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_45000 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TCCCAGGGGCCTCTGATTTTGCTTCCCACCTTCCTGCAGGTGGAAGTCAAGATGGAGGGGGACTCTGTGCTGCTGGAGGTGGATGGGGAGGAGGTGCTGCGCCTGAGACAGGTCTCTGGGCCCCTGACCAGCAAACGCCATCCCATCATGAGGATTGCGCTTGGGGGGCTGCTCTTCCCCGCTTCCAACCTTCGGTTGCCGGTAACTACACCCCAGGGGTGGAACCCTAGCCAAGACTTGGTAAAGCACTGCTGGGTGGCTGGCCGTGGGAATCTAAGTCCACACTTTTAGGGAGAAGGGAAGGGTTGAGAGCTGCAAGG... | TCCCAGGGGCCTCTGATTTTGCTTCCCACCTTCCTGCAGGTGGAAGTCAAGATGGAGGGGGACTCTGTGCTGCTGGAGGTGGATGGGGAGGAGGTGCTGCGCCTGAGACAGGTCTCTGGGCCCCTGACCAGCAAACGCCATCCCATCATGAGGATTGCGCTTGGGGGGCTGCTCTTCCCCGCTTCCAACCTTCGGTTGCCGGTAACTACACCCCAGGGGTGGAACCCTAGCCAAGACTTGGTAAAGCACTGCTGGGTGGCTGGCCGTGGGAATCTAAGTCCACACTTTTAGGGAGAAGGGAAGGGTTGAGAGCTGCAAGG... |
Task1_train_45001 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TGGGCCCAGGGGTCAGAGGCAAGCAGAGGCTGGGGCACAGCAGGCCAGTGTGCAGGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCATGCAGGAACTGTTACACATGTAGTTGTAGTGGATGGTGGTACAGTCAGAGCCAACCTAGGAGATAACACAGGCCCAAGATGAGGCCAGTGCGCCTTGGGGAGACCTGTGGCAAGCAGGGGAGGCCTTTTTTTTTTTTTTTTGAGATGGAATCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATC... | TGGGCCCAGGGGTCAGAGGCAAGCAGAGGCTGGGGCACAGCAGGCCAGTGTGCAGGGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCATGCAGGAACTGTTACACATGTAGTTGTAGTGGATGGTGGTACAGTCAGAGCCAACCTAGGAGATAACACAGGCCCAAGATGAGGCCAGTGCGCCTTGGGGAGACCTGTGGCAAGCAGGGGAGGCCTTTTTTTTTTTTTTTTGAGATGGAATCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATC... |
Task1_train_45002 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TTCAATTGGATTTTCTCCATCTAGCGGAGCCGGGGGCTGCCTGGAAAGATCGCTCCAGGAAGGACAAAGGTCCGGAAGTTGTGGGACCTTAGCAGCTTGGGCTCCCCGGATCACCCCCAAATGATCATTTCGGAATGGAGCCCCAGTTTTCACTAGGATGCCATGGGCTCTAAAATATACAGCTATGAGTTCTCAATGTTTCGAGATCCAAAAGTCTCAGACCTCAATGCTTTGTGCATCTTTTATTTCAGGGATTCCCTACGCCCAGCACCGGGTGGATGTGCAAAGAAGTACGCTTTAGGCCGGCTCAAGGTTCCCCA... | TTCAATTGGATTTTCTCCATCTAGCGGAGCCGGGGGCTGCCTGGAAAGATCGCTCCAGGAAGGACAAAGGTCCGGAAGTTGTGGGACCTTAGCAGCTTGGGCTCCCCGGATCACCCCCAAATGATCATTTCGGAATGGAGCCCCAGTTTTCACTAGGATGCCATGGGCTCTAAAATATACAGCTATGAGTTCTCAATGTTTCGAGATCCAAAAGTCTCAGACCTCAATGCTTTGTGCATCTTTTATTTCAGGGATTCCCTACGCCCAGCACCGGGTGGATGTGCAAAGAAGTACGCTTTAGGCCGGCTCAAGGTTCCCCA... |
Task1_train_45003 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CAACAACCAGACAGAAAACAGACACAGCACATCTTGCTTCTGCCCCTCAGTGAGCTCCTGGCTTCACAGAAAGGTTAGGCCTTATCACCAGAATGTAAACATTGCCATTAGAGATAGAGAACTCAAAAGTAATTAGAACCAGGCTAGAGTTGTCAGGACACACAGGTTTAGGGGAGGGAAAGATCCTCTTTGAACCTGACAGTGTCCAGAAGAGGGTGCCTTCAAAAGCATTCCAAGTGTCTCCCAGAGTGCTGGGGCCCAGGCAGGCTTACCCTCCCTCCTGTCCGCCAGGGCCTGGAGGAGGACCTGGGCTACCTGGT... | CAACAACCAGACAGAAAACAGACACAGCACATCTTGCTTCTGCCCCTCAGTGAGCTCCTGGCTTCACAGAAAGGTTAGGCCTTATCACCAGAATGTAAACATTGCCATTAGAGATAGAGAACTCAAAAGTAATTAGAACCAGGCTAGAGTTGTCAGGACACACAGGTTTAGGGGAGGGAAAGATCCTCTTTGAACCTGACAGTGTCCAGAAGAGGGTGCCTTCAAAAGCATTCCAAGTGTCTCCCAGAGTGCTGGGGCCCAGGCAGGCTTACCCTCCCTCCTGTCCGCCAGGGCCTGGAGGAGGACCTGGGCTACCTGGT... |
Task1_train_45004 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTACCACTGAGAACATCAGGGCCGAGAGGATCAAAAGTGGTGGGATGGCTGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATTGCTTGAGGTCACGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTGGGCGCCTGTAATCACAGCTACTTGGGAGGCTGGGGCAGGAGAATCGCTTGAATCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCACACCATTGCACTCCAGCCTGGGCAACAACAGCGAA... | CTACCACTGAGAACATCAGGGCCGAGAGGATCAAAAGTGGTGGGATGGCTGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATTGCTTGAGGTCACGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTGGGCGCCTGTAATCACAGCTACTTGGGAGGCTGGGGCAGGAGAATCGCTTGAATCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCACACCATTGCACTCCAGCCTGGGCAACAACAGCGAA... |
Task1_train_45005 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TCCGTGGACACAAAGCCTGTGTTGAAGCCCCATTGGCAGATTTCCTGCCATAACTCTGGGAATGGGGGCTTGGGCTGGGATCATGCCTAGGTGTCAGAAAACTTGCTGAGCCTCTATCTCGATGAGTACGAGGAGACACCTTGGGACGCACTTAAGTACCTCATTGCCGGCATCAACTATGGTGGACATGTCACAGATGACTGGGACCGGCGCCTGCTGACCACCTACATCAATGATTATTTCTGTGACCAGTCTCTATCAACTCCCTTCCACCGGTGAGGGGGAGGTGGCCCTGGACAGGGAGCCAGAGGTCACAAGTC... | TCCGTGGACACAAAGCCTGTGTTGAAGCCCCATTGGCAGATTTCCTGCCATAACTCTGGGAATGGGGGCTTGGGCTGGGATCATGCCTAGGTGTCAGAAAACTTGCTGAGCCTCTATCTCGATGAGTACGAGGAGACACCTTGGGACGCACTTAAGTACCTCATTGCCGGCATCAACTATGGTGGACATGTCACAGATGACTGGGACCGGCGCCTGCTGACCACCTACATCAATGATTATTTCTGTGACCAGTCTCTATCAACTCCCTTCCACCGGTGAGGGGGAGGTGGCCCTGGACAGGGAGCCAGAGGTCACAAGTC... |
Task1_train_45006 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GACCCTCCAGGGGCCCGCGCTGCACGGGAAGCCTTTGCCCTTGGGGGCCTGAGCTGTGCTGGGGCCTGGAGCTCCTGCCCGCCTCATCCCCCTCCTCGTAGCGCATGGCTGCCTGGAGGCAGGTGAGAAGTTGGGGCCCTCTGTCTCCAGGCACACCTCTTTCCATCTCTGTATCCCTCAATCTGTGTCATTCTCCATGGGTTCCTGTCATTCTGTGGGCTTCCGTGCATCAGCCCCCTCCTGCCTAGGTAGGACAAGACTGCTCCTTTTTGCCGTATATAACAGACTCCTTCTCTCTCCAGATGCTCAGCCAGCATTGG... | GACCCTCCAGGGGCCCGCGCTGCACGGGAAGCCTTTGCCCTTGGGGGCCTGAGCTGTGCTGGGGCCTGGAGCTCCTGCCCGCCTCATCCCCCTCCTCGTAGCGCATGGCTGCCTGGAGGCAGGTGAGAAGTTGGGGCCCTCTGTCTCCAGGCACACCTCTTTCCATCTCTGTATCCCTCAATCTGTGTCATTCTCCATGGGTTCCTGTCATTCTGTGGGCTTCCGTGCATCAGCCCCCTCCTGCCTAGGTAGGACAAGACTGCTCCTTTTTGCCGTATATAACAGACTCCTTCTCTCTCCAGATGCTCAGCCAGCATTGG... |
Task1_train_45007 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | GGAGGCAGGTGAGAAGTTGGGGCCCTCTGTCTCCAGGCACACCTCTTTCCATCTCTGTATCCCTCAATCTGTGTCATTCTCCATGGGTTCCTGTCATTCTGTGGGCTTCCGTGCATCAGCCCCCTCCTGCCTAGGTAGGACAAGACTGCTCCTTTTTGCCGTATATAACAGACTCCTTCTCTCTCCAGATGCTCAGCCAGCATTGGGCAGCCCCCGCTTCCTGCTCCCCTACCCCCTTCACATGGCAGTAGTTCTGGGCACCCCAGCAAACCATATTATGCTCCAGGGTGAGTGGATATTTGAAGGTTCTGGGAGTGGGA... | GGAGGCAGGTGAGAAGTTGGGGCCCTCTGTCTCCAGGCACACCTCTTTCCATCTCTGTATCCCTCAATCTGTGTCATTCTCCATGGGTTCCTGTCATTCTGTGGGCTTCCGTGCATCAGCCCCCTCCTGCCTAGGTAGGACAAGACTGCTCCTTTTTGCCGTATATAACAGACTCCTTCTCTCTCCAGATGCTCAGCCAGCATTGGGCAGCCCCCGCTTCCTGCTCCCCTACCCCCTTCACATGGCAGTAGTTCTGGGCACCCCAGCAAACCATATTATGCTCCAGGGTGAGTGGATATTTGAAGGTTCTGGGAGTGGGA... |
Task1_train_45008 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | GGTGAGGGCCCGGCGGGCGCGCGGGCAGCGGAGGAGGGCACTGGGGCAGGCTGCAGGGACGGGCTTCGGGAGCCCGGCCGCGCCTTTCCCTGAGCCCCCGCCGGCTTTCTCCCCCCAGGCCCCAGCCAGCACGTCGCGATGAGGCCGGACGCCCCGCCCGCCTGCCTGCCCGCGCAAGGCGCCGCGGGGCCACCAGCACATGCCTGGGCTGGACCTAGGTCCCGCCTGTGGCCGAGAAGGGGGTCGGGCCCAGCCCTTCCACCCCATTGGCAGCTCCCCTCACTTAATTTATTAAGAAAAACTTTTTTTTTTTTTTTAGC... | GGTGAGGGCCCGGCGGGCGCGCGGGCAGCGGAGGAGGGCACTGGGGCAGGCTGCAGGGACGGGCTTCGGGAGCCCGGCCGCGCCTTTCCCTGAGCCCCCGCCGGCTTTCTCCCCCCAGGCCCCAGCCAGCACGTCGCGATGAGGCCGGACGCCCCGCCCGCCTGCCTGCCCGCGCAAGGCGCCGCGGGGCCACCAGCACATGCCTGGGCTGGACCTAGGTCCCGCCTGTGGCCGAGAAGGGGGTCGGGCCCAGCCCTTCCACCCCATTGGCAGCTCCCCTCACTTAATTTATTAAGAAAAACTTTTTTTTTTTTTTTAGC... |
Task1_train_45009 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGCTGGCGGTGGGGTCTATGGGCCACAACTTCAACCCGCCTGGGCTGTTTCCACCCCGTGCACAGTATCGCCTGGTCGGCTTGGGCCTGACGCCTCTTCTCCCACAGTTCCTGCGCTCCCAGGCACCCCCTTGCACCGCGCACCTGCGGGACCCCGGTTTCACGGCCCTACTGGTCACCGGATTCCTGCTCCTCGTGCCGCTGCTCGTGCTTGCTCTGGCCAGCTACCGCCGCCTCTGCCTGCGCCTCCGCCTAGCCGATTGCCTCGTGCCCTACAGCCGAGCCCTTTATCGGCGTCGGCGCGCCCCGCAGCCGCGGCAA... | TGCTGGCGGTGGGGTCTATGGGCCACAACTTCAACCCGCCTGGGCTGTTTCCACCCCGTGCACAGTATCGCCTGGTCGGCTTGGGCCTGACGCCTCTTCTCCCACAGTTCCTGCGCTCCCAGGCACCCCCTTGCACCGCGCACCTGCGGGACCCCGGTTTCACGGCCCTACTGGTCACCGGATTCCTGCTCCTCGTGCCGCTGCTCGTGCTTGCTCTGGCCAGCTACCGCCGCCTCTGCCTGCGCCTCCGCCTAGCCGATTGCCTCGTGCCCTACAGCCGAGCCCTTTATCGGCGTCGGCGCGCCCCGCAGCCGCGGCAA... |
Task1_train_45010 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTGTGCCGAGGAACAGGAAACATGTGCCAGGGCTACAAATGAGCAGAGAGGAGCATCCTTGAGCCCCCTGGCCTTATCGCTTTTGTCCGTTCTTCCTGGCCAGACCTCAGAGATCTGTTCCTGACCCCAGGCACCTCCCCCTCAATAGAGTGGAGGGGCCCAGCCTCGGCCGCCTGCCGCTGCTCCCCTTGGGGACCTGAGCCCGTTCTCTGACCCCAGCTTAGAGGAACTCGGTGTTGCCAGGCCGGGGTGGGAAACAATGGGCCTTCCGGAGCAGGATGACACCCCCTCCCGCCACAATTCTGGAGCAGCAGCCGTGG... | CTGTGCCGAGGAACAGGAAACATGTGCCAGGGCTACAAATGAGCAGAGAGGAGCATCCTTGAGCCCCCTGGCCTTATCGCTTTTGTCCGTTCTTCCTGGCCAGACCTCAGAGATCTGTTCCTGACCCCAGGCACCTCCCCCTCAATAGAGTGGAGGGGCCCAGCCTCGGCCGCCTGCCGCTGCTCCCCTTGGGGACCTGAGCCCGTTCTCTGACCCCAGCTTAGAGGAACTCGGTGTTGCCAGGCCGGGGTGGGAAACAATGGGCCTTCCGGAGCAGGATGACACCCCCTCCCGCCACAATTCTGGAGCAGCAGCCGTGG... |
Task1_train_45011 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | TCCATCTCAAAAAAAAAAAAAAAAAAAAAAAAGAGGTTGAGTTCTTTATAGTAAAATACTATACGTGGAAATCAGATTTTAGTGAGTTGAAGGACTGTGGCTGAGAAAATGGAGACACTTATAGGTTGACTGCTTAAGGAGGAAGAGGCACTGCCATTTATTGAATGTCTACTGGCTTTCAGGTACTCTACTCAGGGTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTGTGTCTCCCAGGTTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCATGCCATT... | TCCATCTCAAAAAAAAAAAAAAAAAAAAAAAAGAGGTTGAGTTCTTTATAGTAAAATACTATACGTGGAAATCAGATTTTAGTGAGTTGAAGGACTGTGGCTGAGAAAATGGAGACACTTATAGGTTGACTGCTTAAGGAGGAAGAGGCACTGCCATTTATTGAATGTCTACTGGCTTTCAGGTACTCTACTCAGGGTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTGTGTCTCCCAGGTTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCATGCCATT... |
Task1_train_45012 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TAATGCTGGAACATTGCCGAGACGTATTGTGCAGCACTGCATAGGTGTAGTATTATGTCCTTCTCAGGGTATCACATCTGGAGGCAAAGAATGTCTCTCTGCCCCTCATGGTTAATTTTGATCACTTGCTTAAAGTATTGCCCCATTTCTCCACTGTACAATGACTGCTTTTTATTTTATTCCCCACTCCCTTCCAACTCATGGCAATCTGGAGGGAGATACTTTCAGACCCTGCAAAAGTTCTGCTCCTCATCCAACATTTCCCCCAGCTTTAGAATCCACTGATGATTCTTACCTGATCCAATCTTTGCCACCAAGTC... | TAATGCTGGAACATTGCCGAGACGTATTGTGCAGCACTGCATAGGTGTAGTATTATGTCCTTCTCAGGGTATCACATCTGGAGGCAAAGAATGTCTCTCTGCCCCTCATGGTTAATTTTGATCACTTGCTTAAAGTATTGCCCCATTTCTCCACTGTACAATGACTGCTTTTTATTTTATTCCCCACTCCCTTCCAACTCATGGCAATCTGGAGGGAGATACTTTCAGACCCTGCAAAAGTTCTGCTCCTCATCCAACATTTCCCCCAGCTTTAGAATCCACTGATGATTCTTACCTGATCCAATCTTTGCCACCAAGTC... |
Task1_train_45013 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TCTCTCTGCCCCTCATGGTTAATTTTGATCACTTGCTTAAAGTATTGCCCCATTTCTCCACTGTACAATGACTGCTTTTTATTTTATTCCCCACTCCCTTCCAACTCATGGCAATCTGGAGGGAGATACTTTCAGACCCTGCAAAAGTTCTGCTCCTCATCCAACATTTCCCCCAGCTTTAGAATCCACTGATGATTCTTACCTGATCCAATCTTTGCCACCAAGTCTGAAAATGATTCATTTAAAAGTTTTTAAGTTTTATTTTTCACATATAGGTCTTTGACCTGGAATAGATTTTGTGTATGGTGTGAGATAGGGAT... | TCTCTCTGCCCCTCATGGTTAATTTTGATCACTTGCTTAAAGTATTGCCCCATTTCTCCACTGTACAATGACTGCTTTTTATTTTATTCCCCACTCCCTTCCAACTCATGGCAATCTGGAGGGAGATACTTTCAGACCCTGCAAAAGTTCTGCTCCTCATCCAACATTTCCCCCAGCTTTAGAATCCACTGATGATTCTTACCTGATCCAATCTTTGCCACCAAGTCTGAAAATGATTCATTTAAAAGTTTTTAAGTTTTATTTTTCACATATAGGTCTTTGACCTGGAATAGATTTTGTGTATGGTGTGAGATAGGGAT... |
Task1_train_45014 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TAGGCTAAACCATACTCAGTATCCAAACAGTGGCCTTTGACTATATTGTTTTTTCCAAAAATAGGACTATGTGTAGAAGAGAGCCCCCGTACATACCTTATCAACCATTTCATCCACCATTTGTAAAAATCTCATCTTCTGGGTCTGGATACTCAAAAACAGATCTTGATTAACAGCCCCTTCCCCACATTGCCCTGGGCAGAAAATGCAAGTCAACTCTCCCCCTCTCAGCTCCAGGAGCTCCGGCATGAGAACGTGGCCCTCTACCTGGGGCTTTTCCTGGCTCGGGGAGCAGAAGGCCCTGCGGCCCTCTGGGAGGG... | TAGGCTAAACCATACTCAGTATCCAAACAGTGGCCTTTGACTATATTGTTTTTTCCAAAAATAGGACTATGTGTAGAAGAGAGCCCCCGTACATACCTTATCAACCATTTCATCCACCATTTGTAAAAATCTCATCTTCTGGGTCTGGATACTCAAAAACAGATCTTGATTAACAGCCCCTTCCCCACATTGCCCTGGGCAGAAAATGCAAGTCAACTCTCCCCCTCTCAGCTCCAGGAGCTCCGGCATGAGAACGTGGCCCTCTACCTGGGGCTTTTCCTGGCTCGGGGAGCAGAAGGCCCTGCGGCCCTCTGGGAGGG... |
Task1_train_45015 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTCAGGGAGAGGAAGGAGCACGCCTGAGCTCCCAGAACAAGCTGCTGGTGGAGCCCAGCAGGAACTCCAGGGCTCAGACCCCTGTCCCAGGCTGCCTCCTCTCATTCTTGTTGCCTCTTTCCAAGTGACTTGCAGGGCTGGTGCCTGTGTGGGGGAAGGTCTGGGGCCAGAACAACCCAGGCCTCCCCTAGCTCTGCCATTTTCCTGCCATGCAGCTGCTGATCCCGCACACCCGATACACCCTGCACATCAACACACTCGCCCGGGAGCTGCTTATCGTGCCAGGGCAGGTGGTGGACAGGGTGAGAGCTGTGTTGGGG... | CTCAGGGAGAGGAAGGAGCACGCCTGAGCTCCCAGAACAAGCTGCTGGTGGAGCCCAGCAGGAACTCCAGGGCTCAGACCCCTGTCCCAGGCTGCCTCCTCTCATTCTTGTTGCCTCTTTCCAAGTGACTTGCAGGGCTGGTGCCTGTGTGGGGGAAGGTCTGGGGCCAGAACAACCCAGGCCTCCCCTAGCTCTGCCATTTTCCTGCCATGCAGCTGCTGATCCCGCACACCCGATACACCCTGCACATCAACACACTCGCCCGGGAGCTGCTTATCGTGCCAGGGCAGGTGGTGGACAGGGTGAGAGCTGTGTTGGGG... |
Task1_train_45016 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | AGGAACTCCAGGGCTCAGACCCCTGTCCCAGGCTGCCTCCTCTCATTCTTGTTGCCTCTTTCCAAGTGACTTGCAGGGCTGGTGCCTGTGTGGGGGAAGGTCTGGGGCCAGAACAACCCAGGCCTCCCCTAGCTCTGCCATTTTCCTGCCATGCAGCTGCTGATCCCGCACACCCGATACACCCTGCACATCAACACACTCGCCCGGGAGCTGCTTATCGTGCCAGGGCAGGTGGTGGACAGGGTGAGAGCTGTGTTGGGGAGGGAGTAGGCAGGCCACTCCTTCAATGTGACGAATTTGAGGTCCTGGGGTAGGAGTGG... | AGGAACTCCAGGGCTCAGACCCCTGTCCCAGGCTGCCTCCTCTCATTCTTGTTGCCTCTTTCCAAGTGACTTGCAGGGCTGGTGCCTGTGTGGGGGAAGGTCTGGGGCCAGAACAACCCAGGCCTCCCCTAGCTCTGCCATTTTCCTGCCATGCAGCTGCTGATCCCGCACACCCGATACACCCTGCACATCAACACACTCGCCCGGGAGCTGCTTATCGTGCCAGGGCAGGTGGTGGACAGGGTGAGAGCTGTGTTGGGGAGGGAGTAGGCAGGCCACTCCTTCAATGTGACGAATTTGAGGTCCTGGGGTAGGAGTGG... |
Task1_train_45017 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | CTCTGGGACCAGATAGGGACAGGACCCAGAGTCCTGCCATTCCCAGGATATAAGGTAGCAAGTTAAAACTTGCCAGGAAGATCAAATATGTGGGATCTTTCTTTTTTTGTTGTTTTTTTGTTTTTTGTTTTTTGTTTTTGTGTCACCCAGGCTGGCGTGCAGTGGCGTGAACATGGCTCACTGCATTTTTTTACTTCCTGGGCTCAAGTGATCCTCCCACTTTAGCTCCCCCCAAGCAGCTGGGACCACAGGCACACACTAATACGCCCGATTAATTTTTGTGTTTTGGGTAGAGACAGGGTTTCACCATGTTTCCTAGG... | CTCTGGGACCAGATAGGGACAGGACCCAGAGTCCTGCCATTCCCAGGATATAAGGTAGCAAGTTAAAACTTGCCAGGAAGATCAAATATGTGGGATCTTTCTTTTTTTGTTGTTTTTTTGTTTTTTGTTTTTTGTTTTTGTGTCACCCAGGCTGGCGTGCAGTGGCGTGAACATGGCTCACTGCATTTTTTTACTTCCTGGGCTCAAGTGATCCTCCCACTTTAGCTCCCCCCAAGCAGCTGGGACCACAGGCACACACTAATACGCCCGATTAATTTTTGTGTTTTGGGTAGAGACAGGGTTTCACCATGTTTCCTAGG... |
Task1_train_45018 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | ATAGCTCTGGAAACTGAAGATGCTCAAGCCCAGCATCTGCAGAAGGCCCCAGAAATTCAACAAGGAATCCTAGCAGCACCTCTCAGGGACCTCATCCACACTAGAAAAGCTAGTAGTAGGGGAGGGAATGGGGCCTCTCCAGCTAAAATCTCTGAGCAGCCAGGGCTTCTCTACCTGTTAAAATCTAATGACTCAGGGTGCAGGTTAGTTCCTCTCTGGGGTCTGGAGGAACTCACTCTGGAGAAGTGCAGAGGGAGGCTGTGGAAAGCAAAGTGCTTCCTATGTGTATGAGAGAAGGGTGCCTGCCTATATGAGTGTAT... | ATAGCTCTGGAAACTGAAGATGCTCAAGCCCAGCATCTGCAGAAGGCCCCAGAAATTCAACAAGGAATCCTAGCAGCACCTCTCAGGGACCTCATCCACACTAGAAAAGCTAGTAGTAGGGGAGGGAATGGGGCCTCTCCAGCTAAAATCTCTGAGCAGCCAGGGCTTCTCTACCTGTTAAAATCTAATGACTCAGGGTGCAGGTTAGTTCCTCTCTGGGGTCTGGAGGAACTCACTCTGGAGAAGTGCAGAGGGAGGCTGTGGAAAGCAAAGTGCTTCCTATGTGTATGAGAGAAGGGTGCCTGCCTATATGAGTGTAT... |
Task1_train_45019 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | TTCCCACCCCCAGCCCACTGTGCTTCCCGAAATGTACTCCCAAGAAGCACCAGTCCACACAGATGCACCTGCGGTCCAACAAGGTTGGACAGTGCCTTGTGCCCTCTACCCAGATGCCGTTACAGGACAGTCACAATGCATATTAGCATAGGATAGGCTGTGAAAAGTTCTGCAAAGACTCACGCGGCTTAATATTCTATAATCCACAGCAAATTTAGTGGAATCAACATTCTTCAGAATTAATGATCCAAGGACATCAAGGAGATCAGCTCTTGGCCTCGATCCCTTGAACTTGAGCTCAATTCTTTTTTCTCCCCCTT... | TTCCCACCCCCAGCCCACTGTGCTTCCCGAAATGTACTCCCAAGAAGCACCAGTCCACACAGATGCACCTGCGGTCCAACAAGGTTGGACAGTGCCTTGTGCCCTCTACCCAGATGCCGTTACAGGACAGTCACAATGCATATTAGCATAGGATAGGCTGTGAAAAGTTCTGCAAAGACTCACGCGGCTTAATATTCTATAATCCACAGCAAATTTAGTGGAATCAACATTCTTCAGAATTAATGATCCAAGGACATCAAGGAGATCAGCTCTTGGCCTCGATCCCTTGAACTTGAGCTCAATTCTTTTTTCTCCCCCTT... |
Task1_train_45020 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | CAGTGCGAGGCCTGTCACCCAGCTCTGCCTGCTCACAAGACCATTCCTAGACCCAACATACACATCCATACACACCTCTTGCTGCTCTCAGTGGTCTCCAGCAGGGCTGAGTCCTTGCCGTTGCCTGAGGAGGAGCTGTGTGAGCTCCGCTGAGATGCGCCTCTAGACTCATGCCCGTTGGACTCATTGCCACTTGAACCATTGCTGTTGGCATCGGTGTCATCGGCCAGGCTGGGGCCTGGGCAAGGCCGGTGCTGTGGGGGCCCAGGGGATGGGACGCCCCCAGGACAAAATGATTCCCCAGGCCTGGGGTCCCCTCC... | CAGTGCGAGGCCTGTCACCCAGCTCTGCCTGCTCACAAGACCATTCCTAGACCCAACATACACATCCATACACACCTCTTGCTGCTCTCAGTGGTCTCCAGCAGGGCTGAGTCCTTGCCGTTGCCTGAGGAGGAGCTGTGTGAGCTCCGCTGAGATGCGCCTCTAGACTCATGCCCGTTGGACTCATTGCCACTTGAACCATTGCTGTTGGCATCGGTGTCATCGGCCAGGCTGGGGCCTGGGCAAGGCCGGTGCTGTGGGGGCCCAGGGGATGGGACGCCCCCAGGACAAAATGATTCCCCAGGCCTGGGGTCCCCTCC... |
Task1_train_45021 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCCAAAGTGTTGGGATTACAGGCCTGAGCCACCACGCCCAGCCCCTACCATACGTTTTTAAATCACATGCTTCCGTTGCTGCTTCTTAAGTTTTCAGTTTTAGGCATGACCTGTTTTTTTCCTGCTATAAAATTCAAGGAATTCACTCTTCCACCCCACTGCCACCATAATTTTGGTTAGATTTATTCATTTGACAGTAGTTACTGAGTGTCCTCTACATTCCGGGTACTGTTCTAGAGGCTTGGTGTAAAGCAATGAATTAAGAAAAAAAAAAAAAAATCAATCAATCCTGCCAGGCGCAGTGGCTCACGCCTGTAATC... | CCCAAAGTGTTGGGATTACAGGCCTGAGCCACCACGCCCAGCCCCTACCATACGTTTTTAAATCACATGCTTCCGTTGCTGCTTCTTAAGTTTTCAGTTTTAGGCATGACCTGTTTTTTTCCTGCTATAAAATTCAAGGAATTCACTCTTCCACCCCACTGCCACCATAATTTTGGTTAGATTTATTCATTTGACAGTAGTTACTGAGTGTCCTCTACATTCCGGGTACTGTTCTAGAGGCTTGGTGTAAAGCAATGAATTAAGAAAAAAAAAAAAAAATCAATCAATCCTGCCAGGCGCAGTGGCTCACGCCTGTAATC... |
Task1_train_45022 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CTTAGGCCAGGCCCTTGGGAAACCTACAGGGCTAACCGTAGCCTGGGGCCCTATAGCACAGTCACCCAGAGTCCTCACCTGCCCCTGCTTGTGCCTGGCACTTGCCTCCCCCTACACCTTCTTTGTGCTTGTGAACACCTCTAGGCATTCATATTTGACTTCCTGCAGGGCCCAGCCTTACTGACTGAGACCATCATAGCTATGCTCTCTGCCTTGCCGCCAACTCCCCAATTTACTTCCTTTACAGACTGATTTTGGTACCATTTCTTCTGCTGGACGAAAAGCTCTTCTCTTCCAAATCACTTTCCACCTTTGGCCCT... | CTTAGGCCAGGCCCTTGGGAAACCTACAGGGCTAACCGTAGCCTGGGGCCCTATAGCACAGTCACCCAGAGTCCTCACCTGCCCCTGCTTGTGCCTGGCACTTGCCTCCCCCTACACCTTCTTTGTGCTTGTGAACACCTCTAGGCATTCATATTTGACTTCCTGCAGGGCCCAGCCTTACTGACTGAGACCATCATAGCTATGCTCTCTGCCTTGCCGCCAACTCCCCAATTTACTTCCTTTACAGACTGATTTTGGTACCATTTCTTCTGCTGGACGAAAAGCTCTTCTCTTCCAAATCACTTTCCACCTTTGGCCCT... |
Task1_train_45023 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TAGAACACTAAATGATTCTGGGTACAATGATAGACACAGAGCATTTTTTATTTGGAGTAGAGAAGCTCCTCTGACTCAACACATCTTGTTGGGATTGGAGAAGACTGTAATGATGGCAAAATCTTCAGAACCAGGGACATGTGGGAGATGCAGATGTGAAGCCAGGAAGTTTAGGGGTTGGGGTCTGGGCACTGACCTGATGGTGGTCTCAGGGGGAAAACTCAGGACCTGCACATAAGTGGATGACCGGAAACAACAATAAACATTGTGAGATCTGCAAGTGGAAGAGGAATAGTGAGTGACCAGGAAGACAAGGCAAA... | TAGAACACTAAATGATTCTGGGTACAATGATAGACACAGAGCATTTTTTATTTGGAGTAGAGAAGCTCCTCTGACTCAACACATCTTGTTGGGATTGGAGAAGACTGTAATGATGGCAAAATCTTCAGAACCAGGGACATGTGGGAGATGCAGATGTGAAGCCAGGAAGTTTAGGGGTTGGGGTCTGGGCACTGACCTGATGGTGGTCTCAGGGGGAAAACTCAGGACCTGCACATAAGTGGATGACCGGAAACAACAATAAACATTGTGAGATCTGCAAGTGGAAGAGGAATAGTGAGTGACCAGGAAGACAAGGCAAA... |
Task1_train_45024 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ATTACAGATGTGAGCCACCATGCCCAGCCCTGCTTAAGCAATTCTTTTTTTTTGTTTTAATAATTTATGGGTCGGAATGGTGGCGCACGCCTGTAATCCCAACGCTTTGGGAGTCCGAGGCGGGCAGATCACTTGAGGTCAGGAGTTGGAGACCAGCCTGGCGAACATAGGGAAACCCCGTCTCTACTAATAATACAAAAATTAGCTGGGCGTGGTGGCGCATGCCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGTGGCAGAAGTTGCAGAGAGCCCAGATTGTGCCACTGCACTCC... | ATTACAGATGTGAGCCACCATGCCCAGCCCTGCTTAAGCAATTCTTTTTTTTTGTTTTAATAATTTATGGGTCGGAATGGTGGCGCACGCCTGTAATCCCAACGCTTTGGGAGTCCGAGGCGGGCAGATCACTTGAGGTCAGGAGTTGGAGACCAGCCTGGCGAACATAGGGAAACCCCGTCTCTACTAATAATACAAAAATTAGCTGGGCGTGGTGGCGCATGCCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGTGGCAGAAGTTGCAGAGAGCCCAGATTGTGCCACTGCACTCC... |
Task1_train_45025 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TCTTCCTGGATTTGTCTCCTAGGTCTGGCTTTAGACTCTTGGGACCTAGACTTCTACACCAAGCGCTTCCAGGAGCTACAGCGGAACCCGAGCACTGTGGAGGCCTTTGACTTGGCGCAGTCCAATAGGTGAGGAGAAATGGGGTTGTTCCCATACCTGAGCCCATGGGTGTTGGGAGAGACCACAGGGGCTCACCTTCATGTTCCTCCCTTGGCTTAGGGGCCTCCCTGAGTCTCTGAGGGCCTGGGCTCCCGTCATCCATCAAGGAGTCTACATTCAAATCTTGGTTTTATCTTCACTTTGGCTCTGGATAGTCCAAA... | TCTTCCTGGATTTGTCTCCTAGGTCTGGCTTTAGACTCTTGGGACCTAGACTTCTACACCAAGCGCTTCCAGGAGCTACAGCGGAACCCGAGCACTGTGGAGGCCTTTGACTTGGCGCAGTCCAATAGGTGAGGAGAAATGGGGTTGTTCCCATACCTGAGCCCATGGGTGTTGGGAGAGACCACAGGGGCTCACCTTCATGTTCCTCCCTTGGCTTAGGGGCCTCCCTGAGTCTCTGAGGGCCTGGGCTCCCGTCATCCATCAAGGAGTCTACATTCAAATCTTGGTTTTATCTTCACTTTGGCTCTGGATAGTCCAAA... |
Task1_train_45026 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATTGTATAGACTTACCATAGTTTACTTAATGAGGTCTCTGTTGTCAGCCTTTAGGTTATTTCATGTACTTGCTAATACAAACGTTACTGTGGTGTTTAATCTTGTAAGTAGGTGATTTTATACCTGTGCAAATAAATCAGCGGGATGACTTCCTCAAAGTGTATTTACCCAATCAGAGACTGTGTGCATTTGTCATTTTGGTTGTTATTGCCAAATCGTCCTCCGTAGTTGATATCAGTTTACTCTCCTATCAACCCAGTCAAGTGGTAAGGCTTCTGGGCTAGGCAGGGTGGCTCACGACTGTAATCCCAACACTTTGG... | ATTGTATAGACTTACCATAGTTTACTTAATGAGGTCTCTGTTGTCAGCCTTTAGGTTATTTCATGTACTTGCTAATACAAACGTTACTGTGGTGTTTAATCTTGTAAGTAGGTGATTTTATACCTGTGCAAATAAATCAGCGGGATGACTTCCTCAAAGTGTATTTACCCAATCAGAGACTGTGTGCATTTGTCATTTTGGTTGTTATTGCCAAATCGTCCTCCGTAGTTGATATCAGTTTACTCTCCTATCAACCCAGTCAAGTGGTAAGGCTTCTGGGCTAGGCAGGGTGGCTCACGACTGTAATCCCAACACTTTGG... |
Task1_train_45027 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GGAGCCAGTCCGAGGCCTGGAGGGGTCTGACTCTCCTGCTGACCCCTGAAGGGAGTTTGGGGGTTCCTCTGCTTCCCAGCCCTGACCCTGCAGCCTTCTTGGGATTGTAGCCTCCTTCCTCGAGGGAGGAAGAGAAACCCAGGCCGCAGCGCCCTGGCCCGACTGGTCCTGTCCTTCGGTTCATTCTCCCAGCCACCTCCCCAGGCCTCTTGGCAAGACCCATGGCTGTGCTGGGCCTCTCTCTGTGACCAGACCCTAGGGCAGGCGGGGATGATCAGACGCAGGACAGGAGAGACCTCGCCAGGACCTCCTCATCTCCG... | GGAGCCAGTCCGAGGCCTGGAGGGGTCTGACTCTCCTGCTGACCCCTGAAGGGAGTTTGGGGGTTCCTCTGCTTCCCAGCCCTGACCCTGCAGCCTTCTTGGGATTGTAGCCTCCTTCCTCGAGGGAGGAAGAGAAACCCAGGCCGCAGCGCCCTGGCCCGACTGGTCCTGTCCTTCGGTTCATTCTCCCAGCCACCTCCCCAGGCCTCTTGGCAAGACCCATGGCTGTGCTGGGCCTCTCTCTGTGACCAGACCCTAGGGCAGGCGGGGATGATCAGACGCAGGACAGGAGAGACCTCGCCAGGACCTCCTCATCTCCG... |
Task1_train_45028 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GATGATCAGACGCAGGACAGGAGAGACCTCGCCAGGACCTCCTCATCTCCGGGGGTCAGAGGCTCCAAGAATCTTGATGGCAGGAAAAGGAGACTAAAAATAATCCGGAAAGGGAGAGTCCGGAGAGAGGAACTGGGAAATGGGGGGCGGAGGGCCAGTGGAGCAGGGAAACAGTGATGCACGCCTCGCAGCCCAGGCCCGGCGGACAGGCGCGCCCACGGCACCCAGACCCAGACAGCGCAGAACACACATGGCACACCCACCCTGGCACCGCTATCTCAGACACTCACACCGAGAACTTCCTAAAGGGCCACACACCA... | GATGATCAGACGCAGGACAGGAGAGACCTCGCCAGGACCTCCTCATCTCCGGGGGTCAGAGGCTCCAAGAATCTTGATGGCAGGAAAAGGAGACTAAAAATAATCCGGAAAGGGAGAGTCCGGAGAGAGGAACTGGGAAATGGGGGGCGGAGGGCCAGTGGAGCAGGGAAACAGTGATGCACGCCTCGCAGCCCAGGCCCGGCGGACAGGCGCGCCCACGGCACCCAGACCCAGACAGCGCAGAACACACATGGCACACCCACCCTGGCACCGCTATCTCAGACACTCACACCGAGAACTTCCTAAAGGGCCACACACCA... |
Task1_train_45029 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | GGTGAGTCCTAGGGAAGGAAGGAGCCCAGGCTGGAGTGGGCAGGAGGGGTCCAGCGGGACCCCTGCTGTCCTTCTGAACGACCTCATCCCTGGGCAGTGGGCAGCGGTTACAGGTTCTGGACTATGCCCATCGCTCCCTGGTCCAGGCCCAGCAGGTTCCGGATCCATCTGGACCCCCTACCTTCCGCCTCTCCCTTCTCAGCAACCACCAGGGCCGCCCCACCCACCGACTACTCCAAGCTTCTTCCCTGTGAGTTGTGTTTCCCTCAGAAAACAACCTTGGGACACTTATCTGACCTCTCAGACCTCCCCCACTTCCC... | GGTGAGTCCTAGGGAAGGAAGGAGCCCAGGCTGGAGTGGGCAGGAGGGGTCCAGCGGGACCCCTGCTGTCCTTCTGAACGACCTCATCCCTGGGCAGTGGGCAGCGGTTACAGGTTCTGGACTATGCCCATCGCTCCCTGGTCCAGGCCCAGCAGGTTCCGGATCCATCTGGACCCCCTACCTTCCGCCTCTCCCTTCTCAGCAACCACCAGGGCCGCCCCACCCACCGACTACTCCAAGCTTCTTCCCTGTGAGTTGTGTTTCCCTCAGAAAACAACCTTGGGACACTTATCTGACCTCTCAGACCTCCCCCACTTCCC... |
Task1_train_45030 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ACTGTCCTAGTCCATTTTGTGTTGCTATAACAGAATACCTGAGGGTGAATAATTTATAAAGAAAAAAGGGCTATTTGGCTCACAATTCTGATGGCCAGAAAGCTCAAGATTGGGCATCTGTTGAGGACGTCAGGCTGCTTTCACTTATGGTGGAGGCAAGGGGGAGCTGGCTTGTGCAGAGATCACAAGGTAAGGGAGGAGCTGAAACTGTGCCCCAAACAGTTAAATAAACCAGTGATTAACAGACATTTTCGAGTTTACAGGATGGCAGCTAAGAAACAGCTTGCTGAAATGCTGAAAAATCCCTTTGCTTATAACAG... | ACTGTCCTAGTCCATTTTGTGTTGCTATAACAGAATACCTGAGGGTGAATAATTTATAAAGAAAAAAGGGCTATTTGGCTCACAATTCTGATGGCCAGAAAGCTCAAGATTGGGCATCTGTTGAGGACGTCAGGCTGCTTTCACTTATGGTGGAGGCAAGGGGGAGCTGGCTTGTGCAGAGATCACAAGGTAAGGGAGGAGCTGAAACTGTGCCCCAAACAGTTAAATAAACCAGTGATTAACAGACATTTTCGAGTTTACAGGATGGCAGCTAAGAAACAGCTTGCTGAAATGCTGAAAAATCCCTTTGCTTATAACAG... |
Task1_train_45031 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TCAGGCTGCTTTCACTTATGGTGGAGGCAAGGGGGAGCTGGCTTGTGCAGAGATCACAAGGTAAGGGAGGAGCTGAAACTGTGCCCCAAACAGTTAAATAAACCAGTGATTAACAGACATTTTCGAGTTTACAGGATGGCAGCTAAGAAACAGCTTGCTGAAATGCTGAAAAATCCCTTTGCTTATAACAGGACTGGCTGAAATCAGTGGGAACCCGTATGGCTGACAGCAATCCGCACAGAACGAGCTTGCTGATGTCACAGCCTGAATTTCCACCTGCTGTTTCATACTAACGCCACCAAATTTGCACATGCAACCCA... | TCAGGCTGCTTTCACTTATGGTGGAGGCAAGGGGGAGCTGGCTTGTGCAGAGATCACAAGGTAAGGGAGGAGCTGAAACTGTGCCCCAAACAGTTAAATAAACCAGTGATTAACAGACATTTTCGAGTTTACAGGATGGCAGCTAAGAAACAGCTTGCTGAAATGCTGAAAAATCCCTTTGCTTATAACAGGACTGGCTGAAATCAGTGGGAACCCGTATGGCTGACAGCAATCCGCACAGAACGAGCTTGCTGATGTCACAGCCTGAATTTCCACCTGCTGTTTCATACTAACGCCACCAAATTTGCACATGCAACCCA... |
Task1_train_45032 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGGGAGGAGCTGAAACTGTGCCCCAAACAGTTAAATAAACCAGTGATTAACAGACATTTTCGAGTTTACAGGATGGCAGCTAAGAAACAGCTTGCTGAAATGCTGAAAAATCCCTTTGCTTATAACAGGACTGGCTGAAATCAGTGGGAACCCGTATGGCTGACAGCAATCCGCACAGAACGAGCTTGCTGATGTCACAGCCTGAATTTCCACCTGCTGTTTCATACTAACGCCACCAAATTTGCACATGCAACCCACGAAGAACCTTGGAGATAACCAGACATGATTAAGGACTTTCTAGACTTCTCCTTTCTTTCCAC... | AGGGAGGAGCTGAAACTGTGCCCCAAACAGTTAAATAAACCAGTGATTAACAGACATTTTCGAGTTTACAGGATGGCAGCTAAGAAACAGCTTGCTGAAATGCTGAAAAATCCCTTTGCTTATAACAGGACTGGCTGAAATCAGTGGGAACCCGTATGGCTGACAGCAATCCGCACAGAACGAGCTTGCTGATGTCACAGCCTGAATTTCCACCTGCTGTTTCATACTAACGCCACCAAATTTGCACATGCAACCCACGAAGAACCTTGGAGATAACCAGACATGATTAAGGACTTTCTAGACTTCTCCTTTCTTTCCAC... |
Task1_train_45033 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | ACAGGACTGGCTGAAATCAGTGGGAACCCGTATGGCTGACAGCAATCCGCACAGAACGAGCTTGCTGATGTCACAGCCTGAATTTCCACCTGCTGTTTCATACTAACGCCACCAAATTTGCACATGCAACCCACGAAGAACCTTGGAGATAACCAGACATGATTAAGGACTTTCTAGACTTCTCCTTTCTTTCCACCAATCACCCGCTAATCCCAGAATCCTCCCCCTAAACCTTTTCTAATAAAAGTACTGCCTTAAGACCAGCAAAGAGAGACAGATTTGAGCTGGATTCCCGTATCCTCGTGGGTCAGCTCACAATA... | ACAGGACTGGCTGAAATCAGTGGGAACCCGTATGGCTGACAGCAATCCGCACAGAACGAGCTTGCTGATGTCACAGCCTGAATTTCCACCTGCTGTTTCATACTAACGCCACCAAATTTGCACATGCAACCCACGAAGAACCTTGGAGATAACCAGACATGATTAAGGACTTTCTAGACTTCTCCTTTCTTTCCACCAATCACCCGCTAATCCCAGAATCCTCCCCCTAAACCTTTTCTAATAAAAGTACTGCCTTAAGACCAGCAAAGAGAGACAGATTTGAGCTGGATTCCCGTATCCTCGTGGGTCAGCTCACAATA... |
Task1_train_45034 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGAATCTTCTGTCTCTCCCAGGTAGCTGGGATTACAGGCACGTGCCACCACTCCTGGCTAATTTTTGTATTTTTAGTAGAGACGCGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCCTGACCTTGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCGTGCCTGGCCACTTCTGTAATCTTGAAATGAGCACAGAGAAGCCCACAAGTGCTTTTAAAGCAGCCCTCTCTATGTCCCAAATA... | GGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGAATCTTCTGTCTCTCCCAGGTAGCTGGGATTACAGGCACGTGCCACCACTCCTGGCTAATTTTTGTATTTTTAGTAGAGACGCGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCCTGACCTTGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCGTGCCTGGCCACTTCTGTAATCTTGAAATGAGCACAGAGAAGCCCACAAGTGCTTTTAAAGCAGCCCTCTCTATGTCCCAAATA... |
Task1_train_45035 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TCTAAGATATATATTTTCCCAACTCTGAATTCAAGACACATCTTACAATTTTTTTTTGGTTTGTTTGTTTTTGAGACGGAGTTTCGCTCTTGTCGCCCAGGCTGGAGTGCAATGGTGCAACCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTTCCGAGTAGCTGGGATTACAGGTGCTTGCCATCACGGCCAGCTAGTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCACACTGGTGTTGAACTCCTGACCTCAGGTGATCCACCTACCTCGGCCTCCCAAAGT... | TCTAAGATATATATTTTCCCAACTCTGAATTCAAGACACATCTTACAATTTTTTTTTGGTTTGTTTGTTTTTGAGACGGAGTTTCGCTCTTGTCGCCCAGGCTGGAGTGCAATGGTGCAACCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTTCCGAGTAGCTGGGATTACAGGTGCTTGCCATCACGGCCAGCTAGTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCACACTGGTGTTGAACTCCTGACCTCAGGTGATCCACCTACCTCGGCCTCCCAAAGT... |
Task1_train_45036 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | CGGATCCGTTTCTGGTCGTTCTCCTGGGGCCCGGGGAGGTGGCGCTGGTCAGGAAGCCTCGCCCAGCCCTCCCGGGGCCCAGGCCTTCCTGGGGCTGGTGGTGCCCTCAGACCCCTCTGTCTGCACAAACCATCCTGGCAACAGGCAGAGATTGCTGGGCCACCCATGGGGCAGAAGAGGGGTGAAGGAAAAGGCTCTCCAGGGGTATTTGAAGCTGGCTGAAGAGATTTCTGTGGACTGAGGTGGGGGCTCAGGGGGCTGTGAGGACAGAGGTTTAATCCAAAGTCGAGAGGTGGCCCTGGGGCTGGAGGGGCAGACAG... | CGGATCCGTTTCTGGTCGTTCTCCTGGGGCCCGGGGAGGTGGCGCTGGTCAGGAAGCCTCGCCCAGCCCTCCCGGGGCCCAGGCCTTCCTGGGGCTGGTGGTGCCCTCAGACCCCTCTGTCTGCACAAACCATCCTGGCAACAGGCAGAGATTGCTGGGCCACCCATGGGGCAGAAGAGGGGTGAAGGAAAAGGCTCTCCAGGGGTATTTGAAGCTGGCTGAAGAGATTTCTGTGGACTGAGGTGGGGGCTCAGGGGGCTGTGAGGACAGAGGTTTAATCCAAAGTCGAGAGGTGGCCCTGGGGCTGGAGGGGCAGACAG... |
Task1_train_45037 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | GACCCCTGCCTGAGGGCAGCCTCTCAGAGAGGAGGGCAGGGGACCTTCCTCAGCTCAGCACCAACAGCCGCCCTGCAGAGAGCCCTGCCTTCCTCAGGAGGCCCCGCTGGACAGAGACCTGCTAAGGGTGCCTCTCAAACCTTCAGGAAGGAGATGATCCAAGTGGTAGCTGGGAGTGGTGGCTCTTGCTTGGAATCCCAGCACTTTGGGAGTCCAGGCAGGAGGATCACTGGAGGCCAGGAGTTAGGGACCAGTCTGGGTAATATGGCAAGACCCCCTCTGAATTTAAAAACAACCCAAGTCTTATGCTAAGGATGTGT... | GACCCCTGCCTGAGGGCAGCCTCTCAGAGAGGAGGGCAGGGGACCTTCCTCAGCTCAGCACCAACAGCCGCCCTGCAGAGAGCCCTGCCTTCCTCAGGAGGCCCCGCTGGACAGAGACCTGCTAAGGGTGCCTCTCAAACCTTCAGGAAGGAGATGATCCAAGTGGTAGCTGGGAGTGGTGGCTCTTGCTTGGAATCCCAGCACTTTGGGAGTCCAGGCAGGAGGATCACTGGAGGCCAGGAGTTAGGGACCAGTCTGGGTAATATGGCAAGACCCCCTCTGAATTTAAAAACAACCCAAGTCTTATGCTAAGGATGTGT... |
Task1_train_45038 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | TGCAGTGAGGCTTCTTCTAAATTCAATATCCTATGTTTAACTAATGATAAGGTCGAAGAATTGGGCCCTGGGACTGGCCTCTGAAATAAATGGCCCTTTATTCCAGGCCCTTCCCCTGGGGGAGTTTGGGAAGGCAGAAGCACTAGTTTGTCACTCCCAAAACCCCACCAAGTGCCTGGGCACAGGTACAGCATGGAGAACCTATAGCACCCTGACCTATGGAGATGTCTGCACCCCAATAAAACAGATGTTAAAATCTCCATGTGCTTTGTGAGGCAGAGCATGCAAAATGTGAGTTCAAAAGACATGAAATTGCCCCT... | TGCAGTGAGGCTTCTTCTAAATTCAATATCCTATGTTTAACTAATGATAAGGTCGAAGAATTGGGCCCTGGGACTGGCCTCTGAAATAAATGGCCCTTTATTCCAGGCCCTTCCCCTGGGGGAGTTTGGGAAGGCAGAAGCACTAGTTTGTCACTCCCAAAACCCCACCAAGTGCCTGGGCACAGGTACAGCATGGAGAACCTATAGCACCCTGACCTATGGAGATGTCTGCACCCCAATAAAACAGATGTTAAAATCTCCATGTGCTTTGTGAGGCAGAGCATGCAAAATGTGAGTTCAAAAGACATGAAATTGCCCCT... |
Task1_train_45039 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | AAGAATGAAACCTATTAACCTCCCACTTCCCCCCCAACACACATACATTTCCCATTATTTTCTCCTGTTGGAAGTACTTGGGTGTGAGTGTGGGCACCTGTATACCAGTGGGAACAGAAAGGAGTTTGTTTTCATTACCATCCTTTTTTTGAGATGGAGTCTTGCTCTGTCACCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCCACCTCCAGGGTTCAAGTGATTCTCTTTCCTCAACCTCCTGAGTAGCTGGGACTACAGGTGCGCGCCACCACGCCCAGCTAATTTTTGTGTCTTTAGTAGAGAC... | AAGAATGAAACCTATTAACCTCCCACTTCCCCCCCAACACACATACATTTCCCATTATTTTCTCCTGTTGGAAGTACTTGGGTGTGAGTGTGGGCACCTGTATACCAGTGGGAACAGAAAGGAGTTTGTTTTCATTACCATCCTTTTTTTGAGATGGAGTCTTGCTCTGTCACCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCCACCTCCAGGGTTCAAGTGATTCTCTTTCCTCAACCTCCTGAGTAGCTGGGACTACAGGTGCGCGCCACCACGCCCAGCTAATTTTTGTGTCTTTAGTAGAGAC... |
Task1_train_45040 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CAGCTTGGGCAGCCATGGGCCCTGTGTGTGCATCCCAGAGCCAGGCTGACCTCAGGCACTGAGGTTGGGTGGTCACAATGACTCTGTGGCCATTGGCTTCGGCTCCATTTGTGGACTTGCAGGATTAGACTGGACCATTCAGATGTTGCCTCCAGGATGTTCCTGCTGGGACCAGGTGGCTTTTTAGGGCCAGCTTCCTAATAACCCATTGTGACAGGGCACCTATGGTTTGTTGTTGCTAATACAGTTGCCTGGGAGCAAGATTTGACCCCAAATTGAGGGCTGTGTCCCCCACTTGTTCTTCCTAAAGGAGCAGAGGA... | CAGCTTGGGCAGCCATGGGCCCTGTGTGTGCATCCCAGAGCCAGGCTGACCTCAGGCACTGAGGTTGGGTGGTCACAATGACTCTGTGGCCATTGGCTTCGGCTCCATTTGTGGACTTGCAGGATTAGACTGGACCATTCAGATGTTGCCTCCAGGATGTTCCTGCTGGGACCAGGTGGCTTTTTAGGGCCAGCTTCCTAATAACCCATTGTGACAGGGCACCTATGGTTTGTTGTTGCTAATACAGTTGCCTGGGAGCAAGATTTGACCCCAAATTGAGGGCTGTGTCCCCCACTTGTTCTTCCTAAAGGAGCAGAGGA... |
Task1_train_45041 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AGAGCCAGGCTGACCTCAGGCACTGAGGTTGGGTGGTCACAATGACTCTGTGGCCATTGGCTTCGGCTCCATTTGTGGACTTGCAGGATTAGACTGGACCATTCAGATGTTGCCTCCAGGATGTTCCTGCTGGGACCAGGTGGCTTTTTAGGGCCAGCTTCCTAATAACCCATTGTGACAGGGCACCTATGGTTTGTTGTTGCTAATACAGTTGCCTGGGAGCAAGATTTGACCCCAAATTGAGGGCTGTGTCCCCCACTTGTTCTTCCTAAAGGAGCAGAGGATGCCTCCGGTGCCTCTCAGATTTGCCCCCGGCCTGA... | AGAGCCAGGCTGACCTCAGGCACTGAGGTTGGGTGGTCACAATGACTCTGTGGCCATTGGCTTCGGCTCCATTTGTGGACTTGCAGGATTAGACTGGACCATTCAGATGTTGCCTCCAGGATGTTCCTGCTGGGACCAGGTGGCTTTTTAGGGCCAGCTTCCTAATAACCCATTGTGACAGGGCACCTATGGTTTGTTGTTGCTAATACAGTTGCCTGGGAGCAAGATTTGACCCCAAATTGAGGGCTGTGTCCCCCACTTGTTCTTCCTAAAGGAGCAGAGGATGCCTCCGGTGCCTCTCAGATTTGCCCCCGGCCTGA... |
Task1_train_45042 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTTTAGTAGAGACAGGGTTTCACCATGCTGGCCAGGCTGGTCTCAAACTCCTGACCTCGTGATCCACCCGCCTCAGCCTGCCAAAGTGCTGTGATTACAGGAATGAGCCACCGTGCCCGGCCTATAAAGCTTACTTTCTTATCAATACTATCACTTAAGGAAGGAACTGACCAATAACTGAATTATATGCAAATACATAAATTAGCCTGTTCGTGTTGGTACCATCAGGGAAAGAACTAAGTTGTCCTCTCTGTGCTGAAACTATTAGAATTGTAAAGAGAGAAGGCTTCTCCATTGGATTTAGTAATCTATTTATTTAT... | CTTTAGTAGAGACAGGGTTTCACCATGCTGGCCAGGCTGGTCTCAAACTCCTGACCTCGTGATCCACCCGCCTCAGCCTGCCAAAGTGCTGTGATTACAGGAATGAGCCACCGTGCCCGGCCTATAAAGCTTACTTTCTTATCAATACTATCACTTAAGGAAGGAACTGACCAATAACTGAATTATATGCAAATACATAAATTAGCCTGTTCGTGTTGGTACCATCAGGGAAAGAACTAAGTTGTCCTCTCTGTGCTGAAACTATTAGAATTGTAAAGAGAGAAGGCTTCTCCATTGGATTTAGTAATCTATTTATTTAT... |
Task1_train_45043 | A sequence alteration has been identified on Chromosome 17. Is it disease-inducing or harmless? | Benign | CCACCTGCTGGGCTTTTTGTAGATTGAAAAGGCTGCTCACATGAGAAGTCATGGAGACTGGAAAGGGAAGATGTATGATCAAAATGGACAGCTCCAGTGCCAAGATCTTTCCTTTCCCCATTTTTTTTTTTTGTTTGTTTTGAGATGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAATGACGCCATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGAGATTCTCCTGCCTCAGGCTCCCGAGTAACTGGGATTACAGGTGCCCGCCACCAAGCCCAGCTAATTTTTTTTTGTATTTTTAGTAGAGATGGGG... | CCACCTGCTGGGCTTTTTGTAGATTGAAAAGGCTGCTCACATGAGAAGTCATGGAGACTGGAAAGGGAAGATGTATGATCAAAATGGACAGCTCCAGTGCCAAGATCTTTCCTTTCCCCATTTTTTTTTTTTGTTTGTTTTGAGATGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAATGACGCCATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGAGATTCTCCTGCCTCAGGCTCCCGAGTAACTGGGATTACAGGTGCCCGCCACCAAGCCCAGCTAATTTTTTTTTGTATTTTTAGTAGAGATGGGG... |
Task1_train_45044 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | GGGATCAGGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGATTACAGGCACACATCACCACGCCCAGCTATTTTTTTGTATTTTTAGTAGAGATGGTATTTCACCAACTCCTGACCTCAGGTGATCTGCCCGCCTCAGCCTTCCAAAATGCTGGGATTACAGGTGTGAGCCACCACGCCTGGCCTGTATTCTTTTTCTTTAAAAAAAAATTTTGGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCTTCTGGGGAAGCTGAGGCAGGATAATCACTTAAAACCCAGGAGGTGGAAGTTGCAGTGAGCTGAGATTG... | GGGATCAGGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGATTACAGGCACACATCACCACGCCCAGCTATTTTTTTGTATTTTTAGTAGAGATGGTATTTCACCAACTCCTGACCTCAGGTGATCTGCCCGCCTCAGCCTTCCAAAATGCTGGGATTACAGGTGTGAGCCACCACGCCTGGCCTGTATTCTTTTTCTTTAAAAAAAAATTTTGGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCTTCTGGGGAAGCTGAGGCAGGATAATCACTTAAAACCCAGGAGGTGGAAGTTGCAGTGAGCTGAGATTG... |
Task1_train_45045 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | GATCAGGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGATTACAGGCACACATCACCACGCCCAGCTATTTTTTTGTATTTTTAGTAGAGATGGTATTTCACCAACTCCTGACCTCAGGTGATCTGCCCGCCTCAGCCTTCCAAAATGCTGGGATTACAGGTGTGAGCCACCACGCCTGGCCTGTATTCTTTTTCTTTAAAAAAAAATTTTGGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCTTCTGGGGAAGCTGAGGCAGGATAATCACTTAAAACCCAGGAGGTGGAAGTTGCAGTGAGCTGAGATTGCG... | GATCAGGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGATTACAGGCACACATCACCACGCCCAGCTATTTTTTTGTATTTTTAGTAGAGATGGTATTTCACCAACTCCTGACCTCAGGTGATCTGCCCGCCTCAGCCTTCCAAAATGCTGGGATTACAGGTGTGAGCCACCACGCCTGGCCTGTATTCTTTTTCTTTAAAAAAAAATTTTGGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCTTCTGGGGAAGCTGAGGCAGGATAATCACTTAAAACCCAGGAGGTGGAAGTTGCAGTGAGCTGAGATTGCG... |
Task1_train_45046 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GTATTCTTTTTCTTTAAAAAAAAATTTTGGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCTTCTGGGGAAGCTGAGGCAGGATAATCACTTAAAACCCAGGAGGTGGAAGTTGCAGTGAGCTGAGATTGCGCCGTTGCAATCCAGCCTGGGCAACGAGAGGGAAATTCCATCTCAAAATAAAAAATAAAATAAAATAAAATAAAATAAGAATACAGACCTCTAGACTCCACCCCGGCTCTCTTAAATTAGAACCTCCAGGACTGGGCACCTGGATATTTCTTTTACAAGTTCCTTGGGTGATACATTTGATAACTGG... | GTATTCTTTTTCTTTAAAAAAAAATTTTGGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCTTCTGGGGAAGCTGAGGCAGGATAATCACTTAAAACCCAGGAGGTGGAAGTTGCAGTGAGCTGAGATTGCGCCGTTGCAATCCAGCCTGGGCAACGAGAGGGAAATTCCATCTCAAAATAAAAAATAAAATAAAATAAAATAAAATAAGAATACAGACCTCTAGACTCCACCCCGGCTCTCTTAAATTAGAACCTCCAGGACTGGGCACCTGGATATTTCTTTTACAAGTTCCTTGGGTGATACATTTGATAACTGG... |
Task1_train_45047 | A sequence alteration has been identified on Chromosome 17. Is it disease-inducing or harmless? | Benign | CTGTGAAAGTTTAGTTCATGTCGGTGGCTGGGCATGGTGTCTCATGCCTATAATCCCAGCACTTTGGGAAGCCGAGGTGGGCAGCTAACTTGAAGTCAGGAGTTCGAGACCAGCCTGGCCAACATAGTGAAACTGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCACATGCCTGTAGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGAGTCGCTTGAGCCTGGGACGTGGAGGTTGCAGTGAGCTGAGATCACGCCATTGTACTCCAGCCTGGGCAATACAGTGAGACTCCATCTCCAAAAAAAAAAAAAA... | CTGTGAAAGTTTAGTTCATGTCGGTGGCTGGGCATGGTGTCTCATGCCTATAATCCCAGCACTTTGGGAAGCCGAGGTGGGCAGCTAACTTGAAGTCAGGAGTTCGAGACCAGCCTGGCCAACATAGTGAAACTGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCACATGCCTGTAGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGAGTCGCTTGAGCCTGGGACGTGGAGGTTGCAGTGAGCTGAGATCACGCCATTGTACTCCAGCCTGGGCAATACAGTGAGACTCCATCTCCAAAAAAAAAAAAAA... |
Task1_train_45048 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CTGTAATTCCAGCTACTTGGGAGGCTGAGACAGGAGAATGCTTGAACTCGGGAGGCGGAGGTTGCAGTGAGCCGAGGTTGAGCCACTGCACTCTAGCCTGGCGACAAGAGTGAAACTCCATCTCTAACAAACAAACAAATAAACAAACATTAGCCAGTGCCCACTATGACCAAGTAGAGATGCAACAGTGACCTTGCCCAATATTTGTATAATTGAATGAATGACACAAGGTCTTGGGGGTTTAATCATCATTGACCCATGTGCACCTGTGAACAATCTAAGCAAACACCTAGGCTGATATAGGCGGAGCAGGGCGGGCG... | CTGTAATTCCAGCTACTTGGGAGGCTGAGACAGGAGAATGCTTGAACTCGGGAGGCGGAGGTTGCAGTGAGCCGAGGTTGAGCCACTGCACTCTAGCCTGGCGACAAGAGTGAAACTCCATCTCTAACAAACAAACAAATAAACAAACATTAGCCAGTGCCCACTATGACCAAGTAGAGATGCAACAGTGACCTTGCCCAATATTTGTATAATTGAATGAATGACACAAGGTCTTGGGGGTTTAATCATCATTGACCCATGTGCACCTGTGAACAATCTAAGCAAACACCTAGGCTGATATAGGCGGAGCAGGGCGGGCG... |
Task1_train_45049 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TTTCAAGAGCCTGGAACCACAGGAGTCTTTGCTCAAACAGTAGCATTTGGGAGTGTGCAACCAGCAGCAGGAAGGAGAGGATCAACAGTCATCTTCCAAGCTCTCCCTGGGTGGTCCATGGGACTCCCCCGGGGCTTGGGATTTCTTGGGAAGAAGCCATACTCAGGTACTTGCTCTTCCCTGGCCCCCTACATCTCAGGTACCTGCTCTTACCTGGTCCCCACATCTCAGGTACCTGCCCTTATCTGGCCTCCCACACTCAGGCATTCGCTCTTACCTGGCCCCCATATTCAATATCTGTTCTTAGCTGGCCCCTATAT... | TTTCAAGAGCCTGGAACCACAGGAGTCTTTGCTCAAACAGTAGCATTTGGGAGTGTGCAACCAGCAGCAGGAAGGAGAGGATCAACAGTCATCTTCCAAGCTCTCCCTGGGTGGTCCATGGGACTCCCCCGGGGCTTGGGATTTCTTGGGAAGAAGCCATACTCAGGTACTTGCTCTTCCCTGGCCCCCTACATCTCAGGTACCTGCTCTTACCTGGTCCCCACATCTCAGGTACCTGCCCTTATCTGGCCTCCCACACTCAGGCATTCGCTCTTACCTGGCCCCCATATTCAATATCTGTTCTTAGCTGGCCCCTATAT... |
Task1_train_45050 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGGTGTTGGGGGGTGGGGCTTTTGGGAGGTGATAAGGTCGTGGGGGTGGAGCCCTTATGAATGGGATTAGTGTTCTTATAATAGAGGCCTGAGAGAACTTGTTCACCCCTTCTACCACATGAGGATGCAATGAGAAGGCACCATCTGTGAGGAACAGGCCTCCGACAGACACCGAATTTGCTGGCACTTTGATCTTGGACTTCCCAGCCTCCAAAATTGTGAGTGATAAATTTCTGTTGTTTATAAATTACCCAGTCTAAAATATTTTGTTACAGAAGCACAAATGGATAAGACAAAGGACGTGAGTAAATTTGAGGAAC... | TGGTGTTGGGGGGTGGGGCTTTTGGGAGGTGATAAGGTCGTGGGGGTGGAGCCCTTATGAATGGGATTAGTGTTCTTATAATAGAGGCCTGAGAGAACTTGTTCACCCCTTCTACCACATGAGGATGCAATGAGAAGGCACCATCTGTGAGGAACAGGCCTCCGACAGACACCGAATTTGCTGGCACTTTGATCTTGGACTTCCCAGCCTCCAAAATTGTGAGTGATAAATTTCTGTTGTTTATAAATTACCCAGTCTAAAATATTTTGTTACAGAAGCACAAATGGATAAGACAAAGGACGTGAGTAAATTTGAGGAAC... |
Task1_train_45051 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GCTTTTGGGAGGTGATAAGGTCGTGGGGGTGGAGCCCTTATGAATGGGATTAGTGTTCTTATAATAGAGGCCTGAGAGAACTTGTTCACCCCTTCTACCACATGAGGATGCAATGAGAAGGCACCATCTGTGAGGAACAGGCCTCCGACAGACACCGAATTTGCTGGCACTTTGATCTTGGACTTCCCAGCCTCCAAAATTGTGAGTGATAAATTTCTGTTGTTTATAAATTACCCAGTCTAAAATATTTTGTTACAGAAGCACAAATGGATAAGACAAAGGACGTGAGTAAATTTGAGGAACTAGAAACAGGCAGAAAT... | GCTTTTGGGAGGTGATAAGGTCGTGGGGGTGGAGCCCTTATGAATGGGATTAGTGTTCTTATAATAGAGGCCTGAGAGAACTTGTTCACCCCTTCTACCACATGAGGATGCAATGAGAAGGCACCATCTGTGAGGAACAGGCCTCCGACAGACACCGAATTTGCTGGCACTTTGATCTTGGACTTCCCAGCCTCCAAAATTGTGAGTGATAAATTTCTGTTGTTTATAAATTACCCAGTCTAAAATATTTTGTTACAGAAGCACAAATGGATAAGACAAAGGACGTGAGTAAATTTGAGGAACTAGAAACAGGCAGAAAT... |
Task1_train_45052 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GTATTTTGAGGGTCTCAAGAGTTCTAGCCTGCCAAATAACAAAAAGGCCAAAGTGGTTGGAAGGAATGCACATCTCCAAGGTATTCCTTTGTAACACCAGGGATCTGTCTCATAAACAAATTGCAATTCAGTAACCTTGTGATGTACAAGGAAGGGTTCTCAACCGAGAATCACAAGACAAAACATGATGGCTTTGCTATGCCACTAATGAACTGCCTGACTGTATAAAATCCATTTTTTCTCTGGGCATTATCTGAGAATAGTTGAGATTGTTTGTGAGGTCTCTTTCATCTCTCTCAGTGCTAATAATTTTCACAGTA... | GTATTTTGAGGGTCTCAAGAGTTCTAGCCTGCCAAATAACAAAAAGGCCAAAGTGGTTGGAAGGAATGCACATCTCCAAGGTATTCCTTTGTAACACCAGGGATCTGTCTCATAAACAAATTGCAATTCAGTAACCTTGTGATGTACAAGGAAGGGTTCTCAACCGAGAATCACAAGACAAAACATGATGGCTTTGCTATGCCACTAATGAACTGCCTGACTGTATAAAATCCATTTTTTCTCTGGGCATTATCTGAGAATAGTTGAGATTGTTTGTGAGGTCTCTTTCATCTCTCTCAGTGCTAATAATTTTCACAGTA... |
Task1_train_45053 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ATAAGGAAATACGTCTATAAATCAGCTAGTCTGTGAGGAAGATGAGGAAGAATATTGACCAGAATAACTGTGACTCTATATGCTTGCTCCTTTAATCAGGAAACCCGTAATAATTGACCCATATGTAATAGAATACACTCTTGACTCTCTACATAAGCAATTATTTAAGTTAGGAGTCAGAATAATAAAGCAATTGCCCAGTGCTTTTGAGGTCAGTAGATTAACTCTACAGAGCTTAATTAAAAAGCGATAATAAATGCTTGCTCTAGGGAGGATATTTCATTAGTCTTCATCATGGCCTGGGTGAAGTATTCCTGATA... | ATAAGGAAATACGTCTATAAATCAGCTAGTCTGTGAGGAAGATGAGGAAGAATATTGACCAGAATAACTGTGACTCTATATGCTTGCTCCTTTAATCAGGAAACCCGTAATAATTGACCCATATGTAATAGAATACACTCTTGACTCTCTACATAAGCAATTATTTAAGTTAGGAGTCAGAATAATAAAGCAATTGCCCAGTGCTTTTGAGGTCAGTAGATTAACTCTACAGAGCTTAATTAAAAAGCGATAATAAATGCTTGCTCTAGGGAGGATATTTCATTAGTCTTCATCATGGCCTGGGTGAAGTATTCCTGATA... |
Task1_train_45054 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TAGGTTGTTAGTTGAAATAATGACAGCATATGACAACCTTAATATAAACATTCAATACTCCATCTGAGGAAAAACTGATTATTGTTAATTGTAATACTCATAATAATTTACCAGAGAGTCTCAATGTCTCAATTTTTCCTTCTATTAAAAGATACTAATTCTATTTAATTCATAAATAATATTCTGATAATTAATAATCCATCTTGGTGGAAAGAAATTTAAGATGCTTCTGGACAAGAATGGGTGGAGGGATCTGGTCTCATTCCATTCTCCAGTGGACATACACTGGGCTTTAAGAAGAAGAATATGGTGGAATCCAC... | TAGGTTGTTAGTTGAAATAATGACAGCATATGACAACCTTAATATAAACATTCAATACTCCATCTGAGGAAAAACTGATTATTGTTAATTGTAATACTCATAATAATTTACCAGAGAGTCTCAATGTCTCAATTTTTCCTTCTATTAAAAGATACTAATTCTATTTAATTCATAAATAATATTCTGATAATTAATAATCCATCTTGGTGGAAAGAAATTTAAGATGCTTCTGGACAAGAATGGGTGGAGGGATCTGGTCTCATTCCATTCTCCAGTGGACATACACTGGGCTTTAAGAAGAAGAATATGGTGGAATCCAC... |
Task1_train_45055 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CCTTCACTGCCTTTACTTTTATTTCTTCCTGCTCCCCTGCACTAAAAGCACATACTTGGCCTCCTCCAGCTCCTCTGTGCGCTGGATGGCGTCCGTCTCGTACTTGGTCCTCCACTGGGCAACCTCACTGTTGGCCTTGGACATTCCCCTCTGCAGCTCAGCCTTGGCTTCCTGCTCCTCCTCATACTGTTCCCGCAGCAGGTCACAGTCATGGCGGGCTGACTGCAGGGCATGGGCCAGAGTGCTCTTGGCCTAGACCAACCAAAAACTATGTGATATAAGTTTATCTTCTGATCATTGAAATTCTCTATGCAAAGTTC... | CCTTCACTGCCTTTACTTTTATTTCTTCCTGCTCCCCTGCACTAAAAGCACATACTTGGCCTCCTCCAGCTCCTCTGTGCGCTGGATGGCGTCCGTCTCGTACTTGGTCCTCCACTGGGCAACCTCACTGTTGGCCTTGGACATTCCCCTCTGCAGCTCAGCCTTGGCTTCCTGCTCCTCCTCATACTGTTCCCGCAGCAGGTCACAGTCATGGCGGGCTGACTGCAGGGCATGGGCCAGAGTGCTCTTGGCCTAGACCAACCAAAAACTATGTGATATAAGTTTATCTTCTGATCATTGAAATTCTCTATGCAAAGTTC... |
Task1_train_45056 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCTTTTATGATCAATTTTCAAATAATTGCATGTCATTTTTCAAGGAAAAGTTTAAAAATGTTGGAATTATATAGTGATTTTGTGTAGACTAAGACATTGGAAGGGAAAAATAATGAGACACAAACCTCTGTTTGAAGTCTGCATAAAGGATTCTGCTTGGGAAGCCTTTCCTGCAGATGCGGATGCCTTCCAGCACACCGTTACACCTCAGCTGATGCAGGACAAGCTCATGCTCCATGGCACCTAAGAGAATGAATCCACATGCCATACTTCGTGGTCTATCGCACACACACTGGAGCTTGTCTGGATATCAGAAATGT... | TCTTTTATGATCAATTTTCAAATAATTGCATGTCATTTTTCAAGGAAAAGTTTAAAAATGTTGGAATTATATAGTGATTTTGTGTAGACTAAGACATTGGAAGGGAAAAATAATGAGACACAAACCTCTGTTTGAAGTCTGCATAAAGGATTCTGCTTGGGAAGCCTTTCCTGCAGATGCGGATGCCTTCCAGCACACCGTTACACCTCAGCTGATGCAGGACAAGCTCATGCTCCATGGCACCTAAGAGAATGAATCCACATGCCATACTTCGTGGTCTATCGCACACACACTGGAGCTTGTCTGGATATCAGAAATGT... |
Task1_train_45057 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CAGACACACACACACAACAAAAACAGCCAGTGAAAATAACAAAGAGAATATTCTTCAAGTTATAATTAGCGTCTTTGAAGGAAATTTTAAAAAATGATATCCATCAAACAAGAATTAGATGCCATTGTACAAAGAAAGCACTATTGGAGAATTATAAAGACCTCTTTTAAATGTAAAATTGTATCATCTATGGCATTCAAAATTCAGTGAGAGGATGGGAAGATAAAGGCAACATCCCAGGATAAAGTTATAAGCAGTATTATGTATTGTGTGTGTGTGTGTATGGTAAAATATTCACACATGCACACACACACAGATAC... | CAGACACACACACACAACAAAAACAGCCAGTGAAAATAACAAAGAGAATATTCTTCAAGTTATAATTAGCGTCTTTGAAGGAAATTTTAAAAAATGATATCCATCAAACAAGAATTAGATGCCATTGTACAAAGAAAGCACTATTGGAGAATTATAAAGACCTCTTTTAAATGTAAAATTGTATCATCTATGGCATTCAAAATTCAGTGAGAGGATGGGAAGATAAAGGCAACATCCCAGGATAAAGTTATAAGCAGTATTATGTATTGTGTGTGTGTGTGTATGGTAAAATATTCACACATGCACACACACACAGATAC... |
Task1_train_45058 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | TCCATCAAACAAGAATTAGATGCCATTGTACAAAGAAAGCACTATTGGAGAATTATAAAGACCTCTTTTAAATGTAAAATTGTATCATCTATGGCATTCAAAATTCAGTGAGAGGATGGGAAGATAAAGGCAACATCCCAGGATAAAGTTATAAGCAGTATTATGTATTGTGTGTGTGTGTGTATGGTAAAATATTCACACATGCACACACACACAGATACAGAAAGTGCGAGAGGTGAGATGATGTATAGAGGATCAATTTAGGTTATCCAACATGTTACCAGTAAGAATTCTAGAAAAAGAACAGAAAGATAACTAGA... | TCCATCAAACAAGAATTAGATGCCATTGTACAAAGAAAGCACTATTGGAGAATTATAAAGACCTCTTTTAAATGTAAAATTGTATCATCTATGGCATTCAAAATTCAGTGAGAGGATGGGAAGATAAAGGCAACATCCCAGGATAAAGTTATAAGCAGTATTATGTATTGTGTGTGTGTGTGTATGGTAAAATATTCACACATGCACACACACACAGATACAGAAAGTGCGAGAGGTGAGATGATGTATAGAGGATCAATTTAGGTTATCCAACATGTTACCAGTAAGAATTCTAGAAAAAGAACAGAAAGATAACTAGA... |
Task1_train_45059 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CAGTAAAGTCCTCATGTCCTCCAGGTTAAAGGGCAGAGAGAAAACAGTGAACTGTGAGAGCCCAGGGGACATGGGGACTTCAGAAGGGACCATGCTGAAGAGATACCATGGAGTGGAATTAAGAAAGGATCATTGGGCTGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCATGAGGTCCGTAGTTCAAGACCAGCCTGGACAATATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGGGCTTGGGCATGGTGGCGGGTGCCTGTAATCCCAGCTACTCGGGAG... | CAGTAAAGTCCTCATGTCCTCCAGGTTAAAGGGCAGAGAGAAAACAGTGAACTGTGAGAGCCCAGGGGACATGGGGACTTCAGAAGGGACCATGCTGAAGAGATACCATGGAGTGGAATTAAGAAAGGATCATTGGGCTGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCATGAGGTCCGTAGTTCAAGACCAGCCTGGACAATATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGGGCTTGGGCATGGTGGCGGGTGCCTGTAATCCCAGCTACTCGGGAG... |
Task1_train_45060 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGGAGAAACCCCATCTCTACTAAAAACACAAAATTAGCCAGGTGTGGTGGTGTATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTAAGCCGAGGTTGCACCACGGCACTCCAGCCTGGGCAACAAGAGTGAAACTCCATCTCAAAAAAAAAGAAGAAAATTAAATTGCCCTTCAAGTATAAGATGGCAGTGCAATAGTATCCAGAGAATGGCCATTCACCCTGGTGCAGCAGCTGACACGGGTCTGTGTGGCCAAAGACTGAACCCCAACCTGTTCCAT... | TGGAGAAACCCCATCTCTACTAAAAACACAAAATTAGCCAGGTGTGGTGGTGTATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTAAGCCGAGGTTGCACCACGGCACTCCAGCCTGGGCAACAAGAGTGAAACTCCATCTCAAAAAAAAAGAAGAAAATTAAATTGCCCTTCAAGTATAAGATGGCAGTGCAATAGTATCCAGAGAATGGCCATTCACCCTGGTGCAGCAGCTGACACGGGTCTGTGTGGCCAAAGACTGAACCCCAACCTGTTCCAT... |
Task1_train_45061 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AGCCAGCACCCTCCCCTGAGGGCCACATCATCCCCCAGGGCATCCTGGAGAACTCCATTAAGATCACCAATGAGCCCCCCACGGGCATGCATGCCAACCTGCACAAGGCCCTGGACAACTTCACTCAGGTACGGCCCCGGGAGGGAGGCAAAAACAGCAGCACACCTCACAGTCAGCTGATGCAAACTGGTGGGGGGAGAGCATGCAACTCAGAAGGGAGTCGGGTGCTGGTTGGGCTACGGAGCAATGCTGATGTGGGTAAAATGTTCCCACCTGATGCCCACTCAGGGCAACCCCACTCTCCATTGCCAGATAACCCC... | AGCCAGCACCCTCCCCTGAGGGCCACATCATCCCCCAGGGCATCCTGGAGAACTCCATTAAGATCACCAATGAGCCCCCCACGGGCATGCATGCCAACCTGCACAAGGCCCTGGACAACTTCACTCAGGTACGGCCCCGGGAGGGAGGCAAAAACAGCAGCACACCTCACAGTCAGCTGATGCAAACTGGTGGGGGGAGAGCATGCAACTCAGAAGGGAGTCGGGTGCTGGTTGGGCTACGGAGCAATGCTGATGTGGGTAAAATGTTCCCACCTGATGCCCACTCAGGGCAACCCCACTCTCCATTGCCAGATAACCCC... |
Task1_train_45062 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GAAATATGTTCATCTTAAGGTAGGTATGCTTAACTGTTTTTAAGAATTCCAAAAGTGGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCAAGGCGGGTGGATCACCTGAGGTCAGGAATTTGAGACCAGCATGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGTCGGGTGTGGTGGTGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTCCTTGAGCTCGGGAGGCAGAGGTTGCCGTGAGCTGAGATCGTGCTACTGCACTCCAGCCTGGGTGA... | GAAATATGTTCATCTTAAGGTAGGTATGCTTAACTGTTTTTAAGAATTCCAAAAGTGGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCAAGGCGGGTGGATCACCTGAGGTCAGGAATTTGAGACCAGCATGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGTCGGGTGTGGTGGTGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTCCTTGAGCTCGGGAGGCAGAGGTTGCCGTGAGCTGAGATCGTGCTACTGCACTCCAGCCTGGGTGA... |
Task1_train_45063 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ATGGGCGGCCAGACTGCAGCTTCGTGGCTCGGATTTCATTTCAAACTCTTCACACAGAAGGGGCTTGCACAGTACAGGAGGGTGGGAAACTGCACATGGAGGGACTTTGCAGCTGCTCCCAGCTGCTACGAAATGCCAATTTCTCCTCCTAGGAATCGAAAGGGCCTCTGCTCAGTATGCCTCTCTAATGGACTTGAAAAACGGGGCCATGATCGTTCGAGGCCAGAAAATTTCAAATTTGGATGAAGTCAGGGGAGCACTAGCTCCTAAACTGTGAGCTGGACAATCTTTGATCTTCCTGTATGCTCTAGAATAAAATG... | ATGGGCGGCCAGACTGCAGCTTCGTGGCTCGGATTTCATTTCAAACTCTTCACACAGAAGGGGCTTGCACAGTACAGGAGGGTGGGAAACTGCACATGGAGGGACTTTGCAGCTGCTCCCAGCTGCTACGAAATGCCAATTTCTCCTCCTAGGAATCGAAAGGGCCTCTGCTCAGTATGCCTCTCTAATGGACTTGAAAAACGGGGCCATGATCGTTCGAGGCCAGAAAATTTCAAATTTGGATGAAGTCAGGGGAGCACTAGCTCCTAAACTGTGAGCTGGACAATCTTTGATCTTCCTGTATGCTCTAGAATAAAATG... |
Task1_train_45064 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | AGACTGAAAACTTGTGGCATATTTCGACCTGGCCAAAATTGGGAAAAGCTGAACTGTTGTGATACATCTTTTAAAATTCTTTGGAGTTCTGTGACTATATCAGTAATAGAGAAATAATTGCTTTAACAGTGTGACCCTCTCATTTTCTTAAATCAGCAGTACATTTAAAAGTCTTTTTTAACAGTTGCACTTCTGAGTAAATTCAAACAATTCGACAGTTTTTATAATTTTCTAGCATTTTATAATAGACATTGATAACATAAGTCAATCCAGGTTGACTCCATGAATTTGTGGGCAATATGGAACTTACTATTAATTGC... | AGACTGAAAACTTGTGGCATATTTCGACCTGGCCAAAATTGGGAAAAGCTGAACTGTTGTGATACATCTTTTAAAATTCTTTGGAGTTCTGTGACTATATCAGTAATAGAGAAATAATTGCTTTAACAGTGTGACCCTCTCATTTTCTTAAATCAGCAGTACATTTAAAAGTCTTTTTTAACAGTTGCACTTCTGAGTAAATTCAAACAATTCGACAGTTTTTATAATTTTCTAGCATTTTATAATAGACATTGATAACATAAGTCAATCCAGGTTGACTCCATGAATTTGTGGGCAATATGGAACTTACTATTAATTGC... |
Task1_train_45065 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GGGCAATATGGAACTTACTATTAATTGCCAGGAAGGCCATTTGCATTTTCTCAGATGGAAAAGGGTCATAGAATGGCAAAATGATAGCTGAAAACTCATAGTGCCAGCCTGAAAGAACGGCAGACTTATAATTTAAAGTCCTATTTTACATTTCTCTCATCTTTAACTTAAAACTTTAAATTAAAATCTTAATAAAACTCGATATGTTGATAAGAGATTTAAATTTCTAGAAATGTTCAGGCTTTTTAAGTTGGGGGTCAAGGATAATGGTGGATATTTAGAGGAGAAATTCAAATATGTGTAATGCCCTTTTTTATGTA... | GGGCAATATGGAACTTACTATTAATTGCCAGGAAGGCCATTTGCATTTTCTCAGATGGAAAAGGGTCATAGAATGGCAAAATGATAGCTGAAAACTCATAGTGCCAGCCTGAAAGAACGGCAGACTTATAATTTAAAGTCCTATTTTACATTTCTCTCATCTTTAACTTAAAACTTTAAATTAAAATCTTAATAAAACTCGATATGTTGATAAGAGATTTAAATTTCTAGAAATGTTCAGGCTTTTTAAGTTGGGGGTCAAGGATAATGGTGGATATTTAGAGGAGAAATTCAAATATGTGTAATGCCCTTTTTTATGTA... |
Task1_train_45066 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TAATCTATAGAGTCTTTCTAGGTACTAGTCACTATGCTGAACACTTTATCCATATAACTTCCTTGAAATCCCCTCAGCCCTATACCCTTGTTATTGGCATCCCCATTTTATAGATGAGAAAACTGAATCTTAGTGTTTACGTAACCTTTTCAGGCCCCTATGGCTGGTAAGCAGCAAAGGACAGGCTCAAACCCAGGCTCTCATTTCTATGCTCTTAACCTTATTATAATATAGTCACTTGTTTACTTGTACCTCTCACTAAAATGTGACCTTTCGATGTTAAGATATATGTCATTACTTCTTTATCTTTGGTACCCAAT... | TAATCTATAGAGTCTTTCTAGGTACTAGTCACTATGCTGAACACTTTATCCATATAACTTCCTTGAAATCCCCTCAGCCCTATACCCTTGTTATTGGCATCCCCATTTTATAGATGAGAAAACTGAATCTTAGTGTTTACGTAACCTTTTCAGGCCCCTATGGCTGGTAAGCAGCAAAGGACAGGCTCAAACCCAGGCTCTCATTTCTATGCTCTTAACCTTATTATAATATAGTCACTTGTTTACTTGTACCTCTCACTAAAATGTGACCTTTCGATGTTAAGATATATGTCATTACTTCTTTATCTTTGGTACCCAAT... |
Task1_train_45067 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | GGCTATCCCAAGGAGCCCATTCAACAGCAGCTTACCTCTTCTCAGCTCCATATTTTCAATGTGACTGGGTCTTATAGTACAGGCTTGTATTCATCACAGATGTTTGGAACTTCAGAATAATACATGGTGCAAATTTGCATTTACCTTCCATTGTAAATCAGTTCCAATAAAAGATAATATAAAAGGCAGAGCTTCTGCCTTGGATTTTGTGTTCTTTAAATTTTTTGGTGCATTCTGTCTTTAAAATATAAGAAGTACCTCACTATATTCAGTGTAACACTCAACCGTCCCTGTCATGAGCTGGGTGACCTTGGTCATTC... | GGCTATCCCAAGGAGCCCATTCAACAGCAGCTTACCTCTTCTCAGCTCCATATTTTCAATGTGACTGGGTCTTATAGTACAGGCTTGTATTCATCACAGATGTTTGGAACTTCAGAATAATACATGGTGCAAATTTGCATTTACCTTCCATTGTAAATCAGTTCCAATAAAAGATAATATAAAAGGCAGAGCTTCTGCCTTGGATTTTGTGTTCTTTAAATTTTTTGGTGCATTCTGTCTTTAAAATATAAGAAGTACCTCACTATATTCAGTGTAACACTCAACCGTCCCTGTCATGAGCTGGGTGACCTTGGTCATTC... |
Task1_train_45068 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGGAGGTGGCCTTGAAATACCACAATACAGCAAAAGAAGGACAAAGCATTCCCTCACCTGCCCAAGAGAAGAAAGTTGCAAAAAGGTGGGGGATACACACAGAAAGCAGAAGCGTAGGAAGAGCCTTCATCTAACTAGATCTCTGGCTGCTGCCTCACACCTAAGGAAGTGAACCGTACATTTAGGAGCCTGGAAAATGGGTCCAACATTTCCAGATCCCTGACTTAGGGAGAAATTACAGGCCCCATGAGTTACAGGGTCACACTGACTTCATTGAGCTTCTCAGATTGCAGTGACTAAAGTGATTAAAATGCAGTTTC... | TGGAGGTGGCCTTGAAATACCACAATACAGCAAAAGAAGGACAAAGCATTCCCTCACCTGCCCAAGAGAAGAAAGTTGCAAAAAGGTGGGGGATACACACAGAAAGCAGAAGCGTAGGAAGAGCCTTCATCTAACTAGATCTCTGGCTGCTGCCTCACACCTAAGGAAGTGAACCGTACATTTAGGAGCCTGGAAAATGGGTCCAACATTTCCAGATCCCTGACTTAGGGAGAAATTACAGGCCCCATGAGTTACAGGGTCACACTGACTTCATTGAGCTTCTCAGATTGCAGTGACTAAAGTGATTAAAATGCAGTTTC... |
Task1_train_45069 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AATACTTCAGAGTAATCTGATGCTCAGGGAAGGCGTAGAAGCCCTTCTGATTCTAAACAAAAATTTATGATGAATTAATTCAAAAAGATCATTAGTGAACTATCAGCCATTCTCAGGATTCCTGGGGATTGTGTGCCTCTGTATGTGTTTTTGTACAGCGGGGAGGGGTTGCAGTAGGAAGTGACAGTGCGCAGGGTGCCCCAAGAAACTCCTCCGCTCACCAGACTTTCAGCTCCTTGATTCTCTAAACTCTTCTACTACAGATGCTGTGGTAGAGAACTACAGCAAGTGCTCATCACATGGGAATAAGTCATGCAAAC... | AATACTTCAGAGTAATCTGATGCTCAGGGAAGGCGTAGAAGCCCTTCTGATTCTAAACAAAAATTTATGATGAATTAATTCAAAAAGATCATTAGTGAACTATCAGCCATTCTCAGGATTCCTGGGGATTGTGTGCCTCTGTATGTGTTTTTGTACAGCGGGGAGGGGTTGCAGTAGGAAGTGACAGTGCGCAGGGTGCCCCAAGAAACTCCTCCGCTCACCAGACTTTCAGCTCCTTGATTCTCTAAACTCTTCTACTACAGATGCTGTGGTAGAGAACTACAGCAAGTGCTCATCACATGGGAATAAGTCATGCAAAC... |
Task1_train_45070 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TAAAAACTATTAAATGCTTAGAAATTTTAAAAAACCAACTGTGCAACCTTCAGTAAGTTACCATACCACTCTGCCCTTGAAGGTATTAAAAGAAATAACCCCAAATTCCAATAATCTCTAGCACTCAATGAGTCTCTGTAATCCATACTTTCCCAAATATAACCTAGAAAGAAACACCCATAAAAGAACAAAAGAGATAAAAAAATTATTGGAGGAATTTATTGCCTGCCTCCATGTCTATAAACGTTCCATGGACACAAAATACAATCATTCAAATTCCCTGGAAACCACCTATATTTTTCGAAGAATTCATTCTGGCC... | TAAAAACTATTAAATGCTTAGAAATTTTAAAAAACCAACTGTGCAACCTTCAGTAAGTTACCATACCACTCTGCCCTTGAAGGTATTAAAAGAAATAACCCCAAATTCCAATAATCTCTAGCACTCAATGAGTCTCTGTAATCCATACTTTCCCAAATATAACCTAGAAAGAAACACCCATAAAAGAACAAAAGAGATAAAAAAATTATTGGAGGAATTTATTGCCTGCCTCCATGTCTATAAACGTTCCATGGACACAAAATACAATCATTCAAATTCCCTGGAAACCACCTATATTTTTCGAAGAATTCATTCTGGCC... |
Task1_train_45071 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TCCTATTTGACCTCTTTGAACTTGTGAGATCACTTTAATTCTATAATTTACTTATTCATTCTTTCACTAAGAATTTGCTGAAAATTTATCATGTGTGAAAATGTCTTGTAAACTCTTTTTTTTTTTTTTCCCTGAGACAGAGTCTTGCTCTGTCGCCCAGAGCTGGAGTGCAATGGCGTGATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACACGCGTGCGCCACCACACCAGGCTAATTTTTGTATTTTTAGTAGACGGGGTTTCGCCATGTTG... | TCCTATTTGACCTCTTTGAACTTGTGAGATCACTTTAATTCTATAATTTACTTATTCATTCTTTCACTAAGAATTTGCTGAAAATTTATCATGTGTGAAAATGTCTTGTAAACTCTTTTTTTTTTTTTTCCCTGAGACAGAGTCTTGCTCTGTCGCCCAGAGCTGGAGTGCAATGGCGTGATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACACGCGTGCGCCACCACACCAGGCTAATTTTTGTATTTTTAGTAGACGGGGTTTCGCCATGTTG... |
Task1_train_45072 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | TGAGGTCAGGAGATCGAGACCCTCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGCGGGCGCCTGCAATCCCAGCTACTCGGGAGGCTGAGGCAGAAGAATAGTATGAACCCGGGAGGTGGAGTTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCAAACAGAGTGAGACTCTGTCTCAAAAAAAATAAATAAATAAAAAAGTAGACATGCGCTAATGAAGTAAATCCATGGATACCATCATCCACCCAGCTGTCCAGTTTGTCTCATTTGAGCAGACG... | TGAGGTCAGGAGATCGAGACCCTCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGCGGGCGCCTGCAATCCCAGCTACTCGGGAGGCTGAGGCAGAAGAATAGTATGAACCCGGGAGGTGGAGTTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCAAACAGAGTGAGACTCTGTCTCAAAAAAAATAAATAAATAAAAAAGTAGACATGCGCTAATGAAGTAAATCCATGGATACCATCATCCACCCAGCTGTCCAGTTTGTCTCATTTGAGCAGACG... |
Task1_train_45073 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | GGAGATCGAGACCCTCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGCGGGCGCCTGCAATCCCAGCTACTCGGGAGGCTGAGGCAGAAGAATAGTATGAACCCGGGAGGTGGAGTTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCAAACAGAGTGAGACTCTGTCTCAAAAAAAATAAATAAATAAAAAAGTAGACATGCGCTAATGAAGTAAATCCATGGATACCATCATCCACCCAGCTGTCCAGTTTGTCTCATTTGAGCAGACGCCGGATAC... | GGAGATCGAGACCCTCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGCGGGCGCCTGCAATCCCAGCTACTCGGGAGGCTGAGGCAGAAGAATAGTATGAACCCGGGAGGTGGAGTTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCAAACAGAGTGAGACTCTGTCTCAAAAAAAATAAATAAATAAAAAAGTAGACATGCGCTAATGAAGTAAATCCATGGATACCATCATCCACCCAGCTGTCCAGTTTGTCTCATTTGAGCAGACGCCGGATAC... |
Task1_train_45074 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCGTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGCACCACCACACCCAGCTCATTTTGTGTTTTTAGTAGAGACAGGGTTTCGCCATGTTGCCCAGGCTGGGCTCAAACTCCAGGACTCAATGATCCACCCACCTCGGCCTCCCAAAGTGCTGGAATTACAAGCACGAGCCACTGCGCCTGGCCTCAAGTTAAAATGCTTTTAAATGAATTTCTGTTCCTGGAGTGAGTGCCATGTACCTAGGGTGCCAAGAAGGTACTCTGCACACAGATGTCTTGAAAT... | CTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCGTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGCACCACCACACCCAGCTCATTTTGTGTTTTTAGTAGAGACAGGGTTTCGCCATGTTGCCCAGGCTGGGCTCAAACTCCAGGACTCAATGATCCACCCACCTCGGCCTCCCAAAGTGCTGGAATTACAAGCACGAGCCACTGCGCCTGGCCTCAAGTTAAAATGCTTTTAAATGAATTTCTGTTCCTGGAGTGAGTGCCATGTACCTAGGGTGCCAAGAAGGTACTCTGCACACAGATGTCTTGAAAT... |
Task1_train_45075 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | CAACCTCCGCCTCCTGGGTTCAAGCGATTCTCGTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGCACCACCACACCCAGCTCATTTTGTGTTTTTAGTAGAGACAGGGTTTCGCCATGTTGCCCAGGCTGGGCTCAAACTCCAGGACTCAATGATCCACCCACCTCGGCCTCCCAAAGTGCTGGAATTACAAGCACGAGCCACTGCGCCTGGCCTCAAGTTAAAATGCTTTTAAATGAATTTCTGTTCCTGGAGTGAGTGCCATGTACCTAGGGTGCCAAGAAGGTACTCTGCACACAGATGTCTTGAAATTCA... | CAACCTCCGCCTCCTGGGTTCAAGCGATTCTCGTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGCACCACCACACCCAGCTCATTTTGTGTTTTTAGTAGAGACAGGGTTTCGCCATGTTGCCCAGGCTGGGCTCAAACTCCAGGACTCAATGATCCACCCACCTCGGCCTCCCAAAGTGCTGGAATTACAAGCACGAGCCACTGCGCCTGGCCTCAAGTTAAAATGCTTTTAAATGAATTTCTGTTCCTGGAGTGAGTGCCATGTACCTAGGGTGCCAAGAAGGTACTCTGCACACAGATGTCTTGAAATTCA... |
Task1_train_45076 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AAATCCAGGGCCTTTCAACAAGGGAGGCAGCAGAAGGCAAGGTTGAGAATTAACAGGCTCTGAGGGATCCCCACTCTCATACGATGACAAAAATCCATTTCCGTTAAATTTAAAAACTAGAGACACAAGGCAATTTTTTAACAATTCTGTAAATGTATGCTAAATCCCCAAGAGAGAGAACAGAGTATGTGGCATTGCCCGGATTTAATTGATCACGGAAACCTTTTTTCTTGGAAAACATCAGAGGAACACAGTTGGGAAGTCCTGTGCACACTGTATTTCTTTTCTTTTGTTTTTTCCCTTAATCAATATCCAGTGAC... | AAATCCAGGGCCTTTCAACAAGGGAGGCAGCAGAAGGCAAGGTTGAGAATTAACAGGCTCTGAGGGATCCCCACTCTCATACGATGACAAAAATCCATTTCCGTTAAATTTAAAAACTAGAGACACAAGGCAATTTTTTAACAATTCTGTAAATGTATGCTAAATCCCCAAGAGAGAGAACAGAGTATGTGGCATTGCCCGGATTTAATTGATCACGGAAACCTTTTTTCTTGGAAAACATCAGAGGAACACAGTTGGGAAGTCCTGTGCACACTGTATTTCTTTTCTTTTGTTTTTTCCCTTAATCAATATCCAGTGAC... |
Task1_train_45077 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CCGTTAAATTTAAAAACTAGAGACACAAGGCAATTTTTTAACAATTCTGTAAATGTATGCTAAATCCCCAAGAGAGAGAACAGAGTATGTGGCATTGCCCGGATTTAATTGATCACGGAAACCTTTTTTCTTGGAAAACATCAGAGGAACACAGTTGGGAAGTCCTGTGCACACTGTATTTCTTTTCTTTTGTTTTTTCCCTTAATCAATATCCAGTGACCATATATTAGGTTCAAAGTCCTGTGCTAGTAGATATCACAGGAAATATAAATAATTATCAGATAAGGACCTTACTTACAATGAGCTTATTGTCCCATAAA... | CCGTTAAATTTAAAAACTAGAGACACAAGGCAATTTTTTAACAATTCTGTAAATGTATGCTAAATCCCCAAGAGAGAGAACAGAGTATGTGGCATTGCCCGGATTTAATTGATCACGGAAACCTTTTTTCTTGGAAAACATCAGAGGAACACAGTTGGGAAGTCCTGTGCACACTGTATTTCTTTTCTTTTGTTTTTTCCCTTAATCAATATCCAGTGACCATATATTAGGTTCAAAGTCCTGTGCTAGTAGATATCACAGGAAATATAAATAATTATCAGATAAGGACCTTACTTACAATGAGCTTATTGTCCCATAAA... |
Task1_train_45078 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AGAAACTTCAGGTTATAGCTTCAGAAACCCATTTAAAGACAGTTTGCCATTTGCCTAAAGACTTGATGAATGCTGATGATTAATCTTAGGAAGCTTATCTGTCAAAAGAAGAATGAAATAATCAGGGGGAAAGGACTGAGAACCATAAAGGAAGGTGGAAAATTTCATATGAAAACAAGAACACCTGGGGCGTGGGTATTACGTGACAGTTCTTAAAAGAACCATTCTTTGAATGAGAAATCAGACAAGTCCACATATTCCAGGTTACTTTAGAGGAGAGGAGTAGGGCCCCTTTCCAGAGGTCACAGGGACTAAAACTC... | AGAAACTTCAGGTTATAGCTTCAGAAACCCATTTAAAGACAGTTTGCCATTTGCCTAAAGACTTGATGAATGCTGATGATTAATCTTAGGAAGCTTATCTGTCAAAAGAAGAATGAAATAATCAGGGGGAAAGGACTGAGAACCATAAAGGAAGGTGGAAAATTTCATATGAAAACAAGAACACCTGGGGCGTGGGTATTACGTGACAGTTCTTAAAAGAACCATTCTTTGAATGAGAAATCAGACAAGTCCACATATTCCAGGTTACTTTAGAGGAGAGGAGTAGGGCCCCTTTCCAGAGGTCACAGGGACTAAAACTC... |
Task1_train_45079 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TATACAATGTCCATGATCTAATAAGGAAGGTGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGGACTTTGGGAGGCCGAGGCGGGTGGATCACGAGGTCAGGAGATCGAGATCATTCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCTTGGTGACGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCTGGGAGGCGGAGCTTGCAGTGAGCCGAGATTGTGCCACTGCACTCCAGCCTGCGCAACAGAGCGAGACTCCGTCTCAAAAAAAA... | TATACAATGTCCATGATCTAATAAGGAAGGTGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGGACTTTGGGAGGCCGAGGCGGGTGGATCACGAGGTCAGGAGATCGAGATCATTCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCTTGGTGACGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCTGGGAGGCGGAGCTTGCAGTGAGCCGAGATTGTGCCACTGCACTCCAGCCTGCGCAACAGAGCGAGACTCCGTCTCAAAAAAAA... |
Task1_train_45080 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TAGCCTTCGAGGAGAAAACGGAGGTTTGGTGATCTGGGATGGACTGGAGACCCTCCTTTCCTAGTAAAATTGATTGCACTGTTTGATGGAGATTATTATTATTATTTGAGATGGAGTCTCGCTCTGTCACCAGGCTGGAGTGAAGTGGCACGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTACTGCAGCCTCCCTAGCAGCTGGGACTACAGTCGCCCGCCACCACACCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGAGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGCC... | TAGCCTTCGAGGAGAAAACGGAGGTTTGGTGATCTGGGATGGACTGGAGACCCTCCTTTCCTAGTAAAATTGATTGCACTGTTTGATGGAGATTATTATTATTATTTGAGATGGAGTCTCGCTCTGTCACCAGGCTGGAGTGAAGTGGCACGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTACTGCAGCCTCCCTAGCAGCTGGGACTACAGTCGCCCGCCACCACACCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGAGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGCC... |
Task1_train_45081 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCTCTCAATGGAGAAACCAGGGTCATCTTTTGGTTCTCATATTGAATCTAGCATAATATGCCTGGTACATAATTGATAGTTACCCTTTACATAAAATACTCCGAATCTGACGACCATTAGAATACTTGTCATTTATCATAGTCAGTTCCCCTCTTAAGTGCATCTCAGGCTTTTGCTCCAGGGCCAGCAGAAACTGGGGGATGAAAGAGAAGTAATTAAGGGAAAGATGTTGAAAAAAATATTTTATGTTTTAGGAAACAGTGACATTCAAGGATGTGGCCATGGACTTTACACCAGAGGAGTGGGGGAAGCTGGATCCT... | TCTCTCAATGGAGAAACCAGGGTCATCTTTTGGTTCTCATATTGAATCTAGCATAATATGCCTGGTACATAATTGATAGTTACCCTTTACATAAAATACTCCGAATCTGACGACCATTAGAATACTTGTCATTTATCATAGTCAGTTCCCCTCTTAAGTGCATCTCAGGCTTTTGCTCCAGGGCCAGCAGAAACTGGGGGATGAAAGAGAAGTAATTAAGGGAAAGATGTTGAAAAAAATATTTTATGTTTTAGGAAACAGTGACATTCAAGGATGTGGCCATGGACTTTACACCAGAGGAGTGGGGGAAGCTGGATCCT... |
Task1_train_45082 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GCAGGGCCTCGCCTCTCCCGCTGTGCCCTGGTCACAGGGTCCTGGGCTTCCTAAGATCACAGGGTGGGGAGGGGCTGCCCACCTCCCTGGGCCTCCCACACCTCTCACCTTACCCCCACTATCCTGGCCTCCTCTGGGTTTCAGGGACACCGAGCTGGGGCAGCAGTGGACTTGGGGCATGAGCAGGTTGATGTCAGAAAATACACCAATAACCTCGGGATTGTGCAGTAAGTCCTCTGTCCCCCCGACCCCAGCCACCAATCTCACCTCAGGGATGGGTTTTGTTTTTAGAAAGGCCTCTCTGAAGCAGGACATGTCTC... | GCAGGGCCTCGCCTCTCCCGCTGTGCCCTGGTCACAGGGTCCTGGGCTTCCTAAGATCACAGGGTGGGGAGGGGCTGCCCACCTCCCTGGGCCTCCCACACCTCTCACCTTACCCCCACTATCCTGGCCTCCTCTGGGTTTCAGGGACACCGAGCTGGGGCAGCAGTGGACTTGGGGCATGAGCAGGTTGATGTCAGAAAATACACCAATAACCTCGGGATTGTGCAGTAAGTCCTCTGTCCCCCCGACCCCAGCCACCAATCTCACCTCAGGGATGGGTTTTGTTTTTAGAAAGGCCTCTCTGAAGCAGGACATGTCTC... |
Task1_train_45083 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GTGGCACGATGGCAGGGCTTGGGAGCCTTCCCAGGCAACACTGACTGCCCAAAATACTAGAAAGGATGCGGGGCCCCGGAAACTCTCATCCATGGCTGGTGGGAACGTGACAGGGCACAGCCATTTTGTAAGTCACATGGGCTGTGGCTCACAAAGCTCAGTGGCCTCGTACCACACATCCCCAAAGTGTGACAGATATTGGCCACACTGATTTGAAAACTGACGTCCAAGTAAAACCCGCATGTGACGTTCACCGCTTGATTGATTGTAACTCACACCCGGAGGCTACGGAGATGATCTTCAACATGGGAACTAGGGAG... | GTGGCACGATGGCAGGGCTTGGGAGCCTTCCCAGGCAACACTGACTGCCCAAAATACTAGAAAGGATGCGGGGCCCCGGAAACTCTCATCCATGGCTGGTGGGAACGTGACAGGGCACAGCCATTTTGTAAGTCACATGGGCTGTGGCTCACAAAGCTCAGTGGCCTCGTACCACACATCCCCAAAGTGTGACAGATATTGGCCACACTGATTTGAAAACTGACGTCCAAGTAAAACCCGCATGTGACGTTCACCGCTTGATTGATTGTAACTCACACCCGGAGGCTACGGAGATGATCTTCAACATGGGAACTAGGGAG... |
Task1_train_45084 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | GATTTTACTGAAAAAAAATTCCTAAAAACTCAGGTGTCCTAAAGAGCTCACTGCTTATTTGGGGGGATCATCTGAACCCAGAATTGTGTTCGTTATTTGGGTTTGTAGACAAAATGAAATTGACAGCGTCTGCACACACACAAAAAAAAAACCCTCTTTCCCCTCTTTTCTAGGCAGCAGGAATTATGTGACATCCTCGTGGCCTATTCTGCATATAACCCTGTGAGTATTCCCGGGCAGCGATATTCCTGGGACATGTGCCCATATTCACAGGCATGGGTGTCTCTTGGGGGTGTTGCAACTTCTTGAAAATTCAGTGT... | GATTTTACTGAAAAAAAATTCCTAAAAACTCAGGTGTCCTAAAGAGCTCACTGCTTATTTGGGGGGATCATCTGAACCCAGAATTGTGTTCGTTATTTGGGTTTGTAGACAAAATGAAATTGACAGCGTCTGCACACACACAAAAAAAAAACCCTCTTTCCCCTCTTTTCTAGGCAGCAGGAATTATGTGACATCCTCGTGGCCTATTCTGCATATAACCCTGTGAGTATTCCCGGGCAGCGATATTCCTGGGACATGTGCCCATATTCACAGGCATGGGTGTCTCTTGGGGGTGTTGCAACTTCTTGAAAATTCAGTGT... |
Task1_train_45085 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | CTGACAGGCTGAATGGGGAAACTCAGCAAAGCCTATCTGTTCCAATGCTTCTTGGCCTCTCTGTGCGGCTCCTTCTAGGGGAGGGGCAGGACCCCTTCTGAAATGCGGGTCTTATGAGTCACAATCAAACAAGGTAGATCAGAGAATTTCTTTATGGACAGCTCCAAGACAGAAAGACAGAGGAAGATATATTTTTAGTTATCATGGCCTGTCTTGGGGAGAAGTAACAAGGGCTATGGGAGTTATGTGCCAGGAACTGTGGACCAAAGCCAACACAGCTGACCCTTGAACAGCACAGGTTTGAACTATGCAGGTCCACT... | CTGACAGGCTGAATGGGGAAACTCAGCAAAGCCTATCTGTTCCAATGCTTCTTGGCCTCTCTGTGCGGCTCCTTCTAGGGGAGGGGCAGGACCCCTTCTGAAATGCGGGTCTTATGAGTCACAATCAAACAAGGTAGATCAGAGAATTTCTTTATGGACAGCTCCAAGACAGAAAGACAGAGGAAGATATATTTTTAGTTATCATGGCCTGTCTTGGGGAGAAGTAACAAGGGCTATGGGAGTTATGTGCCAGGAACTGTGGACCAAAGCCAACACAGCTGACCCTTGAACAGCACAGGTTTGAACTATGCAGGTCCACT... |
Task1_train_45086 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GTATAAGCTAACATCAGTTGGCTTTTTTCCCATCCTTTTTGGAAACAAGTATGTTTGAATACTTGGCTGCACTAATCTTTCAAGCACATATACTTAAGTCTCCTTAATTTTGACTGAGATGAGGAAACAAAGTTGGCTTATTTTTCTCAGTTCCTTAAAAACAGTAACTCAAGATAAACCCTTTCAAAATGCAGTACAGTACTTTTAAAACAAAAGCCATCCAAGTTGAATAAGCGATGGCAGTTTGGGGGCCTGATATGGCTGTTATTTATAAGGTGGCCATTTTTACATCCTAAGAGTAGTTCATTAGTCAATGCATT... | GTATAAGCTAACATCAGTTGGCTTTTTTCCCATCCTTTTTGGAAACAAGTATGTTTGAATACTTGGCTGCACTAATCTTTCAAGCACATATACTTAAGTCTCCTTAATTTTGACTGAGATGAGGAAACAAAGTTGGCTTATTTTTCTCAGTTCCTTAAAAACAGTAACTCAAGATAAACCCTTTCAAAATGCAGTACAGTACTTTTAAAACAAAAGCCATCCAAGTTGAATAAGCGATGGCAGTTTGGGGGCCTGATATGGCTGTTATTTATAAGGTGGCCATTTTTACATCCTAAGAGTAGTTCATTAGTCAATGCATT... |
Task1_train_45087 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GTGGTGCCATCTTAGCTTCCGGGTTTAAGCAATTCTCCTGCCTCACCCTCCCTAGTAGCTGGGATTACAGGCACAAGCCACCATGCCCAGCTAATTTTTGTATTTTTTTTAGTGGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCTAACAGCTGACCAGCCAGCCTCAGCCTCCCAAAGTGCTGGGATTACACCCAGCCACCACGCCCAGCCTTTTGCACTAACCTAATACCTCCTTTTGCAGGCTCCAGTCAGGCCAACACCGACGCGCAGCTGGGAGGAAGACAGGACCCTTGACATCTCCATCTGCACAGAG... | GTGGTGCCATCTTAGCTTCCGGGTTTAAGCAATTCTCCTGCCTCACCCTCCCTAGTAGCTGGGATTACAGGCACAAGCCACCATGCCCAGCTAATTTTTGTATTTTTTTTAGTGGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCTAACAGCTGACCAGCCAGCCTCAGCCTCCCAAAGTGCTGGGATTACACCCAGCCACCACGCCCAGCCTTTTGCACTAACCTAATACCTCCTTTTGCAGGCTCCAGTCAGGCCAACACCGACGCGCAGCTGGGAGGAAGACAGGACCCTTGACATCTCCATCTGCACAGAG... |
Task1_train_45088 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TTTTCATGCAGTTACCATGAACTAATACTACAATAAAGGATGGTCTTGGGTGTCAATTCTTGAAAATGTGTATTTGAAGAAAAAGTAAATTTCGCCTACTGTTGTCAGATATTAGCAGTCCAGATATTCGCTCTAGCTTGTAAACTTCCCTGTGGTCAGCCTAAGCTCTTAACCCCCTATTCTACAGCTTTAGACTGAAGGCAAAAGCTCAAAGCATTTAAGGCCTCCTCAATTTCGGCCCCTGCTGCTCTGTGCTCTGTTCCTTGGTGTAGCTTTGTTCCAGCTCCTGCAGCATTGCACCATTCCTAACCACAACCTTA... | TTTTCATGCAGTTACCATGAACTAATACTACAATAAAGGATGGTCTTGGGTGTCAATTCTTGAAAATGTGTATTTGAAGAAAAAGTAAATTTCGCCTACTGTTGTCAGATATTAGCAGTCCAGATATTCGCTCTAGCTTGTAAACTTCCCTGTGGTCAGCCTAAGCTCTTAACCCCCTATTCTACAGCTTTAGACTGAAGGCAAAAGCTCAAAGCATTTAAGGCCTCCTCAATTTCGGCCCCTGCTGCTCTGTGCTCTGTTCCTTGGTGTAGCTTTGTTCCAGCTCCTGCAGCATTGCACCATTCCTAACCACAACCTTA... |
Task1_train_45089 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TTTTAAGATCACTCTCTAGTGTGAAATCTCTATTTGATGGACACCTTCCTAAGTTACACTCATAAGGCCTCATTAGGATGTACAGTTGACCCTTGAACAACACATTTGAACTGTACAGATCCATTTATACTGGAATTTTTTTTTTCAACTGAACAGAGTTTGAAAGCACATTATTCAGGGATGGGAAACCTGCATAGATGTAGGGCTTTTCATATACACAGGTTCCACCAGGCTGACCGTGCAACTTGAGTATGGGTAGATTTTCGTATACATGGGTGGTCCTGGAACCAATCCCCCGAGTATACCAAAGGATAAGTGTA... | TTTTAAGATCACTCTCTAGTGTGAAATCTCTATTTGATGGACACCTTCCTAAGTTACACTCATAAGGCCTCATTAGGATGTACAGTTGACCCTTGAACAACACATTTGAACTGTACAGATCCATTTATACTGGAATTTTTTTTTTCAACTGAACAGAGTTTGAAAGCACATTATTCAGGGATGGGAAACCTGCATAGATGTAGGGCTTTTCATATACACAGGTTCCACCAGGCTGACCGTGCAACTTGAGTATGGGTAGATTTTCGTATACATGGGTGGTCCTGGAACCAATCCCCCGAGTATACCAAAGGATAAGTGTA... |
Task1_train_45090 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CTGAAGGCTTTTCCACATTCTTCACATTTATAGGGCCTCTCCCCAGTATGAATTCTCTGATGTAGGGTTAGCTGTGATAGAGTAATACAACCCTTTCCACATTCCTTACAGGTGTAGGGTTTTTCTCCAGTGTGTGTTCTCCAATGCACTGTAAGGTAAGAACCCCTCCTGAAGGCTTTTCCACAGACATCACACTTATAGGGCTTCTCTCCACTATGGATTTTCTGATGTTCTGTGACATGTACCATCTGGCTAAATGCTTTCCCACAGTCATTACATTTAAATGGTTTCTCTCCAGTATGTGTTCTTTGATGTGTATT... | CTGAAGGCTTTTCCACATTCTTCACATTTATAGGGCCTCTCCCCAGTATGAATTCTCTGATGTAGGGTTAGCTGTGATAGAGTAATACAACCCTTTCCACATTCCTTACAGGTGTAGGGTTTTTCTCCAGTGTGTGTTCTCCAATGCACTGTAAGGTAAGAACCCCTCCTGAAGGCTTTTCCACAGACATCACACTTATAGGGCTTCTCTCCACTATGGATTTTCTGATGTTCTGTGACATGTACCATCTGGCTAAATGCTTTCCCACAGTCATTACATTTAAATGGTTTCTCTCCAGTATGTGTTCTTTGATGTGTATT... |
Task1_train_45091 | A sequence alteration has been identified on Chromosome 17. Is it disease-inducing or harmless? | Benign | GGCTGGGCACGTTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTCGGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCTGGTCATGGTGGCGGATGCCTGTAATCTTAGCTACTTGGGAGGCTGAGGCAGAAGAATTGCTTGAACTCGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGTGCCATTGCACTCCAGCCTGGGCAACAAGAGTAAAACTATGTCTCAAAAAAAAATATATATATACAATATGTTCACATACTAA... | GGCTGGGCACGTTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTCGGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCTGGTCATGGTGGCGGATGCCTGTAATCTTAGCTACTTGGGAGGCTGAGGCAGAAGAATTGCTTGAACTCGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGTGCCATTGCACTCCAGCCTGGGCAACAAGAGTAAAACTATGTCTCAAAAAAAAATATATATATACAATATGTTCACATACTAA... |
Task1_train_45092 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTTCGAGGACCATCAGGCTTCCACTAACAGTCTCTTTAAAACTCTTCTTGTTTTTGTGCTTATTCTTCTGTAGGTCCTTTCAGCTTCTGATTAGCTCCTGGTCCAATGGTAATCCTACATGTTTTAGTAGTTTTTGTTGTGTTGTTGTTGTGCAATCTATATGTAGTGTCAATATCTGTATCAGTTATTTCTTGGTATATAACAAAATGCAGTGTCTCAAAACAACATCTATTTTGTTCACAATCTGCAGTTTTAGGCAAGGCTCAGTGGGGCCAACTCCCTTTTTCTTTACTTGGCATCAGCTGAGGTGACTTAAAGCT... | CTTCGAGGACCATCAGGCTTCCACTAACAGTCTCTTTAAAACTCTTCTTGTTTTTGTGCTTATTCTTCTGTAGGTCCTTTCAGCTTCTGATTAGCTCCTGGTCCAATGGTAATCCTACATGTTTTAGTAGTTTTTGTTGTGTTGTTGTTGTGCAATCTATATGTAGTGTCAATATCTGTATCAGTTATTTCTTGGTATATAACAAAATGCAGTGTCTCAAAACAACATCTATTTTGTTCACAATCTGCAGTTTTAGGCAAGGCTCAGTGGGGCCAACTCCCTTTTTCTTTACTTGGCATCAGCTGAGGTGACTTAAAGCT... |
Task1_train_45093 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CTGGGCTGCTCAGCGCTGCTGGGGAGAAGCCTGGGGTGACAAGGGTGACCAAGGGCCCTGCAGGCAGTGGGGCTGGCCCCACCACCCTGCCTACAGCCTCAGCTGGCTCTCAGGGCAGTCAGCCTTCAACCCTCAGCCTCCTCCCAGCCACTGCAAAAACCAGGACATGGGATGCCTGGCTGTCCTCCCCCTACTGTCCTGCCTGCCCCGACTCAGCCTCCCGTCCACCTTCTGTGGTGCTGACTGAGCCAGCAGGAAGCAGAGTCTCTGGAGGGCCACGTAGAGCTTGGGGACTGACTGAGTCACCCCCACTGAGGGGT... | CTGGGCTGCTCAGCGCTGCTGGGGAGAAGCCTGGGGTGACAAGGGTGACCAAGGGCCCTGCAGGCAGTGGGGCTGGCCCCACCACCCTGCCTACAGCCTCAGCTGGCTCTCAGGGCAGTCAGCCTTCAACCCTCAGCCTCCTCCCAGCCACTGCAAAAACCAGGACATGGGATGCCTGGCTGTCCTCCCCCTACTGTCCTGCCTGCCCCGACTCAGCCTCCCGTCCACCTTCTGTGGTGCTGACTGAGCCAGCAGGAAGCAGAGTCTCTGGAGGGCCACGTAGAGCTTGGGGACTGACTGAGTCACCCCCACTGAGGGGT... |
Task1_train_45094 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GGGATTTGTGTCCACCTTGTTGTAAGAAGGCAGCTGCTTGCGTGAGGCATGGCGGTGAGGAAACAATGCCACCCGGATCTCACCATTGGCCGTGTGGACTGGCTGTACCATGGGCCAGACGCATGTCTTGGGCAGACACTTTTTAGATGCCAACTTGCCTGTAGACAAAGATGACGCAGAGGTGGCCTCGAGGACGGCCTGTGTGATGGGTTGAATTTGTCCCCCGAAATTCCTGTGTTGATGTCCTAAGCCCCAGTGCTTGAGAATGTGATCTTATTTACAGATATCATCTTATAGAAATAAGTTAAAATGAAAAATGA... | GGGATTTGTGTCCACCTTGTTGTAAGAAGGCAGCTGCTTGCGTGAGGCATGGCGGTGAGGAAACAATGCCACCCGGATCTCACCATTGGCCGTGTGGACTGGCTGTACCATGGGCCAGACGCATGTCTTGGGCAGACACTTTTTAGATGCCAACTTGCCTGTAGACAAAGATGACGCAGAGGTGGCCTCGAGGACGGCCTGTGTGATGGGTTGAATTTGTCCCCCGAAATTCCTGTGTTGATGTCCTAAGCCCCAGTGCTTGAGAATGTGATCTTATTTACAGATATCATCTTATAGAAATAAGTTAAAATGAAAAATGA... |
Task1_train_45095 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | GAGCCTGAGAACGAGCTCTTCTAATAGGCAGATGTCACCTCGGCAGACAGCCCACTACTTCTCAATTCCACATCTCCCTTCCCGCCTGGAAACCCCGTGAGCCTGGGAGCTTAGGAGTCCTCTTCCTAGGGGGCCCGGCCAGCTAGCACCTGGCCTTCTATGGTGTGGAGGTTTTCCTATACGGAAATTGCTGAAGGGTGGCCTGCCCTGGCATTGTTTTGTGGCGCTGTTGGTGGTATTCATAGCTGACAGGAATTGCCATGTGCCAGGCCACTATTAGCTCATTTATATTTCCAGCAGTCTCAGAAGGCGGAGTTAAG... | GAGCCTGAGAACGAGCTCTTCTAATAGGCAGATGTCACCTCGGCAGACAGCCCACTACTTCTCAATTCCACATCTCCCTTCCCGCCTGGAAACCCCGTGAGCCTGGGAGCTTAGGAGTCCTCTTCCTAGGGGGCCCGGCCAGCTAGCACCTGGCCTTCTATGGTGTGGAGGTTTTCCTATACGGAAATTGCTGAAGGGTGGCCTGCCCTGGCATTGTTTTGTGGCGCTGTTGGTGGTATTCATAGCTGACAGGAATTGCCATGTGCCAGGCCACTATTAGCTCATTTATATTTCCAGCAGTCTCAGAAGGCGGAGTTAAG... |
Task1_train_45096 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | TGTAGCTGGCCCGGGTGCCCCCTATAGCTAGGCAGCCAGGACCTGTGACCCAACCTGAGCTGTGTGCTCCTGCACCTTCACAGACACCACTTTCTCCTCCTCCAGGAGCCTGGGCCTGCCAAGGTGGCTGTTACCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCATCCCCAGTGCTGAGAAAGTCCCCACCACCAAGTCCACACTCTGGCAGGAAGAAATGAGGACCAAGGACCAGCCAGATGGCAGCAGCCTGAGTCCAGCTCAGAGTCCCAGCCAGAGCCAGCCTCCTGCTGCCAGCTCCCTGCGGGAACCTGG... | TGTAGCTGGCCCGGGTGCCCCCTATAGCTAGGCAGCCAGGACCTGTGACCCAACCTGAGCTGTGTGCTCCTGCACCTTCACAGACACCACTTTCTCCTCCTCCAGGAGCCTGGGCCTGCCAAGGTGGCTGTTACCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCATCCCCAGTGCTGAGAAAGTCCCCACCACCAAGTCCACACTCTGGCAGGAAGAAATGAGGACCAAGGACCAGCCAGATGGCAGCAGCCTGAGTCCAGCTCAGAGTCCCAGCCAGAGCCAGCCTCCTGCTGCCAGCTCCCTGCGGGAACCTGG... |
Task1_train_45097 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | AGTCATCTAGGCAAGCCTATCTGAACCTGACCGGTTCTGGGCTTCGATGTGTCCGTTCCTCAGACTTCCAGAGTGTTTCTTGGATAGTGAGTCACCTCTGGCTGCTGAGTGGGGGAAGTTGTTTTCCTGGTTGGCCTGCTGGTGACTGGCAGCAAGGACAGCTCCCCATGTAGCCCTAACCCCCCTGCCCTCAGCACAGCGGTTAGTGCCCTGGGAACCCTGGAGCTGCAGGGTGCAGGCCCCGTTTTCTGTGCTGACCAGTAAGGTGCTTGCTGTCCCACCTGCAGCTTCCAGGGCACCAAGTAATAACTTTCCACCTC... | AGTCATCTAGGCAAGCCTATCTGAACCTGACCGGTTCTGGGCTTCGATGTGTCCGTTCCTCAGACTTCCAGAGTGTTTCTTGGATAGTGAGTCACCTCTGGCTGCTGAGTGGGGGAAGTTGTTTTCCTGGTTGGCCTGCTGGTGACTGGCAGCAAGGACAGCTCCCCATGTAGCCCTAACCCCCCTGCCCTCAGCACAGCGGTTAGTGCCCTGGGAACCCTGGAGCTGCAGGGTGCAGGCCCCGTTTTCTGTGCTGACCAGTAAGGTGCTTGCTGTCCCACCTGCAGCTTCCAGGGCACCAAGTAATAACTTTCCACCTC... |
Task1_train_45098 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ATCACCTGAGGTCAGGAGTTTGAGGCCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATCGGCCGGGTGCGGTGGCTCACACCTGTAACCCCGGCACTTTGGGAGGCCGAGGCGGGCAGATCACAAGGTCAGGAGTTGGAGATCAGCCTGGCTAACATAGTGAAACCCTGTCTCTACTAAAAATGCAAAAAAGCTGGGTGTGGTGGTGGGCGCCTGTAATCCCAGCCACTTGGGAGGCTGAGGCAGGGGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGATCCTGCCACTGCA... | ATCACCTGAGGTCAGGAGTTTGAGGCCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATCGGCCGGGTGCGGTGGCTCACACCTGTAACCCCGGCACTTTGGGAGGCCGAGGCGGGCAGATCACAAGGTCAGGAGTTGGAGATCAGCCTGGCTAACATAGTGAAACCCTGTCTCTACTAAAAATGCAAAAAAGCTGGGTGTGGTGGTGGGCGCCTGTAATCCCAGCCACTTGGGAGGCTGAGGCAGGGGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGATCCTGCCACTGCA... |
Task1_train_45099 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGAACCTGCCCAGGTCCAGGGGCGAGGGGGCTGGGGCTGGGGCTGGGGCAAGAGGAGTTCAGGGCTGGCAGCCCTGCCTCCACCATGTGCCCTGGGGGCCAAGGAAGTGGGACAAGAGGCCGTGTGATGAAAGGGTCAGGTTCACTCCTCGGAAGCCCTGTGGCTTCTGACAGCTCTGGCCTGGGGACTCCTGTGCTGGGGGGTGAGTCTCCTTGCACCCGCCTCCAGCCCTCCAAGGAGAGGGCCAGGCTTGCCTGGAAGGCTCAGGAATGCGGCCCGGGACCCCATCTTGGCGGTGTGAGCACGAAGATCCTGGATTG... | GGAACCTGCCCAGGTCCAGGGGCGAGGGGGCTGGGGCTGGGGCTGGGGCAAGAGGAGTTCAGGGCTGGCAGCCCTGCCTCCACCATGTGCCCTGGGGGCCAAGGAAGTGGGACAAGAGGCCGTGTGATGAAAGGGTCAGGTTCACTCCTCGGAAGCCCTGTGGCTTCTGACAGCTCTGGCCTGGGGACTCCTGTGCTGGGGGGTGAGTCTCCTTGCACCCGCCTCCAGCCCTCCAAGGAGAGGGCCAGGCTTGCCTGGAAGGCTCAGGAATGCGGCCCGGGACCCCATCTTGGCGGTGTGAGCACGAAGATCCTGGATTG... |
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