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_48500 | The following genetic variant occurs on Chromosome 22. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TTCTTATAGATTTCACTCAAAGGCCAGTAGCTTCCTCCTGAGCGGTGAGTGCATCATGTCATGGCTTCTGACAGGCCCCCGGTCCTCTCCCAGCCCAGCATCCCCGACCCTCTCCCAACATCTCGCGACCCTGTGCTTTGGTGTTGAGGGAGCAGTGGCAGTCAGGAGGGACTGAGCACCTGTGCTGGGCGGCCAGGGCCAGGCTCTTTTGCTGGTGCTGCCAGAGACGCCTCAGGTCACCCAAGAGTCTCAGGTTCCTCTCCTTCCTCCAGAGGCGGGGCTGGAAATGCTGCTGGCTCTGCTCACACTCCAGGGCTGGG... | TTCTTATAGATTTCACTCAAAGGCCAGTAGCTTCCTCCTGAGCGGTGAGTGCATCATGTCATGGCTTCTGACAGGCCCCCGGTCCTCTCCCAGCCCAGCATCCCCGACCCTCTCCCAACATCTCGCGACCCTGTGCTTTGGTGTTGAGGGAGCAGTGGCAGTCAGGAGGGACTGAGCACCTGTGCTGGGCGGCCAGGGCCAGGCTCTTTTGCTGGTGCTGCCAGAGACGCCTCAGGTCACCCAAGAGTCTCAGGTTCCTCTCCTTCCTCCAGAGGCGGGGCTGGAAATGCTGCTGGCTCTGCTCACACTCCAGGGCTGGG... |
Task1_train_48501 | A variant affecting Chromosome 22 has been observed. Determine if it's benign or associated with disease. | Benign | AATGCAATATCTTCCTGATCCTTCCCTGCTTTGACCAAGTGCTGAGGAATGACCCCAGCACTGACAGATGTTGACCTGCACTGTTCCATGTGATCCCTTACACTTCTCAGAATCTGTGAGCTGACCAGAAGCCTGTGAGCTTTCTATGTGTATTTCACAGTAATGCCCATGCCAACGTCTATTGTTCCGTGTACCTTTTGCTACCCAGAGTTATGTGACCACTGGGGCCCCATCTGATGGTGGGCAATGTTTGGCACACTTATAGGCCATCCACTACCACTACCAGGGGCACGCATAGGTGCTGGAACTCCCTGGTGTGG... | AATGCAATATCTTCCTGATCCTTCCCTGCTTTGACCAAGTGCTGAGGAATGACCCCAGCACTGACAGATGTTGACCTGCACTGTTCCATGTGATCCCTTACACTTCTCAGAATCTGTGAGCTGACCAGAAGCCTGTGAGCTTTCTATGTGTATTTCACAGTAATGCCCATGCCAACGTCTATTGTTCCGTGTACCTTTTGCTACCCAGAGTTATGTGACCACTGGGGCCCCATCTGATGGTGGGCAATGTTTGGCACACTTATAGGCCATCCACTACCACTACCAGGGGCACGCATAGGTGCTGGAACTCCCTGGTGTGG... |
Task1_train_48502 | This alteration occurs on Chromosome 22. Is it associated with a disease or is it a benign variant? | Benign | CAGCTGGTCACACGGTCACCAGCAGCCTCTGAAGGTAGCTGCTTCTCTGAACGCAGCCTCCCCTGAATACTAACACGCTTTTAACTTTTCGCCAACCTGCTGTCTGTGTGGCAGAGAAAATCCTTGTTTCATTTCCACTTTCAAACATACATTTGCGTAACCTTTCACGGGTTCAATACCTGCCTGCGTTTTCCCCAAGTCGCCTCGCAGATCCTGGGCCTTGGGACGCGCTTCCTCCCACCCTGGAGTCTTCCGGCATTTTCCCCTTGGCCAGGGCTGGGATGGCCGTAGCTGTTTCTCCAGACTCACGTTCATGTTAA... | CAGCTGGTCACACGGTCACCAGCAGCCTCTGAAGGTAGCTGCTTCTCTGAACGCAGCCTCCCCTGAATACTAACACGCTTTTAACTTTTCGCCAACCTGCTGTCTGTGTGGCAGAGAAAATCCTTGTTTCATTTCCACTTTCAAACATACATTTGCGTAACCTTTCACGGGTTCAATACCTGCCTGCGTTTTCCCCAAGTCGCCTCGCAGATCCTGGGCCTTGGGACGCGCTTCCTCCCACCCTGGAGTCTTCCGGCATTTTCCCCTTGGCCAGGGCTGGGATGGCCGTAGCTGTTTCTCCAGACTCACGTTCATGTTAA... |
Task1_train_48503 | A genomic change on Chromosome 22 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CTGCTTCTCTGAACGCAGCCTCCCCTGAATACTAACACGCTTTTAACTTTTCGCCAACCTGCTGTCTGTGTGGCAGAGAAAATCCTTGTTTCATTTCCACTTTCAAACATACATTTGCGTAACCTTTCACGGGTTCAATACCTGCCTGCGTTTTCCCCAAGTCGCCTCGCAGATCCTGGGCCTTGGGACGCGCTTCCTCCCACCCTGGAGTCTTCCGGCATTTTCCCCTTGGCCAGGGCTGGGATGGCCGTAGCTGTTTCTCCAGACTCACGTTCATGTTAAAGGAACAAAAACAATCATATACCTTTAAGTCAAAGAGT... | CTGCTTCTCTGAACGCAGCCTCCCCTGAATACTAACACGCTTTTAACTTTTCGCCAACCTGCTGTCTGTGTGGCAGAGAAAATCCTTGTTTCATTTCCACTTTCAAACATACATTTGCGTAACCTTTCACGGGTTCAATACCTGCCTGCGTTTTCCCCAAGTCGCCTCGCAGATCCTGGGCCTTGGGACGCGCTTCCTCCCACCCTGGAGTCTTCCGGCATTTTCCCCTTGGCCAGGGCTGGGATGGCCGTAGCTGTTTCTCCAGACTCACGTTCATGTTAAAGGAACAAAAACAATCATATACCTTTAAGTCAAAGAGT... |
Task1_train_48504 | Given a variant located on Chromosome 22, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAATATGTGGACTCTGGCTGGGGAGAGACTAAAGGAGCTCTGGGGCTCATACTTCTTATAATTCCCACGAGAAGGCTGACATCTGGGGACTTCCCCCACAAGAGGCAAATAGTGAGTTCTGTAAATGGAGACTTAGGTCCCCTGCAAAGCAGAGGGGAGGCTGGGGTCACAGCTGGCCACTGAGAGACCCATCCCCCTCAGCACCGTGGCTTCCCAGCTCTCCCTGTCCTCCTCCCCCCGACATCTGCCCCTTCCCTCCTAACCCCAGGACCAGGGGACCCAGATCTGGAGCTTTGATGAGGAAGCTGCTCACAAATCTG... | AAATATGTGGACTCTGGCTGGGGAGAGACTAAAGGAGCTCTGGGGCTCATACTTCTTATAATTCCCACGAGAAGGCTGACATCTGGGGACTTCCCCCACAAGAGGCAAATAGTGAGTTCTGTAAATGGAGACTTAGGTCCCCTGCAAAGCAGAGGGGAGGCTGGGGTCACAGCTGGCCACTGAGAGACCCATCCCCCTCAGCACCGTGGCTTCCCAGCTCTCCCTGTCCTCCTCCCCCCGACATCTGCCCCTTCCCTCCTAACCCCAGGACCAGGGGACCCAGATCTGGAGCTTTGATGAGGAAGCTGCTCACAAATCTG... |
Task1_train_48505 | A variant was discovered on Chromosome 22. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AGCACACTCAGAGGCGTGCTTCCTTCCGCCCTTGCGGTGGGTGGGGAGGCAATGGCGGGAAAGGGGGGTGGTGCACATGGCGGGGGTCGTCGGGGAAGCGGCTCTGTGAGGAGGCGAAGCCAGCACCTGGAGCGAGTCCCTTAAAGGGAAAACCCGAGCTGAGTCCTGCTCATTCACAAGGGTTCCTCTCGGCCAGAGACCGCCGCATTACCCTGGAGCAGGTTTTTAAGCCGCACAATCTCTTCGCCATTCAATCCGTGATCCTCAAGCTTCAGCGTGCATCAGACACCTGAAACTCTAGCCACAGTTGCAGGGTCCCC... | AGCACACTCAGAGGCGTGCTTCCTTCCGCCCTTGCGGTGGGTGGGGAGGCAATGGCGGGAAAGGGGGGTGGTGCACATGGCGGGGGTCGTCGGGGAAGCGGCTCTGTGAGGAGGCGAAGCCAGCACCTGGAGCGAGTCCCTTAAAGGGAAAACCCGAGCTGAGTCCTGCTCATTCACAAGGGTTCCTCTCGGCCAGAGACCGCCGCATTACCCTGGAGCAGGTTTTTAAGCCGCACAATCTCTTCGCCATTCAATCCGTGATCCTCAAGCTTCAGCGTGCATCAGACACCTGAAACTCTAGCCACAGTTGCAGGGTCCCC... |
Task1_train_48506 | A mutation located on Chromosome 22 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CTGGCTGGAGGCGGGTCGGCCCTGTGCGGTAGCGGAAGGGAAGAGAGGAGCCGGTGGGTGCGGAGGGCGGGGACTGGCTGGGTCCCGTGGGGGCGGGTCCCGGGAGGAGGCTGGGCTGGCGCCCACTTCGTGCTTTGCAGGACTCAAGAGACCAACACTTGGGAGTCACCACACATGGGAGAAAAGTCACCACACATGGGAGATGGATGGAGGGTTCTCCAAGGCAGTTTAAGCAACAGATGTTGGAGCTGTTATGCCCGGGGCACAGTCTTAGCCCATAGGCCCAGTCGCAGCTCTGGGAAAGGGAGAGATGGGAGGGA... | CTGGCTGGAGGCGGGTCGGCCCTGTGCGGTAGCGGAAGGGAAGAGAGGAGCCGGTGGGTGCGGAGGGCGGGGACTGGCTGGGTCCCGTGGGGGCGGGTCCCGGGAGGAGGCTGGGCTGGCGCCCACTTCGTGCTTTGCAGGACTCAAGAGACCAACACTTGGGAGTCACCACACATGGGAGAAAAGTCACCACACATGGGAGATGGATGGAGGGTTCTCCAAGGCAGTTTAAGCAACAGATGTTGGAGCTGTTATGCCCGGGGCACAGTCTTAGCCCATAGGCCCAGTCGCAGCTCTGGGAAAGGGAGAGATGGGAGGGA... |
Task1_train_48507 | Here is a genetic alteration on Chromosome 22. Based on the data, is it a benign variant or a cause of disease? | Benign | TGAGGGGTCCCAGGCAGGGGTGCCAGCCCTGCCCAGTCTCTCTCCATGTCCTCCCAGCGACCATTGCTCTCCTGGCTGAGGATGGCAACCTAGTGAGCCTGGAGGAGGACCTGAAGGAAGGGGCTTCCCGGGCCCAGACCATGGGCAACTCCCTACTGAAGGAGCGAGCCATATATGTCCTCGTTCGGATCATCAGTAAGGTGGCCCAAGGTTCTCTCCCCTGCAGCTATGGTAGAATGTAAGAGGGGGGCATAGCAGACCATAGACCACCCAAGGCCCTGTCCGGCCTCCCACCTCGGCTGGGGACCTAGCCCCAATCC... | TGAGGGGTCCCAGGCAGGGGTGCCAGCCCTGCCCAGTCTCTCTCCATGTCCTCCCAGCGACCATTGCTCTCCTGGCTGAGGATGGCAACCTAGTGAGCCTGGAGGAGGACCTGAAGGAAGGGGCTTCCCGGGCCCAGACCATGGGCAACTCCCTACTGAAGGAGCGAGCCATATATGTCCTCGTTCGGATCATCAGTAAGGTGGCCCAAGGTTCTCTCCCCTGCAGCTATGGTAGAATGTAAGAGGGGGGCATAGCAGACCATAGACCACCCAAGGCCCTGTCCGGCCTCCCACCTCGGCTGGGGACCTAGCCCCAATCC... |
Task1_train_48508 | This genomic variant is located on Chromosome 22. Can you determine its pathogenicity and name any linked disease? | Benign | CCGGGCGCGGTGGCTCACGCCTGTAATCCCAGTACTTTGGGAGGCCGAGGCAGGTGGATCATGAGGTCAGGAGTTCAAGACCAGCCTGGCCAAGATGGATAAACCTCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGAGGCTGGGTGCGGTGGCGCATGCTTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACAAGGTCAGGAGATCGAGACCATCCTGGTAACATGGTGAAATCCCGTTTCTACTAAAAATACAAAAAAATTAGCCGGGCATGGCAGCAAGTGCCTGCAGTCCCAGCTACTCAGG... | CCGGGCGCGGTGGCTCACGCCTGTAATCCCAGTACTTTGGGAGGCCGAGGCAGGTGGATCATGAGGTCAGGAGTTCAAGACCAGCCTGGCCAAGATGGATAAACCTCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGAGGCTGGGTGCGGTGGCGCATGCTTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACAAGGTCAGGAGATCGAGACCATCCTGGTAACATGGTGAAATCCCGTTTCTACTAAAAATACAAAAAAATTAGCCGGGCATGGCAGCAAGTGCCTGCAGTCCCAGCTACTCAGG... |
Task1_train_48509 | A variant was discovered on Chromosome 22. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AAACAGCTTTTGGTATTTTTTTTTTTTTTTCGAGATAGGATGTTGCTCTCTCGCCCAGGCTGGAGTGCAGTGGTTGATCCCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCATGCTTCAGCCTCCTGAGTAGCTGGATTATAGACGTGTGCCACCACGCCTGGCTAACTTTTGTATTTTTGGTAGGGTTGAGGTTTCACCATGTTGGCCAGGCTGGTTTCGAACTCACCTTTTGGTTTTTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTTGCCCAGGCTGGACTGCAATGGTGTAATCTCGGCTC... | AAACAGCTTTTGGTATTTTTTTTTTTTTTTCGAGATAGGATGTTGCTCTCTCGCCCAGGCTGGAGTGCAGTGGTTGATCCCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCATGCTTCAGCCTCCTGAGTAGCTGGATTATAGACGTGTGCCACCACGCCTGGCTAACTTTTGTATTTTTGGTAGGGTTGAGGTTTCACCATGTTGGCCAGGCTGGTTTCGAACTCACCTTTTGGTTTTTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTTGCCCAGGCTGGACTGCAATGGTGTAATCTCGGCTC... |
Task1_train_48510 | Given this context: Chromosome 22 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CTACTGCCAGCTGGGGCCTTGCTGCTCTGAAGTCCCCTGCGGAGGGCCCAGTCCTGTGTGGGCACTGCTGGGCTGTCGCCAGCCTGGGTGCAGGAGGGCTGTTCTAGCTCCAGTGGCACCCATAGCCAGGTCAGCTGGGGCCCTTTCCCACCCCAGCAGGTGCTGTGGCCTGGGCCAGCTCCTGCCTTACAAGCCAGCTGTGAGGAATATGGGAATAGCCCTCCCGGCCTGGTGCCAGCTCTTGGAGTTGACACGGTACAGGGAGGAGACACAGCCCAGGGTCCCTTCCCAGCCCTGCCTCCAAGGAGTTCATGTCCCCT... | CTACTGCCAGCTGGGGCCTTGCTGCTCTGAAGTCCCCTGCGGAGGGCCCAGTCCTGTGTGGGCACTGCTGGGCTGTCGCCAGCCTGGGTGCAGGAGGGCTGTTCTAGCTCCAGTGGCACCCATAGCCAGGTCAGCTGGGGCCCTTTCCCACCCCAGCAGGTGCTGTGGCCTGGGCCAGCTCCTGCCTTACAAGCCAGCTGTGAGGAATATGGGAATAGCCCTCCCGGCCTGGTGCCAGCTCTTGGAGTTGACACGGTACAGGGAGGAGACACAGCCCAGGGTCCCTTCCCAGCCCTGCCTCCAAGGAGTTCATGTCCCCT... |
Task1_train_48511 | This mutation is located on Chromosome 22. Is it associated with a disease or is it a benign polymorphism? | Benign | CATGAACAGGTTTCATTGCTGAGGTGTTTGTTCTGTCCATGAGGTAGGAACCTCGGCAATGAAAGGGTGAGGCAGCCCTGTGTCTCCACAACTGGGGGGATGGAAGGAACCTTGGCTGCCTCACCCCACAGGTCGGGCAGGGCCACCTGGCTGGGAGGTGCCGGGAAGGCTGGGCCCTCACTCCTGACCGCCAGCTCACACCGCCGCAAAGCCATCTCCACAAGGTCTGGCTACAACACGGAGGGCAGACTCAACAGAGAACAGTGTTGTTACCATGAAAATGACAACCTGTCTTTGGAGGAGGCCCCGTGCCACTGAGC... | CATGAACAGGTTTCATTGCTGAGGTGTTTGTTCTGTCCATGAGGTAGGAACCTCGGCAATGAAAGGGTGAGGCAGCCCTGTGTCTCCACAACTGGGGGGATGGAAGGAACCTTGGCTGCCTCACCCCACAGGTCGGGCAGGGCCACCTGGCTGGGAGGTGCCGGGAAGGCTGGGCCCTCACTCCTGACCGCCAGCTCACACCGCCGCAAAGCCATCTCCACAAGGTCTGGCTACAACACGGAGGGCAGACTCAACAGAGAACAGTGTTGTTACCATGAAAATGACAACCTGTCTTTGGAGGAGGCCCCGTGCCACTGAGC... |
Task1_train_48512 | This variant is located on Chromosome 22. Evaluate its biological effect and specify any disease association. | Benign | GGCCGCCCCTACTGGGAAGTGAGGACCCCTCTGCCCGGCCAGCCGCCCCGTCCGGGAGGGAGGTGGGGGGGACAGCCCCCCGCCCAGCCAGCCGCCCTATCCAGGAGGTGAGGGGCGCCTCTGCCCGGCCGTCCCTACTGGGAAGTGAGGAGCCCCTCTGCCTGGCCAGCCGCCCCGTCCGGGAGGGTGGTGGGGGGGTCAGCCCCCCGCCCGGCCAGCCGCCCCATCCGGGAGGTGAGGGGCGCTTCTGCCCGGCCGCCCCTACTGGGAAGTGAGGAGCCCCTCTGCCCGGCCACGACCCCGTCTGGGAGGTGTGCCCA... | GGCCGCCCCTACTGGGAAGTGAGGACCCCTCTGCCCGGCCAGCCGCCCCGTCCGGGAGGGAGGTGGGGGGGACAGCCCCCCGCCCAGCCAGCCGCCCTATCCAGGAGGTGAGGGGCGCCTCTGCCCGGCCGTCCCTACTGGGAAGTGAGGAGCCCCTCTGCCTGGCCAGCCGCCCCGTCCGGGAGGGTGGTGGGGGGGTCAGCCCCCCGCCCGGCCAGCCGCCCCATCCGGGAGGTGAGGGGCGCTTCTGCCCGGCCGCCCCTACTGGGAAGTGAGGAGCCCCTCTGCCCGGCCACGACCCCGTCTGGGAGGTGTGCCCA... |
Task1_train_48513 | This genomic variant is located on Chromosome 22. Can you determine its pathogenicity and name any linked disease? | Benign | TTTCATGTGTCAACAAACCACGCTCACAATTATTTTTGAGACAGGCTTCTCTCCCAAGGCCTAATTGCTGGTATTTAGGGTATGTCAGGCTACCGTGAATCAACGCCCTCAAGCCTCCTAAATGCCCCCTTTTCTAGTTGTGAGGGTCTGTGAGGCACTGCTTTAAGCTATACCCTTGATTTGATCTTTACTATGAGTCCATGGCTTCCTGGCAGTGCTCTGGATTTGATCTTTGCTCACAGGCTGTTACTTAATTTGGGATTCTTTTGCTAGCTGGAGAGGATAGAGGCGAGAAAACATTTTTTGTTGTTGTTTTCAAC... | TTTCATGTGTCAACAAACCACGCTCACAATTATTTTTGAGACAGGCTTCTCTCCCAAGGCCTAATTGCTGGTATTTAGGGTATGTCAGGCTACCGTGAATCAACGCCCTCAAGCCTCCTAAATGCCCCCTTTTCTAGTTGTGAGGGTCTGTGAGGCACTGCTTTAAGCTATACCCTTGATTTGATCTTTACTATGAGTCCATGGCTTCCTGGCAGTGCTCTGGATTTGATCTTTGCTCACAGGCTGTTACTTAATTTGGGATTCTTTTGCTAGCTGGAGAGGATAGAGGCGAGAAAACATTTTTTGTTGTTGTTTTCAAC... |
Task1_train_48514 | Here is a mutation located on Chromosome 22. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTCCACTTGCCTTGTGATATTCTATTACCCTCTTAAGTACTTGATGTCTGTCACTCACACCTGTTCGCACACTCCCTCCCCTTTTGAAAATCCCTAATAAAAACTTGCTGGTTTTTGTGGCTTGTGGGGCATCACGGATCCTACCAACGTGTGACGTCTCCCCCGGATGCCCAGCTTTACAATTTCTCTCTTTTGTACTCTCTCCCTTTATTTCTCAAGCCGGCTGACGGTTAGGAAAAATAGGAAAGAACCTACGTGATTATTGGGGCAGGTCCCCCGATAGAGTGGCACATGATGGGCACAGGGCAGGCTTGGGAAAT... | CTCCACTTGCCTTGTGATATTCTATTACCCTCTTAAGTACTTGATGTCTGTCACTCACACCTGTTCGCACACTCCCTCCCCTTTTGAAAATCCCTAATAAAAACTTGCTGGTTTTTGTGGCTTGTGGGGCATCACGGATCCTACCAACGTGTGACGTCTCCCCCGGATGCCCAGCTTTACAATTTCTCTCTTTTGTACTCTCTCCCTTTATTTCTCAAGCCGGCTGACGGTTAGGAAAAATAGGAAAGAACCTACGTGATTATTGGGGCAGGTCCCCCGATAGAGTGGCACATGATGGGCACAGGGCAGGCTTGGGAAAT... |
Task1_train_48515 | A mutation found on Chromosome 22 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TTAATCGTGCTTTTCAAATTCCCTATTTCCTTGATGGTCTTCTGTAGTTTTTCTATTACTGAAAGTGGGGTATTGAAGTCACCAACTATTATTACTCACAATGTAACCATATTTAACCCTTTACTTTTAAAATTCTTTTTGGAAACTGGAAGGATCTGTAACCACCACCCACTCCCACATCAGACCCTATGCATATGCCAACTGTCTGCTGCTCAGCAGCTGTGATGGTTGTTCCAGTTCTTTATTAGGCAAAGAACAGTTGTTTTTTTGTTTTTTTGTTTTTTTTTTTTTAACATTTCCTTTAAGGAAGGTGGCTCAGA... | TTAATCGTGCTTTTCAAATTCCCTATTTCCTTGATGGTCTTCTGTAGTTTTTCTATTACTGAAAGTGGGGTATTGAAGTCACCAACTATTATTACTCACAATGTAACCATATTTAACCCTTTACTTTTAAAATTCTTTTTGGAAACTGGAAGGATCTGTAACCACCACCCACTCCCACATCAGACCCTATGCATATGCCAACTGTCTGCTGCTCAGCAGCTGTGATGGTTGTTCCAGTTCTTTATTAGGCAAAGAACAGTTGTTTTTTTGTTTTTTTGTTTTTTTTTTTTTAACATTTCCTTTAAGGAAGGTGGCTCAGA... |
Task1_train_48516 | A change on Chromosome 22 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTCCCTGGCAGTCTGCCCCTTTGCTGCTGAACCCCCTCCAGAGCCCTGGCACTGGATGGGCACAGTGGCTCTGGGGAGAGCTGACAGGTGTTGGGGTGCCTGTCTCACCTTGGCTGGCTCTGCAGCCTCATTCCCAGCATCCCCACTTTATAAATGGGGAAGTTGAGGTACAGAGGTGAAGCCTTTCTGAAAGCTCCCTGGCTGGTGACATTCTCTGCTGCCATTGCACACAGGCCACTGGACTGCCCTTCTAGGCACCTCCGGGCTGCATGGGGCCTATGTTGTGCTGGGGCTCGTTCTTCCCTTTCTTTTGCTGCCCC... | CTCCCTGGCAGTCTGCCCCTTTGCTGCTGAACCCCCTCCAGAGCCCTGGCACTGGATGGGCACAGTGGCTCTGGGGAGAGCTGACAGGTGTTGGGGTGCCTGTCTCACCTTGGCTGGCTCTGCAGCCTCATTCCCAGCATCCCCACTTTATAAATGGGGAAGTTGAGGTACAGAGGTGAAGCCTTTCTGAAAGCTCCCTGGCTGGTGACATTCTCTGCTGCCATTGCACACAGGCCACTGGACTGCCCTTCTAGGCACCTCCGGGCTGCATGGGGCCTATGTTGTGCTGGGGCTCGTTCTTCCCTTTCTTTTGCTGCCCC... |
Task1_train_48517 | A variant has been detected on Chromosome 22. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCTGCTGCCATGCATTGGCCCTGGAGGCTCCCACAGCCCTTGAAGCCTCAGGGCCTCCTCCCTGCTTCCCTGGGCCCAGGCCCTCACTCACCCCTCACCTCCCCTGCCCAGTGCACCCCAACAAAGTGTCAATGATGGAGAAGAGCGAGTTGGTGAACGAGACGCGTTGGCAATACTACGGCACCGCCAACACCTCAGGCAACCTCAGCCTGACCTGGCATGTCAAGTCGCTGCCCACGCAGACCATCACCATCGAACTGTGGGGCTACGAGGAGACAGGTGAGGCCAGCTGAGGGCTGGGGTGGCATCAGAGCTTTGGG... | GCTGCTGCCATGCATTGGCCCTGGAGGCTCCCACAGCCCTTGAAGCCTCAGGGCCTCCTCCCTGCTTCCCTGGGCCCAGGCCCTCACTCACCCCTCACCTCCCCTGCCCAGTGCACCCCAACAAAGTGTCAATGATGGAGAAGAGCGAGTTGGTGAACGAGACGCGTTGGCAATACTACGGCACCGCCAACACCTCAGGCAACCTCAGCCTGACCTGGCATGTCAAGTCGCTGCCCACGCAGACCATCACCATCGAACTGTGGGGCTACGAGGAGACAGGTGAGGCCAGCTGAGGGCTGGGGTGGCATCAGAGCTTTGGG... |
Task1_train_48518 | A variant has been detected on Chromosome 22. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGCAAATATTAGTTACAAATCACACAAGGAAAAAGTCACCATGAGGGAGAGTCTGAGAGGCCCCAGCCAGGAAAACTCACTTCTGAAAAATGGCATCAACCACAGACCAGAGACCAAGGTGCTGAGATCCTCAGCCTGGGAGCAGCATAGACAATACCCTGCTCTCTGTCTTGGAGGCCACAGAACTGGCCTGGAGGCCACTGACAGCCTCACCCATCAAGGTCCCCAACTCCTATGGCCCCCAAAGTTGAAGTGTACCTGGCCTAAGAATCTCAGTGACTGAGTTCCTCCCAGGTGGCTTTGAGCAGCACGGATTTGGG... | TGCAAATATTAGTTACAAATCACACAAGGAAAAAGTCACCATGAGGGAGAGTCTGAGAGGCCCCAGCCAGGAAAACTCACTTCTGAAAAATGGCATCAACCACAGACCAGAGACCAAGGTGCTGAGATCCTCAGCCTGGGAGCAGCATAGACAATACCCTGCTCTCTGTCTTGGAGGCCACAGAACTGGCCTGGAGGCCACTGACAGCCTCACCCATCAAGGTCCCCAACTCCTATGGCCCCCAAAGTTGAAGTGTACCTGGCCTAAGAATCTCAGTGACTGAGTTCCTCCCAGGTGGCTTTGAGCAGCACGGATTTGGG... |
Task1_train_48519 | A mutation has occurred on Chromosome 22. What is the medical relevance of this mutation? | Benign | GAGAGGTGAGCACAGAGGGGAGAGATGATGGAGTCAGGAGCATGGGCTTCTGGTGGCCCCAGCAGACCCTGTGGCAGTGTGGCCAGGGGCCTCTGCAAGGAGGGATCTTGGCCAGGATGACGCTGCAGCAGGCCTCTTCCTGAGGCCCCCCAGCCAGTCCGGCCAGGGTCCCAGTGTCCAATGACCCCTGTTCCGCAGCAGCAGCTGGGGCCAGCCCCAGGCTCTCTTCCACTCCCAGCTTCTTAAGACAGGAAGTGGAGAGAGTTGTTTGACAAAACACTGGGGCAAACCACATCCTCTCTCTTCAAGGGACAGTTTGA... | GAGAGGTGAGCACAGAGGGGAGAGATGATGGAGTCAGGAGCATGGGCTTCTGGTGGCCCCAGCAGACCCTGTGGCAGTGTGGCCAGGGGCCTCTGCAAGGAGGGATCTTGGCCAGGATGACGCTGCAGCAGGCCTCTTCCTGAGGCCCCCCAGCCAGTCCGGCCAGGGTCCCAGTGTCCAATGACCCCTGTTCCGCAGCAGCAGCTGGGGCCAGCCCCAGGCTCTCTTCCACTCCCAGCTTCTTAAGACAGGAAGTGGAGAGAGTTGTTTGACAAAACACTGGGGCAAACCACATCCTCTCTCTTCAAGGGACAGTTTGA... |
Task1_train_48520 | A mutation located on Chromosome 22 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ACCATAATAAATACACAAACAGGGTTGTGGCCTGCCCTTGGAGCACACCTGCAGGCCCTGGCTGGCCGCATACTCCGGGTCTGCAGGCTTGGGCGCCTCAAGCAGTAGCAGAGGCGCTTCTGCCCTGGCCTCCCCACATCCCTCCAGCCTGCATCTCTGGCTCTTCTGTCTTCCTGTTCTTATTCTGTCTCTCCCTCCTCCTCACTGATCTTTCCACTTCTCTCCAGCTATTGATCTGAAGCTCCATTTACCAACCGGGAGGGTGCCCTTTTGGCCTGCTCGTGCTCTCCACGGGACGCTGCCTCTCAGCTGCCTGCCAG... | ACCATAATAAATACACAAACAGGGTTGTGGCCTGCCCTTGGAGCACACCTGCAGGCCCTGGCTGGCCGCATACTCCGGGTCTGCAGGCTTGGGCGCCTCAAGCAGTAGCAGAGGCGCTTCTGCCCTGGCCTCCCCACATCCCTCCAGCCTGCATCTCTGGCTCTTCTGTCTTCCTGTTCTTATTCTGTCTCTCCCTCCTCCTCACTGATCTTTCCACTTCTCTCCAGCTATTGATCTGAAGCTCCATTTACCAACCGGGAGGGTGCCCTTTTGGCCTGCTCGTGCTCTCCACGGGACGCTGCCTCTCAGCTGCCTGCCAG... |
Task1_train_48521 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | TATGGGGTCCTCCTGTCTTGCCTGAGCCTGCAGGAAGTTCCTGGTGGAGGAGGGTCAGTGACTGGCCATGTGGGTCCACAGCTCCTGCTTATATCAAAACCAAGAGAGGCCACACAGTCCAGGAGAGCAAGTCCCTGTTGGGGTAAATGCAGGTGTAGGCAAGAGCCAGGGCTAGGGAAGCACTAGAATACAGCCTGAAGATCCAGGAGGACTTCTTGGAGGAGGTGGCGGCTGGGCTGCAGATAACTTTGTTAGGCAGAGAGAGGAAGGGATTCCTAGCAGAGGAACAGCTGGGCTAAGGCCCAGTAGAGGGCGCTTTG... | TATGGGGTCCTCCTGTCTTGCCTGAGCCTGCAGGAAGTTCCTGGTGGAGGAGGGTCAGTGACTGGCCATGTGGGTCCACAGCTCCTGCTTATATCAAAACCAAGAGAGGCCACACAGTCCAGGAGAGCAAGTCCCTGTTGGGGTAAATGCAGGTGTAGGCAAGAGCCAGGGCTAGGGAAGCACTAGAATACAGCCTGAAGATCCAGGAGGACTTCTTGGAGGAGGTGGCGGCTGGGCTGCAGATAACTTTGTTAGGCAGAGAGAGGAAGGGATTCCTAGCAGAGGAACAGCTGGGCTAAGGCCCAGTAGAGGGCGCTTTG... |
Task1_train_48522 | This is a variant located on Chromosome 22. Is this mutation a likely cause of disease or not? | Benign | AAGCAAAAATGGATATGTAGGATCACATCAAGTTAAAAAGCTTCTATGTAGCAAAGGAAACAAAGTAGAGCAACAACTCACAGAATGGGAGAAAATATTTGCAAACTACCTGTCTGACAAGGGATTAATAACCAAAATCTAAGGAAAGCAAACAACTTTATAGGGGAAAAATAATCCAATTAAGAATGGACAAAACACTTGAACAGACATTTCTGAAGACATACAAATAGCAAACAGGCATATGAAAAAGTGCTGATATCAATGATCAGAGAAATGCAAATCAAAACTACAATGAGATATCATCTCACCCCAGTTAAATG... | AAGCAAAAATGGATATGTAGGATCACATCAAGTTAAAAAGCTTCTATGTAGCAAAGGAAACAAAGTAGAGCAACAACTCACAGAATGGGAGAAAATATTTGCAAACTACCTGTCTGACAAGGGATTAATAACCAAAATCTAAGGAAAGCAAACAACTTTATAGGGGAAAAATAATCCAATTAAGAATGGACAAAACACTTGAACAGACATTTCTGAAGACATACAAATAGCAAACAGGCATATGAAAAAGTGCTGATATCAATGATCAGAGAAATGCAAATCAAAACTACAATGAGATATCATCTCACCCCAGTTAAATG... |
Task1_train_48523 | This sequence change occurs on Chromosome 22. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGGATCACATCAAGTTAAAAAGCTTCTATGTAGCAAAGGAAACAAAGTAGAGCAACAACTCACAGAATGGGAGAAAATATTTGCAAACTACCTGTCTGACAAGGGATTAATAACCAAAATCTAAGGAAAGCAAACAACTTTATAGGGGAAAAATAATCCAATTAAGAATGGACAAAACACTTGAACAGACATTTCTGAAGACATACAAATAGCAAACAGGCATATGAAAAAGTGCTGATATCAATGATCAGAGAAATGCAAATCAAAACTACAATGAGATATCATCTCACCCCAGTTAAATGGCTTTTATGCAAGACAAG... | AGGATCACATCAAGTTAAAAAGCTTCTATGTAGCAAAGGAAACAAAGTAGAGCAACAACTCACAGAATGGGAGAAAATATTTGCAAACTACCTGTCTGACAAGGGATTAATAACCAAAATCTAAGGAAAGCAAACAACTTTATAGGGGAAAAATAATCCAATTAAGAATGGACAAAACACTTGAACAGACATTTCTGAAGACATACAAATAGCAAACAGGCATATGAAAAAGTGCTGATATCAATGATCAGAGAAATGCAAATCAAAACTACAATGAGATATCATCTCACCCCAGTTAAATGGCTTTTATGCAAGACAAG... |
Task1_train_48524 | Chromosome 22 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | ATTTGCCTCCATTTTTGAGAATGGTATGAGGAGCAACCAGAAACGAATCAGAATGATTACCGAGAGAGGAGGGGGCAGAGACAGAAGCTACATTTCCTTGAATATGCCTTGCTTCCTAATTTTGATTTTGGAGTAAAAAAAAAACTCTGGTTTTGACTCTGAAGCTAGGTAAACTTTTTACATAATTAAAATCAATTGAATCAAAAAGAAGTTTTTGAAAACACAGAAACACATGAAACTAACCATAAATCAAGTTGGTGACATAACCACACAGGGAAGAAATATTTCAGGTGACTTTGGAACATGATCTTTAACTGTGT... | ATTTGCCTCCATTTTTGAGAATGGTATGAGGAGCAACCAGAAACGAATCAGAATGATTACCGAGAGAGGAGGGGGCAGAGACAGAAGCTACATTTCCTTGAATATGCCTTGCTTCCTAATTTTGATTTTGGAGTAAAAAAAAAACTCTGGTTTTGACTCTGAAGCTAGGTAAACTTTTTACATAATTAAAATCAATTGAATCAAAAAGAAGTTTTTGAAAACACAGAAACACATGAAACTAACCATAAATCAAGTTGGTGACATAACCACACAGGGAAGAAATATTTCAGGTGACTTTGGAACATGATCTTTAACTGTGT... |
Task1_train_48525 | Chromosome 22 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTGAAAACACAGAAACACATGAAACTAACCATAAATCAAGTTGGTGACATAACCACACAGGGAAGAAATATTTCAGGTGACTTTGGAACATGATCTTTAACTGTGTACCCTTGATATGATCCAAGAACACAAAGAGTCACAAAAAAATCTCTAAAATGTATTCTGGAGATTTTTTTCATAGTATTTCATGTATATCTAACTTGAAAAATTGATTCATAATAGTCAACCACCTGGGTGTAAAAGTAATAGGGTTTTTTTATTTTTTGTTTTTTGGTTTTTTTTTTTTTGCCTTTTCCGTGTGTTAACTAATTTTTTGAATG... | TTGAAAACACAGAAACACATGAAACTAACCATAAATCAAGTTGGTGACATAACCACACAGGGAAGAAATATTTCAGGTGACTTTGGAACATGATCTTTAACTGTGTACCCTTGATATGATCCAAGAACACAAAGAGTCACAAAAAAATCTCTAAAATGTATTCTGGAGATTTTTTTCATAGTATTTCATGTATATCTAACTTGAAAAATTGATTCATAATAGTCAACCACCTGGGTGTAAAAGTAATAGGGTTTTTTTATTTTTTGTTTTTTGGTTTTTTTTTTTTTGCCTTTTCCGTGTGTTAACTAATTTTTTGAATG... |
Task1_train_48526 | This mutation is located on Chromosome 22. Is it associated with a disease or is it a benign polymorphism? | Benign | CTACTAAAACCACAAAATTACCTGGGCGTGGTGGCACATGCCTGTAATCCCAGCTACTCCGGAAGCTGAGGCAGGAGAATGGCTTGAACCTGGGAGGCAGAAGTTGCTGTGAGCCAAGGTCGCGCCATTGCACTCCAGCCTGGGCAGCAAGAGTGAAACTTGGTCTCAAAAAAAAAAAAAGACAGAGCTAAGTGGGTGGTGGACTTGAGGTTAGGTTTCAGCTGGGTGATCGTAGGCAAGTCTGGCGACCTCTCTGGGCCCTTTCCCTTCATCTCCATGAGGGAGATAACGATCATTCCTTCATTCTTGACTTTTGGAGT... | CTACTAAAACCACAAAATTACCTGGGCGTGGTGGCACATGCCTGTAATCCCAGCTACTCCGGAAGCTGAGGCAGGAGAATGGCTTGAACCTGGGAGGCAGAAGTTGCTGTGAGCCAAGGTCGCGCCATTGCACTCCAGCCTGGGCAGCAAGAGTGAAACTTGGTCTCAAAAAAAAAAAAAGACAGAGCTAAGTGGGTGGTGGACTTGAGGTTAGGTTTCAGCTGGGTGATCGTAGGCAAGTCTGGCGACCTCTCTGGGCCCTTTCCCTTCATCTCCATGAGGGAGATAACGATCATTCCTTCATTCTTGACTTTTGGAGT... |
Task1_train_48527 | This is a variant located on Chromosome 22. Is this mutation a likely cause of disease or not? | Benign | GACAATGCAACTTCCCCTCCTCGGGCCACCCCAGGAGCATGGCACACCCAGCCTTGGACAGTGGTGCCACCTGCTGTCTCTCAGTGCTGTTACCTTCATCCCGTGTGGATTTGCCTCAATCCACCTTACAACCCTAACATCCTCCATATGACAAGTAATAAAATCACCCCAGAGCTGACAGAAAGCACGATGAAATGCCAGCACACCTGTGGAAAGTTCTGCTCAAGGGAGCAGACTGGTGGTCTTGAGAGTAGGCCCACTTGTCAGGTGTGCCCACCTGTCCTTTCTCAAGGCGAGGGTTTCCCATGACCTGGAGGCTT... | GACAATGCAACTTCCCCTCCTCGGGCCACCCCAGGAGCATGGCACACCCAGCCTTGGACAGTGGTGCCACCTGCTGTCTCTCAGTGCTGTTACCTTCATCCCGTGTGGATTTGCCTCAATCCACCTTACAACCCTAACATCCTCCATATGACAAGTAATAAAATCACCCCAGAGCTGACAGAAAGCACGATGAAATGCCAGCACACCTGTGGAAAGTTCTGCTCAAGGGAGCAGACTGGTGGTCTTGAGAGTAGGCCCACTTGTCAGGTGTGCCCACCTGTCCTTTCTCAAGGCGAGGGTTTCCCATGACCTGGAGGCTT... |
Task1_train_48528 | This sequence change occurs on Chromosome 22. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGGGGTGATGAGAATTTCTAAAGTTAGATTGTGGTGACAATTGCACAGCTCTGTAAATTTATTAAAAATCAAGTTGAAACTTAGCTGAATGTTATGACATACAAATAATACCCCAATATAACTTTAAAAACAAATACCCAAAGGATTATAAATCATACTACTATAAAGACATATACACATGTATGTTTATTGTGGCACTATTCACAATAGCAAAGACTTGGAACGAACCCCAATGTCCATCAGTGATAGACTAGATAAAGAAAATGTGGCACATGTAATACTATGCAGCCGTAAGAGAGAATGAGTTCATGTCCTTTGCA... | TGGGGTGATGAGAATTTCTAAAGTTAGATTGTGGTGACAATTGCACAGCTCTGTAAATTTATTAAAAATCAAGTTGAAACTTAGCTGAATGTTATGACATACAAATAATACCCCAATATAACTTTAAAAACAAATACCCAAAGGATTATAAATCATACTACTATAAAGACATATACACATGTATGTTTATTGTGGCACTATTCACAATAGCAAAGACTTGGAACGAACCCCAATGTCCATCAGTGATAGACTAGATAAAGAAAATGTGGCACATGTAATACTATGCAGCCGTAAGAGAGAATGAGTTCATGTCCTTTGCA... |
Task1_train_48529 | This mutation is located on Chromosome 22. Is it associated with a disease or is it a benign polymorphism? | Benign | TCTCCCAGCCAGCTCGGTTAGCCTTGGCCTTTCCAACCCAGCTGGACACTGATGGCCATACCCTTGACGCCCCCCCGAGGGCTGCCTGGTTGTTTCCTGTTCCACAGGTGGTGGTGGTGGTGGTGGGGGGTGGTAGACCAGCTGTCCCAGCTGGATCCTCATGGCAGCTCTGATGAGCACTGGAGTTTGGGTGGGAGGAGGGGCACATGGGGGACAGAGGCAGGGCTGTCAGCTGCCAGGTTTATGCCACAGGGGTGGGTTTCTGTGGTCCCTGCCTTCGGGCACCATAGAGAACCGGAAACGGGCTCTCCTCCCCAGAT... | TCTCCCAGCCAGCTCGGTTAGCCTTGGCCTTTCCAACCCAGCTGGACACTGATGGCCATACCCTTGACGCCCCCCCGAGGGCTGCCTGGTTGTTTCCTGTTCCACAGGTGGTGGTGGTGGTGGTGGGGGGTGGTAGACCAGCTGTCCCAGCTGGATCCTCATGGCAGCTCTGATGAGCACTGGAGTTTGGGTGGGAGGAGGGGCACATGGGGGACAGAGGCAGGGCTGTCAGCTGCCAGGTTTATGCCACAGGGGTGGGTTTCTGTGGTCCCTGCCTTCGGGCACCATAGAGAACCGGAAACGGGCTCTCCTCCCCAGAT... |
Task1_train_48530 | This sequence change occurs on Chromosome 22. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ACTGCCGTGGGGGAAAAACAGGAGGACTTTGTACTGTACTTGCAAGGATGTGATCTGCTGGGTCCCAAGTCTGCAGCCTCTGTGCATCTTTGGGAGCTCTCTAAGAGCAGCTGTCCTTGAGACAGCAGAGTTTGGGGTTAATGAGTAGGAGTGTTGTGAGCTGTGATTTTGGGGCCCATCTCTTGGAGCTCCTTTGCACCTTTGGAGCTGCTTCCACCTTCCAGGGACTTCGGCGTGAGGACTGATGTCACTTGGACCCCATTGGCCCTCTATGTCTCCTTTCAGGTCTGTGCTCTGGTGTGAACTGTGGTTTTCTTGAA... | ACTGCCGTGGGGGAAAAACAGGAGGACTTTGTACTGTACTTGCAAGGATGTGATCTGCTGGGTCCCAAGTCTGCAGCCTCTGTGCATCTTTGGGAGCTCTCTAAGAGCAGCTGTCCTTGAGACAGCAGAGTTTGGGGTTAATGAGTAGGAGTGTTGTGAGCTGTGATTTTGGGGCCCATCTCTTGGAGCTCCTTTGCACCTTTGGAGCTGCTTCCACCTTCCAGGGACTTCGGCGTGAGGACTGATGTCACTTGGACCCCATTGGCCCTCTATGTCTCCTTTCAGGTCTGTGCTCTGGTGTGAACTGTGGTTTTCTTGAA... |
Task1_train_48531 | This genomic variant is located on Chromosome 22. Can you determine its pathogenicity and name any linked disease? | Benign | TCCAGTCATGTTTATCACGACATCTCTCACTTGCATTCAGCAAGTGTCTAGTGAATGCCTGCTGTGTGTCAGGCAATGTCCAGGTTGCCGGAGAGTCAGAGAGAAACCAGTTACAGGGATATAAACACAGACTCTTCACCCCTTTCCTTTCTTCTCTTCCTTCTTTCTCATTGCAGCTCCCCTACTGCATGCCAATTGCAAAATCTCTTCCTCCTCCCTCTTCAACCTGTTTTCTTTTGCTTTCCTTGTTCTTCCTTATTCTTCCTTAGTTCTCACTTGTCTAGACTTAGGCATGCTGTTTCTCTCTCTCTCTCCTCTTT... | TCCAGTCATGTTTATCACGACATCTCTCACTTGCATTCAGCAAGTGTCTAGTGAATGCCTGCTGTGTGTCAGGCAATGTCCAGGTTGCCGGAGAGTCAGAGAGAAACCAGTTACAGGGATATAAACACAGACTCTTCACCCCTTTCCTTTCTTCTCTTCCTTCTTTCTCATTGCAGCTCCCCTACTGCATGCCAATTGCAAAATCTCTTCCTCCTCCCTCTTCAACCTGTTTTCTTTTGCTTTCCTTGTTCTTCCTTATTCTTCCTTAGTTCTCACTTGTCTAGACTTAGGCATGCTGTTTCTCTCTCTCTCTCCTCTTT... |
Task1_train_48532 | A variant affecting Chromosome 22 has been observed. Determine if it's benign or associated with disease. | Benign | CTGTGTCATCACACAGTGGAAGGGGTGAGGGAGCCCTCTGGGGCCTCTTTTATAAGGGCACTAATCTCATTTACAAGGGCTCCACCCTGGTGACCTAATCACCTCCCAAAAGCCCCACCTCCTAATATCATCATATTGAGGATTAGGTGTCAACATATTAATTTTCGGGGGAGACAAACATTGAATCTATTTCAGCCCCCACCTATTTCCCTGGGAAAGACACTGCTCTCCTACCCCAGCCATTCCCTCCCGTGCCTTCCATGGCCATCACCTCAAGGGAGCTTTGGGTTGGCTTCCTTCCCAGATTCAAAAGCCCATTG... | CTGTGTCATCACACAGTGGAAGGGGTGAGGGAGCCCTCTGGGGCCTCTTTTATAAGGGCACTAATCTCATTTACAAGGGCTCCACCCTGGTGACCTAATCACCTCCCAAAAGCCCCACCTCCTAATATCATCATATTGAGGATTAGGTGTCAACATATTAATTTTCGGGGGAGACAAACATTGAATCTATTTCAGCCCCCACCTATTTCCCTGGGAAAGACACTGCTCTCCTACCCCAGCCATTCCCTCCCGTGCCTTCCATGGCCATCACCTCAAGGGAGCTTTGGGTTGGCTTCCTTCCCAGATTCAAAAGCCCATTG... |
Task1_train_48533 | A genomic change on Chromosome 22 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGGTGTCAACATATTAATTTTCGGGGGAGACAAACATTGAATCTATTTCAGCCCCCACCTATTTCCCTGGGAAAGACACTGCTCTCCTACCCCAGCCATTCCCTCCCGTGCCTTCCATGGCCATCACCTCAAGGGAGCTTTGGGTTGGCTTCCTTCCCAGATTCAAAAGCCCATTGGGTCACTGTGGTCAGTTCTATTTCTCCTAAACTGTCCTGTGTGATCAGGAGTGGAAGTGGTGTTACCCAACTGGGTAAGCAAGAAGTCTTCCTCAAAGTCTTGTAGCAGAATCTCAGTCACCCTTTATACATAGAGTTCTGAAT... | AGGTGTCAACATATTAATTTTCGGGGGAGACAAACATTGAATCTATTTCAGCCCCCACCTATTTCCCTGGGAAAGACACTGCTCTCCTACCCCAGCCATTCCCTCCCGTGCCTTCCATGGCCATCACCTCAAGGGAGCTTTGGGTTGGCTTCCTTCCCAGATTCAAAAGCCCATTGGGTCACTGTGGTCAGTTCTATTTCTCCTAAACTGTCCTGTGTGATCAGGAGTGGAAGTGGTGTTACCCAACTGGGTAAGCAAGAAGTCTTCCTCAAAGTCTTGTAGCAGAATCTCAGTCACCCTTTATACATAGAGTTCTGAAT... |
Task1_train_48534 | A sequence alteration has been identified on Chromosome 22. Is it disease-inducing or harmless? | Benign | ACAAAGCACTCAGAGGCAGGGACCCCATGATTGGAAACCCGCGTGTGCATCGCCCTCAGCATCTCTTCAGGCCTGAGCCCACAGTGGCTTTATCTGCAGTGCCAACACTCTGACATTTGGCAACTTTTTTACTTTTTTAAAAAATAAATTATAACTTTGGTGAGGGGAGGGAATGGGGTCGTTTCTCTTAGAGAGAGGACAAATAGATTTTATTTATTAAAGGAAAGGTTGATGGACTCCAGTCTCTCTCCTTTGAATGATGCCATTTATTTTACAGTCTATAATTTGGTCCCACTGTGAGCCTCCTACTTTTCAGAGGC... | ACAAAGCACTCAGAGGCAGGGACCCCATGATTGGAAACCCGCGTGTGCATCGCCCTCAGCATCTCTTCAGGCCTGAGCCCACAGTGGCTTTATCTGCAGTGCCAACACTCTGACATTTGGCAACTTTTTTACTTTTTTAAAAAATAAATTATAACTTTGGTGAGGGGAGGGAATGGGGTCGTTTCTCTTAGAGAGAGGACAAATAGATTTTATTTATTAAAGGAAAGGTTGATGGACTCCAGTCTCTCTCCTTTGAATGATGCCATTTATTTTACAGTCTATAATTTGGTCCCACTGTGAGCCTCCTACTTTTCAGAGGC... |
Task1_train_48535 | Here is a variant on Chromosome 22. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CCTCTGCCCAGCCTCCAAGCCTCCATGGGTCTTCACACAGTCCTCTGTTCTGAATCTGCCTCGTGACTCTGAATCCTAAAACATTTCTGTGTCTCCCACAAGGTCACTCTTACATTCCTTCAGTTTAAAATGTACCTCCCCCAACCCTGCTTTTACACTGTTGGTGGGAATGTAAATTAATTCAACCATTGTGGAAGATGGTGCTGAGATTCCTCAAAGATCTGGAACCAGAAATAGCATTTGACTCAGCAATCCCATTACTGGGTCCCATTACATATATACCCAAAGGAATATAAATCATTCTGTTACAAAGATACATG... | CCTCTGCCCAGCCTCCAAGCCTCCATGGGTCTTCACACAGTCCTCTGTTCTGAATCTGCCTCGTGACTCTGAATCCTAAAACATTTCTGTGTCTCCCACAAGGTCACTCTTACATTCCTTCAGTTTAAAATGTACCTCCCCCAACCCTGCTTTTACACTGTTGGTGGGAATGTAAATTAATTCAACCATTGTGGAAGATGGTGCTGAGATTCCTCAAAGATCTGGAACCAGAAATAGCATTTGACTCAGCAATCCCATTACTGGGTCCCATTACATATATACCCAAAGGAATATAAATCATTCTGTTACAAAGATACATG... |
Task1_train_48536 | Chromosome 22 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TCCAGCTTCACTACCAGGGTAGGGTCAGGCCAAGGCTGATGAAACATAGGCGTTTGCCTCAGTTTCCCTCTGGAGAAAAGGATTTTAAAACTTTTTGTGCCAGGGACCTCTCTGACAGTTTGGTAAAACCTACAAACCCCTTCTCAGAATAATGTTTTTAAAAGTATAAAATAAAATATATACAATTTTAAAGAAAACGGTATTACTGAGCTGCAGTTATCAAAATACTGTTATAATCTATGATGCCTTAATCTATGTGCTTTTTATTAATTCATTAAACAATGTCTTCTAGTAGTTCTTATAATTGCTGACATTTCAAA... | TCCAGCTTCACTACCAGGGTAGGGTCAGGCCAAGGCTGATGAAACATAGGCGTTTGCCTCAGTTTCCCTCTGGAGAAAAGGATTTTAAAACTTTTTGTGCCAGGGACCTCTCTGACAGTTTGGTAAAACCTACAAACCCCTTCTCAGAATAATGTTTTTAAAAGTATAAAATAAAATATATACAATTTTAAAGAAAACGGTATTACTGAGCTGCAGTTATCAAAATACTGTTATAATCTATGATGCCTTAATCTATGTGCTTTTTATTAATTCATTAAACAATGTCTTCTAGTAGTTCTTATAATTGCTGACATTTCAAA... |
Task1_train_48537 | A variant was discovered on Chromosome 22. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TCTGGCTTCTCTCTGCTACGATGCTGCAAGAATTTTCAGGCCAAATTTCAGTCCCTGGGTAAAGGGAGGGTACAACTTTTCCATTTTTTAAGCTGTGAGAGGGTAGAGTACAAAAGGGATATTTGAAATTGTGCTCCCTGAGTATCAGACTTGTAGAAGCAGAGACCTGGCTGTTCTCATTGTATTAGAAGAAGCAGGATGAACAAAAGGTTTTGGAGAATGCTGGGAAACACGGCTGGGGTTTGAGAGACTTAGGCAGCATGACATTCAGGCCCTTTTAGGTTATTAGGACAATGAGAGTTCCGGGCTCTGTCCCTAAC... | TCTGGCTTCTCTCTGCTACGATGCTGCAAGAATTTTCAGGCCAAATTTCAGTCCCTGGGTAAAGGGAGGGTACAACTTTTCCATTTTTTAAGCTGTGAGAGGGTAGAGTACAAAAGGGATATTTGAAATTGTGCTCCCTGAGTATCAGACTTGTAGAAGCAGAGACCTGGCTGTTCTCATTGTATTAGAAGAAGCAGGATGAACAAAAGGTTTTGGAGAATGCTGGGAAACACGGCTGGGGTTTGAGAGACTTAGGCAGCATGACATTCAGGCCCTTTTAGGTTATTAGGACAATGAGAGTTCCGGGCTCTGTCCCTAAC... |
Task1_train_48538 | This variant is present on Chromosome 22. Is the change likely to result in a pathogenic outcome? | Benign | AGCAGATGCTGACATTTTACTTGTTTCCACCTCCCACAAAACAGACACACACACCCCCAACACAGCCAGTTCCCAAACCAGTGACTGTAGATGCAAGTTGCCTCTGGGTTGCCAGCCTGGGGCAGCTGTGAATTAAAGCCAGAGAAGACACATTTCTGACAGAAAGATCTATTGGAATATTGGCTGGAGACGCTGAGAGGCAGCAGAACACCTGGCGCTCAAGTGTGGCGGGTGACAGGGAATCAGAACCATCCTAATCACCCACCCAGGCTCCCTGTCAGTCCACCACCCATGCCCCTCACACTGGACCACACTGCCCC... | AGCAGATGCTGACATTTTACTTGTTTCCACCTCCCACAAAACAGACACACACACCCCCAACACAGCCAGTTCCCAAACCAGTGACTGTAGATGCAAGTTGCCTCTGGGTTGCCAGCCTGGGGCAGCTGTGAATTAAAGCCAGAGAAGACACATTTCTGACAGAAAGATCTATTGGAATATTGGCTGGAGACGCTGAGAGGCAGCAGAACACCTGGCGCTCAAGTGTGGCGGGTGACAGGGAATCAGAACCATCCTAATCACCCACCCAGGCTCCCTGTCAGTCCACCACCCATGCCCCTCACACTGGACCACACTGCCCC... |
Task1_train_48539 | A variant was discovered on Chromosome 22. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AAGGTGGGCAGATCACTAGGTCAAAACATTGAGACTATCCTGGCCAACATGGTGAAACCCTATCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCAGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATTGCTTGAAACCAGGAGACAGAGGTTGCAATGAGCCGAGACTGAGCCCCTGCACTCCAGCCTGGCGAGAGTGAGACTCCATCTCAAAATAAATAAATAAAAAATAATGCCCTTGACCAGATGGTTCCAAGGACTACGTGGACTAATATACACATTGCCAGCACTGCCCTTGACCT... | AAGGTGGGCAGATCACTAGGTCAAAACATTGAGACTATCCTGGCCAACATGGTGAAACCCTATCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCAGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATTGCTTGAAACCAGGAGACAGAGGTTGCAATGAGCCGAGACTGAGCCCCTGCACTCCAGCCTGGCGAGAGTGAGACTCCATCTCAAAATAAATAAATAAAAAATAATGCCCTTGACCAGATGGTTCCAAGGACTACGTGGACTAATATACACATTGCCAGCACTGCCCTTGACCT... |
Task1_train_48540 | Given this context: Chromosome 22 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | ACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCCGGGCCTGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGTTGAGGTAGGAGAACCGCTTGAACCGGGGAGGCGGAGGTTGCAGTGAGCTCAGATCACACCATTGTACTCCAGCCTGGGCAACAAGAGCGGAACTCCATCTCAAAAAAAAAAAAAAAAAAGAAGAAAAGATTAGCTTTTTCTCTTCCATAAAACTGCAGTCTATTTCCCGGGGCCTAGCCAGCATCAAACCCTGCTTTCCACAGAAGCCCATGGAGGCTGATG... | ACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCCGGGCCTGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGTTGAGGTAGGAGAACCGCTTGAACCGGGGAGGCGGAGGTTGCAGTGAGCTCAGATCACACCATTGTACTCCAGCCTGGGCAACAAGAGCGGAACTCCATCTCAAAAAAAAAAAAAAAAAAGAAGAAAAGATTAGCTTTTTCTCTTCCATAAAACTGCAGTCTATTTCCCGGGGCCTAGCCAGCATCAAACCCTGCTTTCCACAGAAGCCCATGGAGGCTGATG... |
Task1_train_48541 | This variant is located on Chromosome 22. Evaluate its biological effect and specify any disease association. | Benign | AGCATGGATAGACCTTGACAAACCAGGGGATATGGCCATAGAGCACGAGCCACAGAAGGCAGGACACTGACCCCCTTTCTTCAGCTTCCCAGCTATCACTGCAAGGGCAGGGCAGTGGGGGGACAGAGAGGCTGGGGTGGGGAACCAGAAACAAGCAAGAATTCTGGACCTGCCACTTGCAGGAAGTCTTTTCATCTCAATGAGGCTGTTTTCTTACTGGTAAAATGGGAGTTACAATGCCTCCTTCCCAGAACTGTTCTAAGGCTTGGCTAAAACGAGAGATGCGAAGTATTTCACATATAGTTGGTGCAGAATACATC... | AGCATGGATAGACCTTGACAAACCAGGGGATATGGCCATAGAGCACGAGCCACAGAAGGCAGGACACTGACCCCCTTTCTTCAGCTTCCCAGCTATCACTGCAAGGGCAGGGCAGTGGGGGGACAGAGAGGCTGGGGTGGGGAACCAGAAACAAGCAAGAATTCTGGACCTGCCACTTGCAGGAAGTCTTTTCATCTCAATGAGGCTGTTTTCTTACTGGTAAAATGGGAGTTACAATGCCTCCTTCCCAGAACTGTTCTAAGGCTTGGCTAAAACGAGAGATGCGAAGTATTTCACATATAGTTGGTGCAGAATACATC... |
Task1_train_48542 | This mutation is located on Chromosome 22. Is it associated with a disease or is it a benign polymorphism? | Benign | GTCCTGGATCTAAGCGAGGCAATAACAAGGGCCTGCGGGTCCTTCTGGGGAGAGGGTCTGCTCTGGGAATGGGGGCTTGGCTGCTATGGCCAGGATGGTCTTCGAGCTGCTCTTGGGCTCCATGCTGGGTCAGCATCTCAGGAGCAGAGGGAGGGCGCAAGCTGCTGATGGCTGTGTCCTCAGGAGGCGTGGGTTCCAGGCTGCTGGAGGCGCTGAGAGATGCCTTGCAGTAAGGAGCCCTGCCATCTGGAACAGGCACATGTAGGAAGGCAAAATGACCTGAGGCCATTTCCACTTCCTGAGCCTCTGGAATGTGGATT... | GTCCTGGATCTAAGCGAGGCAATAACAAGGGCCTGCGGGTCCTTCTGGGGAGAGGGTCTGCTCTGGGAATGGGGGCTTGGCTGCTATGGCCAGGATGGTCTTCGAGCTGCTCTTGGGCTCCATGCTGGGTCAGCATCTCAGGAGCAGAGGGAGGGCGCAAGCTGCTGATGGCTGTGTCCTCAGGAGGCGTGGGTTCCAGGCTGCTGGAGGCGCTGAGAGATGCCTTGCAGTAAGGAGCCCTGCCATCTGGAACAGGCACATGTAGGAAGGCAAAATGACCTGAGGCCATTTCCACTTCCTGAGCCTCTGGAATGTGGATT... |
Task1_train_48543 | Chromosome 22 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGGACCTGTTTATCTCTGATTTCTGGAGTTCAGCACTAGGTGGGTACCACTTGGCCAATGGTAGGGATTGTGGGGCAGAAAAGAGAATCAGTCCTCATTTGAGGACATTTTGCTTCACAGAGGGATAACTTGCTGGGTTCTAACGCCGCCCGCCCCTTACAGCTGTATGTCTTTTGGCACTTAATTCTGATCCTCAGTTTCTTTATCTGTGAAATGGAGATAATGTGTATATCCTATAGTTTTGAGAATTGAAGCTGTTTAGTTAAATGCTTGCCTGCTGTATACAAGGCAATAAATGTTGTCATTATTATTGCTGAAAT... | AGGACCTGTTTATCTCTGATTTCTGGAGTTCAGCACTAGGTGGGTACCACTTGGCCAATGGTAGGGATTGTGGGGCAGAAAAGAGAATCAGTCCTCATTTGAGGACATTTTGCTTCACAGAGGGATAACTTGCTGGGTTCTAACGCCGCCCGCCCCTTACAGCTGTATGTCTTTTGGCACTTAATTCTGATCCTCAGTTTCTTTATCTGTGAAATGGAGATAATGTGTATATCCTATAGTTTTGAGAATTGAAGCTGTTTAGTTAAATGCTTGCCTGCTGTATACAAGGCAATAAATGTTGTCATTATTATTGCTGAAAT... |
Task1_train_48544 | A genomic variant on Chromosome 22 is under review. What is the biological outcome — benign or pathogenic? | Benign | ACATGGCTAGTGGCTACCGTATGGGACACTGCAGGCAGAGACGATTTCATCAGCATAGATGTCCTTTTAGCCACTGTGTTTACTGAGCCCCAGGATCCATTATTGGAACACACAGGGTCCACAGCACTCACAGAAGCACACAGGCATGCATGCAAACTCACAGGGCTTAGTGAGAGGACTTTTCTTTGCAGTAACAGCCAAGCTATGGCAAAAACTAAACCAGGGATCTAGCACTTGCCAAGACTTGTTGACCGCCCCAGGGAAGAAATCTCTTTGGATGAAAATGAGAGACAGCTTCCATTTTAAATAAACAAACACAA... | ACATGGCTAGTGGCTACCGTATGGGACACTGCAGGCAGAGACGATTTCATCAGCATAGATGTCCTTTTAGCCACTGTGTTTACTGAGCCCCAGGATCCATTATTGGAACACACAGGGTCCACAGCACTCACAGAAGCACACAGGCATGCATGCAAACTCACAGGGCTTAGTGAGAGGACTTTTCTTTGCAGTAACAGCCAAGCTATGGCAAAAACTAAACCAGGGATCTAGCACTTGCCAAGACTTGTTGACCGCCCCAGGGAAGAAATCTCTTTGGATGAAAATGAGAGACAGCTTCCATTTTAAATAAACAAACACAA... |
Task1_train_48545 | 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 | GATCAGTGATGGATAAATGTATAGATGGGTGGATAGATGGAGAGTGGATGGATGGATGAATAGCTGAGTGCATGGATGGATAAATGGATTAATTCATAAGTAAAAAATATAGGATAGATAATGAATGTATAAATAGATAAGCAAATAATAAATAGGGAATTAATTAACAATTGACTTGGTGGAAAGATGGATAAATGAATAAGTGAGTATAATTCAAGTGTGGGTGTGTGGGTAAGTGATCAGACCGGGGTTGCTCAGTGATCAGACTGGGGCTGCTCAGAGAGAAGAGGGCTGCCTCAGTCTTCAGCCTCCCAGTACCC... | GATCAGTGATGGATAAATGTATAGATGGGTGGATAGATGGAGAGTGGATGGATGGATGAATAGCTGAGTGCATGGATGGATAAATGGATTAATTCATAAGTAAAAAATATAGGATAGATAATGAATGTATAAATAGATAAGCAAATAATAAATAGGGAATTAATTAACAATTGACTTGGTGGAAAGATGGATAAATGAATAAGTGAGTATAATTCAAGTGTGGGTGTGTGGGTAAGTGATCAGACCGGGGTTGCTCAGTGATCAGACTGGGGCTGCTCAGAGAGAAGAGGGCTGCCTCAGTCTTCAGCCTCCCAGTACCC... |
Task1_train_48546 | A mutation located on Chromosome 22 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCGCCCACCTTCATGAGGAACCCTGTAGTGAGGTGGGTAGGATTTTAATTTTAGAATTACCTAAAAGATACTTACTTATCTAAATTCTCCAACTAAACTCAGTACTAATACGACTTTCAGCATTTCCTTTCTTTATAAAATAAATTAATGGTTACCCCTAACTAGATGATTCCCTTGTCTTGCCTCAAGCTGGCAACAATTTAAGTTACCGTCAGAGCTGTAGGAGAAGTCCACCTCCACTTTTTAAGATACATCTCTCTCTTCCCGGTTGGCCATAATCCAGGCATACGTCCCAGCAAAAGGCCCTGTTGCTTAGGATC... | CCGCCCACCTTCATGAGGAACCCTGTAGTGAGGTGGGTAGGATTTTAATTTTAGAATTACCTAAAAGATACTTACTTATCTAAATTCTCCAACTAAACTCAGTACTAATACGACTTTCAGCATTTCCTTTCTTTATAAAATAAATTAATGGTTACCCCTAACTAGATGATTCCCTTGTCTTGCCTCAAGCTGGCAACAATTTAAGTTACCGTCAGAGCTGTAGGAGAAGTCCACCTCCACTTTTTAAGATACATCTCTCTCTTCCCGGTTGGCCATAATCCAGGCATACGTCCCAGCAAAAGGCCCTGTTGCTTAGGATC... |
Task1_train_48547 | Chromosome 22 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGCCCAGGTCAATGACTTAAATACCTCACCTAAAATAACTTTGTAAAATGCTTGGCAAATAGTAAGCACTCAATAAATGGCCAGGCCCTGTGCCAAGCTCTTTATTTACAGAGATCATGTCTCATAAGCCTCAGAATCCCCATCTTACAGATGGGGCAACCAAGGCTCAGAAAACAGAAGCCACTTGCCCTAGTCTCCACAGTCAGAAACAAGTGTGTTTCCACTGTGTTCATTTTAATTAGTAAACCCTACTTATTAGCTATGGAACTATTTTTATTCATTAAAATGATAAACAAAAAACATGAACAAGAAGGTGTTCA... | AGCCCAGGTCAATGACTTAAATACCTCACCTAAAATAACTTTGTAAAATGCTTGGCAAATAGTAAGCACTCAATAAATGGCCAGGCCCTGTGCCAAGCTCTTTATTTACAGAGATCATGTCTCATAAGCCTCAGAATCCCCATCTTACAGATGGGGCAACCAAGGCTCAGAAAACAGAAGCCACTTGCCCTAGTCTCCACAGTCAGAAACAAGTGTGTTTCCACTGTGTTCATTTTAATTAGTAAACCCTACTTATTAGCTATGGAACTATTTTTATTCATTAAAATGATAAACAAAAAACATGAACAAGAAGGTGTTCA... |
Task1_train_48548 | This genomic variant is located on Chromosome 22. Can you determine its pathogenicity and name any linked disease? | Benign | TGTTTCCACTGTGTTCATTTTAATTAGTAAACCCTACTTATTAGCTATGGAACTATTTTTATTCATTAAAATGATAAACAAAAAACATGAACAAGAAGGTGTTCAATTAAACTATATAAAGAAAATGTGAAGTCAAATTTCTGCTAATAGAGCAGATACAGGTTCCAACTTCAACAGCAGCCTCGCATATTTACTGAGACTCTGACAAGAGGAGGCTTCAGGGTACTAAAGTTGTTCTGTTACAATTCCAAAAGGATGAATCAAGTAACTCAGCTTCCTGGGCTACACCCTCCACAAGCAAAGAGGAGATAGAATTACAT... | TGTTTCCACTGTGTTCATTTTAATTAGTAAACCCTACTTATTAGCTATGGAACTATTTTTATTCATTAAAATGATAAACAAAAAACATGAACAAGAAGGTGTTCAATTAAACTATATAAAGAAAATGTGAAGTCAAATTTCTGCTAATAGAGCAGATACAGGTTCCAACTTCAACAGCAGCCTCGCATATTTACTGAGACTCTGACAAGAGGAGGCTTCAGGGTACTAAAGTTGTTCTGTTACAATTCCAAAAGGATGAATCAAGTAACTCAGCTTCCTGGGCTACACCCTCCACAAGCAAAGAGGAGATAGAATTACAT... |
Task1_train_48549 | The following genetic variant occurs on Chromosome 22. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GCCACGACACCCGGCTAATTTTTGTATTTTTAATAGAGATGGGGTTTCACCACGTTGGTCAGGCTGGTCTCGAACTCCTGATCTCAAGTTATCTACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCCCGGTGCCCAGCAAACTTTTTTTTTTTTTCTTGAGACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAACCTCCCTCTCCCAGGTTCAAACAATCCTCCCACCTCAACCTCCCGAGTAGCTGGGACTACAGGCACTCACGCTTGGCCTTTTTTTTT... | GCCACGACACCCGGCTAATTTTTGTATTTTTAATAGAGATGGGGTTTCACCACGTTGGTCAGGCTGGTCTCGAACTCCTGATCTCAAGTTATCTACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCCCGGTGCCCAGCAAACTTTTTTTTTTTTTCTTGAGACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAACCTCCCTCTCCCAGGTTCAAACAATCCTCCCACCTCAACCTCCCGAGTAGCTGGGACTACAGGCACTCACGCTTGGCCTTTTTTTTT... |
Task1_train_48550 | This mutation is located on Chromosome 22. Is it associated with a disease or is it a benign polymorphism? | Benign | AGGAGAGTCCCTTCCTGCAAGTGTGAAGAGAAGGAAGTGGGCAGTATTCCATTCCTGTCCGCCAGTGGCAGCCTGTCACCTCCTGCACACTCATGCCACTCAGGGGGACTGTGGTCTGCTGGCCAACCCGAGTCACTTGTGAAAGCACTGAGTGGAGGTCTGTGCAGAAAAGCTCACAAGTGAGTGCAAAATGCCCGTTGTGTCTGGGACTCCCAGTTGCCCTAAGCTGAGACACTAGCCCACTCTCAGCCTTTAAGAGTTTGTTAAAATTTTAGTGCTTTCTTGTTACTTCTCTGGCGGTCACCTCTTCCTCCTGTGTT... | AGGAGAGTCCCTTCCTGCAAGTGTGAAGAGAAGGAAGTGGGCAGTATTCCATTCCTGTCCGCCAGTGGCAGCCTGTCACCTCCTGCACACTCATGCCACTCAGGGGGACTGTGGTCTGCTGGCCAACCCGAGTCACTTGTGAAAGCACTGAGTGGAGGTCTGTGCAGAAAAGCTCACAAGTGAGTGCAAAATGCCCGTTGTGTCTGGGACTCCCAGTTGCCCTAAGCTGAGACACTAGCCCACTCTCAGCCTTTAAGAGTTTGTTAAAATTTTAGTGCTTTCTTGTTACTTCTCTGGCGGTCACCTCTTCCTCCTGTGTT... |
Task1_train_48551 | A mutation has occurred on Chromosome 22. What is the medical relevance of this mutation? | Benign | TGTCACCTCCTGCACACTCATGCCACTCAGGGGGACTGTGGTCTGCTGGCCAACCCGAGTCACTTGTGAAAGCACTGAGTGGAGGTCTGTGCAGAAAAGCTCACAAGTGAGTGCAAAATGCCCGTTGTGTCTGGGACTCCCAGTTGCCCTAAGCTGAGACACTAGCCCACTCTCAGCCTTTAAGAGTTTGTTAAAATTTTAGTGCTTTCTTGTTACTTCTCTGGCGGTCACCTCTTCCTCCTGTGTTCTCTCAAAGATGAAACTGTTTGTGTGGCCTGACTCTCCTTGATGGGGCTTTGATTTTGTAGAATTAAGTTCCC... | TGTCACCTCCTGCACACTCATGCCACTCAGGGGGACTGTGGTCTGCTGGCCAACCCGAGTCACTTGTGAAAGCACTGAGTGGAGGTCTGTGCAGAAAAGCTCACAAGTGAGTGCAAAATGCCCGTTGTGTCTGGGACTCCCAGTTGCCCTAAGCTGAGACACTAGCCCACTCTCAGCCTTTAAGAGTTTGTTAAAATTTTAGTGCTTTCTTGTTACTTCTCTGGCGGTCACCTCTTCCTCCTGTGTTCTCTCAAAGATGAAACTGTTTGTGTGGCCTGACTCTCCTTGATGGGGCTTTGATTTTGTAGAATTAAGTTCCC... |
Task1_train_48552 | A mutation is present on Chromosome 22. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AAAAAAAAAAGAAGTTTTATACATGAGGCCCATGAGGTCCTACTGGGTGCTGGGCACTTTTGTAGGCCAAGCACAAAACAGACAAGGTCCCTGCCCTAGTGGGGCTGATGTTCCAGCCAGGAGGCCAGATGACAGGCAGTGGCCTGGGAAACTGGAGCAGTTAATAACACGCTAGAAGGTAGATAATGCAATGGGAAAAAAAAGAAAACAACAGCAGAGTAGAGGGGAGGGCAGAAGCAGGTGGGGGGAGCAGCCGAAGCTTCATCACAGAGGAAACTCAAATATCCCCAGGTTGCAAGAGATGGCCGCTTCTTTTGGTC... | AAAAAAAAAAGAAGTTTTATACATGAGGCCCATGAGGTCCTACTGGGTGCTGGGCACTTTTGTAGGCCAAGCACAAAACAGACAAGGTCCCTGCCCTAGTGGGGCTGATGTTCCAGCCAGGAGGCCAGATGACAGGCAGTGGCCTGGGAAACTGGAGCAGTTAATAACACGCTAGAAGGTAGATAATGCAATGGGAAAAAAAAGAAAACAACAGCAGAGTAGAGGGGAGGGCAGAAGCAGGTGGGGGGAGCAGCCGAAGCTTCATCACAGAGGAAACTCAAATATCCCCAGGTTGCAAGAGATGGCCGCTTCTTTTGGTC... |
Task1_train_48553 | Given this context: Chromosome 22 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGCACCCCTGGAGAGAGGGGACCTCCTGGGCCACCAGGGCCTCCTGGCCCCCCTGGGCCCCCAGCCCCTGTTGGGCCACCCCATGCCCGGATCTCCCAGCATGGTGAGTCCCCCTGGGATCCCAGCAGGTGGAGGTGGGGGTGGAGTAGCCATCAGCACAGTGCCCGCTACCATCTGCCACGTGCCTTCTGTGTGCCAGCCCTGCTCACGATAGGCCACATGTGACCCAGTCCTCCAGCAGGCGCCGTTGTCCTCCTGTGGTTACAGGTGAGGAACACTGAGGACCAGAGAGGGAAGGTGGCTTGCCAGGGTCCCACAGC... | GGCACCCCTGGAGAGAGGGGACCTCCTGGGCCACCAGGGCCTCCTGGCCCCCCTGGGCCCCCAGCCCCTGTTGGGCCACCCCATGCCCGGATCTCCCAGCATGGTGAGTCCCCCTGGGATCCCAGCAGGTGGAGGTGGGGGTGGAGTAGCCATCAGCACAGTGCCCGCTACCATCTGCCACGTGCCTTCTGTGTGCCAGCCCTGCTCACGATAGGCCACATGTGACCCAGTCCTCCAGCAGGCGCCGTTGTCCTCCTGTGGTTACAGGTGAGGAACACTGAGGACCAGAGAGGGAAGGTGGCTTGCCAGGGTCCCACAGC... |
Task1_train_48554 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | GTGGGTGCCTGTAGTCCCAGCTACTTGGGGGTTGAGGCAGGAGAATGGCGTTAACCTGGGGGGGGCGGAGCTTGCAGTGAGCCAAGATTGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCCGTCTCAAAAAAAAAAACCTGATGTCTATGTCATGGGTTAGACAAGGGATTCTCTAAACTTAGTGTGCTCAGATTACCTGGGGATCTTGTTAAAATGCAGATGCTGAACTGGGAAGTCTCAGGATTGATCCCGCTGGCTTGGGGACTTTGCTGAGTAGCAAAAACACAGAGCAACTTAATTTGAATTTCTCT... | GTGGGTGCCTGTAGTCCCAGCTACTTGGGGGTTGAGGCAGGAGAATGGCGTTAACCTGGGGGGGGCGGAGCTTGCAGTGAGCCAAGATTGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCCGTCTCAAAAAAAAAAACCTGATGTCTATGTCATGGGTTAGACAAGGGATTCTCTAAACTTAGTGTGCTCAGATTACCTGGGGATCTTGTTAAAATGCAGATGCTGAACTGGGAAGTCTCAGGATTGATCCCGCTGGCTTGGGGACTTTGCTGAGTAGCAAAAACACAGAGCAACTTAATTTGAATTTCTCT... |
Task1_train_48555 | This is a variant located on Chromosome 22. Is this mutation a likely cause of disease or not? | Benign | TAGCTCTGCAAGCATTCATTTCTTGGGGATATAAAGTGGAGATGATAATAAGGGCAACCATGTCATAGGGTTGTCAGGAAGATGAGCTAATCCCATTCCCAAGCTAATCCAGGAAGCACAGGTACCACTGGGCTGCTACAGAGGGAACCCTTAGTCAGTGGCAGCCTTGAGAAATCCAGTCTGAGGAATAAGACCGGGGGGAGCAGGGCTAGGGAGCAGGACTGATTCCCTGAGGACTTGTCCCAGTTCTGACTGGTGACCTGTGGCTTCCTACCTCTTGGCTCTCGTCTGTAATCTTGCTACTCAAAGCATGGCACATG... | TAGCTCTGCAAGCATTCATTTCTTGGGGATATAAAGTGGAGATGATAATAAGGGCAACCATGTCATAGGGTTGTCAGGAAGATGAGCTAATCCCATTCCCAAGCTAATCCAGGAAGCACAGGTACCACTGGGCTGCTACAGAGGGAACCCTTAGTCAGTGGCAGCCTTGAGAAATCCAGTCTGAGGAATAAGACCGGGGGGAGCAGGGCTAGGGAGCAGGACTGATTCCCTGAGGACTTGTCCCAGTTCTGACTGGTGACCTGTGGCTTCCTACCTCTTGGCTCTCGTCTGTAATCTTGCTACTCAAAGCATGGCACATG... |
Task1_train_48556 | This alteration occurs on Chromosome 22. Is it associated with a disease or is it a benign variant? | Benign | GAAGGGAAGGGATGCCTGAGCAGTGAAATCTGCAGTTTTGAAACTGACTCTTAAAAGAACATGAGTTAGAGGCTGAAAGGGAAATAAAGGACCCAAAATGAAAGAGAAAGGAAAAGTAGCTGGAAGTGCCATGAGCCCAGACACTCTTGAGTACCAAGCTGTCAGGAACTGCTGGCATTTTCCGAGTCCCAGTCCTGTGCCAGGACTTTATATGAATTACTTCTGCTTCATCATGAGCTAGAAGGTATTACTTTCACCATTTCTGTCTTTAGAAAATAGGGGTCAGGCACAATGGCTCATGCCTGTAATCCCAGCACTTT... | GAAGGGAAGGGATGCCTGAGCAGTGAAATCTGCAGTTTTGAAACTGACTCTTAAAAGAACATGAGTTAGAGGCTGAAAGGGAAATAAAGGACCCAAAATGAAAGAGAAAGGAAAAGTAGCTGGAAGTGCCATGAGCCCAGACACTCTTGAGTACCAAGCTGTCAGGAACTGCTGGCATTTTCCGAGTCCCAGTCCTGTGCCAGGACTTTATATGAATTACTTCTGCTTCATCATGAGCTAGAAGGTATTACTTTCACCATTTCTGTCTTTAGAAAATAGGGGTCAGGCACAATGGCTCATGCCTGTAATCCCAGCACTTT... |
Task1_train_48557 | 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 | TTTCACTATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCACCTCAGCCTCCCAGAATGCTGGGATTATAGGCATGAGCCACTGCGCCCGGCTGTATATTGTTTTTTAAAAACATGATGCTATTGTACACTTAGACTATAGTGCAAACATAACTTTTATACGTACTGGGAAACCAAAAAATTTGTGTCACCTACTTTATTGCAAAGTTTGCTTTATTGTGGTAGTCTGCAACTGAACCTGCAATATCTCTGAGGTATGCCTGTACTTTATGTTGTTTAGGGATGAGATAAAAGGAAGACCGGGTGT... | TTTCACTATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCACCTCAGCCTCCCAGAATGCTGGGATTATAGGCATGAGCCACTGCGCCCGGCTGTATATTGTTTTTTAAAAACATGATGCTATTGTACACTTAGACTATAGTGCAAACATAACTTTTATACGTACTGGGAAACCAAAAAATTTGTGTCACCTACTTTATTGCAAAGTTTGCTTTATTGTGGTAGTCTGCAACTGAACCTGCAATATCTCTGAGGTATGCCTGTACTTTATGTTGTTTAGGGATGAGATAAAAGGAAGACCGGGTGT... |
Task1_train_48558 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | CACATCTGCTAGCTTGCTCTGTCTGCCCTCCCTCCCAAATTACATCCCAAATCTGATCACTGCCCTGCTCCACACCCTAACCTAAATTACCACCCATCAGGCCGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGATGGGAGGATCACCTGAAGTCAGGAGTTTGAGACTAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAAAAAAAATTAGCCAGGCATGGTGGCAGGCGCCTGTAATCCCAGCCACTCGGGAGGCTGAAGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGC... | CACATCTGCTAGCTTGCTCTGTCTGCCCTCCCTCCCAAATTACATCCCAAATCTGATCACTGCCCTGCTCCACACCCTAACCTAAATTACCACCCATCAGGCCGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGATGGGAGGATCACCTGAAGTCAGGAGTTTGAGACTAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAAAAAAAATTAGCCAGGCATGGTGGCAGGCGCCTGTAATCCCAGCCACTCGGGAGGCTGAAGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGC... |
Task1_train_48559 | Given this context: Chromosome 22 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | ATGTTGCCCAGGCTGGTCTCGAACTCCTGGACTCAAGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGACTAGGCATGAGCCGCTGCACCCAGCCCTGATCTTTTCAAAACATAAAATATGCTGGCTTTGTCGGTTCATGGGACCCTTTGCTGTGCTCACTATGGCCTCGGGACCACTGTCCCTGTTGCTCTGCTTGGGAAGCTTCTCCTTCCCTCCTTTGCAGAAGTGACCCCTCCTCACCCTTTAGCTCTCGGTCCCATGTCATGTTCTCAGAGGAGCCTTCTTGACTGGGGTGAAGCCCTACCAAAGGCTCAGA... | ATGTTGCCCAGGCTGGTCTCGAACTCCTGGACTCAAGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGACTAGGCATGAGCCGCTGCACCCAGCCCTGATCTTTTCAAAACATAAAATATGCTGGCTTTGTCGGTTCATGGGACCCTTTGCTGTGCTCACTATGGCCTCGGGACCACTGTCCCTGTTGCTCTGCTTGGGAAGCTTCTCCTTCCCTCCTTTGCAGAAGTGACCCCTCCTCACCCTTTAGCTCTCGGTCCCATGTCATGTTCTCAGAGGAGCCTTCTTGACTGGGGTGAAGCCCTACCAAAGGCTCAGA... |
Task1_train_48560 | A genomic variant on Chromosome 22 is under review. What is the biological outcome — benign or pathogenic? | Benign | CTCATGCCTGTAATCCTAGCACTTTGGGAGGCCGAGACGGGTGGACTGCCTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAACACAGTGAAACCCTGTCTCTACTAAAAAAATTAGCCAGGCGTGGTGGCATGCGCCTGTGGTCCCAGCTACTTAGGAGGCTGAGGTGGGAGGATTACTTGATCCCAGAAGGTCGAGGCTGCAGTGAGCTTGATCAAGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACCCTGTCTCAAAAAATAAAAAATAAAATAAAATAAATTAGGCCAGGCATGGTGCTCATGCCTATAATCC... | CTCATGCCTGTAATCCTAGCACTTTGGGAGGCCGAGACGGGTGGACTGCCTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAACACAGTGAAACCCTGTCTCTACTAAAAAAATTAGCCAGGCGTGGTGGCATGCGCCTGTGGTCCCAGCTACTTAGGAGGCTGAGGTGGGAGGATTACTTGATCCCAGAAGGTCGAGGCTGCAGTGAGCTTGATCAAGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACCCTGTCTCAAAAAATAAAAAATAAAATAAAATAAATTAGGCCAGGCATGGTGCTCATGCCTATAATCC... |
Task1_train_48561 | A variant was discovered on Chromosome 22. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAACACAGTGAAACCCTGTCTCTACTAAAAAAATTAGCCAGGCGTGGTGGCATGCGCCTGTGGTCCCAGCTACTTAGGAGGCTGAGGTGGGAGGATTACTTGATCCCAGAAGGTCGAGGCTGCAGTGAGCTTGATCAAGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACCCTGTCTCAAAAAATAAAAAATAAAATAAAATAAATTAGGCCAGGCATGGTGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATCATCTGAGGTCAGGAGTT... | CCTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAACACAGTGAAACCCTGTCTCTACTAAAAAAATTAGCCAGGCGTGGTGGCATGCGCCTGTGGTCCCAGCTACTTAGGAGGCTGAGGTGGGAGGATTACTTGATCCCAGAAGGTCGAGGCTGCAGTGAGCTTGATCAAGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACCCTGTCTCAAAAAATAAAAAATAAAATAAAATAAATTAGGCCAGGCATGGTGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATCATCTGAGGTCAGGAGTT... |
Task1_train_48562 | The following genetic variant occurs on Chromosome 22. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGCTGGAGTGCAGTGGTGCTATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGAGCTCGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCACGCTGGTCTCGAACTCCTGACCTCAAATGATTCATCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCTACCATACCAGGCCCATTCTCCCTTTTAATGTAAAAACAAAGCATGCTATAAAACAATCAGTTGGGAATTTATCCTGA... | GGCTGGAGTGCAGTGGTGCTATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGAGCTCGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCACGCTGGTCTCGAACTCCTGACCTCAAATGATTCATCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCTACCATACCAGGCCCATTCTCCCTTTTAATGTAAAAACAAAGCATGCTATAAAACAATCAGTTGGGAATTTATCCTGA... |
Task1_train_48563 | A variant on Chromosome 22 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CCAGCACTTTGGGAGGCCAAGGTGGGAGGATCGCTTGAGCCCAGGAGTTCCAGACCAGCCTGGGCAATGTGTTGAAACTCTGTTTCTACCCAAAATGCAAAAACTAACCAAGCGTGGTGGCACATACCTGTAGTCCCAGCTACTTGGGAGGTTGAGGCAGGAGGATCACTTGAGCCTGGAAGGTGGAGGTTGCAGTGATCCAAGATCCATTGCACTCCAGCCTGGATGACAGGGCAAGACCTGTCTCAGGAAAAAAAAAAAAGAAAAGAAAATTTGGCTTTGTCACTTGAGAATTAGCTTTATTAAATTCAGACTGATAG... | CCAGCACTTTGGGAGGCCAAGGTGGGAGGATCGCTTGAGCCCAGGAGTTCCAGACCAGCCTGGGCAATGTGTTGAAACTCTGTTTCTACCCAAAATGCAAAAACTAACCAAGCGTGGTGGCACATACCTGTAGTCCCAGCTACTTGGGAGGTTGAGGCAGGAGGATCACTTGAGCCTGGAAGGTGGAGGTTGCAGTGATCCAAGATCCATTGCACTCCAGCCTGGATGACAGGGCAAGACCTGTCTCAGGAAAAAAAAAAAAGAAAAGAAAATTTGGCTTTGTCACTTGAGAATTAGCTTTATTAAATTCAGACTGATAG... |
Task1_train_48564 | Consider a variant on Chromosome 22. Determine its clinical classification and disease relevance. | Benign | CAGGGCTGAGAATGCTCCAGGGGACCCTTGCCTGGCCTGAGCACCCTGAGGCCTCAGATGTGAGGCTTTGAACCAAGTAGACTAAAGCAGGCCTCAGGCCTGATTGGGACCCAGCAGGCCTAAGCAGGCCCTCTGCCTGCTCTGGAGCCCCCACCATAGGCAGATGGAAGCCAAGCTAAGCCTCCTCCCTGGACTCTCGGGCTTGACACATTCCTGTGAAACACTATGTAGCCACCACATCCTGGCCTATCCCCTGGAGGACTAGGGGAAGGAGGAGCTTCTCAAAGGCTGAGCCCATCTCATCAATGGCAGGTGCAGAC... | CAGGGCTGAGAATGCTCCAGGGGACCCTTGCCTGGCCTGAGCACCCTGAGGCCTCAGATGTGAGGCTTTGAACCAAGTAGACTAAAGCAGGCCTCAGGCCTGATTGGGACCCAGCAGGCCTAAGCAGGCCCTCTGCCTGCTCTGGAGCCCCCACCATAGGCAGATGGAAGCCAAGCTAAGCCTCCTCCCTGGACTCTCGGGCTTGACACATTCCTGTGAAACACTATGTAGCCACCACATCCTGGCCTATCCCCTGGAGGACTAGGGGAAGGAGGAGCTTCTCAAAGGCTGAGCCCATCTCATCAATGGCAGGTGCAGAC... |
Task1_train_48565 | This variant lies on Chromosome 22. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AAGGGGTGCAGGGAGGGATGGCCACATCTGCCATGGGAATCCAGAATGGCTTCTAGGAGGAGGTGGCCTTTGAGCTGGACGCCCATGACAGGCAATTAGTCCATCAGCCAGGGGAAGGACAGGGCAGGCAGAGGGTGAGCCAGGGCCCGGGGCATAGCTGTGCTCTGGGCAATGGGGCCTCACAGGAGTCCTCAGAAGTGTGGTTGAGGGAGTAGGTGACCTGTTGCCTAGTGAAAGGGGCAGGTCTGGGGGCTGTCTTGGCTGGGTCTAACCCTCAAAAGCTCAGCAAGGAGCCAGGAGTTCAGTTGAGAGTCCCCAGG... | AAGGGGTGCAGGGAGGGATGGCCACATCTGCCATGGGAATCCAGAATGGCTTCTAGGAGGAGGTGGCCTTTGAGCTGGACGCCCATGACAGGCAATTAGTCCATCAGCCAGGGGAAGGACAGGGCAGGCAGAGGGTGAGCCAGGGCCCGGGGCATAGCTGTGCTCTGGGCAATGGGGCCTCACAGGAGTCCTCAGAAGTGTGGTTGAGGGAGTAGGTGACCTGTTGCCTAGTGAAAGGGGCAGGTCTGGGGGCTGTCTTGGCTGGGTCTAACCCTCAAAAGCTCAGCAAGGAGCCAGGAGTTCAGTTGAGAGTCCCCAGG... |
Task1_train_48566 | Given a variant located on Chromosome 22, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ACATCTGCCATGGGAATCCAGAATGGCTTCTAGGAGGAGGTGGCCTTTGAGCTGGACGCCCATGACAGGCAATTAGTCCATCAGCCAGGGGAAGGACAGGGCAGGCAGAGGGTGAGCCAGGGCCCGGGGCATAGCTGTGCTCTGGGCAATGGGGCCTCACAGGAGTCCTCAGAAGTGTGGTTGAGGGAGTAGGTGACCTGTTGCCTAGTGAAAGGGGCAGGTCTGGGGGCTGTCTTGGCTGGGTCTAACCCTCAAAAGCTCAGCAAGGAGCCAGGAGTTCAGTTGAGAGTCCCCAGGGTCAGACATGGGCCCAGGGTAGG... | ACATCTGCCATGGGAATCCAGAATGGCTTCTAGGAGGAGGTGGCCTTTGAGCTGGACGCCCATGACAGGCAATTAGTCCATCAGCCAGGGGAAGGACAGGGCAGGCAGAGGGTGAGCCAGGGCCCGGGGCATAGCTGTGCTCTGGGCAATGGGGCCTCACAGGAGTCCTCAGAAGTGTGGTTGAGGGAGTAGGTGACCTGTTGCCTAGTGAAAGGGGCAGGTCTGGGGGCTGTCTTGGCTGGGTCTAACCCTCAAAAGCTCAGCAAGGAGCCAGGAGTTCAGTTGAGAGTCCCCAGGGTCAGACATGGGCCCAGGGTAGG... |
Task1_train_48567 | This variant is located on Chromosome 22. Evaluate its biological effect and specify any disease association. | Benign | GAGGGGCCATGTATATAGCTGAGCTACCACAGCTTTGGTCAGCCCAACTTCCTGCTTCTGAGGGGCCTGGGAGTTCCTGAGGGAGGCTGGGGTGCCCCGGGCACCCCCCTCACAGGGGAGCACCATCCCTCAGCACCCTGAGCCAGAAGGCCTGTGCTCAAGTCCAGGGGAAGGACCTCACAGCTGAGTAGCTCTCTCAGGCGCCCACCAACTCCGTGCCATGTATTCATTAGCTCCCAGTTCTGGCAGTCAGAAGTCCAGGTTCTGTGTGGCTGGGTTTTTTTGCTCCGGGTCCCAGAGGGCTGAAATTGAGGCATCTA... | GAGGGGCCATGTATATAGCTGAGCTACCACAGCTTTGGTCAGCCCAACTTCCTGCTTCTGAGGGGCCTGGGAGTTCCTGAGGGAGGCTGGGGTGCCCCGGGCACCCCCCTCACAGGGGAGCACCATCCCTCAGCACCCTGAGCCAGAAGGCCTGTGCTCAAGTCCAGGGGAAGGACCTCACAGCTGAGTAGCTCTCTCAGGCGCCCACCAACTCCGTGCCATGTATTCATTAGCTCCCAGTTCTGGCAGTCAGAAGTCCAGGTTCTGTGTGGCTGGGTTTTTTTGCTCCGGGTCCCAGAGGGCTGAAATTGAGGCATCTA... |
Task1_train_48568 | 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 | CATGTCCTCGCTGGCTGGCTGTAAGCCAGGTCCTCTCACGGCTCCTAGAGGCCGTCCACCTTCCTTGCCATGGGGCTCCCTCCATCTTCAAGTCAACAACAGAGGATTTCTCATGTGCTGAATCCCCCACATGCTTCAAATCCCTGACTTCCTCCTCTTCTACCAGCAGAAAACTACTTTGAATAGGCTCATGTGGTTAGGGCAAGGCTCACACTCAAATACTTTCCCTATCTTCAGGTCAGCTTGCTATAAGACAGAACCCAACCATGGGCATAAAATCCCTTTGAGAAGCCAGGCGCAGTGGCTCACGTCTGTAATCC... | CATGTCCTCGCTGGCTGGCTGTAAGCCAGGTCCTCTCACGGCTCCTAGAGGCCGTCCACCTTCCTTGCCATGGGGCTCCCTCCATCTTCAAGTCAACAACAGAGGATTTCTCATGTGCTGAATCCCCCACATGCTTCAAATCCCTGACTTCCTCCTCTTCTACCAGCAGAAAACTACTTTGAATAGGCTCATGTGGTTAGGGCAAGGCTCACACTCAAATACTTTCCCTATCTTCAGGTCAGCTTGCTATAAGACAGAACCCAACCATGGGCATAAAATCCCTTTGAGAAGCCAGGCGCAGTGGCTCACGTCTGTAATCC... |
Task1_train_48569 | Consider this mutation on Chromosome 22. Is this a benign change or a disease-causing variant? | Benign | CCACACCTTGGCCTGGGAGCATACGGCCTAGAAACCACAAACTTGGGTTTAAGTCCCAACTCTGCACGTGCCCACCTATGACCACCTCTCCCTCAGGCTCCTCAATAAGTCACCTGACCTGCCTACCTTAGAGGATTGTCCCACACTTAAGTGACAAGCTAGATCTGAAGGTACCTTGTGAGCTCTAAGTTGCTGAACCAATATAAGAGGCTGTGCTTCTTGTTTTTATTTTTTGTTTGTTTGTTTTTTTTTTTTAGAGGGAGTCTTGCTCTGTCGCCCCAGACTGGAGTACAATGGTGTGATCTCAGCTCGCTGCATCC... | CCACACCTTGGCCTGGGAGCATACGGCCTAGAAACCACAAACTTGGGTTTAAGTCCCAACTCTGCACGTGCCCACCTATGACCACCTCTCCCTCAGGCTCCTCAATAAGTCACCTGACCTGCCTACCTTAGAGGATTGTCCCACACTTAAGTGACAAGCTAGATCTGAAGGTACCTTGTGAGCTCTAAGTTGCTGAACCAATATAAGAGGCTGTGCTTCTTGTTTTTATTTTTTGTTTGTTTGTTTTTTTTTTTTAGAGGGAGTCTTGCTCTGTCGCCCCAGACTGGAGTACAATGGTGTGATCTCAGCTCGCTGCATCC... |
Task1_train_48570 | A variant on Chromosome 22 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATGCGAGCCTGGTTAGAAGAGCTCATTAGATAGCACCTTTCAATCCCTCCTTGTTCAGAGGCCCAGAGAGCTCAGGTGTCTCTTCCAAGGTCACACAATGAGGTAAGGATAAATTTGGAACTAAAACTGAGACTCCCTGCCCTTCTGATGCCCACTGGCCTCAGTCCCAGTGGGCACACTTGCTCGCCTCCTGCCTGGGTCTCTGACTTCAGGAGGGCGGAGGGGGCCCGTGTCAGAGCCTTCCGCGCCCCAGCGCATCGCTCCCTACTCCGCCTCTCGGGATCCTTTAAGAGGCGGGGCTTGGCTGCCAGCTCCGCGGC... | ATGCGAGCCTGGTTAGAAGAGCTCATTAGATAGCACCTTTCAATCCCTCCTTGTTCAGAGGCCCAGAGAGCTCAGGTGTCTCTTCCAAGGTCACACAATGAGGTAAGGATAAATTTGGAACTAAAACTGAGACTCCCTGCCCTTCTGATGCCCACTGGCCTCAGTCCCAGTGGGCACACTTGCTCGCCTCCTGCCTGGGTCTCTGACTTCAGGAGGGCGGAGGGGGCCCGTGTCAGAGCCTTCCGCGCCCCAGCGCATCGCTCCCTACTCCGCCTCTCGGGATCCTTTAAGAGGCGGGGCTTGGCTGCCAGCTCCGCGGC... |
Task1_train_48571 | This variant lies on Chromosome 22. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AAGAGCACGGGATCTGGATCCACACTGTTTGGATTCAAATCACAACTTCACCACTTAGCAGCTGTGTGTTCTGGGAAAATGACCCACCTTCTCTGTGCCTCCATTTTCTCACCTGTAAAACGGGCTCCCAGGCTGGTGGGAGGGTTTCAGGTGTAAGACATGGAGAGTCCTTTAGCGAACATGTAGACTGGCAATAAACTCAATAAATGGTGACTGTTATAATTAATCCTCGGAACCATCCTAGGGAGTGGACACTATTGTGTTCCCCATTTTATTTATTACATTAATTTTTTTTTTTTTTTTTTAGTAGAGACGAGGTC... | AAGAGCACGGGATCTGGATCCACACTGTTTGGATTCAAATCACAACTTCACCACTTAGCAGCTGTGTGTTCTGGGAAAATGACCCACCTTCTCTGTGCCTCCATTTTCTCACCTGTAAAACGGGCTCCCAGGCTGGTGGGAGGGTTTCAGGTGTAAGACATGGAGAGTCCTTTAGCGAACATGTAGACTGGCAATAAACTCAATAAATGGTGACTGTTATAATTAATCCTCGGAACCATCCTAGGGAGTGGACACTATTGTGTTCCCCATTTTATTTATTACATTAATTTTTTTTTTTTTTTTTTAGTAGAGACGAGGTC... |
Task1_train_48572 | A mutation is present on Chromosome 22. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AGCTGAGCGTGCAAGTCAGACAAAGCCTGATGTAGGCAGCTCCTATCAGAGGCATGTGGCCTTTGTGGCTGGGGCCCTCAAAAGACAGCCACTGCCAGAAATCTGGAGACTGAATTGTCTGGGTCTCCAGAAGAGAGTCCAACCCCACCACACATCTGCTCCTGTCCAAGGTGCTGAAATCCACCCCACATAGGCTCCTCCTAATCATGTACAGCTGTTGAGTCACCTGCACCCTACCTTCTGGTCCTCCATTCAATGCCACAAATATACACTGAGCATCTACTATATATAGGGAGTGGAAGTAAAAAGGATTTAGATAT... | AGCTGAGCGTGCAAGTCAGACAAAGCCTGATGTAGGCAGCTCCTATCAGAGGCATGTGGCCTTTGTGGCTGGGGCCCTCAAAAGACAGCCACTGCCAGAAATCTGGAGACTGAATTGTCTGGGTCTCCAGAAGAGAGTCCAACCCCACCACACATCTGCTCCTGTCCAAGGTGCTGAAATCCACCCCACATAGGCTCCTCCTAATCATGTACAGCTGTTGAGTCACCTGCACCCTACCTTCTGGTCCTCCATTCAATGCCACAAATATACACTGAGCATCTACTATATATAGGGAGTGGAAGTAAAAAGGATTTAGATAT... |
Task1_train_48573 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGGTGTGGTCTCAGCTCACTGCAACTTCCACCTCATGGTTTCAAGCAGTTCTCTACCTCAGCTTCTTGAGTATCTGGGATTACAGGTGCCCACCACCATGACTGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTCACCACCTTGGCCAGGATGGTCTTGAACTCCTGACCTTGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCCAGCCAACAGCACATTCTTGAAGATCTTCCAGTCATGAGCAGTGAAACTAAGAGTTATCTAATTGCCTCAAGGAGAGTTTAGAGC... | TGGTGTGGTCTCAGCTCACTGCAACTTCCACCTCATGGTTTCAAGCAGTTCTCTACCTCAGCTTCTTGAGTATCTGGGATTACAGGTGCCCACCACCATGACTGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTCACCACCTTGGCCAGGATGGTCTTGAACTCCTGACCTTGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCCAGCCAACAGCACATTCTTGAAGATCTTCCAGTCATGAGCAGTGAAACTAAGAGTTATCTAATTGCCTCAAGGAGAGTTTAGAGC... |
Task1_train_48574 | A sequence alteration has been identified on Chromosome 22. Is it disease-inducing or harmless? | Benign | ATCTCCATGGTGGCTTGCGCTACATGAAGGAATCATGATGGTCATCAGCATATAGAACAGCACACAGCCAGGGAGCAGGCGGCCTGGGAACGGGATCTCGAGCTCCACCTGCAGGGAGGAGCTGTGGCCCACGGACACAGTATGCTCGTACTGCGTCCTCGCCTAGTTGCGGTTGCACAGGTAGCTCTTGGGCCTCTCCATGAACCATGGATTCCATCACACATTATAGCCCCTGAATCCTCAAAGCAGCCCCATGTGGAAGGCAATGTCATCCTCATTTTACAGAGGAGAAAACTGAGGCTTGGAGAGGTGATATGATC... | ATCTCCATGGTGGCTTGCGCTACATGAAGGAATCATGATGGTCATCAGCATATAGAACAGCACACAGCCAGGGAGCAGGCGGCCTGGGAACGGGATCTCGAGCTCCACCTGCAGGGAGGAGCTGTGGCCCACGGACACAGTATGCTCGTACTGCGTCCTCGCCTAGTTGCGGTTGCACAGGTAGCTCTTGGGCCTCTCCATGAACCATGGATTCCATCACACATTATAGCCCCTGAATCCTCAAAGCAGCCCCATGTGGAAGGCAATGTCATCCTCATTTTACAGAGGAGAAAACTGAGGCTTGGAGAGGTGATATGATC... |
Task1_train_48575 | This variant is located on Chromosome 22. Evaluate its biological effect and specify any disease association. | Benign | CATGATGGTCATCAGCATATAGAACAGCACACAGCCAGGGAGCAGGCGGCCTGGGAACGGGATCTCGAGCTCCACCTGCAGGGAGGAGCTGTGGCCCACGGACACAGTATGCTCGTACTGCGTCCTCGCCTAGTTGCGGTTGCACAGGTAGCTCTTGGGCCTCTCCATGAACCATGGATTCCATCACACATTATAGCCCCTGAATCCTCAAAGCAGCCCCATGTGGAAGGCAATGTCATCCTCATTTTACAGAGGAGAAAACTGAGGCTTGGAGAGGTGATATGATCTTTCAGCGGTCACAGAGCAAGGGAGGGGAGGTA... | CATGATGGTCATCAGCATATAGAACAGCACACAGCCAGGGAGCAGGCGGCCTGGGAACGGGATCTCGAGCTCCACCTGCAGGGAGGAGCTGTGGCCCACGGACACAGTATGCTCGTACTGCGTCCTCGCCTAGTTGCGGTTGCACAGGTAGCTCTTGGGCCTCTCCATGAACCATGGATTCCATCACACATTATAGCCCCTGAATCCTCAAAGCAGCCCCATGTGGAAGGCAATGTCATCCTCATTTTACAGAGGAGAAAACTGAGGCTTGGAGAGGTGATATGATCTTTCAGCGGTCACAGAGCAAGGGAGGGGAGGTA... |
Task1_train_48576 | Given this context: Chromosome 22 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CCGGCAAGCCTGTGTTCTTTACTACCCTACAGCTCCATTCCCTCAAAGTCTCCCACTCCTCTCCTGAGACCCTCCTTCCTTCCCTCCCTTTCTGCGTCCCCTGACCCCTGCAAGCCTCACCTCGCAGCCAGCGCAGGAGGAAGTAGTCATCAGCATTGGGCAGTATGGGCAGCAGGTCCTGGAGGTTCTCCCGGAACTGAGCGGAGGAGGATCTGATGGTCGGCGGAGCTCTCATGACCTCGGGGGCCACCAACCCCGCCCCTAACCCTTCCCACATCATCCACCAGTCAACTCCACCAGAAGACCATGCAGGGTGCTGC... | CCGGCAAGCCTGTGTTCTTTACTACCCTACAGCTCCATTCCCTCAAAGTCTCCCACTCCTCTCCTGAGACCCTCCTTCCTTCCCTCCCTTTCTGCGTCCCCTGACCCCTGCAAGCCTCACCTCGCAGCCAGCGCAGGAGGAAGTAGTCATCAGCATTGGGCAGTATGGGCAGCAGGTCCTGGAGGTTCTCCCGGAACTGAGCGGAGGAGGATCTGATGGTCGGCGGAGCTCTCATGACCTCGGGGGCCACCAACCCCGCCCCTAACCCTTCCCACATCATCCACCAGTCAACTCCACCAGAAGACCATGCAGGGTGCTGC... |
Task1_train_48577 | This variant is present on Chromosome 22. Is the change likely to result in a pathogenic outcome? | Benign | TTGGGAGGCTGAGGCAGGTGGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTCGCTAACATGGTGAAACCCCATCTCTACTAAAAAACAAAAATTAGCTAGTTGTGGTGGCGGGCACCTGTAAACCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAGCCCAGGAGGCGGAGGTTACAGTGAGCCAAGATTCTGCCACTGCACTCCAGCCTGGGTGACAGTGAGACTCTGACTCAAAAAAAAAAAAAAAAAAAAGGAAATAATACATAAAAACTGCTGTACCCAGTGCCTGGTACAGAATAAGTGCTCAAAAT... | TTGGGAGGCTGAGGCAGGTGGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTCGCTAACATGGTGAAACCCCATCTCTACTAAAAAACAAAAATTAGCTAGTTGTGGTGGCGGGCACCTGTAAACCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAGCCCAGGAGGCGGAGGTTACAGTGAGCCAAGATTCTGCCACTGCACTCCAGCCTGGGTGACAGTGAGACTCTGACTCAAAAAAAAAAAAAAAAAAAAGGAAATAATACATAAAAACTGCTGTACCCAGTGCCTGGTACAGAATAAGTGCTCAAAAT... |
Task1_train_48578 | A genetic alteration is present on Chromosome 22. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCCTGGCTGATCTGGTCCTCAGCCTTGGACAGTTAGTCCATTAACCTGACCCCACAGGAGCCCCAATCCCTTGGGGTCTGGGGAATCTTGAACTGGGGTTTGGGGTGCAAATATCTGCACTGAGTCACTTAATTGCACCCAGCCTCATTCCTTTATCTGTAAAGTGGGCTAAGAATGCTCCCCTGCCTTCCTCCTCGGTGTAGTACAAGGAAGGATCCCATGACACCTGCTCTCCCAGTTTAAAGCTCTATATGTATGTTGTGAAATTGACAGGGATCGCTGCACAAACGCTAATGCAAAGTGGGCTCCTGTGCTTCCTT... | TCCTGGCTGATCTGGTCCTCAGCCTTGGACAGTTAGTCCATTAACCTGACCCCACAGGAGCCCCAATCCCTTGGGGTCTGGGGAATCTTGAACTGGGGTTTGGGGTGCAAATATCTGCACTGAGTCACTTAATTGCACCCAGCCTCATTCCTTTATCTGTAAAGTGGGCTAAGAATGCTCCCCTGCCTTCCTCCTCGGTGTAGTACAAGGAAGGATCCCATGACACCTGCTCTCCCAGTTTAAAGCTCTATATGTATGTTGTGAAATTGACAGGGATCGCTGCACAAACGCTAATGCAAAGTGGGCTCCTGTGCTTCCTT... |
Task1_train_48579 | A variant affecting Chromosome 22 has been observed. Determine if it's benign or associated with disease. | Benign | TTGAGACGGAGTTGCATTCAGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGCAGCTGGGATTACAGGGGCCCACCATCACACCTGGCTAGTTTTTGTATTTTTAGTAGAAATAGGGTTTCACCATGTGAGCCAGGCTGGTGTCAAACTCCCAACCTCAGGTGATCCACCCACCTCCGCCTCCTCAAGTGCTGGGATTACAGATGTGACCCACCGCGCCCCACCTGTGTTTCTTAAAACCAAAAAAATCCCTCTAAGACT... | TTGAGACGGAGTTGCATTCAGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGCAGCTGGGATTACAGGGGCCCACCATCACACCTGGCTAGTTTTTGTATTTTTAGTAGAAATAGGGTTTCACCATGTGAGCCAGGCTGGTGTCAAACTCCCAACCTCAGGTGATCCACCCACCTCCGCCTCCTCAAGTGCTGGGATTACAGATGTGACCCACCGCGCCCCACCTGTGTTTCTTAAAACCAAAAAAATCCCTCTAAGACT... |
Task1_train_48580 | Consider this mutation on Chromosome 22. Is this a benign change or a disease-causing variant? | Benign | TGCAGGACAGGTGCTGCGGCCAGGACTCAGGGTGTCTCCAAAGGGTGTGCTGGGAGCGAGGGCATTATCAACCTTGTCTGGCACTGCCCTCACTCCACCTGATCCTCCTGACAGCCACCTTTCTCCCCACTCAGAACTGACACTGGGGCTGCGGGCGCCCCCGACCCTACTCAGCACCAGTAGTGGGGGCAAGAGCACCATCACCCGTGTCAACAGCCCTGGGACCCTGGCTCGGCTGGGCAGTGTCACTCATGTCACCAGCTTCAGCCATGCCCCCCCCAGTAGCCGAGGAGGCTGCAGCATCAAGGTGAGCCCCTCCT... | TGCAGGACAGGTGCTGCGGCCAGGACTCAGGGTGTCTCCAAAGGGTGTGCTGGGAGCGAGGGCATTATCAACCTTGTCTGGCACTGCCCTCACTCCACCTGATCCTCCTGACAGCCACCTTTCTCCCCACTCAGAACTGACACTGGGGCTGCGGGCGCCCCCGACCCTACTCAGCACCAGTAGTGGGGGCAAGAGCACCATCACCCGTGTCAACAGCCCTGGGACCCTGGCTCGGCTGGGCAGTGTCACTCATGTCACCAGCTTCAGCCATGCCCCCCCCAGTAGCCGAGGAGGCTGCAGCATCAAGGTGAGCCCCTCCT... |
Task1_train_48581 | Assess the clinical impact of this variant found on Chromosome 22. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CCAGAATAGGTTTCTATTTGGGCTGCAGCTCCAGCTGGCTGGTGGCGGGCTGGGAGGCAGGGGCGGGGCAGGCCCGCTGCCCTTGCCTTTGCCCTCGGACCAGCTGCAAAGACTCAGACACTCAGCCAGAGACAGCAGCCCCTGCCACTGCCCCACCATTACCCCCCATAGAGTCCCCACCAGCACCATGCCGGGGGTACCAGGGCCTGGGCCTGAGCTGGCCGCAGCCCTTGAGGAGCAGTTGGGCCGGGCACTGGAGGAGCTGCGGGCGGTGGCTGAAGCAGGCCGGGTGGCAGTGACCCAGGCAGCCGAGGTAGCTG... | CCAGAATAGGTTTCTATTTGGGCTGCAGCTCCAGCTGGCTGGTGGCGGGCTGGGAGGCAGGGGCGGGGCAGGCCCGCTGCCCTTGCCTTTGCCCTCGGACCAGCTGCAAAGACTCAGACACTCAGCCAGAGACAGCAGCCCCTGCCACTGCCCCACCATTACCCCCCATAGAGTCCCCACCAGCACCATGCCGGGGGTACCAGGGCCTGGGCCTGAGCTGGCCGCAGCCCTTGAGGAGCAGTTGGGCCGGGCACTGGAGGAGCTGCGGGCGGTGGCTGAAGCAGGCCGGGTGGCAGTGACCCAGGCAGCCGAGGTAGCTG... |
Task1_train_48582 | This alteration occurs on Chromosome 22. Is it associated with a disease or is it a benign variant? | Benign | GCTGGTGGCGGGCTGGGAGGCAGGGGCGGGGCAGGCCCGCTGCCCTTGCCTTTGCCCTCGGACCAGCTGCAAAGACTCAGACACTCAGCCAGAGACAGCAGCCCCTGCCACTGCCCCACCATTACCCCCCATAGAGTCCCCACCAGCACCATGCCGGGGGTACCAGGGCCTGGGCCTGAGCTGGCCGCAGCCCTTGAGGAGCAGTTGGGCCGGGCACTGGAGGAGCTGCGGGCGGTGGCTGAAGCAGGCCGGGTGGCAGTGACCCAGGCAGCCGAGGTAGCTGTAGCCACCGTGGAGCCGGTGGCCCGGGCAGCTGAAGA... | GCTGGTGGCGGGCTGGGAGGCAGGGGCGGGGCAGGCCCGCTGCCCTTGCCTTTGCCCTCGGACCAGCTGCAAAGACTCAGACACTCAGCCAGAGACAGCAGCCCCTGCCACTGCCCCACCATTACCCCCCATAGAGTCCCCACCAGCACCATGCCGGGGGTACCAGGGCCTGGGCCTGAGCTGGCCGCAGCCCTTGAGGAGCAGTTGGGCCGGGCACTGGAGGAGCTGCGGGCGGTGGCTGAAGCAGGCCGGGTGGCAGTGACCCAGGCAGCCGAGGTAGCTGTAGCCACCGTGGAGCCGGTGGCCCGGGCAGCTGAAGA... |
Task1_train_48583 | Mutation context: Chromosome 22. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCGGGGTACGTGGGAAGCCCTACAACAAAACTGTCAGTGCCTCTTCCCTGACTGACGCTGACATGGCCATCTTTGGGCAGGCAGGCTGGCAGGCTAGTGGTTATTTCCAAGGCGTGCCAGCAACCCTAGGATCTGCTTCCCTATCCATTGGAGACATGATGAGTTTCACCCATACCCCTGCTTAAAGTCCATGCCCTCTCCCCACCCTGCAGATGGAAGCAGAGCCAGCAGAGCCTCTCGCTGCAGCAGTGGAAGCGGCCAATGGGGCTGAGCAGACCCGAGTGAACAAAGCACCAGAAGGGCGGAGCCCTCTGAGCGCT... | TCGGGGTACGTGGGAAGCCCTACAACAAAACTGTCAGTGCCTCTTCCCTGACTGACGCTGACATGGCCATCTTTGGGCAGGCAGGCTGGCAGGCTAGTGGTTATTTCCAAGGCGTGCCAGCAACCCTAGGATCTGCTTCCCTATCCATTGGAGACATGATGAGTTTCACCCATACCCCTGCTTAAAGTCCATGCCCTCTCCCCACCCTGCAGATGGAAGCAGAGCCAGCAGAGCCTCTCGCTGCAGCAGTGGAAGCGGCCAATGGGGCTGAGCAGACCCGAGTGAACAAAGCACCAGAAGGGCGGAGCCCTCTGAGCGCT... |
Task1_train_48584 | Here is a genetic alteration on Chromosome 22. Based on the data, is it a benign variant or a cause of disease? | Benign | GCTGTGCTCCACCTTTGCTGTGTGACCTTGGCCAAGTTGCTTTTCCTCTCTGAGCCAATGCAAAATGAGGGGGCTTGTCGCTGAAGACTAAAACTGTGACATCTGGGATGGCTAAGTTGTTAGTACTGGAGGCGGTGTGATAGTTGGGGGGAAGCCGGCACACAGTGTGACACTTGGAGCCAAGGAGGGTGCCTAAAATGCCACCTCAAAGAACTGAGTTTGAGAAGGGAGGTGGAGATGGAGTTTTAGGTACTCTGAACTGAGAAGGATACGGGACAGAAACAGAAGTGCGTCTCCAGAGGCAGGGCCTCCCTGCGCCC... | GCTGTGCTCCACCTTTGCTGTGTGACCTTGGCCAAGTTGCTTTTCCTCTCTGAGCCAATGCAAAATGAGGGGGCTTGTCGCTGAAGACTAAAACTGTGACATCTGGGATGGCTAAGTTGTTAGTACTGGAGGCGGTGTGATAGTTGGGGGGAAGCCGGCACACAGTGTGACACTTGGAGCCAAGGAGGGTGCCTAAAATGCCACCTCAAAGAACTGAGTTTGAGAAGGGAGGTGGAGATGGAGTTTTAGGTACTCTGAACTGAGAAGGATACGGGACAGAAACAGAAGTGCGTCTCCAGAGGCAGGGCCTCCCTGCGCCC... |
Task1_train_48585 | Here is a mutation located on Chromosome 22. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GGCTGCCTGGGTTAGCTGCAGGCACTGGTTGTAGAATGACATGGGGCCTCTCAGGGGCTCTGAAGGCCATGGCTGCCTCTCATCTGTGCCTTTATCCTGGAGCTGGTGTCGCCTCTGCTGAAGCCTCCGCAAGTGCCGGGCTGACACCCTGATGGCCCTAGGGTCTCTGGAACAGCTGTAAGGAGAGAAGAGTGGGGCAGATGATCAGGGCTGACAAGGATCCCACCTTACTCTGCAGACAGTGGGCTGAGGCCCAGAGAGAGAGGGGGCTGGGGCCACAGTCACCAGCAAGGCAGAGAGGGGTGGGTTTCACGGAGAAA... | GGCTGCCTGGGTTAGCTGCAGGCACTGGTTGTAGAATGACATGGGGCCTCTCAGGGGCTCTGAAGGCCATGGCTGCCTCTCATCTGTGCCTTTATCCTGGAGCTGGTGTCGCCTCTGCTGAAGCCTCCGCAAGTGCCGGGCTGACACCCTGATGGCCCTAGGGTCTCTGGAACAGCTGTAAGGAGAGAAGAGTGGGGCAGATGATCAGGGCTGACAAGGATCCCACCTTACTCTGCAGACAGTGGGCTGAGGCCCAGAGAGAGAGGGGGCTGGGGCCACAGTCACCAGCAAGGCAGAGAGGGGTGGGTTTCACGGAGAAA... |
Task1_train_48586 | The following genetic variant occurs on Chromosome 22. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGTGGCCCCTTCCGAAGGTGCTGCTTCTGTCGAGGCTTGGGAGGGGCTGGGCTCCGGGAGCTGGGAGTTGGGGAGGTGGCCCGGGAGCTCCAGGAGGCATTGTAGAAGGTCCTGGGCTGCAGGCGAGCGAGGGGCACTGTGCCGTACATCCTACACCTGGGTGGTGGCAGTTGGTGGAAATTGGTGACTGGGAATCCCCCTTCCAGAAGCCCCCAGGGTCGTCTCCATGGAGATCAATGCTCTGCCAGTCCCATCCCCCATCCCGCTGGGTTGTGGGGGACACCCAAGGAGGGTCTGCATCCCGGGCCCTCAGGAGAGGA... | GGTGGCCCCTTCCGAAGGTGCTGCTTCTGTCGAGGCTTGGGAGGGGCTGGGCTCCGGGAGCTGGGAGTTGGGGAGGTGGCCCGGGAGCTCCAGGAGGCATTGTAGAAGGTCCTGGGCTGCAGGCGAGCGAGGGGCACTGTGCCGTACATCCTACACCTGGGTGGTGGCAGTTGGTGGAAATTGGTGACTGGGAATCCCCCTTCCAGAAGCCCCCAGGGTCGTCTCCATGGAGATCAATGCTCTGCCAGTCCCATCCCCCATCCCGCTGGGTTGTGGGGGACACCCAAGGAGGGTCTGCATCCCGGGCCCTCAGGAGAGGA... |
Task1_train_48587 | Consider this mutation on Chromosome 22. Is this a benign change or a disease-causing variant? | Benign | CGAGCGAGGGGCACTGTGCCGTACATCCTACACCTGGGTGGTGGCAGTTGGTGGAAATTGGTGACTGGGAATCCCCCTTCCAGAAGCCCCCAGGGTCGTCTCCATGGAGATCAATGCTCTGCCAGTCCCATCCCCCATCCCGCTGGGTTGTGGGGGACACCCAAGGAGGGTCTGCATCCCGGGCCCTCAGGAGAGGACATGCAGGATGGGACATCATTCCCTGGAAGACAGACAGACAGATAGCTCTCCCTCACCAGGCTTGGAGCCTGGGCTCCCTCTCTGTCTGGAAAGGGACATGAGGGGGTGGCCACGTACCCGCC... | CGAGCGAGGGGCACTGTGCCGTACATCCTACACCTGGGTGGTGGCAGTTGGTGGAAATTGGTGACTGGGAATCCCCCTTCCAGAAGCCCCCAGGGTCGTCTCCATGGAGATCAATGCTCTGCCAGTCCCATCCCCCATCCCGCTGGGTTGTGGGGGACACCCAAGGAGGGTCTGCATCCCGGGCCCTCAGGAGAGGACATGCAGGATGGGACATCATTCCCTGGAAGACAGACAGACAGATAGCTCTCCCTCACCAGGCTTGGAGCCTGGGCTCCCTCTCTGTCTGGAAAGGGACATGAGGGGGTGGCCACGTACCCGCC... |
Task1_train_48588 | A variant was discovered on Chromosome 22. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGCCCCTCTTGACAAGGAGTCTGAGGATTTTAGACCCAGGAAGAATGAGTGATGGGCATATATATATCCTATTACTGAGGCATGAGAAGAGTGGAATGGGTGGGTTGAGGTGGTGTTTTAAGGCCTCTTGCCAGCTTGTTTAACTCTTCTCTGGGGAACGAGGGGGACAACTGTGTACATTGGCTGCTCCAGAATGATGTTGAGCAATCTTGAAGTGCCAGGAGCTGTGCTTTGTCTATTCATGGCCCCTGTGCCTGTGAAACAGGGTTCGGTGACTGTCACTGTGCCTGTGGCAGTCTGTAGTTACCCAGAGAGAACAA... | GGCCCCTCTTGACAAGGAGTCTGAGGATTTTAGACCCAGGAAGAATGAGTGATGGGCATATATATATCCTATTACTGAGGCATGAGAAGAGTGGAATGGGTGGGTTGAGGTGGTGTTTTAAGGCCTCTTGCCAGCTTGTTTAACTCTTCTCTGGGGAACGAGGGGGACAACTGTGTACATTGGCTGCTCCAGAATGATGTTGAGCAATCTTGAAGTGCCAGGAGCTGTGCTTTGTCTATTCATGGCCCCTGTGCCTGTGAAACAGGGTTCGGTGACTGTCACTGTGCCTGTGGCAGTCTGTAGTTACCCAGAGAGAACAA... |
Task1_train_48589 | Given this variant on Chromosome 22, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GGGACGCCTGCACACCTGTCTTTCCTGCTTCAACCTGAAAGATTCCTGATGATGATAATCTGGACACACAAGCCGGGCACGGTGGCTCTAGCCTGTAATCTCAGCACTTTGGGAGGCCTCAGCAGGTGGATCACCTGAGATCAAGAGTTTGAGAACAGCCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCACATACCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTTGAACCCACAAGGCAGAGGTTGCAGTGAGGCGAGATCATGCCATTGCACT... | GGGACGCCTGCACACCTGTCTTTCCTGCTTCAACCTGAAAGATTCCTGATGATGATAATCTGGACACACAAGCCGGGCACGGTGGCTCTAGCCTGTAATCTCAGCACTTTGGGAGGCCTCAGCAGGTGGATCACCTGAGATCAAGAGTTTGAGAACAGCCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCACATACCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTTGAACCCACAAGGCAGAGGTTGCAGTGAGGCGAGATCATGCCATTGCACT... |
Task1_train_48590 | 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 | AAGCTCCAGGCTCTCGAGATAGAGGATCTGGTCACAGTTTCACTCTCCTGCTGCCAGTGGTACTGTACTAAGAAGTAATATAATGGTGCTACTCCAGAAATTTTGGTAAAAGGAGATTAAGGAGGAAAATACATCATCCTTGAGTCACATTTATTTCTCTTTGGGCTTTTATTTATATATCTGTATCTATATCTATCTAGCTATCTGTAGATAGATTTTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCCGTCTCCTGGGTTCAGGTGAT... | AAGCTCCAGGCTCTCGAGATAGAGGATCTGGTCACAGTTTCACTCTCCTGCTGCCAGTGGTACTGTACTAAGAAGTAATATAATGGTGCTACTCCAGAAATTTTGGTAAAAGGAGATTAAGGAGGAAAATACATCATCCTTGAGTCACATTTATTTCTCTTTGGGCTTTTATTTATATATCTGTATCTATATCTATCTAGCTATCTGTAGATAGATTTTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCCGTCTCCTGGGTTCAGGTGAT... |
Task1_train_48591 | This variant is present on Chromosome 22. Is the change likely to result in a pathogenic outcome? | Benign | GATCTGGTCACAGTTTCACTCTCCTGCTGCCAGTGGTACTGTACTAAGAAGTAATATAATGGTGCTACTCCAGAAATTTTGGTAAAAGGAGATTAAGGAGGAAAATACATCATCCTTGAGTCACATTTATTTCTCTTTGGGCTTTTATTTATATATCTGTATCTATATCTATCTAGCTATCTGTAGATAGATTTTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCCGTCTCCTGGGTTCAGGTGATTCTTCTGCCTCAGCCTCCCTAGTA... | GATCTGGTCACAGTTTCACTCTCCTGCTGCCAGTGGTACTGTACTAAGAAGTAATATAATGGTGCTACTCCAGAAATTTTGGTAAAAGGAGATTAAGGAGGAAAATACATCATCCTTGAGTCACATTTATTTCTCTTTGGGCTTTTATTTATATATCTGTATCTATATCTATCTAGCTATCTGTAGATAGATTTTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCCGTCTCCTGGGTTCAGGTGATTCTTCTGCCTCAGCCTCCCTAGTA... |
Task1_train_48592 | An alteration has been detected on Chromosome 22. Is it pathogenic, and if so, what disease is involved? | Benign | CTGTTCAGCTGTCTCCTTTCTAGTACCCTGACCCCAAATTCCAGCCCCTCTGGCAGTCATGAACTCCAGTCTTTGCCTCCTCAGCTCACTGAGACTGAGGGAGGCTCTGCTTAGCCTCCCTTCCCCTCACTGTTTAGAAGGTGCCCCCAGGCAGAAAGTCTGGGCGGCCTAGGGGCTCACCTCGCCCGTGTCCTATCTTTTCAGCATCAGAATCTACACTTACTGTCCAGCGCCTGAAGACAGTTGCCATATGTATTTTGTCTAGTTTTGTCATATATGGCCAGAGGGCAGATCCAGGACCAGTGACTGTGTTCTGACTA... | CTGTTCAGCTGTCTCCTTTCTAGTACCCTGACCCCAAATTCCAGCCCCTCTGGCAGTCATGAACTCCAGTCTTTGCCTCCTCAGCTCACTGAGACTGAGGGAGGCTCTGCTTAGCCTCCCTTCCCCTCACTGTTTAGAAGGTGCCCCCAGGCAGAAAGTCTGGGCGGCCTAGGGGCTCACCTCGCCCGTGTCCTATCTTTTCAGCATCAGAATCTACACTTACTGTCCAGCGCCTGAAGACAGTTGCCATATGTATTTTGTCTAGTTTTGTCATATATGGCCAGAGGGCAGATCCAGGACCAGTGACTGTGTTCTGACTA... |
Task1_train_48593 | A genomic change on Chromosome 22 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CTCCAGAGTAGCGGGGACTACAGGTGTGTGCCACCACGCCAGGCTAATTTTTTGTATTCTTAGTAGAGACAGGATTTCACCGTGTTAGCTGGGATGGTCTCGATCTCCTCACCTCGTGATCCGTCCGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTACACCTGGCCAAGACCTAGTCTCTTTTAAAAAATCTTTGGAAAGATAGTCTAGAACAGGAGTCCATGCCCCTGCTTGCAAGATGCACAGACACGCGGCAGACCCATGGGGAGCTGTCTCCTAACACAGCTAGGGGTCCCATAGTAGGAGAA... | CTCCAGAGTAGCGGGGACTACAGGTGTGTGCCACCACGCCAGGCTAATTTTTTGTATTCTTAGTAGAGACAGGATTTCACCGTGTTAGCTGGGATGGTCTCGATCTCCTCACCTCGTGATCCGTCCGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTACACCTGGCCAAGACCTAGTCTCTTTTAAAAAATCTTTGGAAAGATAGTCTAGAACAGGAGTCCATGCCCCTGCTTGCAAGATGCACAGACACGCGGCAGACCCATGGGGAGCTGTCTCCTAACACAGCTAGGGGTCCCATAGTAGGAGAA... |
Task1_train_48594 | This variant is present on Chromosome 22. Is the change likely to result in a pathogenic outcome? | Benign | CTTTGGGCACCTGACCGTGCAGCTTCAAGCTCCAGAGGCTTTTGGCCAGTTTGGGTCAGCTGCCTTAAGGGTCAGGTGCCCACTCCTGGCCATGGTGGGAAGTTAGAGGCGACGGGTTTGAGTGTTGCCGGAAGCCGCTGCTCTCTGAAGGACTTTCCTTAGAGGGAGGCGGTGGCAGGCTTGGGTTGCCACGTCCATTACAGATGGTATGAGAGGCTTGGGAGACTGGGCTGCAAGACAGTGTACACGTAGTAGGTACACAGTAAATACCTGGGGAACAATTGACTGGCTTGTATTAAGGCCTCAGTGTCTCAGGCACA... | CTTTGGGCACCTGACCGTGCAGCTTCAAGCTCCAGAGGCTTTTGGCCAGTTTGGGTCAGCTGCCTTAAGGGTCAGGTGCCCACTCCTGGCCATGGTGGGAAGTTAGAGGCGACGGGTTTGAGTGTTGCCGGAAGCCGCTGCTCTCTGAAGGACTTTCCTTAGAGGGAGGCGGTGGCAGGCTTGGGTTGCCACGTCCATTACAGATGGTATGAGAGGCTTGGGAGACTGGGCTGCAAGACAGTGTACACGTAGTAGGTACACAGTAAATACCTGGGGAACAATTGACTGGCTTGTATTAAGGCCTCAGTGTCTCAGGCACA... |
Task1_train_48595 | A genetic alteration is present on Chromosome 22. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCTGGGCCTTCTCGCTGCAGGCAAAGGTAATTGGGGCTCTGCATCCTACCATCCCTGCCTCTCCCTCAGGCCTTAGCCCTGCCTTGGGTGGAGGGAGGGCACCTGGTCTGTGGGGGAGCTCTAAGCAGGGAGACCTGGGCCTCACCTCCTGCCCTCCCTGGAGGTGTGGGCCACGTGGCTGGCCTTTGTACTGGAAAGGAGGAGAAAGAAGGCGCGGCTGCAGTGGGCGCTCCAGGCCTACCAGGGGCAGCTCCTCCAGGAGGGTGCCACGCGGCTCCTGCGCTTTGCAGCCAGCATGAAGGCCTCCCGGCAGCAGCTGC... | TCTGGGCCTTCTCGCTGCAGGCAAAGGTAATTGGGGCTCTGCATCCTACCATCCCTGCCTCTCCCTCAGGCCTTAGCCCTGCCTTGGGTGGAGGGAGGGCACCTGGTCTGTGGGGGAGCTCTAAGCAGGGAGACCTGGGCCTCACCTCCTGCCCTCCCTGGAGGTGTGGGCCACGTGGCTGGCCTTTGTACTGGAAAGGAGGAGAAAGAAGGCGCGGCTGCAGTGGGCGCTCCAGGCCTACCAGGGGCAGCTCCTCCAGGAGGGTGCCACGCGGCTCCTGCGCTTTGCAGCCAGCATGAAGGCCTCCCGGCAGCAGCTGC... |
Task1_train_48596 | A sequence alteration has been identified on Chromosome 22. Is it disease-inducing or harmless? | Benign | GTTCAGAGGAACACCGTCGGTATCTTAGCTTCTGAGTCTTCATGGCTGGGGCCAGTTTGGAGGCAAGGATGGACAGCTTGTTTAGTAAGGCTGATTCTTTGGTAGTCTTCCTAAAATTCAGGCTCCTCAAGGGATGGCACGGTGTAGACATCTGCTTTGGTATGTGACTAACCAAGCTCTTGGTAGGTGCTGTTTCAGGTTCTAATCGTGTAGGTGCAGACAGAGTACACAAACTGAGAAGTCTGTGCGCTTTTGTGGGGATGGGATTGGAAGAACTCTTTAAAAAGGCAGAACTTCTGATTTTACCTATTTTTCTCCCA... | GTTCAGAGGAACACCGTCGGTATCTTAGCTTCTGAGTCTTCATGGCTGGGGCCAGTTTGGAGGCAAGGATGGACAGCTTGTTTAGTAAGGCTGATTCTTTGGTAGTCTTCCTAAAATTCAGGCTCCTCAAGGGATGGCACGGTGTAGACATCTGCTTTGGTATGTGACTAACCAAGCTCTTGGTAGGTGCTGTTTCAGGTTCTAATCGTGTAGGTGCAGACAGAGTACACAAACTGAGAAGTCTGTGCGCTTTTGTGGGGATGGGATTGGAAGAACTCTTTAAAAAGGCAGAACTTCTGATTTTACCTATTTTTCTCCCA... |
Task1_train_48597 | Chromosome 22 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGCATACGTTTTCTTCACATGATTTTTTTATTTTGAGAAAGTCCACTGTAGAAGCAGCAGTAACTGGGAAATCTGAATCCTGACCAGTTGTTCCTGTATGTGCAGCATCCAGTTCTCTCCGAGACAAGGTACTCCTGGAGTCCTCTTGAAATGCCAGTTTCTCTTGCCTTGCACCACAATCCAGTAGATTAGATGCCTTCACGTCCAGCACACCTTCTGCAAGCTTATTACTACAGTCCGTGTAGACGATGTCTACCATACCTTCTGTGGACTCATCACAACCAGACATCTTGACAAAGGCTCCTTTCAAATTGCATTTC... | TGCATACGTTTTCTTCACATGATTTTTTTATTTTGAGAAAGTCCACTGTAGAAGCAGCAGTAACTGGGAAATCTGAATCCTGACCAGTTGTTCCTGTATGTGCAGCATCCAGTTCTCTCCGAGACAAGGTACTCCTGGAGTCCTCTTGAAATGCCAGTTTCTCTTGCCTTGCACCACAATCCAGTAGATTAGATGCCTTCACGTCCAGCACACCTTCTGCAAGCTTATTACTACAGTCCGTGTAGACGATGTCTACCATACCTTCTGTGGACTCATCACAACCAGACATCTTGACAAAGGCTCCTTTCAAATTGCATTTC... |
Task1_train_48598 | A genomic change on Chromosome 22 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AATTTTTGTATTTTTAGTGGAGACAGGGTTTCACATGTTGGCCAGGGTTGTCTCAAACTCTTGATTTCAAGTGACCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGCACCCGGCCAGAACTCGAAAAAGTGGTTTTGATGTACTGTGAGAAGAAAAGCAGGCTGTTATGTTTGCAGGCCCCACACCCGAGTGCTCTCACCCCTCTGCCCTTTCCTAGTAGAGCTGAATTCACTGAGGGTTGCTCCATTTGTGGCTGTGTGTCAGGGCCTCTTATTCCCTTTTCTTTTTTTAGGGGGGAGGG... | AATTTTTGTATTTTTAGTGGAGACAGGGTTTCACATGTTGGCCAGGGTTGTCTCAAACTCTTGATTTCAAGTGACCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGCACCCGGCCAGAACTCGAAAAAGTGGTTTTGATGTACTGTGAGAAGAAAAGCAGGCTGTTATGTTTGCAGGCCCCACACCCGAGTGCTCTCACCCCTCTGCCCTTTCCTAGTAGAGCTGAATTCACTGAGGGTTGCTCCATTTGTGGCTGTGTGTCAGGGCCTCTTATTCCCTTTTCTTTTTTTAGGGGGGAGGG... |
Task1_train_48599 | With a mutation on Chromosome 22, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CCCAGGATTTGGGAACAACCCGTTGCTGGCAGAGCTTCCCATCAGTCCACCATGCTGTGCTGCCTCTTGGAGTAAGAAAGCCAAACTGAATTGTCTCCAAGATCTTTATTATGGGTCTGTGATTCTGTGAGTTCCCTGCTGCCCCAGGCCTTCAGGGCTCAATGACTTCATGGGGAAGCCATTTCAGGTTGTGCTGGTCCTCCAACTGTCCCCATTTCAAGTAGGTAACATCCCCGTAGGCAGCACTCCCTCCCTCCCTCAGACACAACCTCATTCCTCCTGAATGAAGAGGTCTAGTGAGGACAGGGACATGCCCTTTT... | CCCAGGATTTGGGAACAACCCGTTGCTGGCAGAGCTTCCCATCAGTCCACCATGCTGTGCTGCCTCTTGGAGTAAGAAAGCCAAACTGAATTGTCTCCAAGATCTTTATTATGGGTCTGTGATTCTGTGAGTTCCCTGCTGCCCCAGGCCTTCAGGGCTCAATGACTTCATGGGGAAGCCATTTCAGGTTGTGCTGGTCCTCCAACTGTCCCCATTTCAAGTAGGTAACATCCCCGTAGGCAGCACTCCCTCCCTCCCTCAGACACAACCTCATTCCTCCTGAATGAAGAGGTCTAGTGAGGACAGGGACATGCCCTTTT... |
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