAGACCTTACCACACTGATGACATTTGTAAGATTTCTGTCCAGCATGGATTCTCTGATGTCTATTGAGGTGTGAATGTGAAGTAAACGCTTTGCCACAATCATCACACTTGTGAGTTTCTCTCCTGTATGAATCCTCCTATGTTTTGCATAGGATGAAACTTGACTGAAGACCTTGCCACAATCATGACATTTATAAGGTTTCTCTCCAGCATGAGTTCGATGATGAATAGC... |
Task1_train_47449 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ACATTTGTAAGGTTTCTCTCCAGTTTGAATTCTAATATGTTTTGCCAGGTATGAATTATATTCAAAAATCTTGTCATAAACCTTACATCTGTGTGGTTTCTCTTCAGCATGCATTTTCTTATGTGTTTCAAGGTTTGATTTGCAACCGAAAACTTTGTCACATTCTTCCTATTTGTAAAGTTTCTCTGCAGTATGAATTCTATGATGACGTGCAAGGGTTGTTTTTTGATTAAAAACCTTGCCACATTCATTACACTTGTAAAGTTTCTCTCCAGTATGAATGGCTTTGTGACTTACAAGGGTTGAATTGTGATGGAAGG... | ACATTTGTAAGGTTTCTCTCCAGTTTGAATTCTAATATGTTTTGCCAGGTATGAATTATATTCAAAAATCTTGTCATAAACCTTACATCTGTGTGGTTTCTCTTCAGCATGCATTTTCTTATGTGTTTCAAGGTTTGATTTGCAACCGAAAACTTTGTCACATTCTTCCTATTTGTAAAGTTTCTCTGCAGTATGAATTCTATGATGACGTGCAAGGGTTGTTTTTTGATTAAAAACCTTGCCACATTCATTACACTTGTAAAGTTTCTCTCCAGTATGAATGGCTTTGTGACTTACAAGGGTTGAATTGTGATGGAAGG... |
Task1_train_47450 | A sequence alteration has been identified on Chromosome 19. Is it disease-inducing or harmless? | Benign | AGGAATCTTGCCTTGGTGGAAAGGATACTTTGGCAGTGGGAGGAAGGAGAGGAGCAGAAAAAATAACTATTGGGCCCGGGCACAGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTGAGGCTGCTGGATCACCTGAAGACAGGAGTTCAACATCAGCCTGGCCAACATGGTGAAACTCTTGTCTCTATTAAAAATACAAAAATTAGCCAGGTATAGTGGCAAGCACCTGTAGTCCCAGCTACTCGAGAGTCTGAAGCAGGAGACACACTTGAACCCGGGAGGTAGAGGTTGCAGTGAGCCGAGATCATGCCATAA... | AGGAATCTTGCCTTGGTGGAAAGGATACTTTGGCAGTGGGAGGAAGGAGAGGAGCAGAAAAAATAACTATTGGGCCCGGGCACAGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTGAGGCTGCTGGATCACCTGAAGACAGGAGTTCAACATCAGCCTGGCCAACATGGTGAAACTCTTGTCTCTATTAAAAATACAAAAATTAGCCAGGTATAGTGGCAAGCACCTGTAGTCCCAGCTACTCGAGAGTCTGAAGCAGGAGACACACTTGAACCCGGGAGGTAGAGGTTGCAGTGAGCCGAGATCATGCCATAA... |
Task1_train_47451 | A mutation on Chromosome 19 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CTGTAATCTCAGCACTTTGGGAGGCTGAGGCTGCTGGATCACCTGAAGACAGGAGTTCAACATCAGCCTGGCCAACATGGTGAAACTCTTGTCTCTATTAAAAATACAAAAATTAGCCAGGTATAGTGGCAAGCACCTGTAGTCCCAGCTACTCGAGAGTCTGAAGCAGGAGACACACTTGAACCCGGGAGGTAGAGGTTGCAGTGAGCCGAGATCATGCCATAATACTCCAGTCTGGGCAACAAGATCATAACTCAGTCTCAAAAAAATAAATAAAAAAAATAACTGTCTGGGCGTGGTGGCTCACGCCTGTAATCCCA... | CTGTAATCTCAGCACTTTGGGAGGCTGAGGCTGCTGGATCACCTGAAGACAGGAGTTCAACATCAGCCTGGCCAACATGGTGAAACTCTTGTCTCTATTAAAAATACAAAAATTAGCCAGGTATAGTGGCAAGCACCTGTAGTCCCAGCTACTCGAGAGTCTGAAGCAGGAGACACACTTGAACCCGGGAGGTAGAGGTTGCAGTGAGCCGAGATCATGCCATAATACTCCAGTCTGGGCAACAAGATCATAACTCAGTCTCAAAAAAATAAATAAAAAAAATAACTGTCTGGGCGTGGTGGCTCACGCCTGTAATCCCA... |
Task1_train_47452 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | TGAGGCTGCTGGATCACCTGAAGACAGGAGTTCAACATCAGCCTGGCCAACATGGTGAAACTCTTGTCTCTATTAAAAATACAAAAATTAGCCAGGTATAGTGGCAAGCACCTGTAGTCCCAGCTACTCGAGAGTCTGAAGCAGGAGACACACTTGAACCCGGGAGGTAGAGGTTGCAGTGAGCCGAGATCATGCCATAATACTCCAGTCTGGGCAACAAGATCATAACTCAGTCTCAAAAAAATAAATAAAAAAAATAACTGTCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCG... | TGAGGCTGCTGGATCACCTGAAGACAGGAGTTCAACATCAGCCTGGCCAACATGGTGAAACTCTTGTCTCTATTAAAAATACAAAAATTAGCCAGGTATAGTGGCAAGCACCTGTAGTCCCAGCTACTCGAGAGTCTGAAGCAGGAGACACACTTGAACCCGGGAGGTAGAGGTTGCAGTGAGCCGAGATCATGCCATAATACTCCAGTCTGGGCAACAAGATCATAACTCAGTCTCAAAAAAATAAATAAAAAAAATAACTGTCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCG... |
Task1_train_47453 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TAAAGTAAGAAATATTTAGGAATAAACATAAAAAGTGAGGTTTGTACCTTGAAATCTATAAACATTGATCAAAATGATTAAAAACATGTATAAATAGATATAAATCCCATACTGATTGGAAAAATGAATATCGCTCAATGATTATATACTCAATTGTGATTTAGATTCGGTACAATACTCATAGAAGTCTCTATAACTTTTTGTTAAAGAAACAAAAAACAGGCCAGGCACAGTGGCTCACTCCTGTAATCTCAGCACTTTGGGAGGTGGAGTCGGGTGGATCATAAAGTCAGAAGATAGAGACCATTCTGGCTAACACG... | TAAAGTAAGAAATATTTAGGAATAAACATAAAAAGTGAGGTTTGTACCTTGAAATCTATAAACATTGATCAAAATGATTAAAAACATGTATAAATAGATATAAATCCCATACTGATTGGAAAAATGAATATCGCTCAATGATTATATACTCAATTGTGATTTAGATTCGGTACAATACTCATAGAAGTCTCTATAACTTTTTGTTAAAGAAACAAAAAACAGGCCAGGCACAGTGGCTCACTCCTGTAATCTCAGCACTTTGGGAGGTGGAGTCGGGTGGATCATAAAGTCAGAAGATAGAGACCATTCTGGCTAACACG... |
Task1_train_47454 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | AACTGTAGTGTCAGCTACTTGGGAGACTGAGGCAGGAGAATTGCTTGAACCTGGGAGGAGGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAACCTGGGCGACAGAGCAAGACTCCATCTCAAAAAAAAAACAAGAAAAAGAAAATAAAGGCTGGGAAAAGTAGCTCCCATCTGTTGGCTAGGCTGTTCTCAAACTCGTGAGCTCCAGTGACCTACCTGTCTTTGCCTCTCAAAGTGCTGGAATTACAGGCATGAGCCATGGCCCCCAGTGCAATCCTCTTAACATAAACAGTTTAATGGCAATTAATGCTTGA... | AACTGTAGTGTCAGCTACTTGGGAGACTGAGGCAGGAGAATTGCTTGAACCTGGGAGGAGGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAACCTGGGCGACAGAGCAAGACTCCATCTCAAAAAAAAAACAAGAAAAAGAAAATAAAGGCTGGGAAAAGTAGCTCCCATCTGTTGGCTAGGCTGTTCTCAAACTCGTGAGCTCCAGTGACCTACCTGTCTTTGCCTCTCAAAGTGCTGGAATTACAGGCATGAGCCATGGCCCCCAGTGCAATCCTCTTAACATAAACAGTTTAATGGCAATTAATGCTTGA... |
Task1_train_47455 | A mutation on Chromosome 19 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GTAAGATTTCTGTCCAGCATGGATTCTCTGATGTCTAATGAGGTGTGAATGTGAAGTAAACGCTTTGCCACAATCATCACACTTGTGAGGTTTCTCTCCTGTATGAATCCTCCTATGTTTTGCATAGGATGAAGCTTGACTGAAGACCTTGCCTCAATCATGACATTTATAAGGTTTCTCTCCAGCATGAGTTCACCAGTGAAATGCAAGGCATGAACGATGTCTGAAAAATTTGCCACATTTATTACACTTGTAAGATCTCTTCACTGTGGATTCTCCAATGATGTGCAATGGTTGTAGCATTACTGAAAACTTTGTGA... | GTAAGATTTCTGTCCAGCATGGATTCTCTGATGTCTAATGAGGTGTGAATGTGAAGTAAACGCTTTGCCACAATCATCACACTTGTGAGGTTTCTCTCCTGTATGAATCCTCCTATGTTTTGCATAGGATGAAGCTTGACTGAAGACCTTGCCTCAATCATGACATTTATAAGGTTTCTCTCCAGCATGAGTTCACCAGTGAAATGCAAGGCATGAACGATGTCTGAAAAATTTGCCACATTTATTACACTTGTAAGATCTCTTCACTGTGGATTCTCCAATGATGTGCAATGGTTGTAGCATTACTGAAAACTTTGTGA... |
Task1_train_47456 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GAAGACCTTGCCTCAATCATGACATTTATAAGGTTTCTCTCCAGCATGAGTTCACCAGTGAAATGCAAGGCATGAACGATGTCTGAAAAATTTGCCACATTTATTACACTTGTAAGATCTCTTCACTGTGGATTCTCCAATGATGTGCAATGGTTGTAGCATTACTGAAAACTTTGTGACAATCATTACATTAGTCAAGTTTCCCTATACCATGGATTGCTTGATGGTGAATAAGTGGTGACTGCCCACTAAAGGGTTTGCCACACTCATTGCACTTGTAAGGTTTCTCTCCAGTGTGAATTCTAGTATGGGGTGCCACG... | GAAGACCTTGCCTCAATCATGACATTTATAAGGTTTCTCTCCAGCATGAGTTCACCAGTGAAATGCAAGGCATGAACGATGTCTGAAAAATTTGCCACATTTATTACACTTGTAAGATCTCTTCACTGTGGATTCTCCAATGATGTGCAATGGTTGTAGCATTACTGAAAACTTTGTGACAATCATTACATTAGTCAAGTTTCCCTATACCATGGATTGCTTGATGGTGAATAAGTGGTGACTGCCCACTAAAGGGTTTGCCACACTCATTGCACTTGTAAGGTTTCTCTCCAGTGTGAATTCTAGTATGGGGTGCCACG... |
Task1_train_47457 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TCTCTCCAGCATGAGTTCACCAGTGAAATGCAAGGCATGAACGATGTCTGAAAAATTTGCCACATTTATTACACTTGTAAGATCTCTTCACTGTGGATTCTCCAATGATGTGCAATGGTTGTAGCATTACTGAAAACTTTGTGACAATCATTACATTAGTCAAGTTTCCCTATACCATGGATTGCTTGATGGTGAATAAGTGGTGACTGCCCACTAAAGGGTTTGCCACACTCATTGCACTTGTAAGGTTTCTCTCCAGTGTGAATTCTAGTATGGGGTGCCACGTGTGAATCATTCCCGAAAGCCTTGTCACAAACCTT... | TCTCTCCAGCATGAGTTCACCAGTGAAATGCAAGGCATGAACGATGTCTGAAAAATTTGCCACATTTATTACACTTGTAAGATCTCTTCACTGTGGATTCTCCAATGATGTGCAATGGTTGTAGCATTACTGAAAACTTTGTGACAATCATTACATTAGTCAAGTTTCCCTATACCATGGATTGCTTGATGGTGAATAAGTGGTGACTGCCCACTAAAGGGTTTGCCACACTCATTGCACTTGTAAGGTTTCTCTCCAGTGTGAATTCTAGTATGGGGTGCCACGTGTGAATCATTCCCGAAAGCCTTGTCACAAACCTT... |
Task1_train_47458 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATCTCTTCACTGTGGATTCTCCAATGATGTGCAATGGTTGTAGCATTACTGAAAACTTTGTGACAATCATTACATTAGTCAAGTTTCCCTATACCATGGATTGCTTGATGGTGAATAAGTGGTGACTGCCCACTAAAGGGTTTGCCACACTCATTGCACTTGTAAGGTTTCTCTCCAGTGTGAATTCTAGTATGGGGTGCCACGTGTGAATCATTCCCGAAAGCCTTGTCACAAACCTTACATTTCTATGGCTTTTCTCCAGTGTGAATTCTCCTATGTATTTGAAGCTGGATTTGTGAATGAAAACTTTGTCACATTGT... | ATCTCTTCACTGTGGATTCTCCAATGATGTGCAATGGTTGTAGCATTACTGAAAACTTTGTGACAATCATTACATTAGTCAAGTTTCCCTATACCATGGATTGCTTGATGGTGAATAAGTGGTGACTGCCCACTAAAGGGTTTGCCACACTCATTGCACTTGTAAGGTTTCTCTCCAGTGTGAATTCTAGTATGGGGTGCCACGTGTGAATCATTCCCGAAAGCCTTGTCACAAACCTTACATTTCTATGGCTTTTCTCCAGTGTGAATTCTCCTATGTATTTGAAGCTGGATTTGTGAATGAAAACTTTGTCACATTGT... |
Task1_train_47459 | Located on Chromosome 19, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CAGTTATGTTGTGACTTTTTAAAAAATTTTTTGTATTTTTGTTTTTTTGAGATAGAGTCTCACTCTGTCACCCAGGCTGGAATGCGATGGCACGATCTTGGCTCACTGCAACCTCCACCTCCTGGGTTCATGCTAGTCTCTTGCCTTAGGTCCTGAGCACCTGGGATTACAGGCATGTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAAATCAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACATGTCTTGGCCTCCAAAAGTCCTGGGATTACAGGTGTGAGCCACTG... | CAGTTATGTTGTGACTTTTTAAAAAATTTTTTGTATTTTTGTTTTTTTGAGATAGAGTCTCACTCTGTCACCCAGGCTGGAATGCGATGGCACGATCTTGGCTCACTGCAACCTCCACCTCCTGGGTTCATGCTAGTCTCTTGCCTTAGGTCCTGAGCACCTGGGATTACAGGCATGTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAAATCAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACATGTCTTGGCCTCCAAAAGTCCTGGGATTACAGGTGTGAGCCACTG... |
Task1_train_47460 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCCTCCTCAGCCCAGGGTCTCACTCTGTTGCCAAGTCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCCACCTCCAGGGTTCTAGTGATTCTCCTGCTTCAACCTCCCAAGTAGCTGGGATTACAGGTGCACACCACCATGCACAGCTAATTTTTGCATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCTAGGCTTGTCTCTAACTCCTGACCTCAAGTGATCAACCTGTTGCAGCCTCCCAAAGTGCTGGGATTAGAGGGGTGAGCCACCGCGGCCAGCCAGTCTAAGCTATTTCTAGCAGGACAGTGAA... | CCCTCCTCAGCCCAGGGTCTCACTCTGTTGCCAAGTCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCCACCTCCAGGGTTCTAGTGATTCTCCTGCTTCAACCTCCCAAGTAGCTGGGATTACAGGTGCACACCACCATGCACAGCTAATTTTTGCATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCTAGGCTTGTCTCTAACTCCTGACCTCAAGTGATCAACCTGTTGCAGCCTCCCAAAGTGCTGGGATTAGAGGGGTGAGCCACCGCGGCCAGCCAGTCTAAGCTATTTCTAGCAGGACAGTGAA... |
Task1_train_47461 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | TATATGTGTTTGTATATATGCATGTATATGTATAGATGTGTGTGTATGTATGTATGTATATATTTATTTATATATAAAGGTTTTAAAAATACAAAAGTAGCAAGATTTGTTTAACTGAAGAGGAATCTCGCCTTGGGGGAAAGGATACTTTGGCAGTGGGAGGAAAGAGAGGAGCAGAAAAAATAACTATCGGGCCCGGGCACAGTGGCTCACACTTGTAATCTCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACCTGAGGACAGGAATTCAACACCAGCCTGGCCAACATGGTGAAACTCTGTCTTTACTAAAAATA... | TATATGTGTTTGTATATATGCATGTATATGTATAGATGTGTGTGTATGTATGTATGTATATATTTATTTATATATAAAGGTTTTAAAAATACAAAAGTAGCAAGATTTGTTTAACTGAAGAGGAATCTCGCCTTGGGGGAAAGGATACTTTGGCAGTGGGAGGAAAGAGAGGAGCAGAAAAAATAACTATCGGGCCCGGGCACAGTGGCTCACACTTGTAATCTCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACCTGAGGACAGGAATTCAACACCAGCCTGGCCAACATGGTGAAACTCTGTCTTTACTAAAAATA... |
Task1_train_47462 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | GGATATTGAGTCATCTGGACATTGTTTTTCTGTAGGAGTTTGTTCTTGCAGGTACTATTAAGCTGCTTTCCTTAACTGTAAACATCTTAAGATCATGACTCATGCGTGAGCAGTAAGGACTACGTCTTGCTAGTTTTAGTAGACTAAAACTTTGTCATTCTAGCTCTCCTAGGATCCTGTTTAACAGTTTTTCCACTCATGCACCACAGCGTTCTAAGCACAATTATGGAGACACCACTCTTTTGTAATGCACTGACACCATGTCACTGCACTTTAGTCTGGGCGACAGAGTGAGATTCCGTCAAAAACAAACAAACAAA... | GGATATTGAGTCATCTGGACATTGTTTTTCTGTAGGAGTTTGTTCTTGCAGGTACTATTAAGCTGCTTTCCTTAACTGTAAACATCTTAAGATCATGACTCATGCGTGAGCAGTAAGGACTACGTCTTGCTAGTTTTAGTAGACTAAAACTTTGTCATTCTAGCTCTCCTAGGATCCTGTTTAACAGTTTTTCCACTCATGCACCACAGCGTTCTAAGCACAATTATGGAGACACCACTCTTTTGTAATGCACTGACACCATGTCACTGCACTTTAGTCTGGGCGACAGAGTGAGATTCCGTCAAAAACAAACAAACAAA... |
Task1_train_47463 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | GATGAACTGCAAGTTATGAACGATGTCTGAAAACTTTGCCACATTTATTAACACTTGTAAGATCTCTCTTCATTACGGATTCTCCAATGATTTGCAACAGTTCTAGCATTACCAAAGGCATTGTGACAATCATTGCATTAGTAAACTTTCCCTACACCATGGATTGCCTGATGGATGGTGAGTAAGTGGTGATTGCCCACTAAAGGCTTTGCCACACTCATTACACTTGTAAGGTTTCTCTCCAGGGTGAATTCTAGTATGTCCTGCAAGGTGTGAATCACACCCAAAATCCTTATCACAAACCTTACATTTGTATGGTT... | GATGAACTGCAAGTTATGAACGATGTCTGAAAACTTTGCCACATTTATTAACACTTGTAAGATCTCTCTTCATTACGGATTCTCCAATGATTTGCAACAGTTCTAGCATTACCAAAGGCATTGTGACAATCATTGCATTAGTAAACTTTCCCTACACCATGGATTGCCTGATGGATGGTGAGTAAGTGGTGATTGCCCACTAAAGGCTTTGCCACACTCATTACACTTGTAAGGTTTCTCTCCAGGGTGAATTCTAGTATGTCCTGCAAGGTGTGAATCACACCCAAAATCCTTATCACAAACCTTACATTTGTATGGTT... |
Task1_train_47464 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTGTAAGATCTCTCTTCATTACGGATTCTCCAATGATTTGCAACAGTTCTAGCATTACCAAAGGCATTGTGACAATCATTGCATTAGTAAACTTTCCCTACACCATGGATTGCCTGATGGATGGTGAGTAAGTGGTGATTGCCCACTAAAGGCTTTGCCACACTCATTACACTTGTAAGGTTTCTCTCCAGGGTGAATTCTAGTATGTCCTGCAAGGTGTGAATCACACCCAAAATCCTTATCACAAACCTTACATTTGTATGGTTTCTCTCCAGTATGAATTCACCTATGTCTTTCAAGCTGTGATTTACGACTGAAAA... | TTGTAAGATCTCTCTTCATTACGGATTCTCCAATGATTTGCAACAGTTCTAGCATTACCAAAGGCATTGTGACAATCATTGCATTAGTAAACTTTCCCTACACCATGGATTGCCTGATGGATGGTGAGTAAGTGGTGATTGCCCACTAAAGGCTTTGCCACACTCATTACACTTGTAAGGTTTCTCTCCAGGGTGAATTCTAGTATGTCCTGCAAGGTGTGAATCACACCCAAAATCCTTATCACAAACCTTACATTTGTATGGTTTCTCTCCAGTATGAATTCACCTATGTCTTTCAAGCTGTGATTTACGACTGAAAA... |
Task1_train_47465 | With a mutation on Chromosome 19, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ACATAGAGATACAACCCATATTGATAGTTTGGAAAAATTAATATTGTTAAGTAATTATATAACCCAATGTGATTTAGATTCAACACGGTACCCATAAAAATGCCTATCAGTTGACATTCCACCACAAAAGAAGTGAAATTGGCTGGTCCCTGCCTTAACTGATGACATTACCTTGTGAAATTCCTTCTCCTGGCTCATCCTGGCTCAAAAACTCCCCCACTGAGCACCTTGTGACCCCCACCTCTGCCAGCCAGAGAACAACCCCCTTTGATTGTAACTTTCCACTACCTACCCAAATCCTATAAAACGGCCCCACCCCA... | ACATAGAGATACAACCCATATTGATAGTTTGGAAAAATTAATATTGTTAAGTAATTATATAACCCAATGTGATTTAGATTCAACACGGTACCCATAAAAATGCCTATCAGTTGACATTCCACCACAAAAGAAGTGAAATTGGCTGGTCCCTGCCTTAACTGATGACATTACCTTGTGAAATTCCTTCTCCTGGCTCATCCTGGCTCAAAAACTCCCCCACTGAGCACCTTGTGACCCCCACCTCTGCCAGCCAGAGAACAACCCCCTTTGATTGTAACTTTCCACTACCTACCCAAATCCTATAAAACGGCCCCACCCCA... |
Task1_train_47466 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | GTCTAATGAGGTGTGAACGTGAAGTAAAGGCTTTGCTCACAATCATCACACTTGTGAGGTTTCTCTCCTGTATGAATTCTCCTGTTTTGCATAGGATGAAGCTTGACTGAAGACCTTGCCTCAATCATGACATTTGTAAGGTTTCTCTCCAGTATGAGTTCACCCATGAACTACAGCGTATGAACGATGTCTGAAAAATTTGCCACATTTACTACACTTGTAAGATCTCTATTCATTATGGATTCTTCAATGATTTGCAATGGTTGTAGCGTTACTGAAGACTTGGTGACAATCATTACATTAGTCAAGTTTCCCTACAC... | GTCTAATGAGGTGTGAACGTGAAGTAAAGGCTTTGCTCACAATCATCACACTTGTGAGGTTTCTCTCCTGTATGAATTCTCCTGTTTTGCATAGGATGAAGCTTGACTGAAGACCTTGCCTCAATCATGACATTTGTAAGGTTTCTCTCCAGTATGAGTTCACCCATGAACTACAGCGTATGAACGATGTCTGAAAAATTTGCCACATTTACTACACTTGTAAGATCTCTATTCATTATGGATTCTTCAATGATTTGCAATGGTTGTAGCGTTACTGAAGACTTGGTGACAATCATTACATTAGTCAAGTTTCCCTACAC... |
Task1_train_47467 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AAAATTAGAGAAGCATCTTTCACATACCTGGGCTAAAGAAACTTCTTTTGCAAGGTTCTGATGCCATTAATTCCTAACATTTAATTTTTCCTTACAAGAAAATTACAGTAACATTTACAAAATGCAAAAGTGTAAACACACAGCTATTGACCTTGAAAATAGGGAGGCCGAGGTAGGTGGATCACCTGAGTTCAGCAATTGTAGACCAGCCTGACCTACATGGAGGAACCCCGTTTCTACTGAAAATACAAAAATTATCCAGGCATGGTGGCGAATGGCTGTAATCCCAGCTACTCAGCAAGGCTGAGGCAGGAGAATCA... | AAAATTAGAGAAGCATCTTTCACATACCTGGGCTAAAGAAACTTCTTTTGCAAGGTTCTGATGCCATTAATTCCTAACATTTAATTTTTCCTTACAAGAAAATTACAGTAACATTTACAAAATGCAAAAGTGTAAACACACAGCTATTGACCTTGAAAATAGGGAGGCCGAGGTAGGTGGATCACCTGAGTTCAGCAATTGTAGACCAGCCTGACCTACATGGAGGAACCCCGTTTCTACTGAAAATACAAAAATTATCCAGGCATGGTGGCGAATGGCTGTAATCCCAGCTACTCAGCAAGGCTGAGGCAGGAGAATCA... |
Task1_train_47468 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | TACATTTGTAAGGCATCTGTCCAGTATGAATTCTCTGATGTCTAATGAGGTGTGAACATGAAGTAAAGGCTTTGCCACAATCATCACACTTGTGAGGTTTCTCTCCTGTATGAATTCTATGTTTTGCATAGGATGAAGCTTGACTGAAGACCTTGTCACAGTCATGATATTTGTAAGGTTTCTCTCCAGTATGAGTTCACTGATGAACTACAAGTTATGAATGACGTCTGAAAAATTTGCCACATTTATTACACTTGTAGATCTCTCTTCAATATGGATTCTGTAATGATTTGCAATGGTTGTAGCATTACTGAAGACTT... | TACATTTGTAAGGCATCTGTCCAGTATGAATTCTCTGATGTCTAATGAGGTGTGAACATGAAGTAAAGGCTTTGCCACAATCATCACACTTGTGAGGTTTCTCTCCTGTATGAATTCTATGTTTTGCATAGGATGAAGCTTGACTGAAGACCTTGTCACAGTCATGATATTTGTAAGGTTTCTCTCCAGTATGAGTTCACTGATGAACTACAAGTTATGAATGACGTCTGAAAAATTTGCCACATTTATTACACTTGTAGATCTCTCTTCAATATGGATTCTGTAATGATTTGCAATGGTTGTAGCATTACTGAAGACTT... |
Task1_train_47469 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AACCAGGGTCAAAAAACCTGGAGAGATGGGTCATCTGGGTCTCAACTCCCTTATGGAAAGACCCCTTTACTGTCTTACTTTCCACCCCAACAGCTATCAACATTTCTGGCATCTCCAGTTGGATACATCAGTCTCAAGTGAAACTGTGGGAAGGTCCCGAAGAACCACAGAAGAACAACAGAATTCAGCACCTGAGCATTCTTGTGAGCCACTGGAGAACTTAAAATTCCACTTCAAGTGAAAAGATAAGTAAAGCCTTCTCTCTGTTCACCCAAAACTAAAGTCAATCTCAGTACGGGGAATCTTGGTTGCGGTGGCAT... | AACCAGGGTCAAAAAACCTGGAGAGATGGGTCATCTGGGTCTCAACTCCCTTATGGAAAGACCCCTTTACTGTCTTACTTTCCACCCCAACAGCTATCAACATTTCTGGCATCTCCAGTTGGATACATCAGTCTCAAGTGAAACTGTGGGAAGGTCCCGAAGAACCACAGAAGAACAACAGAATTCAGCACCTGAGCATTCTTGTGAGCCACTGGAGAACTTAAAATTCCACTTCAAGTGAAAAGATAAGTAAAGCCTTCTCTCTGTTCACCCAAAACTAAAGTCAATCTCAGTACGGGGAATCTTGGTTGCGGTGGCAT... |
Task1_train_47470 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | CCAACACTCTATTTAATTCCAAGAAAAAAAAAAATGGTTCTATCTTTCAGCCTTAAGAGTCTAATGGTGTGTTGTTATTGTCTGTTACAAAGTAACCTACTGAGGTGGGATAAAACTATGTTGGCAGAGAGAACATGATGCATTCATAGTTATGCAAAAATCAGATTAATTAGCACGAGATCTATGATACATTCTGAATAAAACAGTAGCAAAATGTAATACCAGCAGTAAATGTGAATCCTAATCAATAACATGCTATTGTGGTTCATCTCTGAGGTTGTGGTTTCTATTGTGGTTTCAATCTTGGCTATATAACAGCG... | CCAACACTCTATTTAATTCCAAGAAAAAAAAAAATGGTTCTATCTTTCAGCCTTAAGAGTCTAATGGTGTGTTGTTATTGTCTGTTACAAAGTAACCTACTGAGGTGGGATAAAACTATGTTGGCAGAGAGAACATGATGCATTCATAGTTATGCAAAAATCAGATTAATTAGCACGAGATCTATGATACATTCTGAATAAAACAGTAGCAAAATGTAATACCAGCAGTAAATGTGAATCCTAATCAATAACATGCTATTGTGGTTCATCTCTGAGGTTGTGGTTTCTATTGTGGTTTCAATCTTGGCTATATAACAGCG... |
Task1_train_47471 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | ACCTCATGATCCACCCACCTCAGCCACCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGCCCGGTCGTGGTCTGCTCTGTTTCATGGTCAGGTTGCAGGTCATCTCTTTCCTGTAACCCAAAGTGCCGTCTATCAGGAGAACACCCTAAACACAATAAGGATGATGATCAACACCATCATTTTGCATTATTCTCTGCCTGCCCCCATGCTTGGTAATTTGCCAAGGCAGAGTCCTTATTCTTCAAAGAATCTGAATAGAAATGATCCTCATCTAATGCAGTGAGCCCTTCCATCTTACTGATTCTTTCCCAGACATT... | ACCTCATGATCCACCCACCTCAGCCACCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGCCCGGTCGTGGTCTGCTCTGTTTCATGGTCAGGTTGCAGGTCATCTCTTTCCTGTAACCCAAAGTGCCGTCTATCAGGAGAACACCCTAAACACAATAAGGATGATGATCAACACCATCATTTTGCATTATTCTCTGCCTGCCCCCATGCTTGGTAATTTGCCAAGGCAGAGTCCTTATTCTTCAAAGAATCTGAATAGAAATGATCCTCATCTAATGCAGTGAGCCCTTCCATCTTACTGATTCTTTCCCAGACATT... |
Task1_train_47472 | Chromosome 19 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGGATTACAGGTGTGAGCCACTGCGCCCGGTCGTGGTCTGCTCTGTTTCATGGTCAGGTTGCAGGTCATCTCTTTCCTGTAACCCAAAGTGCCGTCTATCAGGAGAACACCCTAAACACAATAAGGATGATGATCAACACCATCATTTTGCATTATTCTCTGCCTGCCCCCATGCTTGGTAATTTGCCAAGGCAGAGTCCTTATTCTTCAAAGAATCTGAATAGAAATGATCCTCATCTAATGCAGTGAGCCCTTCCATCTTACTGATTCTTTCCCAGACATTGCCATGAAAGGCAGGTAAGGAGGCCTATCAACACATT... | GGGATTACAGGTGTGAGCCACTGCGCCCGGTCGTGGTCTGCTCTGTTTCATGGTCAGGTTGCAGGTCATCTCTTTCCTGTAACCCAAAGTGCCGTCTATCAGGAGAACACCCTAAACACAATAAGGATGATGATCAACACCATCATTTTGCATTATTCTCTGCCTGCCCCCATGCTTGGTAATTTGCCAAGGCAGAGTCCTTATTCTTCAAAGAATCTGAATAGAAATGATCCTCATCTAATGCAGTGAGCCCTTCCATCTTACTGATTCTTTCCCAGACATTGCCATGAAAGGCAGGTAAGGAGGCCTATCAACACATT... |
Task1_train_47473 | A variant on Chromosome 19 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCGGCCGGGCGTGGTGGCTCCCACCTGTAATCCCAGCACTTTAGGAGGCTGAGGCAGGCAGATCACGAAGTCAGGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCCGTCTTTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCGCGTGCCTGTAGCCCCAGCTACTCGGGAGGCTGAGGCACGCGAATCGCTTGAACCTAGGAGGTGGAGGTTGCAGTGGGCCAGGATCGCACCACTGCACTCCAGCCTGCCAACAGAGCGAGACACCGTCTCAAAAAAAAAAAAAAGAAAAAGAAAAAGAAAAAGATACTA... | TCGGCCGGGCGTGGTGGCTCCCACCTGTAATCCCAGCACTTTAGGAGGCTGAGGCAGGCAGATCACGAAGTCAGGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCCGTCTTTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCGCGTGCCTGTAGCCCCAGCTACTCGGGAGGCTGAGGCACGCGAATCGCTTGAACCTAGGAGGTGGAGGTTGCAGTGGGCCAGGATCGCACCACTGCACTCCAGCCTGCCAACAGAGCGAGACACCGTCTCAAAAAAAAAAAAAAGAAAAAGAAAAAGAAAAAGATACTA... |
Task1_train_47474 | This mutation on Chromosome 19 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TGGCTCACTGCAACCTCCGCCTCCCGGGTTTACACAATGCTTTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGATGCGTGTCACCATACCTGGCTAAGTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATCTTTGCCAGGCTGGTCTTGAACTACTGACCTTGTGATTCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCCCAGCCTCAACACTTTTAATGTTCCTTTTGAGCAACGTTGTCCAATCCGCAGCCCAGGAAGGCTTTGAATGCAGCCCAACACAAATTCCTAAACTTC... | TGGCTCACTGCAACCTCCGCCTCCCGGGTTTACACAATGCTTTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGATGCGTGTCACCATACCTGGCTAAGTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATCTTTGCCAGGCTGGTCTTGAACTACTGACCTTGTGATTCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCCCAGCCTCAACACTTTTAATGTTCCTTTTGAGCAACGTTGTCCAATCCGCAGCCCAGGAAGGCTTTGAATGCAGCCCAACACAAATTCCTAAACTTC... |
Task1_train_47475 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | TCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTATATAGCTGGGATTACAGGCGCACGCCACCAGGCCTAGCTAATTGTGTACTTTTAGTAGAAATGGGGTTTCGCCATGTTGGTCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCACCTGCCTCGGACTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCACCCAGCCAGTCATTGCATTTTCAAGGAATCTCTCAGGCATAAATTCTCTGACGTTGTCAAAGGAATGAATTCTAACTGCAAAAGTTACCACCTTCATTTGTAAGGTTTCTCTCCACT... | TCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTATATAGCTGGGATTACAGGCGCACGCCACCAGGCCTAGCTAATTGTGTACTTTTAGTAGAAATGGGGTTTCGCCATGTTGGTCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCACCTGCCTCGGACTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCACCCAGCCAGTCATTGCATTTTCAAGGAATCTCTCAGGCATAAATTCTCTGACGTTGTCAAAGGAATGAATTCTAACTGCAAAAGTTACCACCTTCATTTGTAAGGTTTCTCTCCACT... |
Task1_train_47476 | Assess the clinical impact of this variant found on Chromosome 19. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GCAGTTAATGTAAATCCTAGTAACAAACATGGGATTCTGGTTACTTTGATTAAACTTCTTATGCTCGGCCGGCCGGGCACGGTGGCTCCAGCCCGTAATCCCAGCACTTTGGCAGGCCAAGGTGGGCGGATTATGAGGTCAGGAGTTCGAGACCAGCCTGGCAAACATAGTGAAACTCCATCTCTACTAAAAATACAAACATTAGCCAGGCGTGGTGGTGCATGTCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTAAAACCCAGGAGGCGGAGGTTGCGGTGAGCTGAGATTGCATCACTGCACTCC... | GCAGTTAATGTAAATCCTAGTAACAAACATGGGATTCTGGTTACTTTGATTAAACTTCTTATGCTCGGCCGGCCGGGCACGGTGGCTCCAGCCCGTAATCCCAGCACTTTGGCAGGCCAAGGTGGGCGGATTATGAGGTCAGGAGTTCGAGACCAGCCTGGCAAACATAGTGAAACTCCATCTCTACTAAAAATACAAACATTAGCCAGGCGTGGTGGTGCATGTCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTAAAACCCAGGAGGCGGAGGTTGCGGTGAGCTGAGATTGCATCACTGCACTCC... |
Task1_train_47477 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | ATAAGGATGATGAGTGACATCATAGTTCATCATCCTCTGCCCTTTCCAAGTGCTCTCTAATTCAGACTATATTTAATTTTAAAAGGCAGAGTCTTTTTTCTTCAGGAGCTTGGAGAGAAATAATCCTCACCTAATGAAGTGAGTGAGCCCTTCCATCCTTTGATTCTTTCCCGAACAACACCATGTTAGGCGTATAATCATGTATAAAATCAGCACATTGCAAAGTTCTGGTTGGAAGTTATAAATAGTAGCCTTTTCAATAAATCTTAAATACTTCAACAAAACATTTTATAAGCTGAAAGTAATTGGCCATTTCCAAA... | ATAAGGATGATGAGTGACATCATAGTTCATCATCCTCTGCCCTTTCCAAGTGCTCTCTAATTCAGACTATATTTAATTTTAAAAGGCAGAGTCTTTTTTCTTCAGGAGCTTGGAGAGAAATAATCCTCACCTAATGAAGTGAGTGAGCCCTTCCATCCTTTGATTCTTTCCCGAACAACACCATGTTAGGCGTATAATCATGTATAAAATCAGCACATTGCAAAGTTCTGGTTGGAAGTTATAAATAGTAGCCTTTTCAATAAATCTTAAATACTTCAACAAAACATTTTATAAGCTGAAAGTAATTGGCCATTTCCAAA... |
Task1_train_47478 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TGCAATGGCATGATCTCGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGCACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGCGTTTCACCGTGTTGGCCAGCCTGGTCTCGAACTCGAGACCTCAGGTGATCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCGGCGTCCTTTGTAAGGTTTCTATCCACTATGAATTCTTCGATGTTTTGCAAGGTTTGAATTTTGAGTAAAGACCTTG... | TGCAATGGCATGATCTCGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGCACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGCGTTTCACCGTGTTGGCCAGCCTGGTCTCGAACTCGAGACCTCAGGTGATCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCGGCGTCCTTTGTAAGGTTTCTATCCACTATGAATTCTTCGATGTTTTGCAAGGTTTGAATTTTGAGTAAAGACCTTG... |
Task1_train_47479 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AAAACAAAACAAAAAAACCCAGCACAAGTTTATCTCTACCAGTGTTAGATAGATATTATGTCGGACACATCAAGCAATATTCAGCATCTAGATGACCTAGAGAATGAGTGGTGTCTTCAACGATGATAATATCCACAGTGGCTTTGAAGAAAAAACAAGTCAGAGCCTTAAAACTATGATGAGAGCAATAGCAATGACAGGGATTTAAGAACAATGCCCATATGCAAGGTAGTATTTTAAATCCTTTACGTGTACTAACACATACAACACTGTAGCCCATGAGAGAAAGATCTGCTCCCATTTTACTGTGGGGACAACTG... | AAAACAAAACAAAAAAACCCAGCACAAGTTTATCTCTACCAGTGTTAGATAGATATTATGTCGGACACATCAAGCAATATTCAGCATCTAGATGACCTAGAGAATGAGTGGTGTCTTCAACGATGATAATATCCACAGTGGCTTTGAAGAAAAAACAAGTCAGAGCCTTAAAACTATGATGAGAGCAATAGCAATGACAGGGATTTAAGAACAATGCCCATATGCAAGGTAGTATTTTAAATCCTTTACGTGTACTAACACATACAACACTGTAGCCCATGAGAGAAAGATCTGCTCCCATTTTACTGTGGGGACAACTG... |
Task1_train_47480 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCTAGAGAATGAGTGGTGTCTTCAACGATGATAATATCCACAGTGGCTTTGAAGAAAAAACAAGTCAGAGCCTTAAAACTATGATGAGAGCAATAGCAATGACAGGGATTTAAGAACAATGCCCATATGCAAGGTAGTATTTTAAATCCTTTACGTGTACTAACACATACAACACTGTAGCCCATGAGAGAAAGATCTGCTCCCATTTTACTGTGGGGACAACTGTTTCACAGACACACTGAGAAACCTGTCTCAGGTCAAAGGACTAAAAATGACAGAGCAAGTACCTGTACCCAGGTGTCTAGGAATTAAAATTAAAC... | CCTAGAGAATGAGTGGTGTCTTCAACGATGATAATATCCACAGTGGCTTTGAAGAAAAAACAAGTCAGAGCCTTAAAACTATGATGAGAGCAATAGCAATGACAGGGATTTAAGAACAATGCCCATATGCAAGGTAGTATTTTAAATCCTTTACGTGTACTAACACATACAACACTGTAGCCCATGAGAGAAAGATCTGCTCCCATTTTACTGTGGGGACAACTGTTTCACAGACACACTGAGAAACCTGTCTCAGGTCAAAGGACTAAAAATGACAGAGCAAGTACCTGTACCCAGGTGTCTAGGAATTAAAATTAAAC... |
Task1_train_47481 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | GGAGTCTCACCCGTACAGACGGGGTTTCACCGTATTAGCTACGATGTCTCGATCTTTTGACCTTGTGACCCACCCATCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACAGCGCCCAGCCTCTTTCTCTTTTCAATGTATTAAATGCACAAGATTCCATACTTTCAAATTCCATTTTGCAGAATTATTATATTTTCATAGGTTTCCCAAATCAAATATTAATTCAAGTTTCAGTTAGTTGTTTTAAAATAATAAATATATAGTTACATAATCTTTAAAATGATTCGTTTTCTAGCCTAAAATGCTTTATCAC... | GGAGTCTCACCCGTACAGACGGGGTTTCACCGTATTAGCTACGATGTCTCGATCTTTTGACCTTGTGACCCACCCATCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACAGCGCCCAGCCTCTTTCTCTTTTCAATGTATTAAATGCACAAGATTCCATACTTTCAAATTCCATTTTGCAGAATTATTATATTTTCATAGGTTTCCCAAATCAAATATTAATTCAAGTTTCAGTTAGTTGTTTTAAAATAATAAATATATAGTTACATAATCTTTAAAATGATTCGTTTTCTAGCCTAAAATGCTTTATCAC... |
Task1_train_47482 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GTTTGACTATAATTAATTGAATATTTTAGACAGATACATAAAACATTACGAAAAATATACAATAACGAAAAATACATTCTATGTAATTTTAACCAATTAAACAACTAGCATGGCTATGTAAATAACACATGAAATAGACTTCATAGTTGGTTTAACTTGTCACTATTATAATTAATATTTTTCTACATTTCTTAATGTAAACATTTCTAATATTCCTTGGTAGATAGCAAACATAATGCCACTTACTATAAACATACACACAGGTATGTTCCATCTTGCTTTGTGATCTAATGTGCAGTACATAATCCTAAGTGCCTCAT... | GTTTGACTATAATTAATTGAATATTTTAGACAGATACATAAAACATTACGAAAAATATACAATAACGAAAAATACATTCTATGTAATTTTAACCAATTAAACAACTAGCATGGCTATGTAAATAACACATGAAATAGACTTCATAGTTGGTTTAACTTGTCACTATTATAATTAATATTTTTCTACATTTCTTAATGTAAACATTTCTAATATTCCTTGGTAGATAGCAAACATAATGCCACTTACTATAAACATACACACAGGTATGTTCCATCTTGCTTTGTGATCTAATGTGCAGTACATAATCCTAAGTGCCTCAT... |
Task1_train_47483 | A mutation is present on Chromosome 19. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TCTACCTGTCATAATCTCCACACGAACACAGTGGATTCATACTTTCTCCCTCAATATAGCCATTTCTCTGCTATTTCAAGTAAATTTGAAGGAAATGAATGTCTGTGCTCACTTGCTCACCTTAGAGGTAGGAAAACGCAACCCCCAAATCTCTTTCTTTCCAACATGGCCAACTGGCATCTTCACATGATAAAGAAAAAGAGTCTACCATCTACTCGTCTAGATCCTCAAATCTATGCAGTCTCACAGAGTGTGTGTGGTTTTCTGTTGTTGTTATTGTTGTTGTTTGTTTGTTTGCTTTGAGGCCGGGTCTCACTCCC... | TCTACCTGTCATAATCTCCACACGAACACAGTGGATTCATACTTTCTCCCTCAATATAGCCATTTCTCTGCTATTTCAAGTAAATTTGAAGGAAATGAATGTCTGTGCTCACTTGCTCACCTTAGAGGTAGGAAAACGCAACCCCCAAATCTCTTTCTTTCCAACATGGCCAACTGGCATCTTCACATGATAAAGAAAAAGAGTCTACCATCTACTCGTCTAGATCCTCAAATCTATGCAGTCTCACAGAGTGTGTGTGGTTTTCTGTTGTTGTTATTGTTGTTGTTTGTTTGTTTGCTTTGAGGCCGGGTCTCACTCCC... |
Task1_train_47484 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | GTCAATTCTTTTTTTTTTTCTTAGAGACGAAGTCTCACCCTGTCACTCAAGCTGGAGTGCAGTGGTGGGACCTTGGCTCACCACAAACTCTACCTCCTGGGTTCAAACGATTCTCTTGCCTCAGCCTTCTGAGTAGCTGAGATTACAGGCACCCGCCACCACACCCAGCTAATTTTTTTGTATTTTTAGTAGAGTTATGGTTTCACCACGTTGGCCAGGCTATTCTTGAACTCCTGACCTCATGGTCTTCCCACCTCGGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACTGCACCCGGCTGTTAGTGAATTCTTA... | GTCAATTCTTTTTTTTTTTCTTAGAGACGAAGTCTCACCCTGTCACTCAAGCTGGAGTGCAGTGGTGGGACCTTGGCTCACCACAAACTCTACCTCCTGGGTTCAAACGATTCTCTTGCCTCAGCCTTCTGAGTAGCTGAGATTACAGGCACCCGCCACCACACCCAGCTAATTTTTTTGTATTTTTAGTAGAGTTATGGTTTCACCACGTTGGCCAGGCTATTCTTGAACTCCTGACCTCATGGTCTTCCCACCTCGGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACTGCACCCGGCTGTTAGTGAATTCTTA... |
Task1_train_47485 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TGGGAGGCTGAGGTGGCTGGATCACTTGAGGTCATAAGTTCGAGGCCAGCCTGGCCAACATGTTGAAACCCTATCTCTACTAAAAATACAAAAATTAGCCAAACGTGGTAGTGTGTGCGTGTAATCCCAGGTACTCAGGAGGCTGAGGCAGGAGAATGGCTTGAACCCAAAAGGTGGAGGTTGCAGTGAGCTGAGATCGGGCCATTGAACTCCAGGCGGTTGTGACAGAGTGAAACTTCATCTCAAAAATATAAAAATAAAAAATTTGTTTAAAAATGTCAAAATGTGCCTTTTCTGCAAGGATATAGGTAATTTTATGA... | TGGGAGGCTGAGGTGGCTGGATCACTTGAGGTCATAAGTTCGAGGCCAGCCTGGCCAACATGTTGAAACCCTATCTCTACTAAAAATACAAAAATTAGCCAAACGTGGTAGTGTGTGCGTGTAATCCCAGGTACTCAGGAGGCTGAGGCAGGAGAATGGCTTGAACCCAAAAGGTGGAGGTTGCAGTGAGCTGAGATCGGGCCATTGAACTCCAGGCGGTTGTGACAGAGTGAAACTTCATCTCAAAAATATAAAAATAAAAAATTTGTTTAAAAATGTCAAAATGTGCCTTTTCTGCAAGGATATAGGTAATTTTATGA... |
Task1_train_47486 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GTCTCAAAGGCCCCATCTGCAGAACATCCTTTTGGAGAATAAGAACTCTGAACATGGCTTTTGGCCAATATGAACATTCAGACCAGGTAGCCTGCATCATATTTTTTATGTTTTTATTGTGCAATTTGATTTATAAAATGTTTTCTCTGATCTTAGTTTAAAATTTTTCCCAGTGCACATTCTGTGTTTTATATTTTGTGCATAGTGAGCTAGATAATTAAGGTCAACAATGCACAGGTGCAATCTCGGCTTACTACAACCTCCACTTCCTGGGTTCAAATGATTCTCCTGCCTCAGCCTTCCAAGTAGCTGAGATTACA... | GTCTCAAAGGCCCCATCTGCAGAACATCCTTTTGGAGAATAAGAACTCTGAACATGGCTTTTGGCCAATATGAACATTCAGACCAGGTAGCCTGCATCATATTTTTTATGTTTTTATTGTGCAATTTGATTTATAAAATGTTTTCTCTGATCTTAGTTTAAAATTTTTCCCAGTGCACATTCTGTGTTTTATATTTTGTGCATAGTGAGCTAGATAATTAAGGTCAACAATGCACAGGTGCAATCTCGGCTTACTACAACCTCCACTTCCTGGGTTCAAATGATTCTCCTGCCTCAGCCTTCCAAGTAGCTGAGATTACA... |
Task1_train_47487 | A genomic variant on Chromosome 19 is under review. What is the biological outcome — benign or pathogenic? | Benign | ATGTTTTCTCTGATCTTAGTTTAAAATTTTTCCCAGTGCACATTCTGTGTTTTATATTTTGTGCATAGTGAGCTAGATAATTAAGGTCAACAATGCACAGGTGCAATCTCGGCTTACTACAACCTCCACTTCCTGGGTTCAAATGATTCTCCTGCCTCAGCCTTCCAAGTAGCTGAGATTACAGGCACCCACCACCACGACCAGCTAATTTTTTTGTATTTTTAGTAGAGTTGGGATTTCACCATGTTGGCCAAGCTACTCTCGAACTCCTGACTTCATGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGTATTACAGA... | ATGTTTTCTCTGATCTTAGTTTAAAATTTTTCCCAGTGCACATTCTGTGTTTTATATTTTGTGCATAGTGAGCTAGATAATTAAGGTCAACAATGCACAGGTGCAATCTCGGCTTACTACAACCTCCACTTCCTGGGTTCAAATGATTCTCCTGCCTCAGCCTTCCAAGTAGCTGAGATTACAGGCACCCACCACCACGACCAGCTAATTTTTTTGTATTTTTAGTAGAGTTGGGATTTCACCATGTTGGCCAAGCTACTCTCGAACTCCTGACTTCATGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGTATTACAGA... |
Task1_train_47488 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TTGGCTCACTGCAACCTCTGCCCCTTGGGTTCAAACAATTCTTGTGCCTCAGCCTCCCGAGTAGCTGGGACTAGATGTGGGCCACCACGCCTGGCTACATTTTGTAATCTTTTCTTGTCTTCTCAGTGCTATGACTGTTTGACAATACAGAATTTCCATTGATTTTGGTTATCCTTACATGAGCTTGTTGTGGATTATTTACCAATATAGTATATCGTGTGGTCCTTTAGCATTTATTTGTATACAGTAAATATGCTGTAAATATGAAGAATATATACTTTTCATTGATATGACAGTGATATGTTTTTTACAAACTGTTA... | TTGGCTCACTGCAACCTCTGCCCCTTGGGTTCAAACAATTCTTGTGCCTCAGCCTCCCGAGTAGCTGGGACTAGATGTGGGCCACCACGCCTGGCTACATTTTGTAATCTTTTCTTGTCTTCTCAGTGCTATGACTGTTTGACAATACAGAATTTCCATTGATTTTGGTTATCCTTACATGAGCTTGTTGTGGATTATTTACCAATATAGTATATCGTGTGGTCCTTTAGCATTTATTTGTATACAGTAAATATGCTGTAAATATGAAGAATATATACTTTTCATTGATATGACAGTGATATGTTTTTTACAAACTGTTA... |
Task1_train_47489 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TTTAGCATTTATTTGTATACAGTAAATATGCTGTAAATATGAAGAATATATACTTTTCATTGATATGACAGTGATATGTTTTTTACAAACTGTTAGACACTTTAGGGTCACAATGGAAAAATATTCCTTACTTTAGGCTACACATGTTTGTGCCCTGTCAATGTTTTGTCACGATCTTGGAAATAGACTTCCGTAAAAATAATTTGAAGCACATGTAATCGCCCTTTATTTGTTAAAGAATCTTATGCTTTTCTGTTCCTAAACTTTGAGGGTCATGTTTGGAAAGTTTAAAATAACTATTGTTTTTTGTGTCGTATTTA... | TTTAGCATTTATTTGTATACAGTAAATATGCTGTAAATATGAAGAATATATACTTTTCATTGATATGACAGTGATATGTTTTTTACAAACTGTTAGACACTTTAGGGTCACAATGGAAAAATATTCCTTACTTTAGGCTACACATGTTTGTGCCCTGTCAATGTTTTGTCACGATCTTGGAAATAGACTTCCGTAAAAATAATTTGAAGCACATGTAATCGCCCTTTATTTGTTAAAGAATCTTATGCTTTTCTGTTCCTAAACTTTGAGGGTCATGTTTGGAAAGTTTAAAATAACTATTGTTTTTTGTGTCGTATTTA... |
Task1_train_47490 | A variant on Chromosome 19 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATGGTGTTAGCCAGGATGGTCTCGATCTGACCTCGTGATCCTCCTGCCTCAGCCTGCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCAGCCGTTAGTCAATTCTTATTCCTTATAATGCTGTGTATATTTTTGACCTCATAAATTAACATGTAGTGATCTTAACATGTATTTCAGTTCTTATATTGTGTTCTGGTGGTATATAGAAGTTGTGGCTTTTTTCTTAACAGGGAATTGTTTAGAATTCTGCAGGTTGTATAAATGTACTTGTTATTTGCTTGCTAGTTTTATGAGTTACAATATTTTACTAACTAA... | ATGGTGTTAGCCAGGATGGTCTCGATCTGACCTCGTGATCCTCCTGCCTCAGCCTGCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCAGCCGTTAGTCAATTCTTATTCCTTATAATGCTGTGTATATTTTTGACCTCATAAATTAACATGTAGTGATCTTAACATGTATTTCAGTTCTTATATTGTGTTCTGGTGGTATATAGAAGTTGTGGCTTTTTTCTTAACAGGGAATTGTTTAGAATTCTGCAGGTTGTATAAATGTACTTGTTATTTGCTTGCTAGTTTTATGAGTTACAATATTTTACTAACTAA... |
Task1_train_47491 | A variant affecting Chromosome 19 has been observed. Determine if it's benign or associated with disease. | Benign | TGACCTCATAAATTAACATGTAGTGATCTTAACATGTATTTCAGTTCTTATATTGTGTTCTGGTGGTATATAGAAGTTGTGGCTTTTTTCTTAACAGGGAATTGTTTAGAATTCTGCAGGTTGTATAAATGTACTTGTTATTTGCTTGCTAGTTTTATGAGTTACAATATTTTACTAACTAATTTTTATGATTGTACATAAAGCTTTTCGGTATGTGGTATGCAATATAACTGACACAGTCCACTAGTTAATGTCATTTTTTTTTGAGACAGAGTTTCACTGTTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTTGGC... | TGACCTCATAAATTAACATGTAGTGATCTTAACATGTATTTCAGTTCTTATATTGTGTTCTGGTGGTATATAGAAGTTGTGGCTTTTTTCTTAACAGGGAATTGTTTAGAATTCTGCAGGTTGTATAAATGTACTTGTTATTTGCTTGCTAGTTTTATGAGTTACAATATTTTACTAACTAATTTTTATGATTGTACATAAAGCTTTTCGGTATGTGGTATGCAATATAACTGACACAGTCCACTAGTTAATGTCATTTTTTTTTGAGACAGAGTTTCACTGTTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTTGGC... |
Task1_train_47492 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGGTTGTATAAATGTACTTGTTATTTGCTTGCTAGTTTTATGAGTTACAATATTTTACTAACTAATTTTTATGATTGTACATAAAGCTTTTCGGTATGTGGTATGCAATATAACTGACACAGTCCACTAGTTAATGTCATTTTTTTTTGAGACAGAGTTTCACTGTTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTTGGCTCGCTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTTCCCGAGTAGCTGGGATTACAGGCATGAGCCACCACACCCGGCTAATTTTGTATTGTTAGTAGAGAC... | AGGTTGTATAAATGTACTTGTTATTTGCTTGCTAGTTTTATGAGTTACAATATTTTACTAACTAATTTTTATGATTGTACATAAAGCTTTTCGGTATGTGGTATGCAATATAACTGACACAGTCCACTAGTTAATGTCATTTTTTTTTGAGACAGAGTTTCACTGTTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTTGGCTCGCTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTTCCCGAGTAGCTGGGATTACAGGCATGAGCCACCACACCCGGCTAATTTTGTATTGTTAGTAGAGAC... |
Task1_train_47493 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCTGAGGCAAGAGAATGGCTTGAACCCAAAAGGTGGAGGTTGCAGTGAGCCAAGATTGGGCCATAGCACTCCAGCCTGTTGTGACAAAGTGAAACTTCATCTCGAAAATAAAAAAATACAAAAATTTTTAAAAGAACGTCATAACGTGCCTTTTCTGCATAGGTATAGGTAATTTTATGACAGTAATTCAGAAAAATATTGTATTAACTTTTATTTTGAGATTAAGTCTCACTTTGTTACCCAGGCTGAAGTACAGTGTTGCAATCTCAGCTCACTGCAACCTCTGCCTCTTGGGTTCAAGCGATTCTTGTGCCTCAGCC... | GCTGAGGCAAGAGAATGGCTTGAACCCAAAAGGTGGAGGTTGCAGTGAGCCAAGATTGGGCCATAGCACTCCAGCCTGTTGTGACAAAGTGAAACTTCATCTCGAAAATAAAAAAATACAAAAATTTTTAAAAGAACGTCATAACGTGCCTTTTCTGCATAGGTATAGGTAATTTTATGACAGTAATTCAGAAAAATATTGTATTAACTTTTATTTTGAGATTAAGTCTCACTTTGTTACCCAGGCTGAAGTACAGTGTTGCAATCTCAGCTCACTGCAACCTCTGCCTCTTGGGTTCAAGCGATTCTTGTGCCTCAGCC... |
Task1_train_47494 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TACAGAAGATTGTTGGGTCCACCGATAAAAGGGATATAGAGGCTGGGTGTGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGCCGAGAGTTTGAGACCAGCCTGGCCAACATGGTGACACCCCATCTCTACTAAAAAAATACAAAAATTAGCTGGGTGTGGTGGCACACTCCTGTGGTCCCAGCTGCTCAGGAGGCTGAGACACGCAAGGTGGAGGTTGCAGTGAGCTGAGATTGTGCCCCTGCACTCCAGCCTTGGTGACAGAGCCACACTCTCTCAAGAAAAAGGGACTTAGTAATATTTGTTGATTG... | TACAGAAGATTGTTGGGTCCACCGATAAAAGGGATATAGAGGCTGGGTGTGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGCCGAGAGTTTGAGACCAGCCTGGCCAACATGGTGACACCCCATCTCTACTAAAAAAATACAAAAATTAGCTGGGTGTGGTGGCACACTCCTGTGGTCCCAGCTGCTCAGGAGGCTGAGACACGCAAGGTGGAGGTTGCAGTGAGCTGAGATTGTGCCCCTGCACTCCAGCCTTGGTGACAGAGCCACACTCTCTCAAGAAAAAGGGACTTAGTAATATTTGTTGATTG... |
Task1_train_47495 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AAAGTGTTGGGATTACAGGAGTGAGCCACTGCACCTGGCTCATTTATCGTTTGTGTTGGGAATGTTTCAAATCTTCTCTTCTAGCTATTTTGAAATATACAATATATTGCTGTTAACTATAGTCACCCTTCTGTGCTATTGAACACTTGAACTTATTCCTTCTATCCAACTGTGTTTGTGCCCATTAACTATCCCACCCCTTCTAGCCTTTGATAACTGACTCTCTCTTTACCTTCATGAGATCTACTTTTTTAGCTCCTACATGAGTGAGAACATGAAGTTGTAAATAAAGTTTTATTCTAACACCGCCACACCTACTT... | AAAGTGTTGGGATTACAGGAGTGAGCCACTGCACCTGGCTCATTTATCGTTTGTGTTGGGAATGTTTCAAATCTTCTCTTCTAGCTATTTTGAAATATACAATATATTGCTGTTAACTATAGTCACCCTTCTGTGCTATTGAACACTTGAACTTATTCCTTCTATCCAACTGTGTTTGTGCCCATTAACTATCCCACCCCTTCTAGCCTTTGATAACTGACTCTCTCTTTACCTTCATGAGATCTACTTTTTTAGCTCCTACATGAGTGAGAACATGAAGTTGTAAATAAAGTTTTATTCTAACACCGCCACACCTACTT... |
Task1_train_47496 | Mutation context: Chromosome 19. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCAGTCTCCCAAGTAGCGGGGATTACAGGCGCCTGCCACCACGTCCAACTAATTTTTTATTTTTAGTAGAGATGGGATTTCACCATGTTGGTCAGGCTGGTCTTGAACTCTGACCTCAGATGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATGACAGGCGTGAGCCCGGCCGTTTTCTTTTTTGCTTGTTGTGCTTCCTGGAGATGCTCAGTAATTCTTACATTCTTTCCTGGATAGCTGGTCAATCATTATTTATTATTTCCTTGAATTGTTCTAGGAGGAAATGTGGGGTAGAAAGAGTATGGTGGGGTTCTTG... | TCAGTCTCCCAAGTAGCGGGGATTACAGGCGCCTGCCACCACGTCCAACTAATTTTTTATTTTTAGTAGAGATGGGATTTCACCATGTTGGTCAGGCTGGTCTTGAACTCTGACCTCAGATGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATGACAGGCGTGAGCCCGGCCGTTTTCTTTTTTGCTTGTTGTGCTTCCTGGAGATGCTCAGTAATTCTTACATTCTTTCCTGGATAGCTGGTCAATCATTATTTATTATTTCCTTGAATTGTTCTAGGAGGAAATGTGGGGTAGAAAGAGTATGGTGGGGTTCTTG... |
Task1_train_47497 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGGGCACATGTAATCCCAGCTACTCAAGTGGCTGAGGCAGGAGAATTGCTTAAACTCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGCACCACTGCACTCCACCCTGGGCAACAGAGCGAGACTCTGTCTCAAAAACAAAATGAAACAAAACAAAACAAAAAACCAAAACGCTAAGAGATGCAAAGACTGGTAGAAGGAATCTGGTGCTGGTAGATTCATAATTTTCAAAAACAGCCTAGAAATTTTCCAAGGATGTAGTATAACAAAAAGGCAAAGG... | CCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGGGCACATGTAATCCCAGCTACTCAAGTGGCTGAGGCAGGAGAATTGCTTAAACTCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGCACCACTGCACTCCACCCTGGGCAACAGAGCGAGACTCTGTCTCAAAAACAAAATGAAACAAAACAAAACAAAAAACCAAAACGCTAAGAGATGCAAAGACTGGTAGAAGGAATCTGGTGCTGGTAGATTCATAATTTTCAAAAACAGCCTAGAAATTTTCCAAGGATGTAGTATAACAAAAAGGCAAAGG... |
Task1_train_47498 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | GATCACTTGAGGTCAGGAGTTCAAGACCAGTCTGGTCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAACATTAGCCGGACATGGTGGTACGCACCTGTAATCCCAGCTATTCGGGAGGCCGAGGCAGGTGGATCACTTGAGGTCAGGAGTTCGAGACCACCCTGGCCAATTTGGCAAAACTCCATCTCTACTAAAAATACAAAAATTAGCTGGGCGTGATGGCGCACACCTGTAATCCCAGCTACTCAGGAGACTGAGGCACGAGAATCACTTGAACCCGGGAGGCGGATGTTGCAGTGAACCGAGATCACGCCA... | GATCACTTGAGGTCAGGAGTTCAAGACCAGTCTGGTCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAACATTAGCCGGACATGGTGGTACGCACCTGTAATCCCAGCTATTCGGGAGGCCGAGGCAGGTGGATCACTTGAGGTCAGGAGTTCGAGACCACCCTGGCCAATTTGGCAAAACTCCATCTCTACTAAAAATACAAAAATTAGCTGGGCGTGATGGCGCACACCTGTAATCCCAGCTACTCAGGAGACTGAGGCACGAGAATCACTTGAACCCGGGAGGCGGATGTTGCAGTGAACCGAGATCACGCCA... |
Task1_train_47499 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | CAACCCAGGAAGTCCAGCTGGCTTCACGTCTCACTACTACCTTTCTGTAGCTGCTACTACTACAGTGAGTAGACGGCAGTGCTGGGATTCGAACCCTCTGTCTTCTGGCTTGGAAGTCTTAACCACTAATCGCGTCTTCCTTTCAGCTACTCCTTGGGAAAGGCCTGGAAAGAAGCTACAGCACAGGGCACAGCGGGGTCTAAGGACCGTTCCGCGGAGCTCAGCCAGCAGGACTGTGGGGCTGCAGGAAAGGACAGTCCAGCCCAGGGTCCCAGCTTCTCCGCCACTCAGGTTGGAAGTCTCGGGCTGCAGTGCTCCTG... | CAACCCAGGAAGTCCAGCTGGCTTCACGTCTCACTACTACCTTTCTGTAGCTGCTACTACTACAGTGAGTAGACGGCAGTGCTGGGATTCGAACCCTCTGTCTTCTGGCTTGGAAGTCTTAACCACTAATCGCGTCTTCCTTTCAGCTACTCCTTGGGAAAGGCCTGGAAAGAAGCTACAGCACAGGGCACAGCGGGGTCTAAGGACCGTTCCGCGGAGCTCAGCCAGCAGGACTGTGGGGCTGCAGGAAAGGACAGTCCAGCCCAGGGTCCCAGCTTCTCCGCCACTCAGGTTGGAAGTCTCGGGCTGCAGTGCTCCTG... |
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