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_46800 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GAGGCAGAGGTTGCAGTGAGCCGAAATTGCGCCATTGCACTCCAGCCTGGACAAGAGCAAAACTCTGTCTCAAAAAAAAAAAAAAAAAAAGATTAAAGGCGCACACTGTCCACAGGCAAGAGGATTAAATTAGCATTGCATTTCTTTGTTTTTAAAAGAAAAATCTTATTAGATTCTTATACAAAGTGTGGCAAATATAAAACTTGCTTGAAAATATGGAAATTAAATTTTTAAGAGAGTTAATAGTAAACGAATTTAATTTTCTTTTTTTATTTTTACTTTTTATTTTTTAGAGACAGAGTCTTGCTCTGTCTCCCAGG... | GAGGCAGAGGTTGCAGTGAGCCGAAATTGCGCCATTGCACTCCAGCCTGGACAAGAGCAAAACTCTGTCTCAAAAAAAAAAAAAAAAAAAGATTAAAGGCGCACACTGTCCACAGGCAAGAGGATTAAATTAGCATTGCATTTCTTTGTTTTTAAAAGAAAAATCTTATTAGATTCTTATACAAAGTGTGGCAAATATAAAACTTGCTTGAAAATATGGAAATTAAATTTTTAAGAGAGTTAATAGTAAACGAATTTAATTTTCTTTTTTTATTTTTACTTTTTATTTTTTAGAGACAGAGTCTTGCTCTGTCTCCCAGG... |
Task1_train_46801 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | TGAAAATTTTTTGATATATTGGGTTAATTAAATTGTTACAATCAATTCAACCTGTTACTTTTTTTTTTTAAGTTTGGTTACTAGAAAATTTAAAATTTACATATGGCTCACATTTTATTTCAGAAAATTACCTCCGTTCTAAAATTTCAGACGGCCTGCTGAAAGACCAGAAGCCGGGAAGGTCATAAAATCCGAAATTTTAAAATAATTGTTATTATATTCTTTTCATTTGTGAATAGGCATACAGTATGTTATTTATAAATGCATGTGACTTTACACACAAGGTTAAATACAAATTCCCTCTGGGGTGGGCCTGGCTA... | TGAAAATTTTTTGATATATTGGGTTAATTAAATTGTTACAATCAATTCAACCTGTTACTTTTTTTTTTTAAGTTTGGTTACTAGAAAATTTAAAATTTACATATGGCTCACATTTTATTTCAGAAAATTACCTCCGTTCTAAAATTTCAGACGGCCTGCTGAAAGACCAGAAGCCGGGAAGGTCATAAAATCCGAAATTTTAAAATAATTGTTATTATATTCTTTTCATTTGTGAATAGGCATACAGTATGTTATTTATAAATGCATGTGACTTTACACACAAGGTTAAATACAAATTCCCTCTGGGGTGGGCCTGGCTA... |
Task1_train_46802 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | GTTGAACAAAGTTTAAGTAACTGCTTCAGGGTTTTCTCTAGTACAAAATGTGTACAATAAGATCTGTGATACAAATAAAGGTATTACAATCCTCTTTTATTTGTAATGTTTGTCTTCAAAATAAATACTTTAAAAGCTTATATTTTCTGAAATACTTTTTGACAGTAATTAAATTTATAATACTTTTTTTAAGTACTCTCTGATGTTGAGTAAGATGTGAGCAGACATTAATGGCTTTTTCACAGTCTTTATATTGGTACAATTTTTCTCAAGTATAAATGCTTTCCTGGCAATAAGGTGTGAGTATTCATTAAAAATTT... | GTTGAACAAAGTTTAAGTAACTGCTTCAGGGTTTTCTCTAGTACAAAATGTGTACAATAAGATCTGTGATACAAATAAAGGTATTACAATCCTCTTTTATTTGTAATGTTTGTCTTCAAAATAAATACTTTAAAAGCTTATATTTTCTGAAATACTTTTTGACAGTAATTAAATTTATAATACTTTTTTTAAGTACTCTCTGATGTTGAGTAAGATGTGAGCAGACATTAATGGCTTTTTCACAGTCTTTATATTGGTACAATTTTTCTCAAGTATAAATGCTTTCCTGGCAATAAGGTGTGAGTATTCATTAAAAATTT... |
Task1_train_46803 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TACAATAAGATCTGTGATACAAATAAAGGTATTACAATCCTCTTTTATTTGTAATGTTTGTCTTCAAAATAAATACTTTAAAAGCTTATATTTTCTGAAATACTTTTTGACAGTAATTAAATTTATAATACTTTTTTTAAGTACTCTCTGATGTTGAGTAAGATGTGAGCAGACATTAATGGCTTTTTCACAGTCTTTATATTGGTACAATTTTTCTCAAGTATAAATGCTTTCCTGGCAATAAGGTGTGAGTATTCATTAAAAATTTTGCCACATTCTTCACACTTGTAAGAGTTTTTCTAGTAAGAATTATCTTACCT... | TACAATAAGATCTGTGATACAAATAAAGGTATTACAATCCTCTTTTATTTGTAATGTTTGTCTTCAAAATAAATACTTTAAAAGCTTATATTTTCTGAAATACTTTTTGACAGTAATTAAATTTATAATACTTTTTTTAAGTACTCTCTGATGTTGAGTAAGATGTGAGCAGACATTAATGGCTTTTTCACAGTCTTTATATTGGTACAATTTTTCTCAAGTATAAATGCTTTCCTGGCAATAAGGTGTGAGTATTCATTAAAAATTTTGCCACATTCTTCACACTTGTAAGAGTTTTTCTAGTAAGAATTATCTTACCT... |
Task1_train_46804 | 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 | CAAAAAATGAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGCAGAGCTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTTGTCTCAAAAAAAAAATTAACTTATTAAATAATTTAATCAAAAAGTGGTTCTAGAATTGTAGAGCACCAAGCTGTGGTTTTTAGTTTGTGGTCTATGGGAGAGGCTTGAAAGAAAGTCTTTTGTAAAATGCATGATGAAGAAAACCAAATTTAGTAATTGGTTAGGTAC... | CAAAAAATGAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGCAGAGCTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTTGTCTCAAAAAAAAAATTAACTTATTAAATAATTTAATCAAAAAGTGGTTCTAGAATTGTAGAGCACCAAGCTGTGGTTTTTAGTTTGTGGTCTATGGGAGAGGCTTGAAAGAAAGTCTTTTGTAAAATGCATGATGAAGAAAACCAAATTTAGTAATTGGTTAGGTAC... |
Task1_train_46805 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGTGTCAAACTCGTGACCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTGTGGGATTACAGGTGTGAGCTACTGCACCTGGCCACATTGTAATCTTTTATAAAAATTTGAACATTAAAAAGTTACCTGTCACAATCTTTGTAATATGGCTTTCTCCTGGCATACTTTGAACAATTGTCTGAGTTAGAGATTCTGAGAGTCTCTCAAACATGTTCTTTGAGTGTGTCTTGTCTGAAATTTTGTGTTTATTTTTTAGTTAAAGGAAATTATTCATCTTTTTTTTTGGAGATGGAGTCTCAGTCTGTCATGAGGCAGGAGT... | GGTGTCAAACTCGTGACCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTGTGGGATTACAGGTGTGAGCTACTGCACCTGGCCACATTGTAATCTTTTATAAAAATTTGAACATTAAAAAGTTACCTGTCACAATCTTTGTAATATGGCTTTCTCCTGGCATACTTTGAACAATTGTCTGAGTTAGAGATTCTGAGAGTCTCTCAAACATGTTCTTTGAGTGTGTCTTGTCTGAAATTTTGTGTTTATTTTTTAGTTAAAGGAAATTATTCATCTTTTTTTTTGGAGATGGAGTCTCAGTCTGTCATGAGGCAGGAGT... |
Task1_train_46806 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGGAGTCTCAGTCTGTCATGAGGCAGGAGTGCAGTGGCACGATCTCAGTTCACTGCAACCTCCGCCTCCCAGATTCAAGCAATTCTCCTGCCACAGCCTCCTGAATAGCTAGGACTACAGATAAGTGCCACCATGCCCAGCTAAGTTTTGTATTTTCAGTAGAGATGGGGTTTCACCATTTTGGCCAGCATAGTCTTAATCTCTTGAACTCGTGATCCACCCGCCTAGGCCTCGCAAAGTGCTGGGATTATGTGCATGAGCCACTGCACCTGGCCCCTAGTCATCTTTTTTCTTAATACTCAGTAATCACTTGCTACACC... | TGGAGTCTCAGTCTGTCATGAGGCAGGAGTGCAGTGGCACGATCTCAGTTCACTGCAACCTCCGCCTCCCAGATTCAAGCAATTCTCCTGCCACAGCCTCCTGAATAGCTAGGACTACAGATAAGTGCCACCATGCCCAGCTAAGTTTTGTATTTTCAGTAGAGATGGGGTTTCACCATTTTGGCCAGCATAGTCTTAATCTCTTGAACTCGTGATCCACCCGCCTAGGCCTCGCAAAGTGCTGGGATTATGTGCATGAGCCACTGCACCTGGCCCCTAGTCATCTTTTTTCTTAATACTCAGTAATCACTTGCTACACC... |
Task1_train_46807 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTTACTTCCAAAGGCACTGTGTTTTATTGGGGAACAGGAAGAGCTGTGTTGGGTAACTGTAACAGAAATGTTTTTCATTCTATGTGACTCTTTGCATTGTACTCACCTGGGGCGTTGTACACATATAACTTATTGATAAATTATCCACTAATATATTTTGGTTAGTATGTCTTTGTTATATTTATATGTTTATGAAGAAATTAGAATCTGGTATTTTGCTATGCTGTGTTGCTTACGTAGTTTTTATAACTTTAGAGGTTTTGTTTGTGACGTATATATATCTGAGTCTAGTAAGTGAAGTAATTTGTTGTTTTAATTTT... | TTTACTTCCAAAGGCACTGTGTTTTATTGGGGAACAGGAAGAGCTGTGTTGGGTAACTGTAACAGAAATGTTTTTCATTCTATGTGACTCTTTGCATTGTACTCACCTGGGGCGTTGTACACATATAACTTATTGATAAATTATCCACTAATATATTTTGGTTAGTATGTCTTTGTTATATTTATATGTTTATGAAGAAATTAGAATCTGGTATTTTGCTATGCTGTGTTGCTTACGTAGTTTTTATAACTTTAGAGGTTTTGTTTGTGACGTATATATATCTGAGTCTAGTAAGTGAAGTAATTTGTTGTTTTAATTTT... |
Task1_train_46808 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TTCTTTAACTTATTTGCAGTCAAAGCCACTAGCAAAAGAGATTACTAGAGATGTTAATCCATTATGTTACCAAATAGTATACTGTTACCATGTTTTACGTACACCCTTGAGTAAGGTGGAATAGGTTAATGTCTGTGGCATAATAACACTTCACTGAATGCACAATAGTATTTAACATGTTAAAAAGGTTGAATATATTAACATCACATATAATCTGAAATTTAAAAAATATACTGCATTTTATATAAAAGTATTAGTAAAATATACTAATTTTAATTTACTTATAAATGAAATTAAGTTTTCTCATAATGCAGAATATT... | TTCTTTAACTTATTTGCAGTCAAAGCCACTAGCAAAAGAGATTACTAGAGATGTTAATCCATTATGTTACCAAATAGTATACTGTTACCATGTTTTACGTACACCCTTGAGTAAGGTGGAATAGGTTAATGTCTGTGGCATAATAACACTTCACTGAATGCACAATAGTATTTAACATGTTAAAAAGGTTGAATATATTAACATCACATATAATCTGAAATTTAAAAAATATACTGCATTTTATATAAAAGTATTAGTAAAATATACTAATTTTAATTTACTTATAAATGAAATTAAGTTTTCTCATAATGCAGAATATT... |
Task1_train_46809 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GACTTCAGGGTAAAACATTCTCTAATCTAAAATCTAACCTTTTCAATCTCCAACTGCCATTCCCTTCCCACCTTCTCTCTAATCTTTTTTGCTCCACTGTATGAAAGAAAGCCCTCGTCTGCCTAAACTTGGCAATTCTTAAAGTTTTTATAGTTGGTATTCCTCCTGTTCTAATACTTTTTTGGAATTCAAATTTTTTAAATAAATTGAACTTGGTTATACATTACAAAGTCTAGAAACTGCCTTAAAACAATAACAACTTCATCATCAGCAAGACCCTCCCAATCCCCTTTTATGTTAACCTTAACTGCATCTGCCTG... | GACTTCAGGGTAAAACATTCTCTAATCTAAAATCTAACCTTTTCAATCTCCAACTGCCATTCCCTTCCCACCTTCTCTCTAATCTTTTTTGCTCCACTGTATGAAAGAAAGCCCTCGTCTGCCTAAACTTGGCAATTCTTAAAGTTTTTATAGTTGGTATTCCTCCTGTTCTAATACTTTTTTGGAATTCAAATTTTTTAAATAAATTGAACTTGGTTATACATTACAAAGTCTAGAAACTGCCTTAAAACAATAACAACTTCATCATCAGCAAGACCCTCCCAATCCCCTTTTATGTTAACCTTAACTGCATCTGCCTG... |
Task1_train_46810 | A variant on Chromosome 19 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CCAGTTGAGGGGGATTGTGACATATCGTTGGACCAGCACAAGGGAAATTGAAAACTCCTGCCTAGGCCATTCCCATAGAAGGCATTGTGACATATCACTGGTCACAGCACACAGGTAATTTGACTCTCCTTCCTGGGCCTTGCCCATAGGAGATATTGTAGCATATCTTTAGCCCAGCACTTAAAATATGCGACCCTCCTAGTTGGTTTCTTTTCCACAGGTGAGAATTTTACATAAAACTGCACCCAGCACACAGGTGAAATTGTGACTCTTGGATGTTCATCCAGCCAACAGTTATGAGTGTCATCATCGCACATGGA... | CCAGTTGAGGGGGATTGTGACATATCGTTGGACCAGCACAAGGGAAATTGAAAACTCCTGCCTAGGCCATTCCCATAGAAGGCATTGTGACATATCACTGGTCACAGCACACAGGTAATTTGACTCTCCTTCCTGGGCCTTGCCCATAGGAGATATTGTAGCATATCTTTAGCCCAGCACTTAAAATATGCGACCCTCCTAGTTGGTTTCTTTTCCACAGGTGAGAATTTTACATAAAACTGCACCCAGCACACAGGTGAAATTGTGACTCTTGGATGTTCATCCAGCCAACAGTTATGAGTGTCATCATCGCACATGGA... |
Task1_train_46811 | Assess the clinical impact of this variant found on Chromosome 19. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TTCCTTTTTTTGTGGTGCCTTCACTAGATTTTAGTTTCATATATTTCACTGATTTAATATAACAAGTTAGGGTGAAATCCCACCTTGATTTTTTCGAATGCATTCAGTAGGCTTAGGTAAAACTCTTTGCAATGTGGTAAAACTTCGCTGTGATTTCATATGATCCAGGGCTTTTTATGGTTAGTAGGTTTATTATTACTTATACAATGTCATTATACATTTTATACATTTTTGCTCTGCTAAAGACTTCTGTTATTAGGCCAGGCACTGTGGCTCATGCCTGCAATCCCAGGACTTTGGGTGGCCAAGGTGGGCATATC... | TTCCTTTTTTTGTGGTGCCTTCACTAGATTTTAGTTTCATATATTTCACTGATTTAATATAACAAGTTAGGGTGAAATCCCACCTTGATTTTTTCGAATGCATTCAGTAGGCTTAGGTAAAACTCTTTGCAATGTGGTAAAACTTCGCTGTGATTTCATATGATCCAGGGCTTTTTATGGTTAGTAGGTTTATTATTACTTATACAATGTCATTATACATTTTATACATTTTTGCTCTGCTAAAGACTTCTGTTATTAGGCCAGGCACTGTGGCTCATGCCTGCAATCCCAGGACTTTGGGTGGCCAAGGTGGGCATATC... |
Task1_train_46812 | A sequence alteration has been identified on Chromosome 19. Is it disease-inducing or harmless? | Benign | CTTTGCCACATTCTTCATATTTGTAAGGTTTCTCTTCAGTATGAATTTTCTTATGATAACTAAGGGTTGAGGATGACTTATAGGCTTTGCCACATGCTTCACATTTGTAGAATTTCTCTCCAGCATGAGTTTTCTTATGTTTACTAAAGACTGACAACCAGCTGAAGGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTACCTCATGTTTAGTAAGGATGGAGAACATACTAAAACCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTTTCTTATGATAACTAAGGGTT... | CTTTGCCACATTCTTCATATTTGTAAGGTTTCTCTTCAGTATGAATTTTCTTATGATAACTAAGGGTTGAGGATGACTTATAGGCTTTGCCACATGCTTCACATTTGTAGAATTTCTCTCCAGCATGAGTTTTCTTATGTTTACTAAAGACTGACAACCAGCTGAAGGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTACCTCATGTTTAGTAAGGATGGAGAACATACTAAAACCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTTTCTTATGATAACTAAGGGTT... |
Task1_train_46813 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTTATGATAACTAAGGGTTGAGGATGACTTATAGGCTTTGCCACATGCTTCACATTTGTAGAATTTCTCTCCAGCATGAGTTTTCTTATGTTTACTAAAGACTGACAACCAGCTGAAGGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTACCTCATGTTTAGTAAGGATGGAGAACATACTAAAACCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTTTCTTATGATAACTAAGGGTTGAGGGCCATTTATAGGCTTTGCCACATTCTTCACATTTGTAGGGTTTCT... | CTTATGATAACTAAGGGTTGAGGATGACTTATAGGCTTTGCCACATGCTTCACATTTGTAGAATTTCTCTCCAGCATGAGTTTTCTTATGTTTACTAAAGACTGACAACCAGCTGAAGGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTACCTCATGTTTAGTAAGGATGGAGAACATACTAAAACCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTTTCTTATGATAACTAAGGGTTGAGGGCCATTTATAGGCTTTGCCACATTCTTCACATTTGTAGGGTTTCT... |
Task1_train_46814 | A genomic variant on Chromosome 19 is under review. What is the biological outcome — benign or pathogenic? | Benign | GTGGATGTTTGACAAAATATTCTTCTTGGGCCAAAAACATTGGCATTACTGGTGAACTTGTTAGAAATATAGAAACTCAAAACAAAACAAAAAAAATTCAGAAACAGACTTTCTATAAGTCAGAACCAGTTCTCTACTCTCTCATTTGACCTTGAGACATTAAAAATTCTGCCCTGGCTGCTTGGTAAATGTGTATGGGGGTGTGTTTTTTAGAGTCAGAGAATACATTAGAGAATATTTCTGTGTTAAAAAAATATTTTCTTGGATAATTTTGGTCACTCCAATAAGGCAGAACCTGTTCTCTCTGCTCTTTAATTACA... | GTGGATGTTTGACAAAATATTCTTCTTGGGCCAAAAACATTGGCATTACTGGTGAACTTGTTAGAAATATAGAAACTCAAAACAAAACAAAAAAAATTCAGAAACAGACTTTCTATAAGTCAGAACCAGTTCTCTACTCTCTCATTTGACCTTGAGACATTAAAAATTCTGCCCTGGCTGCTTGGTAAATGTGTATGGGGGTGTGTTTTTTAGAGTCAGAGAATACATTAGAGAATATTTCTGTGTTAAAAAAATATTTTCTTGGATAATTTTGGTCACTCCAATAAGGCAGAACCTGTTCTCTCTGCTCTTTAATTACA... |
Task1_train_46815 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGTTGTCTTATATGTAGTAAGCCTTAAGGACTGGTTAAAGGCTTTGCCACATTCCACACAATTATAGGAATTCCCTCCAGTATGAATTACATGAATGTTTAGTAAGGATTGAGGAACAGCTAAAAGGCTTGCCACATTCTTCACATTTGTAGGGTTTCCCTCCTGTATAAATTCCCTTATGTTCAGTAAGGGTTGAGAACTAATGAAAAGCTTTGCCACGTTTTTCACATTTGTAGGGCTTTTCCTCCAGTATGAATTCTTTTATGAGTAGTAAGGTGTGAGGAACAGTTGAAGTCTTTATCACATTCTTCGCATTTGTA... | AGTTGTCTTATATGTAGTAAGCCTTAAGGACTGGTTAAAGGCTTTGCCACATTCCACACAATTATAGGAATTCCCTCCAGTATGAATTACATGAATGTTTAGTAAGGATTGAGGAACAGCTAAAAGGCTTGCCACATTCTTCACATTTGTAGGGTTTCCCTCCTGTATAAATTCCCTTATGTTCAGTAAGGGTTGAGAACTAATGAAAAGCTTTGCCACGTTTTTCACATTTGTAGGGCTTTTCCTCCAGTATGAATTCTTTTATGAGTAGTAAGGTGTGAGGAACAGTTGAAGTCTTTATCACATTCTTCGCATTTGTA... |
Task1_train_46816 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AAAAATGTCTTAATGAGAGAATCAGACATCATGGTTAACATCTGTAATGACAGCTACATGGTATAGAAAGGTTGGAGAATTGCTGCAGGCCAAAACTTTAAGACCAACCTGGGTTATGTAGTGAGACCTTATCTCAAAAATAAGTGCCTTTAAGAGAGCTTTGAGATCCAGTGAGGGAATTGTGAAACTTTGCTAAAGCCCAAGATTGAGGAGCACCCTTTTCAGAAGGCAAGCTTTCATTCAGGTGGCAAACTAGAGGACCCCTGCTCTTGACTACAGACCAGAAAATGTCCCACCCTACTTGGTCCCACAGAGAATTT... | AAAAATGTCTTAATGAGAGAATCAGACATCATGGTTAACATCTGTAATGACAGCTACATGGTATAGAAAGGTTGGAGAATTGCTGCAGGCCAAAACTTTAAGACCAACCTGGGTTATGTAGTGAGACCTTATCTCAAAAATAAGTGCCTTTAAGAGAGCTTTGAGATCCAGTGAGGGAATTGTGAAACTTTGCTAAAGCCCAAGATTGAGGAGCACCCTTTTCAGAAGGCAAGCTTTCATTCAGGTGGCAAACTAGAGGACCCCTGCTCTTGACTACAGACCAGAAAATGTCCCACCCTACTTGGTCCCACAGAGAATTT... |
Task1_train_46817 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TTTAGTAGAGACAGGGTTTCACTATGTTGCCCAGGCTTGGTCTCAAACTCCTGACCTCAGCTGATCCTCCCACCTTGGCCGCCAAAGTGCTAGGATTACAGGTTTGAACCACCAAACTCCTTCTTAATAACCAATAATCACTTGCTATAATTGTTTCCTGTCTGTAGTACCACAGTCTTTCTGCTGCTGTAAAACTTACCTTTCTTATTTATTTATTTCATTATACTTTAAGTCCTAGGGTACATGTGCCCAGCGTGCAGTTATATTACATAGGTATACATGTGCCATGGGTTAATGCTATCCTTCCCCCAGCCCCTCAT... | TTTAGTAGAGACAGGGTTTCACTATGTTGCCCAGGCTTGGTCTCAAACTCCTGACCTCAGCTGATCCTCCCACCTTGGCCGCCAAAGTGCTAGGATTACAGGTTTGAACCACCAAACTCCTTCTTAATAACCAATAATCACTTGCTATAATTGTTTCCTGTCTGTAGTACCACAGTCTTTCTGCTGCTGTAAAACTTACCTTTCTTATTTATTTATTTCATTATACTTTAAGTCCTAGGGTACATGTGCCCAGCGTGCAGTTATATTACATAGGTATACATGTGCCATGGGTTAATGCTATCCTTCCCCCAGCCCCTCAT... |
Task1_train_46818 | A variant has been detected on Chromosome 19. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CAGCTGATCCTCCCACCTTGGCCGCCAAAGTGCTAGGATTACAGGTTTGAACCACCAAACTCCTTCTTAATAACCAATAATCACTTGCTATAATTGTTTCCTGTCTGTAGTACCACAGTCTTTCTGCTGCTGTAAAACTTACCTTTCTTATTTATTTATTTCATTATACTTTAAGTCCTAGGGTACATGTGCCCAGCGTGCAGTTATATTACATAGGTATACATGTGCCATGGGTTAATGCTATCCTTCCCCCAGCCCCTCATACCCCGACAGGCCCTGTTGTGTGATGTTCCCCGCCCTGTGTCCAGGTATTCTCATTG... | CAGCTGATCCTCCCACCTTGGCCGCCAAAGTGCTAGGATTACAGGTTTGAACCACCAAACTCCTTCTTAATAACCAATAATCACTTGCTATAATTGTTTCCTGTCTGTAGTACCACAGTCTTTCTGCTGCTGTAAAACTTACCTTTCTTATTTATTTATTTCATTATACTTTAAGTCCTAGGGTACATGTGCCCAGCGTGCAGTTATATTACATAGGTATACATGTGCCATGGGTTAATGCTATCCTTCCCCCAGCCCCTCATACCCCGACAGGCCCTGTTGTGTGATGTTCCCCGCCCTGTGTCCAGGTATTCTCATTG... |
Task1_train_46819 | 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 | TGTGATGTTCCCCGCCCTGTGTCCAGGTATTCTCATTGCTCAATTCCCACCTATGAGTGAGAACATGTGGTGTTTGGTTTTCTGTCCTTGTGATAGTGTGCTCAGAATGATGGTTTCCAGCTTCATCCATGTCCCTGCAAAGGACATGAACTCATCCTTTTTCATGAATGCATAGTATTCTGTAGTGTATACATGCCACATTTTCTTAATCCATTCTATCATTGATGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCGCAATAAATATACGTGTGCATGTGTCCTTATAGTAGCATGATTTATAAT... | TGTGATGTTCCCCGCCCTGTGTCCAGGTATTCTCATTGCTCAATTCCCACCTATGAGTGAGAACATGTGGTGTTTGGTTTTCTGTCCTTGTGATAGTGTGCTCAGAATGATGGTTTCCAGCTTCATCCATGTCCCTGCAAAGGACATGAACTCATCCTTTTTCATGAATGCATAGTATTCTGTAGTGTATACATGCCACATTTTCTTAATCCATTCTATCATTGATGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCGCAATAAATATACGTGTGCATGTGTCCTTATAGTAGCATGATTTATAAT... |
Task1_train_46820 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TGATGTTCCCCGCCCTGTGTCCAGGTATTCTCATTGCTCAATTCCCACCTATGAGTGAGAACATGTGGTGTTTGGTTTTCTGTCCTTGTGATAGTGTGCTCAGAATGATGGTTTCCAGCTTCATCCATGTCCCTGCAAAGGACATGAACTCATCCTTTTTCATGAATGCATAGTATTCTGTAGTGTATACATGCCACATTTTCTTAATCCATTCTATCATTGATGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCGCAATAAATATACGTGTGCATGTGTCCTTATAGTAGCATGATTTATAATCC... | TGATGTTCCCCGCCCTGTGTCCAGGTATTCTCATTGCTCAATTCCCACCTATGAGTGAGAACATGTGGTGTTTGGTTTTCTGTCCTTGTGATAGTGTGCTCAGAATGATGGTTTCCAGCTTCATCCATGTCCCTGCAAAGGACATGAACTCATCCTTTTTCATGAATGCATAGTATTCTGTAGTGTATACATGCCACATTTTCTTAATCCATTCTATCATTGATGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCGCAATAAATATACGTGTGCATGTGTCCTTATAGTAGCATGATTTATAATCC... |
Task1_train_46821 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | TGGTTTCCAGCTTCATCCATGTCCCTGCAAAGGACATGAACTCATCCTTTTTCATGAATGCATAGTATTCTGTAGTGTATACATGCCACATTTTCTTAATCCATTCTATCATTGATGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCGCAATAAATATACGTGTGCATGTGTCCTTATAGTAGCATGATTTATAATCCTTTGGGTATATACCCAGTAATGGGATGGCTGGCTCAAATGGTATTTCTAGTTCTAGATCCTTGAGGAATCATAACACTGTCTTCCACAATGGTTGAACTAGTTTACAG... | TGGTTTCCAGCTTCATCCATGTCCCTGCAAAGGACATGAACTCATCCTTTTTCATGAATGCATAGTATTCTGTAGTGTATACATGCCACATTTTCTTAATCCATTCTATCATTGATGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCGCAATAAATATACGTGTGCATGTGTCCTTATAGTAGCATGATTTATAATCCTTTGGGTATATACCCAGTAATGGGATGGCTGGCTCAAATGGTATTTCTAGTTCTAGATCCTTGAGGAATCATAACACTGTCTTCCACAATGGTTGAACTAGTTTACAG... |
Task1_train_46822 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TCATCCATGTCCCTGCAAAGGACATGAACTCATCCTTTTTCATGAATGCATAGTATTCTGTAGTGTATACATGCCACATTTTCTTAATCCATTCTATCATTGATGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCGCAATAAATATACGTGTGCATGTGTCCTTATAGTAGCATGATTTATAATCCTTTGGGTATATACCCAGTAATGGGATGGCTGGCTCAAATGGTATTTCTAGTTCTAGATCCTTGAGGAATCATAACACTGTCTTCCACAATGGTTGAACTAGTTTACAGTCCCACCAACAG... | TCATCCATGTCCCTGCAAAGGACATGAACTCATCCTTTTTCATGAATGCATAGTATTCTGTAGTGTATACATGCCACATTTTCTTAATCCATTCTATCATTGATGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCGCAATAAATATACGTGTGCATGTGTCCTTATAGTAGCATGATTTATAATCCTTTGGGTATATACCCAGTAATGGGATGGCTGGCTCAAATGGTATTTCTAGTTCTAGATCCTTGAGGAATCATAACACTGTCTTCCACAATGGTTGAACTAGTTTACAGTCCCACCAACAG... |
Task1_train_46823 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | CGTTTCTATTTCTCCACATCCTCTCCAGCACCTGTTGTCTCCTGACTTTTTAATGATCACCATTCTAACTGGCATGAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCGGATGGCCAGTGATGATGAGCATTTTTCCATGTGTCTGTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCACATCCTTTGCTCACTTTTTGATGGGGTTGTTAGTTTTTTTCTTGTAAATTTGTTTAAGTTCTTTGTAGATTCTGGATGTTTGCCCTTTGTCAGATGGGTAGATTGCATAGATTTTCTCCCATTCTGTAG... | CGTTTCTATTTCTCCACATCCTCTCCAGCACCTGTTGTCTCCTGACTTTTTAATGATCACCATTCTAACTGGCATGAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCGGATGGCCAGTGATGATGAGCATTTTTCCATGTGTCTGTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCACATCCTTTGCTCACTTTTTGATGGGGTTGTTAGTTTTTTTCTTGTAAATTTGTTTAAGTTCTTTGTAGATTCTGGATGTTTGCCCTTTGTCAGATGGGTAGATTGCATAGATTTTCTCCCATTCTGTAG... |
Task1_train_46824 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | TAACTGGCATGAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCGGATGGCCAGTGATGATGAGCATTTTTCCATGTGTCTGTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCACATCCTTTGCTCACTTTTTGATGGGGTTGTTAGTTTTTTTCTTGTAAATTTGTTTAAGTTCTTTGTAGATTCTGGATGTTTGCCCTTTGTCAGATGGGTAGATTGCATAGATTTTCTCCCATTCTGTAGGTTGCCTGTTCATTCTGGTGGTAGTTTCTTTTGCCGTGCAGAAGCTCTTTAGTTTAATTAGATCC... | TAACTGGCATGAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCGGATGGCCAGTGATGATGAGCATTTTTCCATGTGTCTGTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCACATCCTTTGCTCACTTTTTGATGGGGTTGTTAGTTTTTTTCTTGTAAATTTGTTTAAGTTCTTTGTAGATTCTGGATGTTTGCCCTTTGTCAGATGGGTAGATTGCATAGATTTTCTCCCATTCTGTAGGTTGCCTGTTCATTCTGGTGGTAGTTTCTTTTGCCGTGCAGAAGCTCTTTAGTTTAATTAGATCC... |
Task1_train_46825 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCGGATGGCCAGTGATGATGAGCATTTTTCCATGTGTCTGTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCACATCCTTTGCTCACTTTTTGATGGGGTTGTTAGTTTTTTTCTTGTAAATTTGTTTAAGTTCTTTGTAGATTCTGGATGTTTGCCCTTTGTCAGATGGGTAGATTGCATAGATTTTCTCCCATTCTGTAGGTTGCCTGTTCATTCTGGTGGTAGTTTCTTTTGCCGTGCAGAAGCTCTTTAGTTTAATTAGATCCCATTTGTCAA... | GAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCGGATGGCCAGTGATGATGAGCATTTTTCCATGTGTCTGTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCACATCCTTTGCTCACTTTTTGATGGGGTTGTTAGTTTTTTTCTTGTAAATTTGTTTAAGTTCTTTGTAGATTCTGGATGTTTGCCCTTTGTCAGATGGGTAGATTGCATAGATTTTCTCCCATTCTGTAGGTTGCCTGTTCATTCTGGTGGTAGTTTCTTTTGCCGTGCAGAAGCTCTTTAGTTTAATTAGATCCCATTTGTCAA... |
Task1_train_46826 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTATTAAATAGGGAATCCTTTCCCCATTTCTTGTGTTTTGTCAGGTTTGTCAAAGATCAGATAGTTGTAGATGTGTGGTGTTATTTCTGAGGTCTCTATTCTGTTCCATTGGTCTATATATCTGTTTTGGTACCTTACCTTTCATCTCAGCAGCCTCAAACTGTCATTTGAAAGAATACCACTATTTCTTTCAGAACTTTTATGCAATGAGACACAGGAACCAGTGTAAAAGCCCCTGCCATTGAGAAATAAAGATGTATAAGCCATTATTTTACTTGTCTTTTAAAAATGAAACCAGGAGTTGGCAATTTATTTCTAAA... | TTATTAAATAGGGAATCCTTTCCCCATTTCTTGTGTTTTGTCAGGTTTGTCAAAGATCAGATAGTTGTAGATGTGTGGTGTTATTTCTGAGGTCTCTATTCTGTTCCATTGGTCTATATATCTGTTTTGGTACCTTACCTTTCATCTCAGCAGCCTCAAACTGTCATTTGAAAGAATACCACTATTTCTTTCAGAACTTTTATGCAATGAGACACAGGAACCAGTGTAAAAGCCCCTGCCATTGAGAAATAAAGATGTATAAGCCATTATTTTACTTGTCTTTTAAAAATGAAACCAGGAGTTGGCAATTTATTTCTAAA... |
Task1_train_46827 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TTCACATTTGTAGGGTTTTTCTCCAGTACGAATTTTCTTATGTCTAATAAAGTTTAACTGATTAAAAGCATTGCCACATTCTTCACATTTCTAGAGTTTGTCTTCAGTATCAACTATTTTCTGTTGAGTAAGGTCTGAAAACCAGTTAAAAGCTTTGCCACAGTTTTCATATTTGTAGGGTTTCTCTTCAGTATGAATTATCTTATGTTCAGTAAGGTTTGAGGACCAGTTAAAAGTTTTGCCACACTCTTCACATGAGGCGGGTTTCTCTCTAATTTATCTTATATTCAGTAAGATCTGAGAACCCGTTAGAAGCTTTG... | TTCACATTTGTAGGGTTTTTCTCCAGTACGAATTTTCTTATGTCTAATAAAGTTTAACTGATTAAAAGCATTGCCACATTCTTCACATTTCTAGAGTTTGTCTTCAGTATCAACTATTTTCTGTTGAGTAAGGTCTGAAAACCAGTTAAAAGCTTTGCCACAGTTTTCATATTTGTAGGGTTTCTCTTCAGTATGAATTATCTTATGTTCAGTAAGGTTTGAGGACCAGTTAAAAGTTTTGCCACACTCTTCACATGAGGCGGGTTTCTCTCTAATTTATCTTATATTCAGTAAGATCTGAGAACCCGTTAGAAGCTTTG... |
Task1_train_46828 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AGCTTTGCCATATTATTCACATTTGTGGAGTTTATCTTCTTTAGGAATTCTCTCATTTTGAGTAACAGCTGAGCAATGGTTAAAAGCTTTGTCACCTTTATTATATTTGTAGGGTTTTCCTCCAGTATCAATTATTTTATGTGTATTTAAGGTGTGAGGACTGGTTAAAGGCTTTGCCACATTCTTTACATTTGTGGGGTTTCTCTCCAGCATGAATTGTTTTCTGCCTATTAAGGCTTGAGGACTGGTTAAAAGCTTTGCCACATTCTTCACATATGGAGGGTCTGTCTCTAGTATAAATTATCTTATGTGTATTAAGG... | AGCTTTGCCATATTATTCACATTTGTGGAGTTTATCTTCTTTAGGAATTCTCTCATTTTGAGTAACAGCTGAGCAATGGTTAAAAGCTTTGTCACCTTTATTATATTTGTAGGGTTTTCCTCCAGTATCAATTATTTTATGTGTATTTAAGGTGTGAGGACTGGTTAAAGGCTTTGCCACATTCTTTACATTTGTGGGGTTTCTCTCCAGCATGAATTGTTTTCTGCCTATTAAGGCTTGAGGACTGGTTAAAAGCTTTGCCACATTCTTCACATATGGAGGGTCTGTCTCTAGTATAAATTATCTTATGTGTATTAAGG... |
Task1_train_46829 | This mutation on Chromosome 19 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GTATGAATTATCTTATGTTTAGTAAGGGCTGAAAGATGGTTAAAAGCTTTGCCACATTCTTCACATTTGTAGGTTTTCCCTCCAGTATGAATTGTTTTATGTTGAGTAAGGTGTGAGGACTGGTTAAAGGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGAATGAATTATCTTATGTTTAGTAAGGTTTGAGGACTAAATGCTTTACCACACTCTTCACATTTGTAGGGTTTCTTTCCAGTATGAATTATCCTATGTTTAGTAAGGCGTGAGAAATGGCTAAAAGCTTTGCCACGTTCTTCACATTTGTAG... | GTATGAATTATCTTATGTTTAGTAAGGGCTGAAAGATGGTTAAAAGCTTTGCCACATTCTTCACATTTGTAGGTTTTCCCTCCAGTATGAATTGTTTTATGTTGAGTAAGGTGTGAGGACTGGTTAAAGGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGAATGAATTATCTTATGTTTAGTAAGGTTTGAGGACTAAATGCTTTACCACACTCTTCACATTTGTAGGGTTTCTTTCCAGTATGAATTATCCTATGTTTAGTAAGGCGTGAGAAATGGCTAAAAGCTTTGCCACGTTCTTCACATTTGTAG... |
Task1_train_46830 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CATAAGGGTTGAGGAATTGTTAAAAGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTTTCCAGTATAATTATCTCATGTTTTCTAAGGGCTGAGAAATGCTTAAAAGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTACAGTATGAATTACCTTATGTTCCATAAGTTTTGAGACCACTTAAAAGCTTTACCACATTCTTCACATTTGTATGGTTTCTCCCCAGTATGAATTATCTTATGTTTCCTAAGGGCTGAGAAATTGCTAAAAGCTTTGCCACATTCTTCACATTTGTACGATTTCTCCCTAGTATGA... | CATAAGGGTTGAGGAATTGTTAAAAGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTTTCCAGTATAATTATCTCATGTTTTCTAAGGGCTGAGAAATGCTTAAAAGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTACAGTATGAATTACCTTATGTTCCATAAGTTTTGAGACCACTTAAAAGCTTTACCACATTCTTCACATTTGTATGGTTTCTCCCCAGTATGAATTATCTTATGTTTCCTAAGGGCTGAGAAATTGCTAAAAGCTTTGCCACATTCTTCACATTTGTACGATTTCTCCCTAGTATGA... |
Task1_train_46831 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | GGTTTCTTCCCAGTATAAATTATCTTATGTTTCCTAAGGGTTGAGGAATTGTTAAAAGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTTTCCAGTATGAATTATCTCATGTTTTCTAAGGGCTGAGAAATGTTTAAAAGCTTTGCCACATTCTTCACATTTGCAGGGTTTCTCTCCATATGAATTACCTTATGTAAAGTAAGTTTTGAGGACCACTGAAAAGCTTTACCACATTCTTCACATTTGTAGGATTTCTCTCCAGTATGAATTATCTCATGTTTTCTAAGGGTTGAGGAATTGTTAAAAGCTTTGCCACAT... | GGTTTCTTCCCAGTATAAATTATCTTATGTTTCCTAAGGGTTGAGGAATTGTTAAAAGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTTTCCAGTATGAATTATCTCATGTTTTCTAAGGGCTGAGAAATGTTTAAAAGCTTTGCCACATTCTTCACATTTGCAGGGTTTCTCTCCATATGAATTACCTTATGTAAAGTAAGTTTTGAGGACCACTGAAAAGCTTTACCACATTCTTCACATTTGTAGGATTTCTCTCCAGTATGAATTATCTCATGTTTTCTAAGGGTTGAGGAATTGTTAAAAGCTTTGCCACAT... |
Task1_train_46832 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTCATGTTTTCTAAGGGTTGAGGAATTGTTAAAAGCTTTGCCACATTCTTCACATTTATAGGGTTTCTTTCCAGTATGAATTATCTTATGTTTTCTAAGGGCTGAGAAATGCTTAAAAGCTTTGCCACATTCTTCACATTTGCAGGGTTTCTCTGCAGTATGAATTACCTTATGTACAGTAAGTTTTGAGGACCACTTAAAAGCTTTACCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTATCTCATGTTTTCTAAGAGTTGAGGACTGGCTAAAAGCTTTGCCACATTCTTCACATTTGTAGGGTTTCT... | CTCATGTTTTCTAAGGGTTGAGGAATTGTTAAAAGCTTTGCCACATTCTTCACATTTATAGGGTTTCTTTCCAGTATGAATTATCTTATGTTTTCTAAGGGCTGAGAAATGCTTAAAAGCTTTGCCACATTCTTCACATTTGCAGGGTTTCTCTGCAGTATGAATTACCTTATGTACAGTAAGTTTTGAGGACCACTTAAAAGCTTTACCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTATCTCATGTTTTCTAAGAGTTGAGGACTGGCTAAAAGCTTTGCCACATTCTTCACATTTGTAGGGTTTCT... |
Task1_train_46833 | A variant on Chromosome 19 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TGGTTGACGAAGTGAGACCCTATTTCATTAATTAATTAATTAAAAGGAAAAGAAAGAAGATGCCTGAGTGGCTTAAGAAAAGAAGCATACAATATGTTCTCTACAAGAGACCAATTTTAGCACTGAGTCAAATAGTCTGTAAGTAACAGAATTTAAAAAAATCTATATTTCATGCAAATAGTAGCCACAATTGGGTGAGGTAGTCGTAATTATATTGGGCACAATATGCTTTAAGTCAAGTACTAGTACAAGAAAAAGATTGATATTATATAATAGTAAAATGGGTCAATTTACCAGGAATCTATAACTATTATATTTAT... | TGGTTGACGAAGTGAGACCCTATTTCATTAATTAATTAATTAAAAGGAAAAGAAAGAAGATGCCTGAGTGGCTTAAGAAAAGAAGCATACAATATGTTCTCTACAAGAGACCAATTTTAGCACTGAGTCAAATAGTCTGTAAGTAACAGAATTTAAAAAAATCTATATTTCATGCAAATAGTAGCCACAATTGGGTGAGGTAGTCGTAATTATATTGGGCACAATATGCTTTAAGTCAAGTACTAGTACAAGAAAAAGATTGATATTATATAATAGTAAAATGGGTCAATTTACCAGGAATCTATAACTATTATATTTAT... |
Task1_train_46834 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GATTCTCCTTCCTCAGACTCCTGAATAGCTGGGATTATAGACACACACCACCACACATGTCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTTGCCATGTTGGCCAGGCTGATCTTGAACTCCTGACCTAAGGTGATCCATCTGCCGTGGCCTCCCAAAATGCTGGTACTACAGGTGTGAGTCACCACACCTGGCCTGTCATTTTCTTGAATCATATTATTTTCAATGGAAGAAACTGCTTTCAGTATCTTTTATGTATAGGGCACATGCAGTGCCAATATACTTTTTCAGAATTTGATTACTTTGGAAGGTTTTTTTA... | GATTCTCCTTCCTCAGACTCCTGAATAGCTGGGATTATAGACACACACCACCACACATGTCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTTGCCATGTTGGCCAGGCTGATCTTGAACTCCTGACCTAAGGTGATCCATCTGCCGTGGCCTCCCAAAATGCTGGTACTACAGGTGTGAGTCACCACACCTGGCCTGTCATTTTCTTGAATCATATTATTTTCAATGGAAGAAACTGCTTTCAGTATCTTTTATGTATAGGGCACATGCAGTGCCAATATACTTTTTCAGAATTTGATTACTTTGGAAGGTTTTTTTA... |
Task1_train_46835 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CCAGGCTGCAATGCAGTAGCAGCATCTCAGCTTACTGCAACCTCTGGCTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCCAAGTAGCCGGGACTACAGATGTACACCACCATGCTTCGCTAATTTTTTTTATTTCCTTTTAGTAGACATGGGGTTTCACCAAGTTGGCCAGGCTGGTCTTGAACTCAGGTGATCTACCCACCTCGGCATCCCAAAGTGTTGGCCTTACAGATGTAAGCCACTGTGTCTGACAAAAAAAAATCTGTATTTTCAAGACAAAAGTGTACTTTAAATGAAATTATAACTCTTCAAAGATC... | CCAGGCTGCAATGCAGTAGCAGCATCTCAGCTTACTGCAACCTCTGGCTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCCAAGTAGCCGGGACTACAGATGTACACCACCATGCTTCGCTAATTTTTTTTATTTCCTTTTAGTAGACATGGGGTTTCACCAAGTTGGCCAGGCTGGTCTTGAACTCAGGTGATCTACCCACCTCGGCATCCCAAAGTGTTGGCCTTACAGATGTAAGCCACTGTGTCTGACAAAAAAAAATCTGTATTTTCAAGACAAAAGTGTACTTTAAATGAAATTATAACTCTTCAAAGATC... |
Task1_train_46836 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | CTCAGGGTTTTCCTGTAGTACAAAATGTGTACAATAAAACCTGTGATACACGTAAAGGTACTACAACTCTCTTTATATTTATAATGTGTTTCCTCAAAATAAATATTCTTCTGTACTTTAAGGGCTTATATTTTCTGAAAGATCTATTGACAGCAACTGCACTTTTAATGCTTTTATTTAGTATGAACTCTCTGATGCTGAATAAGATGTGAGAAGATATTAATGACATTCACATTTTTTCCCCTAGACAGTCTCCCTCTGTTGCCCAGGCTAGTGTAAATGCTTTCCTTTGCAATTAGGCATGAGCATTGGTTAAATGT... | CTCAGGGTTTTCCTGTAGTACAAAATGTGTACAATAAAACCTGTGATACACGTAAAGGTACTACAACTCTCTTTATATTTATAATGTGTTTCCTCAAAATAAATATTCTTCTGTACTTTAAGGGCTTATATTTTCTGAAAGATCTATTGACAGCAACTGCACTTTTAATGCTTTTATTTAGTATGAACTCTCTGATGCTGAATAAGATGTGAGAAGATATTAATGACATTCACATTTTTTCCCCTAGACAGTCTCCCTCTGTTGCCCAGGCTAGTGTAAATGCTTTCCTTTGCAATTAGGCATGAGCATTGGTTAAATGT... |
Task1_train_46837 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | CACTCATTGAATATTCAATTTTTTATCAATTTTTAAAATTAATGTGTACATCTTTTCTATGGTTTCCTTCTGAAAATTTTATAATATTTTTGATGGAATTATATTGCCCTGTTTTGTATATATTGTAATCTTTAATTGAGATTTGGACATTAAAAAAATCTACCTGTCACAATCTTTATAATGTAGTTCTGTCCTGACATAGTCTAAAAGCAATCGTTTTGGCTAGACATTCTGGGAGTCTCTCACACATGTTCTTAAAATGTGTCTTGTCTAAAATTTTGTGTTTGCTTTTAGTTAAAGGAGTTTGTGTTTCTTCTTAA... | CACTCATTGAATATTCAATTTTTTATCAATTTTTAAAATTAATGTGTACATCTTTTCTATGGTTTCCTTCTGAAAATTTTATAATATTTTTGATGGAATTATATTGCCCTGTTTTGTATATATTGTAATCTTTAATTGAGATTTGGACATTAAAAAAATCTACCTGTCACAATCTTTATAATGTAGTTCTGTCCTGACATAGTCTAAAAGCAATCGTTTTGGCTAGACATTCTGGGAGTCTCTCACACATGTTCTTAAAATGTGTCTTGTCTAAAATTTTGTGTTTGCTTTTAGTTAAAGGAGTTTGTGTTTCTTCTTAA... |
Task1_train_46838 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | TTAATGCTTGTCTTCAAAATAAATACTCTTCTTCACTTTAAAGGCTTATATTTTCTGAAAAATCTATTGACAGTAATTTCATCTTTAATGCTTCTATTAAGTATGAACTCTCTGATATTGAATAAGATGTGAACAGATATTAATGGCTTCTTCACATTCTTTACATTTGCATAATTTTTCTCAAGTATACATCATTTCCTGTCCAATAAAGTGTCAGCATTGGTTAAAAGTTTTGCCACATTCTTCACACTTGTAGAGGTTTCCTCTACTATATTTTACCTACAATCAAGTATGACAACCATTTAAAGGTGTTTAGAAAT... | TTAATGCTTGTCTTCAAAATAAATACTCTTCTTCACTTTAAAGGCTTATATTTTCTGAAAAATCTATTGACAGTAATTTCATCTTTAATGCTTCTATTAAGTATGAACTCTCTGATATTGAATAAGATGTGAACAGATATTAATGGCTTCTTCACATTCTTTACATTTGCATAATTTTTCTCAAGTATACATCATTTCCTGTCCAATAAAGTGTCAGCATTGGTTAAAAGTTTTGCCACATTCTTCACACTTGTAGAGGTTTCCTCTACTATATTTTACCTACAATCAAGTATGACAACCATTTAAAGGTGTTTAGAAAT... |
Task1_train_46839 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTGTTTTGTAGTAAATTAGACACCTCCTTAAAATGATTTTGTTCCAATATTGCTTTTTTCTGCTAAAAATAGTTTCGAACTTAAACACACTCCATAATTTATTTACACCTAAGATTCATCTTAGACTAACAGATGTGTATATTTAACTCTATGTAAATCAATACTAACAGTCCATATGTGCTTGCAGGCAGAGGCCACATGTTCGAAGAAAAATATATGAAAAAATTAAAAAAGATTTATTCGGGACTCAGAAATATATGGATTTTACTTATGTTTGTATATAAGTTTTATTATGACCATAAAAATAATCCTGTAGTCAA... | TTGTTTTGTAGTAAATTAGACACCTCCTTAAAATGATTTTGTTCCAATATTGCTTTTTTCTGCTAAAAATAGTTTCGAACTTAAACACACTCCATAATTTATTTACACCTAAGATTCATCTTAGACTAACAGATGTGTATATTTAACTCTATGTAAATCAATACTAACAGTCCATATGTGCTTGCAGGCAGAGGCCACATGTTCGAAGAAAAATATATGAAAAAATTAAAAAAGATTTATTCGGGACTCAGAAATATATGGATTTTACTTATGTTTGTATATAAGTTTTATTATGACCATAAAAATAATCCTGTAGTCAA... |
Task1_train_46840 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGTTTTGTAGTAAATTAGACACCTCCTTAAAATGATTTTGTTCCAATATTGCTTTTTTCTGCTAAAAATAGTTTCGAACTTAAACACACTCCATAATTTATTTACACCTAAGATTCATCTTAGACTAACAGATGTGTATATTTAACTCTATGTAAATCAATACTAACAGTCCATATGTGCTTGCAGGCAGAGGCCACATGTTCGAAGAAAAATATATGAAAAAATTAAAAAAGATTTATTCGGGACTCAGAAATATATGGATTTTACTTATGTTTGTATATAAGTTTTATTATGACCATAAAAATAATCCTGTAGTCAAC... | TGTTTTGTAGTAAATTAGACACCTCCTTAAAATGATTTTGTTCCAATATTGCTTTTTTCTGCTAAAAATAGTTTCGAACTTAAACACACTCCATAATTTATTTACACCTAAGATTCATCTTAGACTAACAGATGTGTATATTTAACTCTATGTAAATCAATACTAACAGTCCATATGTGCTTGCAGGCAGAGGCCACATGTTCGAAGAAAAATATATGAAAAAATTAAAAAAGATTTATTCGGGACTCAGAAATATATGGATTTTACTTATGTTTGTATATAAGTTTTATTATGACCATAAAAATAATCCTGTAGTCAAC... |
Task1_train_46841 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | TATTTCATAAAAATACAATAAATCATACTAAACTTTAACTAAAATTAAGAATGTTTTTCTTTCATAATAATGCAGAATATTAATCTGAACATCTACCTCATGCATCACTCGATATTATAAGTTAACCATAAAGATCCTCTCTACTTAAATTTTCATCATGCATCTTACATTTTTAATGTCCTTACCTTTCCATAGAAAAGGTCATAAATAATGCCTCTTCATATTTGTAATGCTTTTTCAAAATACTCTTCTGTACTTTAAAGACATATTTTCTGATCAGTCGTTTGACAGTAATTACACTTCTTATTTAGTATGAACGC... | TATTTCATAAAAATACAATAAATCATACTAAACTTTAACTAAAATTAAGAATGTTTTTCTTTCATAATAATGCAGAATATTAATCTGAACATCTACCTCATGCATCACTCGATATTATAAGTTAACCATAAAGATCCTCTCTACTTAAATTTTCATCATGCATCTTACATTTTTAATGTCCTTACCTTTCCATAGAAAAGGTCATAAATAATGCCTCTTCATATTTGTAATGCTTTTTCAAAATACTCTTCTGTACTTTAAAGACATATTTTCTGATCAGTCGTTTGACAGTAATTACACTTCTTATTTAGTATGAACGC... |
Task1_train_46842 | Chromosome 19 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | ATGTCCATTTAGGGTTGAGGATGATATAAATGCTTTGCCACATTCTTCACACTTGTAAGGTTTCTCTCCAGTATGAATTATCTTATGTGTAGTAAGCTTTGAGGATCGATTAAAAGCTTTGCCACATTCTTCACATTTGTATGGTTTCTCTCCAGTGTGCATCCTCGTATGTCTAGTTAGGGTTGAGGATTGGCTAAATGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTATCTTATGTTCAGTAAGAGTTGAAGATTTCCTAAAAGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTC... | ATGTCCATTTAGGGTTGAGGATGATATAAATGCTTTGCCACATTCTTCACACTTGTAAGGTTTCTCTCCAGTATGAATTATCTTATGTGTAGTAAGCTTTGAGGATCGATTAAAAGCTTTGCCACATTCTTCACATTTGTATGGTTTCTCTCCAGTGTGCATCCTCGTATGTCTAGTTAGGGTTGAGGATTGGCTAAATGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTCCAGTATGAATTATCTTATGTTCAGTAAGAGTTGAAGATTTCCTAAAAGCTTTGCCACATTCTTCACATTTGTAGGGTTTCTCTC... |
Task1_train_46843 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TCCAGTGTGTATCCTCTTATGTCTAGTTAGGGTTGAAGACCATATAAATGCTTTGCCACATTCTTTACATTTGAAGGGTTTCTCTCTAGTATGAATTCTTTTATGTTTAGTAAGGCTTGAGGACCAGTTAAATGCTTTGCCACATTCTTCACACTTGTAAGGTTTCTCTCCAGTATGAATAAACTTATGTATAGTAAGATTTGAAGATCGATTAAAAGCTTTGCCACATTCTTCACATTTGTAGAGTTTCTCTCCAGCATGTATTATTTTATGTTTAGTAAGGGTTGAGAGTCGCTTAAAAGTTTTGTCACATTCTTTAC... | TCCAGTGTGTATCCTCTTATGTCTAGTTAGGGTTGAAGACCATATAAATGCTTTGCCACATTCTTTACATTTGAAGGGTTTCTCTCTAGTATGAATTCTTTTATGTTTAGTAAGGCTTGAGGACCAGTTAAATGCTTTGCCACATTCTTCACACTTGTAAGGTTTCTCTCCAGTATGAATAAACTTATGTATAGTAAGATTTGAAGATCGATTAAAAGCTTTGCCACATTCTTCACATTTGTAGAGTTTCTCTCCAGCATGTATTATTTTATGTTTAGTAAGGGTTGAGAGTCGCTTAAAAGTTTTGTCACATTCTTTAC... |
Task1_train_46844 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | ACTTGGGGAGGTTCTGCCCTTCCAGAGGCCTGGAGGAAGACACCCATTTATAGCCATGCAGCAGGCCTGCAGACTTTGGCCTTTACTGTGGTCCCTGAAGCAGGTCCATGATTCAGTTCCAGCTCTCTGAGCCACAGTTCATGGCCGGTTCTGCCTATGTAGAAACCCAAAGTAACGTGGGAAAATCCTCTCTTGTACTAGATGAAAGCCATGCTCATCCACATCCTCATATAAAGCCCACCATATGCAGACCTGACTGCAGAAACCTGCCCTTGGGTCTGCCCTGCAGAGCAAAGTCCTGAAGGATATTCACTCTGTCC... | ACTTGGGGAGGTTCTGCCCTTCCAGAGGCCTGGAGGAAGACACCCATTTATAGCCATGCAGCAGGCCTGCAGACTTTGGCCTTTACTGTGGTCCCTGAAGCAGGTCCATGATTCAGTTCCAGCTCTCTGAGCCACAGTTCATGGCCGGTTCTGCCTATGTAGAAACCCAAAGTAACGTGGGAAAATCCTCTCTTGTACTAGATGAAAGCCATGCTCATCCACATCCTCATATAAAGCCCACCATATGCAGACCTGACTGCAGAAACCTGCCCTTGGGTCTGCCCTGCAGAGCAAAGTCCTGAAGGATATTCACTCTGTCC... |
Task1_train_46845 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGATGGAGTTTCACACTTGTTGCCCAGGCTAGAGTGCAATGGCACGATCTTGACTCACTGCAACCTCTGCCCCTCCAGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGAATTAAAGGCACTCACCACCATGCCTTGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCGCTATGTTGACCAGGCTGGTCTCGAACACCTGACCTCAGGTGATCCATCCACCTCGGCCTCCCAATATGCTGGGATTACAGGTGTGAGCCACTGCGCCCAGCCTGCAGAAA... | AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGATGGAGTTTCACACTTGTTGCCCAGGCTAGAGTGCAATGGCACGATCTTGACTCACTGCAACCTCTGCCCCTCCAGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGAATTAAAGGCACTCACCACCATGCCTTGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCGCTATGTTGACCAGGCTGGTCTCGAACACCTGACCTCAGGTGATCCATCCACCTCGGCCTCCCAATATGCTGGGATTACAGGTGTGAGCCACTGCGCCCAGCCTGCAGAAA... |
Task1_train_46846 | A variant has been detected on Chromosome 19. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTATTTTTTTATATTTTTGTAGAGACTGGGTTTCACCATGTTAGCCAGGATGGGCTTGATCTCCTGACCTCATGATCTGCCTGCCTTGGCCTCCCAAGGTATCTAATAAGTTTTACATTCCATGTTTTAACTTTGTTTTGCAATTATAGATTTTTGTGTTATATATTTTAGGGTATGCCACCACACATTCATTAATTGTGTTTTGATTTTTTAGTATTTATTATAATTATGCATGCTAATTTTTAACATCTTATAATTTAAGGCAGTGTGGAAGAAAGTCAAATATGAATGAGCTATACGTCTTTTTCCAATAGAATTAT... | CTATTTTTTTATATTTTTGTAGAGACTGGGTTTCACCATGTTAGCCAGGATGGGCTTGATCTCCTGACCTCATGATCTGCCTGCCTTGGCCTCCCAAGGTATCTAATAAGTTTTACATTCCATGTTTTAACTTTGTTTTGCAATTATAGATTTTTGTGTTATATATTTTAGGGTATGCCACCACACATTCATTAATTGTGTTTTGATTTTTTAGTATTTATTATAATTATGCATGCTAATTTTTAACATCTTATAATTTAAGGCAGTGTGGAAGAAAGTCAAATATGAATGAGCTATACGTCTTTTTCCAATAGAATTAT... |
Task1_train_46847 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | TGTTTTCCTGTATACAAAAATAAATGTTATCCTTGTATTTTTTTTCTAACTTGTATATTTGTTGTGTAGGTTTGTTGTGAATGGTTTTCTAATTCTGCGTAGATGAGTCATCATAAAATACTCTTTTTTTTTGAGATGGACTCTTGCTCTTCTTGCCCAGGCTGGAGTGTAATGGCGCGATCTCAGCTCACTGCAACTTCTGCCTCCTGGGTTGAAATGATTCTAGTGCCTCAGCCTCCTATGTAGCTGAGATTACAGGCATGTGCCAACATGCCTGGCTAATATTTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATG... | TGTTTTCCTGTATACAAAAATAAATGTTATCCTTGTATTTTTTTTCTAACTTGTATATTTGTTGTGTAGGTTTGTTGTGAATGGTTTTCTAATTCTGCGTAGATGAGTCATCATAAAATACTCTTTTTTTTTGAGATGGACTCTTGCTCTTCTTGCCCAGGCTGGAGTGTAATGGCGCGATCTCAGCTCACTGCAACTTCTGCCTCCTGGGTTGAAATGATTCTAGTGCCTCAGCCTCCTATGTAGCTGAGATTACAGGCATGTGCCAACATGCCTGGCTAATATTTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATG... |
Task1_train_46848 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GTTATTCTAGTTTGTTTGTTGAGCTTTTTTATTTTTACATCTTTTTTTTTTTTTTTACTTTTAGGATCTGTCAGTTTTTTTGTGTATATTTTATCTCCACAATTTGTTTTTTGATATCTTAACTATTTTTTATTCTTGTCCTCATTTTTCTGATTTTCCATAGTTGTTTCTGTTCCCATTTTAATCAGTATTATTCAGTTTATTACCAATTATTAAAATTAATGTATACATCTTTTTTATGATTTCTTTCAGAAAATTTTGTGATATTTTTGGTGGGATTGTATTGCCCTATTTTGTATATATTATAATCCTTGATTAAG... | GTTATTCTAGTTTGTTTGTTGAGCTTTTTTATTTTTACATCTTTTTTTTTTTTTTTACTTTTAGGATCTGTCAGTTTTTTTGTGTATATTTTATCTCCACAATTTGTTTTTTGATATCTTAACTATTTTTTATTCTTGTCCTCATTTTTCTGATTTTCCATAGTTGTTTCTGTTCCCATTTTAATCAGTATTATTCAGTTTATTACCAATTATTAAAATTAATGTATACATCTTTTTTATGATTTCTTTCAGAAAATTTTGTGATATTTTTGGTGGGATTGTATTGCCCTATTTTGTATATATTATAATCCTTGATTAAG... |
Task1_train_46849 | A mutation is present on Chromosome 19. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GTTCTTCACGGCTCCCAGTGAGCTGGGGGAGGATTTTGAGCCACGCGGCAGGGCCTAAGGATGCCCAGAGGGAAGGAGAGGGGCTTTCCTTCCCACCCTGGTGTCCATCCAGTCTCCCCAGTTCAGCCGGCAGGTGTGCACCAGGGCAGCCACCCGTTGGTCAGGCACCATGCTAGCTCCAAAGCCCGCTTCCTCCTGGGAAACTCTTGGAAAGCCGGACGTCCTTTGTGCCCTCAACCCCCATCCCCCGGGCGGTTTCGGTCCTAGCCTGCCGGAGGAGGGTGCCCTTGCCTAAAGGCGGATCCGAGTTCCCCTAGCCA... | GTTCTTCACGGCTCCCAGTGAGCTGGGGGAGGATTTTGAGCCACGCGGCAGGGCCTAAGGATGCCCAGAGGGAAGGAGAGGGGCTTTCCTTCCCACCCTGGTGTCCATCCAGTCTCCCCAGTTCAGCCGGCAGGTGTGCACCAGGGCAGCCACCCGTTGGTCAGGCACCATGCTAGCTCCAAAGCCCGCTTCCTCCTGGGAAACTCTTGGAAAGCCGGACGTCCTTTGTGCCCTCAACCCCCATCCCCCGGGCGGTTTCGGTCCTAGCCTGCCGGAGGAGGGTGCCCTTGCCTAAAGGCGGATCCGAGTTCCCCTAGCCA... |
Task1_train_46850 | A variant has been detected on Chromosome 19. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCTTGAACCCAAGAGGCAGAGGGTGCAGTGAGCCAAGATGGCACCATTGCACTCCAGCCTGGGCAACAGAGGAAAAAAAAAAGAACCTTCCCAGAAGCCTCCAGGAAGTCTCTGTTTGGACGACATCGCACACCCATTCTTGAACCAACTATTTAGAAGGGAGATGCATCACCCCCTTTGCCTGGAGCTAGGGGGTGGGTCAGCTTCCTACAGGCACAGGACTATGTGGTCGCGGGTTAAGCCCCTAAACGAGGGGAAGTGGGGTGGGCAGCAGCCGATCTCCATTACAAGGGACAAGAGTAGGGGCAGCAAGGCCAGAT... | GCTTGAACCCAAGAGGCAGAGGGTGCAGTGAGCCAAGATGGCACCATTGCACTCCAGCCTGGGCAACAGAGGAAAAAAAAAAGAACCTTCCCAGAAGCCTCCAGGAAGTCTCTGTTTGGACGACATCGCACACCCATTCTTGAACCAACTATTTAGAAGGGAGATGCATCACCCCCTTTGCCTGGAGCTAGGGGGTGGGTCAGCTTCCTACAGGCACAGGACTATGTGGTCGCGGGTTAAGCCCCTAAACGAGGGGAAGTGGGGTGGGCAGCAGCCGATCTCCATTACAAGGGACAAGAGTAGGGGCAGCAAGGCCAGAT... |
Task1_train_46851 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TCAGAATCCGGAACATCTCTCGGTGCTTAAGAGTTTTCCTTTAACAATCTTTACCTGTGGGAATGCAGAGACCCCCCCGCCCTGCGAGAGGCCGGCAGCCAGGGATTCCCCGCTCCGCGCCCTCATCACCCCCCGGAAACCACAACCGCTGCGCGCGCGGCTCGGACCCCCACCCGCCGCTCCCCTCCAGCAGACCCTAGGCCTCCGGGAAACCGCGCGGCGACCGCCCCGCGCCCCGCCAGATCCGAACCGCCGGACCCGGCACCCCGGCCACACCCGCCGGTGTCGACGCAGCGAGGCTCGGAGGGTGCATTCTCCGC... | TCAGAATCCGGAACATCTCTCGGTGCTTAAGAGTTTTCCTTTAACAATCTTTACCTGTGGGAATGCAGAGACCCCCCCGCCCTGCGAGAGGCCGGCAGCCAGGGATTCCCCGCTCCGCGCCCTCATCACCCCCCGGAAACCACAACCGCTGCGCGCGCGGCTCGGACCCCCACCCGCCGCTCCCCTCCAGCAGACCCTAGGCCTCCGGGAAACCGCGCGGCGACCGCCCCGCGCCCCGCCAGATCCGAACCGCCGGACCCGGCACCCCGGCCACACCCGCCGGTGTCGACGCAGCGAGGCTCGGAGGGTGCATTCTCCGC... |
Task1_train_46852 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCAGCACCTCTGTTTGCAGCTAGGCCTACAGCCCCGAGTCCTGAGAGTTCTGCTTTATCCTCTCCAGAGAATCAGCCCCTGGCCTTCCTCGGGTTGGGGTGAGTGGCCGTCTGGTGTGGAGTAGTGTAAGGTGATGCAGAGGTTCCCCCCTCTGCCACATTGCTGCAGCCAGGGAGCCTGCCCCTAATTCCTAAGCTTTCTGAAGGTTGTTCTCTGCAGATAGGGTCAGGCCTCCCGCGGCTGGCTCAGGGTCAACTGTCTTGGGGCTGTTACCAGTTTGTCCATCTGTTTTTTAGCTTCCAACATTCTGTTCTGGAATA... | TCAGCACCTCTGTTTGCAGCTAGGCCTACAGCCCCGAGTCCTGAGAGTTCTGCTTTATCCTCTCCAGAGAATCAGCCCCTGGCCTTCCTCGGGTTGGGGTGAGTGGCCGTCTGGTGTGGAGTAGTGTAAGGTGATGCAGAGGTTCCCCCCTCTGCCACATTGCTGCAGCCAGGGAGCCTGCCCCTAATTCCTAAGCTTTCTGAAGGTTGTTCTCTGCAGATAGGGTCAGGCCTCCCGCGGCTGGCTCAGGGTCAACTGTCTTGGGGCTGTTACCAGTTTGTCCATCTGTTTTTTAGCTTCCAACATTCTGTTCTGGAATA... |
Task1_train_46853 | Here is a mutation located on Chromosome 19. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTTTGCCTAGAATGTGAAAAAACTTCTTCTTTACTCCAAGCTCTTGATTTTATTCCAAGTCAGGCACAAAAGACCTTGATCTTCACCTGCTCTGTAGCTGAAACAGAAATAGTGTGTAAGGTGAGTCCATCTCCATATAAAAAATGTTCTGTTTGTTTCAACTGGTCGAATCTCAAGTCATCACAAAATTACTGGGGTGGTTGACTCTGTGGCAGGGAAGTAAAGTTTTACAAGTTTAACATCAATCAGAAGAGGAGGTGGGGTCTTCTCACAGAGCATGCAGGCTGAGGCCTGGATCTGGGGAGGAGCCAGGTGCGGGG... | CTTTGCCTAGAATGTGAAAAAACTTCTTCTTTACTCCAAGCTCTTGATTTTATTCCAAGTCAGGCACAAAAGACCTTGATCTTCACCTGCTCTGTAGCTGAAACAGAAATAGTGTGTAAGGTGAGTCCATCTCCATATAAAAAATGTTCTGTTTGTTTCAACTGGTCGAATCTCAAGTCATCACAAAATTACTGGGGTGGTTGACTCTGTGGCAGGGAAGTAAAGTTTTACAAGTTTAACATCAATCAGAAGAGGAGGTGGGGTCTTCTCACAGAGCATGCAGGCTGAGGCCTGGATCTGGGGAGGAGCCAGGTGCGGGG... |
Task1_train_46854 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AGCGTTCCCCAGGGCAGGGCAGTTTCGTCTTGGTGGAGTATTAAAAGTATCAATTTATAGACATGACAACATCTTCTGTACCCTCTGTTTAAGAAGATTGAGGTGGCTCATGCCTGAATCCTAGCCCTTTGGGAGGCCAAGGTAGGAAGATTGCTGGAAGCCAGGAGTTCAAGACCAGCCTGGGCAACATAGTGAAACCCTGTCTCTACGAAAAAAAAAAAAAAGAAGAAGAAAAAGAAGATTGAGAAGATAACAGTAAAAGATATCATATAGCCAAAAAATCAAATAAATTGGCTAAAGATTTATTCAGTTTTATTTTG... | AGCGTTCCCCAGGGCAGGGCAGTTTCGTCTTGGTGGAGTATTAAAAGTATCAATTTATAGACATGACAACATCTTCTGTACCCTCTGTTTAAGAAGATTGAGGTGGCTCATGCCTGAATCCTAGCCCTTTGGGAGGCCAAGGTAGGAAGATTGCTGGAAGCCAGGAGTTCAAGACCAGCCTGGGCAACATAGTGAAACCCTGTCTCTACGAAAAAAAAAAAAAAGAAGAAGAAAAAGAAGATTGAGAAGATAACAGTAAAAGATATCATATAGCCAAAAAATCAAATAAATTGGCTAAAGATTTATTCAGTTTTATTTTG... |
Task1_train_46855 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CAGGCTTGGTGGCTCATGATTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGAGGATTGCTCAAGCTCAGGAGTTCGAGACCAGCCTGGGCAACATAGCAAGACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGTTTGGTGGTACAAGCCTGTAGTTCTAGCTACTTGGGACACTGAGGTGGGAAGATTGGTTGAGCCCAGGAGGTTTAGGCTGCAGTGAGCTGTGATTGTGCCACTGCACTCCAGCCTGGGTGACAGCAAGACCTTGTCTCAAAAAAAAAAAAAATGACAAAGATAAACATAGTATGATCTAAA... | CAGGCTTGGTGGCTCATGATTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGAGGATTGCTCAAGCTCAGGAGTTCGAGACCAGCCTGGGCAACATAGCAAGACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGTTTGGTGGTACAAGCCTGTAGTTCTAGCTACTTGGGACACTGAGGTGGGAAGATTGGTTGAGCCCAGGAGGTTTAGGCTGCAGTGAGCTGTGATTGTGCCACTGCACTCCAGCCTGGGTGACAGCAAGACCTTGTCTCAAAAAAAAAAAAAATGACAAAGATAAACATAGTATGATCTAAA... |
Task1_train_46856 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTGCTGCCTGCTCTTGCCCTCCTAGCTGTAGCTGTGCTCTGTGCAAGCAAACACGATCTCGGGACCCTAAACTCCCTCTGCCAAAGGGGAAGTTACACGCTGGACCTGGGTCTAAGCCTGTCTGCTTTTGTTCGCAAGCAGACAGCTGTCGCTTCATAGCCCTGGGTCGTAGCCCCGTGTCCTGTTATGTCTCCTGTCACATGTCACTTTATCTTGTGTAAAGCTAGCTTTCCTGAGCTCGAGGGGATGCGTGATTGTCTTTGTCCTGCCCCACCCCCCGCCGCCCTTTCTTCCTCCAGCTTGCTCTCCCTTTTAGACAC... | CTGCTGCCTGCTCTTGCCCTCCTAGCTGTAGCTGTGCTCTGTGCAAGCAAACACGATCTCGGGACCCTAAACTCCCTCTGCCAAAGGGGAAGTTACACGCTGGACCTGGGTCTAAGCCTGTCTGCTTTTGTTCGCAAGCAGACAGCTGTCGCTTCATAGCCCTGGGTCGTAGCCCCGTGTCCTGTTATGTCTCCTGTCACATGTCACTTTATCTTGTGTAAAGCTAGCTTTCCTGAGCTCGAGGGGATGCGTGATTGTCTTTGTCCTGCCCCACCCCCCGCCGCCCTTTCTTCCTCCAGCTTGCTCTCCCTTTTAGACAC... |
Task1_train_46857 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGCTGCCTCTCTCAGACTCCAGAGCAGTTCACATGGAACTGTTTATAAAGCAAAATAAGCCAGAGATAAAGGAAGACCAAGCTCTTCCCTCCCTTAGGAGCCACTGCTCTGTCCCAAACCAAACCAAACTCTAAGCGTGCATAGTGAGCTCATAAGAAACCATTCGCTGGCCGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGATGGGCGAATCTCTTGAGGTTGGGAGTTCAAGACCAGCCTGGCCAACATGGCAAAATCTCATCTCTACTAAAAAAATACAAAAATGAGTGAGCTGAGATTG... | TGCTGCCTCTCTCAGACTCCAGAGCAGTTCACATGGAACTGTTTATAAAGCAAAATAAGCCAGAGATAAAGGAAGACCAAGCTCTTCCCTCCCTTAGGAGCCACTGCTCTGTCCCAAACCAAACCAAACTCTAAGCGTGCATAGTGAGCTCATAAGAAACCATTCGCTGGCCGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGATGGGCGAATCTCTTGAGGTTGGGAGTTCAAGACCAGCCTGGCCAACATGGCAAAATCTCATCTCTACTAAAAAAATACAAAAATGAGTGAGCTGAGATTG... |
Task1_train_46858 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | ATCTCAGGACACCTCACCATCCATCATAGGCCCAGAGTCCATTGTAAAACGCCAGGCTGATGGCTCCCACAGACAGCTGGGCGCCCTCGAAAGAATTATCAAAATTCTTTGTGTTTCCTGTAATGAAGCCAGACAGTGAACGGCGGGTGTCAACCGGGCAGATCTTGAGTGTATCTCCACGGGAAAGATGGGCATGATTGTGACCCCAGCTTAATAAACACGCCCTGAAACTAAGGATCCCTCCCACCGAGTTCCTGCCATGCTTCCTTGGAGATGGGCTCGTGGGGCAAGGCTGCTCCTGCTCCCAGTGGAAGGGCGTT... | ATCTCAGGACACCTCACCATCCATCATAGGCCCAGAGTCCATTGTAAAACGCCAGGCTGATGGCTCCCACAGACAGCTGGGCGCCCTCGAAAGAATTATCAAAATTCTTTGTGTTTCCTGTAATGAAGCCAGACAGTGAACGGCGGGTGTCAACCGGGCAGATCTTGAGTGTATCTCCACGGGAAAGATGGGCATGATTGTGACCCCAGCTTAATAAACACGCCCTGAAACTAAGGATCCCTCCCACCGAGTTCCTGCCATGCTTCCTTGGAGATGGGCTCGTGGGGCAAGGCTGCTCCTGCTCCCAGTGGAAGGGCGTT... |
Task1_train_46859 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ACAGTTTTCAATCCCAGTGAGTCTTTCTACCGCTTGTAAAATAAAATTAAATTACAATGATTCAACTGTTGAACAAGCTTATAGAGTCATAAAAGAACTATGATTTTCTATCTCACCCTTCCGTCTGGCAATCAAAGATCACACGTAGAACTTCTACACATGACCAAGGACCAGTACTGGGGCCTCCTTCCCACCTGAAACAAGGCAGGACTTCACTGCGAGGGGCTCTGAAAAGGAGATGCTGCAGGGTGCCACCCCTGAGTCCCACAGTTAGGGTCCTTTGTAGCCCAATGTCCCCAAGTCCCTCCAGCATGCCTGGG... | ACAGTTTTCAATCCCAGTGAGTCTTTCTACCGCTTGTAAAATAAAATTAAATTACAATGATTCAACTGTTGAACAAGCTTATAGAGTCATAAAAGAACTATGATTTTCTATCTCACCCTTCCGTCTGGCAATCAAAGATCACACGTAGAACTTCTACACATGACCAAGGACCAGTACTGGGGCCTCCTTCCCACCTGAAACAAGGCAGGACTTCACTGCGAGGGGCTCTGAAAAGGAGATGCTGCAGGGTGCCACCCCTGAGTCCCACAGTTAGGGTCCTTTGTAGCCCAATGTCCCCAAGTCCCTCCAGCATGCCTGGG... |
Task1_train_46860 | A variant has been detected on Chromosome 19. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CGTGGGCCATCACACTGGAGCAAAGGGCAGATTTCAAATCCCAACAAATGCAGGATTGGGGAACACTGCGGGGCTGTGGATTTGAAAGCAGGGCCTGCCTTTCTTTCCTTTCTTTCACTGGTTTTATTTTAAGGAAACGCAGACAAGTTGGATTTGTGGCTGTATACAATGCTAGGGAAGGAATCTGGGGTTCCAGAATCTGCCAAGGTCTCTTGAGCCCCAGCCTGGCTAAGCTGCTTTCCAGTCCACTGTTCAAGGAGGGTGCGAGGGGAGACACACTAGGAACCCTGAAGGAAGAAAATCCAAGCTCAGCCAGGGAG... | CGTGGGCCATCACACTGGAGCAAAGGGCAGATTTCAAATCCCAACAAATGCAGGATTGGGGAACACTGCGGGGCTGTGGATTTGAAAGCAGGGCCTGCCTTTCTTTCCTTTCTTTCACTGGTTTTATTTTAAGGAAACGCAGACAAGTTGGATTTGTGGCTGTATACAATGCTAGGGAAGGAATCTGGGGTTCCAGAATCTGCCAAGGTCTCTTGAGCCCCAGCCTGGCTAAGCTGCTTTCCAGTCCACTGTTCAAGGAGGGTGCGAGGGGAGACACACTAGGAACCCTGAAGGAAGAAAATCCAAGCTCAGCCAGGGAG... |
Task1_train_46861 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CTGGGACTACAGGTGTGAGCCACCATGCGCAGCTCCCAAACCTGTTATTATTAATCATTCTTTATAGTAAATTTTCCCTCTTCAAGTCATTGTGTGTGTTCTGACTCCTGATTGGACCTTGACTGATATATGCTACATCAGGCCACACAATGCAGATGTTACACAAGGCAGGAGAGAACCAAATCTGGGGACATAGAAAGACATTTGGCATGTGTTGTGAGATGAAAGAAAGGTAACAAAACAGCATGCACTTTATATACATATACTCTCTAAATTGTTAAAAATCTTATCTGTGGGAGCACAATTAAGTGTGTTTAGCT... | CTGGGACTACAGGTGTGAGCCACCATGCGCAGCTCCCAAACCTGTTATTATTAATCATTCTTTATAGTAAATTTTCCCTCTTCAAGTCATTGTGTGTGTTCTGACTCCTGATTGGACCTTGACTGATATATGCTACATCAGGCCACACAATGCAGATGTTACACAAGGCAGGAGAGAACCAAATCTGGGGACATAGAAAGACATTTGGCATGTGTTGTGAGATGAAAGAAAGGTAACAAAACAGCATGCACTTTATATACATATACTCTCTAAATTGTTAAAAATCTTATCTGTGGGAGCACAATTAAGTGTGTTTAGCT... |
Task1_train_46862 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | AGTCATTATCCTGCCCTTTCGCTGGTGAAAACGTCAACCTAGAGGCCAGGCGTGATGGCTCATGCTTGTAATCCCAGCACTTTGGGAGGCGGAGGCGGGAGGATCACTTGAGGCCAGCAGTTCGAGACCAGCCTGGCCAACATGGCAAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGTGGGTGCATGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCACCTGAACTGAGGAGGTGGAGGTTGCAGTGAGTGGAGATGCTCCATTGCACTCCAGCCTGAGCAACAGGAGCGAAACTTT... | AGTCATTATCCTGCCCTTTCGCTGGTGAAAACGTCAACCTAGAGGCCAGGCGTGATGGCTCATGCTTGTAATCCCAGCACTTTGGGAGGCGGAGGCGGGAGGATCACTTGAGGCCAGCAGTTCGAGACCAGCCTGGCCAACATGGCAAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGTGGGTGCATGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCACCTGAACTGAGGAGGTGGAGGTTGCAGTGAGTGGAGATGCTCCATTGCACTCCAGCCTGAGCAACAGGAGCGAAACTTT... |
Task1_train_46863 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ATCACTTGAGGCCAGCAGTTCGAGACCAGCCTGGCCAACATGGCAAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGTGGGTGCATGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCACCTGAACTGAGGAGGTGGAGGTTGCAGTGAGTGGAGATGCTCCATTGCACTCCAGCCTGAGCAACAGGAGCGAAACTTTGTCTCAAAAAAAGAAAGAAAGAAAGAAAATGTTAACTAGAAGCTGCTTTGTCTCATCCCGTATTTTTGTTAAGCATCAGCACCTTGTGCAAGTTTTTTTTTT... | ATCACTTGAGGCCAGCAGTTCGAGACCAGCCTGGCCAACATGGCAAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGTGGGTGCATGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCACCTGAACTGAGGAGGTGGAGGTTGCAGTGAGTGGAGATGCTCCATTGCACTCCAGCCTGAGCAACAGGAGCGAAACTTTGTCTCAAAAAAAGAAAGAAAGAAAGAAAATGTTAACTAGAAGCTGCTTTGTCTCATCCCGTATTTTTGTTAAGCATCAGCACCTTGTGCAAGTTTTTTTTTT... |
Task1_train_46864 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | CACCCCGGTGCCCTGCAGAGGACCAGCACCAGGAAACACACATTCCATAGGTGACTCAAGGTTCCCAAATCCCGGGAGCTATTTTCCGACTGAGTTTCCCCTGGGGCCCACCTACTTTTTGAGAAGTCTCATGCCCACACTGAAGAAGCACGTAAACCCTTCTCTGAACTGTCTCAAAGTTATTTCTCCTTAAAAAGAAGCATTTCGCTTAGGGTTCTGTTTTGTTTTTGTGTTTTTTGAGACAGGACTTTTTTCTGTTGCCATTACTACAGTCTCGACCTCCCTGGCTCAAGTGATCTTCCCACCTCAGCCTTCTGAGT... | CACCCCGGTGCCCTGCAGAGGACCAGCACCAGGAAACACACATTCCATAGGTGACTCAAGGTTCCCAAATCCCGGGAGCTATTTTCCGACTGAGTTTCCCCTGGGGCCCACCTACTTTTTGAGAAGTCTCATGCCCACACTGAAGAAGCACGTAAACCCTTCTCTGAACTGTCTCAAAGTTATTTCTCCTTAAAAAGAAGCATTTCGCTTAGGGTTCTGTTTTGTTTTTGTGTTTTTTGAGACAGGACTTTTTTCTGTTGCCATTACTACAGTCTCGACCTCCCTGGCTCAAGTGATCTTCCCACCTCAGCCTTCTGAGT... |
Task1_train_46865 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | TGTAGGAGGCCTAATTCTTTTTTTTTTCTTAATTTTTAATTTTTATTTTTTTTTATTATACTTTAAGTTCTAGGGTACATGTGCACAACGTGCAGGTTTGTTACATGTGTATACATGTGCCACGTTCGTGTGCTGCACCTATTAACTCGTCATTTACATAAGGTATATCTCCTAATGCTATCCCTCCCCGCTTCCCCGGGAGGCCTAATTCTTAGCTCCTCTCTTTTCGGTCCTCCCGCACCCTCCCTGACCCTCCTTGGCCCTTAGTGAGTCCTCTCGGCTCTACCCACACGTGTGGGGGTTCTGTCCACTACTCATCT... | TGTAGGAGGCCTAATTCTTTTTTTTTTCTTAATTTTTAATTTTTATTTTTTTTTATTATACTTTAAGTTCTAGGGTACATGTGCACAACGTGCAGGTTTGTTACATGTGTATACATGTGCCACGTTCGTGTGCTGCACCTATTAACTCGTCATTTACATAAGGTATATCTCCTAATGCTATCCCTCCCCGCTTCCCCGGGAGGCCTAATTCTTAGCTCCTCTCTTTTCGGTCCTCCCGCACCCTCCCTGACCCTCCTTGGCCCTTAGTGAGTCCTCTCGGCTCTACCCACACGTGTGGGGGTTCTGTCCACTACTCATCT... |
Task1_train_46866 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | TTTCCAATGTACTGGAGCATAAATGTTATAGCACAAACTTTTTTCACAGTTCTAGAAGATTGCTTGAAAATTTTAAATGGGAGAGCAGTCAGGTCAGTGGTGCGGCCACTTGATGGAACAGAATGCATGTCTTTTTCCAGAATGATGTCGGGGATAAGCAGTCGGCTGTGAAGATGAAGATGTTTGGGAAGCTCACCCGAGACACGTTTGAGTGGCACCCTGACAAGCTTCTATGTAAGAGATTTAATGTCCCTGACCCTTATCCAGAGTAAGTTGGATAAACCTTTACATCAGTACAAAATGTATTCTTGATATTAAAG... | TTTCCAATGTACTGGAGCATAAATGTTATAGCACAAACTTTTTTCACAGTTCTAGAAGATTGCTTGAAAATTTTAAATGGGAGAGCAGTCAGGTCAGTGGTGCGGCCACTTGATGGAACAGAATGCATGTCTTTTTCCAGAATGATGTCGGGGATAAGCAGTCGGCTGTGAAGATGAAGATGTTTGGGAAGCTCACCCGAGACACGTTTGAGTGGCACCCTGACAAGCTTCTATGTAAGAGATTTAATGTCCCTGACCCTTATCCAGAGTAAGTTGGATAAACCTTTACATCAGTACAAAATGTATTCTTGATATTAAAG... |
Task1_train_46867 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | CTATGTGTTCTCACTGTTCAACTCCCACTTATGAATGAGAACGTGTGGTGTTTGGTCTTCTGTTCCTGTGTTAGTTTGCTGAGGATGATGTCCCTGCAAAGGACATGATCTCATTCTTTCTCATGGCTGCATAGTATTCCATGGTGTATATGTACCACATTTTCTTTATCCGGTCTATCATTGATGGGCATTTGGGTTGACACGAAGTCTTTGCTATTGTGAATAATGCTGCAATAAACATACGTGTGCATGTGTATTTATAGAAGAATGATTTATAATCCTCTGGGTATACCTCTGGTTTAAACCTCAATGACAGTGTC... | CTATGTGTTCTCACTGTTCAACTCCCACTTATGAATGAGAACGTGTGGTGTTTGGTCTTCTGTTCCTGTGTTAGTTTGCTGAGGATGATGTCCCTGCAAAGGACATGATCTCATTCTTTCTCATGGCTGCATAGTATTCCATGGTGTATATGTACCACATTTTCTTTATCCGGTCTATCATTGATGGGCATTTGGGTTGACACGAAGTCTTTGCTATTGTGAATAATGCTGCAATAAACATACGTGTGCATGTGTATTTATAGAAGAATGATTTATAATCCTCTGGGTATACCTCTGGTTTAAACCTCAATGACAGTGTC... |
Task1_train_46868 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CGAGTGTGGAGACGGCTCTGATGAGGGCAACTGCTCGGCGCCCGCCTCCGAGCCTCCAGGCAGCCTGTGCCCCGGGGGGACCTTCCCATGCAGCGGGGCGCGCTCCACGCGCTGCCTGCCTGTGGAGCGGCGCTGTGACGGCTTGCAGGACTGCGGCGACGGCTCGGATGAGGCGGGCTGCCCCGACCTGGCGTGCGGCCGGCGGCTGGGCAGCTTCTACGGCTCCTTTGCCTCCCCAGACCTGTTCGGCGCCGCTCGCGGGCCCTCAGACCTTCACTGCACGTGGCTGGTGGACACACAGGACTCCCGGCGGGTGCTGC... | CGAGTGTGGAGACGGCTCTGATGAGGGCAACTGCTCGGCGCCCGCCTCCGAGCCTCCAGGCAGCCTGTGCCCCGGGGGGACCTTCCCATGCAGCGGGGCGCGCTCCACGCGCTGCCTGCCTGTGGAGCGGCGCTGTGACGGCTTGCAGGACTGCGGCGACGGCTCGGATGAGGCGGGCTGCCCCGACCTGGCGTGCGGCCGGCGGCTGGGCAGCTTCTACGGCTCCTTTGCCTCCCCAGACCTGTTCGGCGCCGCTCGCGGGCCCTCAGACCTTCACTGCACGTGGCTGGTGGACACACAGGACTCCCGGCGGGTGCTGC... |
Task1_train_46869 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | GGACTGAGCTGCTACCCCATCCTCGACATCCCTTTAGGGCAGGGGGACTCTGGGTGCCATGGTAGGGAGCGCCTGTGTCAAGCAGCAAAGCCCCCTAATGTCAAGAGCCTCCTCCAGGGCCTGCCACGGCATCTTCCTGGCCAGCAACATGTGTGCACCCACCGAGGTACGCCCCAGCCACTCCCATCTGTGCCCATCAGGGACTCCCCATAGCACGAGCGAACAGCCAGCCCTGTTTATTTATAGGCCTTTTCAGGAAGAGCTAGCAGGGCAGTGCTAAGACAGGAAACCCAGTCCACATTTTAGGGCTTCCTTAAACA... | GGACTGAGCTGCTACCCCATCCTCGACATCCCTTTAGGGCAGGGGGACTCTGGGTGCCATGGTAGGGAGCGCCTGTGTCAAGCAGCAAAGCCCCCTAATGTCAAGAGCCTCCTCCAGGGCCTGCCACGGCATCTTCCTGGCCAGCAACATGTGTGCACCCACCGAGGTACGCCCCAGCCACTCCCATCTGTGCCCATCAGGGACTCCCCATAGCACGAGCGAACAGCCAGCCCTGTTTATTTATAGGCCTTTTCAGGAAGAGCTAGCAGGGCAGTGCTAAGACAGGAAACCCAGTCCACATTTTAGGGCTTCCTTAAACA... |
Task1_train_46870 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCCACGGCATCTTCCTGGCCAGCAACATGTGTGCACCCACCGAGGTACGCCCCAGCCACTCCCATCTGTGCCCATCAGGGACTCCCCATAGCACGAGCGAACAGCCAGCCCTGTTTATTTATAGGCCTTTTCAGGAAGAGCTAGCAGGGCAGTGCTAAGACAGGAAACCCAGTCCACATTTTAGGGCTTCCTTAAACAGGCTTCTGAGAGTCGTATCTTTTTTCTTTTTTTTCCAGAAAAAAACAAAACAAAACTTTTTTGCCAAAACACCTCCTCAATAAACAACATGTAAACAGAAACAACTGCTTCAGTCTCTACAA... | GCCACGGCATCTTCCTGGCCAGCAACATGTGTGCACCCACCGAGGTACGCCCCAGCCACTCCCATCTGTGCCCATCAGGGACTCCCCATAGCACGAGCGAACAGCCAGCCCTGTTTATTTATAGGCCTTTTCAGGAAGAGCTAGCAGGGCAGTGCTAAGACAGGAAACCCAGTCCACATTTTAGGGCTTCCTTAAACAGGCTTCTGAGAGTCGTATCTTTTTTCTTTTTTTTCCAGAAAAAAACAAAACAAAACTTTTTTGCCAAAACACCTCCTCAATAAACAACATGTAAACAGAAACAACTGCTTCAGTCTCTACAA... |
Task1_train_46871 | 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 | GCTACAGTTTTCCACCCCCTCATCCTCATGGTTTCATCTGTGGCATCCTTCTCACTTGTCATCTTTCACCTTGGCTTGGGAACTCTTGGATGGGAGCTCTGTGAGAAGGCAAACCTGGAATGGTGTACAGAATTCTAGAAACCAGCTCCAGGGGTGGGCTGTTCTGCGGGACCCTGGGAGAACTGGACAAGCAGAGGCAAGGACAGATACTTCACCAGGCATGGCTGGGCCCTGGCTGGCTTCCTGCCTGGTAGAATTTGTTCAAGGACTACACTTAGGGAGGACAAGCGGTCTCTGCAAATTGGCTGTGGCGCTGCCTT... | GCTACAGTTTTCCACCCCCTCATCCTCATGGTTTCATCTGTGGCATCCTTCTCACTTGTCATCTTTCACCTTGGCTTGGGAACTCTTGGATGGGAGCTCTGTGAGAAGGCAAACCTGGAATGGTGTACAGAATTCTAGAAACCAGCTCCAGGGGTGGGCTGTTCTGCGGGACCCTGGGAGAACTGGACAAGCAGAGGCAAGGACAGATACTTCACCAGGCATGGCTGGGCCCTGGCTGGCTTCCTGCCTGGTAGAATTTGTTCAAGGACTACACTTAGGGAGGACAAGCGGTCTCTGCAAATTGGCTGTGGCGCTGCCTT... |
Task1_train_46872 | A mutation on Chromosome 19 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GTAATGAAACAGGATGTACTCCACGAGATGTTTCAATATGTTCTCAGTCCAAATTCTACATCTTTCAATTAAAAAATGCATCACCATTGCATTATATACCACAGATCATTAAATACCTATCACTGTCCATATCCAAGTCTCCCAGTGGAAGAGATGGCTGACATTTAGCTAGGAACTTTTAAAACACTTGAGAATAAATTATGACCCAAACTTACTGTTCTTAATGACACGTATAAAGTTCAGCTCTTAAATAAAAGGATTCAGGAATACAGAAACAAAGTCCCCAGCCGTACTAAGGAAATAAAAGTCGTCCAGTTCTT... | GTAATGAAACAGGATGTACTCCACGAGATGTTTCAATATGTTCTCAGTCCAAATTCTACATCTTTCAATTAAAAAATGCATCACCATTGCATTATATACCACAGATCATTAAATACCTATCACTGTCCATATCCAAGTCTCCCAGTGGAAGAGATGGCTGACATTTAGCTAGGAACTTTTAAAACACTTGAGAATAAATTATGACCCAAACTTACTGTTCTTAATGACACGTATAAAGTTCAGCTCTTAAATAAAAGGATTCAGGAATACAGAAACAAAGTCCCCAGCCGTACTAAGGAAATAAAAGTCGTCCAGTTCTT... |
Task1_train_46873 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CATTTTTTTTAAGCAAAACATTATATTTTGGAATAATTATGAGATGTGAGTGCCTAAGCAGAGATGTACAGCAAACATTATCAGGACAGAAAGCATGATGGGAGCACCCGATGTTACATTCTTCAGTTCATGCTGTGACCAGGCGACCTCATAAAAGGAAAAATATAATGTATAAGTACAAACCCCATTTTTTGTTTTGGCTCTTTTATATTTGTATTTTTTGAGACAGAGTCTAGTTTTGTCACCCAGGCTGGATGCAGTGGACCGATCTCGGCTCACTACAACCTCTGCCTCCCAGGCTCAAGCAATCCACCCACTTC... | CATTTTTTTTAAGCAAAACATTATATTTTGGAATAATTATGAGATGTGAGTGCCTAAGCAGAGATGTACAGCAAACATTATCAGGACAGAAAGCATGATGGGAGCACCCGATGTTACATTCTTCAGTTCATGCTGTGACCAGGCGACCTCATAAAAGGAAAAATATAATGTATAAGTACAAACCCCATTTTTTGTTTTGGCTCTTTTATATTTGTATTTTTTGAGACAGAGTCTAGTTTTGTCACCCAGGCTGGATGCAGTGGACCGATCTCGGCTCACTACAACCTCTGCCTCCCAGGCTCAAGCAATCCACCCACTTC... |
Task1_train_46874 | A variant affecting Chromosome 19 has been observed. Determine if it's benign or associated with disease. | Benign | CTTAGAAGATAAACTTGAGAAACAGGAGAAGCCTGTAAATGGTGAAGATAAAGGAGACTCAGGAGTTGATACCCAAAACAGTGAAGGAAATGCCGATGAAGAAGATCCACTTGGACCTAATTGCTATTATGACAAAACTAAATCCTTCTTTGATAATATTTCTTGTGATGACAATAGGTACAGTTTTTAAGCTGTTCTTTTATCTTATGATATTGATTGAAGTGTAAAATGGTTTCATGTAAATTCACGAGGTTTAATGAATACTACCATAATTGTTTTGTTTTGTTTTGAGACAGTCTTACTCTGTTACTCAGGCTGGA... | CTTAGAAGATAAACTTGAGAAACAGGAGAAGCCTGTAAATGGTGAAGATAAAGGAGACTCAGGAGTTGATACCCAAAACAGTGAAGGAAATGCCGATGAAGAAGATCCACTTGGACCTAATTGCTATTATGACAAAACTAAATCCTTCTTTGATAATATTTCTTGTGATGACAATAGGTACAGTTTTTAAGCTGTTCTTTTATCTTATGATATTGATTGAAGTGTAAAATGGTTTCATGTAAATTCACGAGGTTTAATGAATACTACCATAATTGTTTTGTTTTGTTTTGAGACAGTCTTACTCTGTTACTCAGGCTGGA... |
Task1_train_46875 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTGCCTATATTTTTTTGGGGGTGACACTTGTTAATTTGTAAGAGCTCTTTACGTATAGGGACATCAGTTTTCTAACCTGTAAGGAAGTCTTGGCTGGGAGTTGAAACCCCAGGCTAGAAGGCGACCCTTAGACTTTTTAGGTCTGATGGCGGGCCTATGCTGGTGTGGGAATAACACCGCCGGTCTCAGCTGGAGGTCGCCAGCCCTTTGCAAGAGCCTGCCGGTCCCCGCGGGCTGCAGCACACCCCGGCGCGATGTGCCCTGCCTGTGTCTGCCGGAGGCTGTAGTGCGCAGGAGCGGAAACCAGGCCGCCCTTCCCC... | TTGCCTATATTTTTTTGGGGGTGACACTTGTTAATTTGTAAGAGCTCTTTACGTATAGGGACATCAGTTTTCTAACCTGTAAGGAAGTCTTGGCTGGGAGTTGAAACCCCAGGCTAGAAGGCGACCCTTAGACTTTTTAGGTCTGATGGCGGGCCTATGCTGGTGTGGGAATAACACCGCCGGTCTCAGCTGGAGGTCGCCAGCCCTTTGCAAGAGCCTGCCGGTCCCCGCGGGCTGCAGCACACCCCGGCGCGATGTGCCCTGCCTGTGTCTGCCGGAGGCTGTAGTGCGCAGGAGCGGAAACCAGGCCGCCCTTCCCC... |
Task1_train_46876 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCCAAAAGGATATCCCAATTTGCACTCATACCAGTAGCATATGTGCAACTGTTTCACCACAGTCCTGCCAATATTGTAATTTTTAAATAGTAGATAATGCAGTCCATGAAATGTGATATGACTGAACTGGCTTTTCCTTTCTCATTTGAAAGGTAGACCATTTTTCATGTCCTGGCTTCCCTGGGTATTTGCTCTCCCAAATGCTGGCTTCTAGACCCCGCACGGAGTCTCATGCCTGTAATCTCAGCGTTTTGTGTGGTGGTGTGCGCCTGTACTCCTACGTACTCAGGAGTCCGAGGTGGGAGGATTGCTTGAGCCCA... | CCCAAAAGGATATCCCAATTTGCACTCATACCAGTAGCATATGTGCAACTGTTTCACCACAGTCCTGCCAATATTGTAATTTTTAAATAGTAGATAATGCAGTCCATGAAATGTGATATGACTGAACTGGCTTTTCCTTTCTCATTTGAAAGGTAGACCATTTTTCATGTCCTGGCTTCCCTGGGTATTTGCTCTCCCAAATGCTGGCTTCTAGACCCCGCACGGAGTCTCATGCCTGTAATCTCAGCGTTTTGTGTGGTGGTGTGCGCCTGTACTCCTACGTACTCAGGAGTCCGAGGTGGGAGGATTGCTTGAGCCCA... |
Task1_train_46877 | A mutation is present on Chromosome 19. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GCACGAGAATCGCTTGAACTGGGGAGACTGAGGTTGCAGTGAGCCGAGTTCACACCACTGCACTCCAGCCTGGGTGACAGAGCTAGACGCTATCTCAAAAATAAATAAATAAATAAATAAATAAATAAATAAATGAATATAAATAAAACTGGTTAAAAATTGAGTCTCCCTGAAGTAGGTGCTCTTTCCCGTGAAAACTACTTTTTTGGTTTGGTTTGAAGGTAAGAAAGAGCGGGAGAAACTTTGCTCTTTTCATTTAATAATTGTGTTCAGCCTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGA... | GCACGAGAATCGCTTGAACTGGGGAGACTGAGGTTGCAGTGAGCCGAGTTCACACCACTGCACTCCAGCCTGGGTGACAGAGCTAGACGCTATCTCAAAAATAAATAAATAAATAAATAAATAAATAAATAAATGAATATAAATAAAACTGGTTAAAAATTGAGTCTCCCTGAAGTAGGTGCTCTTTCCCGTGAAAACTACTTTTTTGGTTTGGTTTGAAGGTAAGAAAGAGCGGGAGAAACTTTGCTCTTTTCATTTAATAATTGTGTTCAGCCTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGA... |
Task1_train_46878 | A mutation is present on Chromosome 19. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CAATACATGCTTTTTTGGGGAACATAATCAAACCATATGTCTATCAGTCTTTAATATTAAGATGTCTTTTTTTTCTGAACCCATTTTTTGTGAGATTTAGTGAATCTTTCTGAGTATCATATTTGAGAGACAATTGCTTTAGCCTTATTTTTAATTACTTAGCTAGCATGTAAGCTATAAAAGATATAACTAAATACTTGACTCTGTGCTGTCAAATGTCAAATGTTGATTTTTAAAAATTCATATAATTCTAAACTTTTAACAAAATTACTGAAGCAAAGCTCTCATATTTGTCTCTCATTCTTATTGTATAAAAATTC... | CAATACATGCTTTTTTGGGGAACATAATCAAACCATATGTCTATCAGTCTTTAATATTAAGATGTCTTTTTTTTCTGAACCCATTTTTTGTGAGATTTAGTGAATCTTTCTGAGTATCATATTTGAGAGACAATTGCTTTAGCCTTATTTTTAATTACTTAGCTAGCATGTAAGCTATAAAAGATATAACTAAATACTTGACTCTGTGCTGTCAAATGTCAAATGTTGATTTTTAAAAATTCATATAATTCTAAACTTTTAACAAAATTACTGAAGCAAAGCTCTCATATTTGTCTCTCATTCTTATTGTATAAAAATTC... |
Task1_train_46879 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | CTGACATCACATTCCCAGTCATTGTCACAGCTCCTGAATCTTGTTCCATTTCTTCCACAAGCAGGCTAATTTTACCCCTTCTTCAGTGACAGAAGAGGCCTGGGCTATGGCTGAGCCTAAATATATTTGCTATTTCAGGTGACATTTAGTGATGTGGCTATAGACTTCTCTCATGAAGAGTGGGCATGCCTAGATTCTGCTCAGAGGGACTTATACAAGGATGTGATGGTCCAGAATTATGAGAACCTGGTCTCTGTAGGTAAGGATATCACCCCTTCCACTCCAATAGGGGACACCTTTCTTTTGCCACCCTGAATTGC... | CTGACATCACATTCCCAGTCATTGTCACAGCTCCTGAATCTTGTTCCATTTCTTCCACAAGCAGGCTAATTTTACCCCTTCTTCAGTGACAGAAGAGGCCTGGGCTATGGCTGAGCCTAAATATATTTGCTATTTCAGGTGACATTTAGTGATGTGGCTATAGACTTCTCTCATGAAGAGTGGGCATGCCTAGATTCTGCTCAGAGGGACTTATACAAGGATGTGATGGTCCAGAATTATGAGAACCTGGTCTCTGTAGGTAAGGATATCACCCCTTCCACTCCAATAGGGGACACCTTTCTTTTGCCACCCTGAATTGC... |
Task1_train_46880 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | GCATGCCTAGATTCTGCTCAGAGGGACTTATACAAGGATGTGATGGTCCAGAATTATGAGAACCTGGTCTCTGTAGGTAAGGATATCACCCCTTCCACTCCAATAGGGGACACCTTTCTTTTGCCACCCTGAATTGCTGGAGATTCTCCTAAGTAAATGGCTGAATTTCTGTACCATGCTCCCGAGGAAATGTGCAGCTCTGTTGTGCCCTGCCTAAAGCTTATCTTTCCATTTCAGTGAACACCCTTCATCCATTCCTGTGGTCCCTCTTGTGATGGCCTCTCATAATAGAGGACCACAGCTTAAACAATTCTATATTT... | GCATGCCTAGATTCTGCTCAGAGGGACTTATACAAGGATGTGATGGTCCAGAATTATGAGAACCTGGTCTCTGTAGGTAAGGATATCACCCCTTCCACTCCAATAGGGGACACCTTTCTTTTGCCACCCTGAATTGCTGGAGATTCTCCTAAGTAAATGGCTGAATTTCTGTACCATGCTCCCGAGGAAATGTGCAGCTCTGTTGTGCCCTGCCTAAAGCTTATCTTTCCATTTCAGTGAACACCCTTCATCCATTCCTGTGGTCCCTCTTGTGATGGCCTCTCATAATAGAGGACCACAGCTTAAACAATTCTATATTT... |
Task1_train_46881 | 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 | CTCCTTTTCTCCTCTCTGGATTTTCTAGCTTTTGAACTTCTCAGATAGAGGAACCCCAGTGAAGACTGATCAGTTCTTACAATTCTCAAAGCATGGCCCATGTAAGTTGGTGTTTCTTCTTGAAATATGGGGATTTTTATATTACGTGGCTATTTTCCTTAATTGACCTGAAGCATTCTTCATCAGAATGTACCATCTAATTGCCTACTTGATTCCTTCTGTTTGGCGGAATGATGTCAAAGTATCGTTTCCTCCTTACGAGGTCCTCATTTCTAATCGGTGTTCATGAATTCATTGAGCAAGTTACGAAGCAGGTAAAT... | CTCCTTTTCTCCTCTCTGGATTTTCTAGCTTTTGAACTTCTCAGATAGAGGAACCCCAGTGAAGACTGATCAGTTCTTACAATTCTCAAAGCATGGCCCATGTAAGTTGGTGTTTCTTCTTGAAATATGGGGATTTTTATATTACGTGGCTATTTTCCTTAATTGACCTGAAGCATTCTTCATCAGAATGTACCATCTAATTGCCTACTTGATTCCTTCTGTTTGGCGGAATGATGTCAAAGTATCGTTTCCTCCTTACGAGGTCCTCATTTCTAATCGGTGTTCATGAATTCATTGAGCAAGTTACGAAGCAGGTAAAT... |
Task1_train_46882 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | ATGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTTGGCTTACTGCAGCCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAAGTGCCCGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGACTTCATGATCTGCCCACTGGTTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCAGCCTGACTGAAGTTTTTTGACACAAACTCAGGTCCAGTTTCTCTCCTC... | ATGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTTGGCTTACTGCAGCCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAAGTGCCCGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGACTTCATGATCTGCCCACTGGTTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCAGCCTGACTGAAGTTTTTTGACACAAACTCAGGTCCAGTTTCTCTCCTC... |
Task1_train_46883 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTCATGATCTGCCCACTGGTTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCAGCCTGACTGAAGTTTTTTGACACAAACTCAGGTCCAGTTTCTCTCCTCTTTGAATTAAGTTATCTAAAGGTCTCTTTTTCTGACAAGGGGGATGAATGGGCCACAGTGATCCTAGGAGATAACAGGAACCATCCTAAAGGCAGGTATTGAGTTCAGTGAGTTAACATATCTAATCCAGTTTTGCAGTTGGTTTTTGTGTACAAACCCAGTGCTTTAGTGGCCACCCCAGTGATCTCGTCCTATGGGCTTATCAAATAA... | TTCATGATCTGCCCACTGGTTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCAGCCTGACTGAAGTTTTTTGACACAAACTCAGGTCCAGTTTCTCTCCTCTTTGAATTAAGTTATCTAAAGGTCTCTTTTTCTGACAAGGGGGATGAATGGGCCACAGTGATCCTAGGAGATAACAGGAACCATCCTAAAGGCAGGTATTGAGTTCAGTGAGTTAACATATCTAATCCAGTTTTGCAGTTGGTTTTTGTGTACAAACCCAGTGCTTTAGTGGCCACCCCAGTGATCTCGTCCTATGGGCTTATCAAATAA... |
Task1_train_46884 | Chromosome 19 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GTATATCTTGTCATGGTTTTAACAACAAATGATAATTCTCATTGGAATTATAAAATATCATTCTTTGTATGGAGATATTTTATTACGATTATTTCTTTTGTATAGAAGGCCGGACTCATTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGGTGAAGTGGGAGGACGACTTGAGCCTAGGAATTGGAGACCAGCCTGGGCAATGTGGCAAGACCCCATCTCTATAAAAATTACAAAAAAATTAGCTGGACATGGTGGCACACACCTGTAGTCCCAGCTATCCAGGAGGCTGCGGTGGGAGGGAATCACCTGAGCCTGG... | GTATATCTTGTCATGGTTTTAACAACAAATGATAATTCTCATTGGAATTATAAAATATCATTCTTTGTATGGAGATATTTTATTACGATTATTTCTTTTGTATAGAAGGCCGGACTCATTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGGTGAAGTGGGAGGACGACTTGAGCCTAGGAATTGGAGACCAGCCTGGGCAATGTGGCAAGACCCCATCTCTATAAAAATTACAAAAAAATTAGCTGGACATGGTGGCACACACCTGTAGTCCCAGCTATCCAGGAGGCTGCGGTGGGAGGGAATCACCTGAGCCTGG... |
Task1_train_46885 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TTTGTATGGAGATATTTTATTACGATTATTTCTTTTGTATAGAAGGCCGGACTCATTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGGTGAAGTGGGAGGACGACTTGAGCCTAGGAATTGGAGACCAGCCTGGGCAATGTGGCAAGACCCCATCTCTATAAAAATTACAAAAAAATTAGCTGGACATGGTGGCACACACCTGTAGTCCCAGCTATCCAGGAGGCTGCGGTGGGAGGGAATCACCTGAGCCTGGGAGGTTGAGGCTGCATTGAGCTGTGGTTGTGCCACTGCACTCCAGCCGGGGCAAGAGTGAGAT... | TTTGTATGGAGATATTTTATTACGATTATTTCTTTTGTATAGAAGGCCGGACTCATTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGGTGAAGTGGGAGGACGACTTGAGCCTAGGAATTGGAGACCAGCCTGGGCAATGTGGCAAGACCCCATCTCTATAAAAATTACAAAAAAATTAGCTGGACATGGTGGCACACACCTGTAGTCCCAGCTATCCAGGAGGCTGCGGTGGGAGGGAATCACCTGAGCCTGGGAGGTTGAGGCTGCATTGAGCTGTGGTTGTGCCACTGCACTCCAGCCGGGGCAAGAGTGAGAT... |
Task1_train_46886 | A variant affecting Chromosome 19 has been observed. Determine if it's benign or associated with disease. | Benign | CAGACCACAATATTATACCCATAAATTCCTACAATTTTTCCTAGGAGGCCTTGGTGGCAATGCAAATGAGGTCAAATCTGGATTGACAGTTGTTTCTCTGCCATCCTCCTGTCCCCTCCAAGATAATCTGGAGACCCCTTCAGTTTGGTAGATCTTAACTCTGCTCTTGAACCACCCCACACAGTGATCAGAACATGGAAGACTAAAGGCGGCTTTATCATAAGGCCATTATCATCACATGAACCAGGGCAATACACAGGAGATAAGTTGTTGTGTAGAGTAACATGAAGGCTGGACAAATCCTTCACAGGCATAACATG... | CAGACCACAATATTATACCCATAAATTCCTACAATTTTTCCTAGGAGGCCTTGGTGGCAATGCAAATGAGGTCAAATCTGGATTGACAGTTGTTTCTCTGCCATCCTCCTGTCCCCTCCAAGATAATCTGGAGACCCCTTCAGTTTGGTAGATCTTAACTCTGCTCTTGAACCACCCCACACAGTGATCAGAACATGGAAGACTAAAGGCGGCTTTATCATAAGGCCATTATCATCACATGAACCAGGGCAATACACAGGAGATAAGTTGTTGTGTAGAGTAACATGAAGGCTGGACAAATCCTTCACAGGCATAACATG... |
Task1_train_46887 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GCATGAGGTGGGAGAAGAGGAAACCGTGACATCGCAGCGGCCAAGGGAGCCTTCCAGGAGGAAGAAGCGTCTCCCAGGGTCAGGGCTTCTAAGAGCAGTTGGGGAAGACGAGGACTGGAATTTGGATTTGGCCACCTGGGGGTGTTTTCTGAACTTGGAGGAGCATTCTTGTGCCCCTACGATGCTTGCAGCAGCTAAGGACTCCAGACCTGCAGAGTCTGTCCTGAGACAGGTCAGACCTCGGCGGTGGGACGGGAAAGGGGAACTCTCTGTCTAGAGACTTGCGCTCCGATGTAGTTGGAGGTGCTACACTGTGGCTG... | GCATGAGGTGGGAGAAGAGGAAACCGTGACATCGCAGCGGCCAAGGGAGCCTTCCAGGAGGAAGAAGCGTCTCCCAGGGTCAGGGCTTCTAAGAGCAGTTGGGGAAGACGAGGACTGGAATTTGGATTTGGCCACCTGGGGGTGTTTTCTGAACTTGGAGGAGCATTCTTGTGCCCCTACGATGCTTGCAGCAGCTAAGGACTCCAGACCTGCAGAGTCTGTCCTGAGACAGGTCAGACCTCGGCGGTGGGACGGGAAAGGGGAACTCTCTGTCTAGAGACTTGCGCTCCGATGTAGTTGGAGGTGCTACACTGTGGCTG... |
Task1_train_46888 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | TGGGGTTGGGGTGGGAAGAGCTCTAGAGGCGAGGAGCCTGGGGAAGAGGGGATGATGGAGGCAGGAGAGGCCGGGGAGGGGATGGCTCACACAGGGGCTTGTGGGCTGTGGAGAGGGGCTGAGTGTGGGTCAGCCCCGGTTTCAGTGCCCACCTCCCCACAATCCCCCACCCCCAGACCTTTTCTCCCAACCCATTTCTCCTGGAGCTAGCTGGTTTTACAATTTAATGGTGAAAATGACTGCCACCTTAAACTTCTAACTTAGCTGGAATTCTCATTCTACCACCTAGATGCTTGGGTTCCTCCAGCAAGGGACTTTCT... | TGGGGTTGGGGTGGGAAGAGCTCTAGAGGCGAGGAGCCTGGGGAAGAGGGGATGATGGAGGCAGGAGAGGCCGGGGAGGGGATGGCTCACACAGGGGCTTGTGGGCTGTGGAGAGGGGCTGAGTGTGGGTCAGCCCCGGTTTCAGTGCCCACCTCCCCACAATCCCCCACCCCCAGACCTTTTCTCCCAACCCATTTCTCCTGGAGCTAGCTGGTTTTACAATTTAATGGTGAAAATGACTGCCACCTTAAACTTCTAACTTAGCTGGAATTCTCATTCTACCACCTAGATGCTTGGGTTCCTCCAGCAAGGGACTTTCT... |
Task1_train_46889 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GGGCTGAGTGTGGGTCAGCCCCGGTTTCAGTGCCCACCTCCCCACAATCCCCCACCCCCAGACCTTTTCTCCCAACCCATTTCTCCTGGAGCTAGCTGGTTTTACAATTTAATGGTGAAAATGACTGCCACCTTAAACTTCTAACTTAGCTGGAATTCTCATTCTACCACCTAGATGCTTGGGTTCCTCCAGCAAGGGACTTTCTGAGGAAGGGGCACTCGGGTAGCATAAAGTCTGAGTTACCGGCAACGTTGACAGTCCCACTTATGGGGCCTCCCATGTACAAGGCCCTACCTAATGTATGAAAATGGGCCCAGCCA... | GGGCTGAGTGTGGGTCAGCCCCGGTTTCAGTGCCCACCTCCCCACAATCCCCCACCCCCAGACCTTTTCTCCCAACCCATTTCTCCTGGAGCTAGCTGGTTTTACAATTTAATGGTGAAAATGACTGCCACCTTAAACTTCTAACTTAGCTGGAATTCTCATTCTACCACCTAGATGCTTGGGTTCCTCCAGCAAGGGACTTTCTGAGGAAGGGGCACTCGGGTAGCATAAAGTCTGAGTTACCGGCAACGTTGACAGTCCCACTTATGGGGCCTCCCATGTACAAGGCCCTACCTAATGTATGAAAATGGGCCCAGCCA... |
Task1_train_46890 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | TCTCAGCCCAGCGAGATGCCAGCCTTCCTGTCCCGGGTGAGCTGCGCACCCTGCCTGGGGAGCAGGGGAGGAGGGTTGGGGAGCCACAGGCACAGGGCCAGCCTCCCGGTGGCTCTGCTAAGGCCAGACCTCCCGCCACCCCTCTAGGCCAGCGCTCTGACATGCAGAAGGTGACCCTGGGCCTGCTTGTGTTCCTGGCAGGTGAGTACCCATCCCCCGTCTGCCTTTTCCTCTGGATCCCCTGGATGCGGGGATCCAACCTCTGTCTCTCTCCTGTGCTTTTCTACCTCCCCGGGAAGGTGGTAAATGTTAGAACAGCA... | TCTCAGCCCAGCGAGATGCCAGCCTTCCTGTCCCGGGTGAGCTGCGCACCCTGCCTGGGGAGCAGGGGAGGAGGGTTGGGGAGCCACAGGCACAGGGCCAGCCTCCCGGTGGCTCTGCTAAGGCCAGACCTCCCGCCACCCCTCTAGGCCAGCGCTCTGACATGCAGAAGGTGACCCTGGGCCTGCTTGTGTTCCTGGCAGGTGAGTACCCATCCCCCGTCTGCCTTTTCCTCTGGATCCCCTGGATGCGGGGATCCAACCTCTGTCTCTCTCCTGTGCTTTTCTACCTCCCCGGGAAGGTGGTAAATGTTAGAACAGCA... |
Task1_train_46891 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | CATGGTGGAAGCGGGAGGATGGGCTTTGAGCATGATTGGACTTGGGGAAACAGGAATCTGGGAACTGAAACCATCTGTCGTCTTGACCAGAAAAGTCCCCCGCTGCTGCAGGAGGCATGGATTAACCACGTGTCTGGAAACATGAGACCAAATAGTGGCTAAAAACCTCCTAGATTAGAACCCATTTCAGGTGGCAGAATGCTGGCGTGACTCGGAGGTGTGGGGCTGAGTGGGCGAGTCCACATTTCCTCGTTGGGATATGAGGGGATGAGGTGGCTGCTCAGTGACAGGACCCCTGTCCCGCAGGAGACCCTTTCCCA... | CATGGTGGAAGCGGGAGGATGGGCTTTGAGCATGATTGGACTTGGGGAAACAGGAATCTGGGAACTGAAACCATCTGTCGTCTTGACCAGAAAAGTCCCCCGCTGCTGCAGGAGGCATGGATTAACCACGTGTCTGGAAACATGAGACCAAATAGTGGCTAAAAACCTCCTAGATTAGAACCCATTTCAGGTGGCAGAATGCTGGCGTGACTCGGAGGTGTGGGGCTGAGTGGGCGAGTCCACATTTCCTCGTTGGGATATGAGGGGATGAGGTGGCTGCTCAGTGACAGGACCCCTGTCCCGCAGGAGACCCTTTCCCA... |
Task1_train_46892 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GTGTATGTGTGTGTTTGCACACTGGAAAGAAAAGAACTCAATCCACCCTCACAAACGGACCCCATCACTTCCCGCAGGCTCAGCCCAAAGCTGATGAGGACAGACCAGCTGAAATTGGGTGGAGGACCGTTCTCTGTCCCCAGGTCCTGTCTCTGCACAGAAACTTGAACTCCAGGATGGAATTCTTCCTCCTCTGCTGGGACTCCTTTGCATGGCAGGGCCTCATCTCACCTCTCGCAAGAGGGTCTCTTTGTTCAATTTTTTTTAATCTAAAATGATTGTGCCTCTGCCCAAGCAGCCTGGAGACTTCCTATGTGTGC... | GTGTATGTGTGTGTTTGCACACTGGAAAGAAAAGAACTCAATCCACCCTCACAAACGGACCCCATCACTTCCCGCAGGCTCAGCCCAAAGCTGATGAGGACAGACCAGCTGAAATTGGGTGGAGGACCGTTCTCTGTCCCCAGGTCCTGTCTCTGCACAGAAACTTGAACTCCAGGATGGAATTCTTCCTCCTCTGCTGGGACTCCTTTGCATGGCAGGGCCTCATCTCACCTCTCGCAAGAGGGTCTCTTTGTTCAATTTTTTTTAATCTAAAATGATTGTGCCTCTGCCCAAGCAGCCTGGAGACTTCCTATGTGTGC... |
Task1_train_46893 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCCCTCATCATGCCGTTTTATCCCTCAAACATCCCCTGAGTCCCTCCATAACCACGAACCCACACTCAGAGACCATGAACTGCGGAAACGCCTCCCTGGGACCTGGGCCGCTCCGAGCACTGCTCCAGGGACACCATCCCCGCCCTGTGCCGTTCACAGGACATCCTCTCCCAAGGATCCACAACACTGGGCGGGGAGGGTGCACAGCGCATTTATTGAGCTCGGACTCGTCTTGTCCTTGCCTCCGTCGCCCATCTAGAAGGGCACCAGGCTCCCCGCGACACCTCCCGCTGTCCCTCCCTGTGCCCCGGCGCACGCGC... | CCCCTCATCATGCCGTTTTATCCCTCAAACATCCCCTGAGTCCCTCCATAACCACGAACCCACACTCAGAGACCATGAACTGCGGAAACGCCTCCCTGGGACCTGGGCCGCTCCGAGCACTGCTCCAGGGACACCATCCCCGCCCTGTGCCGTTCACAGGACATCCTCTCCCAAGGATCCACAACACTGGGCGGGGAGGGTGCACAGCGCATTTATTGAGCTCGGACTCGTCTTGTCCTTGCCTCCGTCGCCCATCTAGAAGGGCACCAGGCTCCCCGCGACACCTCCCGCTGTCCCTCCCTGTGCCCCGGCGCACGCGC... |
Task1_train_46894 | 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 | AGCAGCAGAGGGGAACCCGCCCAGTGCTGAGTTGTCTTCGAGGTTGGCGCTCCTCCAGGAAAGCGATTGGCTGCGTGGAGTTTAGAATGGGAAAGGAATGCCATCAACCCCTCGGTGCTTTCAGAGGGACCAGCGGGGTAGGAGCGGGTTGAGAGGGGGGCTCCGGGACCTCATGGAGCTCTGCACGTGACCTCCACCTCGACTCCATGCAGTGCACCAGCCTGCACCCCCCAGGTTGCCTTTGATGGGGAATCTGCCCCAGCCGAGATGTCCAGATGTTGCTTTAGACCTGAAGGGCAGCTCGGGAGGTCCAGTAGGCT... | AGCAGCAGAGGGGAACCCGCCCAGTGCTGAGTTGTCTTCGAGGTTGGCGCTCCTCCAGGAAAGCGATTGGCTGCGTGGAGTTTAGAATGGGAAAGGAATGCCATCAACCCCTCGGTGCTTTCAGAGGGACCAGCGGGGTAGGAGCGGGTTGAGAGGGGGGCTCCGGGACCTCATGGAGCTCTGCACGTGACCTCCACCTCGACTCCATGCAGTGCACCAGCCTGCACCCCCCAGGTTGCCTTTGATGGGGAATCTGCCCCAGCCGAGATGTCCAGATGTTGCTTTAGACCTGAAGGGCAGCTCGGGAGGTCCAGTAGGCT... |
Task1_train_46895 | A mutation is present on Chromosome 19. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TGATTCTGCAGTAATGCTTCTCCTTTGTACACGACCGGCTAAGGCTCCCCCTTATTCAGGCCTCAGATCAAACATAGACTACTCTACTGGGATAGGCCCTCCTGACTCCCTGGCAAGGAAGAGCCACACCATACTCAGCTGGTGTCGCATGACTTGTTTTTGAGGGGGATTGTTTCTTTAATGTTTTATCACAATACGAAAGTCAACTCCTTGCTGGTAGAGGCCTGGACCACTACTGGTACAGAGTGAGTGCTCCATAAATTCATATCTCAACAAATACTTAGCGGGCACAGGCTCTATTTCTGGCAATGTTCCAAGCA... | TGATTCTGCAGTAATGCTTCTCCTTTGTACACGACCGGCTAAGGCTCCCCCTTATTCAGGCCTCAGATCAAACATAGACTACTCTACTGGGATAGGCCCTCCTGACTCCCTGGCAAGGAAGAGCCACACCATACTCAGCTGGTGTCGCATGACTTGTTTTTGAGGGGGATTGTTTCTTTAATGTTTTATCACAATACGAAAGTCAACTCCTTGCTGGTAGAGGCCTGGACCACTACTGGTACAGAGTGAGTGCTCCATAAATTCATATCTCAACAAATACTTAGCGGGCACAGGCTCTATTTCTGGCAATGTTCCAAGCA... |
Task1_train_46896 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTCATTTGACAAATATTTATTGAGCACCTACTATGTGCTAGATATTCTGTGCACTGGGGAAACAGCACTGAATAAAACAAGAGGTCACACTCTAGTGGAGAGAGACAAGTTAGTAAATTATATCGTGTGCTAGGAGGTGATACGTGCTTGCAGAAAAGTAGAGGTAATGAGGATTGTTTAAACTGGGTGGTCAGGGAGGGCCTCACTGAGGAGGTGACATTTGGACCAACAAACACTTGGAGGAAATGAGGGAATGAGCTTTGCAGGTGTCTGGGGGCTGAGTGTTGTCTGGTGTGTTTTAAGAATAGCAGGCAGGTGGG... | GTCATTTGACAAATATTTATTGAGCACCTACTATGTGCTAGATATTCTGTGCACTGGGGAAACAGCACTGAATAAAACAAGAGGTCACACTCTAGTGGAGAGAGACAAGTTAGTAAATTATATCGTGTGCTAGGAGGTGATACGTGCTTGCAGAAAAGTAGAGGTAATGAGGATTGTTTAAACTGGGTGGTCAGGGAGGGCCTCACTGAGGAGGTGACATTTGGACCAACAAACACTTGGAGGAAATGAGGGAATGAGCTTTGCAGGTGTCTGGGGGCTGAGTGTTGTCTGGTGTGTTTTAAGAATAGCAGGCAGGTGGG... |
Task1_train_46897 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AACTAATTTTTTAAAAAGGTTTTTAAAATGTTGTGGGTGAAATAAAACACGAGCTATCAGTTAATCTGTATAACCAATGCCAAGTTTCATTACCTCTCTTGTCCAACTTCCTCATCAAGAAAATGAGCATAGCCACATCTTTTTTTGCCTTAAGGGGAGAGGCAGAATTCTAACAATCATAAGACATGATTCCTGATGTGTGCGTGATCCCCACTGAATCTGAGAGTCAAGCACTGTTGCCTCGGTCATACAACATGTATGTGTTGATCCTGACTTTGCACCAGGTCCTATTCTCACCCCAGTGGAGAAGTTAAGGCTCA... | AACTAATTTTTTAAAAAGGTTTTTAAAATGTTGTGGGTGAAATAAAACACGAGCTATCAGTTAATCTGTATAACCAATGCCAAGTTTCATTACCTCTCTTGTCCAACTTCCTCATCAAGAAAATGAGCATAGCCACATCTTTTTTTGCCTTAAGGGGAGAGGCAGAATTCTAACAATCATAAGACATGATTCCTGATGTGTGCGTGATCCCCACTGAATCTGAGAGTCAAGCACTGTTGCCTCGGTCATACAACATGTATGTGTTGATCCTGACTTTGCACCAGGTCCTATTCTCACCCCAGTGGAGAAGTTAAGGCTCA... |
Task1_train_46898 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | GATGTTCCTCTGACATGCTGGGTGCAGTCTTGGCCCTGGCTGTTCCCTCTGTCCCCAGGGCTTCCTCGCCTCCTTTCAGTCTGGGCTGAAATGGCAGCTTCTCAGAGGAGCCTTCCCTGACCCCACCACTTGACACTTTTAACCTCCCCTATTCCCAGCATCCCTTCCTGCTCCGTCACCATCCAAAATACTATAGGTCGGGCACAGTGGCTCAGGTTTGTAATCCCAGCACTTTGGGAGGCCGATGTGGGAGGATCACTTGAGCCCAGGAGTTTGGGCTCAGCCTGGGCAACAAAGTGAGACCTCATCTCTACAAAACT... | GATGTTCCTCTGACATGCTGGGTGCAGTCTTGGCCCTGGCTGTTCCCTCTGTCCCCAGGGCTTCCTCGCCTCCTTTCAGTCTGGGCTGAAATGGCAGCTTCTCAGAGGAGCCTTCCCTGACCCCACCACTTGACACTTTTAACCTCCCCTATTCCCAGCATCCCTTCCTGCTCCGTCACCATCCAAAATACTATAGGTCGGGCACAGTGGCTCAGGTTTGTAATCCCAGCACTTTGGGAGGCCGATGTGGGAGGATCACTTGAGCCCAGGAGTTTGGGCTCAGCCTGGGCAACAAAGTGAGACCTCATCTCTACAAAACT... |
Task1_train_46899 | A variant has been detected on Chromosome 19. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GACACACCCAGCGTGGTGGAAGAACAGAGAGGATATTCCACAGACAATATCATAAAAGCTTGCATTCCCAGCTAGGTACATTGTGGAACTTCTTATTGGATGCTATGGCAGGCACTCTACAGTCTTTAGTCCCCTTAACACATCACAATGACCCTGTGTGGCCAGGGGCTGGCAAGACCTCTGCACTGAGTTAGACAGTGGCCCCCGCAAAATGCATGTCCTTCCCAGAACCTCAGAATGTAACATTATTTGGAAATTGGATCATTGCAGATATAATCAGTTGAGATGAGAGCATATTGGAATAAGGTGGGCCCTCAATC... | GACACACCCAGCGTGGTGGAAGAACAGAGAGGATATTCCACAGACAATATCATAAAAGCTTGCATTCCCAGCTAGGTACATTGTGGAACTTCTTATTGGATGCTATGGCAGGCACTCTACAGTCTTTAGTCCCCTTAACACATCACAATGACCCTGTGTGGCCAGGGGCTGGCAAGACCTCTGCACTGAGTTAGACAGTGGCCCCCGCAAAATGCATGTCCTTCCCAGAACCTCAGAATGTAACATTATTTGGAAATTGGATCATTGCAGATATAATCAGTTGAGATGAGAGCATATTGGAATAAGGTGGGCCCTCAATC... |
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