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_46500 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CAAAAAACCCTGAACGAGTCCCGCGCGCAGCCCTGGTTGGGGTCAATCCAGTATTCCCCTGCCGCAGAGCCAGGCAGGGTGGGTGAGTCCGGATGGGACCCGACGGACCCCAACCCCCCCCACACCCCCACTCCGCCCATCCAAGTGGCGGGGGGACCGGACCTCACCATCAGGCAGGTGCGGGTGGTTGCGGTGCAGCTCGTGGCACACGAGGCCCGGGCGCTCCGCAGTGCCGGGAGGACGCCGCAGCTGCTCCAGCTCCAAGCTCAGCGATGTGAGCGAGGCCAGCACCTCCTCCAGGCCGCCCTCCACGACTGGAA... | CAAAAAACCCTGAACGAGTCCCGCGCGCAGCCCTGGTTGGGGTCAATCCAGTATTCCCCTGCCGCAGAGCCAGGCAGGGTGGGTGAGTCCGGATGGGACCCGACGGACCCCAACCCCCCCCACACCCCCACTCCGCCCATCCAAGTGGCGGGGGGACCGGACCTCACCATCAGGCAGGTGCGGGTGGTTGCGGTGCAGCTCGTGGCACACGAGGCCCGGGCGCTCCGCAGTGCCGGGAGGACGCCGCAGCTGCTCCAGCTCCAAGCTCAGCGATGTGAGCGAGGCCAGCACCTCCTCCAGGCCGCCCTCCACGACTGGAA... |
Task1_train_46501 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | CGTTCATCCATTCACTCATTTATTCATCCATTTATTCATTCACGTATTCATCCATCCACTGAGTTATTCACTTGTCCATTCATTAATTCACTCATTCATACATTCATCCACTCATTCATTAATCCATCCATCCACCCATTCATTCATTCATCCGTGTTCTGGGGGTTACTCATGAGATCAGTAAATTAGAGGATGCAATCCCTGGCTAGAAGTCTGGGAGAGTTTTGGCCGAGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCATGCTGATCACGAGGTCAGGAGATCGAGACCATCCTGGCCA... | CGTTCATCCATTCACTCATTTATTCATCCATTTATTCATTCACGTATTCATCCATCCACTGAGTTATTCACTTGTCCATTCATTAATTCACTCATTCATACATTCATCCACTCATTCATTAATCCATCCATCCACCCATTCATTCATTCATCCGTGTTCTGGGGGTTACTCATGAGATCAGTAAATTAGAGGATGCAATCCCTGGCTAGAAGTCTGGGAGAGTTTTGGCCGAGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCATGCTGATCACGAGGTCAGGAGATCGAGACCATCCTGGCCA... |
Task1_train_46502 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GAGATTGAACCAGATTCTGGGGTTGAGTCCATATTGGATGTTGGCATTGAGGGGAAGACATGGTTGGAGTTGAGATTGAGCCAAATTCTGGGGGTGAGTTCATATTGGATTTTGGTATTGAGGGAAAGACATGGTTGGGTTGGGACTGGGCAGGATTCTGGAGTTGAGTTCACATTGGGTGCTGGTATTGAGGGGGAACACATGGTTGGGTTGGGATTGAATCAGATTCTGGGGTTGAGTTCACATTGGGTGTCAGCATTGAGGGGAAGACATGGTTGGATTGGGATTGAGACAAATTCTAGGGTTGAGTTCATATTGGG... | GAGATTGAACCAGATTCTGGGGTTGAGTCCATATTGGATGTTGGCATTGAGGGGAAGACATGGTTGGAGTTGAGATTGAGCCAAATTCTGGGGGTGAGTTCATATTGGATTTTGGTATTGAGGGAAAGACATGGTTGGGTTGGGACTGGGCAGGATTCTGGAGTTGAGTTCACATTGGGTGCTGGTATTGAGGGGGAACACATGGTTGGGTTGGGATTGAATCAGATTCTGGGGTTGAGTTCACATTGGGTGTCAGCATTGAGGGGAAGACATGGTTGGATTGGGATTGAGACAAATTCTAGGGTTGAGTTCATATTGGG... |
Task1_train_46503 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GCCAATGGAGACAAAAGTGTGCCAGCTGGACCAGGGCTGCCAGCAGAGGGAGCCACCGTGGATGGAGGAGGTGCTGAGTCAGGCTGGCCCTGAAGCCCAGTGGTCAAGGTCAAGGTCCAACATTCAGGGCCAGGCTCCCGGAAGCCTAGCCCACATGTCCTCTCCCAAGGCAGAGTTCAGCGGCCAGCAGGCCACAGTCAGAGAGGGAGTGGCGGCTCCTTCTGGCCTGGACAGCTGCAGAGGAACTGGGTCAAGGTGGGGGTTGGGGGGGTGTGGGAAGAGGGTGGTGGGGTCCCAGGTGAGGGGACAAGGCTGAGGAA... | GCCAATGGAGACAAAAGTGTGCCAGCTGGACCAGGGCTGCCAGCAGAGGGAGCCACCGTGGATGGAGGAGGTGCTGAGTCAGGCTGGCCCTGAAGCCCAGTGGTCAAGGTCAAGGTCCAACATTCAGGGCCAGGCTCCCGGAAGCCTAGCCCACATGTCCTCTCCCAAGGCAGAGTTCAGCGGCCAGCAGGCCACAGTCAGAGAGGGAGTGGCGGCTCCTTCTGGCCTGGACAGCTGCAGAGGAACTGGGTCAAGGTGGGGGTTGGGGGGGTGTGGGAAGAGGGTGGTGGGGTCCCAGGTGAGGGGACAAGGCTGAGGAA... |
Task1_train_46504 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GGTGAGGCTGGCTCATGGCCCGTGGGTCCTCACTCAGCCCTGTGACCTGGAGTCAACGTTATTCATGTAACCTGGGGTCAAGGGTGGCTCAGGAATATGACTTGAGGTCAAAGTCATTCATGCCTGGGATGTGTTGGAGGTCACGGGTCACTTAACCCCATGTCTGGGGGATGAGAATTCACTCTTTCTAGGGATCTGGAGCCAGGAAGGACCCAGCCTGTGTCCTGAGATTAGGAGTCATGGAGTCCCTCACTCACCACTGTGGCTGCCGGTGCCAGGTTGTCACAGTCGGGGAGGTACCGCTCACAAGCCTGGAAGGC... | GGTGAGGCTGGCTCATGGCCCGTGGGTCCTCACTCAGCCCTGTGACCTGGAGTCAACGTTATTCATGTAACCTGGGGTCAAGGGTGGCTCAGGAATATGACTTGAGGTCAAAGTCATTCATGCCTGGGATGTGTTGGAGGTCACGGGTCACTTAACCCCATGTCTGGGGGATGAGAATTCACTCTTTCTAGGGATCTGGAGCCAGGAAGGACCCAGCCTGTGTCCTGAGATTAGGAGTCATGGAGTCCCTCACTCACCACTGTGGCTGCCGGTGCCAGGTTGTCACAGTCGGGGAGGTACCGCTCACAAGCCTGGAAGGC... |
Task1_train_46505 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | TAGATGCTCAATAAATGTCTGTTGAACTCATGGTTGGAAGGATGGATATAGGTACGTGGAGATGCGTGTACACAAGTGTGCACTTGTTGGCTGAGTGATAAATGTAGGTGTGTAAACTTGTGAGTTTCCATCTCTCTGTGACTTGTAACGCAAGATCACAGACACGTGGCGCCCACACCAAGGGGAAAGGAGCTCAGTGCCTGTCCCTGCTTTACTCTCTGCCCCGCAGTCGTGGCCACCATGAGGGACCTGGGGAAGAAGGAGACACTGGAGGCAGCTGCTGGGGAGGCTCTGGGGCAGACCCTCACCGTGGCCCAGCT... | TAGATGCTCAATAAATGTCTGTTGAACTCATGGTTGGAAGGATGGATATAGGTACGTGGAGATGCGTGTACACAAGTGTGCACTTGTTGGCTGAGTGATAAATGTAGGTGTGTAAACTTGTGAGTTTCCATCTCTCTGTGACTTGTAACGCAAGATCACAGACACGTGGCGCCCACACCAAGGGGAAAGGAGCTCAGTGCCTGTCCCTGCTTTACTCTCTGCCCCGCAGTCGTGGCCACCATGAGGGACCTGGGGAAGAAGGAGACACTGGAGGCAGCTGCTGGGGAGGCTCTGGGGCAGACCCTCACCGTGGCCCAGCT... |
Task1_train_46506 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GCAACAAAGTGAAACTCTGTCTCAAAAAAAATAATAATAAAATAAAATAAATTAGCCTGGAGAATTGTGTTCAGAAGGATTCTGAAGTTCAGAAGGAAAAAGTGGCCAGACATGGTGACTCACGTCTATAATCCCAGCACTTTGCGTGGCCTAGGCAGGAGGGCTGTTTGAGCTCAGGAGTTTGAGACCAGCCTGGTCAACACAGGGAGTCCTCATCACTACTAAAAATTTTTTTAGAATTGGGCCAGGCACGGTGACTCATGCCTGTAATCCCAACACTTTGGGAGGCCGAGGCAGGTGGATTACCCAAGATCAGGAGT... | GCAACAAAGTGAAACTCTGTCTCAAAAAAAATAATAATAAAATAAAATAAATTAGCCTGGAGAATTGTGTTCAGAAGGATTCTGAAGTTCAGAAGGAAAAAGTGGCCAGACATGGTGACTCACGTCTATAATCCCAGCACTTTGCGTGGCCTAGGCAGGAGGGCTGTTTGAGCTCAGGAGTTTGAGACCAGCCTGGTCAACACAGGGAGTCCTCATCACTACTAAAAATTTTTTTAGAATTGGGCCAGGCACGGTGACTCATGCCTGTAATCCCAACACTTTGGGAGGCCGAGGCAGGTGGATTACCCAAGATCAGGAGT... |
Task1_train_46507 | A variant on Chromosome 19 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CAACAAAGTGAAACTCTGTCTCAAAAAAAATAATAATAAAATAAAATAAATTAGCCTGGAGAATTGTGTTCAGAAGGATTCTGAAGTTCAGAAGGAAAAAGTGGCCAGACATGGTGACTCACGTCTATAATCCCAGCACTTTGCGTGGCCTAGGCAGGAGGGCTGTTTGAGCTCAGGAGTTTGAGACCAGCCTGGTCAACACAGGGAGTCCTCATCACTACTAAAAATTTTTTTAGAATTGGGCCAGGCACGGTGACTCATGCCTGTAATCCCAACACTTTGGGAGGCCGAGGCAGGTGGATTACCCAAGATCAGGAGTT... | CAACAAAGTGAAACTCTGTCTCAAAAAAAATAATAATAAAATAAAATAAATTAGCCTGGAGAATTGTGTTCAGAAGGATTCTGAAGTTCAGAAGGAAAAAGTGGCCAGACATGGTGACTCACGTCTATAATCCCAGCACTTTGCGTGGCCTAGGCAGGAGGGCTGTTTGAGCTCAGGAGTTTGAGACCAGCCTGGTCAACACAGGGAGTCCTCATCACTACTAAAAATTTTTTTAGAATTGGGCCAGGCACGGTGACTCATGCCTGTAATCCCAACACTTTGGGAGGCCGAGGCAGGTGGATTACCCAAGATCAGGAGTT... |
Task1_train_46508 | Mutation context: Chromosome 19. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GTCTGGGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTCGAGGGGGGTGGAACACGAGGTCAGGGGTTCGAGACCACCCTGACCAACAAGGAGAAACCCCGTCTCTACTAAAAATAAAAAAATTAGCTGGGCCTGGTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGACAAGAGAATCACTTAAACCCGGGAGGCGGAGGTTGCCATGAGCCGAGATTGCACCATTGCACTCCAGCTTGGGCAATGAGCGAAACTCCATCTCAAAAAAAAAAAGCCTAGGTCAAGGCTGGGTGTGGT... | GTCTGGGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTCGAGGGGGGTGGAACACGAGGTCAGGGGTTCGAGACCACCCTGACCAACAAGGAGAAACCCCGTCTCTACTAAAAATAAAAAAATTAGCTGGGCCTGGTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGACAAGAGAATCACTTAAACCCGGGAGGCGGAGGTTGCCATGAGCCGAGATTGCACCATTGCACTCCAGCTTGGGCAATGAGCGAAACTCCATCTCAAAAAAAAAAAGCCTAGGTCAAGGCTGGGTGTGGT... |
Task1_train_46509 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ACTTTGGGAGGCCAAGGCACACAGATGACTGGAGGTCAGGAGTTCCAGACCAGCCTGGCCAACATGGCGAAATCACGTCTCTACCAAAAATACAAAGATTAGCCAGGCGGGCACTTGTAATCTCAGATACTCAGAAGGCTGAGGCAGAAGAATTGCTTGAACCCGAGACGTAGAGGTTGCAGTAAGCAGAGATCATGCCACTGCATTCCAGCCTGGGCGACAGAGTGAGTGAGACTCCATCTCAAAATAAATGAATAAATAAATCTCATAACCAAAGACTTCCTGAAAAGATTTAGAGGAAAAGCCAATTTTTTAAAACC... | ACTTTGGGAGGCCAAGGCACACAGATGACTGGAGGTCAGGAGTTCCAGACCAGCCTGGCCAACATGGCGAAATCACGTCTCTACCAAAAATACAAAGATTAGCCAGGCGGGCACTTGTAATCTCAGATACTCAGAAGGCTGAGGCAGAAGAATTGCTTGAACCCGAGACGTAGAGGTTGCAGTAAGCAGAGATCATGCCACTGCATTCCAGCCTGGGCGACAGAGTGAGTGAGACTCCATCTCAAAATAAATGAATAAATAAATCTCATAACCAAAGACTTCCTGAAAAGATTTAGAGGAAAAGCCAATTTTTTAAAACC... |
Task1_train_46510 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CAGGGTTCTGGGCCACACCTCCTCCAGGAAGCCCCCCTTGATCTCCTTTCCTTCCACATCCCCCGGAGCTACCCTGATTTCTTCTACAGCTGAGCCTCTTTTCTGCCCTGCCGGAATGTGAATGGCATGAGGGCAGGGACCATGTCTGTTGTCTTCTCTGCTGCATTTCCAAGGCCCAGGCGAGGGCAGACACCAACACATGGTGCTTGCAGGGGTCTCCCTGACTGTTGTTGCTCCCAGATCATACTGCTTGCTCCACCGGAGCATGTGCCTGATGCCTTCCTCTCCCGCTTGACCTGAAAGTTCGAACCTCCTGATAA... | CAGGGTTCTGGGCCACACCTCCTCCAGGAAGCCCCCCTTGATCTCCTTTCCTTCCACATCCCCCGGAGCTACCCTGATTTCTTCTACAGCTGAGCCTCTTTTCTGCCCTGCCGGAATGTGAATGGCATGAGGGCAGGGACCATGTCTGTTGTCTTCTCTGCTGCATTTCCAAGGCCCAGGCGAGGGCAGACACCAACACATGGTGCTTGCAGGGGTCTCCCTGACTGTTGTTGCTCCCAGATCATACTGCTTGCTCCACCGGAGCATGTGCCTGATGCCTTCCTCTCCCGCTTGACCTGAAAGTTCGAACCTCCTGATAA... |
Task1_train_46511 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TGAGCCACAGTGCCCACCCCGTAAGCCCCTTCTTTCTTACCTGCAAGGTAGCCAGTTGCTACCCATCCTGTGCTGAGTTACTTGTATTAGCAAGGGATGGGGTGGCTATACTCACCCACCTTACAGATGGGGAAATTGAGGCCCAAAGAGGGGGAAACTACGTGTCTCAGGGAGTGAGGAGCCAGTCTGATTCCTGGAGGGCTGACTGTCTCCACCTGACTTCTTAGGAGGGAGGAGGGCACCAACTTCACATTAAAATCTGGTTGGACACAGTGGCTCACACCTGTAATCCTGGCATTTTGGGAGGCTTAGGCGGGAGG... | TGAGCCACAGTGCCCACCCCGTAAGCCCCTTCTTTCTTACCTGCAAGGTAGCCAGTTGCTACCCATCCTGTGCTGAGTTACTTGTATTAGCAAGGGATGGGGTGGCTATACTCACCCACCTTACAGATGGGGAAATTGAGGCCCAAAGAGGGGGAAACTACGTGTCTCAGGGAGTGAGGAGCCAGTCTGATTCCTGGAGGGCTGACTGTCTCCACCTGACTTCTTAGGAGGGAGGAGGGCACCAACTTCACATTAAAATCTGGTTGGACACAGTGGCTCACACCTGTAATCCTGGCATTTTGGGAGGCTTAGGCGGGAGG... |
Task1_train_46512 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TGACTTTTTTTTTTTTTTAATAGAAACAGGGTCTTTCTTTCCCAGGCTAAAGTACAGTGGCATGATCACAGTTCACTATAGCCTTAAACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTAGCAGGGACTACAGGTGTGCACCACCACACCCAGTTAACCATTCATTCATTCATTCATTCATTTATTTTGAGATGGAGTCTCGCTCTGTCACCTAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGAGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGAGACTA... | TGACTTTTTTTTTTTTTTAATAGAAACAGGGTCTTTCTTTCCCAGGCTAAAGTACAGTGGCATGATCACAGTTCACTATAGCCTTAAACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTAGCAGGGACTACAGGTGTGCACCACCACACCCAGTTAACCATTCATTCATTCATTCATTCATTTATTTTGAGATGGAGTCTCGCTCTGTCACCTAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGAGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGAGACTA... |
Task1_train_46513 | A variant affecting Chromosome 19 has been observed. Determine if it's benign or associated with disease. | Benign | GCCAAGATCATGCCATCACCCTCCAGCCTGGGCGACAGAAGGAGACTCAGTCTAAAAACTTAATTAATTAATTAATTAAAAATAAAAATACAAAAATTAACCTGGTGTGGTGGTGTGTGCCTGTAATCTAAGCTACTCAGGAGGCTGAGGCAGGAGAATCCCCTGAATCCCAGAGGCAGAGGTTGCAGTGAGCCAAGATCGAGCCACTGTTTGCCCAGTCTAGTGCACTGGGCTGCTGAATTTATTTGACCAGACACCTAGCAATAGACTTTGAAGTTCTTTTCCACTTTTCACTCTAAGATGCTGCTGTCATGAATAAG... | GCCAAGATCATGCCATCACCCTCCAGCCTGGGCGACAGAAGGAGACTCAGTCTAAAAACTTAATTAATTAATTAATTAAAAATAAAAATACAAAAATTAACCTGGTGTGGTGGTGTGTGCCTGTAATCTAAGCTACTCAGGAGGCTGAGGCAGGAGAATCCCCTGAATCCCAGAGGCAGAGGTTGCAGTGAGCCAAGATCGAGCCACTGTTTGCCCAGTCTAGTGCACTGGGCTGCTGAATTTATTTGACCAGACACCTAGCAATAGACTTTGAAGTTCTTTTCCACTTTTCACTCTAAGATGCTGCTGTCATGAATAAG... |
Task1_train_46514 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CCTCGCCTCGCTCCCACGCCTCTGCCCCCACCTCGAGCCTGAGTCTTCTCCCCTTCCCCCTCCTCCCCAACACACACCCGAGCCCCAGCTTCCTGACTCCTCGATAGCCCCTACCCGCTTCGAGATCCTAGGTGTTCTTCCGCACCCAACCCTTCGCCCTGGAGACCCAGTGTCTCTCCTGTCCGCTCCCCGGGTACCTCCTTACGCTGTGCTGTGCACCATGGTCCACGGACTGGCATCTTCCCCACTCGCGGTCCGCGAAGACTCCATCTCTCCAACTACCCTGACTCAGAGGCGCTGTTCCCGCTCCACCCAGAGCC... | CCTCGCCTCGCTCCCACGCCTCTGCCCCCACCTCGAGCCTGAGTCTTCTCCCCTTCCCCCTCCTCCCCAACACACACCCGAGCCCCAGCTTCCTGACTCCTCGATAGCCCCTACCCGCTTCGAGATCCTAGGTGTTCTTCCGCACCCAACCCTTCGCCCTGGAGACCCAGTGTCTCTCCTGTCCGCTCCCCGGGTACCTCCTTACGCTGTGCTGTGCACCATGGTCCACGGACTGGCATCTTCCCCACTCGCGGTCCGCGAAGACTCCATCTCTCCAACTACCCTGACTCAGAGGCGCTGTTCCCGCTCCACCCAGAGCC... |
Task1_train_46515 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | GCCTCGTCTCTCCTTTGCCCTTGCCGCAAACGCACTCTCCTCGTATCCCGGCATTCTGCCAGGACCCTGAGAACTGGTTCATCCCCCATCCCCCATCCCGGGTCCCCTTCTCTCAGCCTTGCTGTGTTCATCCAAGAACCCACCTTTCCTCTCCTCTACGCCCTCCCCCCATGCTTTCCCGCCGCTCCATCGGCGCTTTGGAGACCATGGCTCTCTGCTACCACGTCCCAGAGACACCCTCGAGGTTTAGACTCTGGGAGTGCGCCTTTAAACCGGAGGCCTGGGCAGGACGCGGGACGCCTGGGTTCTTTCCCTGGCTG... | GCCTCGTCTCTCCTTTGCCCTTGCCGCAAACGCACTCTCCTCGTATCCCGGCATTCTGCCAGGACCCTGAGAACTGGTTCATCCCCCATCCCCCATCCCGGGTCCCCTTCTCTCAGCCTTGCTGTGTTCATCCAAGAACCCACCTTTCCTCTCCTCTACGCCCTCCCCCCATGCTTTCCCGCCGCTCCATCGGCGCTTTGGAGACCATGGCTCTCTGCTACCACGTCCCAGAGACACCCTCGAGGTTTAGACTCTGGGAGTGCGCCTTTAAACCGGAGGCCTGGGCAGGACGCGGGACGCCTGGGTTCTTTCCCTGGCTG... |
Task1_train_46516 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | CTCAAACTCCTGAGTTTAAGTGATCCTCACACCTCAGCCTCCCTGAGTGCTGGGATTACAGGTGTGAGCCACCACACCCGGCCTGAGTCGGGGGAGGTGTCTATTTTAGTCTGAGTGGTCAAGGAAGGCTTCTCTGAAGAGCTGATGTTGGGGCCAGGCCTCCTCAAGCGATTAGAAGGTGTCAGCCATGGGGAGATGTGGAGGGAGGGTGTTTCAGGCCAAGGAAGGGTAAGATCAAATAATTCAGGGATCTGAGGGCAGAGGAATCTGGACTCCAGTTCTCCCATTCAGGGCTGCCCAGGAGAGACAAAGAGGATCTC... | CTCAAACTCCTGAGTTTAAGTGATCCTCACACCTCAGCCTCCCTGAGTGCTGGGATTACAGGTGTGAGCCACCACACCCGGCCTGAGTCGGGGGAGGTGTCTATTTTAGTCTGAGTGGTCAAGGAAGGCTTCTCTGAAGAGCTGATGTTGGGGCCAGGCCTCCTCAAGCGATTAGAAGGTGTCAGCCATGGGGAGATGTGGAGGGAGGGTGTTTCAGGCCAAGGAAGGGTAAGATCAAATAATTCAGGGATCTGAGGGCAGAGGAATCTGGACTCCAGTTCTCCCATTCAGGGCTGCCCAGGAGAGACAAAGAGGATCTC... |
Task1_train_46517 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | CACCCATGGGTACCTGACTGGGGAGCCCACCTTCTAGTAAGCCCCACGTTGTGTGGGTTCACATGCCTCCCAATTTCCTCCTGCTGATAAAGCTGCCCTCTTCCAAGCCAGCTCATTTATTTTTCTTTTTTTTAGAGATAGTGTCTTGTTCTGTCACCTAGGCTAGAGTGTAGTAGCACAATCATAGCTCACTGCAGCCTCAACCTCCTAGGCTCAAGTGATCCTCCCACCTCAGCCTCCTGCGTAGCTGGGACTACAGGCACGCACCACCATGCCTGGCTAATTTTTAAAAATTTTTTGTAGAGATGAGGGTTTCACTA... | CACCCATGGGTACCTGACTGGGGAGCCCACCTTCTAGTAAGCCCCACGTTGTGTGGGTTCACATGCCTCCCAATTTCCTCCTGCTGATAAAGCTGCCCTCTTCCAAGCCAGCTCATTTATTTTTCTTTTTTTTAGAGATAGTGTCTTGTTCTGTCACCTAGGCTAGAGTGTAGTAGCACAATCATAGCTCACTGCAGCCTCAACCTCCTAGGCTCAAGTGATCCTCCCACCTCAGCCTCCTGCGTAGCTGGGACTACAGGCACGCACCACCATGCCTGGCTAATTTTTAAAAATTTTTTGTAGAGATGAGGGTTTCACTA... |
Task1_train_46518 | With a mutation on Chromosome 19, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CCGGATCCCAGCGTCACTCAGCTCTGGACGGTTCTTCCCCCATTGCTTCTGTCGGCTGCATAGACGTGAGGGGCAGATAGGTGCTCTCCTCCCTAACATGGTAACTGCCGCTCCGTTGGTGCTCCCTGAAGACGTACATTAAGGCCAGTACGATAGTCACCACGCCCAGGGTCAGTAACACCGCCACGAAGACGGGGACAAAGTGGGAGCTCCCAGCTGTGCAGAGAAAGCGCTAAGTCAATATGCGTCCCTTCTGTCTCCAACCCCCCCGCCCCCCGGCTTACCGGTCCAGACCCGCAGCCCCGTGTTAGCTCACCCTC... | CCGGATCCCAGCGTCACTCAGCTCTGGACGGTTCTTCCCCCATTGCTTCTGTCGGCTGCATAGACGTGAGGGGCAGATAGGTGCTCTCCTCCCTAACATGGTAACTGCCGCTCCGTTGGTGCTCCCTGAAGACGTACATTAAGGCCAGTACGATAGTCACCACGCCCAGGGTCAGTAACACCGCCACGAAGACGGGGACAAAGTGGGAGCTCCCAGCTGTGCAGAGAAAGCGCTAAGTCAATATGCGTCCCTTCTGTCTCCAACCCCCCCGCCCCCCGGCTTACCGGTCCAGACCCGCAGCCCCGTGTTAGCTCACCCTC... |
Task1_train_46519 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTAGCACGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCACAAGAATCGCTTGAACCCAGGAGGCAAAATTTGCAGTGAGCTGAGATAGTGCCACTGCACTCCAGCCTGGCGACAGAGAGAGACTCTATGTCAAAAAAAAAAAAAAAAAAAAAAAGGCTGGGCAAGGTGACTCATGCCTGTAATCCCACCACTTTGGGAGGCCGAGGGAGGCGGATCACTTGAGGTCAGGAGTTTGAGACCAACCTGGCCCATATGGCAAAACCCTGTCTCTACTAAAAAT... | CATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTAGCACGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCACAAGAATCGCTTGAACCCAGGAGGCAAAATTTGCAGTGAGCTGAGATAGTGCCACTGCACTCCAGCCTGGCGACAGAGAGAGACTCTATGTCAAAAAAAAAAAAAAAAAAAAAAAGGCTGGGCAAGGTGACTCATGCCTGTAATCCCACCACTTTGGGAGGCCGAGGGAGGCGGATCACTTGAGGTCAGGAGTTTGAGACCAACCTGGCCCATATGGCAAAACCCTGTCTCTACTAAAAAT... |
Task1_train_46520 | A genomic variant on Chromosome 19 is under review. What is the biological outcome — benign or pathogenic? | Benign | TTGAACCCAGGAGGCGGAGGTTGCAATGAGCTGACATCGCGCCATTGTACTCCAGCATGGGGGACAATAGCAAGACTGCGTCTCAAAGAAAAGAAAAGTCAAAAAGTAGGCCAGGCATGGTGGCTCACGCTTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCATTTGAGGCCAGGAGTTTGAGACCAGCCTGGGCAACATGGTGAAATCCTGTCCCTACTAAAAATACAAAAATTAGCTGGGCGTGTTGGCATGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGAAG... | TTGAACCCAGGAGGCGGAGGTTGCAATGAGCTGACATCGCGCCATTGTACTCCAGCATGGGGGACAATAGCAAGACTGCGTCTCAAAGAAAAGAAAAGTCAAAAAGTAGGCCAGGCATGGTGGCTCACGCTTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCATTTGAGGCCAGGAGTTTGAGACCAGCCTGGGCAACATGGTGAAATCCTGTCCCTACTAAAAATACAAAAATTAGCTGGGCGTGTTGGCATGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGAAG... |
Task1_train_46521 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | GAGCTGACATCGCGCCATTGTACTCCAGCATGGGGGACAATAGCAAGACTGCGTCTCAAAGAAAAGAAAAGTCAAAAAGTAGGCCAGGCATGGTGGCTCACGCTTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCATTTGAGGCCAGGAGTTTGAGACCAGCCTGGGCAACATGGTGAAATCCTGTCCCTACTAAAAATACAAAAATTAGCTGGGCGTGTTGGCATGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGAAGGCAGAGGTTGCAGTGAGCCAAGATTGC... | GAGCTGACATCGCGCCATTGTACTCCAGCATGGGGGACAATAGCAAGACTGCGTCTCAAAGAAAAGAAAAGTCAAAAAGTAGGCCAGGCATGGTGGCTCACGCTTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCATTTGAGGCCAGGAGTTTGAGACCAGCCTGGGCAACATGGTGAAATCCTGTCCCTACTAAAAATACAAAAATTAGCTGGGCGTGTTGGCATGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGAAGGCAGAGGTTGCAGTGAGCCAAGATTGC... |
Task1_train_46522 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | GGCGTGATCTCAGCTTATTGCAACCTCTGCCCACCTGGGTTCAAGCAATTCTCTTGCCTCAACACCTCAACCTCCCGAGTAGCTGGGATTACAGGTCCCTGCCACCATGCCCAGCTAATTTTTATATTTTTAGTACAGAGGGGGTTTCACCATGTTAGCCAGCCTGGTCTCAAATTCCTGACCTCAGCTGATCTGCCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCGGCTACCTGATCTCTCTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGC... | GGCGTGATCTCAGCTTATTGCAACCTCTGCCCACCTGGGTTCAAGCAATTCTCTTGCCTCAACACCTCAACCTCCCGAGTAGCTGGGATTACAGGTCCCTGCCACCATGCCCAGCTAATTTTTATATTTTTAGTACAGAGGGGGTTTCACCATGTTAGCCAGCCTGGTCTCAAATTCCTGACCTCAGCTGATCTGCCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCGGCTACCTGATCTCTCTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGC... |
Task1_train_46523 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTGATCTCAGCTTATTGCAACCTCTGCCCACCTGGGTTCAAGCAATTCTCTTGCCTCAACACCTCAACCTCCCGAGTAGCTGGGATTACAGGTCCCTGCCACCATGCCCAGCTAATTTTTATATTTTTAGTACAGAGGGGGTTTCACCATGTTAGCCAGCCTGGTCTCAAATTCCTGACCTCAGCTGATCTGCCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCGGCTACCTGATCTCTCTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGC... | GTGATCTCAGCTTATTGCAACCTCTGCCCACCTGGGTTCAAGCAATTCTCTTGCCTCAACACCTCAACCTCCCGAGTAGCTGGGATTACAGGTCCCTGCCACCATGCCCAGCTAATTTTTATATTTTTAGTACAGAGGGGGTTTCACCATGTTAGCCAGCCTGGTCTCAAATTCCTGACCTCAGCTGATCTGCCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCGGCTACCTGATCTCTCTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGC... |
Task1_train_46524 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGTTGGGAACAGTCAATGATGCAAAGGACATAAATCACTTAGAACAGGGGCTGGCCCACAGCAAGTGCTCAATAAACACTTCTTGGCCTGGTGTTGGTATGGTGCTTCATACCTGTAATCCCAACACTACGGGAGGCCAAAGCCAGAGGATTGTTCAAAGCCAGGAGGTTCGAGACCAGTCTCAGCAACATAGCAAGACCCTGTCTCTACAAAAAAATTTAAAAACTAAAAAATTAGCCATGCGTGGTGCTGCATACCTATAGTCCCAGCTACTCAGGAGGCTGAGATAGGAGGCCTCCTTGAGCCCAAGAGTTGGAGGC... | AGTTGGGAACAGTCAATGATGCAAAGGACATAAATCACTTAGAACAGGGGCTGGCCCACAGCAAGTGCTCAATAAACACTTCTTGGCCTGGTGTTGGTATGGTGCTTCATACCTGTAATCCCAACACTACGGGAGGCCAAAGCCAGAGGATTGTTCAAAGCCAGGAGGTTCGAGACCAGTCTCAGCAACATAGCAAGACCCTGTCTCTACAAAAAAATTTAAAAACTAAAAAATTAGCCATGCGTGGTGCTGCATACCTATAGTCCCAGCTACTCAGGAGGCTGAGATAGGAGGCCTCCTTGAGCCCAAGAGTTGGAGGC... |
Task1_train_46525 | A genomic variant on Chromosome 19 is under review. What is the biological outcome — benign or pathogenic? | Benign | CACGCTGGGCCCAGGGTGCCCCTGAGCTGGAGCAGGAACGCCGGCACCGGCAGATTGTGTCCTGGTTCGCCGACCACCCCCGGGCCCCCTTTGGCCTACACCGGCTGGTGGAGCTTGGGCAGAGCTCAGGCAAGAAGGCAGGTGACTGGTATGGGCCATCGCTAGTGGCACACATCCTCAGGTGAGGGCTGCTGCAGGGATCACGGGAGTTGCTGGGTACCCGCAGGCACTCAGGCCTTCCCTCCTGCCCCCAGGAAAGCCGTGGAGAGCTGCTCCGACGTCACCCGCCTGGTGGTGTACGTTTCTCAGGACTGCACAGG... | CACGCTGGGCCCAGGGTGCCCCTGAGCTGGAGCAGGAACGCCGGCACCGGCAGATTGTGTCCTGGTTCGCCGACCACCCCCGGGCCCCCTTTGGCCTACACCGGCTGGTGGAGCTTGGGCAGAGCTCAGGCAAGAAGGCAGGTGACTGGTATGGGCCATCGCTAGTGGCACACATCCTCAGGTGAGGGCTGCTGCAGGGATCACGGGAGTTGCTGGGTACCCGCAGGCACTCAGGCCTTCCCTCCTGCCCCCAGGAAAGCCGTGGAGAGCTGCTCCGACGTCACCCGCCTGGTGGTGTACGTTTCTCAGGACTGCACAGG... |
Task1_train_46526 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | TTGCGAGCTGTGCCTGGGCATCATGGGTGGGAAACCGCGACACTCACTGTACTTCATTGGCTACCAAGGTAGGCCCACCCCCTCCTCACTCCTCCCACCCCCCACCGCACCCCCACTCACACCTGCACCCCCTGCAGATGACTTCCTGCTGTACCTGGACCCTCACTACTGCCAGCCCACTGTGGATGTCAGCCAGGCCGACTTCCCCCTGGAGGTGAGTGGGAGCCCCAGTGTGTGGTTGGGGCCATGGCGGGTGGGCAGCCCAGCCTCTGAGCCTTCCTCGTCTGTCTGCCCCAGTCCTTCCACTGCACCTCGCCCCG... | TTGCGAGCTGTGCCTGGGCATCATGGGTGGGAAACCGCGACACTCACTGTACTTCATTGGCTACCAAGGTAGGCCCACCCCCTCCTCACTCCTCCCACCCCCCACCGCACCCCCACTCACACCTGCACCCCCTGCAGATGACTTCCTGCTGTACCTGGACCCTCACTACTGCCAGCCCACTGTGGATGTCAGCCAGGCCGACTTCCCCCTGGAGGTGAGTGGGAGCCCCAGTGTGTGGTTGGGGCCATGGCGGGTGGGCAGCCCAGCCTCTGAGCCTTCCTCGTCTGTCTGCCCCAGTCCTTCCACTGCACCTCGCCCCG... |
Task1_train_46527 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CAATTATTGTCTCACTTTACAGATGGGGAGTTGAGGCACAGATAGGGGAATCATTTGTCCAAAGACTCAGCTGGTGAGCAGCCAAGCCAGGGCTTGAACCCACCTAGGCCCCCTGGTTCCAGAGGACACCAAGTCTTTTGTTGAGACAGGGTCTCACTATGTCACCCAGGCTGGAGTGCAGTGGCAGGCTCACAGCTCACAGCAGCCTCAACCTCCTGGACTCAAGCAACCCTCCTACCTCAGCCTCCCAAGTAGCTAGGACTAGATCTCCCTATGTTGCTCAGGTTAGTCTCAGAACTACTGGGCTCAAGTGATCCTCC... | CAATTATTGTCTCACTTTACAGATGGGGAGTTGAGGCACAGATAGGGGAATCATTTGTCCAAAGACTCAGCTGGTGAGCAGCCAAGCCAGGGCTTGAACCCACCTAGGCCCCCTGGTTCCAGAGGACACCAAGTCTTTTGTTGAGACAGGGTCTCACTATGTCACCCAGGCTGGAGTGCAGTGGCAGGCTCACAGCTCACAGCAGCCTCAACCTCCTGGACTCAAGCAACCCTCCTACCTCAGCCTCCCAAGTAGCTAGGACTAGATCTCCCTATGTTGCTCAGGTTAGTCTCAGAACTACTGGGCTCAAGTGATCCTCC... |
Task1_train_46528 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | AGCCCACTCGAGACATAGGAGCTGAGCCCCCTACGATGCCGCCAATGACCCCCTCCTTGGCAACTTTACTCCTACAGCTAGGGCTCCCTACAGCCCTCCCAGCACCTAGCTCCTGAGGTGGGAGGCCCTGCATGTCCAGGATCCTCCGCCAACTCCCCTGCTGTCTACCCTGTGATGTACTGGCCGCCATTCAGTTCCACATATCCACAGTTCTTCGCCGTCCTACCCACCTTCGCCCCTGTGGTGCCCACCACCTGGTGCACTACTCAGGCCCCAGGTCTTTTTTTTTTTTGAAACAGAATTTCGCTCTTGTTGCCCAA... | AGCCCACTCGAGACATAGGAGCTGAGCCCCCTACGATGCCGCCAATGACCCCCTCCTTGGCAACTTTACTCCTACAGCTAGGGCTCCCTACAGCCCTCCCAGCACCTAGCTCCTGAGGTGGGAGGCCCTGCATGTCCAGGATCCTCCGCCAACTCCCCTGCTGTCTACCCTGTGATGTACTGGCCGCCATTCAGTTCCACATATCCACAGTTCTTCGCCGTCCTACCCACCTTCGCCCCTGTGGTGCCCACCACCTGGTGCACTACTCAGGCCCCAGGTCTTTTTTTTTTTTGAAACAGAATTTCGCTCTTGTTGCCCAA... |
Task1_train_46529 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | GAACCCTGGGGGCTGAGTCCTCCCCAGCCCCAGCCACACACCGATGCTGAGTCCGGCTCCTCGAAACGGAAATTGTACTTCTGTTCAAAGTCCTCCTGTTTCTTCAGAAACAGCTCCCCTTCGTCTGAGGAGTCGTCCACAGCCAGCTGGACTGGGGGACCGTGGACCCTGAGGGGCAAGATGTGGTGATGCCAGGGGGCCAGCCAAGTGAGGTCGAGCCCCCCTTTCCTGCACGCCTGGGTACGAAGCGTATGAACTCATTTAATCCTCACAAGAACCCTACAAGGTGCACGCTGCTATTGTCCTCATTTTACAGATGG... | GAACCCTGGGGGCTGAGTCCTCCCCAGCCCCAGCCACACACCGATGCTGAGTCCGGCTCCTCGAAACGGAAATTGTACTTCTGTTCAAAGTCCTCCTGTTTCTTCAGAAACAGCTCCCCTTCGTCTGAGGAGTCGTCCACAGCCAGCTGGACTGGGGGACCGTGGACCCTGAGGGGCAAGATGTGGTGATGCCAGGGGGCCAGCCAAGTGAGGTCGAGCCCCCCTTTCCTGCACGCCTGGGTACGAAGCGTATGAACTCATTTAATCCTCACAAGAACCCTACAAGGTGCACGCTGCTATTGTCCTCATTTTACAGATGG... |
Task1_train_46530 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTTTGTATTTTTAGTAGAGACGGGGTTTCATCATATTGGTCAGGCTGGTCTCGAACTCCTGACCTCAGGTTATCTGCCTGCCTTGGCTTCCCAAACTGCTGGTATTACGGGTGTGAGCCACCACACCCGGCCTATTATTATTATTACTATTATTATTATTTTGACACAGTGTCTCACTCTGTCAGCCAGTGGCAGGATCATAGCTCGCTACAGCCTGGAACTCCTGGGCTTAAGCGATCTTCCCACCTGGGCCTTCCAAAGTGCTGGCACAAGACAGGCCTGAGCCACCCTGCCTGGCCCTATATAAGATATCTTTTTTT... | TTTTGTATTTTTAGTAGAGACGGGGTTTCATCATATTGGTCAGGCTGGTCTCGAACTCCTGACCTCAGGTTATCTGCCTGCCTTGGCTTCCCAAACTGCTGGTATTACGGGTGTGAGCCACCACACCCGGCCTATTATTATTATTACTATTATTATTATTTTGACACAGTGTCTCACTCTGTCAGCCAGTGGCAGGATCATAGCTCGCTACAGCCTGGAACTCCTGGGCTTAAGCGATCTTCCCACCTGGGCCTTCCAAAGTGCTGGCACAAGACAGGCCTGAGCCACCCTGCCTGGCCCTATATAAGATATCTTTTTTT... |
Task1_train_46531 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTGTGATCTGCCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCTGCCGCCAGTGCTGAGTTTTATCATCAGAGAGAGAAACCCAACCGCGGCAGGCAAAGGGTGTCCCTTTATTGTTTTCATAATAGTCTCGTTTTTATTTTATGTATTATATTTATTTTTTTGAGATGGAGTCTCACTCTGTCACCCAGGCTGGAGTACAGTGGTGCGATCTCAGCTCACTGCAACCTCTGTCTCCTGGATTCAAGCGATTCCCCTGCTTTGGCCTCCTGAGTAGCTGGGATTACAGGCATGTGCCACCA... | TTGTGATCTGCCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCTGCCGCCAGTGCTGAGTTTTATCATCAGAGAGAGAAACCCAACCGCGGCAGGCAAAGGGTGTCCCTTTATTGTTTTCATAATAGTCTCGTTTTTATTTTATGTATTATATTTATTTTTTTGAGATGGAGTCTCACTCTGTCACCCAGGCTGGAGTACAGTGGTGCGATCTCAGCTCACTGCAACCTCTGTCTCCTGGATTCAAGCGATTCCCCTGCTTTGGCCTCCTGAGTAGCTGGGATTACAGGCATGTGCCACCA... |
Task1_train_46532 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | TGCTTCTCCTGTCTTGGGGGCTTCCAGGTGGACCTGAATGAGGAGGAAACCATTCTCATCATCCGGCGTCTCCACAAAGTGCTGCGGCCCTTCTTGCTCCGACGACTCAAGAAGGAAGTCGAGGCCCAGTTGCCCGAAAAGGTGATGGAGTTTTGAGGGGAGCCACCAGTGAAGCAGCCTCACGTGGGGGCTTTCTCCAGGGCTGGGCGTGCTCAGGGCCTCTCCCCACAGTCCCAGGCCTGCCCTGGTCAATCCAGCTTGGGGGTGGCGATGACGCCACTGGGTCTGTAAAGCCCTGTGCTGCTGTTGTAGGGATTGAA... | TGCTTCTCCTGTCTTGGGGGCTTCCAGGTGGACCTGAATGAGGAGGAAACCATTCTCATCATCCGGCGTCTCCACAAAGTGCTGCGGCCCTTCTTGCTCCGACGACTCAAGAAGGAAGTCGAGGCCCAGTTGCCCGAAAAGGTGATGGAGTTTTGAGGGGAGCCACCAGTGAAGCAGCCTCACGTGGGGGCTTTCTCCAGGGCTGGGCGTGCTCAGGGCCTCTCCCCACAGTCCCAGGCCTGCCCTGGTCAATCCAGCTTGGGGGTGGCGATGACGCCACTGGGTCTGTAAAGCCCTGTGCTGCTGTTGTAGGGATTGAA... |
Task1_train_46533 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | GTTTGTTTTGAGACAGGGTCTTACTCTCTCGCCCAGTATAGAGTGCAGTGGTGCGGTCTTGGCTCGCTGCAACCTCTGCCTTCCAGGTTCAAGCTATTCTCCTGCCTCAGTCTCCCCAGTAGCTGGGATTACAGACACACATCACCACGCCCTGCTAATTATTTTGCATTTTTAGTAGAGATGGTGTTTCACCATATTGGCCAGGCTGATCTTGAACTCCTGGCCTCAAGTGGTCTGCTCCAAACTGCTGAGATTACAGCCGTGAGCCACTGCTCCCAGCCATCTGCACCTTTCTCATCTTCCCAAATGTAACTATGTCC... | GTTTGTTTTGAGACAGGGTCTTACTCTCTCGCCCAGTATAGAGTGCAGTGGTGCGGTCTTGGCTCGCTGCAACCTCTGCCTTCCAGGTTCAAGCTATTCTCCTGCCTCAGTCTCCCCAGTAGCTGGGATTACAGACACACATCACCACGCCCTGCTAATTATTTTGCATTTTTAGTAGAGATGGTGTTTCACCATATTGGCCAGGCTGATCTTGAACTCCTGGCCTCAAGTGGTCTGCTCCAAACTGCTGAGATTACAGCCGTGAGCCACTGCTCCCAGCCATCTGCACCTTTCTCATCTTCCCAAATGTAACTATGTCC... |
Task1_train_46534 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGTAAAAAACATGTAACATAAAATTTACCTTCTCAAACCTTATTAAGTGCACAGTTCTGTGCCATTAGCAAATTCACACTGTTGTACAACATCACAACCACCATCTCCAGAACTTTTTTTTTTTTTTTTATTCTTTTTGAGACAGAGTCTCACTCGTCGCACGGGCTGGAGTGCAGTGGTGCGATCTCGGTTCACTGCAACCTCCACCTACCAGGTTCAAGCAATTCTCCTGCCTCAGCCCCCTCAGTAGCTGGGATTACAGGTGCCCGTCCTACCACGCCCAGCTAATTTTTGTATTTTCAGTAGAGACTGACTGGGTT... | AGTAAAAAACATGTAACATAAAATTTACCTTCTCAAACCTTATTAAGTGCACAGTTCTGTGCCATTAGCAAATTCACACTGTTGTACAACATCACAACCACCATCTCCAGAACTTTTTTTTTTTTTTTTATTCTTTTTGAGACAGAGTCTCACTCGTCGCACGGGCTGGAGTGCAGTGGTGCGATCTCGGTTCACTGCAACCTCCACCTACCAGGTTCAAGCAATTCTCCTGCCTCAGCCCCCTCAGTAGCTGGGATTACAGGTGCCCGTCCTACCACGCCCAGCTAATTTTTGTATTTTCAGTAGAGACTGACTGGGTT... |
Task1_train_46535 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AGGAGTCAAGGTTATGGTACGATGCCCGTGTTTTCACTCCAGCCACGGAGCTGGGTCTCTGGTCTCGGGGGCAGCTGTGTGACAGAGCGTGCCTCTCCCTACAGTGCTCCTCGTCTTCCTTTGCCTGGGGGTCTTCCTTCTATGGAAGAACTGGCGGCTTAAGAACATCAACAGCATCAACTTTGACAACCCCGTCTATCAGAAGACCACAGAGGATGAGGTCCACATTTGCCACAACCAGGACGGCTACAGCTACCCCTCGGTGAGTGACCCTCTCTAGAAAGCCAGAGCCCATGGCGGCCCCCTCCCAGCTGGAGGCA... | AGGAGTCAAGGTTATGGTACGATGCCCGTGTTTTCACTCCAGCCACGGAGCTGGGTCTCTGGTCTCGGGGGCAGCTGTGTGACAGAGCGTGCCTCTCCCTACAGTGCTCCTCGTCTTCCTTTGCCTGGGGGTCTTCCTTCTATGGAAGAACTGGCGGCTTAAGAACATCAACAGCATCAACTTTGACAACCCCGTCTATCAGAAGACCACAGAGGATGAGGTCCACATTTGCCACAACCAGGACGGCTACAGCTACCCCTCGGTGAGTGACCCTCTCTAGAAAGCCAGAGCCCATGGCGGCCCCCTCCCAGCTGGAGGCA... |
Task1_train_46536 | Located on Chromosome 19, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TTACAGGTGCCCGCCACCATGCCTGGCTAACTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGACTGGTCTTGAACTCCTGATGTCAGGTGACCCACCTGCCTTGGCCTCCCAATGTTGCTGGTACTACAGACATGAGCCACCATGCCTGGTCTCTTCTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCTCGATCTCGGCTCACTGCGAACTCTGCCGCCTGCGTTCACGCCATTCTCCTGCCTCACTCAGCCTCCTGAGTAGCTGGGACTACAGGT... | TTACAGGTGCCCGCCACCATGCCTGGCTAACTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGACTGGTCTTGAACTCCTGATGTCAGGTGACCCACCTGCCTTGGCCTCCCAATGTTGCTGGTACTACAGACATGAGCCACCATGCCTGGTCTCTTCTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCTCGATCTCGGCTCACTGCGAACTCTGCCGCCTGCGTTCACGCCATTCTCCTGCCTCACTCAGCCTCCTGAGTAGCTGGGACTACAGGT... |
Task1_train_46537 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AAGCGATTCTTGTGCTTCAGTCTCCCAAGTAGCTGGGATTACAGGTGCCGGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGGCCTCAAGTGATCTGCCTGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCCAGCTGTCATTATTATTATTAATTATTTTGAGATACAGTTTCACTCTGTCGCCCAGGCTGGAGGGCAGTGGTGTGATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCT... | AAGCGATTCTTGTGCTTCAGTCTCCCAAGTAGCTGGGATTACAGGTGCCGGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGGCCTCAAGTGATCTGCCTGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCCAGCTGTCATTATTATTATTAATTATTTTGAGATACAGTTTCACTCTGTCGCCCAGGCTGGAGGGCAGTGGTGTGATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCT... |
Task1_train_46538 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GAGGTCACTTTCCCTTGCCTGCCTGAAAGAGAAGCTCCCAGGGAAAACAAGAAGAGAAAGGCACCAAGTTAGATTCCTGATGATATCTGAGCACTGAGGCCAGCGTGGTGGCTCATGCTTGTAATCCCAGCACTCTGGGAGGCCAAGACAGGAGCATCATTTGAGCCCAGAAGTTTGAGACCAGCCTGGGCAACATAACAAGACTTTGTCTCTACAAAAAATAAAAAAAATTAACGAGGCACAGTGGTGCATGCCTGTAGACCCAGCTACTTGGGAGGCTAAGGCGGGAGGATTGCTTGAGCCTAGGAAGTCAAGGCTGC... | GAGGTCACTTTCCCTTGCCTGCCTGAAAGAGAAGCTCCCAGGGAAAACAAGAAGAGAAAGGCACCAAGTTAGATTCCTGATGATATCTGAGCACTGAGGCCAGCGTGGTGGCTCATGCTTGTAATCCCAGCACTCTGGGAGGCCAAGACAGGAGCATCATTTGAGCCCAGAAGTTTGAGACCAGCCTGGGCAACATAACAAGACTTTGTCTCTACAAAAAATAAAAAAAATTAACGAGGCACAGTGGTGCATGCCTGTAGACCCAGCTACTTGGGAGGCTAAGGCGGGAGGATTGCTTGAGCCTAGGAAGTCAAGGCTGC... |
Task1_train_46539 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TCACCTTGTGGACACGGGTGATGACCTCCAGGCCCACAGAGCCCACCAAGGCAGTGATGTCGTCCAGGAAGCGTCCGGGGAAGCGCAGCTTGCGGGGTGTGTCTAGTCGCTGGCCAAGCAGCAGGTGCAGCGCCATACTCTTCACCTGGGGGTGGGGTGAGAGGGCTGTGGGTGGGATTTGAAGGGCTGTGGGTAGGACTTGAAGGGCTGTGGGTGGGGCTTGAAGGGCTGTGGGTGGGGCTTGAAGGACTGTGGGTGGGGCTTGAAGGGCTGTGGGTGGAGGAGGCTTGACAGGAGGGGCGGGGCTTTATTAGCAATGG... | TCACCTTGTGGACACGGGTGATGACCTCCAGGCCCACAGAGCCCACCAAGGCAGTGATGTCGTCCAGGAAGCGTCCGGGGAAGCGCAGCTTGCGGGGTGTGTCTAGTCGCTGGCCAAGCAGCAGGTGCAGCGCCATACTCTTCACCTGGGGGTGGGGTGAGAGGGCTGTGGGTGGGATTTGAAGGGCTGTGGGTAGGACTTGAAGGGCTGTGGGTGGGGCTTGAAGGGCTGTGGGTGGGGCTTGAAGGACTGTGGGTGGGGCTTGAAGGGCTGTGGGTGGAGGAGGCTTGACAGGAGGGGCGGGGCTTTATTAGCAATGG... |
Task1_train_46540 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | TGAGAAAAATGGCCAGAGAGGTAAATGGGCTTATAGAAGATCCCTCAGGACCTCAGGACTGAGAAGCCATGTGGATGGGGAAACTGAGGTCTGAGGCCACATTCGCTTACCAATCTGGCCACTGATGATCGGGGGCCTGATGACCAGACGCACGAGCTTGTCCAGCACGTGGTGGGAGAAGGCCACAAGGGGTTCGGGGCTGGCCAGGCGCAGTGCTGCAAGACTGGCCCGCAGCTCCTGCTCCACGTTGCCCTCGCTCAGCACAGTGTCCTTGAGCCGGAATGGGAAGGCTCCCTCCTCCAGGACGTGCACCAGGGTGA... | TGAGAAAAATGGCCAGAGAGGTAAATGGGCTTATAGAAGATCCCTCAGGACCTCAGGACTGAGAAGCCATGTGGATGGGGAAACTGAGGTCTGAGGCCACATTCGCTTACCAATCTGGCCACTGATGATCGGGGGCCTGATGACCAGACGCACGAGCTTGTCCAGCACGTGGTGGGAGAAGGCCACAAGGGGTTCGGGGCTGGCCAGGCGCAGTGCTGCAAGACTGGCCCGCAGCTCCTGCTCCACGTTGCCCTCGCTCAGCACAGTGTCCTTGAGCCGGAATGGGAAGGCTCCCTCCTCCAGGACGTGCACCAGGGTGA... |
Task1_train_46541 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GTAGAACTCGGGGGACCTGGCAGAATCGGGCTGGGGGATCTGCTGGGGGCTGGGGTCCCCACTGTCTGCCCCATCACCTCTGCCATGCCACGCCCTTATTGCTGCTAGGCCCCACTGTCTCTGCTGTCTGCCTCAGCTTCCCTCATTAGCACTCTGGGAGCCTCTACCTCTCTTCTTCCTGTCCCCCATCTTCCCATCGATGCTGCCTTATGTGTATATATAAGGGACATCCTCCTACCCCCATGAGTGCCCCCAAGTTCCTCACGTGTCCCCCTACATACTTGTTATGGTAGACCACCGGTGTGAAGGCCTCGCGGGTA... | GTAGAACTCGGGGGACCTGGCAGAATCGGGCTGGGGGATCTGCTGGGGGCTGGGGTCCCCACTGTCTGCCCCATCACCTCTGCCATGCCACGCCCTTATTGCTGCTAGGCCCCACTGTCTCTGCTGTCTGCCTCAGCTTCCCTCATTAGCACTCTGGGAGCCTCTACCTCTCTTCTTCCTGTCCCCCATCTTCCCATCGATGCTGCCTTATGTGTATATATAAGGGACATCCTCCTACCCCCATGAGTGCCCCCAAGTTCCTCACGTGTCCCCCTACATACTTGTTATGGTAGACCACCGGTGTGAAGGCCTCGCGGGTA... |
Task1_train_46542 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTTTTTTTTTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGGAGTGGTGCGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTTAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACGTGCCACCATGCCCAGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCTATGTATGTATTTATTTATTATATAGAGACGGGGTCTCGCTGTGTTGCCCAGGCTGGTCTCAAACTCTTGGGCTCAAGTGATGCCCCCGCCTCTGCCTCCCAAAGTGCTGGGATAATAGGCATGAGCCAT... | TTTTTTTTTTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGGAGTGGTGCGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTTAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACGTGCCACCATGCCCAGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCTATGTATGTATTTATTTATTATATAGAGACGGGGTCTCGCTGTGTTGCCCAGGCTGGTCTCAAACTCTTGGGCTCAAGTGATGCCCCCGCCTCTGCCTCCCAAAGTGCTGGGATAATAGGCATGAGCCAT... |
Task1_train_46543 | Here is a mutation located on Chromosome 19. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GGGGGTTGAGGGGATCTGACTCCCTGTCCCTTCTACAATGGGAAAAGGCTGCTTCAATGCTGCTTTTCGCAAGTAGAGGGTCTGCAGGGGTCAAAGGGATCACCATCCCACCTTGGAATCCAGAAAGTTCGTGGGGGCAGGCTCAGAGACCAGCCTGCAGGACCTGAGAAAGAGGCGCCGCCTTCCCTGGATGAACTCCAAGAACCCACACTGTGCGAGGAAGATGAACCATCTTCCACCAGCTTGGGAATATCAGTCCTGCCCAACCCAGAAGAGACCTGGAAAATGGTTCTAAGCTAGAAGGCACCACGGATGCCCCT... | GGGGGTTGAGGGGATCTGACTCCCTGTCCCTTCTACAATGGGAAAAGGCTGCTTCAATGCTGCTTTTCGCAAGTAGAGGGTCTGCAGGGGTCAAAGGGATCACCATCCCACCTTGGAATCCAGAAAGTTCGTGGGGGCAGGCTCAGAGACCAGCCTGCAGGACCTGAGAAAGAGGCGCCGCCTTCCCTGGATGAACTCCAAGAACCCACACTGTGCGAGGAAGATGAACCATCTTCCACCAGCTTGGGAATATCAGTCCTGCCCAACCCAGAAGAGACCTGGAAAATGGTTCTAAGCTAGAAGGCACCACGGATGCCCCT... |
Task1_train_46544 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | ATACTACTACTACACTCCACACACCATATCCCACATGGGTGAGGATATCTCTAGGATCAATTTCCAGAAATGGTTTTGCTGGGTTCCCAGGGGATAGGCAGTGGGGCAGTGGGAGTTCCTGCGCGTGGATCCCCTGCAATTAGACGGGACATGTGGCATACACATGGGTATCTTCCTGGGCAGATCCTCAAAGGATCAGTGACTGGGTTGGACCCTGAATCAGAGGATGGGGATGAGGGTTTGGTTCTGGGAGACCAGGGCCTGTGGCCCAGGCTGGGCACTAACCAAGGTCGTCGGCGAGCCTCCGGCCATCCTCAGCA... | ATACTACTACTACACTCCACACACCATATCCCACATGGGTGAGGATATCTCTAGGATCAATTTCCAGAAATGGTTTTGCTGGGTTCCCAGGGGATAGGCAGTGGGGCAGTGGGAGTTCCTGCGCGTGGATCCCCTGCAATTAGACGGGACATGTGGCATACACATGGGTATCTTCCTGGGCAGATCCTCAAAGGATCAGTGACTGGGTTGGACCCTGAATCAGAGGATGGGGATGAGGGTTTGGTTCTGGGAGACCAGGGCCTGTGGCCCAGGCTGGGCACTAACCAAGGTCGTCGGCGAGCCTCCGGCCATCCTCAGCA... |
Task1_train_46545 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | ACAACATCCCAGTAAGGTGACTATTATGACATCTCGTTTTTATAGTTGGGGACACTGAGGCATGGAGAGGTTCAGTAACGCGACCAGTATTACACAGCTGGAAGGGACAGAGCTAGGATTTGAACCCAGGCCATCTAGCTGGAGAGTTTCCCTGCTTAACCGTCATACTCTGCTGTCCCTGGAAGTGAGGACCTCCCTGAGGCAGTGACTCTCGGAGGGGCAGCTTAGGACATTTCAGGCAGAAGAAAAACGTGTACATCACAGGGTGGGTGTGAAGATCCAGTGAATGCTTAGGGGATGCCCGGCACTCAATTAGGTGC... | ACAACATCCCAGTAAGGTGACTATTATGACATCTCGTTTTTATAGTTGGGGACACTGAGGCATGGAGAGGTTCAGTAACGCGACCAGTATTACACAGCTGGAAGGGACAGAGCTAGGATTTGAACCCAGGCCATCTAGCTGGAGAGTTTCCCTGCTTAACCGTCATACTCTGCTGTCCCTGGAAGTGAGGACCTCCCTGAGGCAGTGACTCTCGGAGGGGCAGCTTAGGACATTTCAGGCAGAAGAAAAACGTGTACATCACAGGGTGGGTGTGAAGATCCAGTGAATGCTTAGGGGATGCCCGGCACTCAATTAGGTGC... |
Task1_train_46546 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | GGCCGGCCTACCCCGGGACCCTGACTACTCTGTGTCCTGCCTCTACTCACCTCCCTCACCCTCCAGCATGTGTTTGCCTGCTAACATGAAGTGTGACAAGTACTGGGGTTAGTTAGGGGGCTCCCATAGGGCTGGGGACACTGGGAGGGGCTGGGAATGTGAGGAGTGCCCTGCACTGTCCCTCAAGGAAGCCCTCACCCCTAGGCTCTTCCTCGGACAAGGCTCTGGAGCGTACAGCTCACTGGTCCAGGACTCCAGAGCCAGAGACCTTGGGATGCCCTGCTTCTGGGGACACAGTGAGGACTGCAGACTGCAGGCCA... | GGCCGGCCTACCCCGGGACCCTGACTACTCTGTGTCCTGCCTCTACTCACCTCCCTCACCCTCCAGCATGTGTTTGCCTGCTAACATGAAGTGTGACAAGTACTGGGGTTAGTTAGGGGGCTCCCATAGGGCTGGGGACACTGGGAGGGGCTGGGAATGTGAGGAGTGCCCTGCACTGTCCCTCAAGGAAGCCCTCACCCCTAGGCTCTTCCTCGGACAAGGCTCTGGAGCGTACAGCTCACTGGTCCAGGACTCCAGAGCCAGAGACCTTGGGATGCCCTGCTTCTGGGGACACAGTGAGGACTGCAGACTGCAGGCCA... |
Task1_train_46547 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | GCAAAACTCCCATCTTAAAAAAAAAAAAGAAAAAAGAAAAAGAAAAAGAAAACTCATCCTGTTGGGTGCTGTGGCATGCCTGTTATCTCAGCACTTTGGGAGGCTGAGGTGGTTGGATTGCTTGAGGCCAGAAGTTCAAGACCAGCCTAGGCAACATGGCAAAACCCTGTCTCTACAAAAAACAAAAAAAACAAGAGGGTGTGGTGGCACATGCCTGTAGACTTAGCTACTCAGAAGGCTGAGGTAGGGGGATCACTTGAGCCTTGGAGGTTCAGGGTGCGTTGAGCCCTGATAGTACCATTGCACTCTAGCCTGGGCGA... | GCAAAACTCCCATCTTAAAAAAAAAAAAGAAAAAAGAAAAAGAAAAAGAAAACTCATCCTGTTGGGTGCTGTGGCATGCCTGTTATCTCAGCACTTTGGGAGGCTGAGGTGGTTGGATTGCTTGAGGCCAGAAGTTCAAGACCAGCCTAGGCAACATGGCAAAACCCTGTCTCTACAAAAAACAAAAAAAACAAGAGGGTGTGGTGGCACATGCCTGTAGACTTAGCTACTCAGAAGGCTGAGGTAGGGGGATCACTTGAGCCTTGGAGGTTCAGGGTGCGTTGAGCCCTGATAGTACCATTGCACTCTAGCCTGGGCGA... |
Task1_train_46548 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | CCCTGTATCAACTAAAAGTACAAAAAAAATTAGCTGGGTGTGGTGGCAGGTGCCTGTAGTCTCAGCTACTCAGGAGGCTTAGGCAGGAGAATTGCTTGAACCCAGGAAGCGGAGGTTGCAGTGAGCCGAGATTGTGCCACTACACTCCAGCCTGGGTGACAAAGCGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAGTTTGAGACTTCCTTCTTTTTGCACTCAACGTTGTTACTAAGATTCATCTACATTTTTTTAGTTCATTCCTTTTTCCATATTGCATATAATTCCATGGGTGACTATACCCTGATTTCTTCAT... | CCCTGTATCAACTAAAAGTACAAAAAAAATTAGCTGGGTGTGGTGGCAGGTGCCTGTAGTCTCAGCTACTCAGGAGGCTTAGGCAGGAGAATTGCTTGAACCCAGGAAGCGGAGGTTGCAGTGAGCCGAGATTGTGCCACTACACTCCAGCCTGGGTGACAAAGCGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAGTTTGAGACTTCCTTCTTTTTGCACTCAACGTTGTTACTAAGATTCATCTACATTTTTTTAGTTCATTCCTTTTTCCATATTGCATATAATTCCATGGGTGACTATACCCTGATTTCTTCAT... |
Task1_train_46549 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | AAGTTCAGATAACTTCAGGGTCCCAGTGGTGAACAAACTTAGTTCTCACAAATCTAAGCCCAGATGCCCTTTAGTCTCCCATCCCATCAGGTTGAGCCTGAACAATCTCATGATGCTACAAACTTAAGATCAGACAAACTTCTACACTCCCTTCTCTCACTCGACCCTAGACAATCTATTTTTTCTTTTTTTTTGAGACGGAGTCTCACTCTGTCGCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTTCACCTCCTGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGACTATAGGC... | AAGTTCAGATAACTTCAGGGTCCCAGTGGTGAACAAACTTAGTTCTCACAAATCTAAGCCCAGATGCCCTTTAGTCTCCCATCCCATCAGGTTGAGCCTGAACAATCTCATGATGCTACAAACTTAAGATCAGACAAACTTCTACACTCCCTTCTCTCACTCGACCCTAGACAATCTATTTTTTCTTTTTTTTTGAGACGGAGTCTCACTCTGTCGCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTTCACCTCCTGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGACTATAGGC... |
Task1_train_46550 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | CGCGCCCAGCCAATTTTAATTAATTTAAATAGCGACAGGGGCTAGTGGATACCACAGTGAACTATGGAGCTCTAATGACTTGGAATCAGCTGGAGAAATCATATATATATATATATATATATATATATATATATATATATATACACCTATATATATATACCTTTATATATATATATACCTTTATATATATATACCTTTATATATATATATACCTTTATATATATACCTTTATATATATATACCTTTATATATATATACCTTCATATATATACATATATATATATACCTTCATATATATATATATACCTTTATATATATAT... | CGCGCCCAGCCAATTTTAATTAATTTAAATAGCGACAGGGGCTAGTGGATACCACAGTGAACTATGGAGCTCTAATGACTTGGAATCAGCTGGAGAAATCATATATATATATATATATATATATATATATATATATATATATACACCTATATATATATACCTTTATATATATATATACCTTTATATATATATACCTTTATATATATATATACCTTTATATATATACCTTTATATATATATACCTTTATATATATATACCTTCATATATATACATATATATATATACCTTCATATATATATATATACCTTTATATATATAT... |
Task1_train_46551 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GGGCCTCGGGTGCCAGAGGAATGAGCCCCCTTTTTGCTGGATCCCAGAGGGCCATCACCCTAAACCTAGGTGCCTGTCCACCACTCTGCGCATGTGTGCCGGCTCCTGCCAGGGCTAGCAGACCTTACCTGGGATCTTGGAGGTGGCGGGATAACCAGGGAAGACATGTCATGGCAGAGTGGGCCTGAGGGGGTGCACAGGCCAGACCCAGCAGCCCAGTCTGGCAGCCAGGGCTTCCGGGCCAGCTCAATGTCTCCCCCCGCTGTTCACATCCGTCAGTGCCCTGGGTGGGCCCCAGAGCCGCTCAAACCATGCCTGGC... | GGGCCTCGGGTGCCAGAGGAATGAGCCCCCTTTTTGCTGGATCCCAGAGGGCCATCACCCTAAACCTAGGTGCCTGTCCACCACTCTGCGCATGTGTGCCGGCTCCTGCCAGGGCTAGCAGACCTTACCTGGGATCTTGGAGGTGGCGGGATAACCAGGGAAGACATGTCATGGCAGAGTGGGCCTGAGGGGGTGCACAGGCCAGACCCAGCAGCCCAGTCTGGCAGCCAGGGCTTCCGGGCCAGCTCAATGTCTCCCCCCGCTGTTCACATCCGTCAGTGCCCTGGGTGGGCCCCAGAGCCGCTCAAACCATGCCTGGC... |
Task1_train_46552 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCGCCGCCACGCCTGGCTAATTTTTTTGTAGTTTTAGTAGAGACGGGGTTTCACCATGTTAGTCAGGATGGTCTCGATCTCCTGACCTCGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGGCCGGGTTTTATAATCACATCCATGGATAAGGCAACTTGGTCATGGATGGGGTAAGAGATGGAGGCAAGGAACAGCAGCTCAGGGGAGCCCAGCCACTCTAACCAGGAGAACATAACACACCAGT... | CTATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCGCCGCCACGCCTGGCTAATTTTTTTGTAGTTTTAGTAGAGACGGGGTTTCACCATGTTAGTCAGGATGGTCTCGATCTCCTGACCTCGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGGCCGGGTTTTATAATCACATCCATGGATAAGGCAACTTGGTCATGGATGGGGTAAGAGATGGAGGCAAGGAACAGCAGCTCAGGGGAGCCCAGCCACTCTAACCAGGAGAACATAACACACCAGT... |
Task1_train_46553 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | CCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGGCCGGGTTTTATAATCACATCCATGGATAAGGCAACTTGGTCATGGATGGGGTAAGAGATGGAGGCAAGGAACAGCAGCTCAGGGGAGCCCAGCCACTCTAACCAGGAGAACATAACACACCAGTGGCACTGGTTCAGCCTTGGCAACTATTCTTTTATTGAACATCAGTAACAGAAAGATGCTTGATTTAGGAGGAAGCTTTCCCTCCCTCCCTCCCCCATTGCACCCCGGAACTCAGCAAAGGTGAGCCAGCCACAGAGCATAACACTGTGGCTGGGAC... | CCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGGCCGGGTTTTATAATCACATCCATGGATAAGGCAACTTGGTCATGGATGGGGTAAGAGATGGAGGCAAGGAACAGCAGCTCAGGGGAGCCCAGCCACTCTAACCAGGAGAACATAACACACCAGTGGCACTGGTTCAGCCTTGGCAACTATTCTTTTATTGAACATCAGTAACAGAAAGATGCTTGATTTAGGAGGAAGCTTTCCCTCCCTCCCTCCCCCATTGCACCCCGGAACTCAGCAAAGGTGAGCCAGCCACAGAGCATAACACTGTGGCTGGGAC... |
Task1_train_46554 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TTGCTGTCTCAAGAGTAGCAGAGACTGAAGAAATTCATATGTAAGTAGACCTGTGCAGTTCAAACCTGTGTTGAAGACTCAGCTGTAGTTTGGTGTGTGAATCATGCATGATTGTAGTGTACATAAAATCTTACAGTCTTTCTATAATTTTATAATAATTTATAGTCATTTTTCTGGTTCTAACTTTTAGGAATGATATGGCAAAATCATGATATAGAAGAAGATCAGTACAAAGATCTCAGAAGAAATCTAAGGTAATTTGCACTCACAAGAGAAAGCTGTGTCCTTGAAGTGATTCATAGTATGCCAGAAATTTTATT... | TTGCTGTCTCAAGAGTAGCAGAGACTGAAGAAATTCATATGTAAGTAGACCTGTGCAGTTCAAACCTGTGTTGAAGACTCAGCTGTAGTTTGGTGTGTGAATCATGCATGATTGTAGTGTACATAAAATCTTACAGTCTTTCTATAATTTTATAATAATTTATAGTCATTTTTCTGGTTCTAACTTTTAGGAATGATATGGCAAAATCATGATATAGAAGAAGATCAGTACAAAGATCTCAGAAGAAATCTAAGGTAATTTGCACTCACAAGAGAAAGCTGTGTCCTTGAAGTGATTCATAGTATGCCAGAAATTTTATT... |
Task1_train_46555 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGTATTTTTTAGAGATGGAGTTCCACCACGTTGGCCAGGCTGGTCTCAAACTGCTGACCTCAAGTGATCTTCCCACCTCAACCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCATGCCTGGCTGCTACCATGATTTATTATCATTACTTATCTTAAAACAAAATGTAAAACTTATCAGCTTAAGAAATTTTACATGTACAGTTGAGATAGTTTGACAAATCTACATAAGTTCTCTAAGATGAATTCTATTGTATTTTGCTTTTTTCAATTATCCCGAGGTGTCATGCATGTTGTAGTTTAGTCCAAGATGTTATTT... | TGTATTTTTTAGAGATGGAGTTCCACCACGTTGGCCAGGCTGGTCTCAAACTGCTGACCTCAAGTGATCTTCCCACCTCAACCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCATGCCTGGCTGCTACCATGATTTATTATCATTACTTATCTTAAAACAAAATGTAAAACTTATCAGCTTAAGAAATTTTACATGTACAGTTGAGATAGTTTGACAAATCTACATAAGTTCTCTAAGATGAATTCTATTGTATTTTGCTTTTTTCAATTATCCCGAGGTGTCATGCATGTTGTAGTTTAGTCCAAGATGTTATTT... |
Task1_train_46556 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTAACTTTGTTTTGCCTATGAATTCGTAGGACTCTATCATGACAGGTGCTACAGACCCACAGTCCAAAGAGACATTAGGGACAGCCCAGGCAACCCGCTTTTCTCCCTGGGTTCGGTAAATACATTTCCTATCCTGCTGTGGCTTTAGCCCTTGTTCAGTTCTAGCATCACAATTGCTTTATGAACTAGCCAGGTGTGGTGGCACATGCCTGTGGTCTCAACTACTCAGGAGGCTGAGGCATGAGAATTGCATGAACCCAGGAGTAAGAGGTTGTAGTGAGCCAAGATGGTGCCACTACACTCCAGCCTGGGTAACAGAA... | TTAACTTTGTTTTGCCTATGAATTCGTAGGACTCTATCATGACAGGTGCTACAGACCCACAGTCCAAAGAGACATTAGGGACAGCCCAGGCAACCCGCTTTTCTCCCTGGGTTCGGTAAATACATTTCCTATCCTGCTGTGGCTTTAGCCCTTGTTCAGTTCTAGCATCACAATTGCTTTATGAACTAGCCAGGTGTGGTGGCACATGCCTGTGGTCTCAACTACTCAGGAGGCTGAGGCATGAGAATTGCATGAACCCAGGAGTAAGAGGTTGTAGTGAGCCAAGATGGTGCCACTACACTCCAGCCTGGGTAACAGAA... |
Task1_train_46557 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GCTGTGGGCTCACTCCTGTAATCCCAATCCTTTGAGAAGTGGAGATAGGAGGATAGCTTGAGGCCAGCAGTTCAAGAACAGCCTGGGCAACATAACGAGACCACATATCAACAACAGCAAAAAATTAGCTGGGCATTGTGGTCTGTAGTCCCAGCTACTCAGGAGGCTGAGTGAGGCAGGAGGATCACTTGAGCCAGTAAAGGCTGCAGTAAGCTATGGTGATATCACCACACTCCAGTGTGGGCAACAGGATAAGACCCTGAAACAAAAGAAAAATGACACAGAGTATTTAGTATTTTAAAATAGTTTACATGGGAAGA... | GCTGTGGGCTCACTCCTGTAATCCCAATCCTTTGAGAAGTGGAGATAGGAGGATAGCTTGAGGCCAGCAGTTCAAGAACAGCCTGGGCAACATAACGAGACCACATATCAACAACAGCAAAAAATTAGCTGGGCATTGTGGTCTGTAGTCCCAGCTACTCAGGAGGCTGAGTGAGGCAGGAGGATCACTTGAGCCAGTAAAGGCTGCAGTAAGCTATGGTGATATCACCACACTCCAGTGTGGGCAACAGGATAAGACCCTGAAACAAAAGAAAAATGACACAGAGTATTTAGTATTTTAAAATAGTTTACATGGGAAGA... |
Task1_train_46558 | A sequence alteration has been identified on Chromosome 19. Is it disease-inducing or harmless? | Benign | CTGGAAACTTTCTGGAACCTGACCTCTATAGGTAAGGATGACAATATTCCTTCCCTCAGTGCATTAGTTTACCAATGTTTCTAGCTCACCAATGCTGTTGAGTGATTTGGAACACAGACAGGAAATACTTTGATGAATAAATGAGGCATGGCTGCTGTAAATCATGGGCATAGGTCTAATAATTTTTTCACAATTTTATACTGCCTCAGGATTATTTTTCTGTGTTTGTATTTTAGGAAAAAAGTGGAAAGACCAGAACATTGAATATGAGTACCAAAACCCCAGGAGAAACTTCAGGTAATTTGCACTTATAAGAGAAA... | CTGGAAACTTTCTGGAACCTGACCTCTATAGGTAAGGATGACAATATTCCTTCCCTCAGTGCATTAGTTTACCAATGTTTCTAGCTCACCAATGCTGTTGAGTGATTTGGAACACAGACAGGAAATACTTTGATGAATAAATGAGGCATGGCTGCTGTAAATCATGGGCATAGGTCTAATAATTTTTTCACAATTTTATACTGCCTCAGGATTATTTTTCTGTGTTTGTATTTTAGGAAAAAAGTGGAAAGACCAGAACATTGAATATGAGTACCAAAACCCCAGGAGAAACTTCAGGTAATTTGCACTTATAAGAGAAA... |
Task1_train_46559 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | AATTCCAAAGGCTCTCAAGTGCTTGAGGTGGACCTGGATTCCTTCAAGAGCTTCTCTAGGGAACCGGGTACTGTTTTTGCCTGACCGGCTGGGCCCCAGGCTTAACTTCTGTAGGTACGGGGGTTTGGTTGACTGCCAGCCCTGGAGGGTTGTCTTCTGCCCACACCTTTGACCATCACTTAGCCAGAGCTGGTCTTATCTCTTGACCTGGCTCGGTTAAGAAAAGTCTTCATTCCTCCTCCTGGGGGACAGTAAGGGCCATGATGACTCCCTTTCCGGGTAACTTTAGCTGTAAAAGAGCTGTGCTCTGTAAGAGAGAT... | AATTCCAAAGGCTCTCAAGTGCTTGAGGTGGACCTGGATTCCTTCAAGAGCTTCTCTAGGGAACCGGGTACTGTTTTTGCCTGACCGGCTGGGCCCCAGGCTTAACTTCTGTAGGTACGGGGGTTTGGTTGACTGCCAGCCCTGGAGGGTTGTCTTCTGCCCACACCTTTGACCATCACTTAGCCAGAGCTGGTCTTATCTCTTGACCTGGCTCGGTTAAGAAAAGTCTTCATTCCTCCTCCTGGGGGACAGTAAGGGCCATGATGACTCCCTTTCCGGGTAACTTTAGCTGTAAAAGAGCTGTGCTCTGTAAGAGAGAT... |
Task1_train_46560 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATTCCAAAGGCTCTCAAGTGCTTGAGGTGGACCTGGATTCCTTCAAGAGCTTCTCTAGGGAACCGGGTACTGTTTTTGCCTGACCGGCTGGGCCCCAGGCTTAACTTCTGTAGGTACGGGGGTTTGGTTGACTGCCAGCCCTGGAGGGTTGTCTTCTGCCCACACCTTTGACCATCACTTAGCCAGAGCTGGTCTTATCTCTTGACCTGGCTCGGTTAAGAAAAGTCTTCATTCCTCCTCCTGGGGGACAGTAAGGGCCATGATGACTCCCTTTCCGGGTAACTTTAGCTGTAAAAGAGCTGTGCTCTGTAAGAGAGATG... | ATTCCAAAGGCTCTCAAGTGCTTGAGGTGGACCTGGATTCCTTCAAGAGCTTCTCTAGGGAACCGGGTACTGTTTTTGCCTGACCGGCTGGGCCCCAGGCTTAACTTCTGTAGGTACGGGGGTTTGGTTGACTGCCAGCCCTGGAGGGTTGTCTTCTGCCCACACCTTTGACCATCACTTAGCCAGAGCTGGTCTTATCTCTTGACCTGGCTCGGTTAAGAAAAGTCTTCATTCCTCCTCCTGGGGGACAGTAAGGGCCATGATGACTCCCTTTCCGGGTAACTTTAGCTGTAAAAGAGCTGTGCTCTGTAAGAGAGATG... |
Task1_train_46561 | Chromosome 19 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTTTGTGTCTGACCCATTTTTCTTTCGAGACAAGACAACACTCACACTACAAGAGGGAAAGGGTAAAGGTCACTCACGCGTGGTGGTACATGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCCGGTGGTGAGCCAATATCACGCCATTGTACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAAAAAATAAATAAATAAATAAATTGCTTTATGGAAGAAAGTAAGTATAGATGGAGAGAAAGGGATCTGATAACCGAAGCAGGGAATAAATGTTTGGAGTCCACAGCATCCTGA... | CTTTGTGTCTGACCCATTTTTCTTTCGAGACAAGACAACACTCACACTACAAGAGGGAAAGGGTAAAGGTCACTCACGCGTGGTGGTACATGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCCGGTGGTGAGCCAATATCACGCCATTGTACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAAAAAATAAATAAATAAATAAATTGCTTTATGGAAGAAAGTAAGTATAGATGGAGAGAAAGGGATCTGATAACCGAAGCAGGGAATAAATGTTTGGAGTCCACAGCATCCTGA... |
Task1_train_46562 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | CCAGCCTAAGTGACAGATGGAGACTGTCCCAAACAAAACAAACTAAGCAGAAAAACTAAGGATAGCACCTTCGAATTTGTCCCTAAGTTGTCAAAGTCTTGGACCCCCACTGAAGGAATTCCCTGGTACTTAGACACCAGATAAAGCAGAAGTGAAGACTGCACTCTAATTATCCTCCTTTGTTTTAGGTTTCTTCCTGAAGGACTTGTGAAAAGTCACTTCCTCTACTTTTTTTTCTGCTGACCCCCAAATTTTAAACAAAGCTTTTCTTCCCTAAGGAATTGCAAATCAGAAAATCTTTAAACTGTAAGCCCCAGCTT... | CCAGCCTAAGTGACAGATGGAGACTGTCCCAAACAAAACAAACTAAGCAGAAAAACTAAGGATAGCACCTTCGAATTTGTCCCTAAGTTGTCAAAGTCTTGGACCCCCACTGAAGGAATTCCCTGGTACTTAGACACCAGATAAAGCAGAAGTGAAGACTGCACTCTAATTATCCTCCTTTGTTTTAGGTTTCTTCCTGAAGGACTTGTGAAAAGTCACTTCCTCTACTTTTTTTTCTGCTGACCCCCAAATTTTAAACAAAGCTTTTCTTCCCTAAGGAATTGCAAATCAGAAAATCTTTAAACTGTAAGCCCCAGCTT... |
Task1_train_46563 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GAGTACCTGGGATTACAGGCATACACCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATGTTGAGGCTGGTCTCGAACTCCTGATCTCAAGCGATCCGCACGCCTCAGCCTTCCAAAGTCCTGGGATTACAGGTGTGAGCCACCGCGCCCGGCCCACAGTACTGTTTTTCACAAAATTTCTATTCATGAGTTTTTTATTTAGATAGTTCTGCCTCTCTTATCAGTTGGGTTGGTTGAACCCCTTGCAAAATCCAGTTTTTTTTTTTTGCTTTTGTTGTCTGCTGCTTCAATCAGAATAAAATC... | GAGTACCTGGGATTACAGGCATACACCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATGTTGAGGCTGGTCTCGAACTCCTGATCTCAAGCGATCCGCACGCCTCAGCCTTCCAAAGTCCTGGGATTACAGGTGTGAGCCACCGCGCCCGGCCCACAGTACTGTTTTTCACAAAATTTCTATTCATGAGTTTTTTATTTAGATAGTTCTGCCTCTCTTATCAGTTGGGTTGGTTGAACCCCTTGCAAAATCCAGTTTTTTTTTTTTGCTTTTGTTGTCTGCTGCTTCAATCAGAATAAAATC... |
Task1_train_46564 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | AACAGACATTAAGAGCAGCCCAGGCAGCGCACCTTTCTCCCTGGATTCCATGAAAAGACACATTTTTCTATTCTGCTGTTCGTTTATTGCTTAGTTCTGTTCCAGCATCAGAATTGCTTTAGAGAAGAAAGTAAGTGTAGACAGAGAGTAATGGGTCAGATGACCAAGAAATAGAATAAATGTTTGGAGTCCACAGCATCATGGGAACTTCTTAGGAAGAGGGTATAGACCCCCAGTGCTGTCAGTCTCACCCATCCTCCTCTATACATGTGGGATGTTTCAGGACTTGGTGGCTTTCGAGGATGTGGCTGTGAACTTCA... | AACAGACATTAAGAGCAGCCCAGGCAGCGCACCTTTCTCCCTGGATTCCATGAAAAGACACATTTTTCTATTCTGCTGTTCGTTTATTGCTTAGTTCTGTTCCAGCATCAGAATTGCTTTAGAGAAGAAAGTAAGTGTAGACAGAGAGTAATGGGTCAGATGACCAAGAAATAGAATAAATGTTTGGAGTCCACAGCATCATGGGAACTTCTTAGGAAGAGGGTATAGACCCCCAGTGCTGTCAGTCTCACCCATCCTCCTCTATACATGTGGGATGTTTCAGGACTTGGTGGCTTTCGAGGATGTGGCTGTGAACTTCA... |
Task1_train_46565 | This variant is found on Chromosome 19. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTCACCCATCCTCCTCTATACATGTGGGATGTTTCAGGACTTGGTGGCTTTCGAGGATGTGGCTGTGAACTTCACCCAGGAGGAGTGGTCTTTGCTGGATCCTTCCCAGAAGAATCTCTACAGAGAAGTGATGCAGGAAACCTTGAGGAATCTGGCCTCCATAGGTAAGAATGACAGTATTACGTCCCCCAGTGAATGAGACAAGTGTTTCTAGCTCATTAATGCTATTCCTTGATTTGGAATATGGACAGGCAATACTTTGATGAATAAATGAGGTATGGCTCTAATGTCCCGTGAACATAGAATCTAATCATTTTTTC... | CTCACCCATCCTCCTCTATACATGTGGGATGTTTCAGGACTTGGTGGCTTTCGAGGATGTGGCTGTGAACTTCACCCAGGAGGAGTGGTCTTTGCTGGATCCTTCCCAGAAGAATCTCTACAGAGAAGTGATGCAGGAAACCTTGAGGAATCTGGCCTCCATAGGTAAGAATGACAGTATTACGTCCCCCAGTGAATGAGACAAGTGTTTCTAGCTCATTAATGCTATTCCTTGATTTGGAATATGGACAGGCAATACTTTGATGAATAAATGAGGTATGGCTCTAATGTCCCGTGAACATAGAATCTAATCATTTTTTC... |
Task1_train_46566 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GTGAACTTCACCCAGGAGGAGTGGTCTTTGCTGGATCCTTCCCAGAAGAATCTCTACAGAGAAGTGATGCAGGAAACCTTGAGGAATCTGGCCTCCATAGGTAAGAATGACAGTATTACGTCCCCCAGTGAATGAGACAAGTGTTTCTAGCTCATTAATGCTATTCCTTGATTTGGAATATGGACAGGCAATACTTTGATGAATAAATGAGGTATGGCTCTAATGTCCCGTGAACATAGAATCTAATCATTTTTTCATAATTTTATTTTAATTCAGGATTCTTTTTCTGATTCTGTATTTTAGGAGAAAAATGGAAAGAC... | GTGAACTTCACCCAGGAGGAGTGGTCTTTGCTGGATCCTTCCCAGAAGAATCTCTACAGAGAAGTGATGCAGGAAACCTTGAGGAATCTGGCCTCCATAGGTAAGAATGACAGTATTACGTCCCCCAGTGAATGAGACAAGTGTTTCTAGCTCATTAATGCTATTCCTTGATTTGGAATATGGACAGGCAATACTTTGATGAATAAATGAGGTATGGCTCTAATGTCCCGTGAACATAGAATCTAATCATTTTTTCATAATTTTATTTTAATTCAGGATTCTTTTTCTGATTCTGTATTTTAGGAGAAAAATGGAAAGAC... |
Task1_train_46567 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CACCTTCCAACAATTTAGACAGGGTAGAAAGCCTACACTTTCCTGGATAATGTTGAAAGTGCAAGTTCAGTGGGGAGGGATAGCATTAGGAGATATACCTAATGCTAAATGACGAGTTAATGGGTGCAGCACACCAAATGGGACATGTATACATATGTAACAAACCTGCACGTTGTGCACATGTACCCTAAAACTTAAAGTATATTAATAATAAAATAAAATAAAATAAAATAAAATGCAAGTGTAATCCTTGTTAATAAACATCAAATCACTTATAAACAAACCTTCAATAATGTGTTTCTCATTTTTCACAGAAGTCT... | CACCTTCCAACAATTTAGACAGGGTAGAAAGCCTACACTTTCCTGGATAATGTTGAAAGTGCAAGTTCAGTGGGGAGGGATAGCATTAGGAGATATACCTAATGCTAAATGACGAGTTAATGGGTGCAGCACACCAAATGGGACATGTATACATATGTAACAAACCTGCACGTTGTGCACATGTACCCTAAAACTTAAAGTATATTAATAATAAAATAAAATAAAATAAAATAAAATGCAAGTGTAATCCTTGTTAATAAACATCAAATCACTTATAAACAAACCTTCAATAATGTGTTTCTCATTTTTCACAGAAGTCT... |
Task1_train_46568 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ACAGCAGCTACTACAGATCCACACTACAAATAGACATTAGGGGCAGCCCAGAAAGCACATCTTTCTGTGTGGATTCACCGGAAACTCATACATTTTCCTATTCTGCTGTTCCTTTACCCCATGGTTAAATTGTAGCATCGGAATTGCTTTATGGAAGAAAGTGAGTATAGGCAGCGTAAGAGGTCTGATGACCAAGTCATGAAATCTTTGGAGTCCATAGCATCATGAGAACTTCTTGGGAATAGGGTATAGATGCCCAGTGATATCAGTCTCACCCATCCTTCTCTACACATATGGGATGTTTTAGGACTCAGTGGCCT... | ACAGCAGCTACTACAGATCCACACTACAAATAGACATTAGGGGCAGCCCAGAAAGCACATCTTTCTGTGTGGATTCACCGGAAACTCATACATTTTCCTATTCTGCTGTTCCTTTACCCCATGGTTAAATTGTAGCATCGGAATTGCTTTATGGAAGAAAGTGAGTATAGGCAGCGTAAGAGGTCTGATGACCAAGTCATGAAATCTTTGGAGTCCATAGCATCATGAGAACTTCTTGGGAATAGGGTATAGATGCCCAGTGATATCAGTCTCACCCATCCTTCTCTACACATATGGGATGTTTTAGGACTCAGTGGCCT... |
Task1_train_46569 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGTTCTGGATGACATGCTGAAGAAGAAAACTGGAGTAGAATCATGTGAAAGGAATGTGTGTGAGGTCAGCATGGGTCATTTATCCCTTAATAAGCACACCAGAGCTGACACTGGACACAAGCCATATGAGTATCAGGAATATGGACAGACGCCATATAAATGTACATACTGTAAGAAAGCCTTCAGCTGTCTCCCCTACTTTTGCAGACATGTAATTGCACACACTGGAGAAAAACCCTATGAATGTAAGGATTCTGCGAAGACATTTAGTTTTTCCATTTATTTTCATAGTCATAAAAGAGCTCACTCTGGAGGGAACC... | GGTTCTGGATGACATGCTGAAGAAGAAAACTGGAGTAGAATCATGTGAAAGGAATGTGTGTGAGGTCAGCATGGGTCATTTATCCCTTAATAAGCACACCAGAGCTGACACTGGACACAAGCCATATGAGTATCAGGAATATGGACAGACGCCATATAAATGTACATACTGTAAGAAAGCCTTCAGCTGTCTCCCCTACTTTTGCAGACATGTAATTGCACACACTGGAGAAAAACCCTATGAATGTAAGGATTCTGCGAAGACATTTAGTTTTTCCATTTATTTTCATAGTCATAAAAGAGCTCACTCTGGAGGGAACC... |
Task1_train_46570 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GAGGTCAGGAGTTTAAGACCAGTCTGACCAACATGGTGAAATCCTGTCTCTACTAAAAATATAAAAAATTAGCCTAGCGTGGTGGTGGGTGCCCGTAATCCCAGCTACCCGGGAAGCCAGGAGGTGGAAGTTGCACTGAGCCGAGCTCACACCAACACACTCCAGCCTGGGCAACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAGTTTAGAGGCTGGGCATGGTGGCTCATGCCTGTAAAGCCAGCTACTCGGGAGACTGAGGCAGAAGAATCGCTTGAACCCAGGAGGCAGA... | GAGGTCAGGAGTTTAAGACCAGTCTGACCAACATGGTGAAATCCTGTCTCTACTAAAAATATAAAAAATTAGCCTAGCGTGGTGGTGGGTGCCCGTAATCCCAGCTACCCGGGAAGCCAGGAGGTGGAAGTTGCACTGAGCCGAGCTCACACCAACACACTCCAGCCTGGGCAACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAGTTTAGAGGCTGGGCATGGTGGCTCATGCCTGTAAAGCCAGCTACTCGGGAGACTGAGGCAGAAGAATCGCTTGAACCCAGGAGGCAGA... |
Task1_train_46571 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGTAGATAGGCCTGCAATGGTTGGGTCTGTACTGAACACATATAGATTTTTTTTCTTATGATTCCCTAAACAATACAACTATGTACACAGCTTTTACAATGCATGAGATATTTTAATTAATCTAGACATTTATAGAGTATACAGGAGAATGTGGGTAGGTACATGCGAATATTCCATTTTATAAAAGAGCTGGCATCTGTGGATTTAGGTATACTCAGGGTGTACTGGAACCAATCTTCTTGCATATAGCAGGCAGCAACTCTATTTGAAAGAAATGGAAACTTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTAGCA... | TGTAGATAGGCCTGCAATGGTTGGGTCTGTACTGAACACATATAGATTTTTTTTCTTATGATTCCCTAAACAATACAACTATGTACACAGCTTTTACAATGCATGAGATATTTTAATTAATCTAGACATTTATAGAGTATACAGGAGAATGTGGGTAGGTACATGCGAATATTCCATTTTATAAAAGAGCTGGCATCTGTGGATTTAGGTATACTCAGGGTGTACTGGAACCAATCTTCTTGCATATAGCAGGCAGCAACTCTATTTGAAAGAAATGGAAACTTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTAGCA... |
Task1_train_46572 | Chromosome 19 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GCGAGTGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTTGAATCTGGGAGGTGGAGGTTGCAGTGAGTCGAGATCGCGCCACTGCACTCCAGACTGGGCAATAAGAACGAAACTCAGTCTCAAATGATAAATAAATAAATAAAAATAAAAATAAAATAAAGATTGCCATCCTCAAGTAAGATCCTTCAATGGAACAAAACCTCTGTGTCACCCAAGGGATAACATGCCAACAAACACTGCAAGGATATTTAAAGAAAAAGAACCAGCTTCCTACAACAATGTTTCTAACTAAATATCTGCAAATATG... | GCGAGTGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTTGAATCTGGGAGGTGGAGGTTGCAGTGAGTCGAGATCGCGCCACTGCACTCCAGACTGGGCAATAAGAACGAAACTCAGTCTCAAATGATAAATAAATAAATAAAAATAAAAATAAAATAAAGATTGCCATCCTCAAGTAAGATCCTTCAATGGAACAAAACCTCTGTGTCACCCAAGGGATAACATGCCAACAAACACTGCAAGGATATTTAAAGAAAAAGAACCAGCTTCCTACAACAATGTTTCTAACTAAATATCTGCAAATATG... |
Task1_train_46573 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GAAATAACAACATGCCTATAAACACTGCAAGATTTTTTTTTTAATGAAGCAAAGGAAAAGAAGAACTAGCTTCCTATAACTAAGCATCTGCAAAGAAGATGGAACATTCAATGGTTACAGATCTTCAGCCCTCAAGCCAAACAGATCCTAACATTAGTATTACATAGCCTCCTCAAATGAGTCCACATCTATAATCACAAGTTGGTTCTTCCAACATAGATGATAGTCCTGATGGCCTGTCAAGATTCAAGTTAACCTGATGTCTCACTACTTACCCACAATGCCATACATCTAGTCATCTCAACACATCAAAACACTGG... | GAAATAACAACATGCCTATAAACACTGCAAGATTTTTTTTTTAATGAAGCAAAGGAAAAGAAGAACTAGCTTCCTATAACTAAGCATCTGCAAAGAAGATGGAACATTCAATGGTTACAGATCTTCAGCCCTCAAGCCAAACAGATCCTAACATTAGTATTACATAGCCTCCTCAAATGAGTCCACATCTATAATCACAAGTTGGTTCTTCCAACATAGATGATAGTCCTGATGGCCTGTCAAGATTCAAGTTAACCTGATGTCTCACTACTTACCCACAATGCCATACATCTAGTCATCTCAACACATCAAAACACTGG... |
Task1_train_46574 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | TTACAGATCTTCAGCCCTCAAGCCAAACAGATCCTAACATTAGTATTACATAGCCTCCTCAAATGAGTCCACATCTATAATCACAAGTTGGTTCTTCCAACATAGATGATAGTCCTGATGGCCTGTCAAGATTCAAGTTAACCTGATGTCTCACTACTTACCCACAATGCCATACATCTAGTCATCTCAACACATCAAAACACTGGGCACCACAGAATCATCATCGTTATAATCACTATACTTGGGTTATCAAGAGAGAAGACCCAGGGTTTTGGTAAGTGTTAACACATTAAACAAAAGCAATATGTGAGAGTTGAAAC... | TTACAGATCTTCAGCCCTCAAGCCAAACAGATCCTAACATTAGTATTACATAGCCTCCTCAAATGAGTCCACATCTATAATCACAAGTTGGTTCTTCCAACATAGATGATAGTCCTGATGGCCTGTCAAGATTCAAGTTAACCTGATGTCTCACTACTTACCCACAATGCCATACATCTAGTCATCTCAACACATCAAAACACTGGGCACCACAGAATCATCATCGTTATAATCACTATACTTGGGTTATCAAGAGAGAAGACCCAGGGTTTTGGTAAGTGTTAACACATTAAACAAAAGCAATATGTGAGAGTTGAAAC... |
Task1_train_46575 | A variant affecting Chromosome 19 has been observed. Determine if it's benign or associated with disease. | Benign | ATCATCATCGTTATAATCACTATACTTGGGTTATCAAGAGAGAAGACCCAGGGTTTTGGTAAGTGTTAACACATTAAACAAAAGCAATATGTGAGAGTTGAAACAAAGAAACTTTAATGTTCTGGCTGACTATACTATGTTGATAGGCTGACAATTACTGCATCTATACTGAAAATACATAGACTCTTTTCCTTATCATGAGTCCCTAAACAATACAATAGAACAACTATTTGCATAGCTTTTACAATGCATGAGGTATTTTAAGTAATCTAGACATAATTGAGAGTATACAAGAGGATGTGGGTAAGTTACATACAAAT... | ATCATCATCGTTATAATCACTATACTTGGGTTATCAAGAGAGAAGACCCAGGGTTTTGGTAAGTGTTAACACATTAAACAAAAGCAATATGTGAGAGTTGAAACAAAGAAACTTTAATGTTCTGGCTGACTATACTATGTTGATAGGCTGACAATTACTGCATCTATACTGAAAATACATAGACTCTTTTCCTTATCATGAGTCCCTAAACAATACAATAGAACAACTATTTGCATAGCTTTTACAATGCATGAGGTATTTTAAGTAATCTAGACATAATTGAGAGTATACAAGAGGATGTGGGTAAGTTACATACAAAT... |
Task1_train_46576 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | CCTGTGTCCTGGCAAGAACATAAGAAGGCTTTCTTCTAGCAATGCTTCACTCCTGATGTGATGGAATACCTCAAAGAGAAGGGACTGCCACTCAAGGTCTTCCTCAGAATTGACAACACTCCAGGCCATCTCTCCAATCTCTGTTTTGCCTAAAAGAACATGCAAGTGATATTTCTGCCTCCTAAAACTACATCACTGCTGCGTCACTAGATCAAGGCATCAAGTGCATTCAAGTGACTTACATCCTTGGGTGAATTCATGGAGTCTTGATGCTAACCTTGAATGTACCACAGTGGTTTTATTGAAGAGCTTCACAATTA... | CCTGTGTCCTGGCAAGAACATAAGAAGGCTTTCTTCTAGCAATGCTTCACTCCTGATGTGATGGAATACCTCAAAGAGAAGGGACTGCCACTCAAGGTCTTCCTCAGAATTGACAACACTCCAGGCCATCTCTCCAATCTCTGTTTTGCCTAAAAGAACATGCAAGTGATATTTCTGCCTCCTAAAACTACATCACTGCTGCGTCACTAGATCAAGGCATCAAGTGCATTCAAGTGACTTACATCCTTGGGTGAATTCATGGAGTCTTGATGCTAACCTTGAATGTACCACAGTGGTTTTATTGAAGAGCTTCACAATTA... |
Task1_train_46577 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TACAAATACAATTGTGCTTATTGGGAAGGCTACAGATGCCCTAAAGCCCAGGACAGCCAATACATGTTACAAGCCATCATGGGGTAAGGGAGTCAATGATTTCAAGGACTTCCCTACTATTAATGCAGTTATTAAGAATATGTGAAATGTTGCAAAAAAAGTTGGTGGGGAACGCTGTCTGAAATGACTGAGGATGACGTTAAGGAACACACCGAAAAGCAAAGAGAAACCCTTACCAGCTAGGAACTTCAAAGTCTGCTGAAATCCACTACAGATGATGATGAGCTAGAAAACTTAGAAGACACAGAGCCATTGATTTG... | TACAAATACAATTGTGCTTATTGGGAAGGCTACAGATGCCCTAAAGCCCAGGACAGCCAATACATGTTACAAGCCATCATGGGGTAAGGGAGTCAATGATTTCAAGGACTTCCCTACTATTAATGCAGTTATTAAGAATATGTGAAATGTTGCAAAAAAAGTTGGTGGGGAACGCTGTCTGAAATGACTGAGGATGACGTTAAGGAACACACCGAAAAGCAAAGAGAAACCCTTACCAGCTAGGAACTTCAAAGTCTGCTGAAATCCACTACAGATGATGATGAGCTAGAAAACTTAGAAGACACAGAGCCATTGATTTG... |
Task1_train_46578 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | GCTTATTGGGAAGGCTACAGATGCCCTAAAGCCCAGGACAGCCAATACATGTTACAAGCCATCATGGGGTAAGGGAGTCAATGATTTCAAGGACTTCCCTACTATTAATGCAGTTATTAAGAATATGTGAAATGTTGCAAAAAAAGTTGGTGGGGAACGCTGTCTGAAATGACTGAGGATGACGTTAAGGAACACACCGAAAAGCAAAGAGAAACCCTTACCAGCTAGGAACTTCAAAGTCTGCTGAAATCCACTACAGATGATGATGAGCTAGAAAACTTAGAAGACACAGAGCCATTGATTTGGACACTTGAAAAGTT... | GCTTATTGGGAAGGCTACAGATGCCCTAAAGCCCAGGACAGCCAATACATGTTACAAGCCATCATGGGGTAAGGGAGTCAATGATTTCAAGGACTTCCCTACTATTAATGCAGTTATTAAGAATATGTGAAATGTTGCAAAAAAAGTTGGTGGGGAACGCTGTCTGAAATGACTGAGGATGACGTTAAGGAACACACCGAAAAGCAAAGAGAAACCCTTACCAGCTAGGAACTTCAAAGTCTGCTGAAATCCACTACAGATGATGATGAGCTAGAAAACTTAGAAGACACAGAGCCATTGATTTGGACACTTGAAAAGTT... |
Task1_train_46579 | Located on Chromosome 19, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ATCCACTACAGATGATGATGAGCTAGAAAACTTAGAAGACACAGAGCCATTGATTTGGACACTTGAAAAGTTTGCCACAGTTTTTCAGTAGGCAAAGGTGAAAAAGAGGTACGATCCTCAAAGATCCTATAATGGAACAAAGCTTTCAATCTACCTGAGAAACAACAACATGCCTATAAGCACCACAAGATTTTTTTTTTTAATGAAGCAAAGGAAAAGAAGAACTAGCTTCCTATAGCTAAGCATCTGCAAATAAGACGGAACATTCAATGGTTTTTTCAGTAGGCAAAGGTGAAAAAGAGGTACGATCCTCAAAGATC... | ATCCACTACAGATGATGATGAGCTAGAAAACTTAGAAGACACAGAGCCATTGATTTGGACACTTGAAAAGTTTGCCACAGTTTTTCAGTAGGCAAAGGTGAAAAAGAGGTACGATCCTCAAAGATCCTATAATGGAACAAAGCTTTCAATCTACCTGAGAAACAACAACATGCCTATAAGCACCACAAGATTTTTTTTTTTAATGAAGCAAAGGAAAAGAAGAACTAGCTTCCTATAGCTAAGCATCTGCAAATAAGACGGAACATTCAATGGTTTTTTCAGTAGGCAAAGGTGAAAAAGAGGTACGATCCTCAAAGATC... |
Task1_train_46580 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ACATAGACTCTTTTCCTTATCATGATTCCCTAAACAATACAATAGAACAACTATTTGCATAGCTTTTATAATGCATGAGGTATTTTAAGTAATCTAGACATAATTGAGACTATACAAGAGGATGTGGGTAAGTTACATACAAACATGTCATTTTATAAAAGGGACTGGACATGGCTCACGGAGTGCTGGAACCAATACCCAGCAGGTATCAAGGGATGACTGTACTGGAAAGAAACTGAAACTACTTAAGGCTTTACCAAGTGCTTACATTCACAGGGTCTATCTCCAATGTGTTTCGTACAAGTATCTGAAATGAAATA... | ACATAGACTCTTTTCCTTATCATGATTCCCTAAACAATACAATAGAACAACTATTTGCATAGCTTTTATAATGCATGAGGTATTTTAAGTAATCTAGACATAATTGAGACTATACAAGAGGATGTGGGTAAGTTACATACAAACATGTCATTTTATAAAAGGGACTGGACATGGCTCACGGAGTGCTGGAACCAATACCCAGCAGGTATCAAGGGATGACTGTACTGGAAAGAAACTGAAACTACTTAAGGCTTTACCAAGTGCTTACATTCACAGGGTCTATCTCCAATGTGTTTCGTACAAGTATCTGAAATGAAATA... |
Task1_train_46581 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GGATGTGGGTAAGTTACATACAAACATGTCATTTTATAAAAGGGACTGGACATGGCTCACGGAGTGCTGGAACCAATACCCAGCAGGTATCAAGGGATGACTGTACTGGAAAGAAACTGAAACTACTTAAGGCTTTACCAAGTGCTTACATTCACAGGGTCTATCTCCAATGTGTTTCGTACAAGTATCTGAAATGAAATAAAATTAATAAATGCTTTCCCACATTCCATACATTTAGAGAGAATGCTAGTGAGTCTTTTTATGTCTATGCAAGGAACTGAGAGAAGCAAATGCTTTCCCACATTCCTTACATTCATATG... | GGATGTGGGTAAGTTACATACAAACATGTCATTTTATAAAAGGGACTGGACATGGCTCACGGAGTGCTGGAACCAATACCCAGCAGGTATCAAGGGATGACTGTACTGGAAAGAAACTGAAACTACTTAAGGCTTTACCAAGTGCTTACATTCACAGGGTCTATCTCCAATGTGTTTCGTACAAGTATCTGAAATGAAATAAAATTAATAAATGCTTTCCCACATTCCATACATTTAGAGAGAATGCTAGTGAGTCTTTTTATGTCTATGCAAGGAACTGAGAGAAGCAAATGCTTTCCCACATTCCTTACATTCATATG... |
Task1_train_46582 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | CCTGGGAGGATGTGATTCACTTCTTTGAATAATGTGTGGGTTAGCAAGGATCTGAAACCCCTTATACAAGAGACAAAGACTATATAACTATGCTATAATAGTATAAAACTGTATTATGCATTATAGTATAATAGTAATTATATATTTTAGTTATACATAACATATACCAGTTATGTTTTATATATACAATTATATATCATTATGTAATATATTACATATTATATACACAAATATATCTATAAATGTACATGTAAACACACTATAGGCTATACTAGATAATGCTATACTACATAGTAGAAAATGGTCCAGAAATATCTCTT... | CCTGGGAGGATGTGATTCACTTCTTTGAATAATGTGTGGGTTAGCAAGGATCTGAAACCCCTTATACAAGAGACAAAGACTATATAACTATGCTATAATAGTATAAAACTGTATTATGCATTATAGTATAATAGTAATTATATATTTTAGTTATACATAACATATACCAGTTATGTTTTATATATACAATTATATATCATTATGTAATATATTACATATTATATACACAAATATATCTATAAATGTACATGTAAACACACTATAGGCTATACTAGATAATGCTATACTACATAGTAGAAAATGGTCCAGAAATATCTCTT... |
Task1_train_46583 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAATACCAGCATGCTGAACTTAAGGATTGGCTTATTGAAAATGTCAGGCAAGTTCCTGGCCAGAAAAGCCACATTGAAGCTCCCATGAGCCAAGGAACCCAGGATTCACAGAACAGTCAATAACCAAATCGTGGTTTTATGTGAAGATGACATATTCAGGCTCAGATTATGTATCCACATGCATGAAGGCTGTAGTCATTCCCCATGAAATTCCTCCCACTTCAGCATCCCAAAGTGTTGGGATTACAGAGTCACTTAGATCAGGGAACTGATAGCAATGACAAAATTAGGTACCCCCGACACTAACCCGTGCCTTATCC... | AAATACCAGCATGCTGAACTTAAGGATTGGCTTATTGAAAATGTCAGGCAAGTTCCTGGCCAGAAAAGCCACATTGAAGCTCCCATGAGCCAAGGAACCCAGGATTCACAGAACAGTCAATAACCAAATCGTGGTTTTATGTGAAGATGACATATTCAGGCTCAGATTATGTATCCACATGCATGAAGGCTGTAGTCATTCCCCATGAAATTCCTCCCACTTCAGCATCCCAAAGTGTTGGGATTACAGAGTCACTTAGATCAGGGAACTGATAGCAATGACAAAATTAGGTACCCCCGACACTAACCCGTGCCTTATCC... |
Task1_train_46584 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CCCGCCTCAGCCCACCCACCCCCCGACCTCCCCCACCGCCCCCACCACGCAGTAGCTGGGACTACGGGTGTGCGCCACCAAGCCCTGCCTTGGGGTTCCTTTTCTAAAGTGCCAAATGTGTGGAGGTGGGGAAAAGAAAGGTGGACGCCTCAACGCTGTTATGGTCAAAGATTAAAATGCAACCACACTTTTTATTACACATGATGGGGTAACCGTCTGTTTATAAACAAGGGTCACTATTCCACGAGAGGCCTTACAACATTATGCCAAGCCCCTGGTACCTGGAGGACATCAGACCCTCCTGTTCCTGTGCGGCCTTG... | CCCGCCTCAGCCCACCCACCCCCCGACCTCCCCCACCGCCCCCACCACGCAGTAGCTGGGACTACGGGTGTGCGCCACCAAGCCCTGCCTTGGGGTTCCTTTTCTAAAGTGCCAAATGTGTGGAGGTGGGGAAAAGAAAGGTGGACGCCTCAACGCTGTTATGGTCAAAGATTAAAATGCAACCACACTTTTTATTACACATGATGGGGTAACCGTCTGTTTATAAACAAGGGTCACTATTCCACGAGAGGCCTTACAACATTATGCCAAGCCCCTGGTACCTGGAGGACATCAGACCCTCCTGTTCCTGTGCGGCCTTG... |
Task1_train_46585 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | CCGCCTCAGCCCACCCACCCCCCGACCTCCCCCACCGCCCCCACCACGCAGTAGCTGGGACTACGGGTGTGCGCCACCAAGCCCTGCCTTGGGGTTCCTTTTCTAAAGTGCCAAATGTGTGGAGGTGGGGAAAAGAAAGGTGGACGCCTCAACGCTGTTATGGTCAAAGATTAAAATGCAACCACACTTTTTATTACACATGATGGGGTAACCGTCTGTTTATAAACAAGGGTCACTATTCCACGAGAGGCCTTACAACATTATGCCAAGCCCCTGGTACCTGGAGGACATCAGACCCTCCTGTTCCTGTGCGGCCTTGA... | CCGCCTCAGCCCACCCACCCCCCGACCTCCCCCACCGCCCCCACCACGCAGTAGCTGGGACTACGGGTGTGCGCCACCAAGCCCTGCCTTGGGGTTCCTTTTCTAAAGTGCCAAATGTGTGGAGGTGGGGAAAAGAAAGGTGGACGCCTCAACGCTGTTATGGTCAAAGATTAAAATGCAACCACACTTTTTATTACACATGATGGGGTAACCGTCTGTTTATAAACAAGGGTCACTATTCCACGAGAGGCCTTACAACATTATGCCAAGCCCCTGGTACCTGGAGGACATCAGACCCTCCTGTTCCTGTGCGGCCTTGA... |
Task1_train_46586 | Here is a mutation located on Chromosome 19. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGACAGGGTTTCACTCTGTTGCCAGGATGGAGTACAGTGGGACAATCATTACTCACTGCAACCTCGAACTCCCCAGCTCAAACAAACCTCCCATCTGGGCCTCCCAATTAGCTGGGACAACTCCTGGGCTCAAGTGATCCTCCCGCTTCAGCCTCCCAAAGAGCTAGGAGTAGACACATGAGCAACAATGACTGGCAAAAGCCAAAGTCTTCCTGTTGGTCCTCAAGGCCCTCAAGGTCTGACCTGTCACCCGTTCACCCTGCTTCAGCCACACTGAGCTCCTTGTGGCTCCTGGAATTCTGCACACTCTCCTGCTCGAA... | AGACAGGGTTTCACTCTGTTGCCAGGATGGAGTACAGTGGGACAATCATTACTCACTGCAACCTCGAACTCCCCAGCTCAAACAAACCTCCCATCTGGGCCTCCCAATTAGCTGGGACAACTCCTGGGCTCAAGTGATCCTCCCGCTTCAGCCTCCCAAAGAGCTAGGAGTAGACACATGAGCAACAATGACTGGCAAAAGCCAAAGTCTTCCTGTTGGTCCTCAAGGCCCTCAAGGTCTGACCTGTCACCCGTTCACCCTGCTTCAGCCACACTGAGCTCCTTGTGGCTCCTGGAATTCTGCACACTCTCCTGCTCGAA... |
Task1_train_46587 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | AGACCATGGAGTCGGGGGAGTGAAGGAGGAAGTAGGGGAAGAAACCCTTGAGGCAGGTTCTCGGGGGAGGAAGAGGTTTGGGGGAGGACGTTTTCTGGAATGAAGGAGATGTCCATAAACAGCAATAAATTTTCCTGGGGAAGCGGGGTATTAAAATGGAGGACCAGCCAGGCACGGTGGCTCATGCCTATAATCCAGCAGGCGGAGTTTGAAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAGGGAGGACCACTCACAGGAGGCATATGTTCCCA... | AGACCATGGAGTCGGGGGAGTGAAGGAGGAAGTAGGGGAAGAAACCCTTGAGGCAGGTTCTCGGGGGAGGAAGAGGTTTGGGGGAGGACGTTTTCTGGAATGAAGGAGATGTCCATAAACAGCAATAAATTTTCCTGGGGAAGCGGGGTATTAAAATGGAGGACCAGCCAGGCACGGTGGCTCATGCCTATAATCCAGCAGGCGGAGTTTGAAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAGGGAGGACCACTCACAGGAGGCATATGTTCCCA... |
Task1_train_46588 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ATGTGAGGAAAAGGATGTTTGTTTTGCACGAGCTGTGTCCCCCAATGTACACAGTAGGTGCTCAATAAACTTTTTTTTTTTTTTTTTTTTTTGAGACTGAGTCTGACTCTGTCGCCCAAGCTGGAGTGCAGTGGCACGATCTCAGCTGGCTGCAAACTCCGCCTCCCAGGTTCCAGCGATTCTCCTGCCTCAGCCTGCCGAGTAGCTGGTCTTACAGATGAGTGCCATCACGCCCACCTAATTTGTAGTATTTTTAGTAGAGACAAGGTTTCACCATGTTGGCCAGGCTGGTCTCCAACTCCTGTCTTCAAGTGATCCGC... | ATGTGAGGAAAAGGATGTTTGTTTTGCACGAGCTGTGTCCCCCAATGTACACAGTAGGTGCTCAATAAACTTTTTTTTTTTTTTTTTTTTTTGAGACTGAGTCTGACTCTGTCGCCCAAGCTGGAGTGCAGTGGCACGATCTCAGCTGGCTGCAAACTCCGCCTCCCAGGTTCCAGCGATTCTCCTGCCTCAGCCTGCCGAGTAGCTGGTCTTACAGATGAGTGCCATCACGCCCACCTAATTTGTAGTATTTTTAGTAGAGACAAGGTTTCACCATGTTGGCCAGGCTGGTCTCCAACTCCTGTCTTCAAGTGATCCGC... |
Task1_train_46589 | A mutation on Chromosome 19 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TCACAGTGTGGTTGGTGCGGTAATACCGGCCCTGCAGGCAAGAGGGGAGTCCTGAAGCCAGAGGATCCTGGGCCATCCCTGTGTATAGCTGTGTTTTGATGTATATGGGGTCAAGGATGTTGGGTGCACAGGCATGGGTGGGGGTATGGCACTTGGGAGCGTGGGGACACAGATAAAAGTAGCCACCAGTTGTTGAGCAGTTCTCTTGGACCCACTACCTAGAAGAGGGCATCCAGTCACCATGCCATGCTATCTCTTGCCCAGCCTATGCTATCTCTTCTAATGAGGAATGCACATAAATCCAGGAGGGGGACATTGTG... | TCACAGTGTGGTTGGTGCGGTAATACCGGCCCTGCAGGCAAGAGGGGAGTCCTGAAGCCAGAGGATCCTGGGCCATCCCTGTGTATAGCTGTGTTTTGATGTATATGGGGTCAAGGATGTTGGGTGCACAGGCATGGGTGGGGGTATGGCACTTGGGAGCGTGGGGACACAGATAAAAGTAGCCACCAGTTGTTGAGCAGTTCTCTTGGACCCACTACCTAGAAGAGGGCATCCAGTCACCATGCCATGCTATCTCTTGCCCAGCCTATGCTATCTCTTCTAATGAGGAATGCACATAAATCCAGGAGGGGGACATTGTG... |
Task1_train_46590 | Mutation context: Chromosome 19. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TGGAGTGCAGTGGCATGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTGCCTCGGCCTCCCGAGTCGCTGGGACTACAGGTGCCCACGCACCACGCCTGGCTAATTATTTGGTATTTTTTGTAGAGTCAGGGTCTCCCATGTTGCCCAGGCTGGTCTCGAACTCCTGGGTTCAAGCAATCCTCCTGCCTCGGCCTCCCAAAGTGTTAGGATTACAGGCCTGAGCAACTAACTGCACCCTGGCCCAATAACATTTCTAAGTCAAGTTCTGCAAGAACTCAGCACCAGTGGTGGTTTGAAGCCAC... | TGGAGTGCAGTGGCATGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTGCCTCGGCCTCCCGAGTCGCTGGGACTACAGGTGCCCACGCACCACGCCTGGCTAATTATTTGGTATTTTTTGTAGAGTCAGGGTCTCCCATGTTGCCCAGGCTGGTCTCGAACTCCTGGGTTCAAGCAATCCTCCTGCCTCGGCCTCCCAAAGTGTTAGGATTACAGGCCTGAGCAACTAACTGCACCCTGGCCCAATAACATTTCTAAGTCAAGTTCTGCAAGAACTCAGCACCAGTGGTGGTTTGAAGCCAC... |
Task1_train_46591 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AGGTGCCCACGCACCACGCCTGGCTAATTATTTGGTATTTTTTGTAGAGTCAGGGTCTCCCATGTTGCCCAGGCTGGTCTCGAACTCCTGGGTTCAAGCAATCCTCCTGCCTCGGCCTCCCAAAGTGTTAGGATTACAGGCCTGAGCAACTAACTGCACCCTGGCCCAATAACATTTCTAAGTCAAGTTCTGCAAGAACTCAGCACCAGTGGTGGTTTGAAGCCACATGACAAGTGATTAAGAGTGTGGCCTCTACTTTGTGACCTGGCAAACCATATCACCTCCCTCAGTTCATTCATCAGCAAATTGGGCAGAAAACA... | AGGTGCCCACGCACCACGCCTGGCTAATTATTTGGTATTTTTTGTAGAGTCAGGGTCTCCCATGTTGCCCAGGCTGGTCTCGAACTCCTGGGTTCAAGCAATCCTCCTGCCTCGGCCTCCCAAAGTGTTAGGATTACAGGCCTGAGCAACTAACTGCACCCTGGCCCAATAACATTTCTAAGTCAAGTTCTGCAAGAACTCAGCACCAGTGGTGGTTTGAAGCCACATGACAAGTGATTAAGAGTGTGGCCTCTACTTTGTGACCTGGCAAACCATATCACCTCCCTCAGTTCATTCATCAGCAAATTGGGCAGAAAACA... |
Task1_train_46592 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAGCCTGAGCTTAATGCATGTCCACATTAATGCATAATGCATCTCCTTCATCCTCATCCTAATCACCCACTGGACAGAAGTAGAAACTGAGGCACAGAGAAGTCACACATCTCACTCAAAGTCACACCAAGGTTAGAAAAGTCAGATTCAAATCTATGCGGTCCTGTACCAAAACCTGGGGCCTTAACCAAGATGCCCTACTCAGGCCTCATACCTCCTATCCCCACCTGACTCCTCACCTCATGGGTACTATTTCGCTTAGTGCCTAAGGTCTTGATCAGAACCTGGTT... | GAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAGCCTGAGCTTAATGCATGTCCACATTAATGCATAATGCATCTCCTTCATCCTCATCCTAATCACCCACTGGACAGAAGTAGAAACTGAGGCACAGAGAAGTCACACATCTCACTCAAAGTCACACCAAGGTTAGAAAAGTCAGATTCAAATCTATGCGGTCCTGTACCAAAACCTGGGGCCTTAACCAAGATGCCCTACTCAGGCCTCATACCTCCTATCCCCACCTGACTCCTCACCTCATGGGTACTATTTCGCTTAGTGCCTAAGGTCTTGATCAGAACCTGGTT... |
Task1_train_46593 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCATGTTACCAATCCCGCCTAATTTTTCTATTTTTCGTAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGCTCTCGAACTCCTGACCTCAAGGGATCAGCTGCTTCAGCCTCCCAAAGTGCTGGGATTAGCGGCGTGAGCCACTGCGCCTGGCTGTGCGTAATTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGACTCTTGCCCTGTCGCCTAGGCTGGAGCGCAGTGGCACAATCTCAGCTAACTGCAACCTCCGCCTCC... | CCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCATGTTACCAATCCCGCCTAATTTTTCTATTTTTCGTAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGCTCTCGAACTCCTGACCTCAAGGGATCAGCTGCTTCAGCCTCCCAAAGTGCTGGGATTAGCGGCGTGAGCCACTGCGCCTGGCTGTGCGTAATTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGACTCTTGCCCTGTCGCCTAGGCTGGAGCGCAGTGGCACAATCTCAGCTAACTGCAACCTCCGCCTCC... |
Task1_train_46594 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | GGTGACAGCTGGGAGCAGCTGAGGCTGCAGCATCTAAAGGGTAACCTCAGGCGGCGGGGATGACGATGCCCAAAGGCTCCCCGTTGCCCTACTTCTCCTGCTGGCTGCAAAGGGACCTTCCTCGGCGGGCTGCAAATCTCCACCCAGCTCCGCACTGGAGGCGTCCCCTTGGGCTGGTTACTTTTCTCTAAGGCTCGGTTTACTCTTGGATATATTGAAATAGATACTGCTTTAAAGCAGCTCCCAGGGGAAGAGAGGGTGTGGGCAGGACACTGAAGCTGTCACTCGGGGATAGGTGCCAGGAAGGGCAGAGACAGAGA... | GGTGACAGCTGGGAGCAGCTGAGGCTGCAGCATCTAAAGGGTAACCTCAGGCGGCGGGGATGACGATGCCCAAAGGCTCCCCGTTGCCCTACTTCTCCTGCTGGCTGCAAAGGGACCTTCCTCGGCGGGCTGCAAATCTCCACCCAGCTCCGCACTGGAGGCGTCCCCTTGGGCTGGTTACTTTTCTCTAAGGCTCGGTTTACTCTTGGATATATTGAAATAGATACTGCTTTAAAGCAGCTCCCAGGGGAAGAGAGGGTGTGGGCAGGACACTGAAGCTGTCACTCGGGGATAGGTGCCAGGAAGGGCAGAGACAGAGA... |
Task1_train_46595 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GCCTCGGGCATATTCATTGCTACTGTTGATTTCGTGCTCCTGTTTCTGCCCTAAATGTGTGCCACACTGACGACCACAGTGTAGCCCCTAGTCCCGTCTCCATCTAATCTCTCCCTCATCCTAAAGGCTCAGTCTCCAGAACAAATCCTACATTGTCTACCTGTCACCTCTGTCCTAGCCCAGGACACCCCCCACTCCCTGGACACCTGCTGAGTGTCGTCTCTCGTCCCTCACCCTCCTATCCCCTCCAATCTGTTCCCCAAGCAGCAACAGAAGGTAGTCTTTTTGAAATGCACATCTCGACATTTAGTTTTCCGATC... | GCCTCGGGCATATTCATTGCTACTGTTGATTTCGTGCTCCTGTTTCTGCCCTAAATGTGTGCCACACTGACGACCACAGTGTAGCCCCTAGTCCCGTCTCCATCTAATCTCTCCCTCATCCTAAAGGCTCAGTCTCCAGAACAAATCCTACATTGTCTACCTGTCACCTCTGTCCTAGCCCAGGACACCCCCCACTCCCTGGACACCTGCTGAGTGTCGTCTCTCGTCCCTCACCCTCCTATCCCCTCCAATCTGTTCCCCAAGCAGCAACAGAAGGTAGTCTTTTTGAAATGCACATCTCGACATTTAGTTTTCCGATC... |
Task1_train_46596 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | CGGCTGCCTGGCTAATTTTTGTACTTTTGGTAGAGACGGAGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTCAAGTGAATGAACCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGACACCGTGCCTGGCCCACATTCCCATTTTAAAGATGAAGAAACTGAGGCTCAATCTGGGCAACGTGTGAAACCGAAGTTACAGCATAAGTAAGTGGTAGAGCTGGGTTGTGAACACAGGTGGACGCTACACGGGGTCATTCCCACCAAATTCTGTAGTCTGTACATGTATAATATGGGGTCTT... | CGGCTGCCTGGCTAATTTTTGTACTTTTGGTAGAGACGGAGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTCAAGTGAATGAACCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGACACCGTGCCTGGCCCACATTCCCATTTTAAAGATGAAGAAACTGAGGCTCAATCTGGGCAACGTGTGAAACCGAAGTTACAGCATAAGTAAGTGGTAGAGCTGGGTTGTGAACACAGGTGGACGCTACACGGGGTCATTCCCACCAAATTCTGTAGTCTGTACATGTATAATATGGGGTCTT... |
Task1_train_46597 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CGACTCTATGGTCCCCACCCAGAAGCTGACTCAGCAACTGTTTTCCACAGCTCCAGGATTGCAGCAAGGCACCCATTCCCTAGCCCTCCTGCCCACCAAACTGTTCTTGAATAACCCTAGCCTCTGAATTTTCAGGGAGGCTGATTCAAGTAATAAAACTCCCATCTCCCATTTAGCTGGATGTATGTGGATTAAACTCTCTCTATTGCAATCCCTCTGTCTCGATAAATTGGCTCTATCTGGACAGTGGGCAAGATGAACCCCCTGGGCAGTCATAGGCTGTGAACTCTTAAATCCAGGGAGATGTTTGCTGTCAATGT... | CGACTCTATGGTCCCCACCCAGAAGCTGACTCAGCAACTGTTTTCCACAGCTCCAGGATTGCAGCAAGGCACCCATTCCCTAGCCCTCCTGCCCACCAAACTGTTCTTGAATAACCCTAGCCTCTGAATTTTCAGGGAGGCTGATTCAAGTAATAAAACTCCCATCTCCCATTTAGCTGGATGTATGTGGATTAAACTCTCTCTATTGCAATCCCTCTGTCTCGATAAATTGGCTCTATCTGGACAGTGGGCAAGATGAACCCCCTGGGCAGTCATAGGCTGTGAACTCTTAAATCCAGGGAGATGTTTGCTGTCAATGT... |
Task1_train_46598 | Located on Chromosome 19, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GTAGCTGGGATTACAGGTGCCTGCTACCACGCCACGCTAATTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCATGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTTGCTGGGATTACAGGCACCCACAAGCAGGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCCCCATGTTGGCCAGGCTGGTCCTGACCTCAGGTGACCCACCCTCCTTGGCCTCCCAAAGTGCTGGGATGACAGGCATG... | GTAGCTGGGATTACAGGTGCCTGCTACCACGCCACGCTAATTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCATGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTTGCTGGGATTACAGGCACCCACAAGCAGGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCCCCATGTTGGCCAGGCTGGTCCTGACCTCAGGTGACCCACCCTCCTTGGCCTCCCAAAGTGCTGGGATGACAGGCATG... |
Task1_train_46599 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ATGCCAGGATCCCCAGTCCTTGTTACCCTCATGTGCCACTCCCAGGGCTGCCCCCGAGATGGTTTCTCTGCTGAAGAGGAATAACTGTGGGAAAGCCCTGGACATCGCCCGCCAGGCCCGAGACATGCTGGGGGGGAATGGGATTTCTGACGAGTATCACGTGATCCGGCACGCCATGAACCTGGAGGCCGTGAACACCTACGAAGGTAGGAGCTGGACCTCAGAGGGCTCACTGAGGCCTCAGTGTCTGGGGAGGGGGTACAGGGAGGTGGGACGGGGACAGGTCTGAGTCCAACTCCACCTATCACTAAGTGACAGTG... | ATGCCAGGATCCCCAGTCCTTGTTACCCTCATGTGCCACTCCCAGGGCTGCCCCCGAGATGGTTTCTCTGCTGAAGAGGAATAACTGTGGGAAAGCCCTGGACATCGCCCGCCAGGCCCGAGACATGCTGGGGGGGAATGGGATTTCTGACGAGTATCACGTGATCCGGCACGCCATGAACCTGGAGGCCGTGAACACCTACGAAGGTAGGAGCTGGACCTCAGAGGGCTCACTGAGGCCTCAGTGTCTGGGGAGGGGGTACAGGGAGGTGGGACGGGGACAGGTCTGAGTCCAACTCCACCTATCACTAAGTGACAGTG... |
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