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_45100 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AGAGGCAGCATGGGTAGGAAAGAGGCCCATCTCCCGTCCCCTGATGCTCCCATAACCCAGCCTGGGTGGTGCCGGTGCCTGCCAGGTTCCTCTGGCCTAAATGGATGGAATCTTTTCTCCCTAAGCCACTGCTGAGCTGGAAGCTGCCTGTTCTCCAATGCTGGTCAGCGCTTCATGAGCTGTAAAACCTCGGGCAACCATTGCTTCTTTCCAAGCCTCACTTCCTCCATCTGCACAGTCAGAGTCTTCTCTACCCAGAGACTATAAATGTGAAAATGCTCCCTGGGGCCGGAGAGCCTAGAAGATTGTAAGCATGCAGG... | AGAGGCAGCATGGGTAGGAAAGAGGCCCATCTCCCGTCCCCTGATGCTCCCATAACCCAGCCTGGGTGGTGCCGGTGCCTGCCAGGTTCCTCTGGCCTAAATGGATGGAATCTTTTCTCCCTAAGCCACTGCTGAGCTGGAAGCTGCCTGTTCTCCAATGCTGGTCAGCGCTTCATGAGCTGTAAAACCTCGGGCAACCATTGCTTCTTTCCAAGCCTCACTTCCTCCATCTGCACAGTCAGAGTCTTCTCTACCCAGAGACTATAAATGTGAAAATGCTCCCTGGGGCCGGAGAGCCTAGAAGATTGTAAGCATGCAGG... |
Task1_train_45101 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TTGTGGGCCAGGGCAAGCTGACTCCAGAGAGCAGGAGAGGTGGTCCCAGGACTGGGCTGACGGGCTTCTGGGGGCCATCTGGCTGCCCTGGGCTTGCCCTGCTCTCAGGCAGATGGAGGCCCTCTGTCGCCTTCCCTGCATCCATCCCCAGACACTAAATGAGGAAGGCACTTGTGGTGGGGTCCGGGCCAAGGAAGAAGGGTAAATGGAGCAGCACCCCCAGCTCTCCCCCACTCCCCACCTTTCTGCCTCTTCCCTGTGCCCCTCCCCGACTCTGCGTGCCTCTCCCTCTCTGTGCCCCTCTCCCCCTCTCTTTGTCC... | TTGTGGGCCAGGGCAAGCTGACTCCAGAGAGCAGGAGAGGTGGTCCCAGGACTGGGCTGACGGGCTTCTGGGGGCCATCTGGCTGCCCTGGGCTTGCCCTGCTCTCAGGCAGATGGAGGCCCTCTGTCGCCTTCCCTGCATCCATCCCCAGACACTAAATGAGGAAGGCACTTGTGGTGGGGTCCGGGCCAAGGAAGAAGGGTAAATGGAGCAGCACCCCCAGCTCTCCCCCACTCCCCACCTTTCTGCCTCTTCCCTGTGCCCCTCCCCGACTCTGCGTGCCTCTCCCTCTCTGTGCCCCTCTCCCCCTCTCTTTGTCC... |
Task1_train_45102 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TCTCCCCCACTCCCCACCTTTCTGCCTCTTCCCTGTGCCCCTCCCCGACTCTGCGTGCCTCTCCCTCTCTGTGCCCCTCTCCCCCTCTCTTTGTCCCTTCCTGACCCCTTCAACAACCTGGAATCTTTGTAGCCTGAGGCAAGCCACCCCTTCCTTTTGGAGCATTTGGGAACCAGCACTGGAAAGTCCCCTATCCCCTCCTGGGGGCCTGGGCCACACAGGCCGAGCTGAGCCCCTTTCTTCCTGCCTCCGGGCCAGCATGGTTCTGGGTAAATCCCAAACCCTCTGGGACTCGGCCAATGGCCAGCCCCTCCATGCAC... | TCTCCCCCACTCCCCACCTTTCTGCCTCTTCCCTGTGCCCCTCCCCGACTCTGCGTGCCTCTCCCTCTCTGTGCCCCTCTCCCCCTCTCTTTGTCCCTTCCTGACCCCTTCAACAACCTGGAATCTTTGTAGCCTGAGGCAAGCCACCCCTTCCTTTTGGAGCATTTGGGAACCAGCACTGGAAAGTCCCCTATCCCCTCCTGGGGGCCTGGGCCACACAGGCCGAGCTGAGCCCCTTTCTTCCTGCCTCCGGGCCAGCATGGTTCTGGGTAAATCCCAAACCCTCTGGGACTCGGCCAATGGCCAGCCCCTCCATGCAC... |
Task1_train_45103 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCTGGGGCAGGCTGGACCCCGCCTTATCATCTCTGCTGAGGAAGCCACTGTGGAGAGACAGGTCGGGGAGGTCATGGTGTCAGCTTGGAGACAGTGGAAGGTGTTTGGCTCTTACAGTGAGTGAAGTGGGGACCCCGGGAGGGTCCTGAGCAGAAGTGGGACAGGATGGGACTTAGGATTTCACAGGACCCTGCTGGCTGCGTGAGGATAGACCGTGGAGGCCAGGGGCCGAGGCAAGGATCTAGTAAGATGGCCACTGCTGTACTCCAGTGAGTGATGACCACAGGCCTGGCCGAGGTGGTGGCCACAGGGGCAGATTT... | CCTGGGGCAGGCTGGACCCCGCCTTATCATCTCTGCTGAGGAAGCCACTGTGGAGAGACAGGTCGGGGAGGTCATGGTGTCAGCTTGGAGACAGTGGAAGGTGTTTGGCTCTTACAGTGAGTGAAGTGGGGACCCCGGGAGGGTCCTGAGCAGAAGTGGGACAGGATGGGACTTAGGATTTCACAGGACCCTGCTGGCTGCGTGAGGATAGACCGTGGAGGCCAGGGGCCGAGGCAAGGATCTAGTAAGATGGCCACTGCTGTACTCCAGTGAGTGATGACCACAGGCCTGGCCGAGGTGGTGGCCACAGGGGCAGATTT... |
Task1_train_45104 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GAGCCGGGTGTGGTGGCGGGTGCCTGTAATCCCAGCTACTCCAGAGGCTGAGACAGAAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTTCAGCCTGGGTGACAAGAGCAAAACTCCATCTAAAAAAAATAATAATAAATTAAAAAGAAAACATTTTTCCCCCACTCCTAAAATATGTGCTCTTGCCATAAGGGCAGGGACCCCACAGGCCTTGTTCCCCACTGTATCTTCATAATTTAGCACATGCCGGAGGCCTGCTAGGTGACTAATAGTGTTTGCTGCTAGGTGACTAA... | GAGCCGGGTGTGGTGGCGGGTGCCTGTAATCCCAGCTACTCCAGAGGCTGAGACAGAAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTTCAGCCTGGGTGACAAGAGCAAAACTCCATCTAAAAAAAATAATAATAAATTAAAAAGAAAACATTTTTCCCCCACTCCTAAAATATGTGCTCTTGCCATAAGGGCAGGGACCCCACAGGCCTTGTTCCCCACTGTATCTTCATAATTTAGCACATGCCGGAGGCCTGCTAGGTGACTAATAGTGTTTGCTGCTAGGTGACTAA... |
Task1_train_45105 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CCCCATCCTGGTAAACAACACCCACACACTTTCTACTACTGCTCTAGGGTGAAACCCAAGGCGCTCTAGAGGAGATGAATTATGGATCCGCCCTCCCGGAATCCTGGCTCGGCCCTCCCCACGCCACCCAGGGCCAGTCGGGTCTGCTCACAGCCCGAGGAGGCCGCGTGTCCAGCCGCGGGCAAGAGACAGAGCAGGTCCCTGTGTCTCCAAGTCCCTGAGCCCGTGACACCGGCCCCAGGCCCTGTAGAGAGCAGGCAGCCACCATGGCGAAGGAGGAAGATGAGGAGAAGAAAGCCAAGAAAGGGAAGAAGGGGAAG... | CCCCATCCTGGTAAACAACACCCACACACTTTCTACTACTGCTCTAGGGTGAAACCCAAGGCGCTCTAGAGGAGATGAATTATGGATCCGCCCTCCCGGAATCCTGGCTCGGCCCTCCCCACGCCACCCAGGGCCAGTCGGGTCTGCTCACAGCCCGAGGAGGCCGCGTGTCCAGCCGCGGGCAAGAGACAGAGCAGGTCCCTGTGTCTCCAAGTCCCTGAGCCCGTGACACCGGCCCCAGGCCCTGTAGAGAGCAGGCAGCCACCATGGCGAAGGAGGAAGATGAGGAGAAGAAAGCCAAGAAAGGGAAGAAGGGGAAG... |
Task1_train_45106 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGCTGTTCATGGGCTTCCGCGACCGTACACCCAAGATCTCCAAGAAGGGCCAGTTCCGCAGCGCCTCGGCCTTCTTCTGGGGCCTCCACACCGGCCCCCAGAAGACCAAGCGCAAGAGGAAGGCCCGCACCGTGCTCAAGTCCACGTCAAAGCTCATGACGCAGATGCGCATGGGCAAGAAGAAGCGGGCGATGAAGGGCAAGAAGCCGTCCTTCATGGTGATCCGCTTCCCAGGCCGCCGTGGCTACGGCCGCCTGCGGCCGCGCGCCCGGTCACTCAGCAAAGCGTCCACGGCCATCAACTGGCTCACAAAAAAGTTC... | GGCTGTTCATGGGCTTCCGCGACCGTACACCCAAGATCTCCAAGAAGGGCCAGTTCCGCAGCGCCTCGGCCTTCTTCTGGGGCCTCCACACCGGCCCCCAGAAGACCAAGCGCAAGAGGAAGGCCCGCACCGTGCTCAAGTCCACGTCAAAGCTCATGACGCAGATGCGCATGGGCAAGAAGAAGCGGGCGATGAAGGGCAAGAAGCCGTCCTTCATGGTGATCCGCTTCCCAGGCCGCCGTGGCTACGGCCGCCTGCGGCCGCGCGCCCGGTCACTCAGCAAAGCGTCCACGGCCATCAACTGGCTCACAAAAAAGTTC... |
Task1_train_45107 | 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 | GGAGCCACCACTGGGACCAGGCTTTTTGGACACCTGGCTGGGGGCAGTAACCCCATGGTCTAGCAGACACCTCGGGTAGGTCTCATAGCCCCAGACTAACTTTGGGCCCCCTACCAGGTACTGCTGTCTAGTGGCCCTCAAGCATGACCTGCCGGCTAATGGGGACATGTGTGTGTCAGTGCTGAGTCGCCTGTGCAAAGTCATGCCAAACATGTACCGTGTTGGGGTCAGCAAGGTGAGTCCTGCCCGACAGTCAGCCCTTGGAGACCCCAAGTTTGGGGGGGTCCACAACTACTGAGTCAGAAATGTCCAAGCTAGAG... | GGAGCCACCACTGGGACCAGGCTTTTTGGACACCTGGCTGGGGGCAGTAACCCCATGGTCTAGCAGACACCTCGGGTAGGTCTCATAGCCCCAGACTAACTTTGGGCCCCCTACCAGGTACTGCTGTCTAGTGGCCCTCAAGCATGACCTGCCGGCTAATGGGGACATGTGTGTGTCAGTGCTGAGTCGCCTGTGCAAAGTCATGCCAAACATGTACCGTGTTGGGGTCAGCAAGGTGAGTCCTGCCCGACAGTCAGCCCTTGGAGACCCCAAGTTTGGGGGGGTCCACAACTACTGAGTCAGAAATGTCCAAGCTAGAG... |
Task1_train_45108 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | AGACTCAGTGTCAACCCACCACAGTACTCCAATGCCCACAGGAAGGATGGCGGGAAAGTGTTCATGAAGCGGCCAGACCCTCATGAGGAGGCCCTGATGATCCTGAAAGGGCAGATGACCCACCTGGCAGCTGCACCTGGCACCCAGGTGAGGGGGGAAGGTGGGGCTGAGCCCAGGTGGAACAGAAGACAAAGAGGGGCCTCAGGGATCCTCAGAAACCAGCTACCCCTATAAGCTGTGGCCCTGCCACTGCCCCTCCACAGGGCCTGCCTGTTGCCCCCTGAGCAGTCTCTTTGGGGTGGGACAGGTGTCCAGAGAGG... | AGACTCAGTGTCAACCCACCACAGTACTCCAATGCCCACAGGAAGGATGGCGGGAAAGTGTTCATGAAGCGGCCAGACCCTCATGAGGAGGCCCTGATGATCCTGAAAGGGCAGATGACCCACCTGGCAGCTGCACCTGGCACCCAGGTGAGGGGGGAAGGTGGGGCTGAGCCCAGGTGGAACAGAAGACAAAGAGGGGCCTCAGGGATCCTCAGAAACCAGCTACCCCTATAAGCTGTGGCCCTGCCACTGCCCCTCCACAGGGCCTGCCTGTTGCCCCCTGAGCAGTCTCTTTGGGGTGGGACAGGTGTCCAGAGAGG... |
Task1_train_45109 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCTCCCAAATAGCTGGGATTACAGGTGCCTGCCAGCATGCCCGGCTAATTTTTGCGTTTTTAGTAGAGACGAGGTTTCACCATCTTGGCCAGGCTGGTCCTCAACTCCTGACCTTGTGATCTACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGAGCGAGCCACCGTGCCCAGAGGAGGTGGGTTTTCTTACCCATGGCTGAAGTTTGGCCTGAAGCTGTGGGAAAAGGCAGCCTGGACTCTTCTGCCCCCTGGCTTTCTTGTCCAGGCCTGGCCTTGCACCTCTGGCCTGCCTGATCCCATCCGGCAAGGCGCAG... | CCTCCCAAATAGCTGGGATTACAGGTGCCTGCCAGCATGCCCGGCTAATTTTTGCGTTTTTAGTAGAGACGAGGTTTCACCATCTTGGCCAGGCTGGTCCTCAACTCCTGACCTTGTGATCTACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGAGCGAGCCACCGTGCCCAGAGGAGGTGGGTTTTCTTACCCATGGCTGAAGTTTGGCCTGAAGCTGTGGGAAAAGGCAGCCTGGACTCTTCTGCCCCCTGGCTTTCTTGTCCAGGCCTGGCCTTGCACCTCTGGCCTGCCTGATCCCATCCGGCAAGGCGCAG... |
Task1_train_45110 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | TTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCATGCCATTCTCCTGCCTCAGCCTCCTGAGCAGCTGGGACTACAGGCGCCCGCCACCACACCCAGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCATGATCCACCCGCCTCGGCCTCCCTAAGTCCTGGGATTACAGGCGTGAGCCACCGCACCCGGCCAACAAGACCAGATTAAACCACTTAGAGGTGGCAGTA... | TTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCATGCCATTCTCCTGCCTCAGCCTCCTGAGCAGCTGGGACTACAGGCGCCCGCCACCACACCCAGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCATGATCCACCCGCCTCGGCCTCCCTAAGTCCTGGGATTACAGGCGTGAGCCACCGCACCCGGCCAACAAGACCAGATTAAACCACTTAGAGGTGGCAGTA... |
Task1_train_45111 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CCCCAGACTGGCTGGGGCCCCAAATTGTTGGTCTTCTCTGGACTTTGGGCTCTTCTGAAGAGGTTATCATAGAGGGCTGCTGTGCCCTCTGGGTAGGAACCTTCAGATGAGGCTGCTGCTGAGGACCTGGGCACCTGGCACAGGGAGAATCCGTCAGACTCTGTGGGCGGATGAGAGTCTGGAGGCCTTGCAGTCATGGGTTGGAGACCTTACCACTCACTTGTGAGCTGGCAGCCTGTAGCTCTGTAACATAGGGGTAGTGATGATGACACCCTGGTGATGTCAGAGGTCCTGGAGGGTGGGCTCCAGGGAGAGAGGCC... | CCCCAGACTGGCTGGGGCCCCAAATTGTTGGTCTTCTCTGGACTTTGGGCTCTTCTGAAGAGGTTATCATAGAGGGCTGCTGTGCCCTCTGGGTAGGAACCTTCAGATGAGGCTGCTGCTGAGGACCTGGGCACCTGGCACAGGGAGAATCCGTCAGACTCTGTGGGCGGATGAGAGTCTGGAGGCCTTGCAGTCATGGGTTGGAGACCTTACCACTCACTTGTGAGCTGGCAGCCTGTAGCTCTGTAACATAGGGGTAGTGATGATGACACCCTGGTGATGTCAGAGGTCCTGGAGGGTGGGCTCCAGGGAGAGAGGCC... |
Task1_train_45112 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGTCCTGGAGGGTGGGCTCCAGGGAGAGAGGCCCCTTCCTATACCTGCACAAGCCTCAGGGCCTTTGTGAGCTTCTTTCCAGGCAGCTTTGGGAGAAGGGGCTTGGCAGCTCCCTCATCTCCTCATGAGAGATGGGGGCTTGGGACCCCAAAACCCAAGCTCATATCCCATCCCTGCCCTTTCTCAGGTACTTTACGTGATTTCCCAGGGCCTCGGTGTCCTCCCCTGTGGATGGGTGGCCCCTTTCTCTGAGAAATTCTCAGAAAGCCCCCCTCATGGGCTCAGCTCTGTTACCCAGCATAAGGACAGCTAGAGCACCT... | GGTCCTGGAGGGTGGGCTCCAGGGAGAGAGGCCCCTTCCTATACCTGCACAAGCCTCAGGGCCTTTGTGAGCTTCTTTCCAGGCAGCTTTGGGAGAAGGGGCTTGGCAGCTCCCTCATCTCCTCATGAGAGATGGGGGCTTGGGACCCCAAAACCCAAGCTCATATCCCATCCCTGCCCTTTCTCAGGTACTTTACGTGATTTCCCAGGGCCTCGGTGTCCTCCCCTGTGGATGGGTGGCCCCTTTCTCTGAGAAATTCTCAGAAAGCCCCCCTCATGGGCTCAGCTCTGTTACCCAGCATAAGGACAGCTAGAGCACCT... |
Task1_train_45113 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | GTCCCTGGTGCTTAGTCCAAGCTCTCACTCTTGTGGGCCTCACACTTTGTACCTCAGTCTCTGCCTTCCGGGCTCAAGTGATCCTCCCACCTCAGCCTCCCTACCTATAGGCATGCACCTAATTTTTTGTAGAAATGTTTTTTTTGAGATGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGCTGCGATCCTGGCTCACTGCATCCTCCACCTCCCGGGTTCATGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCACCACGCCTAGCTAATTTTTGTATTTTTTTAGTAGTGATGG... | GTCCCTGGTGCTTAGTCCAAGCTCTCACTCTTGTGGGCCTCACACTTTGTACCTCAGTCTCTGCCTTCCGGGCTCAAGTGATCCTCCCACCTCAGCCTCCCTACCTATAGGCATGCACCTAATTTTTTGTAGAAATGTTTTTTTTGAGATGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGCTGCGATCCTGGCTCACTGCATCCTCCACCTCCCGGGTTCATGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCACCACGCCTAGCTAATTTTTGTATTTTTTTAGTAGTGATGG... |
Task1_train_45114 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | CGGCGTCCCGTAGCCTCGCGTTAAGCCTTGTTCAGAGCGGGGGCTTTTGCTGTCGCAGTGGGTTCCGGAGAGTGCAGGTGATTTCGCAGCAGGTTTCTTGTGCTGGCCGCGCTCGCCGGACGAAGAAGAGAAGGGCAGTTGGGCCTGCGGCCTTGGCGTTCATGAGGCCTCAGAGAGCTCCGGAGGAGCTACAACTGTGAGGGGGCTGCTAGAGTTCTTCTCCTCGGGTGTGTGAGAAGCAGCCTAGGACCCCGGGTTCGGGGAGTCGCAAAGAAGGCCGTAAGGGCTTCACTTCCTTCTCCGGAGGCCTGCCTTCTGCG... | CGGCGTCCCGTAGCCTCGCGTTAAGCCTTGTTCAGAGCGGGGGCTTTTGCTGTCGCAGTGGGTTCCGGAGAGTGCAGGTGATTTCGCAGCAGGTTTCTTGTGCTGGCCGCGCTCGCCGGACGAAGAAGAGAAGGGCAGTTGGGCCTGCGGCCTTGGCGTTCATGAGGCCTCAGAGAGCTCCGGAGGAGCTACAACTGTGAGGGGGCTGCTAGAGTTCTTCTCCTCGGGTGTGTGAGAAGCAGCCTAGGACCCCGGGTTCGGGGAGTCGCAAAGAAGGCCGTAAGGGCTTCACTTCCTTCTCCGGAGGCCTGCCTTCTGCG... |
Task1_train_45115 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | AGCCTAGGACCCCGGGTTCGGGGAGTCGCAAAGAAGGCCGTAAGGGCTTCACTTCCTTCTCCGGAGGCCTGCCTTCTGCGCGTCGATTAACACCGCATTCTTTCCCACTTCCTCTCAATGTTTTCTTCATATATCTGGAAATATGATCAGCGCCCCTGACGTAGTGGCCTTCACCAAAGAGGAAGAGTATGAAGAAGAGCCTTACAATGAGCCGGCCCTGCCTGAGGAGTACTCGGTGCCGCTCTTCCCCTTCGCCAGTCAGGGTGCTAACCCCTGGTCAAAACTGTCCGGGGCCAAGTTTTCGAGGGACTTCATTCTTA... | AGCCTAGGACCCCGGGTTCGGGGAGTCGCAAAGAAGGCCGTAAGGGCTTCACTTCCTTCTCCGGAGGCCTGCCTTCTGCGCGTCGATTAACACCGCATTCTTTCCCACTTCCTCTCAATGTTTTCTTCATATATCTGGAAATATGATCAGCGCCCCTGACGTAGTGGCCTTCACCAAAGAGGAAGAGTATGAAGAAGAGCCTTACAATGAGCCGGCCCTGCCTGAGGAGTACTCGGTGCCGCTCTTCCCCTTCGCCAGTCAGGGTGCTAACCCCTGGTCAAAACTGTCCGGGGCCAAGTTTTCGAGGGACTTCATTCTTA... |
Task1_train_45116 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTGCTCACTGAATGTCTTGCATGTGCTGACTGCTGCCCGCAGTGCTGAACATGCCCCACCGCCCAGGCCCAGCACTGCTTGTTGGGTCAGCATCTAGTGCTGCTGTCACATCTTTGTCTGCACAGCCAGTAGGATTGCCTCAGCCAGGGGGTTTATCAGAAGGTGTGCAAGGCCTTTGGGGGAACTGAGCCCCTATAGTGGGCAGTCTCCTTTACCTTCCCACCTCCCTGAAAAGCACAGAAGACAGTGCCTTGGTTTGTGTTTTGAAGCAAACAAGTCAGCTTTCTGGCTTTGCCCCAAAACTGTGATGGAACATAATA... | CTGCTCACTGAATGTCTTGCATGTGCTGACTGCTGCCCGCAGTGCTGAACATGCCCCACCGCCCAGGCCCAGCACTGCTTGTTGGGTCAGCATCTAGTGCTGCTGTCACATCTTTGTCTGCACAGCCAGTAGGATTGCCTCAGCCAGGGGGTTTATCAGAAGGTGTGCAAGGCCTTTGGGGGAACTGAGCCCCTATAGTGGGCAGTCTCCTTTACCTTCCCACCTCCCTGAAAAGCACAGAAGACAGTGCCTTGGTTTGTGTTTTGAAGCAAACAAGTCAGCTTTCTGGCTTTGCCCCAAAACTGTGATGGAACATAATA... |
Task1_train_45117 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AAATCCCATCTCTATAAAAAATATACAAAAATTATCTGGATGTAGTGGTGCATGCCTGTAGTCAGAGCTACTTGGGAGGCTGAGGTGAGAGGATCACTTGAGCCCGGGAAGTCGAGGCTGCAGTGAGCCGTGATCACTCAACTGCACTCTAGCCTGGGTGACAGAGCAAGACCCTGTCTGTTAAAACAAAACAGAATAGAGCTGGGGCTTCCTTTTCCAGTGGGTGTGGTGCAGGGGGCACTGGGCCTCCCTTGGACCACCCGGTTCTCTGGGGCCCAGCCTCAGCTCTCTGTGGATGGATTGGGTGGCGCTCTTCCCAC... | AAATCCCATCTCTATAAAAAATATACAAAAATTATCTGGATGTAGTGGTGCATGCCTGTAGTCAGAGCTACTTGGGAGGCTGAGGTGAGAGGATCACTTGAGCCCGGGAAGTCGAGGCTGCAGTGAGCCGTGATCACTCAACTGCACTCTAGCCTGGGTGACAGAGCAAGACCCTGTCTGTTAAAACAAAACAGAATAGAGCTGGGGCTTCCTTTTCCAGTGGGTGTGGTGCAGGGGGCACTGGGCCTCCCTTGGACCACCCGGTTCTCTGGGGCCCAGCCTCAGCTCTCTGTGGATGGATTGGGTGGCGCTCTTCCCAC... |
Task1_train_45118 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | ATAAAACAGATAACAAAAGAATCTGGGACCATTACATGCTAAAGTCTGTTACAACTAAATAAAAAAATTAAAAAATTAAAAATGCACTTTCATTATGTCAAAAGCAGGTGGAAAAAATAAACAATTATTTAAGAGTGTTTGTGTCCAAGCACATAGTATAAAATCTCTACACATCATTAAATCTTTGTAATAAAGTAGTTTTATGCCCATCTGTCATAAATAAATGAATAAATTATAAACAATTGAAGCTTAGGGAAAATTATCAGCATTCCAGTTTATAATTAGTAGGTCTAGAATTAGGAAAATAATCCTAAATATGG... | ATAAAACAGATAACAAAAGAATCTGGGACCATTACATGCTAAAGTCTGTTACAACTAAATAAAAAAATTAAAAAATTAAAAATGCACTTTCATTATGTCAAAAGCAGGTGGAAAAAATAAACAATTATTTAAGAGTGTTTGTGTCCAAGCACATAGTATAAAATCTCTACACATCATTAAATCTTTGTAATAAAGTAGTTTTATGCCCATCTGTCATAAATAAATGAATAAATTATAAACAATTGAAGCTTAGGGAAAATTATCAGCATTCCAGTTTATAATTAGTAGGTCTAGAATTAGGAAAATAATCCTAAATATGG... |
Task1_train_45119 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | CCACATCACCCACCAGAGTCCAGGGAGCCTGGCCTGAGAGCTGCCCAGTGCCCTGAGGATGCACCTGGAGCCCATCCCATCTGACACTCCCCATGGGCCTTGCAAGGTCTGACCTCCCAGCGTGCACCTGCCTCTCCCTGCATCCTGGCCGCTCACCCTGCCTGCTCCCCATCTTCCCCCATCCTGCCCAGCCCAGACACTATGACCCTCTCTCCGGCCACTCTGGCCCTTCTGTGACCCTTGTCCTTTCAGAACCTCTGAGTGAGACCTCCCAGATCCGTCCACACCCACGCCTTGGCCACTCTCTGACTGGGCTGCCC... | CCACATCACCCACCAGAGTCCAGGGAGCCTGGCCTGAGAGCTGCCCAGTGCCCTGAGGATGCACCTGGAGCCCATCCCATCTGACACTCCCCATGGGCCTTGCAAGGTCTGACCTCCCAGCGTGCACCTGCCTCTCCCTGCATCCTGGCCGCTCACCCTGCCTGCTCCCCATCTTCCCCCATCCTGCCCAGCCCAGACACTATGACCCTCTCTCCGGCCACTCTGGCCCTTCTGTGACCCTTGTCCTTTCAGAACCTCTGAGTGAGACCTCCCAGATCCGTCCACACCCACGCCTTGGCCACTCTCTGACTGGGCTGCCC... |
Task1_train_45120 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | CAGACACTATGACCCTCTCTCCGGCCACTCTGGCCCTTCTGTGACCCTTGTCCTTTCAGAACCTCTGAGTGAGACCTCCCAGATCCGTCCACACCCACGCCTTGGCCACTCTCTGACTGGGCTGCCCAGCACTGCTGGGGAGACACTCAGGGCAGCAAGGATGACCAAGGGCCCTGCAGGCAGTGGGGCTGGCCCCAGCACTCCTGCTCCAGCCTCAGCTGGCTCTCAGGGTCATTGGCCTTCAGCCCTCAGCCTCCTCCCAGCCACTGCAAAAACCAGGACATGGGATGCTTGGCTGTCCTCCCCTACTGTCCTGCCTG... | CAGACACTATGACCCTCTCTCCGGCCACTCTGGCCCTTCTGTGACCCTTGTCCTTTCAGAACCTCTGAGTGAGACCTCCCAGATCCGTCCACACCCACGCCTTGGCCACTCTCTGACTGGGCTGCCCAGCACTGCTGGGGAGACACTCAGGGCAGCAAGGATGACCAAGGGCCCTGCAGGCAGTGGGGCTGGCCCCAGCACTCCTGCTCCAGCCTCAGCTGGCTCTCAGGGTCATTGGCCTTCAGCCCTCAGCCTCCTCCCAGCCACTGCAAAAACCAGGACATGGGATGCTTGGCTGTCCTCCCCTACTGTCCTGCCTG... |
Task1_train_45121 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATTGTCTTTCTGTTTTTAAATTTGCTAGGGGAAGGACGGTTAACATTTTAACAGAAAAATACCGCAAGTTAATGCATGTGAAAAACTCAGAAAGTCAAAGGAAAACAAACACAAGAACAACACTTAAAACATCCCATAAACCATCGCAATATTAAAACACCACAGAATGGCCGAAGAGGGCTCACGGTGTGCTCTGAACGAGGGTGGGTGGTGCTGAGGGGTGCTGTCCTCCACTGGCAGGCGGCTCACCACCCTGTACAAAGAAGATTTTGCATACTTTTTAGAGTTCTATTCCAAGGGTAAGTGCTTCACCCAGGGTA... | ATTGTCTTTCTGTTTTTAAATTTGCTAGGGGAAGGACGGTTAACATTTTAACAGAAAAATACCGCAAGTTAATGCATGTGAAAAACTCAGAAAGTCAAAGGAAAACAAACACAAGAACAACACTTAAAACATCCCATAAACCATCGCAATATTAAAACACCACAGAATGGCCGAAGAGGGCTCACGGTGTGCTCTGAACGAGGGTGGGTGGTGCTGAGGGGTGCTGTCCTCCACTGGCAGGCGGCTCACCACCCTGTACAAAGAAGATTTTGCATACTTTTTAGAGTTCTATTCCAAGGGTAAGTGCTTCACCCAGGGTA... |
Task1_train_45122 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTGTCCACTTGCTGAGAGCAGATTTGGCAAAGGGTTTTCTCTGTAGGTCTTGTGTCAGTTTGAGGGTCTGCTTTGCCCACTTCCCCTTCCTCAGTGATCCTTCAGCCTGGCACCCAGCTCTGAGATGAGGCCTGCTTAGCACCAGTGAAGTTCCCCACGTTCAAACCAACAACATTCTGTGTGGAGATGAGGGAATCAAAGTTAAAATCCAACCCATCAGCATCCATGAGTTCACTACGGATAATGGACTCCATGTCACATTCCAAGCTCCCATTGAACATGTCCAGGTCCAAGTCGCTGGGGAACTTCTCATGGCCCAT... | CTGTCCACTTGCTGAGAGCAGATTTGGCAAAGGGTTTTCTCTGTAGGTCTTGTGTCAGTTTGAGGGTCTGCTTTGCCCACTTCCCCTTCCTCAGTGATCCTTCAGCCTGGCACCCAGCTCTGAGATGAGGCCTGCTTAGCACCAGTGAAGTTCCCCACGTTCAAACCAACAACATTCTGTGTGGAGATGAGGGAATCAAAGTTAAAATCCAACCCATCAGCATCCATGAGTTCACTACGGATAATGGACTCCATGTCACATTCCAAGCTCCCATTGAACATGTCCAGGTCCAAGTCGCTGGGGAACTTCTCATGGCCCAT... |
Task1_train_45123 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | CTACTATGCCTGGCCACTTTGAATCTGTGTAGCTCAGGTAGTACTGACGCCATCTCTGACTCACGGGTGGGATGTTTGTGCGTGCACGTGAATGTGTGTGTGTGTAGGTATATTCTATAAAGAATTACACTTAAATTTGGCCAATATCTCATCCAGGAATGGGCCTAATACCCCATTAGAGTCAATCCCAGCACTTCTGCAAGAATGACTAGAAGAGAATCTGCCCTTTTTCTCTGGCCTTCAACACAGGAAGATGTAAGCCTAAACTCGTTAGAGGCCAACACTAGGAGAAAAACTTGTTTGGCCATAAAACCCATGGA... | CTACTATGCCTGGCCACTTTGAATCTGTGTAGCTCAGGTAGTACTGACGCCATCTCTGACTCACGGGTGGGATGTTTGTGCGTGCACGTGAATGTGTGTGTGTGTAGGTATATTCTATAAAGAATTACACTTAAATTTGGCCAATATCTCATCCAGGAATGGGCCTAATACCCCATTAGAGTCAATCCCAGCACTTCTGCAAGAATGACTAGAAGAGAATCTGCCCTTTTTCTCTGGCCTTCAACACAGGAAGATGTAAGCCTAAACTCGTTAGAGGCCAACACTAGGAGAAAAACTTGTTTGGCCATAAAACCCATGGA... |
Task1_train_45124 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | GTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCAGGAAGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAACTTGCAGTGAGCCTAGATGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAACGAGACTCTGTCTCAAAAAAAAAGAAAAAAAGAAAATATACAAAGTTCCAGAAAAAGAATTTAAAATAATAATCTTAAGGAAACAGTGGAATTCAAGAGCATACAGTTACACAATTCAATGAAATCAAGAAAATTCATAATTTGAATGAGAAATTTAACAGAGATATAAAAAAGAACCACACAGAAAACTTG... | GTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCAGGAAGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAACTTGCAGTGAGCCTAGATGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAACGAGACTCTGTCTCAAAAAAAAAGAAAAAAAGAAAATATACAAAGTTCCAGAAAAAGAATTTAAAATAATAATCTTAAGGAAACAGTGGAATTCAAGAGCATACAGTTACACAATTCAATGAAATCAAGAAAATTCATAATTTGAATGAGAAATTTAACAGAGATATAAAAAAGAACCACACAGAAAACTTG... |
Task1_train_45125 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GTCCAGCTACCTAACCTCAAGGAAGCCAACAGGCGATGGAAAAGTTGGCATAAAAATGAGAATGTAGGCTGGACGTAATCCCACCTGTAATAACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGACGGCAGATTGCTTGAGGCCAGGAGTTTGAGACCAGCCTGGGCAACGTAGTAAGCTCCTATCTCTACAAAAAATATAAAAATTAGTTGGGCATGAAGGCATGCACCTGTGGTTTCTGCTACTTCGGAGGCTGAGGTGGAAGATCGTTTGAGCCTGGGATGTCAAAGCTGCAGTGAGCCAAGATTGTGTCACTCC... | GTCCAGCTACCTAACCTCAAGGAAGCCAACAGGCGATGGAAAAGTTGGCATAAAAATGAGAATGTAGGCTGGACGTAATCCCACCTGTAATAACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGACGGCAGATTGCTTGAGGCCAGGAGTTTGAGACCAGCCTGGGCAACGTAGTAAGCTCCTATCTCTACAAAAAATATAAAAATTAGTTGGGCATGAAGGCATGCACCTGTGGTTTCTGCTACTTCGGAGGCTGAGGTGGAAGATCGTTTGAGCCTGGGATGTCAAAGCTGCAGTGAGCCAAGATTGTGTCACTCC... |
Task1_train_45126 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ATAAACAACTCGAGAAATTTTACAATGGGGGCGTGCTGAAAAGCTAACAGGAAGCTTTCTGAGATTTTTGCATAGAAGTTTGGAGGCCCCAAATAAAAACAGACATAACTGCTCTGGTCCATTCTGTACATCTTTAAAAGAAGGAAGAAAAAATGAAAAAGTTTCTCTCCACCTCATTTTCCTCAACACACCCGCTTCAAGAGCAACCTTGTCTTGGTCTTCTGTGTTTCAGGGCTCAATCAAGACATCACAGATGTGTGTTTTTCCCCTGAGAAAGACCACAGCTCCAAGTCTGCGACCTCACAAGTCTATTGGACAGC... | ATAAACAACTCGAGAAATTTTACAATGGGGGCGTGCTGAAAAGCTAACAGGAAGCTTTCTGAGATTTTTGCATAGAAGTTTGGAGGCCCCAAATAAAAACAGACATAACTGCTCTGGTCCATTCTGTACATCTTTAAAAGAAGGAAGAAAAAATGAAAAAGTTTCTCTCCACCTCATTTTCCTCAACACACCCGCTTCAAGAGCAACCTTGTCTTGGTCTTCTGTGTTTCAGGGCTCAATCAAGACATCACAGATGTGTGTTTTTCCCCTGAGAAAGACCACAGCTCCAAGTCTGCGACCTCACAAGTCTATTGGACAGC... |
Task1_train_45127 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CCATTCTGTACATCTTTAAAAGAAGGAAGAAAAAATGAAAAAGTTTCTCTCCACCTCATTTTCCTCAACACACCCGCTTCAAGAGCAACCTTGTCTTGGTCTTCTGTGTTTCAGGGCTCAATCAAGACATCACAGATGTGTGTTTTTCCCCTGAGAAAGACCACAGCTCCAAGTCTGCGACCTCACAAGTCTATTGGACAGCCAAAACTCAGCACACATCCCTTCCTTTGTCCAAAGCCCCAGAAAATGAACACTTGCTTGGGGCAGCATCTAACCCTGGTAAGTGAACTTTCAGCAAGAAAGCCAATATGGGCTAGGTG... | CCATTCTGTACATCTTTAAAAGAAGGAAGAAAAAATGAAAAAGTTTCTCTCCACCTCATTTTCCTCAACACACCCGCTTCAAGAGCAACCTTGTCTTGGTCTTCTGTGTTTCAGGGCTCAATCAAGACATCACAGATGTGTGTTTTTCCCCTGAGAAAGACCACAGCTCCAAGTCTGCGACCTCACAAGTCTATTGGACAGCCAAAACTCAGCACACATCCCTTCCTTTGTCCAAAGCCCCAGAAAATGAACACTTGCTTGGGGCAGCATCTAACCCTGGTAAGTGAACTTTCAGCAAGAAAGCCAATATGGGCTAGGTG... |
Task1_train_45128 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TGATGGGCTTGATGAGTCTTTGCTTCTGTGATGGGGAGCAGAACTCCACTGTAACCTTTCCTTTTCCCCCTTTTTCCCCACTCCCATGTCTTCCTCTCTCTCCCTCCTGTTCAGTATGGGATGTAGACACAGGGAAGTGCCTGAAGACGTTTAGACACAAAGACCCCATCTTGGCCACCAGGATCAATGATACCTACATTGTGAGCAGCTGTGAGCGAGGGCTGGTGAAAGTGTGGCACATTGCCATGGCCCAGTTGGTAAAGGTAAGTGGGCAGTGGGCTACCTTGGCGGAAAGGGCACTGGGGAGGAGATGGGTGGGC... | TGATGGGCTTGATGAGTCTTTGCTTCTGTGATGGGGAGCAGAACTCCACTGTAACCTTTCCTTTTCCCCCTTTTTCCCCACTCCCATGTCTTCCTCTCTCTCCCTCCTGTTCAGTATGGGATGTAGACACAGGGAAGTGCCTGAAGACGTTTAGACACAAAGACCCCATCTTGGCCACCAGGATCAATGATACCTACATTGTGAGCAGCTGTGAGCGAGGGCTGGTGAAAGTGTGGCACATTGCCATGGCCCAGTTGGTAAAGGTAAGTGGGCAGTGGGCTACCTTGGCGGAAAGGGCACTGGGGAGGAGATGGGTGGGC... |
Task1_train_45129 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | TACCTGTACAGGTATACCTGAAGGGTAAAGTCCTACGAGTGAAATTGCTAAGCCAAAGGATAAGTGCATTCAAAAACTAGAAAGATATTGCCAAGGTTGTCCTGAAAAATACTGTATCAATTTACACTCCTACTTGCAATATATGAGAGACCCCACTGCATTTGTGCCAACTCTGGGTGTTAGCTGGCATTTTGTAGTTGCTTGTATAAGTAAAAATGGGGTCCGCATTTTCTTCTAGGTTGACCATTAACAAACTAAATGTCCATCAATGGGCAATGGCTAAGTAATAAAAAAATCTATTGTATGGAATATTATATACA... | TACCTGTACAGGTATACCTGAAGGGTAAAGTCCTACGAGTGAAATTGCTAAGCCAAAGGATAAGTGCATTCAAAAACTAGAAAGATATTGCCAAGGTTGTCCTGAAAAATACTGTATCAATTTACACTCCTACTTGCAATATATGAGAGACCCCACTGCATTTGTGCCAACTCTGGGTGTTAGCTGGCATTTTGTAGTTGCTTGTATAAGTAAAAATGGGGTCCGCATTTTCTTCTAGGTTGACCATTAACAAACTAAATGTCCATCAATGGGCAATGGCTAAGTAATAAAAAAATCTATTGTATGGAATATTATATACA... |
Task1_train_45130 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTTGGATAAGAAGAGGAGGAGTTGTGAGAAGGGGTCATGGAACTAAGGATGCAGTCAGATGATTTTGTGAAGGAGCCAGAAACCTTGAGATTATCCCCAGTAGCCTCGGCTTGCTCTGTGACTTGGGAGAGAACAGGTGAGGAGGACAGGTGTTAAGTTGTAGTAGCCTCATCTGCACCCTAGAGTTTTCTCAGATGGTGCAGCCTAGGGGCAGGGATGGAGGAGCTGAGACTTCGATTATTCTCTGGGTTTTTTGCCAGATGATTTGAGGAGGCGGGTGGAGGATCTGCATGTGTCCTTTTCCTAGGTTTTGAATTCCT... | CTTGGATAAGAAGAGGAGGAGTTGTGAGAAGGGGTCATGGAACTAAGGATGCAGTCAGATGATTTTGTGAAGGAGCCAGAAACCTTGAGATTATCCCCAGTAGCCTCGGCTTGCTCTGTGACTTGGGAGAGAACAGGTGAGGAGGACAGGTGTTAAGTTGTAGTAGCCTCATCTGCACCCTAGAGTTTTCTCAGATGGTGCAGCCTAGGGGCAGGGATGGAGGAGCTGAGACTTCGATTATTCTCTGGGTTTTTTGCCAGATGATTTGAGGAGGCGGGTGGAGGATCTGCATGTGTCCTTTTCCTAGGTTTTGAATTCCT... |
Task1_train_45131 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | TATTTGGGAAGGGAGTGGTTTAGGGAAGACTCGAAAGTGACAATGGAGCTATCAAGTTCAAGAAGGAGTTAGTAGGGGAGGAGGCTGCAGGAAGAAGTGCACGCCTGGAGGCAGGAACAGCATGTGTCCCGGTAGTTCAGGGTGGCGGGCCCAGGCGGGTGAGAAAGGGCAATGGAGAAGGAAGGAGAGGAGACCGTGCAGACACTGCAAGTGCCAGAAACCCGATCCACACTGGCTTCAGAGGGTGGAGGGGAGGTTCTTCTTGGCTTCCATAATAGAAATGTCCAGGGACCTACCGACTTCAGATTCAGCGCAAACTC... | TATTTGGGAAGGGAGTGGTTTAGGGAAGACTCGAAAGTGACAATGGAGCTATCAAGTTCAAGAAGGAGTTAGTAGGGGAGGAGGCTGCAGGAAGAAGTGCACGCCTGGAGGCAGGAACAGCATGTGTCCCGGTAGTTCAGGGTGGCGGGCCCAGGCGGGTGAGAAAGGGCAATGGAGAAGGAAGGAGAGGAGACCGTGCAGACACTGCAAGTGCCAGAAACCCGATCCACACTGGCTTCAGAGGGTGGAGGGGAGGTTCTTCTTGGCTTCCATAATAGAAATGTCCAGGGACCTACCGACTTCAGATTCAGCGCAAACTC... |
Task1_train_45132 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GAAGACTCGAAAGTGACAATGGAGCTATCAAGTTCAAGAAGGAGTTAGTAGGGGAGGAGGCTGCAGGAAGAAGTGCACGCCTGGAGGCAGGAACAGCATGTGTCCCGGTAGTTCAGGGTGGCGGGCCCAGGCGGGTGAGAAAGGGCAATGGAGAAGGAAGGAGAGGAGACCGTGCAGACACTGCAAGTGCCAGAAACCCGATCCACACTGGCTTCAGAGGGTGGAGGGGAGGTTCTTCTTGGCTTCCATAATAGAAATGTCCAGGGACCTACCGACTTCAGATTCAGCGCAAACTCATCTGGGCCCGGTCTGTATCCCTC... | GAAGACTCGAAAGTGACAATGGAGCTATCAAGTTCAAGAAGGAGTTAGTAGGGGAGGAGGCTGCAGGAAGAAGTGCACGCCTGGAGGCAGGAACAGCATGTGTCCCGGTAGTTCAGGGTGGCGGGCCCAGGCGGGTGAGAAAGGGCAATGGAGAAGGAAGGAGAGGAGACCGTGCAGACACTGCAAGTGCCAGAAACCCGATCCACACTGGCTTCAGAGGGTGGAGGGGAGGTTCTTCTTGGCTTCCATAATAGAAATGTCCAGGGACCTACCGACTTCAGATTCAGCGCAAACTCATCTGGGCCCGGTCTGTATCCCTC... |
Task1_train_45133 | 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 | GGCTCACACCTGTAATCCCAGCACTTTGTGGGGGTCAAGGTGGGTGGATCACTTGAGACCAGAAGTTTGAGACCAACCTGGGCAACATGGCAAAACCCCATCTTTACCAAAGATAAAGAAATTAGCCAGGGTTGGTGGCACACAGCTGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGAAGATCACTTGAGTCCGGGAGGTGGAGGTTGCAGTGAGCTGGGATCACGCCGCTGCACTCCAGCCCGGGCAACAGAGCAAGACCTTGTCTCAAAAAAAAAAAAAAAAGAAAAGGAAAAGAAAATTAACTTAACAATTAAGG... | GGCTCACACCTGTAATCCCAGCACTTTGTGGGGGTCAAGGTGGGTGGATCACTTGAGACCAGAAGTTTGAGACCAACCTGGGCAACATGGCAAAACCCCATCTTTACCAAAGATAAAGAAATTAGCCAGGGTTGGTGGCACACAGCTGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGAAGATCACTTGAGTCCGGGAGGTGGAGGTTGCAGTGAGCTGGGATCACGCCGCTGCACTCCAGCCCGGGCAACAGAGCAAGACCTTGTCTCAAAAAAAAAAAAAAAAGAAAAGGAAAAGAAAATTAACTTAACAATTAAGG... |
Task1_train_45134 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | AGGAAGCTCCAGGTGGCTCATGGGACTGTACGGAGTGGCTGGGTCACAGCTGTAGCCAGAGACTCAGGGAGGAACCTGGGGTCAGCAGGTGAAGTCCTGGCCCTGGGAGCCCCTATCTGGCCCATCGCTGGGCGGGGGATCTGTCTGTCTGCAGACCCTCTGGCTGTTCCCATCTGCCTCCTTCCTGTCGCTGACAAGGAGGGGAGGCACAGAGGAGTGGGAACCTTGGCACAGCAGGTCCCCCTACCCATGGCCTCAGTTTCCCTATTTTCAAGATGGAAGTGGAGGCTGGGTAATGGGATCCCAGCAGGCTCTCTGTG... | AGGAAGCTCCAGGTGGCTCATGGGACTGTACGGAGTGGCTGGGTCACAGCTGTAGCCAGAGACTCAGGGAGGAACCTGGGGTCAGCAGGTGAAGTCCTGGCCCTGGGAGCCCCTATCTGGCCCATCGCTGGGCGGGGGATCTGTCTGTCTGCAGACCCTCTGGCTGTTCCCATCTGCCTCCTTCCTGTCGCTGACAAGGAGGGGAGGCACAGAGGAGTGGGAACCTTGGCACAGCAGGTCCCCCTACCCATGGCCTCAGTTTCCCTATTTTCAAGATGGAAGTGGAGGCTGGGTAATGGGATCCCAGCAGGCTCTCTGTG... |
Task1_train_45135 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CACCCTGATGGTGGCATGGGAGGGAGTGGCATTCCAGGCAGAAGGAGCAGCCTCTGGGTTTGGGGGTCCTCTGGCAGCCAGGTAAGAAGGCTGGGTAAGAAAGCGAGGGCCTGGCTGGAGTGGCCCCAGCCCTGGCACAGAGATGCAGAGTCTGGTGTTGGGCGGGAGAGCTGTGTGCAGAGGGCGGGGTGGGCAGGCGTTAATGGAGGCCCGCCTGGGCCTTTGATGAGGGCAGCGCCCGCCTGCCTGCCTGGCTAGGGGTTAATTAGCCTTAATCAAGGTGGCACCTCCTTCCTCCACCCTCTCCCTCAGGCCTAGAA... | CACCCTGATGGTGGCATGGGAGGGAGTGGCATTCCAGGCAGAAGGAGCAGCCTCTGGGTTTGGGGGTCCTCTGGCAGCCAGGTAAGAAGGCTGGGTAAGAAAGCGAGGGCCTGGCTGGAGTGGCCCCAGCCCTGGCACAGAGATGCAGAGTCTGGTGTTGGGCGGGAGAGCTGTGTGCAGAGGGCGGGGTGGGCAGGCGTTAATGGAGGCCCGCCTGGGCCTTTGATGAGGGCAGCGCCCGCCTGCCTGCCTGGCTAGGGGTTAATTAGCCTTAATCAAGGTGGCACCTCCTTCCTCCACCCTCTCCCTCAGGCCTAGAA... |
Task1_train_45136 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | TGGGGGCTCAGGCAGGTGCAGGGCAGGCGAAGGAACAGCTGGCTGTCACCAGGGTGGAGACCTTGCCAGGTGAGCATAAACGAAGGATGGAGGGCACTATGGGAAGTGCATGCAGATGACCAAGAGTTCTAAACTGGGCTGGGAGGAAAGCAAGGAAAGAGGGGCTGATGGTTGGCGAAAAGGGGCTGGGCCAGGAGCTTGGAGGGCCTGGTGGTTTGAAGAGCACAGGGAAGCGCCACATGAGGGAGGGCCTGGCCTGAGGGAGGGATGCCTCAATCCAGACTTTGGAGGCAGTGCCTTCACCAGTAACAAGAGATATG... | TGGGGGCTCAGGCAGGTGCAGGGCAGGCGAAGGAACAGCTGGCTGTCACCAGGGTGGAGACCTTGCCAGGTGAGCATAAACGAAGGATGGAGGGCACTATGGGAAGTGCATGCAGATGACCAAGAGTTCTAAACTGGGCTGGGAGGAAAGCAAGGAAAGAGGGGCTGATGGTTGGCGAAAAGGGGCTGGGCCAGGAGCTTGGAGGGCCTGGTGGTTTGAAGAGCACAGGGAAGCGCCACATGAGGGAGGGCCTGGCCTGAGGGAGGGATGCCTCAATCCAGACTTTGGAGGCAGTGCCTTCACCAGTAACAAGAGATATG... |
Task1_train_45137 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CACTCCTGTAATCCGAGCACTTTGGGAGGCTAAGGTGGGAAGATCGCTTGAGCCCAGGAGTTCAAAACCAGCCTGGTCAACATAATGAGACCCTGTGTCTACAAAAGAAAAAAAGGTTAGCTGGGTATGGTGGCACATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAAGCCAGAAGGATCACTTGAGCCCAGGAGTTCAAGGCTGCAATGAGCCATTATTGCATCACTGTGCTCCAGCCTGAGTGACAGCATAAGACTCTGTCTCAAAAAAACAAAAAAAGAGAAAATTGGCTGGGCACAGTGGCTCACTCCTGTAATC... | CACTCCTGTAATCCGAGCACTTTGGGAGGCTAAGGTGGGAAGATCGCTTGAGCCCAGGAGTTCAAAACCAGCCTGGTCAACATAATGAGACCCTGTGTCTACAAAAGAAAAAAAGGTTAGCTGGGTATGGTGGCACATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAAGCCAGAAGGATCACTTGAGCCCAGGAGTTCAAGGCTGCAATGAGCCATTATTGCATCACTGTGCTCCAGCCTGAGTGACAGCATAAGACTCTGTCTCAAAAAAACAAAAAAAGAGAAAATTGGCTGGGCACAGTGGCTCACTCCTGTAATC... |
Task1_train_45138 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CGGGTCCTTTGCCCCCACGAGCAGCACTATGACATCACCAGGGCGTTTTGTGTTGACTACTGCATCGTCTCACAAAGTGGCCCCTGCCCGAGATAGTGAAGCTAGTCTGGGAAGAGACGGCATCAGCTCCCCATATCTGAGCCACTGTGCCGACAAGGCCCAGCCTCCTCAGGCTCTCCTTGGCTGGACACACCAGAGATGGAGCTGACCTCCCCAAGTCTAAAAGGAAGACAAGTGTCACCCTGACACCGTGCATGGCCTCCTGGCACAAGGCCCCACCAGCTGATGAGAGGCCTTTGCTGGTACATCAGTGACCACAC... | CGGGTCCTTTGCCCCCACGAGCAGCACTATGACATCACCAGGGCGTTTTGTGTTGACTACTGCATCGTCTCACAAAGTGGCCCCTGCCCGAGATAGTGAAGCTAGTCTGGGAAGAGACGGCATCAGCTCCCCATATCTGAGCCACTGTGCCGACAAGGCCCAGCCTCCTCAGGCTCTCCTTGGCTGGACACACCAGAGATGGAGCTGACCTCCCCAAGTCTAAAAGGAAGACAAGTGTCACCCTGACACCGTGCATGGCCTCCTGGCACAAGGCCCCACCAGCTGATGAGAGGCCTTTGCTGGTACATCAGTGACCACAC... |
Task1_train_45139 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AGCTAATTTTGTATTTTTAGTAGAGATGAGGTTTCTCCATGTTGGTCAGGCTGGCCTTGAACTACCGATCTCAGGTGATCTGCCTGCCTCAGCCCCCACAAAGTGCTGGGATTATAGACGTGAGCTACCACGCCCGGCCCCCATTTCTGGTATTTTTTATTTTAAGAAATTCCATTTGGTTCTTTTAAAACTATTTTGCATTTTTCTCATTATACTCTTGTTTTCTTTAACTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTGTTGTCCAGGCTGGAGTACAAGTGGCACAATCTCGGCTTACTGCAACCTCAAC... | AGCTAATTTTGTATTTTTAGTAGAGATGAGGTTTCTCCATGTTGGTCAGGCTGGCCTTGAACTACCGATCTCAGGTGATCTGCCTGCCTCAGCCCCCACAAAGTGCTGGGATTATAGACGTGAGCTACCACGCCCGGCCCCCATTTCTGGTATTTTTTATTTTAAGAAATTCCATTTGGTTCTTTTAAAACTATTTTGCATTTTTCTCATTATACTCTTGTTTTCTTTAACTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTGTTGTCCAGGCTGGAGTACAAGTGGCACAATCTCGGCTTACTGCAACCTCAAC... |
Task1_train_45140 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTATATTAAAAGTCTATGATATACTCTTGGCTTTCCAGAAACTTAATTTGAAGAAGTTAATTTAAAAACCATAGTTTTCTATATATTAATTTGACAGTTCAGCCTTTATTAGGTCAAAGTTTCAAAAGAGCTCAGCTGTTAGATGTTTAGTAATGAATGCCATCAGCCTTTATGTCATCAGGATTCAGGATGTTTAGGTGTGTGTTTGCTCAGGGCTCAGAAATAGTCTTGGTGGTGGGTTTACAGCTGCCCATCTTGTTAGGTGTGGAACCTGCCTTAGCGCTGGGGCTGCTGCCAGTCTATGGGAACATTCCCTCCCG... | CTATATTAAAAGTCTATGATATACTCTTGGCTTTCCAGAAACTTAATTTGAAGAAGTTAATTTAAAAACCATAGTTTTCTATATATTAATTTGACAGTTCAGCCTTTATTAGGTCAAAGTTTCAAAAGAGCTCAGCTGTTAGATGTTTAGTAATGAATGCCATCAGCCTTTATGTCATCAGGATTCAGGATGTTTAGGTGTGTGTTTGCTCAGGGCTCAGAAATAGTCTTGGTGGTGGGTTTACAGCTGCCCATCTTGTTAGGTGTGGAACCTGCCTTAGCGCTGGGGCTGCTGCCAGTCTATGGGAACATTCCCTCCCG... |
Task1_train_45141 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CCCCCGTGGAGGGAGGTCACCATGCAGCAATTCCTGAGGCATGGCTGGGCCTACTCTGCAAGTGTAAACTTAATGAGCTGTGCTTAAATAGCTAATTTGTGCTTGATTGTGTGACAAGCATTTTGTTTTTCATATTTACTGTATGTATTTACCATTTTGGGCATTTTTCATGCAAGGACTTGTTGGACCCTCATGGAGGTCCTGCAAGGTGGATGCACTCTATAAGAGGAAACTGAGGCACATGGCTTATGAGCGGGAAAGGCAAGAGGCAAGGCCAGGCAGGCAGCTCCAGAGCGCATGCCGTCAACCACCCTGACAGC... | CCCCCGTGGAGGGAGGTCACCATGCAGCAATTCCTGAGGCATGGCTGGGCCTACTCTGCAAGTGTAAACTTAATGAGCTGTGCTTAAATAGCTAATTTGTGCTTGATTGTGTGACAAGCATTTTGTTTTTCATATTTACTGTATGTATTTACCATTTTGGGCATTTTTCATGCAAGGACTTGTTGGACCCTCATGGAGGTCCTGCAAGGTGGATGCACTCTATAAGAGGAAACTGAGGCACATGGCTTATGAGCGGGAAAGGCAAGAGGCAAGGCCAGGCAGGCAGCTCCAGAGCGCATGCCGTCAACCACCCTGACAGC... |
Task1_train_45142 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | ACAGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAGCATTTCCCATGTGCCTCCTCTGTGAAAACAGCCCAAATTAATGACAGCAGATGCTGAAGTCTGAGATGGTCAGATGTTAGGAAGGGGATTGGCTGTGACCACCTGGGACCTGCCCACCTGGCTCATGAGGCTACGGCCCAAAGTTGCCAGCTCCTCAGATTTTTCCAGAGCAGCTGGAACCTGCATTGTTTTGTAAAATCTTCAGAATTCAGGTTTTCTGAAAACCCTATGATGGTCCCACCAGTCCCGGTGTGGGCTGAATCTGCTT... | ACAGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAGCATTTCCCATGTGCCTCCTCTGTGAAAACAGCCCAAATTAATGACAGCAGATGCTGAAGTCTGAGATGGTCAGATGTTAGGAAGGGGATTGGCTGTGACCACCTGGGACCTGCCCACCTGGCTCATGAGGCTACGGCCCAAAGTTGCCAGCTCCTCAGATTTTTCCAGAGCAGCTGGAACCTGCATTGTTTTGTAAAATCTTCAGAATTCAGGTTTTCTGAAAACCCTATGATGGTCCCACCAGTCCCGGTGTGGGCTGAATCTGCTT... |
Task1_train_45143 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTTGGGGCCTCAGTGTCTTCGTAACTGAGTAATGTGGCTGCAGGTGTGCTAAGGGAGAAGGCTTTGTCTAGCTCTGAGGTTATGGTGTGACTGGACTGGGACTGGGGGTGCTGGGTCCCTGTGGGCGGGGAGGGGTGGGCCTGTCCAGCTCCTCCGTCGGGGCTAATGCTGGAAGGCCCAGGTCTCCCTGCTTCCAGCCTAGCCCAGCCAAGGCAGGCTGCCATCCAGATGTGGCTGTGGGCCAGGCGGTGCCATAGCCCCTAGCTTGCAGATGCCCTAGCCTGTCACTGACAGGCCGGTGTGGGGCCTTTAGTGGGGGC... | CTTGGGGCCTCAGTGTCTTCGTAACTGAGTAATGTGGCTGCAGGTGTGCTAAGGGAGAAGGCTTTGTCTAGCTCTGAGGTTATGGTGTGACTGGACTGGGACTGGGGGTGCTGGGTCCCTGTGGGCGGGGAGGGGTGGGCCTGTCCAGCTCCTCCGTCGGGGCTAATGCTGGAAGGCCCAGGTCTCCCTGCTTCCAGCCTAGCCCAGCCAAGGCAGGCTGCCATCCAGATGTGGCTGTGGGCCAGGCGGTGCCATAGCCCCTAGCTTGCAGATGCCCTAGCCTGTCACTGACAGGCCGGTGTGGGGCCTTTAGTGGGGGC... |
Task1_train_45144 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GGGGCCTCAGTGTCTTCGTAACTGAGTAATGTGGCTGCAGGTGTGCTAAGGGAGAAGGCTTTGTCTAGCTCTGAGGTTATGGTGTGACTGGACTGGGACTGGGGGTGCTGGGTCCCTGTGGGCGGGGAGGGGTGGGCCTGTCCAGCTCCTCCGTCGGGGCTAATGCTGGAAGGCCCAGGTCTCCCTGCTTCCAGCCTAGCCCAGCCAAGGCAGGCTGCCATCCAGATGTGGCTGTGGGCCAGGCGGTGCCATAGCCCCTAGCTTGCAGATGCCCTAGCCTGTCACTGACAGGCCGGTGTGGGGCCTTTAGTGGGGGCAGC... | GGGGCCTCAGTGTCTTCGTAACTGAGTAATGTGGCTGCAGGTGTGCTAAGGGAGAAGGCTTTGTCTAGCTCTGAGGTTATGGTGTGACTGGACTGGGACTGGGGGTGCTGGGTCCCTGTGGGCGGGGAGGGGTGGGCCTGTCCAGCTCCTCCGTCGGGGCTAATGCTGGAAGGCCCAGGTCTCCCTGCTTCCAGCCTAGCCCAGCCAAGGCAGGCTGCCATCCAGATGTGGCTGTGGGCCAGGCGGTGCCATAGCCCCTAGCTTGCAGATGCCCTAGCCTGTCACTGACAGGCCGGTGTGGGGCCTTTAGTGGGGGCAGC... |
Task1_train_45145 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | TCAGTCCCTTCTCACAGGCTGTAAAGAAATACCTGAAACTGGATTGGTTATTTATTTATTTATGAGACGGCCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTTGTGCCTCAGCCTCCCAAGTAGCTGGGACTACCAGTATGCACCACCACACCTGGTTAATTTTTGTATTTTTAGTAGACACAGGGTTTTGCCATGTTGGCCAGGTTGGTCTCGAACTCCTGACCTGGTGATCTGCAGGACTGGATAATTTATATAAAAAAGAGGTTTACTTGGCTTATGGTTCTGCA... | TCAGTCCCTTCTCACAGGCTGTAAAGAAATACCTGAAACTGGATTGGTTATTTATTTATTTATGAGACGGCCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTTGTGCCTCAGCCTCCCAAGTAGCTGGGACTACCAGTATGCACCACCACACCTGGTTAATTTTTGTATTTTTAGTAGACACAGGGTTTTGCCATGTTGGCCAGGTTGGTCTCGAACTCCTGACCTGGTGATCTGCAGGACTGGATAATTTATATAAAAAAGAGGTTTACTTGGCTTATGGTTCTGCA... |
Task1_train_45146 | 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 | CAGCCTCTCAAAGACTCCTTCCTGCCCCTCCCAGTCAGAGACCCCCAAGGGTGACGCCATTCTGGCCTGTTGTTCAACTTGACTTGAACAACACTTCAAGTCAAGTTTGGATCTGGCTTCTTCTGCTCAGTTGCGAGGCCCATTGATGTTTCCTGTGGCCTAGCTCCTTTTTATTGCCGAGGGCTACTCTGTTGTATGAAAACCACAATTCATTTCTCCCTTCTCCTTTGGTGAACATTTGCACTGTTTCCAGCCTGGGGCAATGATGAGTAAAGCTGTTAAAAACAGGCACATATGTTTTCCTTTCTCTTGGGTAATTT... | CAGCCTCTCAAAGACTCCTTCCTGCCCCTCCCAGTCAGAGACCCCCAAGGGTGACGCCATTCTGGCCTGTTGTTCAACTTGACTTGAACAACACTTCAAGTCAAGTTTGGATCTGGCTTCTTCTGCTCAGTTGCGAGGCCCATTGATGTTTCCTGTGGCCTAGCTCCTTTTTATTGCCGAGGGCTACTCTGTTGTATGAAAACCACAATTCATTTCTCCCTTCTCCTTTGGTGAACATTTGCACTGTTTCCAGCCTGGGGCAATGATGAGTAAAGCTGTTAAAAACAGGCACATATGTTTTCCTTTCTCTTGGGTAATTT... |
Task1_train_45147 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTAATGGATGCTGGGCTTGATACCAAGGTGATGGGTTGATCTCTGCAGCAAACCACCATGGCACCCGTTTACCTAGTTAACAAATCTGCACATCCTGTACTTGCACCCTGGAACTTAAAATCAAAGTTGAAGGGGATGGAAATGGCAGATCACGCCTATAATCTCAGCACTTTGGGAGGCTGAGGAGGGCGGATCGCTTCAGGTCAGGAGTCCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTATGGTGGTGGGCTCCTGTAATCCCAGCTACTCGGGAGGCTGAGG... | CTAATGGATGCTGGGCTTGATACCAAGGTGATGGGTTGATCTCTGCAGCAAACCACCATGGCACCCGTTTACCTAGTTAACAAATCTGCACATCCTGTACTTGCACCCTGGAACTTAAAATCAAAGTTGAAGGGGATGGAAATGGCAGATCACGCCTATAATCTCAGCACTTTGGGAGGCTGAGGAGGGCGGATCGCTTCAGGTCAGGAGTCCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTATGGTGGTGGGCTCCTGTAATCCCAGCTACTCGGGAGGCTGAGG... |
Task1_train_45148 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GCTGGGCTTGATACCAAGGTGATGGGTTGATCTCTGCAGCAAACCACCATGGCACCCGTTTACCTAGTTAACAAATCTGCACATCCTGTACTTGCACCCTGGAACTTAAAATCAAAGTTGAAGGGGATGGAAATGGCAGATCACGCCTATAATCTCAGCACTTTGGGAGGCTGAGGAGGGCGGATCGCTTCAGGTCAGGAGTCCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTATGGTGGTGGGCTCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCACGAGAAT... | GCTGGGCTTGATACCAAGGTGATGGGTTGATCTCTGCAGCAAACCACCATGGCACCCGTTTACCTAGTTAACAAATCTGCACATCCTGTACTTGCACCCTGGAACTTAAAATCAAAGTTGAAGGGGATGGAAATGGCAGATCACGCCTATAATCTCAGCACTTTGGGAGGCTGAGGAGGGCGGATCGCTTCAGGTCAGGAGTCCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTATGGTGGTGGGCTCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCACGAGAAT... |
Task1_train_45149 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TCCTGAAACAGCCTCCCTCAGCACCTTGAGTATTATGCCCTAACAGGCTCTTGCATGCAGTGAGAGGGAGGCCCCGAGGCCAGCTGTCTCTGTTCAGAAAGACCTGGGGGTCTCCTTGACCATGGGCTTAGGGCTCAGACCCCAACACAAACAAGCCCCATGTGCTGCAGAGAAGCAGGTACCTTTGCTGAGGTCCAAAGGCTGTGAGTCCTGCACGAGCCTGTAGTGGTGCGGGTCCCAGGTCACATTGGAGGTGTAGAGCTTGGGGATCTGAATGTGCTGTTTGCCTCGGACATCAAACGTCTCACAGGCTGCCTGGA... | TCCTGAAACAGCCTCCCTCAGCACCTTGAGTATTATGCCCTAACAGGCTCTTGCATGCAGTGAGAGGGAGGCCCCGAGGCCAGCTGTCTCTGTTCAGAAAGACCTGGGGGTCTCCTTGACCATGGGCTTAGGGCTCAGACCCCAACACAAACAAGCCCCATGTGCTGCAGAGAAGCAGGTACCTTTGCTGAGGTCCAAAGGCTGTGAGTCCTGCACGAGCCTGTAGTGGTGCGGGTCCCAGGTCACATTGGAGGTGTAGAGCTTGGGGATCTGAATGTGCTGTTTGCCTCGGACATCAAACGTCTCACAGGCTGCCTGGA... |
Task1_train_45150 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ATGGGTAAACAAATATATAAGAAATAAAAACAAGATGATGTGTTAGACTGAGGGTAAGGGGGCCTCCTCTAGCTTGAGTGGTCAGAGAGCCTTCTCAGAGGAGGTGACATTATAGGAAATACCTTTTGACAAGAAGAAATGAGCCTAGAAAAATTCTGAGGAAAAGGCATGTCATGCAAAGGGAACAGGGAGTACAAAGGCTGTGAGTCAGGACTGAATTTGGTTCATTCAACGGCCAGGAAGAAGAGCCCAGCCCAATGTCTGCTACAGAGTAAATCTCAATACGCAGAGGTATTTTTGCAATTATGAGAACTGCCTAG... | ATGGGTAAACAAATATATAAGAAATAAAAACAAGATGATGTGTTAGACTGAGGGTAAGGGGGCCTCCTCTAGCTTGAGTGGTCAGAGAGCCTTCTCAGAGGAGGTGACATTATAGGAAATACCTTTTGACAAGAAGAAATGAGCCTAGAAAAATTCTGAGGAAAAGGCATGTCATGCAAAGGGAACAGGGAGTACAAAGGCTGTGAGTCAGGACTGAATTTGGTTCATTCAACGGCCAGGAAGAAGAGCCCAGCCCAATGTCTGCTACAGAGTAAATCTCAATACGCAGAGGTATTTTTGCAATTATGAGAACTGCCTAG... |
Task1_train_45151 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GCCCTATCCTCCAGTTCTCAGCATATAGAAGGGAGCTCTCTCATCTGCTAGCCACTCCTGCCTCACTGTGCCATGCTTTCTGTAATGCACTCTGGGTCCAGGGACTGCTTGGCAGGAGGTGGGAAGAACAAGAAGTTTAGGGCCTTCCCAGTTTCTTAGGGCCTGTCTGGAGAGGGAACTAGCGTTTACTGAGTTTTTACGATGTGTTACACACCATGTAAAGCCCTTTACCTACATTATTTCTTATACCCCAAACAGAGAGCAAATAAGTATCCCCATTTTTTAGTCACATAGAGTTCCAGAGTTGCCACAGTTACATC... | GCCCTATCCTCCAGTTCTCAGCATATAGAAGGGAGCTCTCTCATCTGCTAGCCACTCCTGCCTCACTGTGCCATGCTTTCTGTAATGCACTCTGGGTCCAGGGACTGCTTGGCAGGAGGTGGGAAGAACAAGAAGTTTAGGGCCTTCCCAGTTTCTTAGGGCCTGTCTGGAGAGGGAACTAGCGTTTACTGAGTTTTTACGATGTGTTACACACCATGTAAAGCCCTTTACCTACATTATTTCTTATACCCCAAACAGAGAGCAAATAAGTATCCCCATTTTTTAGTCACATAGAGTTCCAGAGTTGCCACAGTTACATC... |
Task1_train_45152 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCCTCAAGAGCCAGATGGACTTCCTGGGGTTCGGAACCTGGAACCAGAGGAGGTTCCACAGGTGCAGTTGAGGGGTTCTAAGAAAGATGATAAAGATGTTTATGTGTACAGTATTCTCTTCCTTGGATATATTCTGAGCCACTTTTTCTTAAATTTTGAAAATTTTTTTCTTTTTTCTTTTTTTTTCAAGATGGAGTCTTGCTTTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCCACCTCCCGAGTTCAAGCAACTCCACCTCCTGCCTCTTCCTCCGGAGTAGCTGGGGTTACAGGCGC... | CCCTCAAGAGCCAGATGGACTTCCTGGGGTTCGGAACCTGGAACCAGAGGAGGTTCCACAGGTGCAGTTGAGGGGTTCTAAGAAAGATGATAAAGATGTTTATGTGTACAGTATTCTCTTCCTTGGATATATTCTGAGCCACTTTTTCTTAAATTTTGAAAATTTTTTTCTTTTTTCTTTTTTTTTCAAGATGGAGTCTTGCTTTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCCACCTCCCGAGTTCAAGCAACTCCACCTCCTGCCTCTTCCTCCGGAGTAGCTGGGGTTACAGGCGC... |
Task1_train_45153 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | TCCTGTGCTAGGCGCTGGCCCCACTGAGCGAGATTAAGTCCCACCTTACAGCCTGGCATTCCAGACGTGGGAAGGCAAGACCTCGGAGCTCTTCTGACCCTGTGGACTGTCCCTGTCCTCCCATTAGCCTCTTGCAGCCTCTGTCAGGGTCCTCCCCCAACTTTCCCTCCCTGCCAGGAGCAAGGTTCCCTCTGCCCCAAGCCACTGGACTGGAAGGGGCAGGAAGAGGGCTAAGGTTGTCCAGGGACCTCCTGAGAGAGGTCAGGAAGGCAGGAGTCAGTGCGGTCAAAGATTTTTGCTCCCACCAAGCCCCAAATTTC... | TCCTGTGCTAGGCGCTGGCCCCACTGAGCGAGATTAAGTCCCACCTTACAGCCTGGCATTCCAGACGTGGGAAGGCAAGACCTCGGAGCTCTTCTGACCCTGTGGACTGTCCCTGTCCTCCCATTAGCCTCTTGCAGCCTCTGTCAGGGTCCTCCCCCAACTTTCCCTCCCTGCCAGGAGCAAGGTTCCCTCTGCCCCAAGCCACTGGACTGGAAGGGGCAGGAAGAGGGCTAAGGTTGTCCAGGGACCTCCTGAGAGAGGTCAGGAAGGCAGGAGTCAGTGCGGTCAAAGATTTTTGCTCCCACCAAGCCCCAAATTTC... |
Task1_train_45154 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACTCTTGAGGCTGAGGCAGGAAAATCACTTGAACTCAGGAGGTGGAGGTTGAAGTGAGCCGAGAGCATGCCACCGCACTCCAGCCTAGGCAACAGAGGGAGACTCCGTCTCCAAAAAAACAAATAAATAAAAATAAAAACAAAAATACAAAAAATAGCCAGGTGTGGTGGTACAAGCCTGTAGTCCCAGCTACTCTTGAGGCTGAGGCAGGAGAGTTGCTTGAACCCGGGAGGCAGAGGTTGCAGTAAGCCAAGATGATGCCACTGCACTCCAGCCTGGGTGACAGAGAGAGACTCCATCTCAAAAAAAAAAAAAAAGTG... | ACTCTTGAGGCTGAGGCAGGAAAATCACTTGAACTCAGGAGGTGGAGGTTGAAGTGAGCCGAGAGCATGCCACCGCACTCCAGCCTAGGCAACAGAGGGAGACTCCGTCTCCAAAAAAACAAATAAATAAAAATAAAAACAAAAATACAAAAAATAGCCAGGTGTGGTGGTACAAGCCTGTAGTCCCAGCTACTCTTGAGGCTGAGGCAGGAGAGTTGCTTGAACCCGGGAGGCAGAGGTTGCAGTAAGCCAAGATGATGCCACTGCACTCCAGCCTGGGTGACAGAGAGAGACTCCATCTCAAAAAAAAAAAAAAAGTG... |
Task1_train_45155 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TGGAGAGGAGCACCTGGCAGTGGGACTCATCTTCTCCAAGTCTCCAGACTGCAGCCTGCAAGTGGCTGGGTTTCTGGTCAACTGAAGCAGAGGAGGCTGGACCTGGCAGGGGGAGCTTCCCACTTGCTCTCTGCCATCCAGAGAATGGGGAAAGAGGGATGTCCTTGCCCCTGTCTCCCTCCTCCTGGTGCTCCAAACATGGTCCAACTGACCTCATCATCAAACCACTCTTGGCAGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCTGAGGTGGGCAGATCACCTGAGGTCAGGCATTCGAGACCAG... | TGGAGAGGAGCACCTGGCAGTGGGACTCATCTTCTCCAAGTCTCCAGACTGCAGCCTGCAAGTGGCTGGGTTTCTGGTCAACTGAAGCAGAGGAGGCTGGACCTGGCAGGGGGAGCTTCCCACTTGCTCTCTGCCATCCAGAGAATGGGGAAAGAGGGATGTCCTTGCCCCTGTCTCCCTCCTCCTGGTGCTCCAAACATGGTCCAACTGACCTCATCATCAAACCACTCTTGGCAGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCTGAGGTGGGCAGATCACCTGAGGTCAGGCATTCGAGACCAG... |
Task1_train_45156 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ATATGAAAGGTCTTTGATGATCTACCCCAGCTTTCCTTTCCAGTCCTTTCTCTCACTCCTCTCCCTTAGTTACTCTCTGTCTACTAAAAGAGACTGTTTACTCTCTGTGATACTGTGAAATATATATTTGGTCTTCCCTGCTTCCTGGCATATAAAATCTAAAATCATTAGTGCCTCCTAAGTGATGTCTTTTTGTGTGCTGAGTTGACTAGTTGCTGGCAGCCCCTAAGTAGCTTCCAGATGGTGGCTGGTCACTGGAAAGACCCAGGCAGGATTAGAGGGTTATAATTTTCAGCCCCCCACCCAACCCACACTTCCTG... | ATATGAAAGGTCTTTGATGATCTACCCCAGCTTTCCTTTCCAGTCCTTTCTCTCACTCCTCTCCCTTAGTTACTCTCTGTCTACTAAAAGAGACTGTTTACTCTCTGTGATACTGTGAAATATATATTTGGTCTTCCCTGCTTCCTGGCATATAAAATCTAAAATCATTAGTGCCTCCTAAGTGATGTCTTTTTGTGTGCTGAGTTGACTAGTTGCTGGCAGCCCCTAAGTAGCTTCCAGATGGTGGCTGGTCACTGGAAAGACCCAGGCAGGATTAGAGGGTTATAATTTTCAGCCCCCCACCCAACCCACACTTCCTG... |
Task1_train_45157 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TTCCCGGAGCCTCCCATTATATTGCAGGATGCTCACTTACTTGGTATGTTCCAGAGATGCCACATCATTCAGGTTGAAGACAATGATGATGGCTGGAAGAGTGGCAGAAACAGCCCCAGGTTGACAGGGAAGACACTACTGCTCATTTCCCCAATCCTTCCAGCTCCATATGAGAAGCCATGTGCACTCTGAGACCCACCTACCCCACTTCACCCAGCCCCTTACCTTGAGCTCCTCTATAGTAGGTTGATGCAATGCATTTGAACCTCTCCTGCCCAGCGGTATCCCAACTGGAAGGAAGGAAGAGTGAAGCACAGGTA... | TTCCCGGAGCCTCCCATTATATTGCAGGATGCTCACTTACTTGGTATGTTCCAGAGATGCCACATCATTCAGGTTGAAGACAATGATGATGGCTGGAAGAGTGGCAGAAACAGCCCCAGGTTGACAGGGAAGACACTACTGCTCATTTCCCCAATCCTTCCAGCTCCATATGAGAAGCCATGTGCACTCTGAGACCCACCTACCCCACTTCACCCAGCCCCTTACCTTGAGCTCCTCTATAGTAGGTTGATGCAATGCATTTGAACCTCTCCTGCCCAGCGGTATCCCAACTGGAAGGAAGGAAGAGTGAAGCACAGGTA... |
Task1_train_45158 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGTGCCACGTTTTCTTAATCCATCTATCATTGTTGGACATTTAGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCACAATAAACATACGTGTGCATGTGTCTTTATAGCAGCATGATTTATAATCCTTTGGGTATACACCCAGTAATGGGATGGCTGGGTCAAATGGTATTTCTAGTTCTAGATCCCTGAGGAATCGCCACACTGACTTCCACAATGGTTGAACTAGTTTACAGTCCCACCAACAGTGTAAAAGTGTTCCTATTTCTCCACATCCTCTCCAGCACTTGTTGTTTCCTGACTTTTTAAAGATCACCA... | TGTGCCACGTTTTCTTAATCCATCTATCATTGTTGGACATTTAGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCACAATAAACATACGTGTGCATGTGTCTTTATAGCAGCATGATTTATAATCCTTTGGGTATACACCCAGTAATGGGATGGCTGGGTCAAATGGTATTTCTAGTTCTAGATCCCTGAGGAATCGCCACACTGACTTCCACAATGGTTGAACTAGTTTACAGTCCCACCAACAGTGTAAAAGTGTTCCTATTTCTCCACATCCTCTCCAGCACTTGTTGTTTCCTGACTTTTTAAAGATCACCA... |
Task1_train_45159 | 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 | GATTGATTTTGAGATCCAAAGTGAGCCTGAAGCCATGTTTTGGAATGAAAATTCCCAGTGGATTTATCACCCCTCTCCAAGGGTTGGCAGCTGTGAGGCCTGGCTCAGGGCTTCTATCCCCTTCTATCTCTTCAGTAACCAGTTCTACCAAATCTGCACGCAGGCTGAAAAAATCAGCACTGATAGTGGGAAGATAGAGAAGAGAAATTCCTCCAGCTCCAGGCCTCCAAGCTGTCAGGCACCAGGACCCCCGTCCCCCAGCTCCTGAGAGCAAGGAGCTGCACAACCCGGTGGCTTGCAAGGTGTCAGCCGCTTCTCAA... | GATTGATTTTGAGATCCAAAGTGAGCCTGAAGCCATGTTTTGGAATGAAAATTCCCAGTGGATTTATCACCCCTCTCCAAGGGTTGGCAGCTGTGAGGCCTGGCTCAGGGCTTCTATCCCCTTCTATCTCTTCAGTAACCAGTTCTACCAAATCTGCACGCAGGCTGAAAAAATCAGCACTGATAGTGGGAAGATAGAGAAGAGAAATTCCTCCAGCTCCAGGCCTCCAAGCTGTCAGGCACCAGGACCCCCGTCCCCCAGCTCCTGAGAGCAAGGAGCTGCACAACCCGGTGGCTTGCAAGGTGTCAGCCGCTTCTCAA... |
Task1_train_45160 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTAGAATTACTGCCTCCACTGGGACAGGGCAGGAGGCAGAACTGTCCAGAACTTTAGAGAACTAGAGACCTCCCAAGAGGCTGATGTTGGCATGCCAGGACTACCCAGAGGTCACCGTTGAGAGGAGTTTTGGCCATTGGTGATGGCGCTGTGAGGAGTACCCTGGTGCAGTTCCCACCATGGTCAAGTTAATCCTGCTGCAGGTTGCCATGCCAGGGCGGGATGGTGGTCATGTGGAGAAAGGTACTCCTGCTCTGCTAGTGTGTTCCAGGCTGGTCCAGGGCATGAGGAGGCTCAGGATGCTGGCTGTTGATGCTTGT... | CTAGAATTACTGCCTCCACTGGGACAGGGCAGGAGGCAGAACTGTCCAGAACTTTAGAGAACTAGAGACCTCCCAAGAGGCTGATGTTGGCATGCCAGGACTACCCAGAGGTCACCGTTGAGAGGAGTTTTGGCCATTGGTGATGGCGCTGTGAGGAGTACCCTGGTGCAGTTCCCACCATGGTCAAGTTAATCCTGCTGCAGGTTGCCATGCCAGGGCGGGATGGTGGTCATGTGGAGAAAGGTACTCCTGCTCTGCTAGTGTGTTCCAGGCTGGTCCAGGGCATGAGGAGGCTCAGGATGCTGGCTGTTGATGCTTGT... |
Task1_train_45161 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGTCCCCCCATTTGTCCCCTTCCCATCTATTAGGTTCGATAAAAACTGATTGGCCATCTACCAGGAATGAAATACTTAGAGTACGTGGCTGATAACCCCATGAAAAGTATCATCCCCATTTCACAGATGAGGAAACTGAGGCTATAAGAGGTGAAGGAACTTTGAAGATACTAGCTAATAACAGCTACAGTCTGGTTCAGAATCCAGGAGAGAGGTTTGGAGTTTGTGTTGGGAAGGGGAGCGTGGGGAACAGGTATACTCACCCCTCTGGCATGAGGGCAGGTCCTCACTCCAAGTTAGGTCCCACTGGCACATGAGGA... | TGTCCCCCCATTTGTCCCCTTCCCATCTATTAGGTTCGATAAAAACTGATTGGCCATCTACCAGGAATGAAATACTTAGAGTACGTGGCTGATAACCCCATGAAAAGTATCATCCCCATTTCACAGATGAGGAAACTGAGGCTATAAGAGGTGAAGGAACTTTGAAGATACTAGCTAATAACAGCTACAGTCTGGTTCAGAATCCAGGAGAGAGGTTTGGAGTTTGTGTTGGGAAGGGGAGCGTGGGGAACAGGTATACTCACCCCTCTGGCATGAGGGCAGGTCCTCACTCCAAGTTAGGTCCCACTGGCACATGAGGA... |
Task1_train_45162 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GAAAAGTATCATCCCCATTTCACAGATGAGGAAACTGAGGCTATAAGAGGTGAAGGAACTTTGAAGATACTAGCTAATAACAGCTACAGTCTGGTTCAGAATCCAGGAGAGAGGTTTGGAGTTTGTGTTGGGAAGGGGAGCGTGGGGAACAGGTATACTCACCCCTCTGGCATGAGGGCAGGTCCTCACTCCAAGTTAGGTCCCACTGGCACATGAGGACACTGGATCCCACTACCTGGTAGCCAGGGTAGCACTGGTAAGTGACCACGGTGCCGTGCACTAGCTCAGGCTGCGATGGGCTCTTCCAGCCATTGGGGATC... | GAAAAGTATCATCCCCATTTCACAGATGAGGAAACTGAGGCTATAAGAGGTGAAGGAACTTTGAAGATACTAGCTAATAACAGCTACAGTCTGGTTCAGAATCCAGGAGAGAGGTTTGGAGTTTGTGTTGGGAAGGGGAGCGTGGGGAACAGGTATACTCACCCCTCTGGCATGAGGGCAGGTCCTCACTCCAAGTTAGGTCCCACTGGCACATGAGGACACTGGATCCCACTACCTGGTAGCCAGGGTAGCACTGGTAAGTGACCACGGTGCCGTGCACTAGCTCAGGCTGCGATGGGCTCTTCCAGCCATTGGGGATC... |
Task1_train_45163 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AACCCTGTCTCCACTAAAAATACAAAAAATTAGCTGGGCATGGTGGCGGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGTGGAGCTTGCAGTGAGCCGAGATTGCGCCACTGCAGTTCAGCCTGGGCGACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAATCATTACAATGTTGTATATATATATTTTTTCTCAAATCACATAAGACAGGGGAGACCTTTATGTTGAATAGACACCTTCTATGGGCCAGGTATTTGGGGACTGATGAATAAGGTGACATCATAGCCTG... | AACCCTGTCTCCACTAAAAATACAAAAAATTAGCTGGGCATGGTGGCGGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGTGGAGCTTGCAGTGAGCCGAGATTGCGCCACTGCAGTTCAGCCTGGGCGACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAATCATTACAATGTTGTATATATATATTTTTTCTCAAATCACATAAGACAGGGGAGACCTTTATGTTGAATAGACACCTTCTATGGGCCAGGTATTTGGGGACTGATGAATAAGGTGACATCATAGCCTG... |
Task1_train_45164 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | GAAAAAAAAGAACAAGTGCCTGGGAGTTCTGGGGTTATTTCTTCCCACCTGCCTATCTTGAGCACCAAATGGCCCTATTATCCCACTTGCCCTCTGGACCCTTCCCCAGGCCCAGGTGACAGGTGGCTAAACTCCAGGTCAGGGCATGTCTCAGCTCCCATCTCCTCCCTTGTGAGAGGAGGAGGGACGGGGAGGAGGGACGGGGAGGAGGGAGGGGAGGGCAGCCGCCCGGGAACAGGACCACGACACTCCCCACCTGCTTATGGGTTCTCCAGAGCGACCAACAGTTCTGCCCATACCCTGCCCAAAATGCCCATGCC... | GAAAAAAAAGAACAAGTGCCTGGGAGTTCTGGGGTTATTTCTTCCCACCTGCCTATCTTGAGCACCAAATGGCCCTATTATCCCACTTGCCCTCTGGACCCTTCCCCAGGCCCAGGTGACAGGTGGCTAAACTCCAGGTCAGGGCATGTCTCAGCTCCCATCTCCTCCCTTGTGAGAGGAGGAGGGACGGGGAGGAGGGACGGGGAGGAGGGAGGGGAGGGCAGCCGCCCGGGAACAGGACCACGACACTCCCCACCTGCTTATGGGTTCTCCAGAGCGACCAACAGTTCTGCCCATACCCTGCCCAAAATGCCCATGCC... |
Task1_train_45165 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | CCAGGAGAGGGCCCAGTTCTCCTGCCTAGTGTGTAGAGCCTTCTAGGGTGGCTGGAGAAGAGTGGGGAACTCTGGCGGAAGACAGCCTTCTCTTGTCACCCCAAGAGGAGTCACTTATATAGCAATAACCACTGCCCTAGCAACTAAGGCTGGGGGATGGGCATGGGCCCCCAAGAAACGAGCAGGGAGAAGGTATGGGAGCAGGACCTGGGAAATGTTGCTTATTCAGAGATTCAGAATGGAAAAATATATTACAGAGTTGACATGCATCATTCCTGGGCCCAATACCAGCCAGGAGGAGGGCCATGAATATCTGTCCT... | CCAGGAGAGGGCCCAGTTCTCCTGCCTAGTGTGTAGAGCCTTCTAGGGTGGCTGGAGAAGAGTGGGGAACTCTGGCGGAAGACAGCCTTCTCTTGTCACCCCAAGAGGAGTCACTTATATAGCAATAACCACTGCCCTAGCAACTAAGGCTGGGGGATGGGCATGGGCCCCCAAGAAACGAGCAGGGAGAAGGTATGGGAGCAGGACCTGGGAAATGTTGCTTATTCAGAGATTCAGAATGGAAAAATATATTACAGAGTTGACATGCATCATTCCTGGGCCCAATACCAGCCAGGAGGAGGGCCATGAATATCTGTCCT... |
Task1_train_45166 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | CATTCTGCCATCTCCTAAGAAAGCCAGAGTGCAGGCTAGGAATGTCACCTGAGCCCAGGAACTCAAGGCTGCAATGAGTGGTGATTCCACCACTGCACTCCAGCCTGGGCGACAGAGTAAGATCTTGCCTCAAAAAACAAACAAACAGCTGGGCACGGTGGCTCACACCTGTAATCCTAGCACTTTGAAAGCTGGGGCAGGCGGATCACTTGACATTAGGGGTTCCAGACCAGCCTGGCAAACATGGAGAAACCCCGTCTCTACCAAAAAAAATATTAAAAATTAGCTGGGTGTGGTGGTGCACGCCTGTAGTCCCCAGC... | CATTCTGCCATCTCCTAAGAAAGCCAGAGTGCAGGCTAGGAATGTCACCTGAGCCCAGGAACTCAAGGCTGCAATGAGTGGTGATTCCACCACTGCACTCCAGCCTGGGCGACAGAGTAAGATCTTGCCTCAAAAAACAAACAAACAGCTGGGCACGGTGGCTCACACCTGTAATCCTAGCACTTTGAAAGCTGGGGCAGGCGGATCACTTGACATTAGGGGTTCCAGACCAGCCTGGCAAACATGGAGAAACCCCGTCTCTACCAAAAAAAATATTAAAAATTAGCTGGGTGTGGTGGTGCACGCCTGTAGTCCCCAGC... |
Task1_train_45167 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | CGAGAGCTCGGAGTGACGGCCTGGGACCTGCCACTGTGGCGTGCGGCTCCTCCCCGCGCCGCGAGGCCGCGACCTCTGCCACGTGGACCGCGCGCGGGGCGCTCCCTGGTGGCGATGGCGCGGCACTGGCCGAGCACTGCGGGGGCTTTCCTCCTTGTTGGTTGCTGAGTGGGCGGCCAAGGGGAGAAAAGGAGCCGCTTCTGCCTCCCTTGCCAAAACTCCGTTTCTAATTAAATTATTTTTAGTAGACTCTGGAGTTGAGCTTGTGCATCTGCCGCACAGAGACTCCCACCCGGACCCTCGTCCTAGGCCATGGAGGT... | CGAGAGCTCGGAGTGACGGCCTGGGACCTGCCACTGTGGCGTGCGGCTCCTCCCCGCGCCGCGAGGCCGCGACCTCTGCCACGTGGACCGCGCGCGGGGCGCTCCCTGGTGGCGATGGCGCGGCACTGGCCGAGCACTGCGGGGGCTTTCCTCCTTGTTGGTTGCTGAGTGGGCGGCCAAGGGGAGAAAAGGAGCCGCTTCTGCCTCCCTTGCCAAAACTCCGTTTCTAATTAAATTATTTTTAGTAGACTCTGGAGTTGAGCTTGTGCATCTGCCGCACAGAGACTCCCACCCGGACCCTCGTCCTAGGCCATGGAGGT... |
Task1_train_45168 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGAATCACATGGTATTATAGAAGGGGTTGGTTGTCCGTTTTTTGTCATTTGCCTTTTTCAGTCTCCTAAGGGGGTGAGTTCTGCCGTGTTGCTGACGGGGTGCCACGGCCAGCCCTGGAGCTGGGCATGCACACTGCAGTCCCTGGGTCTGTAGCACGGGAAGGCCTCCTTCAGAACTAGTCAATTCAAGTCCTGCCCTGGGGAGCAAATACTGCTGACTAGAACCAAATTCTTTGGCATACTGCACAAGGGGCCTCTCCACTGGCTTGCTCTGCACAATACACTCTGTTGTTGTGAGTTGTTCTACAAAAGACTTGGTG... | AGAATCACATGGTATTATAGAAGGGGTTGGTTGTCCGTTTTTTGTCATTTGCCTTTTTCAGTCTCCTAAGGGGGTGAGTTCTGCCGTGTTGCTGACGGGGTGCCACGGCCAGCCCTGGAGCTGGGCATGCACACTGCAGTCCCTGGGTCTGTAGCACGGGAAGGCCTCCTTCAGAACTAGTCAATTCAAGTCCTGCCCTGGGGAGCAAATACTGCTGACTAGAACCAAATTCTTTGGCATACTGCACAAGGGGCCTCTCCACTGGCTTGCTCTGCACAATACACTCTGTTGTTGTGAGTTGTTCTACAAAAGACTTGGTG... |
Task1_train_45169 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TCTTCTCACCCAGGCTGGAGTGCAGTGGCATGATCATGACTCACTGCAGCCTCAACCTCCCAGGTGGGAGATGATTCTCCCACCTCAGCCACCTGAGTAGCTGGGACTACAGGTGTGCACCACCATGCCCAGCTAATTTTTTGTATTTTTAATAGAGAGAAGGTTTCACCCTGTTGCCAAGGATAGTCTCAAATGCCTGGGTGCTGGGATTGTAGGTGTAAGCCACCGTACCCAGCCTGGTAATTCCATTTTTAATGCCCAACTTAAAATTATAAGATGTATAAGAACAGTATTTCCTTTTCCCAAGCATTTACTTATAC... | TCTTCTCACCCAGGCTGGAGTGCAGTGGCATGATCATGACTCACTGCAGCCTCAACCTCCCAGGTGGGAGATGATTCTCCCACCTCAGCCACCTGAGTAGCTGGGACTACAGGTGTGCACCACCATGCCCAGCTAATTTTTTGTATTTTTAATAGAGAGAAGGTTTCACCCTGTTGCCAAGGATAGTCTCAAATGCCTGGGTGCTGGGATTGTAGGTGTAAGCCACCGTACCCAGCCTGGTAATTCCATTTTTAATGCCCAACTTAAAATTATAAGATGTATAAGAACAGTATTTCCTTTTCCCAAGCATTTACTTATAC... |
Task1_train_45170 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | TTTTCTGAAGAATTGGGTAAGCATATCATTATGTAGTGGTTCGATCTGTAGTAATGCTTTTTGTCTTAAAGCCTATTTCCAGGGCTGTGGTGTTCCACAGCTCCAGGGAGGACATTCACATTACAGTTTATGCAAATAAACTGAAATTAGACAGTCTGTTTCGTTACTTTGGAGTGGCCTTAATTCTGTGGGTTATGAGTATAACTTCTCAGTTTTATTTTGGTTAGTATCTGCCTGATGTATCTTTTCCATCCTTTCTTATATTGTAGGTTGCCTATGTCTCTCTCTTGTCATCACATATGGCTGGATTTCTTTTAAAA... | TTTTCTGAAGAATTGGGTAAGCATATCATTATGTAGTGGTTCGATCTGTAGTAATGCTTTTTGTCTTAAAGCCTATTTCCAGGGCTGTGGTGTTCCACAGCTCCAGGGAGGACATTCACATTACAGTTTATGCAAATAAACTGAAATTAGACAGTCTGTTTCGTTACTTTGGAGTGGCCTTAATTCTGTGGGTTATGAGTATAACTTCTCAGTTTTATTTTGGTTAGTATCTGCCTGATGTATCTTTTCCATCCTTTCTTATATTGTAGGTTGCCTATGTCTCTCTCTTGTCATCACATATGGCTGGATTTCTTTTAAAA... |
Task1_train_45171 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTGGGAGGAGGTAGTATTTGAGAAGAGACTTAAATGGACTGGGCCGTACGTAAATCTTGGGGTTATGTGTTTATTAAAAACTAAGGAAGAGGAGCTGGTCATGGTGGTATGTACCTGTAGTTCCAGCTACATAGGAGGCTGAGGTGGGAGGATTGTTTGAGCCCAGGAGTTCAAGGCAGCAATGAGCTATGATCATGCCACTGTACTCTGGCCTGAGTGACAAAGTGAGATCCCATCTTTTTTTTTTTTTTTTTTTTTTAGGCTGGAGTCTCACTGTGTCACCCAGGCAGGAGTGCAGTGGCGCAATCTCTGCTCACTGC... | CTGGGAGGAGGTAGTATTTGAGAAGAGACTTAAATGGACTGGGCCGTACGTAAATCTTGGGGTTATGTGTTTATTAAAAACTAAGGAAGAGGAGCTGGTCATGGTGGTATGTACCTGTAGTTCCAGCTACATAGGAGGCTGAGGTGGGAGGATTGTTTGAGCCCAGGAGTTCAAGGCAGCAATGAGCTATGATCATGCCACTGTACTCTGGCCTGAGTGACAAAGTGAGATCCCATCTTTTTTTTTTTTTTTTTTTTTTAGGCTGGAGTCTCACTGTGTCACCCAGGCAGGAGTGCAGTGGCGCAATCTCTGCTCACTGC... |
Task1_train_45172 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCCACCATTCATTCTGCACACATTGTGTCAGGCAAGATGCTCAGTATCAGACACAGAATATAGGAAAGTACAAGTAACCAGCTGGGTGTGGTCACTCATGCCTATAATCCCAGCACTTTGGAAGGCCAAGGCTGGGGAGGACTGCTTGAGGCCAGGAGTTTGAGACCAGTCTGGACAACACAGCAAGACCCTCATTCTCTACAAAAAATATTTTTAAAAAAGTTTTTAAAAGAAAGTACAAGAAGGTACACATACCCTTTCACAAGTCACAGTGATATCTTACTAAAATGCCTGGAGCCACAAGAAGCCTGTTTTCCCTT... | TCCACCATTCATTCTGCACACATTGTGTCAGGCAAGATGCTCAGTATCAGACACAGAATATAGGAAAGTACAAGTAACCAGCTGGGTGTGGTCACTCATGCCTATAATCCCAGCACTTTGGAAGGCCAAGGCTGGGGAGGACTGCTTGAGGCCAGGAGTTTGAGACCAGTCTGGACAACACAGCAAGACCCTCATTCTCTACAAAAAATATTTTTAAAAAAGTTTTTAAAAGAAAGTACAAGAAGGTACACATACCCTTTCACAAGTCACAGTGATATCTTACTAAAATGCCTGGAGCCACAAGAAGCCTGTTTTCCCTT... |
Task1_train_45173 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GCTTTCTCATTGCCTCTTTCCGTGTTCGATTCGGCTGATCTGGGCCCAGCCTCCGCTCCCGCTCTCTGTCGGTGGGCGCGGGGGAATCCGAAACGGCTCAGCAGAATCCCAGCAGCTTGCTGCTACTGGAGCGGGCCGCCTCCATGGCCTCCAGGCAGGCCGGGCTGGACCGCGTGAGGTCCTAGGAGACGGGATTCCGGGAAGCGGGGAGTATGGTGGGGGTCCTGGCCATGGCGGCTGCAGCTGCTCCGCCTCCCGTGAAGGACTGCGAGATTGAGGTGAGGTTGAGTCGAGGATCTGTTGAGTTCCTTCCTCTATCT... | GCTTTCTCATTGCCTCTTTCCGTGTTCGATTCGGCTGATCTGGGCCCAGCCTCCGCTCCCGCTCTCTGTCGGTGGGCGCGGGGGAATCCGAAACGGCTCAGCAGAATCCCAGCAGCTTGCTGCTACTGGAGCGGGCCGCCTCCATGGCCTCCAGGCAGGCCGGGCTGGACCGCGTGAGGTCCTAGGAGACGGGATTCCGGGAAGCGGGGAGTATGGTGGGGGTCCTGGCCATGGCGGCTGCAGCTGCTCCGCCTCCCGTGAAGGACTGCGAGATTGAGGTGAGGTTGAGTCGAGGATCTGTTGAGTTCCTTCCTCTATCT... |
Task1_train_45174 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGAGTTCCTTCCTCTATCTTTTGGGGGATTGGAAGGTGGGTCTTGGCGGAAGGTGATCCTGACTTTGTAAGGGGAAAGGTGGGACATTGTGAGGACCCACAGCTGTGACACATTGTGTGCAACAGTTGCCAGAGTGTGTCGTTTAGAGTCGTGTCAAGTCCTGATAAACATTTGGATTCTGAGATATTTGCGGGGTCACAGTAAATTGGGGACTTAAGATAACACGGCCAGTTCCCAGATCCCGAAATGTTGGTGGAACGTGATGTTTTGGACTTCCGACATGTCACAGAGGATCCCAGGGTCAAGTTCTGGGTTCGTGA... | TGAGTTCCTTCCTCTATCTTTTGGGGGATTGGAAGGTGGGTCTTGGCGGAAGGTGATCCTGACTTTGTAAGGGGAAAGGTGGGACATTGTGAGGACCCACAGCTGTGACACATTGTGTGCAACAGTTGCCAGAGTGTGTCGTTTAGAGTCGTGTCAAGTCCTGATAAACATTTGGATTCTGAGATATTTGCGGGGTCACAGTAAATTGGGGACTTAAGATAACACGGCCAGTTCCCAGATCCCGAAATGTTGGTGGAACGTGATGTTTTGGACTTCCGACATGTCACAGAGGATCCCAGGGTCAAGTTCTGGGTTCGTGA... |
Task1_train_45175 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | GCTGAAGAAGATCTTTAAGTTAAACTAGTTCATACATCCACCTGTGCTTGGAATGCCACTTTAGAATGTCACTACAGAAATCAAGCAAGGTACTTAAAGAAAACAGTTTCTCATGGCTTAGTATCTGCGGTTAGGAATCGCAGTGTAACATGTTCTTTTGGGTTTATCAGGTTTCAGTGACAGGCACTAAGCGGTCATTATAAAGAGATTCTAATGCCATGAAGTAGTGGGCTAGCATCTTAAGGTAGACTTGTTATATTTTACACCTTTTCATCTCAGACTAGCATTCTAACTGAAGCATGTATCTTGGCGTCCTTGAA... | GCTGAAGAAGATCTTTAAGTTAAACTAGTTCATACATCCACCTGTGCTTGGAATGCCACTTTAGAATGTCACTACAGAAATCAAGCAAGGTACTTAAAGAAAACAGTTTCTCATGGCTTAGTATCTGCGGTTAGGAATCGCAGTGTAACATGTTCTTTTGGGTTTATCAGGTTTCAGTGACAGGCACTAAGCGGTCATTATAAAGAGATTCTAATGCCATGAAGTAGTGGGCTAGCATCTTAAGGTAGACTTGTTATATTTTACACCTTTTCATCTCAGACTAGCATTCTAACTGAAGCATGTATCTTGGCGTCCTTGAA... |
Task1_train_45176 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | AACATGCGAGATGCCAGCTGATTGTACTACAGCTAAAGGTTGAAAGTCTCTTTGGTGAACTTTGTCCCACATATTTTATTCTTCTTGATTTCATTCTAGAGGACAGCTTCAACTTTAATTTTTTTAGAGATAATTATACCTTGGTTTGCCTCATGTACTACTTAAAATTGGGATTTAATAGTAAATTTTCCAGCAAGAGAAGTCTCAAAATTAAATGTATCCAAATTGGGACCTTTATCCAAACTTACTTAGATCAGTTATTTTATCTCATACTCTGTCAATGGACTTCTTACCACAGGGCCCTTGTTGTTCACTGAAGA... | AACATGCGAGATGCCAGCTGATTGTACTACAGCTAAAGGTTGAAAGTCTCTTTGGTGAACTTTGTCCCACATATTTTATTCTTCTTGATTTCATTCTAGAGGACAGCTTCAACTTTAATTTTTTTAGAGATAATTATACCTTGGTTTGCCTCATGTACTACTTAAAATTGGGATTTAATAGTAAATTTTCCAGCAAGAGAAGTCTCAAAATTAAATGTATCCAAATTGGGACCTTTATCCAAACTTACTTAGATCAGTTATTTTATCTCATACTCTGTCAATGGACTTCTTACCACAGGGCCCTTGTTGTTCACTGAAGA... |
Task1_train_45177 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | GAGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGTGGAGCTTGTAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGGCGACGGAGCGAGACCCTGTCTCAAAAAAATAAAATAAAATAAAATAAAATAAATAAATGACTGGCTTAACCTTCTGTACTGGTAGAATAAATAAATATAGTAATATTTGGATGTACATAGTATTTTTAAGAATGAAAGAAAATTTCTGTGTCTTTGATTTTTAACTGTTAAGAGTAGAAATACAGAATGTGGCTAACTGTCTTGCTACCTG... | GAGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGTGGAGCTTGTAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGGCGACGGAGCGAGACCCTGTCTCAAAAAAATAAAATAAAATAAAATAAAATAAATAAATGACTGGCTTAACCTTCTGTACTGGTAGAATAAATAAATATAGTAATATTTGGATGTACATAGTATTTTTAAGAATGAAAGAAAATTTCTGTGTCTTTGATTTTTAACTGTTAAGAGTAGAAATACAGAATGTGGCTAACTGTCTTGCTACCTG... |
Task1_train_45178 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CAAGCATGAGCCACCACAACTGTCAGTTTCTTAGGTTTTTCTGTGTACTCAATCATGTTATCTGCGAACAGAGATAGTTTTCTTTCCTTTGTTTTTTCTGCCTTTTATTTCTTTTTGTTGCCTTATTTCATTGGGTAGGACCTTCAATATGTTAAGTAGAAGTGGTAACAATGGATATCCTTAGCTTGTACTTGATCTTAGATGGAAAGTGTTTACTATTTTACTGTTGAATACAAAGTTAGCTATAGGCTTTTCATACCTTCTTTTTATCAGATTAAGGAAATTTCTTTTATTCCAACTTTCTTTTTTTTTTTTTTTTT... | CAAGCATGAGCCACCACAACTGTCAGTTTCTTAGGTTTTTCTGTGTACTCAATCATGTTATCTGCGAACAGAGATAGTTTTCTTTCCTTTGTTTTTTCTGCCTTTTATTTCTTTTTGTTGCCTTATTTCATTGGGTAGGACCTTCAATATGTTAAGTAGAAGTGGTAACAATGGATATCCTTAGCTTGTACTTGATCTTAGATGGAAAGTGTTTACTATTTTACTGTTGAATACAAAGTTAGCTATAGGCTTTTCATACCTTCTTTTTATCAGATTAAGGAAATTTCTTTTATTCCAACTTTCTTTTTTTTTTTTTTTTT... |
Task1_train_45179 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | TTTGTGTGTGGCAACAGGTCTAGAGTGTATACCAACTCTAGGGAGTTGGAGGTGCTAGAGAAGGGAGGGCTTCAATTTCTTGCTTTATGTTTCAGATTATTTGAAGTTTTTTCAACAAATATATTTCACTTTTAGATTATAGAAAATGTTTATGTTACAGAAAATATTTAATACTTTTTTTTTTTAAGACATGGGGACTTGCTACATTGCCCAGTCTGGCTTCAAATCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTTCCAAGTAGCTGGCAGGCATGCACCAATGATATTTAATACTTTGACATCAAAGAGACTTAG... | TTTGTGTGTGGCAACAGGTCTAGAGTGTATACCAACTCTAGGGAGTTGGAGGTGCTAGAGAAGGGAGGGCTTCAATTTCTTGCTTTATGTTTCAGATTATTTGAAGTTTTTTCAACAAATATATTTCACTTTTAGATTATAGAAAATGTTTATGTTACAGAAAATATTTAATACTTTTTTTTTTTAAGACATGGGGACTTGCTACATTGCCCAGTCTGGCTTCAAATCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTTCCAAGTAGCTGGCAGGCATGCACCAATGATATTTAATACTTTGACATCAAAGAGACTTAG... |
Task1_train_45180 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GTTCTGGCCAGGGCAATCAGGCAAGAGAAAGAAATAAAGGGTATTCGGTTAGGAAAAGAGAAAGTCAAATTGCCTCTGTTTGCAGATGACATGGTTGTATGTTTAGAAAACCCCATCGTCTCAGCCCAAAATCTCCTTAAGCTGATAAGCAACTTCAGCAAAGTCTCAGGATACAAAATCAATGTGCAAAAATCACAAGCATTCCTATACACCAATAACAGACAAACAGAGAGCCAAATCATGAGTGAACTCCCATTCACAACTGCTACAAAGAGAATAAAATACCTAGGAATCCAACTTACAAGGGATGTGAAGGACCT... | GTTCTGGCCAGGGCAATCAGGCAAGAGAAAGAAATAAAGGGTATTCGGTTAGGAAAAGAGAAAGTCAAATTGCCTCTGTTTGCAGATGACATGGTTGTATGTTTAGAAAACCCCATCGTCTCAGCCCAAAATCTCCTTAAGCTGATAAGCAACTTCAGCAAAGTCTCAGGATACAAAATCAATGTGCAAAAATCACAAGCATTCCTATACACCAATAACAGACAAACAGAGAGCCAAATCATGAGTGAACTCCCATTCACAACTGCTACAAAGAGAATAAAATACCTAGGAATCCAACTTACAAGGGATGTGAAGGACCT... |
Task1_train_45181 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ATGGTGTGTTAAATCTGCACTAAAACTGCTTCTTTACATGTTTTTAAATTTTTTCATTATGTTTTTAACACTTTTCTTACATGCAAAAAACACAACCGTTAAACTTTTCTTATTAAAATGCAAAGCCTAGTGTCTTCTAGCTTTTTGAAGAGCTTTTGTCCATTATATAATCTGTCAAGTAGCCAAGAGTTCCTCAGAAGCAGGACATCATTTAGATTTAAAACAATTATGGCTTGTCTGTAAAATAATGTTGTAGCATAACCATTCATGGGATGGCAGCTACGATTTTACTTCAGTAAAATATCCTTGGATACTACCGC... | ATGGTGTGTTAAATCTGCACTAAAACTGCTTCTTTACATGTTTTTAAATTTTTTCATTATGTTTTTAACACTTTTCTTACATGCAAAAAACACAACCGTTAAACTTTTCTTATTAAAATGCAAAGCCTAGTGTCTTCTAGCTTTTTGAAGAGCTTTTGTCCATTATATAATCTGTCAAGTAGCCAAGAGTTCCTCAGAAGCAGGACATCATTTAGATTTAAAACAATTATGGCTTGTCTGTAAAATAATGTTGTAGCATAACCATTCATGGGATGGCAGCTACGATTTTACTTCAGTAAAATATCCTTGGATACTACCGC... |
Task1_train_45182 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CAGCCTCAAACTCCTGGGCTCAAGTGATCCTCTTCAGCCTCCCAAGTAGCTGGGACTACAGGTACGTGCCACCACACCTGCCTAATGTTTTTATTTCTAATTTTTTGGTAGGGATGGGGTCTTGCTGTGTTGTCCAATCTGGCCTCAAATACCTTGCTGTGTTGTCCAAGCTGGCCTCAAATACCTAGCCACAAGTAACCCTCCTGCTTTGGCCTCTCATAGGCACTGGGATTACAGGCATGAGCCGCCACATCCAACCAACATGTGTGTTCTATATGATACACCACAGTGCTCCTGTGTGTTAGAGACTGTGGGAGCGG... | CAGCCTCAAACTCCTGGGCTCAAGTGATCCTCTTCAGCCTCCCAAGTAGCTGGGACTACAGGTACGTGCCACCACACCTGCCTAATGTTTTTATTTCTAATTTTTTGGTAGGGATGGGGTCTTGCTGTGTTGTCCAATCTGGCCTCAAATACCTTGCTGTGTTGTCCAAGCTGGCCTCAAATACCTAGCCACAAGTAACCCTCCTGCTTTGGCCTCTCATAGGCACTGGGATTACAGGCATGAGCCGCCACATCCAACCAACATGTGTGTTCTATATGATACACCACAGTGCTCCTGTGTGTTAGAGACTGTGGGAGCGG... |
Task1_train_45183 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | CTTTCTCTACTAAAGATACAAAAAATTAGCCAGGCGTGGTGGCATGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGATTCCGGGAGGTGGAGGTTGCAGTGAGCCAAGATCGTGCTATTGCACTCCAGCCTGGGCGACAGGGTGAGACTCCATCTCAAAAAAAGAAAAAAAAGGTTACAGTCCCATTAACAGTGTATAAGAGTTCCCTTTTCTCCACATCCTTGCCAGCATTTGTTATTTTCTGTCTCTTTGATGATAGCCATTCTTATTAGGGTGAGGTGGTATCTCATTGTGGTTTTGAT... | CTTTCTCTACTAAAGATACAAAAAATTAGCCAGGCGTGGTGGCATGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGATTCCGGGAGGTGGAGGTTGCAGTGAGCCAAGATCGTGCTATTGCACTCCAGCCTGGGCGACAGGGTGAGACTCCATCTCAAAAAAAGAAAAAAAAGGTTACAGTCCCATTAACAGTGTATAAGAGTTCCCTTTTCTCCACATCCTTGCCAGCATTTGTTATTTTCTGTCTCTTTGATGATAGCCATTCTTATTAGGGTGAGGTGGTATCTCATTGTGGTTTTGAT... |
Task1_train_45184 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | GCAAATTAGTGGTTGCCAAGAGCTCAGAGAAGGAAGGAATGGAGAATGACTACTTGGTGAGCACAGGGTTTCCTTTTAGGGTGATGAAAAGATTCTGGAACTAGGTAGTGGTGATGGTTGCACAACACTGCCATTGTGCTAAAAGGCTACTGAATTATATGCGTTAAAATGGTTACATGGTAAATTTAGGTTATGCATCTTTTACCACAATTTTTAAATTGTTTTTATTTAACTGTTCTGTGCCTCAACTTCCACATCTGTAAAATGAAGATAGGGTTGTTGTGAGAGTTAAAAGAAAAAAAAAGGCCAGGCACGGTGGC... | GCAAATTAGTGGTTGCCAAGAGCTCAGAGAAGGAAGGAATGGAGAATGACTACTTGGTGAGCACAGGGTTTCCTTTTAGGGTGATGAAAAGATTCTGGAACTAGGTAGTGGTGATGGTTGCACAACACTGCCATTGTGCTAAAAGGCTACTGAATTATATGCGTTAAAATGGTTACATGGTAAATTTAGGTTATGCATCTTTTACCACAATTTTTAAATTGTTTTTATTTAACTGTTCTGTGCCTCAACTTCCACATCTGTAAAATGAAGATAGGGTTGTTGTGAGAGTTAAAAGAAAAAAAAAGGCCAGGCACGGTGGC... |
Task1_train_45185 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CCAAAGGAATACGAGTCACTTGTGATTATTCCTCTATAGGTTTGAAAGATGTATCAGGCCAACTTACTGGATACAGTTTTAATTTAAAACTCTATACATCATACCCCCAACTCACAGACTTCATGTATCCATTGAATACTCTTCTGTTTCCACAGTCTTAATGTGGCCCTAACAAAGTCATCCTTTTAGAGGACTCAAAAGAGGCCCCCCCTACAACTTCTATAATGTAATATTTACAGTAGTTAACATTTATTGATCACTCAGTGTGTGCCAGACATTTTTCAGGTAGGGATTCATTTAATCCTCAAAACTCATTTGAG... | CCAAAGGAATACGAGTCACTTGTGATTATTCCTCTATAGGTTTGAAAGATGTATCAGGCCAACTTACTGGATACAGTTTTAATTTAAAACTCTATACATCATACCCCCAACTCACAGACTTCATGTATCCATTGAATACTCTTCTGTTTCCACAGTCTTAATGTGGCCCTAACAAAGTCATCCTTTTAGAGGACTCAAAAGAGGCCCCCCCTACAACTTCTATAATGTAATATTTACAGTAGTTAACATTTATTGATCACTCAGTGTGTGCCAGACATTTTTCAGGTAGGGATTCATTTAATCCTCAAAACTCATTTGAG... |
Task1_train_45186 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | ACTTCTAAAATGTGACTGCTTGAATACAGGTATCTACCAGTGATATGGGGTGGATAATTAATAATGCTTGGCTACTTCTATAAAGACAGTGTTGCTTATTTTTCAAAACTTTTTCTTTTTTTCTTTTTTTTTTTTTTTTTTACCAATTATATTCTTCCCTTCTCCCCAAGAGGTGGGCAGAAAAGCATTGTTAATCTCCTTTTACAGGTGAGGAAAAACAAGATCAGAGGTGCTAAGTGCTGTAGCCTAGTGCCAGGTCTTCTGTCCCCAATTCTGGGTTCTCCCCAAGCCCATGTTTCTCCTTTCTCGCAATCTTTACT... | ACTTCTAAAATGTGACTGCTTGAATACAGGTATCTACCAGTGATATGGGGTGGATAATTAATAATGCTTGGCTACTTCTATAAAGACAGTGTTGCTTATTTTTCAAAACTTTTTCTTTTTTTCTTTTTTTTTTTTTTTTTTACCAATTATATTCTTCCCTTCTCCCCAAGAGGTGGGCAGAAAAGCATTGTTAATCTCCTTTTACAGGTGAGGAAAAACAAGATCAGAGGTGCTAAGTGCTGTAGCCTAGTGCCAGGTCTTCTGTCCCCAATTCTGGGTTCTCCCCAAGCCCATGTTTCTCCTTTCTCGCAATCTTTACT... |
Task1_train_45187 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AACCTGGGAGGCGGAGGTTGTAGTGAGCCAAGATTGTGCCACTGCACTCCAGCCTGGGCAACAAAGTGAGACTCCGTCTCAAAAAAAAAAAAAAGTCGAAAAAACTGAACTCCCCTTTTACTTTCTTCTACTTCTATTTTTTTTTTTTTAAATTTTACTTTAAGTTCTGGGATACATGTGCAGGTTTGTTGCATAGGTCAACCCATCATCTAGGTTTTAAGACCCGCATGCATTAGGTATTTGTCCTAATGCTCTCCCTCCCCTTGCCCCTCACCCCCTGACAGGCCCCTGTGTGTGATGTTCCCCTCCCTGTGTCCATG... | AACCTGGGAGGCGGAGGTTGTAGTGAGCCAAGATTGTGCCACTGCACTCCAGCCTGGGCAACAAAGTGAGACTCCGTCTCAAAAAAAAAAAAAAGTCGAAAAAACTGAACTCCCCTTTTACTTTCTTCTACTTCTATTTTTTTTTTTTTAAATTTTACTTTAAGTTCTGGGATACATGTGCAGGTTTGTTGCATAGGTCAACCCATCATCTAGGTTTTAAGACCCGCATGCATTAGGTATTTGTCCTAATGCTCTCCCTCCCCTTGCCCCTCACCCCCTGACAGGCCCCTGTGTGTGATGTTCCCCTCCCTGTGTCCATG... |
Task1_train_45188 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | GAATGGCATGAACCCAGGAGGCAGAGCTTGCAGTGAGCCGAGATCACACCACCGCATGGATGGTGTGAGAGAGACTGCCTGGATGACAGAAAGAGACTCCATCTCAAAAAAAAAAAAAAAAGAAAAAAGAAAAAAAACAGAAAACCTGGGATCCCATATCCTAGTCCTGAGGGTTTTGGAGCAGAATAGGTCTCTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCGTTGTGTCACCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCAGCCACCACCTCCTGGGTTCAAGCGATTCTCCTTCCTCAGCCC... | GAATGGCATGAACCCAGGAGGCAGAGCTTGCAGTGAGCCGAGATCACACCACCGCATGGATGGTGTGAGAGAGACTGCCTGGATGACAGAAAGAGACTCCATCTCAAAAAAAAAAAAAAAAGAAAAAAGAAAAAAAACAGAAAACCTGGGATCCCATATCCTAGTCCTGAGGGTTTTGGAGCAGAATAGGTCTCTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCGTTGTGTCACCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCAGCCACCACCTCCTGGGTTCAAGCGATTCTCCTTCCTCAGCCC... |
Task1_train_45189 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TCGCTGCCCTCATTCCTTCAGCTTCGTGGAACTCAGAATTGTGCTTGGAGTCCTGGAAGAAATCACTTAGAAGCATATGTTAACAGCATCTCCTACTTGCCAAAGCAGGGAGCCATCAGGTAGATATTCTTTAAAAGCCAGCTGAAAATCTCAGGAAATAAGGAATGTTTTCGGAGTGGATAATTCAGGGCTACTAAATATACAAGCTTAAAGCAAAGCCAGCAGGACAAGATTGAAGCCAGGATTGCCTTCCTAGACAAGGAATAATCCAATCAGCCAATGAGAGACCTGGTCTGACCGGCATCATGCCAACACTTGTT... | TCGCTGCCCTCATTCCTTCAGCTTCGTGGAACTCAGAATTGTGCTTGGAGTCCTGGAAGAAATCACTTAGAAGCATATGTTAACAGCATCTCCTACTTGCCAAAGCAGGGAGCCATCAGGTAGATATTCTTTAAAAGCCAGCTGAAAATCTCAGGAAATAAGGAATGTTTTCGGAGTGGATAATTCAGGGCTACTAAATATACAAGCTTAAAGCAAAGCCAGCAGGACAAGATTGAAGCCAGGATTGCCTTCCTAGACAAGGAATAATCCAATCAGCCAATGAGAGACCTGGTCTGACCGGCATCATGCCAACACTTGTT... |
Task1_train_45190 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGAGTTGGAAGGCCTTCTGCAGACGGACCCATTCCACCTGAATCTCCATGACATATTGGACTTCTCCATATAATTTCATTTGGAAAGAAACTTGAGCATCTAAATAAAATGTTTGGAAACCACCATGCTACAAGACCAGCATGTGCTGTCTAGTTCTTACCCTCTGCAACAGTAAGATTCTGGGGCATTAAGACTTAGTTCCAGGATTCTGTCATTCTGCCAACGTTCTGTGGCTGGGGTTCTAAAGGAGCTTGCCTGGCTTAGAACTGCAAGTGACTCTAGTGTGATGGAGAGCACCAGCAAAGCCTTAGGGCCCATCC... | AGAGTTGGAAGGCCTTCTGCAGACGGACCCATTCCACCTGAATCTCCATGACATATTGGACTTCTCCATATAATTTCATTTGGAAAGAAACTTGAGCATCTAAATAAAATGTTTGGAAACCACCATGCTACAAGACCAGCATGTGCTGTCTAGTTCTTACCCTCTGCAACAGTAAGATTCTGGGGCATTAAGACTTAGTTCCAGGATTCTGTCATTCTGCCAACGTTCTGTGGCTGGGGTTCTAAAGGAGCTTGCCTGGCTTAGAACTGCAAGTGACTCTAGTGTGATGGAGAGCACCAGCAAAGCCTTAGGGCCCATCC... |
Task1_train_45191 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCATGTTTTGCAAGAGAATCTAAGGAAAATGGATCAATTCCCTATAATCAAATTAACATAAAAATTATAAACATGTTTTAAACCAGTATTTCTCAAACCTTTTGGTCTCAGCACCACTTTACTCTCTTAAAAATGATTAAGCACCCAAAAAGCTTTTGTTTATGTAAGCTCTATCTATAATATTTGTATTATAAAAACTGAGAAATTTTTAAAATATTTATTAATTCATTTAAATAATAAGCCCATTTTATGTTAATACACATAACATTTTAAATGAAAATTTACTACACTTTTGAAAACAAAAATATATATAGTGAGCT... | CCATGTTTTGCAAGAGAATCTAAGGAAAATGGATCAATTCCCTATAATCAAATTAACATAAAAATTATAAACATGTTTTAAACCAGTATTTCTCAAACCTTTTGGTCTCAGCACCACTTTACTCTCTTAAAAATGATTAAGCACCCAAAAAGCTTTTGTTTATGTAAGCTCTATCTATAATATTTGTATTATAAAAACTGAGAAATTTTTAAAATATTTATTAATTCATTTAAATAATAAGCCCATTTTATGTTAATACACATAACATTTTAAATGAAAATTTACTACACTTTTGAAAACAAAAATATATATAGTGAGCT... |
Task1_train_45192 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TTTTTTTTTTTTTTTTTGTAGAGACGGTTTTCACCATGTTGCCCAGCCTGGTCTTGAACTCCTGGGCTCAAGCAATTTGGCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGAGTGAGCTACCACACCCGGCCAAAAAAATTTTTTTATTGAGGTCTAATTCAACAGTCTTCAGCATATCTCAAGACTGCAGTATTTAGCTCACAGCCTTGGCTTAAAGATACACAAGTTCTACTATGCTTCTAATTAAGGCTTATTAAGGTTTATTAAAGTCAGCAGCATCAGCTCACCATCTCATCGAGCAGCACATTGCCATCTT... | TTTTTTTTTTTTTTTTTGTAGAGACGGTTTTCACCATGTTGCCCAGCCTGGTCTTGAACTCCTGGGCTCAAGCAATTTGGCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGAGTGAGCTACCACACCCGGCCAAAAAAATTTTTTTATTGAGGTCTAATTCAACAGTCTTCAGCATATCTCAAGACTGCAGTATTTAGCTCACAGCCTTGGCTTAAAGATACACAAGTTCTACTATGCTTCTAATTAAGGCTTATTAAGGTTTATTAAAGTCAGCAGCATCAGCTCACCATCTCATCGAGCAGCACATTGCCATCTT... |
Task1_train_45193 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCCCAGATGGACAGATTATGGAGATTTCATTCCAAATGGACTATTTACAGGTTTAAAGATAAAAGCACTTGATGAGTTACGAACTGTGGTTTGGTCAAAGAATACTTGGAAGTCTACAAAGCACAAATTCGCAAATTTCCTGCAGGTTTTAATTTTGGTGAATGTTTTCATTCATTCAGTCACTCAACTTAGTTTCCCTCATCCCTGCATTTATTAGATCACCAAGTTCTATCAATTCTACTACCTAAATATCTCTTGAATCTGCCACCTTCTCTCCATCTCCACTGTTATCATCTCTACTTTGGATGGCATCCGGATAT... | CCCCAGATGGACAGATTATGGAGATTTCATTCCAAATGGACTATTTACAGGTTTAAAGATAAAAGCACTTGATGAGTTACGAACTGTGGTTTGGTCAAAGAATACTTGGAAGTCTACAAAGCACAAATTCGCAAATTTCCTGCAGGTTTTAATTTTGGTGAATGTTTTCATTCATTCAGTCACTCAACTTAGTTTCCCTCATCCCTGCATTTATTAGATCACCAAGTTCTATCAATTCTACTACCTAAATATCTCTTGAATCTGCCACCTTCTCTCCATCTCCACTGTTATCATCTCTACTTTGGATGGCATCCGGATAT... |
Task1_train_45194 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TTTTCATTCATTCAGTCACTCAACTTAGTTTCCCTCATCCCTGCATTTATTAGATCACCAAGTTCTATCAATTCTACTACCTAAATATCTCTTGAATCTGCCACCTTCTCTCCATCTCCACTGTTATCATCTCTACTTTGGATGGCATCCGGATATCTCCAAACTTAAATATACCCTCCACACATTTTTCTTTCTAAAAGGCAACGTGATTCAGTCAGTTCCCTGATCAAAAGTCCTCCAATGATTTTTATGTTTTCCATCATTTTCAAGTTAAAATCCAAACACAGCAATGACATACTTGACCTTTCCCAATATCTTCC... | TTTTCATTCATTCAGTCACTCAACTTAGTTTCCCTCATCCCTGCATTTATTAGATCACCAAGTTCTATCAATTCTACTACCTAAATATCTCTTGAATCTGCCACCTTCTCTCCATCTCCACTGTTATCATCTCTACTTTGGATGGCATCCGGATATCTCCAAACTTAAATATACCCTCCACACATTTTTCTTTCTAAAAGGCAACGTGATTCAGTCAGTTCCCTGATCAAAAGTCCTCCAATGATTTTTATGTTTTCCATCATTTTCAAGTTAAAATCCAAACACAGCAATGACATACTTGACCTTTCCCAATATCTTCC... |
Task1_train_45195 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGCTGGAGTGCAGTGGCATGATCTCAGCTAACTGCAACCTCTGCCTCCTCGGTTCAAACGATTCTCATGCCTCAGCTTCCTAAGTAGCTGTGACTATGGGTGCACACATTGGGTGCACACTACGGGTGCTAATTTTTGTATTTTTAGCAGAGACGGGGTTTTACCGTGTTGGCCAGGCTGGTCTCGAAATCCGGCCTCAAGTGATCTGGCCACTTTGGCCTCCCAAAATGCCAGGATTACAGGCATGAGCCACCAAGCCTAGCCTGTGCCATCTTTCTAACCATAATTTTCTGTCTTTACACAAGCAGGAGAATCCTCCT... | GGCTGGAGTGCAGTGGCATGATCTCAGCTAACTGCAACCTCTGCCTCCTCGGTTCAAACGATTCTCATGCCTCAGCTTCCTAAGTAGCTGTGACTATGGGTGCACACATTGGGTGCACACTACGGGTGCTAATTTTTGTATTTTTAGCAGAGACGGGGTTTTACCGTGTTGGCCAGGCTGGTCTCGAAATCCGGCCTCAAGTGATCTGGCCACTTTGGCCTCCCAAAATGCCAGGATTACAGGCATGAGCCACCAAGCCTAGCCTGTGCCATCTTTCTAACCATAATTTTCTGTCTTTACACAAGCAGGAGAATCCTCCT... |
Task1_train_45196 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CGCGGGGGCTCACACCTGTAATTCCAGCACTTTGGAAAGCCGAGGCAGGCAGATCATGAGGTCAAGAGTTCGTAGACCAGCATGGCCAATATGGTGAAACCTTGTCTCTACTAAAAATACAAAAATCAGCTGGGCGTGGTGGGATGTGCCTGTAGTCCCAGCTACTTGGGAGGCCAAGGCAGGAGAATTGCTTGAACCCCGGAGGCCGACATTGCAGCAAGCCGAGATTGCGCCACTGCACTCCAGCCTGAGTGACACAGCAAGACTCCGTCTCAAACAAACAAACAAACAAACAAACAATTTTTTTTTTTTAGAGATAG... | CGCGGGGGCTCACACCTGTAATTCCAGCACTTTGGAAAGCCGAGGCAGGCAGATCATGAGGTCAAGAGTTCGTAGACCAGCATGGCCAATATGGTGAAACCTTGTCTCTACTAAAAATACAAAAATCAGCTGGGCGTGGTGGGATGTGCCTGTAGTCCCAGCTACTTGGGAGGCCAAGGCAGGAGAATTGCTTGAACCCCGGAGGCCGACATTGCAGCAAGCCGAGATTGCGCCACTGCACTCCAGCCTGAGTGACACAGCAAGACTCCGTCTCAAACAAACAAACAAACAAACAAACAATTTTTTTTTTTTAGAGATAG... |
Task1_train_45197 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTTAATAATCAGCTCAGGGCTGGGTGCGGTGACGCACGCCTGTGATCCCAGCACTTTGGGAGGCCCAGGCGGGCAGATCACTTGAGCCCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCAGCTCTACTAAAAATACAAAAATTAGCCAGGCTTGGTGGCACACGCCTTTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGACAGAAGTTGCAGTGAGCCGAGATCGCACCACTGGTGCGACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAGAAGAAGAAAGAAAAAG... | TTTAATAATCAGCTCAGGGCTGGGTGCGGTGACGCACGCCTGTGATCCCAGCACTTTGGGAGGCCCAGGCGGGCAGATCACTTGAGCCCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCAGCTCTACTAAAAATACAAAAATTAGCCAGGCTTGGTGGCACACGCCTTTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGACAGAAGTTGCAGTGAGCCGAGATCGCACCACTGGTGCGACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAGAAGAAGAAAGAAAAAG... |
Task1_train_45198 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | AACGGTACTGAGGACAAACCTTGAATACACCCCTACCCCCGTGACCCTCATCACCCTGAAATACTTTCTGTTCTTTTGTTTTTGAGACAGGGTCTCACTCTCACCCATGCTGGGGTGCATTGCTGTAATAATGGCTCACTGCAGCCTCAAACTCCAGGGCTCAAGTGATCCTCCCACCACAGCCTCCGAAAGTGCTGGAATTATAGGTGTCAGCCACCATGCTTGGCCCTGAGCTACTTTCAAATTTTCCTGAGCTACAAAATCAACAATGTCCTCAAGGATCAAGAGATAAACTACATCTTAATTTAGGCAGGGTACTA... | AACGGTACTGAGGACAAACCTTGAATACACCCCTACCCCCGTGACCCTCATCACCCTGAAATACTTTCTGTTCTTTTGTTTTTGAGACAGGGTCTCACTCTCACCCATGCTGGGGTGCATTGCTGTAATAATGGCTCACTGCAGCCTCAAACTCCAGGGCTCAAGTGATCCTCCCACCACAGCCTCCGAAAGTGCTGGAATTATAGGTGTCAGCCACCATGCTTGGCCCTGAGCTACTTTCAAATTTTCCTGAGCTACAAAATCAACAATGTCCTCAAGGATCAAGAGATAAACTACATCTTAATTTAGGCAGGGTACTA... |
Task1_train_45199 | 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 | CCAGGGCTCAAGTGATCCTCCCACCACAGCCTCCGAAAGTGCTGGAATTATAGGTGTCAGCCACCATGCTTGGCCCTGAGCTACTTTCAAATTTTCCTGAGCTACAAAATCAACAATGTCCTCAAGGATCAAGAGATAAACTACATCTTAATTTAGGCAGGGTACTATTATAAGGTGATAGCAAACTTCAATGCAAAGGGCTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGACTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCCTCCTCCCAGGTTCAAGCAATTCTTCTGCTTCAGCCTCCCAA... | CCAGGGCTCAAGTGATCCTCCCACCACAGCCTCCGAAAGTGCTGGAATTATAGGTGTCAGCCACCATGCTTGGCCCTGAGCTACTTTCAAATTTTCCTGAGCTACAAAATCAACAATGTCCTCAAGGATCAAGAGATAAACTACATCTTAATTTAGGCAGGGTACTATTATAAGGTGATAGCAAACTTCAATGCAAAGGGCTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGACTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCCTCCTCCCAGGTTCAAGCAATTCTTCTGCTTCAGCCTCCCAA... |
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