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_48400 | This mutation is located on Chromosome 22. Is it associated with a disease or is it a benign polymorphism? | Benign | CACACACAAAAGAAAAAAGCTATGGAACAATGATATAAATGAAGATATATTTAGTACAGCTGTACAATGTGTTGTGTTTTAAACTAAGTGCTATTACAAAAGAGTAAAAAATTTTAAAAATTAAAAACTTGGTAAAGCAAGAAAGTTAAACTAAGGTTAATTTTCTTTTTTTTTTTTTTTGATAAGAGTCAGGATCTGTTGCCCGGGCTGGAGTGCAATGGCCCGATCTCCGCTCACCGCAACCTCCCTCCCAGGTTCAAGGGCTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAAGTAATAGATCCATTACAT... | CACACACAAAAGAAAAAAGCTATGGAACAATGATATAAATGAAGATATATTTAGTACAGCTGTACAATGTGTTGTGTTTTAAACTAAGTGCTATTACAAAAGAGTAAAAAATTTTAAAAATTAAAAACTTGGTAAAGCAAGAAAGTTAAACTAAGGTTAATTTTCTTTTTTTTTTTTTTTGATAAGAGTCAGGATCTGTTGCCCGGGCTGGAGTGCAATGGCCCGATCTCCGCTCACCGCAACCTCCCTCCCAGGTTCAAGGGCTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAAGTAATAGATCCATTACAT... |
Task1_train_48401 | A variant was discovered on Chromosome 22. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ATAATTGATGAGAAACCTTGATAGAAAACTAAACCCACATTTTATAGTAACATAAAGGCAATAATGGATGACGTTAATCCTTCTCTGTCCGCCATCAGAAGATTTGATACATCTTTGTTGAGGTATTATATGATCGTCCTCTAAACTTTGAAATAATTAACAGAAGGTAAGTCCTGCTGTGATGGCCATATAAAAGTTTACTTAAACCTTTTTTTTGTTTGTTTAAATAAAAGGCGATGTAGATACTGGTAGAGCTTGTTGCTCATGTTACAGAATATACAGCTTTATAAACTTTAATTTCTCAACAAATAAATTGACTA... | ATAATTGATGAGAAACCTTGATAGAAAACTAAACCCACATTTTATAGTAACATAAAGGCAATAATGGATGACGTTAATCCTTCTCTGTCCGCCATCAGAAGATTTGATACATCTTTGTTGAGGTATTATATGATCGTCCTCTAAACTTTGAAATAATTAACAGAAGGTAAGTCCTGCTGTGATGGCCATATAAAAGTTTACTTAAACCTTTTTTTTGTTTGTTTAAATAAAAGGCGATGTAGATACTGGTAGAGCTTGTTGCTCATGTTACAGAATATACAGCTTTATAAACTTTAATTTCTCAACAAATAAATTGACTA... |
Task1_train_48402 | A variant found on Chromosome 22 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TCTGTCACCCAAGCAGGAGTGCAGTAGGGCAAACATGGCTCACTGCAACCTCAAATTCTTGGGCTCAAGGGATCCTCCTCCCTCAGTCCCAAGTAGCTGGGACTATCGGCATGTGCGACCATACCTGGCTAATGTTTTCTTTTTGGTAGGGACGGGTGTCTCACTTTCTTGCCCAGTCCAGTCTTGGAACTCCTGGGCTCAAGTGATCCTCCTGCCTTGGCCTCCCAAAGTGCTGGGATCACAGGCATAAGTTACTGTGCTCAGCCTGGTTTGACTTAATAGTCCTAGAGGCCCTGTCCCAACCATACAACCTTGGGCAT... | TCTGTCACCCAAGCAGGAGTGCAGTAGGGCAAACATGGCTCACTGCAACCTCAAATTCTTGGGCTCAAGGGATCCTCCTCCCTCAGTCCCAAGTAGCTGGGACTATCGGCATGTGCGACCATACCTGGCTAATGTTTTCTTTTTGGTAGGGACGGGTGTCTCACTTTCTTGCCCAGTCCAGTCTTGGAACTCCTGGGCTCAAGTGATCCTCCTGCCTTGGCCTCCCAAAGTGCTGGGATCACAGGCATAAGTTACTGTGCTCAGCCTGGTTTGACTTAATAGTCCTAGAGGCCCTGTCCCAACCATACAACCTTGGGCAT... |
Task1_train_48403 | This sequence variant lies on Chromosome 22. Is it clinically significant, and what condition might it cause if any? | Benign | GACTTCCTGACAAAAGAAGCAAGAGTCTCCGTGTCTGCAGCATTTCTCCATTCTGTCTCTGCCATCAGAGGAATTTTAAAGCAAAGCTCTGATTATAATTTTGTACCTCAGAGATGTCAGTGACAAACCATCGCCTGTTGGATAAAGTCCATATTTCTTAGCTGTCATTCAGGTTCCTCCATGGTCCTGTCCTCACTGACCTTCTATTCTTCATGGGCACTCTGCATTAATTAAACAGGGCTCTGTCCTTATCTTCTTTTTTTTCTGTCTCTGTGCTTTTGCCTGCATTGTGTCTTCTGTGTACCCTTCGCCTGCCAAAA... | GACTTCCTGACAAAAGAAGCAAGAGTCTCCGTGTCTGCAGCATTTCTCCATTCTGTCTCTGCCATCAGAGGAATTTTAAAGCAAAGCTCTGATTATAATTTTGTACCTCAGAGATGTCAGTGACAAACCATCGCCTGTTGGATAAAGTCCATATTTCTTAGCTGTCATTCAGGTTCCTCCATGGTCCTGTCCTCACTGACCTTCTATTCTTCATGGGCACTCTGCATTAATTAAACAGGGCTCTGTCCTTATCTTCTTTTTTTTCTGTCTCTGTGCTTTTGCCTGCATTGTGTCTTCTGTGTACCCTTCGCCTGCCAAAA... |
Task1_train_48404 | A variant has been detected on Chromosome 22. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTGCAGTCCGGGAACCCAGAGGAGAAAGCAGCTCACTACCTCTTCTCACTCGAGCAAGGGCGGGTAAAGAAAGCAGGAGATGCGGGCTGGGCGCGGTGGCTCAGGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACCTGAAGTCAGGAGTTGGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAACACAAAAATTAGCTGGGTGGGGTGGTGGGTACCCGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCAAAAT... | CTGCAGTCCGGGAACCCAGAGGAGAAAGCAGCTCACTACCTCTTCTCACTCGAGCAAGGGCGGGTAAAGAAAGCAGGAGATGCGGGCTGGGCGCGGTGGCTCAGGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACCTGAAGTCAGGAGTTGGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAACACAAAAATTAGCTGGGTGGGGTGGTGGGTACCCGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCAAAAT... |
Task1_train_48405 | This mutation on Chromosome 22 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CAAAAGGGAGGCAGGAAGCAGGAGACAGCCGGGTTGCCCCCAGCCAGGAGGAGGAGCACAGGCCCCAGGGCTGGACAGTGGAGGTGGGGTGACATGATACTCCGCAGAGCTCCGCCCACCCTGTATGCTGACAGGTGCCTGTTAGAGTGTGCTCTGATTCCTCTCCCTCCACCTTCACTGGATCCACCCAAAGTCCTGGGCTCTGGAAAGTGAGGGGCTGAGTCAGACCTAGCAGCCCTGCAGGTCAGTTCCTGGACCAGTCCTTTAAGACGACAAACCCTCCCTAACTATCAAACCCACCAAACGGGCAGGACCAGGCA... | CAAAAGGGAGGCAGGAAGCAGGAGACAGCCGGGTTGCCCCCAGCCAGGAGGAGGAGCACAGGCCCCAGGGCTGGACAGTGGAGGTGGGGTGACATGATACTCCGCAGAGCTCCGCCCACCCTGTATGCTGACAGGTGCCTGTTAGAGTGTGCTCTGATTCCTCTCCCTCCACCTTCACTGGATCCACCCAAAGTCCTGGGCTCTGGAAAGTGAGGGGCTGAGTCAGACCTAGCAGCCCTGCAGGTCAGTTCCTGGACCAGTCCTTTAAGACGACAAACCCTCCCTAACTATCAAACCCACCAAACGGGCAGGACCAGGCA... |
Task1_train_48406 | Assess the clinical impact of this variant found on Chromosome 22. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GAGCCATGATCATGCCACTGCACTATTGCCCATGCCAGTCTGGGCAAGAGACTGAGACCCTGTCTCAAAAAAAAAAAAAAAAATCACTGAATAGTTCCATGCTTCCTAGAATCCCAAAGACTAAATCAAGCAGATGCAGGCCTTATATTCCAGCTTTCTCCCTGATCTGACCTGCAGACAGTATTTCCCAAACCATGTTCCACAGGACCTGCTGTCACAGTTGGCTTTGCAGCATTCTCCATGTGGTTCACACACCACAGGCTGTCTGCATGGACGCTGTAAATTTCTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCC... | GAGCCATGATCATGCCACTGCACTATTGCCCATGCCAGTCTGGGCAAGAGACTGAGACCCTGTCTCAAAAAAAAAAAAAAAAATCACTGAATAGTTCCATGCTTCCTAGAATCCCAAAGACTAAATCAAGCAGATGCAGGCCTTATATTCCAGCTTTCTCCCTGATCTGACCTGCAGACAGTATTTCCCAAACCATGTTCCACAGGACCTGCTGTCACAGTTGGCTTTGCAGCATTCTCCATGTGGTTCACACACCACAGGCTGTCTGCATGGACGCTGTAAATTTCTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCC... |
Task1_train_48407 | A mutation on Chromosome 22 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CATGTCCGCATCCCAGAAGTGACCGCTAGGACAGTGGTGCTGTTGGCGATAACACTGCCCTTCCTCCAGCAGTGTCTGACAACTCGTGGAGGGATTTTTGGTGTCTTCATAGGTGGTGGAGGCTGCACGGACACTCCAAGGGCCGAGGCCAAGAATGTTAAACCTTCTGCAAGGGAAAGAGCTGTCCTGCCCCAAATGCCAGTAGCCCCTCGGTGAGAAACACACACTTCCAGAAACATGTAGGAAGGACAACTCAGGCTGCTCAACGATCTCTTGTACTTGAAGAGACGCCTGCAGCTCGGGCTGGATTTGACTGGTGT... | CATGTCCGCATCCCAGAAGTGACCGCTAGGACAGTGGTGCTGTTGGCGATAACACTGCCCTTCCTCCAGCAGTGTCTGACAACTCGTGGAGGGATTTTTGGTGTCTTCATAGGTGGTGGAGGCTGCACGGACACTCCAAGGGCCGAGGCCAAGAATGTTAAACCTTCTGCAAGGGAAAGAGCTGTCCTGCCCCAAATGCCAGTAGCCCCTCGGTGAGAAACACACACTTCCAGAAACATGTAGGAAGGACAACTCAGGCTGCTCAACGATCTCTTGTACTTGAAGAGACGCCTGCAGCTCGGGCTGGATTTGACTGGTGT... |
Task1_train_48408 | A mutation on Chromosome 22 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TAAAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTTTTGGCCTCAAGTGATCCGCCCACCTCAGCCTCCCAAAGCGTTGGGATTACAGGCGTGAGCCACCGCACCCGGCTCTTCACTTTTAAGAGACTGTTTTTCATTCTGTATAGCACTGAATGCTACTTTTAATTATCTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACCATCTCCCAGGCTGGAGTGTACTGGTGTGATCTCAGATCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGTGTGAGCCACCGTGCCTGGCCTTTAT... | TAAAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTTTTGGCCTCAAGTGATCCGCCCACCTCAGCCTCCCAAAGCGTTGGGATTACAGGCGTGAGCCACCGCACCCGGCTCTTCACTTTTAAGAGACTGTTTTTCATTCTGTATAGCACTGAATGCTACTTTTAATTATCTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACCATCTCCCAGGCTGGAGTGTACTGGTGTGATCTCAGATCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGTGTGAGCCACCGTGCCTGGCCTTTAT... |
Task1_train_48409 | A genomic change on Chromosome 22 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AAACGTTTGAGGTGATGAATACCTTCATTACCCTGATTTGATCATTGCACATTGTATGCATGTATCAAAGTATCACATGTAACACATAAATATGTACAATTACTATGTATCTATAAAAATAAGAAACAAAGGAAAACAGTTGCTGTATAAACAATACTGGGATAACTGTCAAAATTTAAATATTGAATATATTATATATGGGAAAATTGTACGGATATGAAATTATCTGAATTTGGTAATAATTGCACTGGGGTTATGTATGAAAACATCTTTGATCCTATGAGGTTCATATTGAATTATTTAGAGCTGAAGAATGTCAA... | AAACGTTTGAGGTGATGAATACCTTCATTACCCTGATTTGATCATTGCACATTGTATGCATGTATCAAAGTATCACATGTAACACATAAATATGTACAATTACTATGTATCTATAAAAATAAGAAACAAAGGAAAACAGTTGCTGTATAAACAATACTGGGATAACTGTCAAAATTTAAATATTGAATATATTATATATGGGAAAATTGTACGGATATGAAATTATCTGAATTTGGTAATAATTGCACTGGGGTTATGTATGAAAACATCTTTGATCCTATGAGGTTCATATTGAATTATTTAGAGCTGAAGAATGTCAA... |
Task1_train_48410 | A mutation on Chromosome 22 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AAACAGTTGCTGTATAAACAATACTGGGATAACTGTCAAAATTTAAATATTGAATATATTATATATGGGAAAATTGTACGGATATGAAATTATCTGAATTTGGTAATAATTGCACTGGGGTTATGTATGAAAACATCTTTGATCCTATGAGGTTCATATTGAATTATTTAGAGCTGAAGAATGTCAATCTCTTCAATTTACTCTCAAGTAGTCCAGCAAAAGAAAAAAAGTGATTGTGTAAATATATACACATATATACTGTGTACTCACACATACACATAGATGTGTGTGTATGAGAGAGAAAATTAGTGAAGGAAGGC... | AAACAGTTGCTGTATAAACAATACTGGGATAACTGTCAAAATTTAAATATTGAATATATTATATATGGGAAAATTGTACGGATATGAAATTATCTGAATTTGGTAATAATTGCACTGGGGTTATGTATGAAAACATCTTTGATCCTATGAGGTTCATATTGAATTATTTAGAGCTGAAGAATGTCAATCTCTTCAATTTACTCTCAAGTAGTCCAGCAAAAGAAAAAAAGTGATTGTGTAAATATATACACATATATACTGTGTACTCACACATACACATAGATGTGTGTGTATGAGAGAGAAAATTAGTGAAGGAAGGC... |
Task1_train_48411 | A mutation on Chromosome 22 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGCCCGGTAGAAAACCGCCATTGCTCACTCCCCCCACCCCCACAACACACCTTATGAAAATGCCCCTCTCTCCTCCAAAGGAGAAATGGCACATTAAAAGGCAGGATGTGTCTTGCTCCTTGCCCCAGGCTGGCTTCAGAATAAATTCACATTTGTGTATAAAACCTTTTGTATCACATTTTTTTTTGTATCAGAGTTAGTTGAGCTCTACACGCAGTGAGCAGCTCCTCAGCTTTTCGCTGCATAGGTACTGTGTTCAGCTTTCCTTCCGTCCTCAGTCTGGAGAACCTCAATCAACCTAGCTCCAGGTTTATGGATTC... | TGCCCGGTAGAAAACCGCCATTGCTCACTCCCCCCACCCCCACAACACACCTTATGAAAATGCCCCTCTCTCCTCCAAAGGAGAAATGGCACATTAAAAGGCAGGATGTGTCTTGCTCCTTGCCCCAGGCTGGCTTCAGAATAAATTCACATTTGTGTATAAAACCTTTTGTATCACATTTTTTTTTGTATCAGAGTTAGTTGAGCTCTACACGCAGTGAGCAGCTCCTCAGCTTTTCGCTGCATAGGTACTGTGTTCAGCTTTCCTTCCGTCCTCAGTCTGGAGAACCTCAATCAACCTAGCTCCAGGTTTATGGATTC... |
Task1_train_48412 | This sequence change occurs on Chromosome 22. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGGAGAGAATGGCTAATGAGGCTCTAGGGATCAGCACAGCCAGCTGCTGGAGGTCCCAGAGGACGGGTGACTCAGCAGGAATGGGGGAGTCTGAGGGGTTGACAGAGTGCCCAATTCTCACCTCCTCCTGCACCTTCCAGAGAGACGGGCTGCAGGGAGTGATTGAGTGGATGAACATGACTAGAGGGACCCAGTCTTCTCCTCAGCAGCTGCTTGAGGACAGTATTAGCGGTCCCCTCAATCCCCCCCCCAACACATGCACACATGCACTGACCTGCAGGGGCCAGATCCCGGTGGACCCGGGGACACAGCTTCCAGGG... | GGGAGAGAATGGCTAATGAGGCTCTAGGGATCAGCACAGCCAGCTGCTGGAGGTCCCAGAGGACGGGTGACTCAGCAGGAATGGGGGAGTCTGAGGGGTTGACAGAGTGCCCAATTCTCACCTCCTCCTGCACCTTCCAGAGAGACGGGCTGCAGGGAGTGATTGAGTGGATGAACATGACTAGAGGGACCCAGTCTTCTCCTCAGCAGCTGCTTGAGGACAGTATTAGCGGTCCCCTCAATCCCCCCCCCAACACATGCACACATGCACTGACCTGCAGGGGCCAGATCCCGGTGGACCCGGGGACACAGCTTCCAGGG... |
Task1_train_48413 | Mutation context: Chromosome 22. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CCTCCACAATTTGCTGAGGGAGGCCCCAGAGTCCAGGGCACCCAGAGTGCTAACTAGCCCCTGGGGGTACAGGGAGAACAGCATGCTGTGTGGGGGATACTACTCTCTGCCCATACCTAGGGCCCTGTGGCGGCCACAGGCAGCACTGCTTATGCAGAGGCACTGGGGTGAGAAGGAGTAGGGTGCAGTAGTGAGGGCTCCACAGAGGGTGGAAGGGCTGCAGGGGAAGGCAGACCAGCAGGGATGCCATGAGGGCCTCAGATGCCAGGCTGCAGAGGTGGACGGGCTGGCCAGCTCCTCTCCCCAGCCTCCTACTGTAA... | CCTCCACAATTTGCTGAGGGAGGCCCCAGAGTCCAGGGCACCCAGAGTGCTAACTAGCCCCTGGGGGTACAGGGAGAACAGCATGCTGTGTGGGGGATACTACTCTCTGCCCATACCTAGGGCCCTGTGGCGGCCACAGGCAGCACTGCTTATGCAGAGGCACTGGGGTGAGAAGGAGTAGGGTGCAGTAGTGAGGGCTCCACAGAGGGTGGAAGGGCTGCAGGGGAAGGCAGACCAGCAGGGATGCCATGAGGGCCTCAGATGCCAGGCTGCAGAGGTGGACGGGCTGGCCAGCTCCTCTCCCCAGCCTCCTACTGTAA... |
Task1_train_48414 | This genomic variant is located on Chromosome 22. Can you determine its pathogenicity and name any linked disease? | Benign | GCTCTGGAACCTGGCTGCCCTGCCCCAGTGCATGTGGGATCCACGGCATGCTTCCTGCTTCGTCCTCTGCAGCCAGTAGGGGACTCCTGTGGCCAGGACTTCCTTGTTAAGTAGCAGCCCTTCTCCAAGGGGAGCACAAGCCTGCCCGCACACAGCCTCCAGCATCATGCTCCAGCAGGCCAAGCTCAGGGACAGGCAATTCAGTAACAAAACTCACAGCTCTGGACAGTTCTGGCACAAAGGTCAAGTCTGTCTGTGGGCAACTCAAGATTCTCATTCCACATGGGATGGAAAAAATGGGTCTCCAGCCACAGTGTGAG... | GCTCTGGAACCTGGCTGCCCTGCCCCAGTGCATGTGGGATCCACGGCATGCTTCCTGCTTCGTCCTCTGCAGCCAGTAGGGGACTCCTGTGGCCAGGACTTCCTTGTTAAGTAGCAGCCCTTCTCCAAGGGGAGCACAAGCCTGCCCGCACACAGCCTCCAGCATCATGCTCCAGCAGGCCAAGCTCAGGGACAGGCAATTCAGTAACAAAACTCACAGCTCTGGACAGTTCTGGCACAAAGGTCAAGTCTGTCTGTGGGCAACTCAAGATTCTCATTCCACATGGGATGGAAAAAATGGGTCTCCAGCCACAGTGTGAG... |
Task1_train_48415 | A variant was discovered on Chromosome 22. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GGGCAGTCCCTCCCAGGTACCACTGTTCCCAGAACCAAGCCAGGTCCAGCTGCATTTTCTTGAGGCCCAATAACGAGAAGCAGACAAACTAGGAAAGAAGGGAGTTTATCACTGTAACTGGATACAGGGAGAAGGCTGGAGATAATTCCAGCAGACCAACTCAAAGTGCTACAATTTTCTTACTGTTTATATAGGTTGGGGTTATGTGCCTACATGCAGTACAGCAATCACCTAAGTCTACTGGTAACTAATTTTGTTCCAAGGAGAAGGTCAGAGGCAAAAAAAATGCTTGCTAAGTCCGATTAAAAGGGGCCCAGTGC... | GGGCAGTCCCTCCCAGGTACCACTGTTCCCAGAACCAAGCCAGGTCCAGCTGCATTTTCTTGAGGCCCAATAACGAGAAGCAGACAAACTAGGAAAGAAGGGAGTTTATCACTGTAACTGGATACAGGGAGAAGGCTGGAGATAATTCCAGCAGACCAACTCAAAGTGCTACAATTTTCTTACTGTTTATATAGGTTGGGGTTATGTGCCTACATGCAGTACAGCAATCACCTAAGTCTACTGGTAACTAATTTTGTTCCAAGGAGAAGGTCAGAGGCAAAAAAAATGCTTGCTAAGTCCGATTAAAAGGGGCCCAGTGC... |
Task1_train_48416 | This variant is located on Chromosome 22. Evaluate its biological effect and specify any disease association. | Benign | CTTGAGGCCCGACCACCGGCCCGACCACAAGCTTGGAGCCAAAACCCAGCACCGGCTGCTGGTGGTGCCCGAGAACGAGAACAGGATGGAGGACAGGCTGGCCGAGACCTCCAGGGCCAAAGACCATCACATCTCCGGAGCTGAGGTGGGGAAAGCAAGCACCTAGCATGACAATGGCCCCGTTGTGTGTGGTGGGGGTCGGGGTTGGGGGGCATGGTGCAGTCGGCCTTCACGTAAACTAAGTAGGCAGGTAGGATCTGAAGAAGGCACAGGTGCAAGTAAAATTCGTCAATTAAACCACTATTTTGATTACGTTCCAT... | CTTGAGGCCCGACCACCGGCCCGACCACAAGCTTGGAGCCAAAACCCAGCACCGGCTGCTGGTGGTGCCCGAGAACGAGAACAGGATGGAGGACAGGCTGGCCGAGACCTCCAGGGCCAAAGACCATCACATCTCCGGAGCTGAGGTGGGGAAAGCAAGCACCTAGCATGACAATGGCCCCGTTGTGTGTGGTGGGGGTCGGGGTTGGGGGGCATGGTGCAGTCGGCCTTCACGTAAACTAAGTAGGCAGGTAGGATCTGAAGAAGGCACAGGTGCAAGTAAAATTCGTCAATTAAACCACTATTTTGATTACGTTCCAT... |
Task1_train_48417 | Here is a mutation located on Chromosome 22. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GCATGAAAACCCCAGGAGGAAGCAGGGGACCCTCACCCATGGGCAGGTTCACAGTAGCCTAGAGGCCAGGGCTGGACCCCAGGGGTCCAAGGCCACCATCCGTGGAGCAGTCCCCTCTGCTGGGGAGCACCCTGGTGCAGAGACTGAGGATCGCTGAGCTGTGCTCCTCTCAAAGACAGCTGTACCCTAAATACCCCCTCGCTGGGAAGGAAGAAGAAGGGACAGCTCCTTGTTGGGTGTGGGAGTGGAGCCAAGGTGGACTTGAGACTCTGGGCGGCTTCTGTGGTATTTGAAGTTGCTAGTTTCTCAGTATCAGCGCG... | GCATGAAAACCCCAGGAGGAAGCAGGGGACCCTCACCCATGGGCAGGTTCACAGTAGCCTAGAGGCCAGGGCTGGACCCCAGGGGTCCAAGGCCACCATCCGTGGAGCAGTCCCCTCTGCTGGGGAGCACCCTGGTGCAGAGACTGAGGATCGCTGAGCTGTGCTCCTCTCAAAGACAGCTGTACCCTAAATACCCCCTCGCTGGGAAGGAAGAAGAAGGGACAGCTCCTTGTTGGGTGTGGGAGTGGAGCCAAGGTGGACTTGAGACTCTGGGCGGCTTCTGTGGTATTTGAAGTTGCTAGTTTCTCAGTATCAGCGCG... |
Task1_train_48418 | This mutation occurs on Chromosome 22. Does this change lead to a known medical condition, or is it benign? | Benign | CCAAGAAGTCCAGGTGGCGTCACCTCTCAAGATCACCTGAGGTCAGGAGTTTGAGAACAGCCTGCCCAACATGGTAAAACCCTGTATCTATTAAAAATACAAAAATGAGCCGGGCGTGGTGGCAGGCACCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTCGAGGCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGAGTGACAGAGTGAGACTCCGTTTCAAGAAAAATAATAATAAAACAAAAAAAGAAGAGAAAACTGAAGCTGAGATTCCGCCACAAGCTCCA... | CCAAGAAGTCCAGGTGGCGTCACCTCTCAAGATCACCTGAGGTCAGGAGTTTGAGAACAGCCTGCCCAACATGGTAAAACCCTGTATCTATTAAAAATACAAAAATGAGCCGGGCGTGGTGGCAGGCACCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTCGAGGCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGAGTGACAGAGTGAGACTCCGTTTCAAGAAAAATAATAATAAAACAAAAAAAGAAGAGAAAACTGAAGCTGAGATTCCGCCACAAGCTCCA... |
Task1_train_48419 | A variant has been detected on Chromosome 22. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CCACAAGCTCCAGGATAGCTGGTTGGCGTGCTGTGCTGCACAACCTGAAAGAAGCGCCCACCGGATGCCAGGCACCTGCCATGGACCACTTGGTCGGGAGGAAACATGATGTCCATTGTATGGATGGGATAACGAGGTTCACAGCGGTGACACCCCTAGCCCACATGGAGAGAGACAGTGAATGGCTGAGCTGGGGTGCCCCCCGTGTGAGTTAGCAAGCTCCCCTGCTCAGGCTGCTGCTGGCCCAGCCCTATGGCTAAGTGGATTCCTGCTATCGTGTGCCCCAAATACAGATTGGATGTCGTCCATCTGATTGGACC... | CCACAAGCTCCAGGATAGCTGGTTGGCGTGCTGTGCTGCACAACCTGAAAGAAGCGCCCACCGGATGCCAGGCACCTGCCATGGACCACTTGGTCGGGAGGAAACATGATGTCCATTGTATGGATGGGATAACGAGGTTCACAGCGGTGACACCCCTAGCCCACATGGAGAGAGACAGTGAATGGCTGAGCTGGGGTGCCCCCCGTGTGAGTTAGCAAGCTCCCCTGCTCAGGCTGCTGCTGGCCCAGCCCTATGGCTAAGTGGATTCCTGCTATCGTGTGCCCCAAATACAGATTGGATGTCGTCCATCTGATTGGACC... |
Task1_train_48420 | This variant is located on Chromosome 22. Evaluate its biological effect and specify any disease association. | Benign | CTCCATTTTGCCTGGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGAGATTACAGGCCCTTCACCCCCTTGTTTTCTTTTTGTTTGTTTGTTTTTTAAAGACAGGGTCTCGCTCTTTGCCTAGGCTGGAGTGCAGTGCCCCGATCACAGCTCACCCCGATCACAGCTCACTGCAGCCTTGACCTCCTGGGCTCAGGTGATCTTCCCACTTCAGCCTTCCAAGTAGCTGTGATTACAAGTGCATGCCACACACTCGGCTAATATTTTTTAGTTTTTTGATAGAGATGGGGGTCT... | CTCCATTTTGCCTGGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGAGATTACAGGCCCTTCACCCCCTTGTTTTCTTTTTGTTTGTTTGTTTTTTAAAGACAGGGTCTCGCTCTTTGCCTAGGCTGGAGTGCAGTGCCCCGATCACAGCTCACCCCGATCACAGCTCACTGCAGCCTTGACCTCCTGGGCTCAGGTGATCTTCCCACTTCAGCCTTCCAAGTAGCTGTGATTACAAGTGCATGCCACACACTCGGCTAATATTTTTTAGTTTTTTGATAGAGATGGGGGTCT... |
Task1_train_48421 | This mutation on Chromosome 22 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AGCCAGACACATTTACCCTCCAGTTATGTCTCACTGGGAACTCAGACTCCAGATAACGTCTAGGAGGTCTTGATTATGCTCACTAAGCAGATCCATAGCTCAGAAGGGAGGAGGGGAGGGGCAGAGCCACACTCAGGCCACCTCCCTTAGAAAAGACTTTGCCAGGAGACAGAATGCTTGTTCTGGACATCAGAGAGGTCGGTGCCACAATCAACTTGAAACACCAGAAGATCCCTGGGAATTGTGGGCCTGTCACTCACTTTAAAATTACTACAGTGGCGATATTGAGATATCTAGTGTGCTTAAATGACCTCATCTTG... | AGCCAGACACATTTACCCTCCAGTTATGTCTCACTGGGAACTCAGACTCCAGATAACGTCTAGGAGGTCTTGATTATGCTCACTAAGCAGATCCATAGCTCAGAAGGGAGGAGGGGAGGGGCAGAGCCACACTCAGGCCACCTCCCTTAGAAAAGACTTTGCCAGGAGACAGAATGCTTGTTCTGGACATCAGAGAGGTCGGTGCCACAATCAACTTGAAACACCAGAAGATCCCTGGGAATTGTGGGCCTGTCACTCACTTTAAAATTACTACAGTGGCGATATTGAGATATCTAGTGTGCTTAAATGACCTCATCTTG... |
Task1_train_48422 | This is a variant located on Chromosome 22. Is this mutation a likely cause of disease or not? | Benign | ACAATAACCATAAGTATAGGGGAATCTAGGTCCTCCAGGTGGCTTCACACTTAGGGTCTTACTTCTCCCCCAGCATGCTGCAGTAAGAATTCGGCCTCTCAATCAGTCTTGTAGTAGTGAAGTTCTGCTATCATTATATTCTAATTCAAAATACTCAAATTCACAGATGAAGGCTAGAAATGGTTTGTTCACAACTACCCCTTGAAAGACAAGAAAAATTCTTTCAAGGACAAGCAACTTGAAAGTCTTTATCTACTCAGGAACAGATCCAGTCTCTGAACAATTTATCCAAATGAAATAAACCCAAGAAAAAGCCATAT... | ACAATAACCATAAGTATAGGGGAATCTAGGTCCTCCAGGTGGCTTCACACTTAGGGTCTTACTTCTCCCCCAGCATGCTGCAGTAAGAATTCGGCCTCTCAATCAGTCTTGTAGTAGTGAAGTTCTGCTATCATTATATTCTAATTCAAAATACTCAAATTCACAGATGAAGGCTAGAAATGGTTTGTTCACAACTACCCCTTGAAAGACAAGAAAAATTCTTTCAAGGACAAGCAACTTGAAAGTCTTTATCTACTCAGGAACAGATCCAGTCTCTGAACAATTTATCCAAATGAAATAAACCCAAGAAAAAGCCATAT... |
Task1_train_48423 | Chromosome 22 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CCTTTGCCTGTCAACAGTCAGACAGGCCAGAATCAGGCCCTGGGCTGGAGGAGTCTCCCTGGGTTGATTTCTGTGCTACAGTGCTGTCAGCAGAGTGGGGTGGGGGAGGGGGAGGCGCGCTTTTTTCATCTACCCGGGGAGCAAACACCAACTCCTGCAGCAGTTCTGCCAACAAGGCAGAACTATGACGAAACTGATTACCACTAGCCTCTCTGTATCAGAGTCAAGATATGGGGTGGATGAGTCCGTTCCCCAAGGGTGTGCTTTGGAGCCACTGCCACAGAGCTAAGAAGCCCCTCTGCTAGAACACACCTGTGCCC... | CCTTTGCCTGTCAACAGTCAGACAGGCCAGAATCAGGCCCTGGGCTGGAGGAGTCTCCCTGGGTTGATTTCTGTGCTACAGTGCTGTCAGCAGAGTGGGGTGGGGGAGGGGGAGGCGCGCTTTTTTCATCTACCCGGGGAGCAAACACCAACTCCTGCAGCAGTTCTGCCAACAAGGCAGAACTATGACGAAACTGATTACCACTAGCCTCTCTGTATCAGAGTCAAGATATGGGGTGGATGAGTCCGTTCCCCAAGGGTGTGCTTTGGAGCCACTGCCACAGAGCTAAGAAGCCCCTCTGCTAGAACACACCTGTGCCC... |
Task1_train_48424 | A variant affecting Chromosome 22 has been observed. Determine if it's benign or associated with disease. | Benign | AGGAGTAACCTGGACAAGCTGTACCATGGCCTGGAACTCGCCAAGAAGCAGCTGCGAGCCACCCAGCAGACCATTGCCAGCTGCCTTTGCACCAACCTCGTCATCTCCCAGGGGCCTTTCCTGTACTGCTCTCTCATGGAGGTCAGGCTTCCCACAGAGCACAGGCGCCTGGTCACAGCACCAGTGGCTTCGTCTGACCATCTGTCTCGCCTCCGCAGGGCACTCCAGATGTCATGCTGTTCTCTAGGCCGGCATCCCTAAGCCTGCTCAGCAAACACCTGCTCAAGTCCTTTGTGTGTTCGGTGAGGGGCCAGGCGGGT... | AGGAGTAACCTGGACAAGCTGTACCATGGCCTGGAACTCGCCAAGAAGCAGCTGCGAGCCACCCAGCAGACCATTGCCAGCTGCCTTTGCACCAACCTCGTCATCTCCCAGGGGCCTTTCCTGTACTGCTCTCTCATGGAGGTCAGGCTTCCCACAGAGCACAGGCGCCTGGTCACAGCACCAGTGGCTTCGTCTGACCATCTGTCTCGCCTCCGCAGGGCACTCCAGATGTCATGCTGTTCTCTAGGCCGGCATCCCTAAGCCTGCTCAGCAAACACCTGCTCAAGTCCTTTGTGTGTTCGGTGAGGGGCCAGGCGGGT... |
Task1_train_48425 | Mutation context: Chromosome 22. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CCGATGAGGAGAGCGGCCTCTGGTCAGGGGTCGCACAGCCTAGTGGGCCTGGGCCCTGGGAGAGGGGTCGCCCTCCTTCTCTCACCCCACTCCTGATTTTATGCAGGAAGCTTTTTTAATGGAAAAGATGGGGCCCTGCAAGGGGGCTGGAGAAAGAGGCTTTATGGAGTCCAGGCCAGTGAGGTCGCTGGGCAGGCACCTAAGGAAAGAGAACCTAAACCCAGATCTTTTGCCACTTGGAGCTCATTCCTGGCAGTTGCCAATGGGTCACAGCCTCCTCTTGGCCCAGTGACCCAGCCTCATCTTGGAATTAAGGGTTT... | CCGATGAGGAGAGCGGCCTCTGGTCAGGGGTCGCACAGCCTAGTGGGCCTGGGCCCTGGGAGAGGGGTCGCCCTCCTTCTCTCACCCCACTCCTGATTTTATGCAGGAAGCTTTTTTAATGGAAAAGATGGGGCCCTGCAAGGGGGCTGGAGAAAGAGGCTTTATGGAGTCCAGGCCAGTGAGGTCGCTGGGCAGGCACCTAAGGAAAGAGAACCTAAACCCAGATCTTTTGCCACTTGGAGCTCATTCCTGGCAGTTGCCAATGGGTCACAGCCTCCTCTTGGCCCAGTGACCCAGCCTCATCTTGGAATTAAGGGTTT... |
Task1_train_48426 | A mutation has occurred on Chromosome 22. What is the medical relevance of this mutation? | Benign | TCCCCCTACCCCACAACAGTCCCCGGAGTGTGATGTTCCCCTTCCTGTGTCCGTGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCGGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGTTTCATCCATGTCCCTATGAAGGACATGAGCTCTTCATTTTTTATGGCTGCATAGTATTCCATGGTGTATATGTGCCACATTTTCTTAATCCAGTCTATCGTTGTTGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCTGCAATAAACATACGTGTGCAT... | TCCCCCTACCCCACAACAGTCCCCGGAGTGTGATGTTCCCCTTCCTGTGTCCGTGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCGGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGTTTCATCCATGTCCCTATGAAGGACATGAGCTCTTCATTTTTTATGGCTGCATAGTATTCCATGGTGTATATGTGCCACATTTTCTTAATCCAGTCTATCGTTGTTGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCTGCAATAAACATACGTGTGCAT... |
Task1_train_48427 | This variant is found on Chromosome 22. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCTCCTCCTGGCCCATGCAACACAGGGCTCAGCAGGGGAAACGCCTCTCCTTCGATGTGCACCATGGGCCGATGCCCTGCCCAGCACGCCACAGCCACGCCAACCACTCCCTGTTCCTGGTTCTCCCTTCTGCTCTCACTTTCCAATTCATTAATACCTGGTCCCCCTTTTGCTTTAACTTTTCAATTCATCAATCCGGTCAAGTTCATCTCTGGACTGGAACATGCCCCATAAATTACAGTCCTAAGTTCCAGCAGCTGTTTCCCAAACACACCAGGAGAGACGAGGCAGATCTGGGCCAGGACGGCAGGAGGGCCCCT... | CCTCCTCCTGGCCCATGCAACACAGGGCTCAGCAGGGGAAACGCCTCTCCTTCGATGTGCACCATGGGCCGATGCCCTGCCCAGCACGCCACAGCCACGCCAACCACTCCCTGTTCCTGGTTCTCCCTTCTGCTCTCACTTTCCAATTCATTAATACCTGGTCCCCCTTTTGCTTTAACTTTTCAATTCATCAATCCGGTCAAGTTCATCTCTGGACTGGAACATGCCCCATAAATTACAGTCCTAAGTTCCAGCAGCTGTTTCCCAAACACACCAGGAGAGACGAGGCAGATCTGGGCCAGGACGGCAGGAGGGCCCCT... |
Task1_train_48428 | This sequence change occurs on Chromosome 22. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ACAGAACAATCTGAGGAATTAAAGTCATATTTTTATTGCACCATAAAAACATGTGAAGGCGGCAGGACGGCGGCCGCGGGGCCAGGCGGAGAGCACCCGGCTCTGGCCCCACCCTGCACTCCCTGGGCCGTCTCCAGGGAGACGCAGGATCGAAACCACTGTTGGCCCAGCACACCGGTCCCACGCTGGGCAAGGGAGACCGGGAGAGCGGCCGCTTTGCCCACATTGCCCTGCTGGGCCCTGGTTCCTGCCCTGGCTGTGCAGCTGCCTGGGTGGGGGCTCTGGGCCAGTGTCCCACCAGAGTAGTGAGGTGTGGGGAT... | ACAGAACAATCTGAGGAATTAAAGTCATATTTTTATTGCACCATAAAAACATGTGAAGGCGGCAGGACGGCGGCCGCGGGGCCAGGCGGAGAGCACCCGGCTCTGGCCCCACCCTGCACTCCCTGGGCCGTCTCCAGGGAGACGCAGGATCGAAACCACTGTTGGCCCAGCACACCGGTCCCACGCTGGGCAAGGGAGACCGGGAGAGCGGCCGCTTTGCCCACATTGCCCTGCTGGGCCCTGGTTCCTGCCCTGGCTGTGCAGCTGCCTGGGTGGGGGCTCTGGGCCAGTGTCCCACCAGAGTAGTGAGGTGTGGGGAT... |
Task1_train_48429 | Consider a variant on Chromosome 22. Determine its clinical classification and disease relevance. | Benign | GCCATGCTCTGCAGGACAGACCCTGTCCCACCCAGGCCTGGGACCCCCGTAAACCACAGCAGCAGAGCAGGCATCAGGCAATCCAAGCAGCCAGGCCAGGCACAGCAAACCTGGGTGGACGTAGCTCACCCACAACAAATGGTGGAGGCAAGAATGGGTGAGCAGGAGGCCACCTGGGCTCCCTCAGGCACCCTGGTGTTTGCTTGGCCCTCACTGGAGCAAGGCCGCTGTGGCCACACCGGAGCCGGAGCTGTTGGACAAAGGCTTTCAGCACCCCTGAAGGGCTCGACAGCGTGTCCGGGGCTGCGGCCAAGTAAAAA... | GCCATGCTCTGCAGGACAGACCCTGTCCCACCCAGGCCTGGGACCCCCGTAAACCACAGCAGCAGAGCAGGCATCAGGCAATCCAAGCAGCCAGGCCAGGCACAGCAAACCTGGGTGGACGTAGCTCACCCACAACAAATGGTGGAGGCAAGAATGGGTGAGCAGGAGGCCACCTGGGCTCCCTCAGGCACCCTGGTGTTTGCTTGGCCCTCACTGGAGCAAGGCCGCTGTGGCCACACCGGAGCCGGAGCTGTTGGACAAAGGCTTTCAGCACCCCTGAAGGGCTCGACAGCGTGTCCGGGGCTGCGGCCAAGTAAAAA... |
Task1_train_48430 | This variant is found on Chromosome 22. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTGTGACCTGAACCCCTGGGCTTCTGCCTCAGGCCTCCTGTGCTCTGCTCTCTGCCTGCTGGGTCCCCTCACCAGGCTTCTGTCTGGTTCCCAGGCTACCTGCCTGGAGGGTCACACCAGGAGGATTTCAAACAGGTTTCAAGTGGGGTCACTTGCCATCACTGTGCCCCACGAGGTACACTGTTGTGGGCGGCAGGGCTGGCCTTTCTCATCTGGGACATGCCACGTTGCTGTTCCCAAGGGGAGTGGTGAGTGGGTCTGTCCTGGTGTGCCTGGCCTGGGGACTGCCAGTGTCCTTACTTGGACACTCAATGAAAAGG... | CTGTGACCTGAACCCCTGGGCTTCTGCCTCAGGCCTCCTGTGCTCTGCTCTCTGCCTGCTGGGTCCCCTCACCAGGCTTCTGTCTGGTTCCCAGGCTACCTGCCTGGAGGGTCACACCAGGAGGATTTCAAACAGGTTTCAAGTGGGGTCACTTGCCATCACTGTGCCCCACGAGGTACACTGTTGTGGGCGGCAGGGCTGGCCTTTCTCATCTGGGACATGCCACGTTGCTGTTCCCAAGGGGAGTGGTGAGTGGGTCTGTCCTGGTGTGCCTGGCCTGGGGACTGCCAGTGTCCTTACTTGGACACTCAATGAAAAGG... |
Task1_train_48431 | Chromosome 22 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TCTACCCGAGGGCACCAGAGGGCACGAGAAGGCTGGCTCCCTGGCGCTGACACGTCAGGCAACTGAGGCACAAGGCTGGCATTTCTGAACCTTGCCCCTCTGCAAACACAAGGGGGCGATGGTGGCACTCCAAGCAAAGGGGCGTGTGGGTGCTGCAGGAGGAGCACAGAGCACTGGCGCCCCTCCCCTCCCGCCCTGCAGATGCCGGAGGCCCCGCCTCTGCTGTTGGCAGCTGTGTTGCTGGGCCTGGTGCTGCTGGTGGTGCTGCTGCTGCTTCTGAGGCACTGGGGCTGGGGCCTGTGCCTTATCGGCTGGAACGA... | TCTACCCGAGGGCACCAGAGGGCACGAGAAGGCTGGCTCCCTGGCGCTGACACGTCAGGCAACTGAGGCACAAGGCTGGCATTTCTGAACCTTGCCCCTCTGCAAACACAAGGGGGCGATGGTGGCACTCCAAGCAAAGGGGCGTGTGGGTGCTGCAGGAGGAGCACAGAGCACTGGCGCCCCTCCCCTCCCGCCCTGCAGATGCCGGAGGCCCCGCCTCTGCTGTTGGCAGCTGTGTTGCTGGGCCTGGTGCTGCTGGTGGTGCTGCTGCTGCTTCTGAGGCACTGGGGCTGGGGCCTGTGCCTTATCGGCTGGAACGA... |
Task1_train_48432 | This sequence change occurs on Chromosome 22. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTACGGCAGGAGGAGCGCTTGAGGCCAGGAGAGTTCGAGACCAGCCTGGGCAACATGGCAAAAGAAAAAATATATATATATATTTTAGATGGAGTCTTGCTCTGTCACCAGGCTGGAGTGCAGTGGCACGATCACGGCTCACTGCAACCTCCACCTCTTGGGTTCAAGCGATTACCCTGCCTTAGCCTCCTGAGTAGCTGGGACTACAGGCGCGCGCTGCCACACCCGGCTAGTTTTTTGTAGTTTAGTAGAGATGGGGTTTCACCACATTGGCCAGGATGGTCTCAATATCCTGACTTCGTGATCCGCCCGCCTCGGCC... | CTACGGCAGGAGGAGCGCTTGAGGCCAGGAGAGTTCGAGACCAGCCTGGGCAACATGGCAAAAGAAAAAATATATATATATATTTTAGATGGAGTCTTGCTCTGTCACCAGGCTGGAGTGCAGTGGCACGATCACGGCTCACTGCAACCTCCACCTCTTGGGTTCAAGCGATTACCCTGCCTTAGCCTCCTGAGTAGCTGGGACTACAGGCGCGCGCTGCCACACCCGGCTAGTTTTTTGTAGTTTAGTAGAGATGGGGTTTCACCACATTGGCCAGGATGGTCTCAATATCCTGACTTCGTGATCCGCCCGCCTCGGCC... |
Task1_train_48433 | Chromosome 22 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGCTGCTTTAATTTTTAAATTTTCTTACAAAAATTTAGGTGTTTACCAATAGTCTTATTTTGGCTTATTTTTAATGCTTTTTCTCAGTGTTTTTCTTCTGTTTCTGAGTCACGAACAGCAGGCACTGAAAGCAGTCCCCCAGCCACTGCCGAAGGTCAGTCCCGGAGGTGCTGCCCAGGCTCCAGGCAGATGCGGCAGCCCCGGCCCCAGCCAGCATGGGCTGGAGAAAGGCTCTCTACTGCACAGGGGCCTCACGTGACTGCAGGGCTCTGGGGAGGTGGGGCACCTGTAGCCTGACCCCCACCTTGCTGCTTCCAAAG... | TGCTGCTTTAATTTTTAAATTTTCTTACAAAAATTTAGGTGTTTACCAATAGTCTTATTTTGGCTTATTTTTAATGCTTTTTCTCAGTGTTTTTCTTCTGTTTCTGAGTCACGAACAGCAGGCACTGAAAGCAGTCCCCCAGCCACTGCCGAAGGTCAGTCCCGGAGGTGCTGCCCAGGCTCCAGGCAGATGCGGCAGCCCCGGCCCCAGCCAGCATGGGCTGGAGAAAGGCTCTCTACTGCACAGGGGCCTCACGTGACTGCAGGGCTCTGGGGAGGTGGGGCACCTGTAGCCTGACCCCCACCTTGCTGCTTCCAAAG... |
Task1_train_48434 | This mutation is located on Chromosome 22. Is it associated with a disease or is it a benign polymorphism? | Benign | CAGCTCTCACAAGGCACAAGCCCCACCACTGCACGGTTGGGGTGGGAACCAAGGAGGTGGGTCCCAGGAGAGTTTCTGTGGGGGCAGGAGGTGTGAAGGCAGGAGGTGAGGGGACATGCCCGAGGGGCGCAGCGTCAGCCTCCCTGCTATGGTAGAGACTGGGGAACCTGTCACAGTGTCTGGGCCTGATGCCTGGCTCCTGGGGCAAGCGTCTCAGCAGCTGCACTCCTGCCTACCGGGTGCTTTCCCAGGCGGTCGCAGGCCGAGTGGCCTCGTTCCTCCCGGGTTGAGCCTCACACTCTTCTCTTCCCAGGGGATGT... | CAGCTCTCACAAGGCACAAGCCCCACCACTGCACGGTTGGGGTGGGAACCAAGGAGGTGGGTCCCAGGAGAGTTTCTGTGGGGGCAGGAGGTGTGAAGGCAGGAGGTGAGGGGACATGCCCGAGGGGCGCAGCGTCAGCCTCCCTGCTATGGTAGAGACTGGGGAACCTGTCACAGTGTCTGGGCCTGATGCCTGGCTCCTGGGGCAAGCGTCTCAGCAGCTGCACTCCTGCCTACCGGGTGCTTTCCCAGGCGGTCGCAGGCCGAGTGGCCTCGTTCCTCCCGGGTTGAGCCTCACACTCTTCTCTTCCCAGGGGATGT... |
Task1_train_48435 | This variant is found on Chromosome 22. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCTCAGTCTGGCCTGATTTCATGGTCCCCAGCTGTACCCCGTGTTAGGTGGGTGGCAGGTGGCAATTTGCCCTGACATGGCACAGCAGGGCCTCTGCATGGCCCGCTGATTGCTCCTCACAGGCACCTACGGGCTGAGCAACGCGCTGCTGGAGACTCCCTGGAGGAAGCTGTGCTTTGGGAAGCAGCTCTTCCTGGAGGCTGTGGAACGGAGCCAGGCGCTGCCCAAGGATGTGCTCATCGCCAGCCTCCTGGATGTGCTCAACAATGAAGAGGCGTGAGTGGGCGGGTCCTGCTGGGGTGAGCCCCAGTGTCCCGCCA... | CCTCAGTCTGGCCTGATTTCATGGTCCCCAGCTGTACCCCGTGTTAGGTGGGTGGCAGGTGGCAATTTGCCCTGACATGGCACAGCAGGGCCTCTGCATGGCCCGCTGATTGCTCCTCACAGGCACCTACGGGCTGAGCAACGCGCTGCTGGAGACTCCCTGGAGGAAGCTGTGCTTTGGGAAGCAGCTCTTCCTGGAGGCTGTGGAACGGAGCCAGGCGCTGCCCAAGGATGTGCTCATCGCCAGCCTCCTGGATGTGCTCAACAATGAAGAGGCGTGAGTGGGCGGGTCCTGCTGGGGTGAGCCCCAGTGTCCCGCCA... |
Task1_train_48436 | Located on Chromosome 22, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GAGGGAGTGGCTGCTGTCTGGTGTGCAGGGGTCGGTGGGTTCCTCAGGGGCATTTCTGCCGACTTGGGCTGAGTCAGAGGCTTGGGAAGAGGGGGCGGCCGATGGTCTGTGGCTGGGAAGTGTGAGGGTCTCTCGCCTTGGGTCTGTGTCAGTTCTGGCAGTGACAGGGTGTTTGGGGGAAAGACTTGGGTCTGCCGCTACCCACAGGGGACTCTCAGGAACCCGAGAGCTTGGGGAGATGAAATGGGGGTGCATAGGGGCCACCTGTTGGCTCAGGGCCCTGTGGGGGCCGCTGAACCTGCTGGAACTCTCCTGCCTGC... | GAGGGAGTGGCTGCTGTCTGGTGTGCAGGGGTCGGTGGGTTCCTCAGGGGCATTTCTGCCGACTTGGGCTGAGTCAGAGGCTTGGGAAGAGGGGGCGGCCGATGGTCTGTGGCTGGGAAGTGTGAGGGTCTCTCGCCTTGGGTCTGTGTCAGTTCTGGCAGTGACAGGGTGTTTGGGGGAAAGACTTGGGTCTGCCGCTACCCACAGGGGACTCTCAGGAACCCGAGAGCTTGGGGAGATGAAATGGGGGTGCATAGGGGCCACCTGTTGGCTCAGGGCCCTGTGGGGGCCGCTGAACCTGCTGGAACTCTCCTGCCTGC... |
Task1_train_48437 | Here’s a variant located on Chromosome 22. What is the predicted biological effect — harmless or disease-causing? | Benign | TGGCAGTGACAGGGTGTTTGGGGGAAAGACTTGGGTCTGCCGCTACCCACAGGGGACTCTCAGGAACCCGAGAGCTTGGGGAGATGAAATGGGGGTGCATAGGGGCCACCTGTTGGCTCAGGGCCCTGTGGGGGCCGCTGAACCTGCTGGAACTCTCCTGCCTGCCACATGCCAGGGGCAGGGCTGAGGGAGTGTGAGGGATGCACAGCTGTTCAGGGCTGAGACATTCTGGGCTGGGGCTGTCCCAGCGTGGGAGGCGTGCGGGCTGTAGGGCCCCGAAGCTGACCTCCACCTTTCTGCTTCTCTCTCACGGACGCCGC... | TGGCAGTGACAGGGTGTTTGGGGGAAAGACTTGGGTCTGCCGCTACCCACAGGGGACTCTCAGGAACCCGAGAGCTTGGGGAGATGAAATGGGGGTGCATAGGGGCCACCTGTTGGCTCAGGGCCCTGTGGGGGCCGCTGAACCTGCTGGAACTCTCCTGCCTGCCACATGCCAGGGGCAGGGCTGAGGGAGTGTGAGGGATGCACAGCTGTTCAGGGCTGAGACATTCTGGGCTGGGGCTGTCCCAGCGTGGGAGGCGTGCGGGCTGTAGGGCCCCGAAGCTGACCTCCACCTTTCTGCTTCTCTCTCACGGACGCCGC... |
Task1_train_48438 | Consider a variant on Chromosome 22. Determine its clinical classification and disease relevance. | Benign | CTGAACACATACCTGAACCAGAAAGCAAGAAAGTGCTCACAGAATGATGGGGCGGCATCTAAAGGTGCCTGGAGCGCCCCCAACTGGCCACACATGGCACAGTCTGGGCATTAAGGAATAATGAGCCATGCGCTTGGGATTAGTAAACTACATACATCTTACAGCTCAATAAAAAATTTTAAAAAGACAATCGCCCAGACATTTAGGGGAAGAAGTAATGCCAATTCTACACAAACTCTTCTGGAAAACTGAAGAGGAGAGAACACTTCGAAACTCATCCTATAAGGCTGGCAAAAACCCTGATACCCAAACCAGATATT... | CTGAACACATACCTGAACCAGAAAGCAAGAAAGTGCTCACAGAATGATGGGGCGGCATCTAAAGGTGCCTGGAGCGCCCCCAACTGGCCACACATGGCACAGTCTGGGCATTAAGGAATAATGAGCCATGCGCTTGGGATTAGTAAACTACATACATCTTACAGCTCAATAAAAAATTTTAAAAAGACAATCGCCCAGACATTTAGGGGAAGAAGTAATGCCAATTCTACACAAACTCTTCTGGAAAACTGAAGAGGAGAGAACACTTCGAAACTCATCCTATAAGGCTGGCAAAAACCCTGATACCCAAACCAGATATT... |
Task1_train_48439 | Chromosome 22 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTGCTAATGATACCGACAAGGCACGCTAACGCGGACACTGTACACGACATCGCTAATGAGGACACCGTATAAGACATCGCTAGTAACTATCGCAAGAACAAAAAACCAAACACTGCATATTCTCACTCATAGGTGGGAATTGAACAATGAGATCACATGGACACAGGAAGGGGAATATCACACTCTGGGGACTGTTGTGGGGTGGGGGGGGGAGGGATAGCATCGGGAGATATACCTAATGCTAGATGACGAGTTAGTGCGTGCAGCACACCAGCATGGCACATGTATACATATGTAACTAGCCTGCACAATGTGCACAT... | TTGCTAATGATACCGACAAGGCACGCTAACGCGGACACTGTACACGACATCGCTAATGAGGACACCGTATAAGACATCGCTAGTAACTATCGCAAGAACAAAAAACCAAACACTGCATATTCTCACTCATAGGTGGGAATTGAACAATGAGATCACATGGACACAGGAAGGGGAATATCACACTCTGGGGACTGTTGTGGGGTGGGGGGGGGAGGGATAGCATCGGGAGATATACCTAATGCTAGATGACGAGTTAGTGCGTGCAGCACACCAGCATGGCACATGTATACATATGTAACTAGCCTGCACAATGTGCACAT... |
Task1_train_48440 | A variant affecting Chromosome 22 has been observed. Determine if it's benign or associated with disease. | Benign | CCAGCTGGCTCCAGGGAAGCAGTATGGCCCAGAGGCAGGGATCCCACATTCCACGTGCTGCCTGTTTGTGTCCTGCCAGCTGCTCTGGACGGCCGACCCAGGGCAGGACGCAGTCTCCACTCAGATGGCTGGGCCTTCTGAGATGGGTGACCCCTCTAAGATGGGTGACCAAAGTTGACCTCCGTGGGGCATCTGGTCAGAGGATGAGAGTGTGCCCAGGACGAGAGCCCCAAGTTGCCAGCGTGAGACCAATGAGTGCTGTGTGGCGGCTGCAGGGTGATCAGAAGATCCTGGCAGCAGGGGAAGACTTTGAGCTGGGC... | CCAGCTGGCTCCAGGGAAGCAGTATGGCCCAGAGGCAGGGATCCCACATTCCACGTGCTGCCTGTTTGTGTCCTGCCAGCTGCTCTGGACGGCCGACCCAGGGCAGGACGCAGTCTCCACTCAGATGGCTGGGCCTTCTGAGATGGGTGACCCCTCTAAGATGGGTGACCAAAGTTGACCTCCGTGGGGCATCTGGTCAGAGGATGAGAGTGTGCCCAGGACGAGAGCCCCAAGTTGCCAGCGTGAGACCAATGAGTGCTGTGTGGCGGCTGCAGGGTGATCAGAAGATCCTGGCAGCAGGGGAAGACTTTGAGCTGGGC... |
Task1_train_48441 | A genomic variant on Chromosome 22 is under review. What is the biological outcome — benign or pathogenic? | Benign | CTGGAGAATGGGTAGAGGTGAACCCAGAAAAGAAACATGGGCACAACATGTGTTAAGGTGCAAGGCAAGTGTGTGCATCCAGGGAGCTGGAAAAGGTTGGGCTGACGTGTTGAGAAAAGGCCAGAAAGGTGGGAGACGGGGCTGAAGAAGACACCTGGCTGGGACAGGCCACCAAGGCCTCCAAGCTCTGTTTTAGGCCCTGCCTTGTGCGAATAAGGAAGCCTTGGAGCACTTCTGAGCCCAAATGCGCAGTGGCAGGGCTGCCCTTTGGCTCAGCCCATCTCAGCAAGCTGCACCCTAGGCCTGGCCTCCAGAGATGC... | CTGGAGAATGGGTAGAGGTGAACCCAGAAAAGAAACATGGGCACAACATGTGTTAAGGTGCAAGGCAAGTGTGTGCATCCAGGGAGCTGGAAAAGGTTGGGCTGACGTGTTGAGAAAAGGCCAGAAAGGTGGGAGACGGGGCTGAAGAAGACACCTGGCTGGGACAGGCCACCAAGGCCTCCAAGCTCTGTTTTAGGCCCTGCCTTGTGCGAATAAGGAAGCCTTGGAGCACTTCTGAGCCCAAATGCGCAGTGGCAGGGCTGCCCTTTGGCTCAGCCCATCTCAGCAAGCTGCACCCTAGGCCTGGCCTCCAGAGATGC... |
Task1_train_48442 | This genomic variant is located on Chromosome 22. Can you determine its pathogenicity and name any linked disease? | Benign | TCGGTGCGGCGCCTTCTTCCTCCCAAGCGAAAGCTCCCTGCGGGGGCGGGGTCTGAGCGGAGGGGCGGGGCCGGGGCGGGGCCCAGGGGCGATTAGATCTCGGCCGGAGCCAAGCACAGAAGGGGCGGGGCCACGTCCGGGGCAGGGGCGCGGAAGGGTTGGATCTGGGTCCGGTGGCACCCAGAGGGTGCGGCCTGAACCCAGGCGAAAGCGGGGCAGTATCTGGGCTCACCGGCGCGTAGGGTCCTTGCCGCGGCAAGCGCAGCAGCAGCCGAGCAGCGAGAGCAGCAGGCAGACGAGCAGGACGAGCAGCGCGCCCG... | TCGGTGCGGCGCCTTCTTCCTCCCAAGCGAAAGCTCCCTGCGGGGGCGGGGTCTGAGCGGAGGGGCGGGGCCGGGGCGGGGCCCAGGGGCGATTAGATCTCGGCCGGAGCCAAGCACAGAAGGGGCGGGGCCACGTCCGGGGCAGGGGCGCGGAAGGGTTGGATCTGGGTCCGGTGGCACCCAGAGGGTGCGGCCTGAACCCAGGCGAAAGCGGGGCAGTATCTGGGCTCACCGGCGCGTAGGGTCCTTGCCGCGGCAAGCGCAGCAGCAGCCGAGCAGCGAGAGCAGCAGGCAGACGAGCAGGACGAGCAGCGCGCCCG... |
Task1_train_48443 | A genetic alteration is present on Chromosome 22. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TAAAAACTTTAAAAGTATGTGTGGTAACTGTAGAACCCAGAAAGTGGAGAGGAACAGAAGTAAGAGAACCATTCCATGAGAGAGAAGGTCTGGTGTCCTTTCTGGTTGTTTCCCATAGTCAAGGTCATGCTATCCTGGGGTTTTTTGTGCAGCATCTTCCACATCAATAGGGGATGAAATGTTCTCCTTTAATTAGAAAGCCCTGGTCGGCACGAAGGAACTCTTGTCATACCCCTCTGTGAATGTCTCTTGCCATCCTCAGTTACCATCTTGTTCTTGGACCTTGTAATAATTTCCGATTTTTTGCTATTACCAGTGAC... | TAAAAACTTTAAAAGTATGTGTGGTAACTGTAGAACCCAGAAAGTGGAGAGGAACAGAAGTAAGAGAACCATTCCATGAGAGAGAAGGTCTGGTGTCCTTTCTGGTTGTTTCCCATAGTCAAGGTCATGCTATCCTGGGGTTTTTTGTGCAGCATCTTCCACATCAATAGGGGATGAAATGTTCTCCTTTAATTAGAAAGCCCTGGTCGGCACGAAGGAACTCTTGTCATACCCCTCTGTGAATGTCTCTTGCCATCCTCAGTTACCATCTTGTTCTTGGACCTTGTAATAATTTCCGATTTTTTGCTATTACCAGTGAC... |
Task1_train_48444 | A change on Chromosome 22 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ACATAAGGTATAGAAAATGGAATGAAAGCCCCACCCATAACCCCCCACCTGATACGATGGCCTCAGTGTGGCTCTGTGCTCTGCATCCTCCCTGCTGGGCTGGGGTCAAGGAACTGACCTTTTCTTTGCCCCTGTGCCCTGCTATGCCTGGGCCTGAGCTGAGGGCTGGGACTTGGGGCTGGGGAGGGGACCTGGCCAGCGTGGAGGATTTAGCAGAGCATGAGATGATGGATGGGCTGGGCAGCCAGGAGAGGCAACTCCTGAGCCTTGTCTGGGTAGATAGGAAGGATGGCAGCCCCAGCCCAGGGGACAGCTCAGGC... | ACATAAGGTATAGAAAATGGAATGAAAGCCCCACCCATAACCCCCCACCTGATACGATGGCCTCAGTGTGGCTCTGTGCTCTGCATCCTCCCTGCTGGGCTGGGGTCAAGGAACTGACCTTTTCTTTGCCCCTGTGCCCTGCTATGCCTGGGCCTGAGCTGAGGGCTGGGACTTGGGGCTGGGGAGGGGACCTGGCCAGCGTGGAGGATTTAGCAGAGCATGAGATGATGGATGGGCTGGGCAGCCAGGAGAGGCAACTCCTGAGCCTTGTCTGGGTAGATAGGAAGGATGGCAGCCCCAGCCCAGGGGACAGCTCAGGC... |
Task1_train_48445 | Mutation context: Chromosome 22. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GCAGGACTGGCGACATGTCCTGGCTTACGGGGAAAGGATCCTGAGCTCACATGCAGTAGACTTGGGCAGGCAAAGGGGGCACCAAGGGCACAGGCCAAGCCTTGGGGGCAGGTGCCAATCTCCAGTCCCAGGATCCCCCAGGGCAGAACCTGAGCCCTCCCAGTGCTTGCCTTCAGCCACCTGGCTCCCCTCCTGGGAGGCCTCTGCTGGATCCAGAAGATGCTCAACCCTCAAGGCCTCTGCTGCCACTGACAGCTGGCACTGGAGGCAGGACAAGCCCTGCCTCTTCTCCCTCTATTGGGACTGGTCCCCTGAAGAAC... | GCAGGACTGGCGACATGTCCTGGCTTACGGGGAAAGGATCCTGAGCTCACATGCAGTAGACTTGGGCAGGCAAAGGGGGCACCAAGGGCACAGGCCAAGCCTTGGGGGCAGGTGCCAATCTCCAGTCCCAGGATCCCCCAGGGCAGAACCTGAGCCCTCCCAGTGCTTGCCTTCAGCCACCTGGCTCCCCTCCTGGGAGGCCTCTGCTGGATCCAGAAGATGCTCAACCCTCAAGGCCTCTGCTGCCACTGACAGCTGGCACTGGAGGCAGGACAAGCCCTGCCTCTTCTCCCTCTATTGGGACTGGTCCCCTGAAGAAC... |
Task1_train_48446 | Given this context: Chromosome 22 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGCCAGTGTGAGGACGCAGGTCCAGGCAGAGTGGAGACGGCAGAGCTCTGCTGAGGCCTGGGGCCCAGCCGAAGGCAAGAGAGGCAGGGGAGCCCTTTCCTGCTGTGGAGCCGGCCGTGGACAGTTGCAGGTGCTGAGGCTGGAGCCAGGCTGTATTTTCAGGGTGGGGTAGCGGCTGCTTCCTCTCCTCAGCCAGGCCCACCTGCCTCCTGGGCCCTGAGGGTCAGCATGGGCCAGGTGGGGACCTCAGGGTCGGCCTGCACAGCCACACTGGGGCCACCCTGCTGTCTGCAACATCTAGTCTCACTGGGCCCCTCTTG... | GGCCAGTGTGAGGACGCAGGTCCAGGCAGAGTGGAGACGGCAGAGCTCTGCTGAGGCCTGGGGCCCAGCCGAAGGCAAGAGAGGCAGGGGAGCCCTTTCCTGCTGTGGAGCCGGCCGTGGACAGTTGCAGGTGCTGAGGCTGGAGCCAGGCTGTATTTTCAGGGTGGGGTAGCGGCTGCTTCCTCTCCTCAGCCAGGCCCACCTGCCTCCTGGGCCCTGAGGGTCAGCATGGGCCAGGTGGGGACCTCAGGGTCGGCCTGCACAGCCACACTGGGGCCACCCTGCTGTCTGCAACATCTAGTCTCACTGGGCCCCTCTTG... |
Task1_train_48447 | Here is a mutation located on Chromosome 22. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GCCAGTGTGAGGACGCAGGTCCAGGCAGAGTGGAGACGGCAGAGCTCTGCTGAGGCCTGGGGCCCAGCCGAAGGCAAGAGAGGCAGGGGAGCCCTTTCCTGCTGTGGAGCCGGCCGTGGACAGTTGCAGGTGCTGAGGCTGGAGCCAGGCTGTATTTTCAGGGTGGGGTAGCGGCTGCTTCCTCTCCTCAGCCAGGCCCACCTGCCTCCTGGGCCCTGAGGGTCAGCATGGGCCAGGTGGGGACCTCAGGGTCGGCCTGCACAGCCACACTGGGGCCACCCTGCTGTCTGCAACATCTAGTCTCACTGGGCCCCTCTTGC... | GCCAGTGTGAGGACGCAGGTCCAGGCAGAGTGGAGACGGCAGAGCTCTGCTGAGGCCTGGGGCCCAGCCGAAGGCAAGAGAGGCAGGGGAGCCCTTTCCTGCTGTGGAGCCGGCCGTGGACAGTTGCAGGTGCTGAGGCTGGAGCCAGGCTGTATTTTCAGGGTGGGGTAGCGGCTGCTTCCTCTCCTCAGCCAGGCCCACCTGCCTCCTGGGCCCTGAGGGTCAGCATGGGCCAGGTGGGGACCTCAGGGTCGGCCTGCACAGCCACACTGGGGCCACCCTGCTGTCTGCAACATCTAGTCTCACTGGGCCCCTCTTGC... |
Task1_train_48448 | A mutation has occurred on Chromosome 22. What is the medical relevance of this mutation? | Benign | TCCTGATGCCGCCAGGAGCGCCGAGGAGAGGGCAGGGGGCTGGAGACGCCCCGCAGAGGGCTACGTGCCCTGCTGGACAGAGGTCTCCTGCCTCCTCGGCGGCGCCAGCCCACCTCCCACAACCCCTGCGGGAGAAGCCCCCAAGGGGAGGAGACGGGCCTGGCCCCTGCCCCGAGCACCTTCCGTCTCTAGGTCGGAGTCTGAATCGGCCTTGGGACCCTGCTTGGCTTCGGGGACCCCTGCAAGACGTCCACAGGCCGCCGTCGCCTCTTCCTCCTGCTTTTTATCCTCCCCAGACCTCTGGCAGGAACCGCTCATCG... | TCCTGATGCCGCCAGGAGCGCCGAGGAGAGGGCAGGGGGCTGGAGACGCCCCGCAGAGGGCTACGTGCCCTGCTGGACAGAGGTCTCCTGCCTCCTCGGCGGCGCCAGCCCACCTCCCACAACCCCTGCGGGAGAAGCCCCCAAGGGGAGGAGACGGGCCTGGCCCCTGCCCCGAGCACCTTCCGTCTCTAGGTCGGAGTCTGAATCGGCCTTGGGACCCTGCTTGGCTTCGGGGACCCCTGCAAGACGTCCACAGGCCGCCGTCGCCTCTTCCTCCTGCTTTTTATCCTCCCCAGACCTCTGGCAGGAACCGCTCATCG... |
Task1_train_48449 | This sequence change occurs on Chromosome 22. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CACGTGGGCTCAGAGGCAGGGTGCTCAGTTTCCTGCACATTGGGATGCACCACTTGGGCTGCTGGGCATAGGTGGATGAGGGTATGGGAAGACGTGGGGGCCCCACTGGTGGTCACTGTGGGGTCTAGTTGGAGGAGACGGTAGCCCAGCTGGGGTGAAGAGGAGAGGCAGACACAGGACATAGGTAGGGACAAAGAAGCAGAGCATGTGGCTCTGCTCCGACCTCCACCCAATCACGACGGCCCTGTCTTTCAGAAAGTCCCACCGCCTCATTCTGGCTTCTCAGAGGCCCTCAGCCTTCCTTGCGCCCCTGGTGCTGG... | CACGTGGGCTCAGAGGCAGGGTGCTCAGTTTCCTGCACATTGGGATGCACCACTTGGGCTGCTGGGCATAGGTGGATGAGGGTATGGGAAGACGTGGGGGCCCCACTGGTGGTCACTGTGGGGTCTAGTTGGAGGAGACGGTAGCCCAGCTGGGGTGAAGAGGAGAGGCAGACACAGGACATAGGTAGGGACAAAGAAGCAGAGCATGTGGCTCTGCTCCGACCTCCACCCAATCACGACGGCCCTGTCTTTCAGAAAGTCCCACCGCCTCATTCTGGCTTCTCAGAGGCCCTCAGCCTTCCTTGCGCCCCTGGTGCTGG... |
Task1_train_48450 | Consider this mutation on Chromosome 22. Is this a benign change or a disease-causing variant? | Benign | CCCTTGAAGAGTGGGCAAAGACAGCAAGAGAGCTGCAGCCTGGGCCCGAGCTCAGAAACAGCTGTCGCCTCAGTCTGCGCACAGGCATGCACCCCAGGGTAGTGCCTGCAGGGATGCATGTGTCCCCGTGGGGGTGCCTGTGCCAGGCAGGCCTCAGGTGCATGCCATGCTCAGAACCCTGCTGCCCTTTCTAGGCAGCCTCCTTGGGGCCCAAGCTCTGCTCCCTGGATCTGCCACCTAGCAGACGTGGGGAGCCTGACCCCATGCCTGTCATGGAACCCTCCTTGCCTGGTGTGTGTGGCTCCCCTCTTCACTGGGCA... | CCCTTGAAGAGTGGGCAAAGACAGCAAGAGAGCTGCAGCCTGGGCCCGAGCTCAGAAACAGCTGTCGCCTCAGTCTGCGCACAGGCATGCACCCCAGGGTAGTGCCTGCAGGGATGCATGTGTCCCCGTGGGGGTGCCTGTGCCAGGCAGGCCTCAGGTGCATGCCATGCTCAGAACCCTGCTGCCCTTTCTAGGCAGCCTCCTTGGGGCCCAAGCTCTGCTCCCTGGATCTGCCACCTAGCAGACGTGGGGAGCCTGACCCCATGCCTGTCATGGAACCCTCCTTGCCTGGTGTGTGTGGCTCCCCTCTTCACTGGGCA... |
Task1_train_48451 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | CCCCGGGCCTTGCCTGGCTCCTCCCGCAGGCGCTGCCCCTCTCCCACCCCGTTTTGATCTCTTTGCCCTGCACCCTCAGATGACCCTGTTCCACAGCGTGCCCCAGGCTGGACCCTCCCACTTTCACCCCATACCGCTCACGGGTAACTTCCGCCCACAGCAGCCTCTTTTTTTTTTTGAGACGGGGTCTTGCTGTGTCGCCCAGGCTGGAGTGCAGTGTTGGAATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCCGCCATCACGCC... | CCCCGGGCCTTGCCTGGCTCCTCCCGCAGGCGCTGCCCCTCTCCCACCCCGTTTTGATCTCTTTGCCCTGCACCCTCAGATGACCCTGTTCCACAGCGTGCCCCAGGCTGGACCCTCCCACTTTCACCCCATACCGCTCACGGGTAACTTCCGCCCACAGCAGCCTCTTTTTTTTTTTGAGACGGGGTCTTGCTGTGTCGCCCAGGCTGGAGTGCAGTGTTGGAATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCCGCCATCACGCC... |
Task1_train_48452 | An alteration has been detected on Chromosome 22. Is it pathogenic, and if so, what disease is involved? | Benign | GCTGCTGTCGACTCTGCTCATCCCTCCTTCCCTCCCTGAGTGACAGTAGCCACTCATATAGCATCTGTGCAGACCCCCAGGTCTCTCCTGCCCACCCACACCTCTCCTGAGCCTAAAGCTGCACAACCAGCTGCCTCCTCCTCTCAGAACACTTCCATAACAGAAGCCCCTCAAGGGAGCTACGTCTGTATCCCCGGCTAACTTCAGGCCACCCCTCTCCCAGCCTTAGCCAGCAGCCTGCAGGAGTGTGGCCAGATCTCAGCAGGCTGAGGCGAGGAGGTGGAGGCTAGGCAGCAGGAGGAGCAACTGTACAGTGATTC... | GCTGCTGTCGACTCTGCTCATCCCTCCTTCCCTCCCTGAGTGACAGTAGCCACTCATATAGCATCTGTGCAGACCCCCAGGTCTCTCCTGCCCACCCACACCTCTCCTGAGCCTAAAGCTGCACAACCAGCTGCCTCCTCCTCTCAGAACACTTCCATAACAGAAGCCCCTCAAGGGAGCTACGTCTGTATCCCCGGCTAACTTCAGGCCACCCCTCTCCCAGCCTTAGCCAGCAGCCTGCAGGAGTGTGGCCAGATCTCAGCAGGCTGAGGCGAGGAGGTGGAGGCTAGGCAGCAGGAGGAGCAACTGTACAGTGATTC... |
Task1_train_48453 | A mutation located on Chromosome 22 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TATTGGAAGAACACTCAAGCCCATTTACAGTGTGGGACTAATGCTGAGAGGTTGAGTCACATTGGCAGGAAAGAGCAGAGCCAGGAACTGAAGCTAGGTCTGTGACTTAGAGCCGGCACTCTTTCCACTGCAGAGGGGAGAGGTCTCAAGGCAGAACCTGGGGCTGTGCACACCGCGGGAAGGGCAGAGGCCCCTGGAAACGAACAGGAGCAGGAGGCCCAGGGCTGCGCAGCAACCAAGGAGGACACGAGGAAGGTGCTTGTGCCACCGGTGGAAGACGTGGCTTTGGCTTTTAGGCTCCCCTCGGGGCAGGAGCAGAT... | TATTGGAAGAACACTCAAGCCCATTTACAGTGTGGGACTAATGCTGAGAGGTTGAGTCACATTGGCAGGAAAGAGCAGAGCCAGGAACTGAAGCTAGGTCTGTGACTTAGAGCCGGCACTCTTTCCACTGCAGAGGGGAGAGGTCTCAAGGCAGAACCTGGGGCTGTGCACACCGCGGGAAGGGCAGAGGCCCCTGGAAACGAACAGGAGCAGGAGGCCCAGGGCTGCGCAGCAACCAAGGAGGACACGAGGAAGGTGCTTGTGCCACCGGTGGAAGACGTGGCTTTGGCTTTTAGGCTCCCCTCGGGGCAGGAGCAGAT... |
Task1_train_48454 | Consider this mutation on Chromosome 22. Is this a benign change or a disease-causing variant? | Benign | CAGAGCCAGGAACTGAAGCTAGGTCTGTGACTTAGAGCCGGCACTCTTTCCACTGCAGAGGGGAGAGGTCTCAAGGCAGAACCTGGGGCTGTGCACACCGCGGGAAGGGCAGAGGCCCCTGGAAACGAACAGGAGCAGGAGGCCCAGGGCTGCGCAGCAACCAAGGAGGACACGAGGAAGGTGCTTGTGCCACCGGTGGAAGACGTGGCTTTGGCTTTTAGGCTCCCCTCGGGGCAGGAGCAGATCAAAGAGCCTAGCCCCAGCTTCGGTGGTGGGTGGGGGGTCCTCCCGGCAGCGGGGAGCGTGGGCACCAGCATCCT... | CAGAGCCAGGAACTGAAGCTAGGTCTGTGACTTAGAGCCGGCACTCTTTCCACTGCAGAGGGGAGAGGTCTCAAGGCAGAACCTGGGGCTGTGCACACCGCGGGAAGGGCAGAGGCCCCTGGAAACGAACAGGAGCAGGAGGCCCAGGGCTGCGCAGCAACCAAGGAGGACACGAGGAAGGTGCTTGTGCCACCGGTGGAAGACGTGGCTTTGGCTTTTAGGCTCCCCTCGGGGCAGGAGCAGATCAAAGAGCCTAGCCCCAGCTTCGGTGGTGGGTGGGGGGTCCTCCCGGCAGCGGGGAGCGTGGGCACCAGCATCCT... |
Task1_train_48455 | A variant on Chromosome 22 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AGCCAGGAACTGAAGCTAGGTCTGTGACTTAGAGCCGGCACTCTTTCCACTGCAGAGGGGAGAGGTCTCAAGGCAGAACCTGGGGCTGTGCACACCGCGGGAAGGGCAGAGGCCCCTGGAAACGAACAGGAGCAGGAGGCCCAGGGCTGCGCAGCAACCAAGGAGGACACGAGGAAGGTGCTTGTGCCACCGGTGGAAGACGTGGCTTTGGCTTTTAGGCTCCCCTCGGGGCAGGAGCAGATCAAAGAGCCTAGCCCCAGCTTCGGTGGTGGGTGGGGGGTCCTCCCGGCAGCGGGGAGCGTGGGCACCAGCATCCTCAG... | AGCCAGGAACTGAAGCTAGGTCTGTGACTTAGAGCCGGCACTCTTTCCACTGCAGAGGGGAGAGGTCTCAAGGCAGAACCTGGGGCTGTGCACACCGCGGGAAGGGCAGAGGCCCCTGGAAACGAACAGGAGCAGGAGGCCCAGGGCTGCGCAGCAACCAAGGAGGACACGAGGAAGGTGCTTGTGCCACCGGTGGAAGACGTGGCTTTGGCTTTTAGGCTCCCCTCGGGGCAGGAGCAGATCAAAGAGCCTAGCCCCAGCTTCGGTGGTGGGTGGGGGGTCCTCCCGGCAGCGGGGAGCGTGGGCACCAGCATCCTCAG... |
Task1_train_48456 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | CAGGAGCAGATCAAAGAGCCTAGCCCCAGCTTCGGTGGTGGGTGGGGGGTCCTCCCGGCAGCGGGGAGCGTGGGCACCAGCATCCTCAGCCTGCGGCTCCCAGGCGAGTGTGGGAGGGCAGAGCCCAGAGAATTGGAGGTGGGGCCAATGTGGGCCCCGCCCCCAACCATTGTGTCGGAGAGGGAAGTGGACGAGCTCCTCGGTAAGAACCAATGAGGATGTGGTATGCAAATAAGCAAGTGGAGGCCGCCAGCCGACTTCCTCGCACTGTGCAGCTGCTCCAGTGAGGGCGCAGACTGTACTGGCCTGTGCGGAGCAAG... | CAGGAGCAGATCAAAGAGCCTAGCCCCAGCTTCGGTGGTGGGTGGGGGGTCCTCCCGGCAGCGGGGAGCGTGGGCACCAGCATCCTCAGCCTGCGGCTCCCAGGCGAGTGTGGGAGGGCAGAGCCCAGAGAATTGGAGGTGGGGCCAATGTGGGCCCCGCCCCCAACCATTGTGTCGGAGAGGGAAGTGGACGAGCTCCTCGGTAAGAACCAATGAGGATGTGGTATGCAAATAAGCAAGTGGAGGCCGCCAGCCGACTTCCTCGCACTGTGCAGCTGCTCCAGTGAGGGCGCAGACTGTACTGGCCTGTGCGGAGCAAG... |
Task1_train_48457 | A change on Chromosome 22 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GGGCCATGGAGCAGAGGAAGGGCTGGATGCATGAAGGAGGCGGGGTGCGGGGAGCGAGGGACCCGCAGACTCCAGGGCCACAGATGCGTGGACCTATTGGAGACCCTCAGGTTGTCTCCCCACCCCACGCAGAGAGGAATGCGCAGCTGAAGAGAGAGGTGGGCAGCAGGCCCGGTCACCTGCCAGGTGACCACATGGCCAGGTGCCGCCACCACTCGGGTTACCTGGCCGATGACGAGGCCAGCCACTCCATGTGCAGTGCACGGGTAAGTGTGCCCAGCAGGGCGCCGACCCTTGAGGCCACAACATGTTCCCCACCA... | GGGCCATGGAGCAGAGGAAGGGCTGGATGCATGAAGGAGGCGGGGTGCGGGGAGCGAGGGACCCGCAGACTCCAGGGCCACAGATGCGTGGACCTATTGGAGACCCTCAGGTTGTCTCCCCACCCCACGCAGAGAGGAATGCGCAGCTGAAGAGAGAGGTGGGCAGCAGGCCCGGTCACCTGCCAGGTGACCACATGGCCAGGTGCCGCCACCACTCGGGTTACCTGGCCGATGACGAGGCCAGCCACTCCATGTGCAGTGCACGGGTAAGTGTGCCCAGCAGGGCGCCGACCCTTGAGGCCACAACATGTTCCCCACCA... |
Task1_train_48458 | A sequence alteration has been identified on Chromosome 22. Is it disease-inducing or harmless? | Benign | GCTGGGTAGCCAGACCAGCTTTCAGTGGACACAGGAGCAGCCCTTGTCCTGGTTCTCAGGGCTGCTGGGCTCAAGCTCTGGCGTGCCTGAAGCATCAGAGCCGAGGCCTGGAGAACAGGAGCCAATCTTCCGCAAGCGAGAGTTCAATAAGGAGATCAAGTCATTACTGAGCCAGCTGGAGTCCCTCGACCTGCCTGGCTACTGTCCGCTCCGTGAGCCCCATCGCACGCTGAACTTCCTGGCTGACCACCGCCTCTTCCCTGCCCTGCAAAGCGTGGTCAGCCAGGCTGTGGATAAGCTCCGTGGCGCCCACTGCCGCG... | GCTGGGTAGCCAGACCAGCTTTCAGTGGACACAGGAGCAGCCCTTGTCCTGGTTCTCAGGGCTGCTGGGCTCAAGCTCTGGCGTGCCTGAAGCATCAGAGCCGAGGCCTGGAGAACAGGAGCCAATCTTCCGCAAGCGAGAGTTCAATAAGGAGATCAAGTCATTACTGAGCCAGCTGGAGTCCCTCGACCTGCCTGGCTACTGTCCGCTCCGTGAGCCCCATCGCACGCTGAACTTCCTGGCTGACCACCGCCTCTTCCCTGCCCTGCAAAGCGTGGTCAGCCAGGCTGTGGATAAGCTCCGTGGCGCCCACTGCCGCG... |
Task1_train_48459 | A mutation is present on Chromosome 22. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AATACAAAAATTAGCCAGGCGTGGTGGTGCGTGCCTGTAATCCCAGCTACTTAGGAGCCTGAGGCAGGAGAATTGCTTGAACGCAGGAGGCGGAGGTTGCAGTGAGCTGAGACAGCGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCCGTCTCGAAAAAAAAAAAAAAAAGTTGAGAGAGTCCTGGCACCGACCAACCATGTCCTTGGTGTGGCCCTGTGGCTTGTCTCTGGCCCTGTGTTTGGCACTTAAAAAAAAAGAGGCACTTTTTATTAAAGTAAACATGTACAAAACTGGAGATGACAGCGAACACCC... | AATACAAAAATTAGCCAGGCGTGGTGGTGCGTGCCTGTAATCCCAGCTACTTAGGAGCCTGAGGCAGGAGAATTGCTTGAACGCAGGAGGCGGAGGTTGCAGTGAGCTGAGACAGCGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCCGTCTCGAAAAAAAAAAAAAAAAGTTGAGAGAGTCCTGGCACCGACCAACCATGTCCTTGGTGTGGCCCTGTGGCTTGTCTCTGGCCCTGTGTTTGGCACTTAAAAAAAAAGAGGCACTTTTTATTAAAGTAAACATGTACAAAACTGGAGATGACAGCGAACACCC... |
Task1_train_48460 | Here is a genetic alteration on Chromosome 22. Based on the data, is it a benign variant or a cause of disease? | Benign | ACGAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAATTCCTAACCTGAAGTGATCCGCCGGCCTCTGCCTCCCAAAGTGCCGGGATTACAGGCGTGAGCCACTGTGCCCAGCCTCAATAAAGCAGTTACGCCTGCTTCAGAGAATCCCTTTTCTACTCTGAGGCTGCCTTGAGCTCAGAGGCCTTTGTCACTTCCTGGGGCTGAGGTGAGAGGCCAGGAGTGGAGGCTTGCCTGCTTTTCACTGGGGTCCTTGCAGCTGCAGAGATTGCATGGTTTTCTATTGAGATGCAAAGCCTGGCTCTGCTAATTTCCATGAAGGT... | ACGAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAATTCCTAACCTGAAGTGATCCGCCGGCCTCTGCCTCCCAAAGTGCCGGGATTACAGGCGTGAGCCACTGTGCCCAGCCTCAATAAAGCAGTTACGCCTGCTTCAGAGAATCCCTTTTCTACTCTGAGGCTGCCTTGAGCTCAGAGGCCTTTGTCACTTCCTGGGGCTGAGGTGAGAGGCCAGGAGTGGAGGCTTGCCTGCTTTTCACTGGGGTCCTTGCAGCTGCAGAGATTGCATGGTTTTCTATTGAGATGCAAAGCCTGGCTCTGCTAATTTCCATGAAGGT... |
Task1_train_48461 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCAGAGGGCAGCTGCCACCAGCACCTGGCACCACACGGCAGTCTGGCCTACAGGGTATTTTCTAAACCTGGCATGTGAATGGGTTCCATGGGGCACCCAGCTGCCTCTAAGACCATAAGGGCTTGTTGTGAGAATGGGAATTGCAGCAGGTCCTGGGAAGCTGCCAGACGCACACGGGCACCATGTACAGGGCTTCTCAGAGATGGGAGCAGGGAGCAGGGGACGGAGAAGTGTGGGGTCAAGAGCGTGGCCCTGAGCAGGGGGCTGCAGCGAAGACCAAGGGGATTCATAAGCCAGATCCGGGGAGGGGGTCTCCCAGC... | TCAGAGGGCAGCTGCCACCAGCACCTGGCACCACACGGCAGTCTGGCCTACAGGGTATTTTCTAAACCTGGCATGTGAATGGGTTCCATGGGGCACCCAGCTGCCTCTAAGACCATAAGGGCTTGTTGTGAGAATGGGAATTGCAGCAGGTCCTGGGAAGCTGCCAGACGCACACGGGCACCATGTACAGGGCTTCTCAGAGATGGGAGCAGGGAGCAGGGGACGGAGAAGTGTGGGGTCAAGAGCGTGGCCCTGAGCAGGGGGCTGCAGCGAAGACCAAGGGGATTCATAAGCCAGATCCGGGGAGGGGGTCTCCCAGC... |
Task1_train_48462 | Mutation context: Chromosome 22. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TATGAGTCACCTGGCATCTGGGCCAATCTTCAGCCTTGTGGGCGTTAGTCGGTGTGTGCACACCCCACAGTGCACGAGGGCACATCTGGGCCTTCACAGGGAAGGCCAGGTCCTGAATGGAGGCCTCAGGAGGGGATGCCCGCTGTGGACCTGCCTGGCTGGCCACACACTGGGTCACCAGTTTCCAGATACCAGCCCATGGAGGGGTGCTGGGCTGGGCACACAGGGCTGGCGGGGCAGCTTTGTGAGTAGACTCGAAGCCTGAGTACTGGAGACGGAGCCGGCTCTGGGGCCTGGGCAGGCGCACCCACCGATGCCAT... | TATGAGTCACCTGGCATCTGGGCCAATCTTCAGCCTTGTGGGCGTTAGTCGGTGTGTGCACACCCCACAGTGCACGAGGGCACATCTGGGCCTTCACAGGGAAGGCCAGGTCCTGAATGGAGGCCTCAGGAGGGGATGCCCGCTGTGGACCTGCCTGGCTGGCCACACACTGGGTCACCAGTTTCCAGATACCAGCCCATGGAGGGGTGCTGGGCTGGGCACACAGGGCTGGCGGGGCAGCTTTGTGAGTAGACTCGAAGCCTGAGTACTGGAGACGGAGCCGGCTCTGGGGCCTGGGCAGGCGCACCCACCGATGCCAT... |
Task1_train_48463 | A mutation is present on Chromosome 22. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GATCCCTTCCTTACACCTTATACAAAAATCAATTCAAGATGGATTAAAGACTTAAATGTTAGACCTAAAACCATAAAAACCCTAAGAAGAAAACCTAGGCATTACCATTCAGGACATAGGCATGGGCAAGGACTTCACGTCTAAAACACCAAAAGCAATGGCAACAAAAGCCAAAATTGACAAATGGGATCTGATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTACCATCAGAGTGAACAGGCAACCTACAAAATGGGAGAAAATTTTCACAACCTACTCATCTGACAAAGGGGCTAATATCCAGAATCTACAAT... | GATCCCTTCCTTACACCTTATACAAAAATCAATTCAAGATGGATTAAAGACTTAAATGTTAGACCTAAAACCATAAAAACCCTAAGAAGAAAACCTAGGCATTACCATTCAGGACATAGGCATGGGCAAGGACTTCACGTCTAAAACACCAAAAGCAATGGCAACAAAAGCCAAAATTGACAAATGGGATCTGATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTACCATCAGAGTGAACAGGCAACCTACAAAATGGGAGAAAATTTTCACAACCTACTCATCTGACAAAGGGGCTAATATCCAGAATCTACAAT... |
Task1_train_48464 | This mutation on Chromosome 22 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TCAATTCAAGATGGATTAAAGACTTAAATGTTAGACCTAAAACCATAAAAACCCTAAGAAGAAAACCTAGGCATTACCATTCAGGACATAGGCATGGGCAAGGACTTCACGTCTAAAACACCAAAAGCAATGGCAACAAAAGCCAAAATTGACAAATGGGATCTGATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTACCATCAGAGTGAACAGGCAACCTACAAAATGGGAGAAAATTTTCACAACCTACTCATCTGACAAAGGGGCTAATATCCAGAATCTACAATGAACTCAAACAAATTTACAAGAAAAAAA... | TCAATTCAAGATGGATTAAAGACTTAAATGTTAGACCTAAAACCATAAAAACCCTAAGAAGAAAACCTAGGCATTACCATTCAGGACATAGGCATGGGCAAGGACTTCACGTCTAAAACACCAAAAGCAATGGCAACAAAAGCCAAAATTGACAAATGGGATCTGATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTACCATCAGAGTGAACAGGCAACCTACAAAATGGGAGAAAATTTTCACAACCTACTCATCTGACAAAGGGGCTAATATCCAGAATCTACAATGAACTCAAACAAATTTACAAGAAAAAAA... |
Task1_train_48465 | A sequence alteration has been identified on Chromosome 22. Is it disease-inducing or harmless? | Benign | TGAGACCCTTATATACCCTGAGCTGCATGCTGTGGAGAGAGGGTCTGTGGAAGACCTTGGCTCTTAGCCATCGACTCCTCTGGGGAACACCATGAAATCCTCAGACTGGGGATGTCCTCTGGAGCCATCTTTATCCTCTTCTTCTTCCCAGTATCTCCTGCTCCATGATCTGGGTCCTGTCCCTGGCCCTGTTGCATCTCCAGTGTCTGATCCATGCCAGCCCTTCCTTAAATATGTGTTGAACCCATTTCCCATTTGCCCAAGAAATGAGTGCTGGCAACGAGCTGCACTTTTTTTTTTCTAAATGGGAAATGGGTCAA... | TGAGACCCTTATATACCCTGAGCTGCATGCTGTGGAGAGAGGGTCTGTGGAAGACCTTGGCTCTTAGCCATCGACTCCTCTGGGGAACACCATGAAATCCTCAGACTGGGGATGTCCTCTGGAGCCATCTTTATCCTCTTCTTCTTCCCAGTATCTCCTGCTCCATGATCTGGGTCCTGTCCCTGGCCCTGTTGCATCTCCAGTGTCTGATCCATGCCAGCCCTTCCTTAAATATGTGTTGAACCCATTTCCCATTTGCCCAAGAAATGAGTGCTGGCAACGAGCTGCACTTTTTTTTTTCTAAATGGGAAATGGGTCAA... |
Task1_train_48466 | This mutation on Chromosome 22 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GTTGACAAAATATCAAAATCTATAAACTCTGGGTTTAAAAAACAATGAAATACACAGTACACATAAGAAAATAGTGTCAAAGCTCACTACTATAAGAGACAATGATCAATATTGAAATTTTCTCTTACATGAAGACGCTCAAAACATTTTAGCAGTGACTAGTGAGGTTGTATCCATTCTCTTATGTTTATATTTATGTTTAAAATATTGTCCTTGAGAAGGAGTGTAGGTAGGTATAAGCAGAGGTGGCTGTGCGGATCCAAGATTCTAGCCTGCCCCCTTGATACAGCCCATTACCCTAGTCCCATCCAATCTCACAC... | GTTGACAAAATATCAAAATCTATAAACTCTGGGTTTAAAAAACAATGAAATACACAGTACACATAAGAAAATAGTGTCAAAGCTCACTACTATAAGAGACAATGATCAATATTGAAATTTTCTCTTACATGAAGACGCTCAAAACATTTTAGCAGTGACTAGTGAGGTTGTATCCATTCTCTTATGTTTATATTTATGTTTAAAATATTGTCCTTGAGAAGGAGTGTAGGTAGGTATAAGCAGAGGTGGCTGTGCGGATCCAAGATTCTAGCCTGCCCCCTTGATACAGCCCATTACCCTAGTCCCATCCAATCTCACAC... |
Task1_train_48467 | Here is a genetic alteration on Chromosome 22. Based on the data, is it a benign variant or a cause of disease? | Benign | TTTATGTTTAAAATATTGTCCTTGAGAAGGAGTGTAGGTAGGTATAAGCAGAGGTGGCTGTGCGGATCCAAGATTCTAGCCTGCCCCCTTGATACAGCCCATTACCCTAGTCCCATCCAATCTCACACATGGCCCATCATCATCTTCTGACTTGAGCGGGGAGAGAGACGGTGGGTAGAGAGGGAGGAAAGGAGTTAGTTCAGAGCATAGGAGACGTGGTCAGAGAGTTGGCAGAGGGAGGGAGGGAGGCAGATACTGTGGGTTCACGTGGTGCTTTGACAACTGTGGATTTACTTCTGAATGAAGCATGAAGTCATTGA... | TTTATGTTTAAAATATTGTCCTTGAGAAGGAGTGTAGGTAGGTATAAGCAGAGGTGGCTGTGCGGATCCAAGATTCTAGCCTGCCCCCTTGATACAGCCCATTACCCTAGTCCCATCCAATCTCACACATGGCCCATCATCATCTTCTGACTTGAGCGGGGAGAGAGACGGTGGGTAGAGAGGGAGGAAAGGAGTTAGTTCAGAGCATAGGAGACGTGGTCAGAGAGTTGGCAGAGGGAGGGAGGGAGGCAGATACTGTGGGTTCACGTGGTGCTTTGACAACTGTGGATTTACTTCTGAATGAAGCATGAAGTCATTGA... |
Task1_train_48468 | Chromosome 22 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGGTCATAGATGTGGTTGCAGCTGTTACTGGACAGAGTGGTCAAGACATCCTGTGTCTGCAGAGGCCCTCCCCAGCCCTCACCTGGGCAGTGGAGCTGTTGGCCAGAGAGGCAGTGGGAAGAAGGGTGGGGCTCCCAGAGTCGACCCTGCGGGCTGAAACTGGTGCAGCCTGCACCTCACCAGGCAGAGAATGGATGTGGGGCAGCTTGACACCGAGCAGGGGCTCATCTGAGCCTCAGGGGTGGTTGCTCTATCAAAGTGTTTGCAAGTAAACAGTCCCAGTGCACACCCAGCTGCTCAGTGCCACCTCGTGCACCCAG... | AGGTCATAGATGTGGTTGCAGCTGTTACTGGACAGAGTGGTCAAGACATCCTGTGTCTGCAGAGGCCCTCCCCAGCCCTCACCTGGGCAGTGGAGCTGTTGGCCAGAGAGGCAGTGGGAAGAAGGGTGGGGCTCCCAGAGTCGACCCTGCGGGCTGAAACTGGTGCAGCCTGCACCTCACCAGGCAGAGAATGGATGTGGGGCAGCTTGACACCGAGCAGGGGCTCATCTGAGCCTCAGGGGTGGTTGCTCTATCAAAGTGTTTGCAAGTAAACAGTCCCAGTGCACACCCAGCTGCTCAGTGCCACCTCGTGCACCCAG... |
Task1_train_48469 | A variant has been detected on Chromosome 22. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | ATGTACCAATTGTATTTTACTGCTTCGTTGATCTGTTGTAAAAATCACCCAGTGAGGGAGTAAGCTGATGGGTAAAATGGGTTGAAAAATTAAACAAGATGAACCACATTGATGATGGTCAAATTTGGCTGATGGGTGCAAACAATTCATTAGAAAAGTATCTGTATATTTGTATGGTTCAAAAGTTTCCATGCTATCCAGTGTTTAAAATATCCTTGTTTGTAACTGTTCTGCTTTTAACCGGTGTACAATGTGGACAAAATGTAAGCTTACACTCTGACTTTGAGTAGAAGCCCATCTTCTCCCAACAGGCAGAGGAG... | ATGTACCAATTGTATTTTACTGCTTCGTTGATCTGTTGTAAAAATCACCCAGTGAGGGAGTAAGCTGATGGGTAAAATGGGTTGAAAAATTAAACAAGATGAACCACATTGATGATGGTCAAATTTGGCTGATGGGTGCAAACAATTCATTAGAAAAGTATCTGTATATTTGTATGGTTCAAAAGTTTCCATGCTATCCAGTGTTTAAAATATCCTTGTTTGTAACTGTTCTGCTTTTAACCGGTGTACAATGTGGACAAAATGTAAGCTTACACTCTGACTTTGAGTAGAAGCCCATCTTCTCCCAACAGGCAGAGGAG... |
Task1_train_48470 | A mutation is present on Chromosome 22. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TGAAAAATTAAACAAGATGAACCACATTGATGATGGTCAAATTTGGCTGATGGGTGCAAACAATTCATTAGAAAAGTATCTGTATATTTGTATGGTTCAAAAGTTTCCATGCTATCCAGTGTTTAAAATATCCTTGTTTGTAACTGTTCTGCTTTTAACCGGTGTACAATGTGGACAAAATGTAAGCTTACACTCTGACTTTGAGTAGAAGCCCATCTTCTCCCAACAGGCAGAGGAGAAGCTGGTGTGGAGAACATGGAAAACACAGGAGCTCAGGGTTTCCCAGGACAGAGAAGCGAGTGAGCCTGGAGCCCTAAAAG... | TGAAAAATTAAACAAGATGAACCACATTGATGATGGTCAAATTTGGCTGATGGGTGCAAACAATTCATTAGAAAAGTATCTGTATATTTGTATGGTTCAAAAGTTTCCATGCTATCCAGTGTTTAAAATATCCTTGTTTGTAACTGTTCTGCTTTTAACCGGTGTACAATGTGGACAAAATGTAAGCTTACACTCTGACTTTGAGTAGAAGCCCATCTTCTCCCAACAGGCAGAGGAGAAGCTGGTGTGGAGAACATGGAAAACACAGGAGCTCAGGGTTTCCCAGGACAGAGAAGCGAGTGAGCCTGGAGCCCTAAAAG... |
Task1_train_48471 | A mutation on Chromosome 22 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTGGCTGATGGGTGCAAACAATTCATTAGAAAAGTATCTGTATATTTGTATGGTTCAAAAGTTTCCATGCTATCCAGTGTTTAAAATATCCTTGTTTGTAACTGTTCTGCTTTTAACCGGTGTACAATGTGGACAAAATGTAAGCTTACACTCTGACTTTGAGTAGAAGCCCATCTTCTCCCAACAGGCAGAGGAGAAGCTGGTGTGGAGAACATGGAAAACACAGGAGCTCAGGGTTTCCCAGGACAGAGAAGCGAGTGAGCCTGGAGCCCTAAAAGCAAGGGTGGGGCTGTGAGTTGGGCTGTGGGTGTGTGCAGGGG... | TTGGCTGATGGGTGCAAACAATTCATTAGAAAAGTATCTGTATATTTGTATGGTTCAAAAGTTTCCATGCTATCCAGTGTTTAAAATATCCTTGTTTGTAACTGTTCTGCTTTTAACCGGTGTACAATGTGGACAAAATGTAAGCTTACACTCTGACTTTGAGTAGAAGCCCATCTTCTCCCAACAGGCAGAGGAGAAGCTGGTGTGGAGAACATGGAAAACACAGGAGCTCAGGGTTTCCCAGGACAGAGAAGCGAGTGAGCCTGGAGCCCTAAAAGCAAGGGTGGGGCTGTGAGTTGGGCTGTGGGTGTGTGCAGGGG... |
Task1_train_48472 | This variant lies on Chromosome 22. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TATTTGTATGGTTCAAAAGTTTCCATGCTATCCAGTGTTTAAAATATCCTTGTTTGTAACTGTTCTGCTTTTAACCGGTGTACAATGTGGACAAAATGTAAGCTTACACTCTGACTTTGAGTAGAAGCCCATCTTCTCCCAACAGGCAGAGGAGAAGCTGGTGTGGAGAACATGGAAAACACAGGAGCTCAGGGTTTCCCAGGACAGAGAAGCGAGTGAGCCTGGAGCCCTAAAAGCAAGGGTGGGGCTGTGAGTTGGGCTGTGGGTGTGTGCAGGGGCCACAGTGTGAAGGGCATGCTTCAGAGGCCACAGGATTTGGA... | TATTTGTATGGTTCAAAAGTTTCCATGCTATCCAGTGTTTAAAATATCCTTGTTTGTAACTGTTCTGCTTTTAACCGGTGTACAATGTGGACAAAATGTAAGCTTACACTCTGACTTTGAGTAGAAGCCCATCTTCTCCCAACAGGCAGAGGAGAAGCTGGTGTGGAGAACATGGAAAACACAGGAGCTCAGGGTTTCCCAGGACAGAGAAGCGAGTGAGCCTGGAGCCCTAAAAGCAAGGGTGGGGCTGTGAGTTGGGCTGTGGGTGTGTGCAGGGGCCACAGTGTGAAGGGCATGCTTCAGAGGCCACAGGATTTGGA... |
Task1_train_48473 | A mutation on Chromosome 22 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AACTGTTCTGCTTTTAACCGGTGTACAATGTGGACAAAATGTAAGCTTACACTCTGACTTTGAGTAGAAGCCCATCTTCTCCCAACAGGCAGAGGAGAAGCTGGTGTGGAGAACATGGAAAACACAGGAGCTCAGGGTTTCCCAGGACAGAGAAGCGAGTGAGCCTGGAGCCCTAAAAGCAAGGGTGGGGCTGTGAGTTGGGCTGTGGGTGTGTGCAGGGGCCACAGTGTGAAGGGCATGCTTCAGAGGCCACAGGATTTGGATTTTATAATAAGAATGATGAGTTACTGAAGGGGTTTAAGCCAGGTAGTACCTTCCCT... | AACTGTTCTGCTTTTAACCGGTGTACAATGTGGACAAAATGTAAGCTTACACTCTGACTTTGAGTAGAAGCCCATCTTCTCCCAACAGGCAGAGGAGAAGCTGGTGTGGAGAACATGGAAAACACAGGAGCTCAGGGTTTCCCAGGACAGAGAAGCGAGTGAGCCTGGAGCCCTAAAAGCAAGGGTGGGGCTGTGAGTTGGGCTGTGGGTGTGTGCAGGGGCCACAGTGTGAAGGGCATGCTTCAGAGGCCACAGGATTTGGATTTTATAATAAGAATGATGAGTTACTGAAGGGGTTTAAGCCAGGTAGTACCTTCCCT... |
Task1_train_48474 | A change on Chromosome 22 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GACTGCTCATATTCTGTGCCATAAGCCAACAGCTACTGATCCCAAGATCTTGTAATCCCTCTGTAAAACTGGTGCTGTACTGCATACCTTGCCAGCTGGGACTTTTTATCTTACTGCATTTTCCAGGAATAAATAACCTTGTCCCAAAAACAAACATATTTAAAGACATTTCCTTCTGTGGACACTGATTCCATGCTATCTGTTTTCCAAGGAAGTGGTGAGCCCGTTTCTGAGAACACCTGGTATCAATGGCTGTCCCTTCCAAACCAAGCAAAAAGTGATTTCTTGTCGGTGTGGATTTGGTTTTGTTATTAATTTTA... | GACTGCTCATATTCTGTGCCATAAGCCAACAGCTACTGATCCCAAGATCTTGTAATCCCTCTGTAAAACTGGTGCTGTACTGCATACCTTGCCAGCTGGGACTTTTTATCTTACTGCATTTTCCAGGAATAAATAACCTTGTCCCAAAAACAAACATATTTAAAGACATTTCCTTCTGTGGACACTGATTCCATGCTATCTGTTTTCCAAGGAAGTGGTGAGCCCGTTTCTGAGAACACCTGGTATCAATGGCTGTCCCTTCCAAACCAAGCAAAAAGTGATTTCTTGTCGGTGTGGATTTGGTTTTGTTATTAATTTTA... |
Task1_train_48475 | This sequence variant lies on Chromosome 22. Is it clinically significant, and what condition might it cause if any? | Benign | CTGTTCCCCCTAATCTGTGTGGCTCAGGAAGTAGAGCTCCAGAGACTTCTCTACCATGGCCTGAATCCCTCTGCTGCTCACCCTCCTCAGTCTCTGCACAGGAGGCTGGAGATAGAAAGGCAGGGACTGGCACTGGGAGGACCAGGGCTCTGCCTTGCTCCCCCGGCTCACCGAGCCACTTCCCACACCCTGTGTCTCTGTCCTGACTCTTAGGGTCCTGGGCAGTCAGGGCTCACTTGGTGGCCTGCACAGTTTGTCTGTGACTAAACCAGCCACCATCTCCTGCACTGGAAACAGCAGCAATAACGTCCTTGGAATTG... | CTGTTCCCCCTAATCTGTGTGGCTCAGGAAGTAGAGCTCCAGAGACTTCTCTACCATGGCCTGAATCCCTCTGCTGCTCACCCTCCTCAGTCTCTGCACAGGAGGCTGGAGATAGAAAGGCAGGGACTGGCACTGGGAGGACCAGGGCTCTGCCTTGCTCCCCCGGCTCACCGAGCCACTTCCCACACCCTGTGTCTCTGTCCTGACTCTTAGGGTCCTGGGCAGTCAGGGCTCACTTGGTGGCCTGCACAGTTTGTCTGTGACTAAACCAGCCACCATCTCCTGCACTGGAAACAGCAGCAATAACGTCCTTGGAATTG... |
Task1_train_48476 | This alteration occurs on Chromosome 22. Is it associated with a disease or is it a benign variant? | Benign | AAATGCAATAAACATTTTTTGAAAGCTATAAAAATTATGTAAAGGAACATGGCTTACACTAAAAGGAACACTTAAAATAATGACACCCTTGAAATGCAATCCCAAAACACAGCATACATTTTATTTCAGTTCCATATATGGACTGGTTTTATTTAAATGTCTATATTAAATCTCACTATTCCATTTTTAAATGGAGCACTTAAAATCTCATTCTACGGCAACTGCCTGGTGATACATTCACCAGTGGAAATATCAACAAAACCATCCAGCTGTTTTCCTCCATCCCCATAGAATTCCCCAAACTAGTAATTATTAAGAGC... | AAATGCAATAAACATTTTTTGAAAGCTATAAAAATTATGTAAAGGAACATGGCTTACACTAAAAGGAACACTTAAAATAATGACACCCTTGAAATGCAATCCCAAAACACAGCATACATTTTATTTCAGTTCCATATATGGACTGGTTTTATTTAAATGTCTATATTAAATCTCACTATTCCATTTTTAAATGGAGCACTTAAAATCTCATTCTACGGCAACTGCCTGGTGATACATTCACCAGTGGAAATATCAACAAAACCATCCAGCTGTTTTCCTCCATCCCCATAGAATTCCCCAAACTAGTAATTATTAAGAGC... |
Task1_train_48477 | A variant has been detected on Chromosome 22. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GATCACAGAACAGGAAGTCAGCTAGTACCAGGCACCATTCTATTAATTTTATTGCTATTTCACCTCAAACCAATGATACATGACGGCTGTTTGATGTCTGCAGGGGCCCTTCACCAAACAAAAGCATTTTACTTTGAATGGTTTGGCTTCCTTGGATGTTTTCAGGTAGGTAAAGACACTCTGAAGCAGTGTTCCTTTTGACCTGGCCCCAAGACTAGAATGAATGTGTGCCTATACTTCAACTAGAACAAAGAACCACTGCTCTCCCTCAACTAACCTCCGCCTTCTTGGTCTCTGCTCACGCAGCAGCTTCTCTTTCA... | GATCACAGAACAGGAAGTCAGCTAGTACCAGGCACCATTCTATTAATTTTATTGCTATTTCACCTCAAACCAATGATACATGACGGCTGTTTGATGTCTGCAGGGGCCCTTCACCAAACAAAAGCATTTTACTTTGAATGGTTTGGCTTCCTTGGATGTTTTCAGGTAGGTAAAGACACTCTGAAGCAGTGTTCCTTTTGACCTGGCCCCAAGACTAGAATGAATGTGTGCCTATACTTCAACTAGAACAAAGAACCACTGCTCTCCCTCAACTAACCTCCGCCTTCTTGGTCTCTGCTCACGCAGCAGCTTCTCTTTCA... |
Task1_train_48478 | A mutation located on Chromosome 22 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GCCCCAGCACCCTTCCCAGTCGACAGCCCAGTTTTTAAAAAGGTAGGAGGGGGCAAAACTTGAATAGACATTTAATAAAAAGAAATACTCACGTGGCCGATAACTATATAATCTCAAGGTCCATTAATCATCAGGGAAGTGCAAATTAAAGCCACAATAAGGTACCACTACAATTTCAAGAGAAGGGCACTTACTAAAAGGACTGACAGTACCAAGTGCTGGATCAGTAGCAATGGAATTCGCAGTATCGGTGGTGGGAATGTAAATCGTTTCAATCACTCTGGAAATGTATTTGGCAGTATCTACACTAGACAGCTAAA... | GCCCCAGCACCCTTCCCAGTCGACAGCCCAGTTTTTAAAAAGGTAGGAGGGGGCAAAACTTGAATAGACATTTAATAAAAAGAAATACTCACGTGGCCGATAACTATATAATCTCAAGGTCCATTAATCATCAGGGAAGTGCAAATTAAAGCCACAATAAGGTACCACTACAATTTCAAGAGAAGGGCACTTACTAAAAGGACTGACAGTACCAAGTGCTGGATCAGTAGCAATGGAATTCGCAGTATCGGTGGTGGGAATGTAAATCGTTTCAATCACTCTGGAAATGTATTTGGCAGTATCTACACTAGACAGCTAAA... |
Task1_train_48479 | This sequence change occurs on Chromosome 22. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCCTTCCCAGTCGACAGCCCAGTTTTTAAAAAGGTAGGAGGGGGCAAAACTTGAATAGACATTTAATAAAAAGAAATACTCACGTGGCCGATAACTATATAATCTCAAGGTCCATTAATCATCAGGGAAGTGCAAATTAAAGCCACAATAAGGTACCACTACAATTTCAAGAGAAGGGCACTTACTAAAAGGACTGACAGTACCAAGTGCTGGATCAGTAGCAATGGAATTCGCAGTATCGGTGGTGGGAATGTAAATCGTTTCAATCACTCTGGAAATGTATTTGGCAGTATCTACACTAGACAGCTAAATATATGCAG... | CCCTTCCCAGTCGACAGCCCAGTTTTTAAAAAGGTAGGAGGGGGCAAAACTTGAATAGACATTTAATAAAAAGAAATACTCACGTGGCCGATAACTATATAATCTCAAGGTCCATTAATCATCAGGGAAGTGCAAATTAAAGCCACAATAAGGTACCACTACAATTTCAAGAGAAGGGCACTTACTAAAAGGACTGACAGTACCAAGTGCTGGATCAGTAGCAATGGAATTCGCAGTATCGGTGGTGGGAATGTAAATCGTTTCAATCACTCTGGAAATGTATTTGGCAGTATCTACACTAGACAGCTAAATATATGCAG... |
Task1_train_48480 | A sequence alteration has been identified on Chromosome 22. Is it disease-inducing or harmless? | Benign | ACTTCTCATAGCTATATATACCCACGAGAAATGATTACATGCTTACCAAAAGACACGCACAAGCTCATAGCAGCTTTATTCAAAATTGCCAAAGAATCAGCCTCAAAGTCCATCAACAGTGAAATAAATTTATACAAAACTGCCACAGTCACTCAACAAAATTCTACCCAGCAATGAAAAAGAATGTGCTACTGCTACACACAGCAAAAATGCATCTCACTTATTTTATTTCATTTTACTTTATTTTGAGACAGTCATGCTCTGTCACCCAGGCTGGAGGGCAGTGGCGCGATCTCAGCTCAGTGCAAACTCCCCCCTCC... | ACTTCTCATAGCTATATATACCCACGAGAAATGATTACATGCTTACCAAAAGACACGCACAAGCTCATAGCAGCTTTATTCAAAATTGCCAAAGAATCAGCCTCAAAGTCCATCAACAGTGAAATAAATTTATACAAAACTGCCACAGTCACTCAACAAAATTCTACCCAGCAATGAAAAAGAATGTGCTACTGCTACACACAGCAAAAATGCATCTCACTTATTTTATTTCATTTTACTTTATTTTGAGACAGTCATGCTCTGTCACCCAGGCTGGAGGGCAGTGGCGCGATCTCAGCTCAGTGCAAACTCCCCCCTCC... |
Task1_train_48481 | Given a variant located on Chromosome 22, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CACACAGCAAAAATGCATCTCACTTATTTTATTTCATTTTACTTTATTTTGAGACAGTCATGCTCTGTCACCCAGGCTGGAGGGCAGTGGCGCGATCTCAGCTCAGTGCAAACTCCCCCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCACGCTTGGCTAATTTTTCTATTTTATGCAGAGAAGGGGTTTCACTATGTTGGCCAGCCTGGTCTCAAACTTCTGACCCCAAGTGATCCACCCACCTCAGTCTCCCAAAGTGCTGGGATTACAGGCATGAGCCAT... | CACACAGCAAAAATGCATCTCACTTATTTTATTTCATTTTACTTTATTTTGAGACAGTCATGCTCTGTCACCCAGGCTGGAGGGCAGTGGCGCGATCTCAGCTCAGTGCAAACTCCCCCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCACGCTTGGCTAATTTTTCTATTTTATGCAGAGAAGGGGTTTCACTATGTTGGCCAGCCTGGTCTCAAACTTCTGACCCCAAGTGATCCACCCACCTCAGTCTCCCAAAGTGCTGGGATTACAGGCATGAGCCAT... |
Task1_train_48482 | A mutation has occurred on Chromosome 22. What is the medical relevance of this mutation? | Benign | TAAGTGTTAGAAAGGGCTGATAAGCTTCACATAAACCATGGAAAAACAGGAAAACTGAGTAAGTCCAACAGTTAGGGAAGCTTCCATGGGATCCCCGCTTCCAGGAGATCCAAGGGAGGAGGAGGAACCGCGATCAAGTGTGAGTTGTGTAATCTCTGAGCTGTGCAATCTCCCTGTGAGGCAGTGACACTCCTCTGTCCAGCTTCACACTGCCAGTTTGTCCAGTGGCACTGGAGGAAGCAGCACCAGGGGCACATTTGCACAAAGGTGCTGTCCTTCCTCCCAGTATAAGGGAGAAGTGAAAAGACTGGGGCCCAGCA... | TAAGTGTTAGAAAGGGCTGATAAGCTTCACATAAACCATGGAAAAACAGGAAAACTGAGTAAGTCCAACAGTTAGGGAAGCTTCCATGGGATCCCCGCTTCCAGGAGATCCAAGGGAGGAGGAGGAACCGCGATCAAGTGTGAGTTGTGTAATCTCTGAGCTGTGCAATCTCCCTGTGAGGCAGTGACACTCCTCTGTCCAGCTTCACACTGCCAGTTTGTCCAGTGGCACTGGAGGAAGCAGCACCAGGGGCACATTTGCACAAAGGTGCTGTCCTTCCTCCCAGTATAAGGGAGAAGTGAAAAGACTGGGGCCCAGCA... |
Task1_train_48483 | Here is a mutation located on Chromosome 22. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GTCGCGGGAGGAACAGGTGCCCACAATGGCGGCAGATCTGCCCGTGGATCACTGAAGATTCCTGCTCTCCTGCTGAGGTGGAGATTGCAGTGAGCTGAGATCGCACCATTGCACTCCAGCCTGGGCAACAGAGTCAGACTCTCTCTTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCCCTCTGTCGCCCAGGCTGGATTCCAGTGGCCTGATCTCTGGGCTCACCGCAAGCTCCGCCTACCGGGTTCACGCCATTCTCCTGCCTCAGCCTCTGGAGTAGTTGGGACTACAGGCGCCCGCCACCACACCCGGCT... | GTCGCGGGAGGAACAGGTGCCCACAATGGCGGCAGATCTGCCCGTGGATCACTGAAGATTCCTGCTCTCCTGCTGAGGTGGAGATTGCAGTGAGCTGAGATCGCACCATTGCACTCCAGCCTGGGCAACAGAGTCAGACTCTCTCTTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCCCTCTGTCGCCCAGGCTGGATTCCAGTGGCCTGATCTCTGGGCTCACCGCAAGCTCCGCCTACCGGGTTCACGCCATTCTCCTGCCTCAGCCTCTGGAGTAGTTGGGACTACAGGCGCCCGCCACCACACCCGGCT... |
Task1_train_48484 | Chromosome 22 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGGTGCCCACAATGGCGGCAGATCTGCCCGTGGATCACTGAAGATTCCTGCTCTCCTGCTGAGGTGGAGATTGCAGTGAGCTGAGATCGCACCATTGCACTCCAGCCTGGGCAACAGAGTCAGACTCTCTCTTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCCCTCTGTCGCCCAGGCTGGATTCCAGTGGCCTGATCTCTGGGCTCACCGCAAGCTCCGCCTACCGGGTTCACGCCATTCTCCTGCCTCAGCCTCTGGAGTAGTTGGGACTACAGGCGCCCGCCACCACACCCGGCTAATTTTTTGTATTT... | AGGTGCCCACAATGGCGGCAGATCTGCCCGTGGATCACTGAAGATTCCTGCTCTCCTGCTGAGGTGGAGATTGCAGTGAGCTGAGATCGCACCATTGCACTCCAGCCTGGGCAACAGAGTCAGACTCTCTCTTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCCCTCTGTCGCCCAGGCTGGATTCCAGTGGCCTGATCTCTGGGCTCACCGCAAGCTCCGCCTACCGGGTTCACGCCATTCTCCTGCCTCAGCCTCTGGAGTAGTTGGGACTACAGGCGCCCGCCACCACACCCGGCTAATTTTTTGTATTT... |
Task1_train_48485 | A mutation located on Chromosome 22 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GGATGATCTCCATCTCCTGACGTCATGATCCGCCCTCCCAAAGTGCTGGCATTACAGGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGTGTTGAAACTCCCTTGAGGCATTTTCTTCGGCCTTCGGGTCCATCCTCTGTCTCCTCCTTGACCTCCTCATCTCCTCCTCGCCACTGCCTTGGGGACCTTGGCCAGGCTCATGGCATCCAGCAGCCACTCAATGTCAATACCTCCATGTTCATCTCTCAGCCCGCCCTTGCCCGTGAACCCATGCTTATTTATTTATTTTTTTTATACGTGC... | GGATGATCTCCATCTCCTGACGTCATGATCCGCCCTCCCAAAGTGCTGGCATTACAGGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGTGTTGAAACTCCCTTGAGGCATTTTCTTCGGCCTTCGGGTCCATCCTCTGTCTCCTCCTTGACCTCCTCATCTCCTCCTCGCCACTGCCTTGGGGACCTTGGCCAGGCTCATGGCATCCAGCAGCCACTCAATGTCAATACCTCCATGTTCATCTCTCAGCCCGCCCTTGCCCGTGAACCCATGCTTATTTATTTATTTTTTTTATACGTGC... |
Task1_train_48486 | Located on Chromosome 22, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AACATGCGGTGATTGCAGTGAATCATAGCTGCTCTTACTGGGTGGGAGGTGCACCAGTTTGCTTCCTAAGTGCATAGAAAGCCTGGCACGCACGTCTCTCTGGACTTTGAAAGCTTGGCAGAAGAGCTTCAGTTGACTTACTCTAATTAGTCCTGACGGAACAAAACCACTAGAGTAGGGCATTTCAACCCTGAGACACTTCTGTAGCAATTGTTCCTGCCCCACATCCCTGCACTGCATGTGTGACCTCTCTGTGGTGGGCTGGGCAGGGCAGATTGGGCCACACTGGCACAGAATGGGGCTGGACTCTCTGGTCCTCA... | AACATGCGGTGATTGCAGTGAATCATAGCTGCTCTTACTGGGTGGGAGGTGCACCAGTTTGCTTCCTAAGTGCATAGAAAGCCTGGCACGCACGTCTCTCTGGACTTTGAAAGCTTGGCAGAAGAGCTTCAGTTGACTTACTCTAATTAGTCCTGACGGAACAAAACCACTAGAGTAGGGCATTTCAACCCTGAGACACTTCTGTAGCAATTGTTCCTGCCCCACATCCCTGCACTGCATGTGTGACCTCTCTGTGGTGGGCTGGGCAGGGCAGATTGGGCCACACTGGCACAGAATGGGGCTGGACTCTCTGGTCCTCA... |
Task1_train_48487 | Consider this mutation on Chromosome 22. Is this a benign change or a disease-causing variant? | Benign | TGCACCTGCCCCACCCCACTGAACTGCGTGTGTTACCTCTCTGTGCTGGGCTGGGCAGGGCAGATTGGGTCACACTGGCACAGAATGGGGCTGGACTCTCTGGTCCTCAACTTCTGAGGTGACAGGTGCTGTGGGGTCACCTGGAAGAAGAAAGCTCCTGGGCTGAGTCTCCTCCACCAGTTGGGGGCAGCAGAGCTGCAGCCAGGAGCAGTGAGGAGAGAGGCTGGGGCTGCCCAGCTGGGGCGAAGAGGAAGGCCAGCCTGGGGTTCAACAGGTGTCCAAGAGTCAGTCTTCAGACTGAAAATGAAGACAGTTCATCC... | TGCACCTGCCCCACCCCACTGAACTGCGTGTGTTACCTCTCTGTGCTGGGCTGGGCAGGGCAGATTGGGTCACACTGGCACAGAATGGGGCTGGACTCTCTGGTCCTCAACTTCTGAGGTGACAGGTGCTGTGGGGTCACCTGGAAGAAGAAAGCTCCTGGGCTGAGTCTCCTCCACCAGTTGGGGGCAGCAGAGCTGCAGCCAGGAGCAGTGAGGAGAGAGGCTGGGGCTGCCCAGCTGGGGCGAAGAGGAAGGCCAGCCTGGGGTTCAACAGGTGTCCAAGAGTCAGTCTTCAGACTGAAAATGAAGACAGTTCATCC... |
Task1_train_48488 | This mutation occurs on Chromosome 22. Does this change lead to a known medical condition, or is it benign? | Benign | CCTCTCTGTGCTGGGCTGGGCAGGGCAGATTGGGTCACACTGGCACAGAATGGGGCTGGACTCTCTGGTCCTCAACTTCTGAGGTGACAGGTGCTGTGGGGTCACCTGGAAGAAGAAAGCTCCTGGGCTGAGTCTCCTCCACCAGTTGGGGGCAGCAGAGCTGCAGCCAGGAGCAGTGAGGAGAGAGGCTGGGGCTGCCCAGCTGGGGCGAAGAGGAAGGCCAGCCTGGGGTTCAACAGGTGTCCAAGAGTCAGTCTTCAGACTGAAAATGAAGACAGTTCATCCTATCCCCTCGGGCTGCAGTGACCACGTTCTGAGGG... | CCTCTCTGTGCTGGGCTGGGCAGGGCAGATTGGGTCACACTGGCACAGAATGGGGCTGGACTCTCTGGTCCTCAACTTCTGAGGTGACAGGTGCTGTGGGGTCACCTGGAAGAAGAAAGCTCCTGGGCTGAGTCTCCTCCACCAGTTGGGGGCAGCAGAGCTGCAGCCAGGAGCAGTGAGGAGAGAGGCTGGGGCTGCCCAGCTGGGGCGAAGAGGAAGGCCAGCCTGGGGTTCAACAGGTGTCCAAGAGTCAGTCTTCAGACTGAAAATGAAGACAGTTCATCCTATCCCCTCGGGCTGCAGTGACCACGTTCTGAGGG... |
Task1_train_48489 | Consider this mutation on Chromosome 22. Is this a benign change or a disease-causing variant? | Benign | GGCTGGGGCTGCCCAGCTGGGGCGAAGAGGAAGGCCAGCCTGGGGTTCAACAGGTGTCCAAGAGTCAGTCTTCAGACTGAAAATGAAGACAGTTCATCCTATCCCCTCGGGCTGCAGTGACCACGTTCTGAGGGTCAGATTCATACAGTGTCACCCAAGGACACCGACAGAAGCCCGGCACAGTGAAGGCCTCACCTGGGAAATGCAACTAGAAGAGGCTGGGCCCAGGTGTCAGCTTGGGCAGCTTCCTTAGGAAGGGGATTCCCTGGGAGAAGTCCTGAGGCCGAGGTGCTCTAGGAGGGGCACAATGTGAGGTGACA... | GGCTGGGGCTGCCCAGCTGGGGCGAAGAGGAAGGCCAGCCTGGGGTTCAACAGGTGTCCAAGAGTCAGTCTTCAGACTGAAAATGAAGACAGTTCATCCTATCCCCTCGGGCTGCAGTGACCACGTTCTGAGGGTCAGATTCATACAGTGTCACCCAAGGACACCGACAGAAGCCCGGCACAGTGAAGGCCTCACCTGGGAAATGCAACTAGAAGAGGCTGGGCCCAGGTGTCAGCTTGGGCAGCTTCCTTAGGAAGGGGATTCCCTGGGAGAAGTCCTGAGGCCGAGGTGCTCTAGGAGGGGCACAATGTGAGGTGACA... |
Task1_train_48490 | A genomic change on Chromosome 22 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGTCTGCAGGGCTTCAGGTTACAGGGGCTGTGGAGTGACCTGGTGCAGGAAGCCCCGTCTCCTTCCATAGGACATCAGTGTGAACCCAGGGAGAGGCGCTGGTATGAGAGAGATGAGAACACAGGTGTGAACCACCTGCTTGTGCAGGGGACTGAGCCTTCACTTGGAGCCAAAGTTTTCTTTCCCAGGTTCAATCCTGAACAAGAGGGCCTTCTGGACTTCTTTTTGTTTTCAGGCTTGTGCCCCTTCAGGTTTGGGGCTGTCTGGATCCCAGCCAGGGGACACTGAGGAAATCCAGGAGTCTCACACTGACTGTTCTA... | GGTCTGCAGGGCTTCAGGTTACAGGGGCTGTGGAGTGACCTGGTGCAGGAAGCCCCGTCTCCTTCCATAGGACATCAGTGTGAACCCAGGGAGAGGCGCTGGTATGAGAGAGATGAGAACACAGGTGTGAACCACCTGCTTGTGCAGGGGACTGAGCCTTCACTTGGAGCCAAAGTTTTCTTTCCCAGGTTCAATCCTGAACAAGAGGGCCTTCTGGACTTCTTTTTGTTTTCAGGCTTGTGCCCCTTCAGGTTTGGGGCTGTCTGGATCCCAGCCAGGGGACACTGAGGAAATCCAGGAGTCTCACACTGACTGTTCTA... |
Task1_train_48491 | Given this context: Chromosome 22 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CCTCTCAGCACAAACTCTGAGAAGTATGGAATGAAATAAAGACAAACAAGAAATTAATGGTGCCGACGGTGGTGATGTTAGCTCACAGCTAAGCTGCAGAACCAGAAACATGCGGTGATGGGCTGAGTCTCCTCCACCAGCTGGGGGCAGCAGAGCTGCAGCCAGGAGCTTTCAGGAGAGAGGCTGGGGCTGCCCAGCTGGGGCAAAGAGAAGGCCAGCCTGGGGTTCAACAGGTGTCCAAGAATCTGTCTTCAGACTGAAAGTGAGTGCAGTTCATCCTATCCCCTCAGGCTTCAGTGACCACGCTCTGAGGGTCAGAC... | CCTCTCAGCACAAACTCTGAGAAGTATGGAATGAAATAAAGACAAACAAGAAATTAATGGTGCCGACGGTGGTGATGTTAGCTCACAGCTAAGCTGCAGAACCAGAAACATGCGGTGATGGGCTGAGTCTCCTCCACCAGCTGGGGGCAGCAGAGCTGCAGCCAGGAGCTTTCAGGAGAGAGGCTGGGGCTGCCCAGCTGGGGCAAAGAGAAGGCCAGCCTGGGGTTCAACAGGTGTCCAAGAATCTGTCTTCAGACTGAAAGTGAGTGCAGTTCATCCTATCCCCTCAGGCTTCAGTGACCACGCTCTGAGGGTCAGAC... |
Task1_train_48492 | A mutation is present on Chromosome 22. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GAGTATCTGCTGGGTCTGTAAACCCAATCTGCCTACTGCACTGATCCAGCAACAGGACAGGAAACTCCTCAGAGCAAGGACTGTGTCTTCCTCATGCTGAATTCCTAAAATGCATTCTTGCCAGGACAGAGTGGGTCAGGGTGAATATTTGTTGGGTGAATGAGCTTCTGTCTCTGTTGTATTGCAGGAGTCACCACCAGTGCACATTGGCCCTGTATTTGTATCCAGAACCAATCAAAGCCACCCCTGAGTCCTGCATCTCTCAGTACCAAGCTCCAGTCCCCCTTCAAGACCACCCACCACACAGACGTGCAGGGAGC... | GAGTATCTGCTGGGTCTGTAAACCCAATCTGCCTACTGCACTGATCCAGCAACAGGACAGGAAACTCCTCAGAGCAAGGACTGTGTCTTCCTCATGCTGAATTCCTAAAATGCATTCTTGCCAGGACAGAGTGGGTCAGGGTGAATATTTGTTGGGTGAATGAGCTTCTGTCTCTGTTGTATTGCAGGAGTCACCACCAGTGCACATTGGCCCTGTATTTGTATCCAGAACCAATCAAAGCCACCCCTGAGTCCTGCATCTCTCAGTACCAAGCTCCAGTCCCCCTTCAAGACCACCCACCACACAGACGTGCAGGGAGC... |
Task1_train_48493 | A variant on Chromosome 22 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CAGTGACCATGACCTGAGACCTGGAGGGAAAGAGGTTCCTCTTTTCTTAGAATATTTGTCATTGACACTGATGTTTAAATTCTTCTGACCTCCTGTCTCTCAGATTTGACTCTTGGAAATGGTGCTTATTTTTCTGATACAGATTCAGACAATTTGCCTCTTCTCATTGCCCTGGCCCCCATCTCACTGTCACACATGCCATTCCATTCTGTAGTCACGCGTGTCCCACCTCCCTGCCCTTTTCTCTGGTAGCTCGTCCTGCAGACACAGGGGCTTCTCCTTCCCTGGCCACTCCTCCACGTCCACTGTCCCCAGTCTTT... | CAGTGACCATGACCTGAGACCTGGAGGGAAAGAGGTTCCTCTTTTCTTAGAATATTTGTCATTGACACTGATGTTTAAATTCTTCTGACCTCCTGTCTCTCAGATTTGACTCTTGGAAATGGTGCTTATTTTTCTGATACAGATTCAGACAATTTGCCTCTTCTCATTGCCCTGGCCCCCATCTCACTGTCACACATGCCATTCCATTCTGTAGTCACGCGTGTCCCACCTCCCTGCCCTTTTCTCTGGTAGCTCGTCCTGCAGACACAGGGGCTTCTCCTTCCCTGGCCACTCCTCCACGTCCACTGTCCCCAGTCTTT... |
Task1_train_48494 | This mutation is located on Chromosome 22. Is it associated with a disease or is it a benign polymorphism? | Benign | CTTGAAAAGATAATCCACAATCAGTGCCTTTGCCCGAGAGACATGCAGAAATGCAGAGATCCATAGTAGACCACTGTCTCCCAACAACCATCAACTTTATCAATGAAATGAAGTCTCAGGCTATTTGTCTGTTACCATAGCCCACAAAAATGTCTGGCTTGATTGTCACCAAATGTATCAAGGAAGTTAAGGAGTATCTGACACAAAATGTGAACCAAGCAATTCTCAAAGGAGCCTCCCAGGAAATTCACTTTAGGAAGTCCTAGGAGGCTCCTCTGAGAGTTGCTAAAACAAAACATTGAGAGTCCTAGAGGGCTGCA... | CTTGAAAAGATAATCCACAATCAGTGCCTTTGCCCGAGAGACATGCAGAAATGCAGAGATCCATAGTAGACCACTGTCTCCCAACAACCATCAACTTTATCAATGAAATGAAGTCTCAGGCTATTTGTCTGTTACCATAGCCCACAAAAATGTCTGGCTTGATTGTCACCAAATGTATCAAGGAAGTTAAGGAGTATCTGACACAAAATGTGAACCAAGCAATTCTCAAAGGAGCCTCCCAGGAAATTCACTTTAGGAAGTCCTAGGAGGCTCCTCTGAGAGTTGCTAAAACAAAACATTGAGAGTCCTAGAGGGCTGCA... |
Task1_train_48495 | Chromosome 22 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CCCCGCCACCGCCAAGTTGACCTCAGTACAGCAAGGGCCCAGCCTGAGGTCCCTATCCTGGGCCTTAGTCCTTCACCCACCTGAAAACTGAGGCCAGGGGCTCCCCAGGTGGACACCAGGACTCTGACCCCCTGCCCCTCATCCACCCCGCAGGTCAGCCCAAGGCTGCCCCATCGGTCACTCTGTTCCCGCCCTCCTCTGAGGAGCTTCAAGCCAACAAGGCCACACTGGTGTGCCTGATCAGTGACTTCTACCCGGGAGCTGTGAAAGTGGCCTGGAAGGCAGATGGCAGCCCCGTCAACACGGGAGTGGAGACCACC... | CCCCGCCACCGCCAAGTTGACCTCAGTACAGCAAGGGCCCAGCCTGAGGTCCCTATCCTGGGCCTTAGTCCTTCACCCACCTGAAAACTGAGGCCAGGGGCTCCCCAGGTGGACACCAGGACTCTGACCCCCTGCCCCTCATCCACCCCGCAGGTCAGCCCAAGGCTGCCCCATCGGTCACTCTGTTCCCGCCCTCCTCTGAGGAGCTTCAAGCCAACAAGGCCACACTGGTGTGCCTGATCAGTGACTTCTACCCGGGAGCTGTGAAAGTGGCCTGGAAGGCAGATGGCAGCCCCGTCAACACGGGAGTGGAGACCACC... |
Task1_train_48496 | A mutation on Chromosome 22 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TCAAGTACCTAATGTCCAGTTATCCACGGATGGTCAGTGGGGCTGGGGAGGTCAAAGTCAATCATGAGATTCCAGAGTGGTGCCATAGACGTGCCTGTAAACCAATTGGTCTTTTTAAGAGCTGTATGTGGGATCTAAGAACCGGGTTGATGATTGTCCCAGGAGGTAGCACAGGATGGGGGGCCTGGGCTATGAGACAAACACACATACATACATGTTCACAAACATAAACACACATGAACACCTCATAGGCACACAGGTATTCACAAACAAACATGCCTGCATGCAAATACATACACACACACTCTCCTGTGCTATTT... | TCAAGTACCTAATGTCCAGTTATCCACGGATGGTCAGTGGGGCTGGGGAGGTCAAAGTCAATCATGAGATTCCAGAGTGGTGCCATAGACGTGCCTGTAAACCAATTGGTCTTTTTAAGAGCTGTATGTGGGATCTAAGAACCGGGTTGATGATTGTCCCAGGAGGTAGCACAGGATGGGGGGCCTGGGCTATGAGACAAACACACATACATACATGTTCACAAACATAAACACACATGAACACCTCATAGGCACACAGGTATTCACAAACAAACATGCCTGCATGCAAATACATACACACACACTCTCCTGTGCTATTT... |
Task1_train_48497 | A sequence alteration has been identified on Chromosome 22. Is it disease-inducing or harmless? | Benign | AACTTTCTTCCCACCTTGAAAGTGGGAAGCTCAGCTAGGTGCAGTGGCTCATGCCTGTAATCCCAGCATTTTAGGAGGCCGAGGCAGGCAGATCACTTGAGGCCAGGAATTTGAAACCAGGCTGGCCAACGTGGTGAAACCAGTCTCTACTAAAAATACAAAAATTAGCTGAGCGTGATGACACATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCACAAGAATTGCTTGAACCCAAAGAGGCAGGGGCTGCAGTGAGCTGAGATCGTGTCACCGTACTCCAGCCTGGGTGACAGAGTGAGAGACTGTCTCAAAAAA... | AACTTTCTTCCCACCTTGAAAGTGGGAAGCTCAGCTAGGTGCAGTGGCTCATGCCTGTAATCCCAGCATTTTAGGAGGCCGAGGCAGGCAGATCACTTGAGGCCAGGAATTTGAAACCAGGCTGGCCAACGTGGTGAAACCAGTCTCTACTAAAAATACAAAAATTAGCTGAGCGTGATGACACATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCACAAGAATTGCTTGAACCCAAAGAGGCAGGGGCTGCAGTGAGCTGAGATCGTGTCACCGTACTCCAGCCTGGGTGACAGAGTGAGAGACTGTCTCAAAAAA... |
Task1_train_48498 | A variant was discovered on Chromosome 22. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGCTCCTGCTTCATCTTCCTCGTGGGAACCAAGAAGGACCTTCTGGTGAGCAGAGTGGCACTGGTGGTCTGGGTGGCCCTTGGGAAAATGCCTCCCCTTACAGCCCTCATTGGAGGAGCCATGGGGAGGGAGGGAGGCAGCACAGTGGGAAGCAGGCAGCTGCCTATCCCCCTGGGCCTCCCTGCAGGAGAGCCGGGACGCTGGGTCAACAAGGGCCATTTCTCCCAGTCAGGGGCCGCATGTGAGCAGGCCGAAGCAGACGCTGTGCACCTGGCCAGGGAGATGCAGGCCGAGTACTGGTCAGTGTCGGCCAAGACTGG... | GGCTCCTGCTTCATCTTCCTCGTGGGAACCAAGAAGGACCTTCTGGTGAGCAGAGTGGCACTGGTGGTCTGGGTGGCCCTTGGGAAAATGCCTCCCCTTACAGCCCTCATTGGAGGAGCCATGGGGAGGGAGGGAGGCAGCACAGTGGGAAGCAGGCAGCTGCCTATCCCCCTGGGCCTCCCTGCAGGAGAGCCGGGACGCTGGGTCAACAAGGGCCATTTCTCCCAGTCAGGGGCCGCATGTGAGCAGGCCGAAGCAGACGCTGTGCACCTGGCCAGGGAGATGCAGGCCGAGTACTGGTCAGTGTCGGCCAAGACTGG... |
Task1_train_48499 | A mutation on Chromosome 22 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AGACGGGATTTCGCCATGTTGGCCAGGCTGGTAATTTTTGTATCTTTAGTAGAGACGGGGTTTTGCCACGTTAGCCAGGCTGGTCTCTTAACTCCTGATCCAAGTGATCCACCTACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGGAACCACTGTGCCTGGCCTTTGCATTGGTTTTCTTGCTGCTCCTGTTTTGCTCTCCCCCTCCCCATCCCTCAGTCTTGCCTCTGGGAGTACTCGTCCCAAACAAGCTCCAAGTACAACAGCCTTTCTTTGAGGCCTGCTTGCAGGGAGCCCAAGCCAAAACAGATGTTACAG... | AGACGGGATTTCGCCATGTTGGCCAGGCTGGTAATTTTTGTATCTTTAGTAGAGACGGGGTTTTGCCACGTTAGCCAGGCTGGTCTCTTAACTCCTGATCCAAGTGATCCACCTACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGGAACCACTGTGCCTGGCCTTTGCATTGGTTTTCTTGCTGCTCCTGTTTTGCTCTCCCCCTCCCCATCCCTCAGTCTTGCCTCTGGGAGTACTCGTCCCAAACAAGCTCCAAGTACAACAGCCTTTCTTTGAGGCCTGCTTGCAGGGAGCCCAAGCCAAAACAGATGTTACAG... |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.