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_47300 | 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 | TCCGCCCACCTCGGCCTCCCAAAGTGCTGGGACTGCAGGTGTGAGCCACCGCATCCGGCCTCTCTGTTCTTTAGGACTCTGTTGATTTATCTGAGTGTCCATGTCCCTAGTTTTCCAGCCTCTGTCTTCACTCTTCAGATCACCAACTTGCTAGAGTGCAATGGTGTGATCTCCTGATGCCCCTTTTCCTCACAGGGTGGCCTCAGGCTCCTCATCCAGGAGTCTGTGTGGGATGAAGCCATGAGACGGCTGCAGGAGCGGATGGGGCGGCTTCGGAGTGGCCGAGGGCTGGATGGGGCCGTGGACATGGGGGCCCGGGG... | TCCGCCCACCTCGGCCTCCCAAAGTGCTGGGACTGCAGGTGTGAGCCACCGCATCCGGCCTCTCTGTTCTTTAGGACTCTGTTGATTTATCTGAGTGTCCATGTCCCTAGTTTTCCAGCCTCTGTCTTCACTCTTCAGATCACCAACTTGCTAGAGTGCAATGGTGTGATCTCCTGATGCCCCTTTTCCTCACAGGGTGGCCTCAGGCTCCTCATCCAGGAGTCTGTGTGGGATGAAGCCATGAGACGGCTGCAGGAGCGGATGGGGCGGCTTCGGAGTGGCCGAGGGCTGGATGGGGCCGTGGACATGGGGGCCCGGGG... |
Task1_train_47301 | A variant has been detected on Chromosome 19. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CCCCGCTGCGGGGCGTCCGGAGAACGCGCCATCTGCGGCGTGAGCGGCCGCCTCTCACCACCAGGGGGCGCGCTCCGCCTGGGCCCAGATTCCACCCCTTGACTGTCTCCCCCCAAAAATTTCCTTTCACTTTCGGTCTCTGGCTGTCACCCGGCTTGGCCCCTTCCACACCCAACTGGGGCAAGCCTGGTGCGTGAGGAGACTTGGACTCTAGGTCCCCAAGGGGCGGAGCCAGGGTCCCCACTCCTGGGGCAGGGGGAGCAGAGGGTGGGGGGCTGGGTTCCCGGGTCCCTAACCTGGGGAGGGTTCTGGGGACCAGA... | CCCCGCTGCGGGGCGTCCGGAGAACGCGCCATCTGCGGCGTGAGCGGCCGCCTCTCACCACCAGGGGGCGCGCTCCGCCTGGGCCCAGATTCCACCCCTTGACTGTCTCCCCCCAAAAATTTCCTTTCACTTTCGGTCTCTGGCTGTCACCCGGCTTGGCCCCTTCCACACCCAACTGGGGCAAGCCTGGTGCGTGAGGAGACTTGGACTCTAGGTCCCCAAGGGGCGGAGCCAGGGTCCCCACTCCTGGGGCAGGGGGAGCAGAGGGTGGGGGGCTGGGTTCCCGGGTCCCTAACCTGGGGAGGGTTCTGGGGACCAGA... |
Task1_train_47302 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | GTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCACGCCCAGCCTATCTTTTTTTTTTTTTTTAAGAAAAGGTAATACATTGAGCAGTTTTCCTCCCAACCTAGTCCCTGTCCAATCTGTTTCCTGTCTTAAATTTATTTTTTATTATAATTTTTTTTTTTTTTTTTTTTTGTGAGACAGACTTTTGCTCTTGTTAGCCAGGCTGGAGTGCAGTGGTGCTATCTTGACTCACGGCAACCTCCACCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCTGGAGTAGCTTGGATTACAAG... | GTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCACGCCCAGCCTATCTTTTTTTTTTTTTTTAAGAAAAGGTAATACATTGAGCAGTTTTCCTCCCAACCTAGTCCCTGTCCAATCTGTTTCCTGTCTTAAATTTATTTTTTATTATAATTTTTTTTTTTTTTTTTTTTTGTGAGACAGACTTTTGCTCTTGTTAGCCAGGCTGGAGTGCAGTGGTGCTATCTTGACTCACGGCAACCTCCACCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCTGGAGTAGCTTGGATTACAAG... |
Task1_train_47303 | A sequence alteration has been identified on Chromosome 19. Is it disease-inducing or harmless? | Benign | TCGCGCCATTGCACTTCAGTCTGGGCAACAAGAGCGAAACTCCATCTTAAAAAAAAAAAAAAAAGATGGGGTCTTGCCCTGTCGCCCAGGCTGGAGTGCAGTGGGGTGATCTTGGCTCACTGCAGCCTTGACCTCCTGGGCTCAAGGGATCCTCCCACCTCAGCCTCCCAAGTAGCTGAGACTCCAGGCACAGTGCGGCCTCTGGAGATACTTCTGGTTGTCACTTCTAGAGGGGTGAGGATGCTACTGACGTCTCCTGGATAGAGCCCAGAGATGCTCCTTAGCATTCTCCGGTGCACAGGACAGGCCCTGACAACAAG... | TCGCGCCATTGCACTTCAGTCTGGGCAACAAGAGCGAAACTCCATCTTAAAAAAAAAAAAAAAAGATGGGGTCTTGCCCTGTCGCCCAGGCTGGAGTGCAGTGGGGTGATCTTGGCTCACTGCAGCCTTGACCTCCTGGGCTCAAGGGATCCTCCCACCTCAGCCTCCCAAGTAGCTGAGACTCCAGGCACAGTGCGGCCTCTGGAGATACTTCTGGTTGTCACTTCTAGAGGGGTGAGGATGCTACTGACGTCTCCTGGATAGAGCCCAGAGATGCTCCTTAGCATTCTCCGGTGCACAGGACAGGCCCTGACAACAAG... |
Task1_train_47304 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGAAGAGCCTGGCTTGGGGACCCAGGCATCCTGGCTCCCCGCCCCTCCGAGACCCAGAAGTTTGGGGCTCCTAGGCCCAGGAGTCCAGGGCCCCTGCCCACTTAGGTCCCTAGACCCAATAATATAACTAATCCCCTGCCTCTGCCTCTCTCGTAATCTTTGTTGTCTGTGGGTGGATGTGACAATGAGCACAGAAAGAGGCACAAGTGGAAATTACCAGGAAGGGAAGACTCCAGATCACCAGTGGACATGTTTATAAGCATCTGTGTCAGGTGCTGTAGACACAGTGGGGAAAGAAAGATAAGCTGCCTGCTCCTTGC... | GGAAGAGCCTGGCTTGGGGACCCAGGCATCCTGGCTCCCCGCCCCTCCGAGACCCAGAAGTTTGGGGCTCCTAGGCCCAGGAGTCCAGGGCCCCTGCCCACTTAGGTCCCTAGACCCAATAATATAACTAATCCCCTGCCTCTGCCTCTCTCGTAATCTTTGTTGTCTGTGGGTGGATGTGACAATGAGCACAGAAAGAGGCACAAGTGGAAATTACCAGGAAGGGAAGACTCCAGATCACCAGTGGACATGTTTATAAGCATCTGTGTCAGGTGCTGTAGACACAGTGGGGAAAGAAAGATAAGCTGCCTGCTCCTTGC... |
Task1_train_47305 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTCTTCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTACCTGTAGCACCACACCCAGCTATTAAAAACATTTTTTTCCAGCTGGGTGAGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCACGAGGTCAAGAGATCGAGATCATCCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATATAAAAATTAGCTGGATGTGGTGGTGCACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCGGAGGTTGCGGTGAGCCGAGATTGCGCCAC... | TTCTTCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTACCTGTAGCACCACACCCAGCTATTAAAAACATTTTTTTCCAGCTGGGTGAGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCACGAGGTCAAGAGATCGAGATCATCCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATATAAAAATTAGCTGGATGTGGTGGTGCACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCGGAGGTTGCGGTGAGCCGAGATTGCGCCAC... |
Task1_train_47306 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | TTTTGTTTGTTTGTTTGTTTTGTTTTTTTTTATTTTGAGATGAAGTCTCACTCTTGTTGCCCTGGCTGGAGAGCAATGGCTCAATCTCGGCTCACTAAAACATCCACCTCCTGAGTTCAAGCGATTCTCCTGTGTCAGCCTCCCAGATAACTGGGATTACAGGCATATACCACCATGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAGCTCCTGACCTCAAACGATCCACCTGCCTAGGCCTCCCAAGTGCTGGGATTACAGGCATGAGCCACTACATCCAGCC... | TTTTGTTTGTTTGTTTGTTTTGTTTTTTTTTATTTTGAGATGAAGTCTCACTCTTGTTGCCCTGGCTGGAGAGCAATGGCTCAATCTCGGCTCACTAAAACATCCACCTCCTGAGTTCAAGCGATTCTCCTGTGTCAGCCTCCCAGATAACTGGGATTACAGGCATATACCACCATGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAGCTCCTGACCTCAAACGATCCACCTGCCTAGGCCTCCCAAGTGCTGGGATTACAGGCATGAGCCACTACATCCAGCC... |
Task1_train_47307 | A mutation is present on Chromosome 19. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GAGGGCGCATGGGACAGACCCTCAGCAGGACTTCCAGCCTGAGAGCAGCTGGACGGCCAGAGAGGTTAGGCTGGCAGCAGAGGCGAGTGGAGGTGGAGGTTCCGCAGGTACTCACTGGCCCTTGCTGTGTCTTCCCCCGCTGTCGCCACCCCACCAGTATCTGAAGAAGCTGCACACGCAGGAGCGGGCGGTGGAGGAGGTGAAGCTGGCCATCAAGCCATACTATCAGAAGAAGGACATCACCAAGGAGGAGTACAAGGACATCCTGAGGAAGGCCGTCCACAAGGTGGGCACCCGGAGAGAGGGGCAGACACAGGCCG... | GAGGGCGCATGGGACAGACCCTCAGCAGGACTTCCAGCCTGAGAGCAGCTGGACGGCCAGAGAGGTTAGGCTGGCAGCAGAGGCGAGTGGAGGTGGAGGTTCCGCAGGTACTCACTGGCCCTTGCTGTGTCTTCCCCCGCTGTCGCCACCCCACCAGTATCTGAAGAAGCTGCACACGCAGGAGCGGGCGGTGGAGGAGGTGAAGCTGGCCATCAAGCCATACTATCAGAAGAAGGACATCACCAAGGAGGAGTACAAGGACATCCTGAGGAAGGCCGTCCACAAGGTGGGCACCCGGAGAGAGGGGCAGACACAGGCCG... |
Task1_train_47308 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | TCACCTTCCCCCGGCACCAACAGCCGCTTCAGTGGGTTCTCAGAGGGCCCCAGGTTTGGGAAGGGAGTGGGATTGTCCAAGCTGGGGCTCCGCAGGGGCTGAGGGCAGGGCTCAGGGGCTACAGCCAGGCTTGGGGGTCCCGGATCTGGGAGTGGGGCCAACACCATGTTACCCAGTAACTCATCCAGAATGTCTTCCTGGAGGGAAACAAAAAAAGAGAATCAGGCATTTCCATATCCTTTTCTGGAGACTTCATATGGACCAGGTCTGTTCTCAGCAACGCAGGGAGGTCAGGCTTGAGCTCTGCCTTCAAGGGGCTT... | TCACCTTCCCCCGGCACCAACAGCCGCTTCAGTGGGTTCTCAGAGGGCCCCAGGTTTGGGAAGGGAGTGGGATTGTCCAAGCTGGGGCTCCGCAGGGGCTGAGGGCAGGGCTCAGGGGCTACAGCCAGGCTTGGGGGTCCCGGATCTGGGAGTGGGGCCAACACCATGTTACCCAGTAACTCATCCAGAATGTCTTCCTGGAGGGAAACAAAAAAAGAGAATCAGGCATTTCCATATCCTTTTCTGGAGACTTCATATGGACCAGGTCTGTTCTCAGCAACGCAGGGAGGTCAGGCTTGAGCTCTGCCTTCAAGGGGCTT... |
Task1_train_47309 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | AGCCTCCCAAGTAGCTGGGATTACAGGTGCTCACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTCTCACCATGTTGGCCAGGCTGGTCTCAAACTCCCGACCTCAGTGATCTGCCCGTCTTGGCCTCCCAAAGTGCTGGGATAACAGGTGTGAGCCACTGCGTCCACCCTTTTTATTTTATTTTTATTTTATTGAGACACAGTTTCACTCTACCTACTAGGCTGGAGTGCAGTAGCGTGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTCCAAGTGAATTTCTTTTTTTTTTTTTTTTTTTTTT... | AGCCTCCCAAGTAGCTGGGATTACAGGTGCTCACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTCTCACCATGTTGGCCAGGCTGGTCTCAAACTCCCGACCTCAGTGATCTGCCCGTCTTGGCCTCCCAAAGTGCTGGGATAACAGGTGTGAGCCACTGCGTCCACCCTTTTTATTTTATTTTTATTTTATTGAGACACAGTTTCACTCTACCTACTAGGCTGGAGTGCAGTAGCGTGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTCCAAGTGAATTTCTTTTTTTTTTTTTTTTTTTTTT... |
Task1_train_47310 | A genomic variant on Chromosome 19 is under review. What is the biological outcome — benign or pathogenic? | Benign | TGAGCCAGGGTCTGGCTCTGTGGCCCAGGCTGGAGTGCAGCAGCACCATCATAGCTCTCTGAAGCTTTGAACTCCTGGGCTCAAGCGATCACTCCTGCCTCAGCCTCCCGAGTGGCTAGGACTACCAGGGTGCGACACCACACCACTCCCAGCTAATTTTTAAATTGTTTGTAGAGATGGGGTCTCCGCTATGTGGCCCAGGCTTGTCTTGCACTCCTGGCCTCAAGTAATCCGCCCACGTCGGCCTCCCAATGTGCTGGGATTATAGATGTGAGCCACCTCACTGGGCCACCTTTTGTAGATTACTGTTTGGAATGCCC... | TGAGCCAGGGTCTGGCTCTGTGGCCCAGGCTGGAGTGCAGCAGCACCATCATAGCTCTCTGAAGCTTTGAACTCCTGGGCTCAAGCGATCACTCCTGCCTCAGCCTCCCGAGTGGCTAGGACTACCAGGGTGCGACACCACACCACTCCCAGCTAATTTTTAAATTGTTTGTAGAGATGGGGTCTCCGCTATGTGGCCCAGGCTTGTCTTGCACTCCTGGCCTCAAGTAATCCGCCCACGTCGGCCTCCCAATGTGCTGGGATTATAGATGTGAGCCACCTCACTGGGCCACCTTTTGTAGATTACTGTTTGGAATGCCC... |
Task1_train_47311 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CAATCTGGTTTGTGTATAAACAACTGTCTTGCATTAATTTCATTAGTTTGATAGTAAATTAAACAAGAACTTCTGGCATAAACAGGTTTGGATCAAACAGCTACCTTTCAGGAAGTAAACAGCTTGAGAGATGGAAGTGGAATTGCTTAGTCATAATAGTAGCCTGCTAGCCCCAGCAGTGGGCTTCACAGATGAAAAGGAAAGTGTCTTTCAAGTTGGTGGACCGAGTTAAGTGAGATGGTTTCAGAGAGTTTTGTTGCAGTATTACTGATAGAATTTCAGCCTACATTTTCATTTCACTTTCTGACATGAGTTCCCAT... | CAATCTGGTTTGTGTATAAACAACTGTCTTGCATTAATTTCATTAGTTTGATAGTAAATTAAACAAGAACTTCTGGCATAAACAGGTTTGGATCAAACAGCTACCTTTCAGGAAGTAAACAGCTTGAGAGATGGAAGTGGAATTGCTTAGTCATAATAGTAGCCTGCTAGCCCCAGCAGTGGGCTTCACAGATGAAAAGGAAAGTGTCTTTCAAGTTGGTGGACCGAGTTAAGTGAGATGGTTTCAGAGAGTTTTGTTGCAGTATTACTGATAGAATTTCAGCCTACATTTTCATTTCACTTTCTGACATGAGTTCCCAT... |
Task1_train_47312 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | GCAGCACTCCAGGGTTGGGCTGGTTGAGGGGTAGAGATGACATTTTCTGAGGTAGGGAGGACAGGGGAGCCGTGCTTCCTAGGGCCACCGGGAGGCTGGAGGGAGGGAATTTGTGTAAAGCGCTTGAGATGGTGACTTTAGTACCTAGTGAGTGCTGGGTGAACCCAGCTGGTGAGGCTGTTCAGGTGACTGAGATTCTGGCGCAGGGCAGGTCAGAAAGGGGGCTTGGGCTGTGAAAGATGGCAGGTGCTGGAGAGGAGGCAGGGGTGGGGTGGGAGCGAGTTGTCTGCCCAGAGGACCTGGCTCTGGGACATTCCCAG... | GCAGCACTCCAGGGTTGGGCTGGTTGAGGGGTAGAGATGACATTTTCTGAGGTAGGGAGGACAGGGGAGCCGTGCTTCCTAGGGCCACCGGGAGGCTGGAGGGAGGGAATTTGTGTAAAGCGCTTGAGATGGTGACTTTAGTACCTAGTGAGTGCTGGGTGAACCCAGCTGGTGAGGCTGTTCAGGTGACTGAGATTCTGGCGCAGGGCAGGTCAGAAAGGGGGCTTGGGCTGTGAAAGATGGCAGGTGCTGGAGAGGAGGCAGGGGTGGGGTGGGAGCGAGTTGTCTGCCCAGAGGACCTGGCTCTGGGACATTCCCAG... |
Task1_train_47313 | 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 | TCAGGAACTATGCCACGTGCTTTTTTTATGGATTCAGCATCGTAGAGATGAGACACATGGGACTCAGAATGTGGTGGTAACAGCATTTGAACTCAAGTCTCTCTGGACATAAAAAATCCTCATCGTAATAGCTCCTACTGAGACAGTCATGGTCATTGCTGATTACTGGGTGGTCACTGTGGGTAACGCAGGAGCTGACATATATCATTCTCCCCACTGCTTAACTGCTTACAACGATCCCTGCATTTATCATTAGGCCCATTTCTCAGAAAAGTAAGTAGAGGCTAAAAAGTTGAGAGCACGCAACAAACGTGGGATTG... | TCAGGAACTATGCCACGTGCTTTTTTTATGGATTCAGCATCGTAGAGATGAGACACATGGGACTCAGAATGTGGTGGTAACAGCATTTGAACTCAAGTCTCTCTGGACATAAAAAATCCTCATCGTAATAGCTCCTACTGAGACAGTCATGGTCATTGCTGATTACTGGGTGGTCACTGTGGGTAACGCAGGAGCTGACATATATCATTCTCCCCACTGCTTAACTGCTTACAACGATCCCTGCATTTATCATTAGGCCCATTTCTCAGAAAAGTAAGTAGAGGCTAAAAAGTTGAGAGCACGCAACAAACGTGGGATTG... |
Task1_train_47314 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGTGACTCATGCTGGACTCTAACCCACGAGGGTTTCTCAGAGTCAGCAGCTGGGGGATGAAGAAGTGAAAAGTGACTGGCAGGAAATTCTGCAAGCAAGGAAAGGGAAAGAGAAATGAACTGGTGCAGGTCTGCGGGAAGAGAATGAGGCTGGATCCTCAAAATCACAGGAGGAAGCAGGCCCAGACCTCAGAGGCAGAAAGAGAAAGAAACCAGAGCTTAGAGTCAGGAGGAGGAAACCAGACCCCGGAGCCACAAGGAGAGGGCTGGATCCCCGGCTCAGAGGGAAGAGGTCGGATCCCCAGCTGAGAGGGAGGAGGG... | TGTGACTCATGCTGGACTCTAACCCACGAGGGTTTCTCAGAGTCAGCAGCTGGGGGATGAAGAAGTGAAAAGTGACTGGCAGGAAATTCTGCAAGCAAGGAAAGGGAAAGAGAAATGAACTGGTGCAGGTCTGCGGGAAGAGAATGAGGCTGGATCCTCAAAATCACAGGAGGAAGCAGGCCCAGACCTCAGAGGCAGAAAGAGAAAGAAACCAGAGCTTAGAGTCAGGAGGAGGAAACCAGACCCCGGAGCCACAAGGAGAGGGCTGGATCCCCGGCTCAGAGGGAAGAGGTCGGATCCCCAGCTGAGAGGGAGGAGGG... |
Task1_train_47315 | A variant affecting Chromosome 19 has been observed. Determine if it's benign or associated with disease. | Benign | TCCAGTTCAAACTTGGAAAGGGTGGTCTCCAGATTCTCTCTTTAAGGACTGGTTTTCATTTTGCAGAGGGTTCAAGACTTTAATAAAAGTGGTTCTGGCCATACTAGGAAGTTGCCGAATACTCCCTTGTCTCTTAGCTCTCCTTGTTGGAAGCATTCAATCAACTATAAAGGCAATAGCAGCTAGGCAAACTACCACTCAGCTAACGGCTCTGCATAAATATCAACCTTTGTCTAAAGAAAAAAAGTGTCTCTTCATGCAGAATTAAGTAATAGTAATGCCTTCTATTAAACTTCTTTTATAAAAAACATCAAAAGGGG... | TCCAGTTCAAACTTGGAAAGGGTGGTCTCCAGATTCTCTCTTTAAGGACTGGTTTTCATTTTGCAGAGGGTTCAAGACTTTAATAAAAGTGGTTCTGGCCATACTAGGAAGTTGCCGAATACTCCCTTGTCTCTTAGCTCTCCTTGTTGGAAGCATTCAATCAACTATAAAGGCAATAGCAGCTAGGCAAACTACCACTCAGCTAACGGCTCTGCATAAATATCAACCTTTGTCTAAAGAAAAAAAGTGTCTCTTCATGCAGAATTAAGTAATAGTAATGCCTTCTATTAAACTTCTTTTATAAAAAACATCAAAAGGGG... |
Task1_train_47316 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GCCCAGAGGGTGCTGAGCGTGGCAGGTGAACTCTCCTTCGTGCTCCATTTGAATGGGTGGCAGCTCCAGGACCCCGGGGTCTGAGGGCTGGGAGGGGCCCACGGTCTGTCCCCACCGGGTCCAGCTCAGCCTGGCTGGGGGGCTGCTGTGGGTGACACAGACCAGGCGCAGGCTTTGGCCCTCCAGGACCGGGAGGGATGTGCCGTTCCCGAGGTTTTCCAGGACTAGGGAAGGAAGAGGCAGAATCGACGTGCAGCTCAGGGCTCAGGGACCCTCCTGTGTGGGGACCCTCCAGACTCCTGGGCCCCCAGTTTGGCACT... | GCCCAGAGGGTGCTGAGCGTGGCAGGTGAACTCTCCTTCGTGCTCCATTTGAATGGGTGGCAGCTCCAGGACCCCGGGGTCTGAGGGCTGGGAGGGGCCCACGGTCTGTCCCCACCGGGTCCAGCTCAGCCTGGCTGGGGGGCTGCTGTGGGTGACACAGACCAGGCGCAGGCTTTGGCCCTCCAGGACCGGGAGGGATGTGCCGTTCCCGAGGTTTTCCAGGACTAGGGAAGGAAGAGGCAGAATCGACGTGCAGCTCAGGGCTCAGGGACCCTCCTGTGTGGGGACCCTCCAGACTCCTGGGCCCCCAGTTTGGCACT... |
Task1_train_47317 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | CGGGAGGGATGTGCCGTTCCCGAGGTTTTCCAGGACTAGGGAAGGAAGAGGCAGAATCGACGTGCAGCTCAGGGCTCAGGGACCCTCCTGTGTGGGGACCCTCCAGACTCCTGGGCCCCCAGTTTGGCACTGAGAGGCCCTGGCTCCTCTGTCTCCTTTCCTACCTGTCCTGTTTGCTTGGGAAACCATCACTCTCAGGTTCTCTGGAGGATCTGAAATGGAGACAGGGGACCGGCTCTAGACAGACCAGGGGCTTCCCTCTGGGTAAAGGGAACTATCCTGGACACTGAGGTGGGGGAAGTGGGTGGGATAGAAGGGCA... | CGGGAGGGATGTGCCGTTCCCGAGGTTTTCCAGGACTAGGGAAGGAAGAGGCAGAATCGACGTGCAGCTCAGGGCTCAGGGACCCTCCTGTGTGGGGACCCTCCAGACTCCTGGGCCCCCAGTTTGGCACTGAGAGGCCCTGGCTCCTCTGTCTCCTTTCCTACCTGTCCTGTTTGCTTGGGAAACCATCACTCTCAGGTTCTCTGGAGGATCTGAAATGGAGACAGGGGACCGGCTCTAGACAGACCAGGGGCTTCCCTCTGGGTAAAGGGAACTATCCTGGACACTGAGGTGGGGGAAGTGGGTGGGATAGAAGGGCA... |
Task1_train_47318 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | GGGGACCCTGAGTTGACATAAGTGGAGGTGAGGATCCTGTGGGCAGGGATTGGATGGTCATGTCTTCTTTGCCTCCCCCCACTGCATGGAGTAGATTTTGCCTGGAGAATGAATGAATGAATGAATGGGACTCTGCATCCATCACTTCACCTGCAGCCATGACTCACCTGTGTCCCCTGACAGTCCCCTCCTAGCACTGCCCACCTCCGAGGCTGGCCAGGGTGGCTCCTTCCTGGTTTGGGGCTGGTCCTCATGCCCTCTGCCCTGCTGCTTCCCCTGTGAAAGGAGAAGTTGGGAGGCGAGCTTTCAGGACATTGCGG... | GGGGACCCTGAGTTGACATAAGTGGAGGTGAGGATCCTGTGGGCAGGGATTGGATGGTCATGTCTTCTTTGCCTCCCCCCACTGCATGGAGTAGATTTTGCCTGGAGAATGAATGAATGAATGAATGGGACTCTGCATCCATCACTTCACCTGCAGCCATGACTCACCTGTGTCCCCTGACAGTCCCCTCCTAGCACTGCCCACCTCCGAGGCTGGCCAGGGTGGCTCCTTCCTGGTTTGGGGCTGGTCCTCATGCCCTCTGCCCTGCTGCTTCCCCTGTGAAAGGAGAAGTTGGGAGGCGAGCTTTCAGGACATTGCGG... |
Task1_train_47319 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GGACCCTGAGTTGACATAAGTGGAGGTGAGGATCCTGTGGGCAGGGATTGGATGGTCATGTCTTCTTTGCCTCCCCCCACTGCATGGAGTAGATTTTGCCTGGAGAATGAATGAATGAATGAATGGGACTCTGCATCCATCACTTCACCTGCAGCCATGACTCACCTGTGTCCCCTGACAGTCCCCTCCTAGCACTGCCCACCTCCGAGGCTGGCCAGGGTGGCTCCTTCCTGGTTTGGGGCTGGTCCTCATGCCCTCTGCCCTGCTGCTTCCCCTGTGAAAGGAGAAGTTGGGAGGCGAGCTTTCAGGACATTGCGGTT... | GGACCCTGAGTTGACATAAGTGGAGGTGAGGATCCTGTGGGCAGGGATTGGATGGTCATGTCTTCTTTGCCTCCCCCCACTGCATGGAGTAGATTTTGCCTGGAGAATGAATGAATGAATGAATGGGACTCTGCATCCATCACTTCACCTGCAGCCATGACTCACCTGTGTCCCCTGACAGTCCCCTCCTAGCACTGCCCACCTCCGAGGCTGGCCAGGGTGGCTCCTTCCTGGTTTGGGGCTGGTCCTCATGCCCTCTGCCCTGCTGCTTCCCCTGTGAAAGGAGAAGTTGGGAGGCGAGCTTTCAGGACATTGCGGTT... |
Task1_train_47320 | 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 | CCTGAGTTGACATAAGTGGAGGTGAGGATCCTGTGGGCAGGGATTGGATGGTCATGTCTTCTTTGCCTCCCCCCACTGCATGGAGTAGATTTTGCCTGGAGAATGAATGAATGAATGAATGGGACTCTGCATCCATCACTTCACCTGCAGCCATGACTCACCTGTGTCCCCTGACAGTCCCCTCCTAGCACTGCCCACCTCCGAGGCTGGCCAGGGTGGCTCCTTCCTGGTTTGGGGCTGGTCCTCATGCCCTCTGCCCTGCTGCTTCCCCTGTGAAAGGAGAAGTTGGGAGGCGAGCTTTCAGGACATTGCGGTTCCCG... | CCTGAGTTGACATAAGTGGAGGTGAGGATCCTGTGGGCAGGGATTGGATGGTCATGTCTTCTTTGCCTCCCCCCACTGCATGGAGTAGATTTTGCCTGGAGAATGAATGAATGAATGAATGGGACTCTGCATCCATCACTTCACCTGCAGCCATGACTCACCTGTGTCCCCTGACAGTCCCCTCCTAGCACTGCCCACCTCCGAGGCTGGCCAGGGTGGCTCCTTCCTGGTTTGGGGCTGGTCCTCATGCCCTCTGCCCTGCTGCTTCCCCTGTGAAAGGAGAAGTTGGGAGGCGAGCTTTCAGGACATTGCGGTTCCCG... |
Task1_train_47321 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | CTCCTACCCCCGGGATGGCTGGGACGAGTCTACTGCTGCTTATGGCTACTGGTTCAAAGGATGGACCAGCCCAAAGACGGGTGCTCCTGTGGCCACTAACAACCAGAGTCGAGAGGTGGAAATGAGCACCCGGGACCGATTCCAGCTCACTGGGGATCCCGGCAAAGGGAGCTGCTCCTTGGTGATCAGAGACGCGCAGAGGGAGGATGAGGCATGGTACTTCTTTCGGGTGGAGAGAGGAAGCCGTGTGAGACATAGTTTCGTGAACAATTTGTTCTAAAAGTAACAGGTATGGAATGGGGTGGGAACCCCTGCCTGTC... | CTCCTACCCCCGGGATGGCTGGGACGAGTCTACTGCTGCTTATGGCTACTGGTTCAAAGGATGGACCAGCCCAAAGACGGGTGCTCCTGTGGCCACTAACAACCAGAGTCGAGAGGTGGAAATGAGCACCCGGGACCGATTCCAGCTCACTGGGGATCCCGGCAAAGGGAGCTGCTCCTTGGTGATCAGAGACGCGCAGAGGGAGGATGAGGCATGGTACTTCTTTCGGGTGGAGAGAGGAAGCCGTGTGAGACATAGTTTCGTGAACAATTTGTTCTAAAAGTAACAGGTATGGAATGGGGTGGGAACCCCTGCCTGTC... |
Task1_train_47322 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CTACCCCCGGGATGGCTGGGACGAGTCTACTGCTGCTTATGGCTACTGGTTCAAAGGATGGACCAGCCCAAAGACGGGTGCTCCTGTGGCCACTAACAACCAGAGTCGAGAGGTGGAAATGAGCACCCGGGACCGATTCCAGCTCACTGGGGATCCCGGCAAAGGGAGCTGCTCCTTGGTGATCAGAGACGCGCAGAGGGAGGATGAGGCATGGTACTTCTTTCGGGTGGAGAGAGGAAGCCGTGTGAGACATAGTTTCGTGAACAATTTGTTCTAAAAGTAACAGGTATGGAATGGGGTGGGAACCCCTGCCTGTCACA... | CTACCCCCGGGATGGCTGGGACGAGTCTACTGCTGCTTATGGCTACTGGTTCAAAGGATGGACCAGCCCAAAGACGGGTGCTCCTGTGGCCACTAACAACCAGAGTCGAGAGGTGGAAATGAGCACCCGGGACCGATTCCAGCTCACTGGGGATCCCGGCAAAGGGAGCTGCTCCTTGGTGATCAGAGACGCGCAGAGGGAGGATGAGGCATGGTACTTCTTTCGGGTGGAGAGAGGAAGCCGTGTGAGACATAGTTTCGTGAACAATTTGTTCTAAAAGTAACAGGTATGGAATGGGGTGGGAACCCCTGCCTGTCACA... |
Task1_train_47323 | A sequence alteration has been identified on Chromosome 19. Is it disease-inducing or harmless? | Benign | GATAGGGTTAAAGCTGAAGAGAGCCAGAGACAGATGAGACGCAGAGTGGAACATCACTTACGCAAATCACACACAGCACCACGGCCAGCATGCGATTTTGAGGGTACAAATACATCTAAGTGAACACATCAGAACACATGTTAAGTGTGCTTGAGCAGCTGTCCATGGTTGAGAGAAGGAAGTTGGGAGACACGAAGGGAGTAAAATAAAACGAGAAAGGCTTCATGTGAGGGAAGGACTGGGAAGGACTTCACGGCACACTAAGGACAGGGAAACATGAGGGACTCAACGCCATTTACTGGAGGGTTCACCCTCTTCCC... | GATAGGGTTAAAGCTGAAGAGAGCCAGAGACAGATGAGACGCAGAGTGGAACATCACTTACGCAAATCACACACAGCACCACGGCCAGCATGCGATTTTGAGGGTACAAATACATCTAAGTGAACACATCAGAACACATGTTAAGTGTGCTTGAGCAGCTGTCCATGGTTGAGAGAAGGAAGTTGGGAGACACGAAGGGAGTAAAATAAAACGAGAAAGGCTTCATGTGAGGGAAGGACTGGGAAGGACTTCACGGCACACTAAGGACAGGGAAACATGAGGGACTCAACGCCATTTACTGGAGGGTTCACCCTCTTCCC... |
Task1_train_47324 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | TAAGCACTATGAAATAAATAGAGATTTGGAGACAGATGGGAACCTGAGCCCAGAGATCTTCCAGAGTGGGCAGGAGCTGGCTCTTACCTGACTCTGGTCCTCTGGATCCACAAAGATATTTTCAGCTGTCACATTTCCATGAACATACTCATTCTCATGGAGGAACTCCAGGGCATCCAGCTGGGGGAAGAAGCAAGTCAGTGTCTGCATGAGCAGTACGACTAACACAGAGAGGCTATGGTGCAGACCAGGAGGGAGCCCCACTATTAAGGCCTGGGGTTGTCCGACACTGTGACTGGGGGTTAAACCTGACTAAATCC... | TAAGCACTATGAAATAAATAGAGATTTGGAGACAGATGGGAACCTGAGCCCAGAGATCTTCCAGAGTGGGCAGGAGCTGGCTCTTACCTGACTCTGGTCCTCTGGATCCACAAAGATATTTTCAGCTGTCACATTTCCATGAACATACTCATTCTCATGGAGGAACTCCAGGGCATCCAGCTGGGGGAAGAAGCAAGTCAGTGTCTGCATGAGCAGTACGACTAACACAGAGAGGCTATGGTGCAGACCAGGAGGGAGCCCCACTATTAAGGCCTGGGGTTGTCCGACACTGTGACTGGGGGTTAAACCTGACTAAATCC... |
Task1_train_47325 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCAGAGTGGGCAGGAGCTGGCTCTTACCTGACTCTGGTCCTCTGGATCCACAAAGATATTTTCAGCTGTCACATTTCCATGAACATACTCATTCTCATGGAGGAACTCCAGGGCATCCAGCTGGGGGAAGAAGCAAGTCAGTGTCTGCATGAGCAGTACGACTAACACAGAGAGGCTATGGTGCAGACCAGGAGGGAGCCCCACTATTAAGGCCTGGGGTTGTCCGACACTGTGACTGGGGGTTAAACCTGACTAAATCCGGGGTAGCATGAGGAGCCCGCTGTGACAGCACATTGAGCACGCCTCTAATCAGGCTCTCA... | CCAGAGTGGGCAGGAGCTGGCTCTTACCTGACTCTGGTCCTCTGGATCCACAAAGATATTTTCAGCTGTCACATTTCCATGAACATACTCATTCTCATGGAGGAACTCCAGGGCATCCAGCTGGGGGAAGAAGCAAGTCAGTGTCTGCATGAGCAGTACGACTAACACAGAGAGGCTATGGTGCAGACCAGGAGGGAGCCCCACTATTAAGGCCTGGGGTTGTCCGACACTGTGACTGGGGGTTAAACCTGACTAAATCCGGGGTAGCATGAGGAGCCCGCTGTGACAGCACATTGAGCACGCCTCTAATCAGGCTCTCA... |
Task1_train_47326 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | AAATAACTTGTAAGCAAATATTCATGGCAGCGTTACTCATAACAGCCCAAAGCGGAAACTACCCAAACGCCCATCAGCTGCTAAGTGGCTAAGCCACATGGGGTGTTCCCATACAGCAGAATATCACGCAGCCATAAAAGGAGTGCGGCAGTGACGCGCCACAGCATGGATGCACCTTGAGCACACGCCGCTGGGTGAGGGATGCCAGACACAAGAGGCCACACAGCGCAGGACTCCACTTCTGTGAACACCCAGAAGGGGCAAATCCACGGAGGGAGAAAGGCGGTTAGTGGCTGCCAGTGGACTGGGGGAAGAATCAG... | AAATAACTTGTAAGCAAATATTCATGGCAGCGTTACTCATAACAGCCCAAAGCGGAAACTACCCAAACGCCCATCAGCTGCTAAGTGGCTAAGCCACATGGGGTGTTCCCATACAGCAGAATATCACGCAGCCATAAAAGGAGTGCGGCAGTGACGCGCCACAGCATGGATGCACCTTGAGCACACGCCGCTGGGTGAGGGATGCCAGACACAAGAGGCCACACAGCGCAGGACTCCACTTCTGTGAACACCCAGAAGGGGCAAATCCACGGAGGGAGAAAGGCGGTTAGTGGCTGCCAGTGGACTGGGGGAAGAATCAG... |
Task1_train_47327 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GGGATGCCAGACACAAGAGGCCACACAGCGCAGGACTCCACTTCTGTGAACACCCAGAAGGGGCAAATCCACGGAGGGAGAAAGGCGGTTAGTGGCTGCCAGTGGACTGGGGGAAGAATCAGAGTGATGGCTCAGAACTACTGGGTTTCTTTTTGGGGTGACAGAAACGTCCTGGAATTAGATAGTGACGATGGTTGCATAACACTCTGAATATCCTGAAGGCCACTCAGTTGCACCCTTTAAAAGAATGAATTTTCGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTAGGTGGATCACTTGAGGT... | GGGATGCCAGACACAAGAGGCCACACAGCGCAGGACTCCACTTCTGTGAACACCCAGAAGGGGCAAATCCACGGAGGGAGAAAGGCGGTTAGTGGCTGCCAGTGGACTGGGGGAAGAATCAGAGTGATGGCTCAGAACTACTGGGTTTCTTTTTGGGGTGACAGAAACGTCCTGGAATTAGATAGTGACGATGGTTGCATAACACTCTGAATATCCTGAAGGCCACTCAGTTGCACCCTTTAAAAGAATGAATTTTCGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTAGGTGGATCACTTGAGGT... |
Task1_train_47328 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GAGGGGCACACTTCACACAGGGCACATGCCAACTGGCCGCAGTCCCCGCCACTCCCAACTGCCTTACTCCAGCCTGCTGCACTCATTCCCACTATTGCCCGGCCCTGCAGGTGGGTAGGTATAGAGTCCAAGGTCTAAGAGAAAGTTGCCTAGCGACAGGTCTGCAGCTAGGGATGTGGCTTCCATTCCCATTCTCAGAACGGGGTCCCCTCCCACTGTCCTGGTGCTGAGACGACCCAGTCCCTGGCCGCCCATGGACAGAGTGTACCTTCATAGAGAATGCCCTGGTTGTCCCTGGTCTGGAAGGACTTCAGCTTCCA... | GAGGGGCACACTTCACACAGGGCACATGCCAACTGGCCGCAGTCCCCGCCACTCCCAACTGCCTTACTCCAGCCTGCTGCACTCATTCCCACTATTGCCCGGCCCTGCAGGTGGGTAGGTATAGAGTCCAAGGTCTAAGAGAAAGTTGCCTAGCGACAGGTCTGCAGCTAGGGATGTGGCTTCCATTCCCATTCTCAGAACGGGGTCCCCTCCCACTGTCCTGGTGCTGAGACGACCCAGTCCCTGGCCGCCCATGGACAGAGTGTACCTTCATAGAGAATGCCCTGGTTGTCCCTGGTCTGGAAGGACTTCAGCTTCCA... |
Task1_train_47329 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CCTAAGCGGCTCTCAGGGCTTACATTTTTAAAGTTTAACCTGGGACCCTGTTAGAACTCCATACCTCCTCTCCTACTCATCTTGTCTGTCGCTCCCTCACGTTCTAACTACCATTGTATCATTCAGAGCGGGAGCTGTGTGAGGACAGGGCGTGTCCCCAGTGTTTGGAACGAACAGTACCTGCTCTAGGGCCCAGCAGACAGCTCTAAACTAATGAATGATTGAGTAGCAGCTCTTAGGACTTGCTTGTTCAATCCTCCAGTCACCCCATGAAGAAGCTGGGTTGTCCCTCTTTTGCCGATTGGTCTGAAACTGAGGTT... | CCTAAGCGGCTCTCAGGGCTTACATTTTTAAAGTTTAACCTGGGACCCTGTTAGAACTCCATACCTCCTCTCCTACTCATCTTGTCTGTCGCTCCCTCACGTTCTAACTACCATTGTATCATTCAGAGCGGGAGCTGTGTGAGGACAGGGCGTGTCCCCAGTGTTTGGAACGAACAGTACCTGCTCTAGGGCCCAGCAGACAGCTCTAAACTAATGAATGATTGAGTAGCAGCTCTTAGGACTTGCTTGTTCAATCCTCCAGTCACCCCATGAAGAAGCTGGGTTGTCCCTCTTTTGCCGATTGGTCTGAAACTGAGGTT... |
Task1_train_47330 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ATATACCTCCATATCCTCTAGTAGTGACACTTGAGTTGCATAGTTACCACATAAGCGTCTTTCCCCTTTAACAGCATGCCGCTCTTGGAAGCAGGGCTTAGCTGATTCACCCTGTATTCCCAGCTCCTGACATCATGCTTGGCATATAAGGGGTGCCTATTACATGTCTGTTGGTGCATTTGAGGCCGAGGGAACAACATGAGCACAAGTGTGGTGAGGAGAGTGAGCTGGATATCTGTGGGAGAGATGAGCAGAGGCAAAGGTGACAATTCAGAACAAGATGTGGTTTCAGAAGGCTTTCATTTGCAAGTTTTAATTCC... | ATATACCTCCATATCCTCTAGTAGTGACACTTGAGTTGCATAGTTACCACATAAGCGTCTTTCCCCTTTAACAGCATGCCGCTCTTGGAAGCAGGGCTTAGCTGATTCACCCTGTATTCCCAGCTCCTGACATCATGCTTGGCATATAAGGGGTGCCTATTACATGTCTGTTGGTGCATTTGAGGCCGAGGGAACAACATGAGCACAAGTGTGGTGAGGAGAGTGAGCTGGATATCTGTGGGAGAGATGAGCAGAGGCAAAGGTGACAATTCAGAACAAGATGTGGTTTCAGAAGGCTTTCATTTGCAAGTTTTAATTCC... |
Task1_train_47331 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | ATGAGCAGAGGCAAAGGTGACAATTCAGAACAAGATGTGGTTTCAGAAGGCTTTCATTTGCAAGTTTTAATTCCAGGCAGAGAGACTTTAAGCAGTCTCATAGATACTCAGATGGTGAGCCAAGAACTGCACAAGGGACAGGCTGGAAAAGGTATGATGATGGAGGAGAGGAGAGATGGGGAGACTGGAGGCATACAGCAGAGCAGTGACATTCATGTTTTGTGAAGGATCCCAGAGAGCATACAGCTTGGTAGTTAAGAATATGGGGGCCAGGCGTGGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGGCGAGGC... | ATGAGCAGAGGCAAAGGTGACAATTCAGAACAAGATGTGGTTTCAGAAGGCTTTCATTTGCAAGTTTTAATTCCAGGCAGAGAGACTTTAAGCAGTCTCATAGATACTCAGATGGTGAGCCAAGAACTGCACAAGGGACAGGCTGGAAAAGGTATGATGATGGAGGAGAGGAGAGATGGGGAGACTGGAGGCATACAGCAGAGCAGTGACATTCATGTTTTGTGAAGGATCCCAGAGAGCATACAGCTTGGTAGTTAAGAATATGGGGGCCAGGCGTGGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGGCGAGGC... |
Task1_train_47332 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | TGGGGAGACTGGAGGCATACAGCAGAGCAGTGACATTCATGTTTTGTGAAGGATCCCAGAGAGCATACAGCTTGGTAGTTAAGAATATGGGGGCCAGGCGTGGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGGCGAGGCAGGCCGGTCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGCTGAAACTCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGAGGGCACCTGCAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCGTTGAG... | TGGGGAGACTGGAGGCATACAGCAGAGCAGTGACATTCATGTTTTGTGAAGGATCCCAGAGAGCATACAGCTTGGTAGTTAAGAATATGGGGGCCAGGCGTGGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGGCGAGGCAGGCCGGTCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGCTGAAACTCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGAGGGCACCTGCAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCGTTGAG... |
Task1_train_47333 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGTTAAGAATATGGGGGCCAGGCGTGGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGGCGAGGCAGGCCGGTCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGCTGAAACTCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGAGGGCACCTGCAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCGTTGAGCTGAGATCGTGCAGCACTTCAGCCTGGGCAACAGGGCAAGACTCAGTCTCCAAAAAAAAAAAAAAAAATATATATA... | AGTTAAGAATATGGGGGCCAGGCGTGGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGGCGAGGCAGGCCGGTCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGCTGAAACTCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGAGGGCACCTGCAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCGTTGAGCTGAGATCGTGCAGCACTTCAGCCTGGGCAACAGGGCAAGACTCAGTCTCCAAAAAAAAAAAAAAAAATATATATA... |
Task1_train_47334 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCGTTGAGCTGAGATCGTGCAGCACTTCAGCCTGGGCAACAGGGCAAGACTCAGTCTCCAAAAAAAAAAAAAAAAATATATATATATATATATATATATATAGTCAGAGGGGTTCAAATCCTCAGTCTTCTGCTCACTTACCTGTAAGAAAGCAGAAACGTGCCTACCTTACAGGAGGTTGTCGAGTGTAACAGAGTGCCTGAGGCACTCCTGCCTGTGAACAAGCATACCATGAATGGGAATTACTCTGTCCTGTGAATCTTTCTC... | GCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCGTTGAGCTGAGATCGTGCAGCACTTCAGCCTGGGCAACAGGGCAAGACTCAGTCTCCAAAAAAAAAAAAAAAAATATATATATATATATATATATATATAGTCAGAGGGGTTCAAATCCTCAGTCTTCTGCTCACTTACCTGTAAGAAAGCAGAAACGTGCCTACCTTACAGGAGGTTGTCGAGTGTAACAGAGTGCCTGAGGCACTCCTGCCTGTGAACAAGCATACCATGAATGGGAATTACTCTGTCCTGTGAATCTTTCTC... |
Task1_train_47335 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | TTTGGTGACAGTACAGGATAGAGTGGAGAGTAGAAGCAGGTGAGTCCAGGCGATTTTTTAGGGAACTTGGTCAGTCACTTAGGTGTGAAGGTAATGGTAGAATCTCCCTCCTCGTTGAACCCTATGGTTTCCCAACTCCCTTCTTGACCCTCCTGGGAATGGGCTCTGTCTGTTTTCTGTGATGCCAGTTCCACATGGGTCACCCCTTTGGGTCCCTTGATGGATAGGCTGGACTCAAGATCTATCACCCCTACTTGCTCTTGTCTGTGTTCTCACCCTTAGTGAACAGGAGACATTTGCACTTGCTCTTTCAGATGTGA... | TTTGGTGACAGTACAGGATAGAGTGGAGAGTAGAAGCAGGTGAGTCCAGGCGATTTTTTAGGGAACTTGGTCAGTCACTTAGGTGTGAAGGTAATGGTAGAATCTCCCTCCTCGTTGAACCCTATGGTTTCCCAACTCCCTTCTTGACCCTCCTGGGAATGGGCTCTGTCTGTTTTCTGTGATGCCAGTTCCACATGGGTCACCCCTTTGGGTCCCTTGATGGATAGGCTGGACTCAAGATCTATCACCCCTACTTGCTCTTGTCTGTGTTCTCACCCTTAGTGAACAGGAGACATTTGCACTTGCTCTTTCAGATGTGA... |
Task1_train_47336 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGGAGAGTAGAAGCAGGTGAGTCCAGGCGATTTTTTAGGGAACTTGGTCAGTCACTTAGGTGTGAAGGTAATGGTAGAATCTCCCTCCTCGTTGAACCCTATGGTTTCCCAACTCCCTTCTTGACCCTCCTGGGAATGGGCTCTGTCTGTTTTCTGTGATGCCAGTTCCACATGGGTCACCCCTTTGGGTCCCTTGATGGATAGGCTGGACTCAAGATCTATCACCCCTACTTGCTCTTGTCTGTGTTCTCACCCTTAGTGAACAGGAGACATTTGCACTTGCTCTTTCAGATGTGACTGAGACCAAGAACTCTCCTCTG... | TGGAGAGTAGAAGCAGGTGAGTCCAGGCGATTTTTTAGGGAACTTGGTCAGTCACTTAGGTGTGAAGGTAATGGTAGAATCTCCCTCCTCGTTGAACCCTATGGTTTCCCAACTCCCTTCTTGACCCTCCTGGGAATGGGCTCTGTCTGTTTTCTGTGATGCCAGTTCCACATGGGTCACCCCTTTGGGTCCCTTGATGGATAGGCTGGACTCAAGATCTATCACCCCTACTTGCTCTTGTCTGTGTTCTCACCCTTAGTGAACAGGAGACATTTGCACTTGCTCTTTCAGATGTGACTGAGACCAAGAACTCTCCTCTG... |
Task1_train_47337 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | CTGTCTCAAAAAACAAAAACAAACAAACAAACAAACAAACAAACAAACAAAAAAACCCAACAAACCCACCAAACATACCATATTTGGTTTCTGTAAAAAAATAAAAAAGAGAGAGAGAATTTTTAAAAAACAAAAACCATACTATCTAATTTACATTTTTAATCTTTTTATCTGTCTCCTGGGATTACAGCAGCTCTGTCAAATAGCAATATAATACAGGCCAGATGTGTAATGTAACATTTTCTAGTAGCCACATTTAATGATAAAAGTAAAAAAGGAACGGGTAACATTAATTTAATGATATATTTTATTTAACCCAG... | CTGTCTCAAAAAACAAAAACAAACAAACAAACAAACAAACAAACAAACAAAAAAACCCAACAAACCCACCAAACATACCATATTTGGTTTCTGTAAAAAAATAAAAAAGAGAGAGAGAATTTTTAAAAAACAAAAACCATACTATCTAATTTACATTTTTAATCTTTTTATCTGTCTCCTGGGATTACAGCAGCTCTGTCAAATAGCAATATAATACAGGCCAGATGTGTAATGTAACATTTTCTAGTAGCCACATTTAATGATAAAAGTAAAAAAGGAACGGGTAACATTAATTTAATGATATATTTTATTTAACCCAG... |
Task1_train_47338 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AATTTCTGAATTGCCTGTTGTGATATCTAGAGAGGTGTTAGACTTCCTGAGTTGGCTGAGAGCGATGGGAACAGGGATGGAGACTTCCTGGAAGGTGGAGGAGAGCAGGATCTGCTAGGTGGTTGGTAGAACTGCTAGAGTGGGTTGGATGTCAGGGTAACTGAGTGGGCATAGGATTTTCTGACTGTGTGTGACAGGCCTCTGGGAGGGAAAGTGGAGACTTCTTGGAAACTTCTTGGATGTTGGGTGGGACTTCTGAGCATAATACTGAACTTCCTAGCAGGTGAGTGGGACTTCCTGGATTAAATCGGGCAATTCCT... | AATTTCTGAATTGCCTGTTGTGATATCTAGAGAGGTGTTAGACTTCCTGAGTTGGCTGAGAGCGATGGGAACAGGGATGGAGACTTCCTGGAAGGTGGAGGAGAGCAGGATCTGCTAGGTGGTTGGTAGAACTGCTAGAGTGGGTTGGATGTCAGGGTAACTGAGTGGGCATAGGATTTTCTGACTGTGTGTGACAGGCCTCTGGGAGGGAAAGTGGAGACTTCTTGGAAACTTCTTGGATGTTGGGTGGGACTTCTGAGCATAATACTGAACTTCCTAGCAGGTGAGTGGGACTTCCTGGATTAAATCGGGCAATTCCT... |
Task1_train_47339 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TCTGTGCCTTAAAATTCATAACACCAGACACATAAACCAAAAGTCAATTTGACTTCTTTTTTTTGAGATGGAGTCTTGCCCTGTTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCACACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGCTTTTGCCAAGTTGGCTAGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTTAGATT... | TCTGTGCCTTAAAATTCATAACACCAGACACATAAACCAAAAGTCAATTTGACTTCTTTTTTTTGAGATGGAGTCTTGCCCTGTTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCACACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGCTTTTGCCAAGTTGGCTAGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTTAGATT... |
Task1_train_47340 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | ATACAGCATGTCCCTTTTGGGGTCTGGCTTCCCTCACTCAACATGAAGTGTGTGTCAGTGTTTGTCCTTTTTCCTTGCTGTATAGTACTCTATCTATGATCAGCCCACACCACAGTCTGTTTATCCCTTCTTCTGTTGATGACACCTGGGCTGTTTCCAGTTGGAGACTCATAATAAAGCTGCTGGGATGATTCTGGAACAAGGCTATTTTGTGCACATCCATTTTCAGTTCTCTTGATTAAATGCCAAGGAGTGAGACTGCCAGGTCCTAGGCATGGTGTGGATCTAGCTTTAGTTTTTCCTAGACTCGAGTTCTTGAA... | ATACAGCATGTCCCTTTTGGGGTCTGGCTTCCCTCACTCAACATGAAGTGTGTGTCAGTGTTTGTCCTTTTTCCTTGCTGTATAGTACTCTATCTATGATCAGCCCACACCACAGTCTGTTTATCCCTTCTTCTGTTGATGACACCTGGGCTGTTTCCAGTTGGAGACTCATAATAAAGCTGCTGGGATGATTCTGGAACAAGGCTATTTTGTGCACATCCATTTTCAGTTCTCTTGATTAAATGCCAAGGAGTGAGACTGCCAGGTCCTAGGCATGGTGTGGATCTAGCTTTAGTTTTTCCTAGACTCGAGTTCTTGAA... |
Task1_train_47341 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | TGAGGGTGATGGTTCCTTCTTCACAGGGTTGTTTTGAAGATTAGAGATTATGTTTGTCCATCACAGGTATGGGCCTAGCACATGGTGGATGCTCCATCCATTCATCCATTCACCTTTCAGTTAATTAATCAAGTGATCGACCAGTTTAGGCTTCCAGCCAGCCAGTAACTCATCCGCCCATCCAGCTGATGATTTTTTCATCAACTAATTGGTTAATTCACCCAGCCATCCACTCGTCCAGTAATTAATCTGTTTGTCCATTTATCCATCAACCAATTTAGTTATCCATTCATCCAGAAACACATCATTTACCCACTTCA... | TGAGGGTGATGGTTCCTTCTTCACAGGGTTGTTTTGAAGATTAGAGATTATGTTTGTCCATCACAGGTATGGGCCTAGCACATGGTGGATGCTCCATCCATTCATCCATTCACCTTTCAGTTAATTAATCAAGTGATCGACCAGTTTAGGCTTCCAGCCAGCCAGTAACTCATCCGCCCATCCAGCTGATGATTTTTTCATCAACTAATTGGTTAATTCACCCAGCCATCCACTCGTCCAGTAATTAATCTGTTTGTCCATTTATCCATCAACCAATTTAGTTATCCATTCATCCAGAAACACATCATTTACCCACTTCA... |
Task1_train_47342 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AACCACTGTGGCCAGCTAATTTTATAATTTGTAGAGATGGGGTCTTGCTATGTTGTCCAGGCTGGTCTTGAACTCCTAGGCTCAAGTGATTCTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGCCCAGACTGGACTTGCTCACTTTTCACCCACTTCCTGTTAGCTCCTCTGACCAGAGCCCAAGTCTCAGACAATCAATCACATCTTGCCTTTGGCTTCCTGCCTTTTTCCTTCTTTCTTTCTTTTTTTTTCTTTCTTTCCTGAGACCAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCA... | AACCACTGTGGCCAGCTAATTTTATAATTTGTAGAGATGGGGTCTTGCTATGTTGTCCAGGCTGGTCTTGAACTCCTAGGCTCAAGTGATTCTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGCCCAGACTGGACTTGCTCACTTTTCACCCACTTCCTGTTAGCTCCTCTGACCAGAGCCCAAGTCTCAGACAATCAATCACATCTTGCCTTTGGCTTCCTGCCTTTTTCCTTCTTTCTTTCTTTTTTTTTCTTTCTTTCCTGAGACCAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCA... |
Task1_train_47343 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CTTCTTCCCTCCCTCCATCTCTCTCTTTTCTTTCTCTCCCTCTCTTTTTGTTTTTGAGATGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACACACCAACACACCCGGCTTTTTTGTATTTTTAGTAGATGGGGTTTCACCATATTGGCCAGGATGGTCTCGAACTCCTGACCTCGTGATCTGCCCGCTTCAGCCTCCCAAAGTGCTGGGATTACAGGAGTGAGCCAC... | CTTCTTCCCTCCCTCCATCTCTCTCTTTTCTTTCTCTCCCTCTCTTTTTGTTTTTGAGATGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACACACCAACACACCCGGCTTTTTTGTATTTTTAGTAGATGGGGTTTCACCATATTGGCCAGGATGGTCTCGAACTCCTGACCTCGTGATCTGCCCGCTTCAGCCTCCCAAAGTGCTGGGATTACAGGAGTGAGCCAC... |
Task1_train_47344 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | TACTAAAAATACAAAAATTTGCCGGGCATGGTGGCGGGCACCTGTAATCGCAGCTACTCAGGAGGCTGAGGCTGGAGAATCGTTTGAACCTGGGAGGCAGAAGTTGCAGTGAGCTGAGATTGTACCACTGCACTCCAGCCTGGGCAATAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAGAAGAAGAAAAGAAAAATTGGCCAGGCATAGTGGCGTGCACCTATAGTCCCAGAGGATTGCTTGAGCCCAGGAGTTTGAGGCTGCAAGTGAGCTATGATTACACCACTGCACTCCAGCCGGGTGACAG... | TACTAAAAATACAAAAATTTGCCGGGCATGGTGGCGGGCACCTGTAATCGCAGCTACTCAGGAGGCTGAGGCTGGAGAATCGTTTGAACCTGGGAGGCAGAAGTTGCAGTGAGCTGAGATTGTACCACTGCACTCCAGCCTGGGCAATAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAGAAGAAGAAAAGAAAAATTGGCCAGGCATAGTGGCGTGCACCTATAGTCCCAGAGGATTGCTTGAGCCCAGGAGTTTGAGGCTGCAAGTGAGCTATGATTACACCACTGCACTCCAGCCGGGTGACAG... |
Task1_train_47345 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GGCTTTTCGAAGCTGTTGGAGAATTCCAGAGGCGGAGGCAGCGGTTCCACGAAAAGGAATTCGCCATCTTCCACATCCACCGAGGGGGCGGGAGGCGGCAGGACCAGCAGGGGCAGCCCGTTCTCTTCGCTGGCCCTCGGGGAGGTCGGGGAGGGGGGCACGGACCGGCGTGGGCTGGGCGGCGGGACCCCCGGCCCGTCCTCCGAGGGGGGACCCCTTCCGCTCGTCACAGGGGCCCGGGGCTGGCAGTTTTCAAGGAACCGCACGTGCAGCGGCAGCCGCTCGGGTTCTTCGGGGGCTGCGGACCTCCAGGGCTTGCT... | GGCTTTTCGAAGCTGTTGGAGAATTCCAGAGGCGGAGGCAGCGGTTCCACGAAAAGGAATTCGCCATCTTCCACATCCACCGAGGGGGCGGGAGGCGGCAGGACCAGCAGGGGCAGCCCGTTCTCTTCGCTGGCCCTCGGGGAGGTCGGGGAGGGGGGCACGGACCGGCGTGGGCTGGGCGGCGGGACCCCCGGCCCGTCCTCCGAGGGGGGACCCCTTCCGCTCGTCACAGGGGCCCGGGGCTGGCAGTTTTCAAGGAACCGCACGTGCAGCGGCAGCCGCTCGGGTTCTTCGGGGGCTGCGGACCTCCAGGGCTTGCT... |
Task1_train_47346 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CACACAGAGAAGCAGAGGAGACCAACGGACCGGACAGAGACGAGGAGAGGAACAGGAAGAGAGAAGCTGGGAGAATCGGGAACCTGGGGGCTAGTGACCTGCACACAGGGCAGGGGCACTCGGCAGTTCCCAGAGGCCACCCCTCCCACCCCAGACATCCAGACATCTGGAACTTTGGGTGCCAAGAGTCCAGCTTAATGCAGGCAGCCTGGCTTTTGGGGGCTTTGGTGGTCCCCCAGCTCTTGGGCTTTGGCCATGGGGCTCGGGGAGCAGAGAGGGAGTGGGAGGGAGGCTGGGGAGGTGCCCAGGAGGAGGAGCGG... | CACACAGAGAAGCAGAGGAGACCAACGGACCGGACAGAGACGAGGAGAGGAACAGGAAGAGAGAAGCTGGGAGAATCGGGAACCTGGGGGCTAGTGACCTGCACACAGGGCAGGGGCACTCGGCAGTTCCCAGAGGCCACCCCTCCCACCCCAGACATCCAGACATCTGGAACTTTGGGTGCCAAGAGTCCAGCTTAATGCAGGCAGCCTGGCTTTTGGGGGCTTTGGTGGTCCCCCAGCTCTTGGGCTTTGGCCATGGGGCTCGGGGAGCAGAGAGGGAGTGGGAGGGAGGCTGGGGAGGTGCCCAGGAGGAGGAGCGG... |
Task1_train_47347 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TGGGTTAATCCACGCACTGTGCTTACAATAGTGCCTGGTGTACAGTGAGGGCCTTGCCAGGGTTTGAGGCTACACATTTGGCAACTCCTCCCCACAGTCCTATAATCAGAAAACCCAAAACCTGGGCAGCGGGAGCTGACCTGAAATGATGCAATGCTTTTTTTTTTTTTTTTTTTTTTGGAGACAGGATCTCACTCTGTCACCCAGGCTGGAGTGCAATGGCATTATCATAGCTCACTGCAGCCTCCATCTCCCTGGCTATAGGAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGGCAGGCAGGGGCACACCATCAT... | TGGGTTAATCCACGCACTGTGCTTACAATAGTGCCTGGTGTACAGTGAGGGCCTTGCCAGGGTTTGAGGCTACACATTTGGCAACTCCTCCCCACAGTCCTATAATCAGAAAACCCAAAACCTGGGCAGCGGGAGCTGACCTGAAATGATGCAATGCTTTTTTTTTTTTTTTTTTTTTTGGAGACAGGATCTCACTCTGTCACCCAGGCTGGAGTGCAATGGCATTATCATAGCTCACTGCAGCCTCCATCTCCCTGGCTATAGGAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGGCAGGCAGGGGCACACCATCAT... |
Task1_train_47348 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGGTTAATCCACGCACTGTGCTTACAATAGTGCCTGGTGTACAGTGAGGGCCTTGCCAGGGTTTGAGGCTACACATTTGGCAACTCCTCCCCACAGTCCTATAATCAGAAAACCCAAAACCTGGGCAGCGGGAGCTGACCTGAAATGATGCAATGCTTTTTTTTTTTTTTTTTTTTTTGGAGACAGGATCTCACTCTGTCACCCAGGCTGGAGTGCAATGGCATTATCATAGCTCACTGCAGCCTCCATCTCCCTGGCTATAGGAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGGCAGGCAGGGGCACACCATCATG... | GGGTTAATCCACGCACTGTGCTTACAATAGTGCCTGGTGTACAGTGAGGGCCTTGCCAGGGTTTGAGGCTACACATTTGGCAACTCCTCCCCACAGTCCTATAATCAGAAAACCCAAAACCTGGGCAGCGGGAGCTGACCTGAAATGATGCAATGCTTTTTTTTTTTTTTTTTTTTTTGGAGACAGGATCTCACTCTGTCACCCAGGCTGGAGTGCAATGGCATTATCATAGCTCACTGCAGCCTCCATCTCCCTGGCTATAGGAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGGCAGGCAGGGGCACACCATCATG... |
Task1_train_47349 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CTAACCCAGTGGACTCCACAACTCCAAAAATTAACTTCCTAGGGACAGGTAGAGAGCAGGGAAAACCGATGACACTCTCGGCTGTGCACTGTAACTGCTACAAGTAATGTGGAGGCGCTGGCCAATACAGTAGCCATGACCATGTATGGCTATTTAAATTTAGGTTAAATAAAATGGAGTGTTCAGCTCCCAACCATCACATGGGCCACACATCCACCACTGCAATCATTTCTCAGATGCTGATGAGAGCTACTCCTCCCACACTCATGCAGCAGCAGGCGCTGTGGAGCACCTGCACGGGTGCCCTTTGAGCCCCTGGC... | CTAACCCAGTGGACTCCACAACTCCAAAAATTAACTTCCTAGGGACAGGTAGAGAGCAGGGAAAACCGATGACACTCTCGGCTGTGCACTGTAACTGCTACAAGTAATGTGGAGGCGCTGGCCAATACAGTAGCCATGACCATGTATGGCTATTTAAATTTAGGTTAAATAAAATGGAGTGTTCAGCTCCCAACCATCACATGGGCCACACATCCACCACTGCAATCATTTCTCAGATGCTGATGAGAGCTACTCCTCCCACACTCATGCAGCAGCAGGCGCTGTGGAGCACCTGCACGGGTGCCCTTTGAGCCCCTGGC... |
Task1_train_47350 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | CCTGACGCTCTTTTCAGTTAACGGCAAGGCGGTGCACCCAAGTCCGGTGGTGTCCTACCTGGTGACCTCCTACCTGTGCTGGGACGCCAGCGACTTGATGCTGCACTCCGGTGAGGGCGGGGCCTCGGGAGGAGGGCGGGGCCTCGGGAAGCGGGTGGGGCCTAGGGTGGGACTCGGAGTACAGCGGCCCACCTAGCCATCTCCCAGGAGCCGTGTCCTACCTAAGCCCAGTGGGCATGTGAAGCAGAGGGCAGCCCTTGAATGCGCGGCGGCTGAGCTACCGCGGGTGGGCCGTGCAGCAGGGCGCAGCGAGGCGGACA... | CCTGACGCTCTTTTCAGTTAACGGCAAGGCGGTGCACCCAAGTCCGGTGGTGTCCTACCTGGTGACCTCCTACCTGTGCTGGGACGCCAGCGACTTGATGCTGCACTCCGGTGAGGGCGGGGCCTCGGGAGGAGGGCGGGGCCTCGGGAAGCGGGTGGGGCCTAGGGTGGGACTCGGAGTACAGCGGCCCACCTAGCCATCTCCCAGGAGCCGTGTCCTACCTAAGCCCAGTGGGCATGTGAAGCAGAGGGCAGCCCTTGAATGCGCGGCGGCTGAGCTACCGCGGGTGGGCCGTGCAGCAGGGCGCAGCGAGGCGGACA... |
Task1_train_47351 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | AAGCAGAGGGCAGCCCTTGAATGCGCGGCGGCTGAGCTACCGCGGGTGGGCCGTGCAGCAGGGCGCAGCGAGGCGGACATCCAAACAGCGGAACTCAGACGCTGACTCCGAGCGCACCCCGGGCCTTCCCATTTCATACACCCTCGAGGATGAGACCCAAGCACCTCCAAGGAATAGCACCCGAGGTCTTCAGGACACCGACCGGTAGCCATGGCCAGATGCCCGGCCAACCCCTTCAGCGTGGCCACGCCCTGGATATTCGACCTCCCCTGAGGCCCCACCCCCTGATATCAGGCCACGCCCTCCGAGGGGACCGGTGG... | AAGCAGAGGGCAGCCCTTGAATGCGCGGCGGCTGAGCTACCGCGGGTGGGCCGTGCAGCAGGGCGCAGCGAGGCGGACATCCAAACAGCGGAACTCAGACGCTGACTCCGAGCGCACCCCGGGCCTTCCCATTTCATACACCCTCGAGGATGAGACCCAAGCACCTCCAAGGAATAGCACCCGAGGTCTTCAGGACACCGACCGGTAGCCATGGCCAGATGCCCGGCCAACCCCTTCAGCGTGGCCACGCCCTGGATATTCGACCTCCCCTGAGGCCCCACCCCCTGATATCAGGCCACGCCCTCCGAGGGGACCGGTGG... |
Task1_train_47352 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | CAGGCTGGCCTCGAACTCCTGACCTGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTCAGCCACCGCGCCCAGCCACTTTTGTCAAATTCTTGAGACACAGCTCGGGCTGGATCAAGTGAGCTACTCTGGTTTTATTGAACAGCTGAAATAACCAACTTTTTGGAAATTGATGAAATCTTACGGAGTTAACAGTGGAGGTACCAGGGCTCTTAAGAGTTCCCGATTCTCTTCTGAGACTACAAATTGTGATTTTGCATGCCACCTTAATCTTTTTTTTTTTTTTTTTAAATCGAGGTTTCAGTCT... | CAGGCTGGCCTCGAACTCCTGACCTGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTCAGCCACCGCGCCCAGCCACTTTTGTCAAATTCTTGAGACACAGCTCGGGCTGGATCAAGTGAGCTACTCTGGTTTTATTGAACAGCTGAAATAACCAACTTTTTGGAAATTGATGAAATCTTACGGAGTTAACAGTGGAGGTACCAGGGCTCTTAAGAGTTCCCGATTCTCTTCTGAGACTACAAATTGTGATTTTGCATGCCACCTTAATCTTTTTTTTTTTTTTTTTAAATCGAGGTTTCAGTCT... |
Task1_train_47353 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | TCCATCTCCTATCCGAGTCCCCCAGTTCCTCCTGTCAACCCTGATTCCCCTGATCTAGCACCCCCTCTGCAGGTGCTGCACCCCTCATCCTGTCTCGGATTGTGGGAGGCTGGGAGTGCGAGAAGCATTCCCAACCCTGGCAGGTGCTTGTGGCCTCTCGTGGCAGGGCAGTCTGCGGCGGTGTTCTGGTGCACCCCCAGTGGGTCCTCACAGCTGCCCACTGCATCAGGAAGTGAGTAGGGGCCTGGGGTCTGGGGAGCAGGTGTCTGTGTCCCAGAGGAATAACAGCTGGGCATTTTCCCCAGGATAACCTCTAAGGC... | TCCATCTCCTATCCGAGTCCCCCAGTTCCTCCTGTCAACCCTGATTCCCCTGATCTAGCACCCCCTCTGCAGGTGCTGCACCCCTCATCCTGTCTCGGATTGTGGGAGGCTGGGAGTGCGAGAAGCATTCCCAACCCTGGCAGGTGCTTGTGGCCTCTCGTGGCAGGGCAGTCTGCGGCGGTGTTCTGGTGCACCCCCAGTGGGTCCTCACAGCTGCCCACTGCATCAGGAAGTGAGTAGGGGCCTGGGGTCTGGGGAGCAGGTGTCTGTGTCCCAGAGGAATAACAGCTGGGCATTTTCCCCAGGATAACCTCTAAGGC... |
Task1_train_47354 | 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 | AATAGCCAGGTCTGGCTGGGTCGGCACAACCTGTTTGAGCCTGAAGACACAGGCCAGAGGGTCCCTGTCAGCCACAGCTTCCCACACCCGCTCTACAATATGAGCCTTCTGAAGCATCAAAGCCTTAGACCAGATGAAGACTCCAGCCATGACCTCATGCTGCTCCGCCTGTCAGAGCCTGCCAAGATCACAGATGTTGTGAAGGTCCTGGGCCTGCCCACCCAGGAGCCAGCACTGGGGACCACCTGCTACGCCTCAGGCTGGGGCAGCATCGAACCAGAGGAGTGTACGCCTGGGCCAGATGGTGTAGCTGGGAGCCC... | AATAGCCAGGTCTGGCTGGGTCGGCACAACCTGTTTGAGCCTGAAGACACAGGCCAGAGGGTCCCTGTCAGCCACAGCTTCCCACACCCGCTCTACAATATGAGCCTTCTGAAGCATCAAAGCCTTAGACCAGATGAAGACTCCAGCCATGACCTCATGCTGCTCCGCCTGTCAGAGCCTGCCAAGATCACAGATGTTGTGAAGGTCCTGGGCCTGCCCACCCAGGAGCCAGCACTGGGGACCACCTGCTACGCCTCAGGCTGGGGCAGCATCGAACCAGAGGAGTGTACGCCTGGGCCAGATGGTGTAGCTGGGAGCCC... |
Task1_train_47355 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TGTTTATCTGTCTCAGTGTCTCTGCATCTCTTTGTAAAGTCTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTTACTCTGTTGCCCCAGCTGGAGTATAGTGGTGTGATCTCAACTCACTTCAACCTCTGCCTCCCATATTCAAGCAATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCTGCCACCATATCCAGCTAACTTTTGTATTTTTAGTACAGACAGGATTTCACCATTTTGGCCAGGCTGGTCTTGAACTCCTTACCTCAAGTGATCTGCCTGCCTCGCCTCCCAAAGTGCTGGGATTACAG... | TGTTTATCTGTCTCAGTGTCTCTGCATCTCTTTGTAAAGTCTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTTACTCTGTTGCCCCAGCTGGAGTATAGTGGTGTGATCTCAACTCACTTCAACCTCTGCCTCCCATATTCAAGCAATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCTGCCACCATATCCAGCTAACTTTTGTATTTTTAGTACAGACAGGATTTCACCATTTTGGCCAGGCTGGTCTTGAACTCCTTACCTCAAGTGATCTGCCTGCCTCGCCTCCCAAAGTGCTGGGATTACAG... |
Task1_train_47356 | Chromosome 19 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTTTCTTCACCATGGATGACAGCCTGGCCTGGCTATTGAGCTTCACGAGCATGAGGTCATTAACATGGGTCTGTGTGGAGTAGCCGGGGTGGCGGAATGACTTCGAGGCCTTGATCCTCTGAGCTCTCCTGTCGCCCAGCGTATCACTGCCCAGGTGCACGGTGTACTCACTGCGAGGAGTGACATTCACAGATTCAGAAGAGACACTGTGACAGAGAGGGTGTGCAAAGACCTGGGGGACGGGGTGGGGACAGAGACCCAGAGAGAGGAGGGGGGACAGAGACACAGAGAGAGGAGGGGAGACAGAGACCCAGAGAGAG... | CTTTCTTCACCATGGATGACAGCCTGGCCTGGCTATTGAGCTTCACGAGCATGAGGTCATTAACATGGGTCTGTGTGGAGTAGCCGGGGTGGCGGAATGACTTCGAGGCCTTGATCCTCTGAGCTCTCCTGTCGCCCAGCGTATCACTGCCCAGGTGCACGGTGTACTCACTGCGAGGAGTGACATTCACAGATTCAGAAGAGACACTGTGACAGAGAGGGTGTGCAAAGACCTGGGGGACGGGGTGGGGACAGAGACCCAGAGAGAGGAGGGGGGACAGAGACACAGAGAGAGGAGGGGAGACAGAGACCCAGAGAGAG... |
Task1_train_47357 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | GGAGTTTTCCAGCTGCATGGGGGAATTTTCTGACACTGTGCACAGGGGACATCACTTCTCACCACATTAAACGAAGCTGTACTTGTTGCTATTGGGCTTTCTCCATCTAGAGAGGGGCCCTTGGATCTCACGTGTTTTTTCTTACCCTGAGCCATTTTCAAATCAAGGGGCTGGGGGTTACTTGGAGGTGCCCCTTTATGATACCTCTGACCCTCTCTTTCCAGTCTTCCTGCCCTCAGACAACCGGGTCCTCAATCTGTGCTAAATCCTGCTCCTTCCAAGTGTCACCTCCTCCTGGAAGCCTTCCCTGACCACTCGAA... | GGAGTTTTCCAGCTGCATGGGGGAATTTTCTGACACTGTGCACAGGGGACATCACTTCTCACCACATTAAACGAAGCTGTACTTGTTGCTATTGGGCTTTCTCCATCTAGAGAGGGGCCCTTGGATCTCACGTGTTTTTTCTTACCCTGAGCCATTTTCAAATCAAGGGGCTGGGGGTTACTTGGAGGTGCCCCTTTATGATACCTCTGACCCTCTCTTTCCAGTCTTCCTGCCCTCAGACAACCGGGTCCTCAATCTGTGCTAAATCCTGCTCCTTCCAAGTGTCACCTCCTCCTGGAAGCCTTCCCTGACCACTCGAA... |
Task1_train_47358 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTTTCCCAATCTTCACTACCCCCTCGGCCCTCTGGTCTTAGAGGCTGGGATAGAAGCAAGGTGAGGTCCCTTGAGTTCAGTGGCCTCATGAAGGCAGAGAAGGTGCTAATGACTCAGGGCCAGCCTAGCTCGGAGGAACTGGTGTTGGGTGGAACCAGAAGTGGGAAACAGTGGGAGATGAGAAGGAAGTGGTTAAAAGGTGTTTCCTGGGACTTGGAACTAGGGTGAGGAAAATGATTCTTCCATCATCCCTAAGGGTTGGGGATGGAAGGTTGGGACTGGGGGCTACCCTGTGCACTTCTTCCCTGGACACACGCTTT... | GTTTCCCAATCTTCACTACCCCCTCGGCCCTCTGGTCTTAGAGGCTGGGATAGAAGCAAGGTGAGGTCCCTTGAGTTCAGTGGCCTCATGAAGGCAGAGAAGGTGCTAATGACTCAGGGCCAGCCTAGCTCGGAGGAACTGGTGTTGGGTGGAACCAGAAGTGGGAAACAGTGGGAGATGAGAAGGAAGTGGTTAAAAGGTGTTTCCTGGGACTTGGAACTAGGGTGAGGAAAATGATTCTTCCATCATCCCTAAGGGTTGGGGATGGAAGGTTGGGACTGGGGGCTACCCTGTGCACTTCTTCCCTGGACACACGCTTT... |
Task1_train_47359 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GACTCAGGGCCAGCCTAGCTCGGAGGAACTGGTGTTGGGTGGAACCAGAAGTGGGAAACAGTGGGAGATGAGAAGGAAGTGGTTAAAAGGTGTTTCCTGGGACTTGGAACTAGGGTGAGGAAAATGATTCTTCCATCATCCCTAAGGGTTGGGGATGGAAGGTTGGGACTGGGGGCTACCCTGTGCACTTCTTCCCTGGACACACGCTTTCACCGGGACGTGGTCAGATCACGACAACAGGTAACCTTTAGTCAGAACTCACCACCCACTGTGTTAAGCCTTACATGACAATCACCATGAAGATTTACATACACATGTTA... | GACTCAGGGCCAGCCTAGCTCGGAGGAACTGGTGTTGGGTGGAACCAGAAGTGGGAAACAGTGGGAGATGAGAAGGAAGTGGTTAAAAGGTGTTTCCTGGGACTTGGAACTAGGGTGAGGAAAATGATTCTTCCATCATCCCTAAGGGTTGGGGATGGAAGGTTGGGACTGGGGGCTACCCTGTGCACTTCTTCCCTGGACACACGCTTTCACCGGGACGTGGTCAGATCACGACAACAGGTAACCTTTAGTCAGAACTCACCACCCACTGTGTTAAGCCTTACATGACAATCACCATGAAGATTTACATACACATGTTA... |
Task1_train_47360 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CTCGGAGGAACTGGTGTTGGGTGGAACCAGAAGTGGGAAACAGTGGGAGATGAGAAGGAAGTGGTTAAAAGGTGTTTCCTGGGACTTGGAACTAGGGTGAGGAAAATGATTCTTCCATCATCCCTAAGGGTTGGGGATGGAAGGTTGGGACTGGGGGCTACCCTGTGCACTTCTTCCCTGGACACACGCTTTCACCGGGACGTGGTCAGATCACGACAACAGGTAACCTTTAGTCAGAACTCACCACCCACTGTGTTAAGCCTTACATGACAATCACCATGAAGATTTACATACACATGTTATATCATAGTCTCCTCACA... | CTCGGAGGAACTGGTGTTGGGTGGAACCAGAAGTGGGAAACAGTGGGAGATGAGAAGGAAGTGGTTAAAAGGTGTTTCCTGGGACTTGGAACTAGGGTGAGGAAAATGATTCTTCCATCATCCCTAAGGGTTGGGGATGGAAGGTTGGGACTGGGGGCTACCCTGTGCACTTCTTCCCTGGACACACGCTTTCACCGGGACGTGGTCAGATCACGACAACAGGTAACCTTTAGTCAGAACTCACCACCCACTGTGTTAAGCCTTACATGACAATCACCATGAAGATTTACATACACATGTTATATCATAGTCTCCTCACA... |
Task1_train_47361 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | GTAGTTCATGGAAGGTGAGGGGATGAAAATGGGCTTGGAGATGGGAATGGGGTGGGGTTGGGATGGAAATGGGATTGAGGATAGGGATGAGGAGGGGGTTAGGTCTGGGTAAGAGTTGGGGTCAAGGATGGGTTTGGGAATGGAGTTGGGGATCGGGCACAGGGTCTGCTCTTTTCCCATAACCTCCCTGTCCTCCCTCCCAGGAGTCAGAGACTCTCCCTGTTCAGACCCTACCTGGCAAGGGTCCTGGCCCCGGTCCAGTCCAGCACATATCATGTTGTTGGTGACCACGCCAGGGTAGAAGACCTCACACTCTTTAG... | GTAGTTCATGGAAGGTGAGGGGATGAAAATGGGCTTGGAGATGGGAATGGGGTGGGGTTGGGATGGAAATGGGATTGAGGATAGGGATGAGGAGGGGGTTAGGTCTGGGTAAGAGTTGGGGTCAAGGATGGGTTTGGGAATGGAGTTGGGGATCGGGCACAGGGTCTGCTCTTTTCCCATAACCTCCCTGTCCTCCCTCCCAGGAGTCAGAGACTCTCCCTGTTCAGACCCTACCTGGCAAGGGTCCTGGCCCCGGTCCAGTCCAGCACATATCATGTTGTTGGTGACCACGCCAGGGTAGAAGACCTCACACTCTTTAG... |
Task1_train_47362 | 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 | TTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCAGAGATAGCACCACTGTACTCCAGCCTGGGTGACAGAGCGAGACTCTGTCAAAAAATAAAATAAAATAAAAGCCATTGGATCAGGGTCTAGCACATAGTAAGCACTCAGTAGATTCACTCATTTAGCAAATATTTATTGAAACCTTGATATATGGCCAGGAGCTGTCTTTGGGGCTGGGGATACAACAGAGAACAAACCAGGTGTTGTCATTCCCAGAGTCACAATATTTCAAGGCAGAATTTGAATCCAGGTCTCACTGAT... | TTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCAGAGATAGCACCACTGTACTCCAGCCTGGGTGACAGAGCGAGACTCTGTCAAAAAATAAAATAAAATAAAAGCCATTGGATCAGGGTCTAGCACATAGTAAGCACTCAGTAGATTCACTCATTTAGCAAATATTTATTGAAACCTTGATATATGGCCAGGAGCTGTCTTTGGGGCTGGGGATACAACAGAGAACAAACCAGGTGTTGTCATTCCCAGAGTCACAATATTTCAAGGCAGAATTTGAATCCAGGTCTCACTGAT... |
Task1_train_47363 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGAGCATGGTGTTAGCCAGGGAGGAGGTGGGGACGGTGCTTAGGAGTGGGGCCGAGACAGGATGGGTAGGCACTGGGAAAGGTGATAGGTTTAGCGATAAAGCTGGGATTATGGGTGGGATAAAGGATGGGGTTAGGCTCAAAAACGAGTTTGGGGATGGTTGGAGCTGGAAATGGTGTGGAAACGGGGATGGAGCTGAAGTTTGTGCTGAGGTCAGAAACGGGAACAGGGGAAGAGATGGATTGGGAGTTGCAGGGGTCGGCGGGTTGAGGTTGGGGATGAAATTGTGGATGTCGGTAAAGATGTCATTGAAGCTGGGG... | TGAGCATGGTGTTAGCCAGGGAGGAGGTGGGGACGGTGCTTAGGAGTGGGGCCGAGACAGGATGGGTAGGCACTGGGAAAGGTGATAGGTTTAGCGATAAAGCTGGGATTATGGGTGGGATAAAGGATGGGGTTAGGCTCAAAAACGAGTTTGGGGATGGTTGGAGCTGGAAATGGTGTGGAAACGGGGATGGAGCTGAAGTTTGTGCTGAGGTCAGAAACGGGAACAGGGGAAGAGATGGATTGGGAGTTGCAGGGGTCGGCGGGTTGAGGTTGGGGATGAAATTGTGGATGTCGGTAAAGATGTCATTGAAGCTGGGG... |
Task1_train_47364 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGCATCCAGGCCCTCATGACCACTGCTCCAGTTCAGGTGCCTTATGGGTTGTTCTGTAATTTGGAATCAGCCCTGTCACTGTCCAGACACAGAGGGTTAGGGGATCCCAGAGATTCAAGAGGGAGGATCCTGCCCTGCCCCCATCCCCTGCGTACCTGTTGCCAGAGCAAGCAGGATTAACTGCAGAATCCTCATGGCCTGGAGGGGGGAGGAGCGGGCCCCAGGTTCCTCTGGGAACAAGGAGGGACATGGGGCCGCATCACTTTACGGGGAAATCGGGAGGGGGGGGCTGGCTCATGCCCTCTCCTCTCTCCCTCACC... | GGCATCCAGGCCCTCATGACCACTGCTCCAGTTCAGGTGCCTTATGGGTTGTTCTGTAATTTGGAATCAGCCCTGTCACTGTCCAGACACAGAGGGTTAGGGGATCCCAGAGATTCAAGAGGGAGGATCCTGCCCTGCCCCCATCCCCTGCGTACCTGTTGCCAGAGCAAGCAGGATTAACTGCAGAATCCTCATGGCCTGGAGGGGGGAGGAGCGGGCCCCAGGTTCCTCTGGGAACAAGGAGGGACATGGGGCCGCATCACTTTACGGGGAAATCGGGAGGGGGGGGCTGGCTCATGCCCTCTCCTCTCTCCCTCACC... |
Task1_train_47365 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | CTCCTTTTTTTTTTTTTTTTTTTTTTCAAGACCGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACCATCTTGGCTCACTACAACCTCCACCTCCCAGGTTCAAGCAATTCACCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGAAGCATGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATAAGGTTTCACCATGTGTGTCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCAGGCCTCTCTTTCTGA... | CTCCTTTTTTTTTTTTTTTTTTTTTTCAAGACCGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACCATCTTGGCTCACTACAACCTCCACCTCCCAGGTTCAAGCAATTCACCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGAAGCATGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATAAGGTTTCACCATGTGTGTCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCAGGCCTCTCTTTCTGA... |
Task1_train_47366 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | GCGGGCTGCTGTAGCTGCAGCAGCATGAGGTCGTTGTCGTGGGTCCGGGAGTTGTAGTTGGGGTGCGTCACCTGACGAACCACGCGCAGCACCTGCTGGGTGGCCTCCCACCTCCTCAGGTTGTGCTTGCCCAGGGCAACCTGAAGGATCCTGGCCACGACCCCCAAGAGAAGCGCTGCTCAGGGTCTGAGCCAGAGACTCCTCCCCACCCTCCAGCCCGGTTCCCTGGCCGGGTGACGAGTCTTCCCCGAGGTCTAGCCTGCTTCTCACTAACTGCAGGCCGAGCATTCTTGGCCTCCTGTGCCCTTCCCCATGGCCAG... | GCGGGCTGCTGTAGCTGCAGCAGCATGAGGTCGTTGTCGTGGGTCCGGGAGTTGTAGTTGGGGTGCGTCACCTGACGAACCACGCGCAGCACCTGCTGGGTGGCCTCCCACCTCCTCAGGTTGTGCTTGCCCAGGGCAACCTGAAGGATCCTGGCCACGACCCCCAAGAGAAGCGCTGCTCAGGGTCTGAGCCAGAGACTCCTCCCCACCCTCCAGCCCGGTTCCCTGGCCGGGTGACGAGTCTTCCCCGAGGTCTAGCCTGCTTCTCACTAACTGCAGGCCGAGCATTCTTGGCCTCCTGTGCCCTTCCCCATGGCCAG... |
Task1_train_47367 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TGGGGTGCGTCACCTGACGAACCACGCGCAGCACCTGCTGGGTGGCCTCCCACCTCCTCAGGTTGTGCTTGCCCAGGGCAACCTGAAGGATCCTGGCCACGACCCCCAAGAGAAGCGCTGCTCAGGGTCTGAGCCAGAGACTCCTCCCCACCCTCCAGCCCGGTTCCCTGGCCGGGTGACGAGTCTTCCCCGAGGTCTAGCCTGCTTCTCACTAACTGCAGGCCGAGCATTCTTGGCCTCCTGTGCCCTTCCCCATGGCCAGGGCATTCTCTCGGCCCAGCCCCAGCTGCCTCTCCTTCCGCTCTTGGGCTGGGCTCCAG... | TGGGGTGCGTCACCTGACGAACCACGCGCAGCACCTGCTGGGTGGCCTCCCACCTCCTCAGGTTGTGCTTGCCCAGGGCAACCTGAAGGATCCTGGCCACGACCCCCAAGAGAAGCGCTGCTCAGGGTCTGAGCCAGAGACTCCTCCCCACCCTCCAGCCCGGTTCCCTGGCCGGGTGACGAGTCTTCCCCGAGGTCTAGCCTGCTTCTCACTAACTGCAGGCCGAGCATTCTTGGCCTCCTGTGCCCTTCCCCATGGCCAGGGCATTCTCTCGGCCCAGCCCCAGCTGCCTCTCCTTCCGCTCTTGGGCTGGGCTCCAG... |
Task1_train_47368 | This mutation on Chromosome 19 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TGCTGGGTGGCCTCCCACCTCCTCAGGTTGTGCTTGCCCAGGGCAACCTGAAGGATCCTGGCCACGACCCCCAAGAGAAGCGCTGCTCAGGGTCTGAGCCAGAGACTCCTCCCCACCCTCCAGCCCGGTTCCCTGGCCGGGTGACGAGTCTTCCCCGAGGTCTAGCCTGCTTCTCACTAACTGCAGGCCGAGCATTCTTGGCCTCCTGTGCCCTTCCCCATGGCCAGGGCATTCTCTCGGCCCAGCCCCAGCTGCCTCTCCTTCCGCTCTTGGGCTGGGCTCCAGCTCCTGGCTTGGGAAGAAGGTGATGATTGGGAGAG... | TGCTGGGTGGCCTCCCACCTCCTCAGGTTGTGCTTGCCCAGGGCAACCTGAAGGATCCTGGCCACGACCCCCAAGAGAAGCGCTGCTCAGGGTCTGAGCCAGAGACTCCTCCCCACCCTCCAGCCCGGTTCCCTGGCCGGGTGACGAGTCTTCCCCGAGGTCTAGCCTGCTTCTCACTAACTGCAGGCCGAGCATTCTTGGCCTCCTGTGCCCTTCCCCATGGCCAGGGCATTCTCTCGGCCCAGCCCCAGCTGCCTCTCCTTCCGCTCTTGGGCTGGGCTCCAGCTCCTGGCTTGGGAAGAAGGTGATGATTGGGAGAG... |
Task1_train_47369 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TTTGCTTCTGTAGGTCTGTGCATAACGTCACTTCCTCCAAGGCCCTTCCTTCCCTGACCCCTGTGGAAACAAGCTCTTCCTGTCTCTCTCTCTCATCATTTTTTTTTTAATTTGTAGCATTCATCACTACCTGACATTACATATTGATGTGCTTGCTGTCCGTTTCTCCCAGACTGAACTTCATGAGGGCAGAGACTTGTCTCCTGTTCACTGCCATGTTCCTAGAACCCAGAGGAGTGCCTGATGCAAAGGAGATGCTCATACACGTTTTGAGTGAATCATCTAGTCCTTGGCCTCCAGCCCAAGTTTGGGTGGCCACA... | TTTGCTTCTGTAGGTCTGTGCATAACGTCACTTCCTCCAAGGCCCTTCCTTCCCTGACCCCTGTGGAAACAAGCTCTTCCTGTCTCTCTCTCTCATCATTTTTTTTTTAATTTGTAGCATTCATCACTACCTGACATTACATATTGATGTGCTTGCTGTCCGTTTCTCCCAGACTGAACTTCATGAGGGCAGAGACTTGTCTCCTGTTCACTGCCATGTTCCTAGAACCCAGAGGAGTGCCTGATGCAAAGGAGATGCTCATACACGTTTTGAGTGAATCATCTAGTCCTTGGCCTCCAGCCCAAGTTTGGGTGGCCACA... |
Task1_train_47370 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTTTTCTAGGGAAGCCGAAGGATTGTTCCCCGAGTTCCAGGTGGGGCTGAGCTGTCCTGTCCCGCCTGAGTTAGAATTGAAGTGGCCGATGCTAATCTGAGGCCCGTGTTGGCTCTGCAGGTGTGGAGGGCCCCAGGGGAGCAGTGCTGAGAGGCCTGACTGAGCCCCTCCTGCTCAAGACAGAACTCAGATGTGGACACCCAGCCCTGCAGAACAGATGCAGGACAACACTGTCAGCCATGGCTCAGCCCTTCTGACCATTGCAGTTGAGATGCTGCAACTTCCCAGGGAGCGACTGGGCAAACATGGGGGCCTGAGGT... | CTTTTCTAGGGAAGCCGAAGGATTGTTCCCCGAGTTCCAGGTGGGGCTGAGCTGTCCTGTCCCGCCTGAGTTAGAATTGAAGTGGCCGATGCTAATCTGAGGCCCGTGTTGGCTCTGCAGGTGTGGAGGGCCCCAGGGGAGCAGTGCTGAGAGGCCTGACTGAGCCCCTCCTGCTCAAGACAGAACTCAGATGTGGACACCCAGCCCTGCAGAACAGATGCAGGACAACACTGTCAGCCATGGCTCAGCCCTTCTGACCATTGCAGTTGAGATGCTGCAACTTCCCAGGGAGCGACTGGGCAAACATGGGGGCCTGAGGT... |
Task1_train_47371 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AATCTGAGGCCCGTGTTGGCTCTGCAGGTGTGGAGGGCCCCAGGGGAGCAGTGCTGAGAGGCCTGACTGAGCCCCTCCTGCTCAAGACAGAACTCAGATGTGGACACCCAGCCCTGCAGAACAGATGCAGGACAACACTGTCAGCCATGGCTCAGCCCTTCTGACCATTGCAGTTGAGATGCTGCAACTTCCCAGGGAGCGACTGGGCAAACATGGGGGCCTGAGGTATTCACGGCAACGTGCACAGATGATAAAACTACCTAGAAAAGCATGGAGACCATTAGCGTTAAAGTGAGGCTGGGGCTGCTTCAGGAGGAAGT... | AATCTGAGGCCCGTGTTGGCTCTGCAGGTGTGGAGGGCCCCAGGGGAGCAGTGCTGAGAGGCCTGACTGAGCCCCTCCTGCTCAAGACAGAACTCAGATGTGGACACCCAGCCCTGCAGAACAGATGCAGGACAACACTGTCAGCCATGGCTCAGCCCTTCTGACCATTGCAGTTGAGATGCTGCAACTTCCCAGGGAGCGACTGGGCAAACATGGGGGCCTGAGGTATTCACGGCAACGTGCACAGATGATAAAACTACCTAGAAAAGCATGGAGACCATTAGCGTTAAAGTGAGGCTGGGGCTGCTTCAGGAGGAAGT... |
Task1_train_47372 | Here is a mutation located on Chromosome 19. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CAGACCAGGATGCTCCAGTGGCCACAAACAACCCAGCTCGGGCAGTGTGGGAGGAGACTCGGGACCGATTCCACCTCCTTGGGGACCCACATACCAAGAATTGCACCCTGAGCATCAGAGATGCCAGAAGAAGTGATGCGGGGAGATACTTCTTTCGTATGGAGAAAGGAAGTATAAAATGGAATTATAAACATCACCGGCTCTCTGTGAATGTGACAGGTAAGGCACAGGCTCCAGGAAAGGCCACAGGGAAAGGTCATGGGGGCGGCAGGGAAAGGCTGGGATGGAGCCCCTGCCCCAGGAGAGGGCTTAGGGTGAAG... | CAGACCAGGATGCTCCAGTGGCCACAAACAACCCAGCTCGGGCAGTGTGGGAGGAGACTCGGGACCGATTCCACCTCCTTGGGGACCCACATACCAAGAATTGCACCCTGAGCATCAGAGATGCCAGAAGAAGTGATGCGGGGAGATACTTCTTTCGTATGGAGAAAGGAAGTATAAAATGGAATTATAAACATCACCGGCTCTCTGTGAATGTGACAGGTAAGGCACAGGCTCCAGGAAAGGCCACAGGGAAAGGTCATGGGGGCGGCAGGGAAAGGCTGGGATGGAGCCCCTGCCCCAGGAGAGGGCTTAGGGTGAAG... |
Task1_train_47373 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ACCAGGATGCTCCAGTGGCCACAAACAACCCAGCTCGGGCAGTGTGGGAGGAGACTCGGGACCGATTCCACCTCCTTGGGGACCCACATACCAAGAATTGCACCCTGAGCATCAGAGATGCCAGAAGAAGTGATGCGGGGAGATACTTCTTTCGTATGGAGAAAGGAAGTATAAAATGGAATTATAAACATCACCGGCTCTCTGTGAATGTGACAGGTAAGGCACAGGCTCCAGGAAAGGCCACAGGGAAAGGTCATGGGGGCGGCAGGGAAAGGCTGGGATGGAGCCCCTGCCCCAGGAGAGGGCTTAGGGTGAAGCGA... | ACCAGGATGCTCCAGTGGCCACAAACAACCCAGCTCGGGCAGTGTGGGAGGAGACTCGGGACCGATTCCACCTCCTTGGGGACCCACATACCAAGAATTGCACCCTGAGCATCAGAGATGCCAGAAGAAGTGATGCGGGGAGATACTTCTTTCGTATGGAGAAAGGAAGTATAAAATGGAATTATAAACATCACCGGCTCTCTGTGAATGTGACAGGTAAGGCACAGGCTCCAGGAAAGGCCACAGGGAAAGGTCATGGGGGCGGCAGGGAAAGGCTGGGATGGAGCCCCTGCCCCAGGAGAGGGCTTAGGGTGAAGCGA... |
Task1_train_47374 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CACTGGGTGCTGGGTCCCGGAATCTGGGCTGGTGGTGGGGTCAGGAGGACACTGGCTCTGCCTTCCCTGTTTATGCGGCTCCTGGGGACAGACAGGGCCAGTGTCCCCAGCCCTCACAGTGATGCGGGTCTCCATGTCTTTCTGTCCCAGACCCGCCTCAGAACTTGACCATGACTGTCTTCCAAGGAGACGGCACAGGTAGGATGGAGCTCCCTCCCTGGGGCTGGAGGAGCAGGGCCTTCAGGTCAGGATGGGGCTGGCTTATTCCTCAACCTGGACTCACTTTGGCAAACAGGGATGTCCTTGTGGGTGAACTCAGG... | CACTGGGTGCTGGGTCCCGGAATCTGGGCTGGTGGTGGGGTCAGGAGGACACTGGCTCTGCCTTCCCTGTTTATGCGGCTCCTGGGGACAGACAGGGCCAGTGTCCCCAGCCCTCACAGTGATGCGGGTCTCCATGTCTTTCTGTCCCAGACCCGCCTCAGAACTTGACCATGACTGTCTTCCAAGGAGACGGCACAGGTAGGATGGAGCTCCCTCCCTGGGGCTGGAGGAGCAGGGCCTTCAGGTCAGGATGGGGCTGGCTTATTCCTCAACCTGGACTCACTTTGGCAAACAGGGATGTCCTTGTGGGTGAACTCAGG... |
Task1_train_47375 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ACCAACTTTGGGGTATACTGATCTTTTGTAGGAATTTTCGTATCTCAATTTTATTCATTTCAGCTCTGATTTTGGTTATTTGTTTTATTCTGCTAGCTTTGGGGTTGACTTGCTCTTGTTTTTCTAATTCCTCTAGGTGTAATGTTAAGTTGCTAATTTGGGATCTTTCTAACTTTTTGATATGGGTATTCTGGTACATTGCATCTTTACTTTCCTGGATGCTAGGACCAAACTGGACTAGAGTAAATTACGTGGTTCCTTCTGTCCCAAAGAAAGATGTATTTTTAACTCAGGAGCTACATCAGCCCCATCTGGCTACA... | ACCAACTTTGGGGTATACTGATCTTTTGTAGGAATTTTCGTATCTCAATTTTATTCATTTCAGCTCTGATTTTGGTTATTTGTTTTATTCTGCTAGCTTTGGGGTTGACTTGCTCTTGTTTTTCTAATTCCTCTAGGTGTAATGTTAAGTTGCTAATTTGGGATCTTTCTAACTTTTTGATATGGGTATTCTGGTACATTGCATCTTTACTTTCCTGGATGCTAGGACCAAACTGGACTAGAGTAAATTACGTGGTTCCTTCTGTCCCAAAGAAAGATGTATTTTTAACTCAGGAGCTACATCAGCCCCATCTGGCTACA... |
Task1_train_47376 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TCAGGCCGGTGCACTCCAGCCTGGGCAACAAAGCAAGACCCTGTCTTAAAAAAAAAAGCACTAAATGTATTGAATTTTCTATTACGTGCCACATGCTAAATATTTAAATAACTTACAACAGATATTATTTACTGGAGACTTAATTTGTTGTATATCAAATGAGGATGCAGCTACCTCTCTATTAGTAAGGATGAATGAAGAGTTATCTAGATACTATTGTGTGTAGAGATTTGACAAAGGTATGGTGGCAAGTACTAATATGTCCCAGGGATCAACGGTTTGCTGGATGCATACTACACAGAGTGATATGGAAAACCATG... | TCAGGCCGGTGCACTCCAGCCTGGGCAACAAAGCAAGACCCTGTCTTAAAAAAAAAAGCACTAAATGTATTGAATTTTCTATTACGTGCCACATGCTAAATATTTAAATAACTTACAACAGATATTATTTACTGGAGACTTAATTTGTTGTATATCAAATGAGGATGCAGCTACCTCTCTATTAGTAAGGATGAATGAAGAGTTATCTAGATACTATTGTGTGTAGAGATTTGACAAAGGTATGGTGGCAAGTACTAATATGTCCCAGGGATCAACGGTTTGCTGGATGCATACTACACAGAGTGATATGGAAAACCATG... |
Task1_train_47377 | With a mutation on Chromosome 19, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ACCAAATGCTCCATGCAGCTGTGTGAATTCCTGGCAGCTCTTCCAACTGTGCTCAGAGCTTGTGAGGACTGTAAGATTAACCTGTAGTAAGGAATGTAGGTATCTGCAGTGGCACTGGAGGTTGGTTGGATTCCTCTGCTTATCATTTCCCTACAAGGGGAAATCCTTCCTGTCTCTGGGACAAACCAATCTGGGCTGGGGAGATGGAGCTGCAAAGCCCGGGTGCCTCCATGCTGCCCTCCTGGGTTTCCAATTACCACAGGTAACTCTCCACTCCCTTGCTGCACTACACTACTCTCCCTTCGACACTCCACTCAAAT... | ACCAAATGCTCCATGCAGCTGTGTGAATTCCTGGCAGCTCTTCCAACTGTGCTCAGAGCTTGTGAGGACTGTAAGATTAACCTGTAGTAAGGAATGTAGGTATCTGCAGTGGCACTGGAGGTTGGTTGGATTCCTCTGCTTATCATTTCCCTACAAGGGGAAATCCTTCCTGTCTCTGGGACAAACCAATCTGGGCTGGGGAGATGGAGCTGCAAAGCCCGGGTGCCTCCATGCTGCCCTCCTGGGTTTCCAATTACCACAGGTAACTCTCCACTCCCTTGCTGCACTACACTACTCTCCCTTCGACACTCCACTCAAAT... |
Task1_train_47378 | A variant affecting Chromosome 19 has been observed. Determine if it's benign or associated with disease. | Benign | AAATGCTCCATGCAGCTGTGTGAATTCCTGGCAGCTCTTCCAACTGTGCTCAGAGCTTGTGAGGACTGTAAGATTAACCTGTAGTAAGGAATGTAGGTATCTGCAGTGGCACTGGAGGTTGGTTGGATTCCTCTGCTTATCATTTCCCTACAAGGGGAAATCCTTCCTGTCTCTGGGACAAACCAATCTGGGCTGGGGAGATGGAGCTGCAAAGCCCGGGTGCCTCCATGCTGCCCTCCTGGGTTTCCAATTACCACAGGTAACTCTCCACTCCCTTGCTGCACTACACTACTCTCCCTTCGACACTCCACTCAAATCTT... | AAATGCTCCATGCAGCTGTGTGAATTCCTGGCAGCTCTTCCAACTGTGCTCAGAGCTTGTGAGGACTGTAAGATTAACCTGTAGTAAGGAATGTAGGTATCTGCAGTGGCACTGGAGGTTGGTTGGATTCCTCTGCTTATCATTTCCCTACAAGGGGAAATCCTTCCTGTCTCTGGGACAAACCAATCTGGGCTGGGGAGATGGAGCTGCAAAGCCCGGGTGCCTCCATGCTGCCCTCCTGGGTTTCCAATTACCACAGGTAACTCTCCACTCCCTTGCTGCACTACACTACTCTCCCTTCGACACTCCACTCAAATCTT... |
Task1_train_47379 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | CCGCCAGGCAGGCGTAGGTGCCTGCGTGGCCCGGTCCGACCGCGGGCAGCAGGAGGCGCGACCCCGCGGGCACCGCGGCCTCGGCCGGGTCCGCCAGGCTCCACGTGATGTCGGCGGGCGGCCGCGAGGCGGCGGCGCAGCGCAAGGTCACGTTACTGCCCGCGGTGACAAAGCGGGCAGGCGCGGCGTCGCGGTCCGAGGAGACCGTGATGGTCGGCGGGTCCGGGCCGTCTGGAGGGAGGAGGGGTCGGGACCGCGAGTGTCAGGGTCACCTGGGACGCCGCTAGGACTCCCGGAGACTGGGTCCCCAGCCCGCTTCT... | CCGCCAGGCAGGCGTAGGTGCCTGCGTGGCCCGGTCCGACCGCGGGCAGCAGGAGGCGCGACCCCGCGGGCACCGCGGCCTCGGCCGGGTCCGCCAGGCTCCACGTGATGTCGGCGGGCGGCCGCGAGGCGGCGGCGCAGCGCAAGGTCACGTTACTGCCCGCGGTGACAAAGCGGGCAGGCGCGGCGTCGCGGTCCGAGGAGACCGTGATGGTCGGCGGGTCCGGGCCGTCTGGAGGGAGGAGGGGTCGGGACCGCGAGTGTCAGGGTCACCTGGGACGCCGCTAGGACTCCCGGAGACTGGGTCCCCAGCCCGCTTCT... |
Task1_train_47380 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | GGCAGACCCAGGCACTGTCCTTGCCTCCTCCCTGCCCTCCCTCCCCATGCTAAGCCCAGTCTCTCCTGCCACATCATGTCTCTGCTCTGTCCTGTCACCTTTGGCTGAGGCCTCATTCTCCCCCATGTGACCATCACCTCGGCCTCCCAGCCTCTAAACTCACCCAAAAGGATCTTTCTTCTTTTTTTCTTTTTGAGACAGAGTCTCGCTCTGCTCCCAGGCAGGAGTGCAGTGGTGCCTGGAGTGCAGTGGTGCGATCTTGTATCACTGCAACCTCCGCCTCCCAGGTTCCAGTGATTCTCATGCCTCAGCCTCCCAAG... | GGCAGACCCAGGCACTGTCCTTGCCTCCTCCCTGCCCTCCCTCCCCATGCTAAGCCCAGTCTCTCCTGCCACATCATGTCTCTGCTCTGTCCTGTCACCTTTGGCTGAGGCCTCATTCTCCCCCATGTGACCATCACCTCGGCCTCCCAGCCTCTAAACTCACCCAAAAGGATCTTTCTTCTTTTTTTCTTTTTGAGACAGAGTCTCGCTCTGCTCCCAGGCAGGAGTGCAGTGGTGCCTGGAGTGCAGTGGTGCGATCTTGTATCACTGCAACCTCCGCCTCCCAGGTTCCAGTGATTCTCATGCCTCAGCCTCCCAAG... |
Task1_train_47381 | 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 | CACCACCAGGAGGATGGTCCCCACCCAGGCACAGAACAGGCCACCACCCATGAAGCTGTACATGGTGATCTGTGGGGAAGGGGAGAGATGGGATTGGGAGCTGAATTCCCGGGACTTGAAGGGAGGAACTGGGGGGAGAGAGGGCTCAGGAGTGGGATGCCAAGTGCTTGGGAGAAGGAGATGGAGACCTAGACGCCTGGGTCCTGGGCGAGGAGGGGACTGGAGCCCGGACTCCTGGGTCTGAGGGAGGAGGATGGTAGGGATCCTGGAAAGACAACAGGGAGAGCGGGGCTGGGTTCTGGGAAGAAAAGGCCGGGGGC... | CACCACCAGGAGGATGGTCCCCACCCAGGCACAGAACAGGCCACCACCCATGAAGCTGTACATGGTGATCTGTGGGGAAGGGGAGAGATGGGATTGGGAGCTGAATTCCCGGGACTTGAAGGGAGGAACTGGGGGGAGAGAGGGCTCAGGAGTGGGATGCCAAGTGCTTGGGAGAAGGAGATGGAGACCTAGACGCCTGGGTCCTGGGCGAGGAGGGGACTGGAGCCCGGACTCCTGGGTCTGAGGGAGGAGGATGGTAGGGATCCTGGAAAGACAACAGGGAGAGCGGGGCTGGGTTCTGGGAAGAAAAGGCCGGGGGC... |
Task1_train_47382 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GAAACCCTGCCACACCCCGGCCCAGGTGTTAGGACTTCCCATTGTGTTTTCCTGTCTACATACAGATGCCACGGGTCTGCTGTGTCCCTCCAAGCTCCTGCTCCAACCACAGGACCCTACTCTTTGCCCCAGTCAGCTTCTCCTCCAAGAACCTTGGCATCCAGGCGGCCCCCTAACCTGGCAGCTGCAGGATGGATCCACTCTGGGCCCCATGGACGTTCCAGGCCTCACAGCGGAGCCTGAGGCCGGAGCTGAGCCCTCCATGGAGGCTCAGGGAGCTGTTGGCCCAGGGCCCGGCTGAGCTGGGGGTGACCTCGAAG... | GAAACCCTGCCACACCCCGGCCCAGGTGTTAGGACTTCCCATTGTGTTTTCCTGTCTACATACAGATGCCACGGGTCTGCTGTGTCCCTCCAAGCTCCTGCTCCAACCACAGGACCCTACTCTTTGCCCCAGTCAGCTTCTCCTCCAAGAACCTTGGCATCCAGGCGGCCCCCTAACCTGGCAGCTGCAGGATGGATCCACTCTGGGCCCCATGGACGTTCCAGGCCTCACAGCGGAGCCTGAGGCCGGAGCTGAGCCCTCCATGGAGGCTCAGGGAGCTGTTGGCCCAGGGCCCGGCTGAGCTGGGGGTGACCTCGAAG... |
Task1_train_47383 | Mutation context: Chromosome 19. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCCTGTCTACATACAGATGCCACGGGTCTGCTGTGTCCCTCCAAGCTCCTGCTCCAACCACAGGACCCTACTCTTTGCCCCAGTCAGCTTCTCCTCCAAGAACCTTGGCATCCAGGCGGCCCCCTAACCTGGCAGCTGCAGGATGGATCCACTCTGGGCCCCATGGACGTTCCAGGCCTCACAGCGGAGCCTGAGGCCGGAGCTGAGCCCTCCATGGAGGCTCAGGGAGCTGTTGGCCCAGGGCCCGGCTGAGCTGGGGGTGACCTCGAAGGAGTCCTGGCTGCTGTTCCCCTCCAGCAGCTCCTCCCCAAGCCACCAGC... | TCCTGTCTACATACAGATGCCACGGGTCTGCTGTGTCCCTCCAAGCTCCTGCTCCAACCACAGGACCCTACTCTTTGCCCCAGTCAGCTTCTCCTCCAAGAACCTTGGCATCCAGGCGGCCCCCTAACCTGGCAGCTGCAGGATGGATCCACTCTGGGCCCCATGGACGTTCCAGGCCTCACAGCGGAGCCTGAGGCCGGAGCTGAGCCCTCCATGGAGGCTCAGGGAGCTGTTGGCCCAGGGCCCGGCTGAGCTGGGGGTGACCTCGAAGGAGTCCTGGCTGCTGTTCCCCTCCAGCAGCTCCTCCCCAAGCCACCAGC... |
Task1_train_47384 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | GGGATGGGTCCCTGGTAGCCGGGGAAAGGGGAGACATTGGTCCAAGTTTTGGTTAGACAGGAGGAGGGAGCCCTGGTGACCTACTGCATAGCATGGGGCTCTAGAGGGTTCTTGTTCTATGAGAATCAGCCTCTGACTTCTTTGCTGGAGGGGTTGTGATTCCTCAAACAGGCCTGAGTCTCTGCAGTTTCTCGCTTGTGGATCTTGATCTCCGAGTATTCACTGTCAGTGGCCTCCTGTCCCTGCGGGTCCTGAGGCTTCACTTTATGGAAGCTGAGGGTTGCATAATGGAGCTCTCCTTCCTCCCCTGACGAGGGGGC... | GGGATGGGTCCCTGGTAGCCGGGGAAAGGGGAGACATTGGTCCAAGTTTTGGTTAGACAGGAGGAGGGAGCCCTGGTGACCTACTGCATAGCATGGGGCTCTAGAGGGTTCTTGTTCTATGAGAATCAGCCTCTGACTTCTTTGCTGGAGGGGTTGTGATTCCTCAAACAGGCCTGAGTCTCTGCAGTTTCTCGCTTGTGGATCTTGATCTCCGAGTATTCACTGTCAGTGGCCTCCTGTCCCTGCGGGTCCTGAGGCTTCACTTTATGGAAGCTGAGGGTTGCATAATGGAGCTCTCCTTCCTCCCCTGACGAGGGGGC... |
Task1_train_47385 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTGGCCCTCAAGGACTGAAAGAGATGAGCCATTTCCCAGGGCTGTGGATGCTGCAGAGAAAGAGACAGAGGGTCATCCCATTACTGGGTATATACCCAAAGGATTATAAATCATGCTGCTATAAAGACACATGCACATGTATGTTTATTGTGGCACTATTCACAATAGCAAAGACTTGGAACCAGCCCAAATGTCCAACAATGATAGACTGGATTAAGAAAATGTGGCACATATACACCATGGAATACTATGCAGCCACAAAAAATGATGAGTTCATGTCCTTTGTAGGGACATGGATGAAGCTGGAAACCATCATTCTC... | CTGGCCCTCAAGGACTGAAAGAGATGAGCCATTTCCCAGGGCTGTGGATGCTGCAGAGAAAGAGACAGAGGGTCATCCCATTACTGGGTATATACCCAAAGGATTATAAATCATGCTGCTATAAAGACACATGCACATGTATGTTTATTGTGGCACTATTCACAATAGCAAAGACTTGGAACCAGCCCAAATGTCCAACAATGATAGACTGGATTAAGAAAATGTGGCACATATACACCATGGAATACTATGCAGCCACAAAAAATGATGAGTTCATGTCCTTTGTAGGGACATGGATGAAGCTGGAAACCATCATTCTC... |
Task1_train_47386 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | ACTCCAGTGAATTTAGATGCAAAATCAAAGACATGTAGAAATTCTCGGGGGAGTATTTCTCACCCAGACAATCATTACTGAACTCCCCCTGTGTCCAGCCTGTGCTCAGGGGCGCTGGGGACTCAGTGGTGACTGAGACAGGGCAGTCCTGCCCTCCTGGAGCCCACAGTCCAGGGCGAGATATAGATATGTGCCCAGACTCTGAGGACCCCCAGAGGTCATGGCTGGGATGGGGGGAGCCCAGGAGGAGCTGGGGGAGCCCAGAGGGGACACCTGACCCAGGCTGGGGTGGAGGAGACATCCAAGCTGAGACCTGAGTG... | ACTCCAGTGAATTTAGATGCAAAATCAAAGACATGTAGAAATTCTCGGGGGAGTATTTCTCACCCAGACAATCATTACTGAACTCCCCCTGTGTCCAGCCTGTGCTCAGGGGCGCTGGGGACTCAGTGGTGACTGAGACAGGGCAGTCCTGCCCTCCTGGAGCCCACAGTCCAGGGCGAGATATAGATATGTGCCCAGACTCTGAGGACCCCCAGAGGTCATGGCTGGGATGGGGGGAGCCCAGGAGGAGCTGGGGGAGCCCAGAGGGGACACCTGACCCAGGCTGGGGTGGAGGAGACATCCAAGCTGAGACCTGAGTG... |
Task1_train_47387 | 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 | GCCCTTCTCAGCTCCCTTGCCAGGATGCCAGATCTTATCTTACAGCTCTTGGCTTCTCTCCAACATGCCCAGAAGTCCCCTGGAGAGGAGCAGAGCTTGGGGAAGCAGACCCCACTTGTAATTTTTTTCTCTTTCCTGCTTCACCCAGAGTTGGGAAGCAATCTGGGCATCTCCGTCAATGCCAGCTCCCTGGTGGAGAACATGGATTCTGTGGCTGCTGACTGCCTCACAAATGTCACCAACATCACGTGGTATGTGAATGATGTGCCTACCTCTAGTAGTGACCGGATGACAATTTCCCCAGACGGCAAGACCCTCGT... | GCCCTTCTCAGCTCCCTTGCCAGGATGCCAGATCTTATCTTACAGCTCTTGGCTTCTCTCCAACATGCCCAGAAGTCCCCTGGAGAGGAGCAGAGCTTGGGGAAGCAGACCCCACTTGTAATTTTTTTCTCTTTCCTGCTTCACCCAGAGTTGGGAAGCAATCTGGGCATCTCCGTCAATGCCAGCTCCCTGGTGGAGAACATGGATTCTGTGGCTGCTGACTGCCTCACAAATGTCACCAACATCACGTGGTATGTGAATGATGTGCCTACCTCTAGTAGTGACCGGATGACAATTTCCCCAGACGGCAAGACCCTCGT... |
Task1_train_47388 | Chromosome 19 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TCAGAAACATAGCCTGGGCCTCCTACCCTGTCTCTACAGATGGGCCCGACTATGTGCTGCTGAGGAGCAATCCTGATGATTTCAACGGCATTGTGACAGCTGAGATCGGCTCCCAAGTGGAAATGGAGTGTATCTGCTATTCCTTCCTGGATCTCAAGTACCACTGGATCCACAATGGCTCCCTCCTGAACTTCTCAGATGCAAAGATGAACCTCTCGAGTCTTGCCTGGGAGCAGATGGGCCGTTACCGATGCACTGTGGAGAACCCCGTGACACAGCTGATCATGTACATGGACGTCAGGATCCAGGCCCCCCATGAG... | TCAGAAACATAGCCTGGGCCTCCTACCCTGTCTCTACAGATGGGCCCGACTATGTGCTGCTGAGGAGCAATCCTGATGATTTCAACGGCATTGTGACAGCTGAGATCGGCTCCCAAGTGGAAATGGAGTGTATCTGCTATTCCTTCCTGGATCTCAAGTACCACTGGATCCACAATGGCTCCCTCCTGAACTTCTCAGATGCAAAGATGAACCTCTCGAGTCTTGCCTGGGAGCAGATGGGCCGTTACCGATGCACTGTGGAGAACCCCGTGACACAGCTGATCATGTACATGGACGTCAGGATCCAGGCCCCCCATGAG... |
Task1_train_47389 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGGATGGATGGATGGATGGATGGATGGATGGACAGACGGGTGGGTGGATGGATGGATGGATGGATGGATGGATGGATGGGTGGGTGGGTGGGTGGATGGATGGATGGATGGATGGATGGATGGACTGACGGGTGGGTGGGTGGTTGGATGGATGGACGGACGGACAGACGGACAGATGGATGGATGGATGAATGGTTGGATGAATAAACAAAAATAAACCCACAAGCCTTCTCCTTGGAACTTCCTATTTCTTCTACATTGCATTTTCCCTAAAGCATATATCTATCTTTATATTTTATTCATTTGTTGTTTTATTAGTT... | TGGATGGATGGATGGATGGATGGATGGATGGACAGACGGGTGGGTGGATGGATGGATGGATGGATGGATGGATGGATGGGTGGGTGGGTGGGTGGATGGATGGATGGATGGATGGATGGATGGACTGACGGGTGGGTGGGTGGTTGGATGGATGGACGGACGGACAGACGGACAGATGGATGGATGGATGAATGGTTGGATGAATAAACAAAAATAAACCCACAAGCCTTCTCCTTGGAACTTCCTATTTCTTCTACATTGCATTTTCCCTAAAGCATATATCTATCTTTATATTTTATTCATTTGTTGTTTTATTAGTT... |
Task1_train_47390 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGAAAGCCTGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAAGCTGAGGCAGGCGATCACCTGAGGTTGGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACTCCGTCTCTACTAAAAATACAAAATTAGCCGGGCATGGTGGCTCGTGTATGTAATCCCAGCTACTCGAGAGACTGAGGCAGAATTACTTGAACCCGGGAGGTGGAGGTTGTGGTGAGCTGAGATCGCACCATCGCACTTCAGCCTGGGCAACAAGATCAAAACTCTGTCTCAAAATAAATAAATAAATAAAAATAAAAACAAAAAATT... | GGAAAGCCTGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAAGCTGAGGCAGGCGATCACCTGAGGTTGGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACTCCGTCTCTACTAAAAATACAAAATTAGCCGGGCATGGTGGCTCGTGTATGTAATCCCAGCTACTCGAGAGACTGAGGCAGAATTACTTGAACCCGGGAGGTGGAGGTTGTGGTGAGCTGAGATCGCACCATCGCACTTCAGCCTGGGCAACAAGATCAAAACTCTGTCTCAAAATAAATAAATAAATAAAAATAAAAACAAAAAATT... |
Task1_train_47391 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | CCTGGTTATTTGGAGCCTCTTTCCCCAAAAGAAAACCATCTCCCCACTCCCTATGGAGAGTACAGAAGTAATTAAGAGGTCCAGGTGCTCACATGAGCCCAAGAGTTGGACCACGGTTTCAAAGAGACCCCTTGCTTGGTTCAGCTGGTCAACGGGGTAATTCACACCACCACTACCCTCCCTTTCCTCACTCTCGACTTTCCCAATCACCCCATTTTCCTCCACTCAGGTTTTCTGAGATTCTGCCACCTGTGTGCCCTTCCCACATGAAGTCTTTCTGTGCCTCCCTGGAGCCCACTCTCACCTGAAGATGAAGCAAA... | CCTGGTTATTTGGAGCCTCTTTCCCCAAAAGAAAACCATCTCCCCACTCCCTATGGAGAGTACAGAAGTAATTAAGAGGTCCAGGTGCTCACATGAGCCCAAGAGTTGGACCACGGTTTCAAAGAGACCCCTTGCTTGGTTCAGCTGGTCAACGGGGTAATTCACACCACCACTACCCTCCCTTTCCTCACTCTCGACTTTCCCAATCACCCCATTTTCCTCCACTCAGGTTTTCTGAGATTCTGCCACCTGTGTGCCCTTCCCACATGAAGTCTTTCTGTGCCTCCCTGGAGCCCACTCTCACCTGAAGATGAAGCAAA... |
Task1_train_47392 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCCTATGGAGAGTACAGAAGTAATTAAGAGGTCCAGGTGCTCACATGAGCCCAAGAGTTGGACCACGGTTTCAAAGAGACCCCTTGCTTGGTTCAGCTGGTCAACGGGGTAATTCACACCACCACTACCCTCCCTTTCCTCACTCTCGACTTTCCCAATCACCCCATTTTCCTCCACTCAGGTTTTCTGAGATTCTGCCACCTGTGTGCCCTTCCCACATGAAGTCTTTCTGTGCCTCCCTGGAGCCCACTCTCACCTGAAGATGAAGCAAACACAGAGGAAAACCAGGGTTGTGATGCTAGCTCCCCAGACTGCTCCCA... | CCCTATGGAGAGTACAGAAGTAATTAAGAGGTCCAGGTGCTCACATGAGCCCAAGAGTTGGACCACGGTTTCAAAGAGACCCCTTGCTTGGTTCAGCTGGTCAACGGGGTAATTCACACCACCACTACCCTCCCTTTCCTCACTCTCGACTTTCCCAATCACCCCATTTTCCTCCACTCAGGTTTTCTGAGATTCTGCCACCTGTGTGCCCTTCCCACATGAAGTCTTTCTGTGCCTCCCTGGAGCCCACTCTCACCTGAAGATGAAGCAAACACAGAGGAAAACCAGGGTTGTGATGCTAGCTCCCCAGACTGCTCCCA... |
Task1_train_47393 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ACTGAGGACGTTGTGCCCCCAGCCACTCTTGTCTGGGCCTTGGAAACATCTTCTCCAAGCTTCATTTCTCTGGAGCAGTTAGGGGTTGAATTATGTCTCCCCACAATTCCTATTTTGAAGTCCTAACCCCCAGCACCTCAGAGCATGACCTGATTTGGAGAAGGGTCATAGCTGATGTAATTAGTTATAATGAGGTGTTCCTGGATCAGGGTGAGCCCTAATCCAATATGACTGTTGTCCTTATAAAAAGGGGAAAATGTGGGTCGGGTGCAGTGGTTCACACCTGTAATCCCATCATTTTGGGAGGCCAAGGCTAGCAG... | ACTGAGGACGTTGTGCCCCCAGCCACTCTTGTCTGGGCCTTGGAAACATCTTCTCCAAGCTTCATTTCTCTGGAGCAGTTAGGGGTTGAATTATGTCTCCCCACAATTCCTATTTTGAAGTCCTAACCCCCAGCACCTCAGAGCATGACCTGATTTGGAGAAGGGTCATAGCTGATGTAATTAGTTATAATGAGGTGTTCCTGGATCAGGGTGAGCCCTAATCCAATATGACTGTTGTCCTTATAAAAAGGGGAAAATGTGGGTCGGGTGCAGTGGTTCACACCTGTAATCCCATCATTTTGGGAGGCCAAGGCTAGCAG... |
Task1_train_47394 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGAATAGACATGTCTTCAAAGATGATATACAAGTGGCCAATAATAGGAAAAAATGCTCAACTTCACTAATTATGTGGGAAATGCAAATCAAAACCACTGGGTGATATCCCTTTACATCCATTAGAATGGCTACAATTAAAAAAACAGAATAACAAGTGTTGGCAAGGATATAGAGAAACTGGAATCCTTGTGTATTACTAGTGGGAATGTAAAATGGTGTAGTCCTATGGAAAACAGGATGATGATTTCTCAAAAATTAAACATAAAATTACCATATGATCCAGCAACTCCACTTCTGGGTAGATACCCACAAGAATTGA... | TGAATAGACATGTCTTCAAAGATGATATACAAGTGGCCAATAATAGGAAAAAATGCTCAACTTCACTAATTATGTGGGAAATGCAAATCAAAACCACTGGGTGATATCCCTTTACATCCATTAGAATGGCTACAATTAAAAAAACAGAATAACAAGTGTTGGCAAGGATATAGAGAAACTGGAATCCTTGTGTATTACTAGTGGGAATGTAAAATGGTGTAGTCCTATGGAAAACAGGATGATGATTTCTCAAAAATTAAACATAAAATTACCATATGATCCAGCAACTCCACTTCTGGGTAGATACCCACAAGAATTGA... |
Task1_train_47395 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | GTGGCCAATAATAGGAAAAAATGCTCAACTTCACTAATTATGTGGGAAATGCAAATCAAAACCACTGGGTGATATCCCTTTACATCCATTAGAATGGCTACAATTAAAAAAACAGAATAACAAGTGTTGGCAAGGATATAGAGAAACTGGAATCCTTGTGTATTACTAGTGGGAATGTAAAATGGTGTAGTCCTATGGAAAACAGGATGATGATTTCTCAAAAATTAAACATAAAATTACCATATGATCCAGCAACTCCACTTCTGGGTAGATACCCACAAGAATTGAAAGCAAGGACCCAAACAGCTGTTTGTACACTC... | GTGGCCAATAATAGGAAAAAATGCTCAACTTCACTAATTATGTGGGAAATGCAAATCAAAACCACTGGGTGATATCCCTTTACATCCATTAGAATGGCTACAATTAAAAAAACAGAATAACAAGTGTTGGCAAGGATATAGAGAAACTGGAATCCTTGTGTATTACTAGTGGGAATGTAAAATGGTGTAGTCCTATGGAAAACAGGATGATGATTTCTCAAAAATTAAACATAAAATTACCATATGATCCAGCAACTCCACTTCTGGGTAGATACCCACAAGAATTGAAAGCAAGGACCCAAACAGCTGTTTGTACACTC... |
Task1_train_47396 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | ACCTCTCTCTCCTCCTGGATAATATATGGATATTGGGACATGTAAAATACACTTACCTTGGTACTTAACTATTGTGATTGTCAGGAATTCTAAACTATCTTTTGTTTTTATTAAAGCTCCCCCATTTACTTGCTCTGAAAGATCATTATTGCTTTCTCATTTTTGAGTTGACTTTACTGAGTATAGATTGCAAATTGATGTTAGAAATAGTATTTGCCTTCTTCTACTCTCCAGGTTGCTACTGATAATTCAGTTGTCAATTAAATGACTTTTCTTTTGAAGGTGATCCTTTTTCTCTGGTAGCTGTTCAGATTTTTTTC... | ACCTCTCTCTCCTCCTGGATAATATATGGATATTGGGACATGTAAAATACACTTACCTTGGTACTTAACTATTGTGATTGTCAGGAATTCTAAACTATCTTTTGTTTTTATTAAAGCTCCCCCATTTACTTGCTCTGAAAGATCATTATTGCTTTCTCATTTTTGAGTTGACTTTACTGAGTATAGATTGCAAATTGATGTTAGAAATAGTATTTGCCTTCTTCTACTCTCCAGGTTGCTACTGATAATTCAGTTGTCAATTAAATGACTTTTCTTTTGAAGGTGATCCTTTTTCTCTGGTAGCTGTTCAGATTTTTTTC... |
Task1_train_47397 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | GAAACTCCATCTCAAAAACAAACAAACAAACAAACAAAACAAAGAAGGTTGAATGGGACATAATGATTTCCTGGCTCTGGGATATGAAGGGGGAGAACAGGAGAGAAGAGAACTCCCAGGTGATGAGGGAGGAGTGGGTTTGGTGGAATGCTGAAGAGCTCAGCCTGGACTTTCCGAGTGGACATGCACATGAGAAGATCCCCAAACCACTCACCGAGGTGATGGTACCCATAATGGGGTCTTCATCATCCATTTTCTCTGGTCTCCCAGCTGCTTGCTTCCTGCGGGCTTTCACTCTAAGGAAAGAAACCAGCACAGTG... | GAAACTCCATCTCAAAAACAAACAAACAAACAAACAAAACAAAGAAGGTTGAATGGGACATAATGATTTCCTGGCTCTGGGATATGAAGGGGGAGAACAGGAGAGAAGAGAACTCCCAGGTGATGAGGGAGGAGTGGGTTTGGTGGAATGCTGAAGAGCTCAGCCTGGACTTTCCGAGTGGACATGCACATGAGAAGATCCCCAAACCACTCACCGAGGTGATGGTACCCATAATGGGGTCTTCATCATCCATTTTCTCTGGTCTCCCAGCTGCTTGCTTCCTGCGGGCTTTCACTCTAAGGAAAGAAACCAGCACAGTG... |
Task1_train_47398 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CAGGTTCAAGCGATTGTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACATGCCACCATGCCTGGCTAATTTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCACGCTGGTCTCGAACTCGTGACCTCAAGTGGTCTCCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCTCAGCCAAATTGTACACTTTGAGTGAGTGAACTCTGTGCGAGATAAATTGGAGACAAATATGGACAACTCTCCCAAGGAAATTTGCTATTAACCGAAATAGAAATGGAACAGTTG... | CAGGTTCAAGCGATTGTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACATGCCACCATGCCTGGCTAATTTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCACGCTGGTCTCGAACTCGTGACCTCAAGTGGTCTCCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCTCAGCCAAATTGTACACTTTGAGTGAGTGAACTCTGTGCGAGATAAATTGGAGACAAATATGGACAACTCTCCCAAGGAAATTTGCTATTAACCGAAATAGAAATGGAACAGTTG... |
Task1_train_47399 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TCCAGTTGAGCTGTGCTGACTCTGGGCTCATAGAAACTATGAGATAATAAATGTGTTTCGTTCAAGCTGCCAAACATATGGTAACTTGTTATGCAGCAATGGAAAACTAATATAATGCATTAGAATTGCTACACCAGGCCAGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAAGTGGGCAGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTAGCCAACATGGTGAAACCCTGTCCCTGCAAAAATACAAAAATTAGCCAGGCATGATGACAGGTGCCTGTAATACCAGCTACTGGGGAGGCTGA... | TCCAGTTGAGCTGTGCTGACTCTGGGCTCATAGAAACTATGAGATAATAAATGTGTTTCGTTCAAGCTGCCAAACATATGGTAACTTGTTATGCAGCAATGGAAAACTAATATAATGCATTAGAATTGCTACACCAGGCCAGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAAGTGGGCAGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTAGCCAACATGGTGAAACCCTGTCCCTGCAAAAATACAAAAATTAGCCAGGCATGATGACAGGTGCCTGTAATACCAGCTACTGGGGAGGCTGA... |
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