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_33600 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCCAGTCCTGTGCGCCCGCCTCTTAAGCAGTGCTCCTGTCTGCAGTGCCCCGAGTGGTGAAGTTTATGTCTGGGCTGAGCACCGTGGTCGCAGAGGAGGGCGGCGAGGCCACCTTCCAGTGCGTGGTGTCCCCCAGTGATGTGGCAGTCGTGTGGTTCCGGGACGGTGCCCTGCTTCAGCCCAGCGAGAAGTTTGCCATATCACAGAGTGGCGCCAGCCACAGCCTGACCATCTCAGACCTGGTGCTGGAGGACGCGGGCCAGATCACCGTGGAGGCTGAGGGCGCCTCATCCTCTGCTGCCCTGAGGGTCCGAGGTGAG... | GCCAGTCCTGTGCGCCCGCCTCTTAAGCAGTGCTCCTGTCTGCAGTGCCCCGAGTGGTGAAGTTTATGTCTGGGCTGAGCACCGTGGTCGCAGAGGAGGGCGGCGAGGCCACCTTCCAGTGCGTGGTGTCCCCCAGTGATGTGGCAGTCGTGTGGTTCCGGGACGGTGCCCTGCTTCAGCCCAGCGAGAAGTTTGCCATATCACAGAGTGGCGCCAGCCACAGCCTGACCATCTCAGACCTGGTGCTGGAGGACGCGGGCCAGATCACCGTGGAGGCTGAGGGCGCCTCATCCTCTGCTGCCCTGAGGGTCCGAGGTGAG... |
Task1_train_33601 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCAGGGCCGCGCTGTTTGGATTGGGATCCCGGGGCGCGGTGCCGGCAGCTCTGCCTGGGCCCGGCTCAGGGCAGGCGCCGGGGCTGTGCGGGCCCTCTGTACCTTGGCTTGTCCGTGGAGGAGGGCGAGGGCCGCCGTGACCTCCCCTCTCCTGCGACCCCAGAGGCGCCTGTGCTGTTCAAAAAGAAGCTGGAGCCGCAGACGGTGGAGGAGCGGAGCTCGGTGACCCTGGAGGTGGAGCTGACGCGGCCGTGGCCGGAGCTGAGGTGGACACGGAACGCGACGGCCCTGGCGCCGGGAAAGAACGTGGAGATCCACGC... | CCAGGGCCGCGCTGTTTGGATTGGGATCCCGGGGCGCGGTGCCGGCAGCTCTGCCTGGGCCCGGCTCAGGGCAGGCGCCGGGGCTGTGCGGGCCCTCTGTACCTTGGCTTGTCCGTGGAGGAGGGCGAGGGCCGCCGTGACCTCCCCTCTCCTGCGACCCCAGAGGCGCCTGTGCTGTTCAAAAAGAAGCTGGAGCCGCAGACGGTGGAGGAGCGGAGCTCGGTGACCCTGGAGGTGGAGCTGACGCGGCCGTGGCCGGAGCTGAGGTGGACACGGAACGCGACGGCCCTGGCGCCGGGAAAGAACGTGGAGATCCACGC... |
Task1_train_33602 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | CGCCCGCTGCGGGACAAGATTGCCATGGAGAAGCACCGCGGTGTGCTGGAGTGTCAGGTGTCCCGGGCCAGCGCCCAGGTGCGGTGGTTCAAGGGCAGTCAGGAGCTGCAGCCCGGGCCCAAGTACGAGCTGGTCAGTGATGGCCTCTACCGCAAGCTGATCATCAGTGATGTCCACGCAGAGGACGAGGACACCTACACCTGTGACGCCGGTGATGTCAAGACCAGTGCACAGTTCTTCGTGGAAGGTGCAGGCAGGGAGGGCAGCTCTGCAGGTTGCTTTTGTTGGGGGGAGTCTCCCAGGTCCATGGTTTGCCCTAC... | CGCCCGCTGCGGGACAAGATTGCCATGGAGAAGCACCGCGGTGTGCTGGAGTGTCAGGTGTCCCGGGCCAGCGCCCAGGTGCGGTGGTTCAAGGGCAGTCAGGAGCTGCAGCCCGGGCCCAAGTACGAGCTGGTCAGTGATGGCCTCTACCGCAAGCTGATCATCAGTGATGTCCACGCAGAGGACGAGGACACCTACACCTGTGACGCCGGTGATGTCAAGACCAGTGCACAGTTCTTCGTGGAAGGTGCAGGCAGGGAGGGCAGCTCTGCAGGTTGCTTTTGTTGGGGGGAGTCTCCCAGGTCCATGGTTTGCCCTAC... |
Task1_train_33603 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGGACCTGGAGGATGTGGATGTGCAGGAGGGCTCCTCGGCCACCTTCCGTTGCCGGATCTCCCCGGCCAACTACGAGCCTGTGCACTGGTTCCTGGACAAGACACCCCTGCATGCCAACGAGCTCAATGAGATCGATGCCCAGCCCGGGGGCTACCACGTGCTGACCCTGCGGCAGCTGGCGCTCAAGGACTCGGGCACCATCTACTTTGAGGCGGGTGACCAGCGGGCCTCGGCCGCCCTGCGGGTCACTGGTGGGTTGCATGCCCGCATTGCACATGTTGCTCAGAGCTGCAGACAGGTGGAGAGGTGGATGGCAGCT... | AGGACCTGGAGGATGTGGATGTGCAGGAGGGCTCCTCGGCCACCTTCCGTTGCCGGATCTCCCCGGCCAACTACGAGCCTGTGCACTGGTTCCTGGACAAGACACCCCTGCATGCCAACGAGCTCAATGAGATCGATGCCCAGCCCGGGGGCTACCACGTGCTGACCCTGCGGCAGCTGGCGCTCAAGGACTCGGGCACCATCTACTTTGAGGCGGGTGACCAGCGGGCCTCGGCCGCCCTGCGGGTCACTGGTGGGTTGCATGCCCGCATTGCACATGTTGCTCAGAGCTGCAGACAGGTGGAGAGGTGGATGGCAGCT... |
Task1_train_33604 | Here is a variant on Chromosome 1. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GTGTCTTTTCTGTGTCATCCATGTCCTGTCTCTTCTGTGGGCTCAGAGGCATGATTGTGTCCATATCTTCTGACCTCCCCAGCCCTGCCCGCCAAGTTCACAAAGGGTCTGAGGAATGAAGAGGCCACAGAAGGGGCCACGGCTATGTTGCAGTGTGAGCTGAGCAAGGTGGCCCCTGTTGAGTGGAGGAAGGGACCTGAAACCCTCAGAGATGGGGACAGATACAACCTGAGGCAGGATGGGACCAGATGTGAGCTGCAGATTCATGGCCTGTCCGTGGCAGACACTGGGGAGTACTCATGTGTATGTGGTCAGGAGAA... | GTGTCTTTTCTGTGTCATCCATGTCCTGTCTCTTCTGTGGGCTCAGAGGCATGATTGTGTCCATATCTTCTGACCTCCCCAGCCCTGCCCGCCAAGTTCACAAAGGGTCTGAGGAATGAAGAGGCCACAGAAGGGGCCACGGCTATGTTGCAGTGTGAGCTGAGCAAGGTGGCCCCTGTTGAGTGGAGGAAGGGACCTGAAACCCTCAGAGATGGGGACAGATACAACCTGAGGCAGGATGGGACCAGATGTGAGCTGCAGATTCATGGCCTGTCCGTGGCAGACACTGGGGAGTACTCATGTGTATGTGGTCAGGAGAA... |
Task1_train_33605 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TCTGGGCTTTGCCAACTGCAGTTTCTCTCTCTTTGTGAGGAGGCTCACAGGATGGTCTCAGAAAGTTTCTTGGGCAAGCAAGGATGGAGGGCATCTCTGTTGCCCGATCCCAGGCAGCAGGTGGTGGAATAAGCCTTTGGTTCTGTCTTCCTCCCTTGCCTGTGGGGTGTGGGGTTCAACTCTGTGGGCAGCAGTAGCCTGGGCACATTCTCCTATCTGCCGTGACCACCCTGAGTTTCCATCTGAGAAGTGGGTGGGAGGGAGGAGGAGAGTGTGGAAGGCACAGGGCAGGCAGTGACCACAAACATGTCTGGGAAGCT... | TCTGGGCTTTGCCAACTGCAGTTTCTCTCTCTTTGTGAGGAGGCTCACAGGATGGTCTCAGAAAGTTTCTTGGGCAAGCAAGGATGGAGGGCATCTCTGTTGCCCGATCCCAGGCAGCAGGTGGTGGAATAAGCCTTTGGTTCTGTCTTCCTCCCTTGCCTGTGGGGTGTGGGGTTCAACTCTGTGGGCAGCAGTAGCCTGGGCACATTCTCCTATCTGCCGTGACCACCCTGAGTTTCCATCTGAGAAGTGGGTGGGAGGGAGGAGGAGAGTGTGGAAGGCACAGGGCAGGCAGTGACCACAAACATGTCTGGGAAGCT... |
Task1_train_33606 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ATGCTTCCTGCGGGCTCCTGGGATCAGGAATTGGCCCCCAGGGCCACAGAGTGGGCACCACTCTATGCATGCTGTCTGCCTGCAGTGGCACAGGTGGGCATGGAGGGTGGATGAGAAGTCTGGGCTTAGGGAGTGGTATAGCTGGACACCAACCTGTGCCCTGCTGGCTACCACCTTGCTGGCCGCACGTGCCCAGCCATGAAACCCAGTCCCTTGTGAAGGCAAGAGCAGCCCCTGCTGAGCCTACCCCTGCTGTCACCTGCTTCCTCCGCTGTGGGCTCAGGCTGGGTTTCTGCCCTTCTGGGAAAGAGCTGGCCGTA... | ATGCTTCCTGCGGGCTCCTGGGATCAGGAATTGGCCCCCAGGGCCACAGAGTGGGCACCACTCTATGCATGCTGTCTGCCTGCAGTGGCACAGGTGGGCATGGAGGGTGGATGAGAAGTCTGGGCTTAGGGAGTGGTATAGCTGGACACCAACCTGTGCCCTGCTGGCTACCACCTTGCTGGCCGCACGTGCCCAGCCATGAAACCCAGTCCCTTGTGAAGGCAAGAGCAGCCCCTGCTGAGCCTACCCCTGCTGTCACCTGCTTCCTCCGCTGTGGGCTCAGGCTGGGTTTCTGCCCTTCTGGGAAAGAGCTGGCCGTA... |
Task1_train_33607 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATGGACGAGCGGGAGGTGCACACGGATGGGCACCGTGTCATCATAGAGCAGGACTGGAACGTGGCCAGGCTGACCTTCAGGCCGGCCTTGCCCTGTGACAGTGGCATCTATTCTTGTGAGGCTGCGGGCACCCGCGTAGTGGCCCTGCTGCAAGTGCAAGGTGAGGCCGCCTGGTGAGCAGCCCTAGGCCCGGGGCAGCTTTGGCACAGCTTGGGCTGTGCAGTGATAGTGGAATGGCAGGCAGTGTCCGGTGGCGCTGGGACACAGGTGGCTCGGACAGGTGGGAACAGGCCCCGTAGGTGGCAAGCTCGCTGCACCAG... | ATGGACGAGCGGGAGGTGCACACGGATGGGCACCGTGTCATCATAGAGCAGGACTGGAACGTGGCCAGGCTGACCTTCAGGCCGGCCTTGCCCTGTGACAGTGGCATCTATTCTTGTGAGGCTGCGGGCACCCGCGTAGTGGCCCTGCTGCAAGTGCAAGGTGAGGCCGCCTGGTGAGCAGCCCTAGGCCCGGGGCAGCTTTGGCACAGCTTGGGCTGTGCAGTGATAGTGGAATGGCAGGCAGTGTCCGGTGGCGCTGGGACACAGGTGGCTCGGACAGGTGGGAACAGGCCCCGTAGGTGGCAAGCTCGCTGCACCAG... |
Task1_train_33608 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GGCCAGGCCCTCTGCTCCGCCAGCCTGCACGTCTCGGGCCGTGAGTGGGGGTGGGGGGATGGGGGGATGGGGGGCTGGGGCATGGGGGGTGGGCACTGGGTGGCTTTGGGGTCTCCTTGGGGCACACTGCCCATCACCACCATCTTGGCTGGGACCCTGTGGGACCCCCTCCTTCCTCTTTTCATTCTCTGACAGCACCAGGGAGACCCCAAAATGGGTCAGGCCCTGGTGGTGCTGGTGGTTTTGAGCCTCAGAGTCGCCTCTGGGCCCAGGCCCCGTGGGTTCTGCACCGCTGGCTCCAGAGACATTTCCTGAAGCCC... | GGCCAGGCCCTCTGCTCCGCCAGCCTGCACGTCTCGGGCCGTGAGTGGGGGTGGGGGGATGGGGGGATGGGGGGCTGGGGCATGGGGGGTGGGCACTGGGTGGCTTTGGGGTCTCCTTGGGGCACACTGCCCATCACCACCATCTTGGCTGGGACCCTGTGGGACCCCCTCCTTCCTCTTTTCATTCTCTGACAGCACCAGGGAGACCCCAAAATGGGTCAGGCCCTGGTGGTGCTGGTGGTTTTGAGCCTCAGAGTCGCCTCTGGGCCCAGGCCCCGTGGGTTCTGCACCGCTGGCTCCAGAGACATTTCCTGAAGCCC... |
Task1_train_33609 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GAGCTCCGTGGTCCCTTACGGCAGCCCCCTCCTGCCCAGCTCTGTGATCCAGGAGCTGCTGAGTTCTGAGCAGGCCTTCGTGGAGGAGCTGCAGTTCCTGCAGAGCCACCACCTGCAGCACCTGGAGCGCTGCCCCCACGTGCCCATAGCTGTGGCCGGCCAGAAGGCAGTCATCTTCCGCAATGTGCGGGACATCGGCCGCTTCCACAGCAGGTGGGTGGGTGGGGCCACACACACACACACACACACACACACACACACACGTCCATGCATGGACACACTGTAGGGCCAGGCCTCCTGCAGGTGGGTTGGAGCCAAGG... | GAGCTCCGTGGTCCCTTACGGCAGCCCCCTCCTGCCCAGCTCTGTGATCCAGGAGCTGCTGAGTTCTGAGCAGGCCTTCGTGGAGGAGCTGCAGTTCCTGCAGAGCCACCACCTGCAGCACCTGGAGCGCTGCCCCCACGTGCCCATAGCTGTGGCCGGCCAGAAGGCAGTCATCTTCCGCAATGTGCGGGACATCGGCCGCTTCCACAGCAGGTGGGTGGGTGGGGCCACACACACACACACACACACACACACACACACACGTCCATGCATGGACACACTGTAGGGCCAGGCCTCCTGCAGGTGGGTTGGAGCCAAGG... |
Task1_train_33610 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | AGATGGAGCCCTGAGTTAGATGAAAGCAAAACTAAATGAGAGAGAGACAGTACTTTGGACAAAGCAGACAGCTGGCAGTAGCTCACTTGGTGACGACTTTGTCACCTCATACATGCCACATCCCTTGTCTTGAGCCTGAGGGAAGTGCAAGGCTGAGGGCAAAATGAGTAACAGGCAGGGAACTGGTATGTGTTGTGTGTTACTCAGCACGTTCTGCTTCCCTACGTGTTAACTCAGTTTGCTCTCAGTGCTCAGCAAGGTCAGGGGCACCGGGCACCAGAGGAGGACCTGGGCTGACTGCTCTGCTTCTCCCTCTTGGC... | AGATGGAGCCCTGAGTTAGATGAAAGCAAAACTAAATGAGAGAGAGACAGTACTTTGGACAAAGCAGACAGCTGGCAGTAGCTCACTTGGTGACGACTTTGTCACCTCATACATGCCACATCCCTTGTCTTGAGCCTGAGGGAAGTGCAAGGCTGAGGGCAAAATGAGTAACAGGCAGGGAACTGGTATGTGTTGTGTGTTACTCAGCACGTTCTGCTTCCCTACGTGTTAACTCAGTTTGCTCTCAGTGCTCAGCAAGGTCAGGGGCACCGGGCACCAGAGGAGGACCTGGGCTGACTGCTCTGCTTCTCCCTCTTGGC... |
Task1_train_33611 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | CAACTTCGGGACAGTGGGGGAGACGGTCACCCTTCACATCTGCCCAGACAGGGATGGGGATGAGGCGGCACAGCCCTGATGCTGCTGCCATGGTGGCTTGGGGCAGCGGGGAGAAAGGAGTGTCCTTGAGGCCTAGGACGCTGCCCGGCCTCAGCAGCAGCCCTGGGAGCCTCCTGAGGGCCCTCCCTGTCCCTGGCCACGGGCCCTTCTTACCTCACTCAACTTCAGCCAGGAGGACTGGGTGGTGCTTGCAATGTTGGAATGACCGGCTCAAAGACCTCAGCTCTGGGCTGTTTCCTGTCAGCCTGGCAGGAGCCTCA... | CAACTTCGGGACAGTGGGGGAGACGGTCACCCTTCACATCTGCCCAGACAGGGATGGGGATGAGGCGGCACAGCCCTGATGCTGCTGCCATGGTGGCTTGGGGCAGCGGGGAGAAAGGAGTGTCCTTGAGGCCTAGGACGCTGCCCGGCCTCAGCAGCAGCCCTGGGAGCCTCCTGAGGGCCCTCCCTGTCCCTGGCCACGGGCCCTTCTTACCTCACTCAACTTCAGCCAGGAGGACTGGGTGGTGCTTGCAATGTTGGAATGACCGGCTCAAAGACCTCAGCTCTGGGCTGTTTCCTGTCAGCCTGGCAGGAGCCTCA... |
Task1_train_33612 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | ATCAGGGTCAGCCCCACACTATGCAGGGGGAGCCTGAGGCCAACAGGGGCAGGGCCTCTGGGCAACAGGGCATGTGAGCACAGAACTGTGGCTGTGGCCCGACCTCTGCCCAGCCCAGAGGACGTTTGTCCCTGTGCGTTAGTGAGAGGGCTGTGGGAACCTCAGGCTGGAACCACATTTCAGTGCCCCAGCCCCCAACCCCCAGCAGGAGGCAGGGAGAACTGCAAGGAGCTCAGGGACAGGGGGTCGCTGTCACCTCTGACCTCTGGCCTTTGCCATCTGCCCCACCTGGACATCTTGGGTGAGGGCTGTGGTGTCCT... | ATCAGGGTCAGCCCCACACTATGCAGGGGGAGCCTGAGGCCAACAGGGGCAGGGCCTCTGGGCAACAGGGCATGTGAGCACAGAACTGTGGCTGTGGCCCGACCTCTGCCCAGCCCAGAGGACGTTTGTCCCTGTGCGTTAGTGAGAGGGCTGTGGGAACCTCAGGCTGGAACCACATTTCAGTGCCCCAGCCCCCAACCCCCAGCAGGAGGCAGGGAGAACTGCAAGGAGCTCAGGGACAGGGGGTCGCTGTCACCTCTGACCTCTGGCCTTTGCCATCTGCCCCACCTGGACATCTTGGGTGAGGGCTGTGGTGTCCT... |
Task1_train_33613 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | GAGAACTGAGTTTCTCGGGCGCATGACCCATTGCACCATCTTCCCACGTTCCTTCCATGCCCATCCCTCCAGCCTATGCAGGAGTGGGCTGCTTCCCGTTCCATGCCTCAATCAAAGTCGAGTTACAAGCACAACACAGTTCCCTGGGGCGTGTTTCTGAGGTGGTCAGGATGGGGGCTACAGGCCTAGCTCTGGGACCCCTGGCCCAATGCCCAGAGTGGGCCGGCCTGCTTGAACCTGTGCAGGGCAACCCAGTGAAGCCCAGCAGCCCCACCAAGGGCCCTTCTGACCAGAGGCTCGGCCCCTGCACAGGGTTCTGG... | GAGAACTGAGTTTCTCGGGCGCATGACCCATTGCACCATCTTCCCACGTTCCTTCCATGCCCATCCCTCCAGCCTATGCAGGAGTGGGCTGCTTCCCGTTCCATGCCTCAATCAAAGTCGAGTTACAAGCACAACACAGTTCCCTGGGGCGTGTTTCTGAGGTGGTCAGGATGGGGGCTACAGGCCTAGCTCTGGGACCCCTGGCCCAATGCCCAGAGTGGGCCGGCCTGCTTGAACCTGTGCAGGGCAACCCAGTGAAGCCCAGCAGCCCCACCAAGGGCCCTTCTGACCAGAGGCTCGGCCCCTGCACAGGGTTCTGG... |
Task1_train_33614 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CAGGACATTCCAGAACACCTGGAAACTATGGAGACAGTGAAAACATCAGTGGTGGCCAGGAGTTAGGGGAGATGAATGAATGAGCGGAGCACGGAGGATTAAGGGCAGTGACATTATTTTGTATGATACTATGACAGATATGTGGCATTATATATTTATCTAGAACCATGGGACACCATGCCAAGAGTGAGCCCTCATGAAAACTGCACTCTGGGTGCTGACGGCATTGTCAACGGAAGTTCATCAAACATGGTGGACGTTCCTTCTGGTGTAGGGTTTTTATGCTGGGGGAAGGTGTGTGAGGGGGTTAGGGGAAGATG... | CAGGACATTCCAGAACACCTGGAAACTATGGAGACAGTGAAAACATCAGTGGTGGCCAGGAGTTAGGGGAGATGAATGAATGAGCGGAGCACGGAGGATTAAGGGCAGTGACATTATTTTGTATGATACTATGACAGATATGTGGCATTATATATTTATCTAGAACCATGGGACACCATGCCAAGAGTGAGCCCTCATGAAAACTGCACTCTGGGTGCTGACGGCATTGTCAACGGAAGTTCATCAAACATGGTGGACGTTCCTTCTGGTGTAGGGTTTTTATGCTGGGGGAAGGTGTGTGAGGGGGTTAGGGGAAGATG... |
Task1_train_33615 | Consider a variant on Chromosome 1. Determine its clinical classification and disease relevance. | Benign | TGGCCAACATAGTGAAAACCTGTCTCTACTAAAAATACAAAAACTAGCCGGGAGTGGTGGCACCCACCTATAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGAATCGCTTGAACCGGGAGGCAAAGGTTGCAGTGAGCCAAGACCATGCCATTGTACTCCAGCCTGGGTGACAGAGTGAGACTCAGTCTCAAAAAAAAATAAAAAGAAAAAAGAAAAATGTCTGTATTATATGCCCATAGTGGGCTGTCCTAGCAGTAGTCCTACATTTCCAAAAGTCTGGTAAAGACAAAAACAGGTAAACTGTATTTAATTAAAACG... | TGGCCAACATAGTGAAAACCTGTCTCTACTAAAAATACAAAAACTAGCCGGGAGTGGTGGCACCCACCTATAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGAATCGCTTGAACCGGGAGGCAAAGGTTGCAGTGAGCCAAGACCATGCCATTGTACTCCAGCCTGGGTGACAGAGTGAGACTCAGTCTCAAAAAAAAATAAAAAGAAAAAAGAAAAATGTCTGTATTATATGCCCATAGTGGGCTGTCCTAGCAGTAGTCCTACATTTCCAAAAGTCTGGTAAAGACAAAAACAGGTAAACTGTATTTAATTAAAACG... |
Task1_train_33616 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GTTTTCCAGCAATAACACTTTCTCCTAATAAGCTATTCTATTGAAACTAAGACAACTTAGACGAGCAAAGTTCTGGAAGTCTGTTTAATATTGTTCATTCCTACTTTCTATCAACAACAGCAAGAATTACTGCTCTCTGGTTCCAAAGGATGCAGGGCAGCAGATTTTTTAAATGGCTAGGATGGCATGTTCAGAAGGAATTACTCTACAATGGGACAGAGGCCTTGTAAATGGACTCCCCTATTCAAACAATAAGGCACTTAGTATTCTATACCAAGGCCATCATCTGGCCCTGTTTTGGTCAAGGGTATCTCTGAGGA... | GTTTTCCAGCAATAACACTTTCTCCTAATAAGCTATTCTATTGAAACTAAGACAACTTAGACGAGCAAAGTTCTGGAAGTCTGTTTAATATTGTTCATTCCTACTTTCTATCAACAACAGCAAGAATTACTGCTCTCTGGTTCCAAAGGATGCAGGGCAGCAGATTTTTTAAATGGCTAGGATGGCATGTTCAGAAGGAATTACTCTACAATGGGACAGAGGCCTTGTAAATGGACTCCCCTATTCAAACAATAAGGCACTTAGTATTCTATACCAAGGCCATCATCTGGCCCTGTTTTGGTCAAGGGTATCTCTGAGGA... |
Task1_train_33617 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TTTCTTTCTTAATGTTCAGATCATCAATGAGAGAGTAGCTGAGTTCTCTCTTTCGGGATCCCAAAGAAACATCTGTGCTGTCCTTCGATGTTGCCAGGGCATCCTGTCGACACCTGCCCTGGCTGTCATCTACACGGCCAAACAGGAGCTGATGGTGGCCTTGCTGAGCCAGCTTTGCTGGTCGGCCTGCAGGCAGCCCGAAGGAGCTGTGGTAGCCCAGTTGTTTGAGGTCATTCACCTGGCCCTTGGCCATTATCTCTTGATCCTGCAGCAGCAGGTCAACCCAAGACGTGCCTTTGGGGATGTGACTGCTCACCTGC... | TTTCTTTCTTAATGTTCAGATCATCAATGAGAGAGTAGCTGAGTTCTCTCTTTCGGGATCCCAAAGAAACATCTGTGCTGTCCTTCGATGTTGCCAGGGCATCCTGTCGACACCTGCCCTGGCTGTCATCTACACGGCCAAACAGGAGCTGATGGTGGCCTTGCTGAGCCAGCTTTGCTGGTCGGCCTGCAGGCAGCCCGAAGGAGCTGTGGTAGCCCAGTTGTTTGAGGTCATTCACCTGGCCCTTGGCCATTATCTCTTGATCCTGCAGCAGCAGGTCAACCCAAGACGTGCCTTTGGGGATGTGACTGCTCACCTGC... |
Task1_train_33618 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TGGCCCTTGGCCATTATCTCTTGATCCTGCAGCAGCAGGTCAACCCAAGACGTGCCTTTGGGGATGTGACTGCTCACCTGCTCCAGCCGTGCCTGGTCCTGAGGCACTTACTCTCTGGGGGCACATGGACGCAGGCTGGCCAGGGCCAGCTGAGGCAGGTGCTGAGCCGGGACATCAGGAGTCAGATTGAGGCCATGTTCCGAGGAGGGATTTTTCAGCCTGAGCTACTGTCATCCTACAAGGAGGGGCTCTTGGACCAGCAGCAAGGGGATGTGAAGACGGGAGCCATGAAGAACCTTCTGGCTCCCATGGACACCGTG... | TGGCCCTTGGCCATTATCTCTTGATCCTGCAGCAGCAGGTCAACCCAAGACGTGCCTTTGGGGATGTGACTGCTCACCTGCTCCAGCCGTGCCTGGTCCTGAGGCACTTACTCTCTGGGGGCACATGGACGCAGGCTGGCCAGGGCCAGCTGAGGCAGGTGCTGAGCCGGGACATCAGGAGTCAGATTGAGGCCATGTTCCGAGGAGGGATTTTTCAGCCTGAGCTACTGTCATCCTACAAGGAGGGGCTCTTGGACCAGCAGCAAGGGGATGTGAAGACGGGAGCCATGAAGAACCTTCTGGCTCCCATGGACACCGTG... |
Task1_train_33619 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | GCTCCTGTGGGCCAGCAGATAACAGCCCCCACGAGGCTCCCTCCTCCCAGCTAGGTTAATCACATGTGAAACGGAAGTAATAATGCTGCTGCCCCACGTCCCTCCGGAGGATTCATGGCAGAAACACCTTTCTGAGCATTATTTCCACACCCAGCCTCTTGTTTTAAGCGAATACGAGCTCCCCATCTGGAGGGACCTGCTGATAACCTCGTGAGAAGACCTATAGATCCGCTGGGGTGGAGGAGCCATCTGCACTTCATCTTCTTAAAGGGACTGTCAGGCAGGTCGTGCCTTAATGCGGCACATTCCTTATTCTAAAT... | GCTCCTGTGGGCCAGCAGATAACAGCCCCCACGAGGCTCCCTCCTCCCAGCTAGGTTAATCACATGTGAAACGGAAGTAATAATGCTGCTGCCCCACGTCCCTCCGGAGGATTCATGGCAGAAACACCTTTCTGAGCATTATTTCCACACCCAGCCTCTTGTTTTAAGCGAATACGAGCTCCCCATCTGGAGGGACCTGCTGATAACCTCGTGAGAAGACCTATAGATCCGCTGGGGTGGAGGAGCCATCTGCACTTCATCTTCTTAAAGGGACTGTCAGGCAGGTCGTGCCTTAATGCGGCACATTCCTTATTCTAAAT... |
Task1_train_33620 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GTTCTTGATTTAGCTGATGCTTTGACACATGACAGGCAGTCCCTCCAGTGGCCAGAATCAGATTCCGTTCATTCCGAATTCTTTGTTGAGAAGATTCCTGGCTGCTCAGAGTAACAGGGCAGCCTCAATACATACACACTTTACATGACAATGGGGAAAAACAGCATGAGGGGTGATTGACAGCAACGAGGGAGCTGGAAATGAAAGAGGCAATGACAGGCACTTAGCAAAAGCCTCCCCGGCTCCTCTGATTGCACTGTCTTTCCCTGCTGGCAAGAACTCCAGGTGAGCAGGTGGACGGAAATAAGGAAAGCAGGGTA... | GTTCTTGATTTAGCTGATGCTTTGACACATGACAGGCAGTCCCTCCAGTGGCCAGAATCAGATTCCGTTCATTCCGAATTCTTTGTTGAGAAGATTCCTGGCTGCTCAGAGTAACAGGGCAGCCTCAATACATACACACTTTACATGACAATGGGGAAAAACAGCATGAGGGGTGATTGACAGCAACGAGGGAGCTGGAAATGAAAGAGGCAATGACAGGCACTTAGCAAAAGCCTCCCCGGCTCCTCTGATTGCACTGTCTTTCCCTGCTGGCAAGAACTCCAGGTGAGCAGGTGGACGGAAATAAGGAAAGCAGGGTA... |
Task1_train_33621 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AATATGGGGTAATTAATATGCTGCTTGGCCTTTGCAGTACCCTCTCTGTTTCCTCTGTACCACCTAAGATGAAGTCTAGTTTTGCTACTTTTGTTTAGTAATCATAAGGATTTAGTTGGATTTGGGGATAAGAACATAGTAGAAATCATGATGTAAAATGAAGCCATAGATATGAAACAATCAGCCATTAGATTTGACAGGGCCAGTCTGGGTCCAGAGATGTCAAGCTTCAAAGCTTTAGTGGATCTTTTCCACAGTTTTTAGTGTGGGGGAATTCATGTAGAAGGCTTAGAGATTTGAGGAATCTGAACTGTACCTTG... | AATATGGGGTAATTAATATGCTGCTTGGCCTTTGCAGTACCCTCTCTGTTTCCTCTGTACCACCTAAGATGAAGTCTAGTTTTGCTACTTTTGTTTAGTAATCATAAGGATTTAGTTGGATTTGGGGATAAGAACATAGTAGAAATCATGATGTAAAATGAAGCCATAGATATGAAACAATCAGCCATTAGATTTGACAGGGCCAGTCTGGGTCCAGAGATGTCAAGCTTCAAAGCTTTAGTGGATCTTTTCCACAGTTTTTAGTGTGGGGGAATTCATGTAGAAGGCTTAGAGATTTGAGGAATCTGAACTGTACCTTG... |
Task1_train_33622 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | TTGTTATTTCTTTGTAGTTAATGCCTTTTTTCTCTGGCTGCTTTTAAGATCTTCTGTGTGACTTTGGTGTGCTAAGTAAGTTCTGCTATGATATGTCCAGTAGAACTTCTTTTTTTATTATTATCCTTAGGATTTGATAGGTTTTCTGAATCTGAGAATTGGTATCTTTCATCCATTCTGGAACATTTTTATATATTATTTCTTCAATTGTGCTTTTCTTTCATTCCTCTATCATCTCCATCTAGATCTCTTGTTTAGACAGGCTCACCCTATCCTCTGTATTTGCTGCATTCTCGATAATTTCACAGTCTGTCTTCTAG... | TTGTTATTTCTTTGTAGTTAATGCCTTTTTTCTCTGGCTGCTTTTAAGATCTTCTGTGTGACTTTGGTGTGCTAAGTAAGTTCTGCTATGATATGTCCAGTAGAACTTCTTTTTTTATTATTATCCTTAGGATTTGATAGGTTTTCTGAATCTGAGAATTGGTATCTTTCATCCATTCTGGAACATTTTTATATATTATTTCTTCAATTGTGCTTTTCTTTCATTCCTCTATCATCTCCATCTAGATCTCTTGTTTAGACAGGCTCACCCTATCCTCTGTATTTGCTGCATTCTCGATAATTTCACAGTCTGTCTTCTAG... |
Task1_train_33623 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GAGGATCCTGGGCTTCCTTTGAGTCCCGATGTGGTTGGCTTTTTTATTCTTCCTCCTCTTCCTCCTGGCCTGGCTCTGCGGTCTGGGTCAGGTGGATGTGCTCTCTTTCGAAGGGAGACCCATTTCAGATGCCACTGGCTTTCTTGCCTTTGCCTTCTGCAGGACCCTCCTTCTCAGTGAGCGCTCCTCCCAGCACTTCTCCTAGGGACAGCAGGCTAAGTCCATGTGTCCCTGCTCTGCCCTGCACAGTGTGCTGCCACCCTCAACCGGGCAACCCTCGGGCTGGCCTCTGCCCCTGTGACCAGTCAGTGCCAGGGCTG... | GAGGATCCTGGGCTTCCTTTGAGTCCCGATGTGGTTGGCTTTTTTATTCTTCCTCCTCTTCCTCCTGGCCTGGCTCTGCGGTCTGGGTCAGGTGGATGTGCTCTCTTTCGAAGGGAGACCCATTTCAGATGCCACTGGCTTTCTTGCCTTTGCCTTCTGCAGGACCCTCCTTCTCAGTGAGCGCTCCTCCCAGCACTTCTCCTAGGGACAGCAGGCTAAGTCCATGTGTCCCTGCTCTGCCCTGCACAGTGTGCTGCCACCCTCAACCGGGCAACCCTCGGGCTGGCCTCTGCCCCTGTGACCAGTCAGTGCCAGGGCTG... |
Task1_train_33624 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CAAGAAAATGAACAGCCGTGATCTGTTGCCACCCACAATAAGAACTAGAACATCTGGTCATGTAGAGTGCTCACACCTGTAATCGCAGCGCTTTGGGAGGGGGAGGTGGGAAGATCTCTTGAGCCCAGGAGTTTTAGACTAGCCTGGGCAACATAGCAAGACCACATCTCTATCAAAAAAAAAAAAAAAACTAGAACACACTTGGAACAGCATCAAGGCATGCTGTTATCTGCAGGGGGTGGGGGTAGGGGTGGAGCTGGGTGAGTGTGAGGGGATGGAGCATGGCGAGAGGGAGGTTGGATTGCTGGATCAAGAGCGAC... | CAAGAAAATGAACAGCCGTGATCTGTTGCCACCCACAATAAGAACTAGAACATCTGGTCATGTAGAGTGCTCACACCTGTAATCGCAGCGCTTTGGGAGGGGGAGGTGGGAAGATCTCTTGAGCCCAGGAGTTTTAGACTAGCCTGGGCAACATAGCAAGACCACATCTCTATCAAAAAAAAAAAAAAAACTAGAACACACTTGGAACAGCATCAAGGCATGCTGTTATCTGCAGGGGGTGGGGGTAGGGGTGGAGCTGGGTGAGTGTGAGGGGATGGAGCATGGCGAGAGGGAGGTTGGATTGCTGGATCAAGAGCGAC... |
Task1_train_33625 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GGTTTAGGTTCCCCAGATTTGTGGAACACATGCAGGGTGCTTGAGAGATTCCCAAGCTGTCAAATTAGAAATTACAGATAAACTTTGAATTTTGAAGTACAGGGGACTTTGAGTTAGGGGGTTACAAGAGAGGAGCAAAAACTGCAGGAAGAAAGCTGAGTTCTGGAATTAGTACCATCACAGTAATTGCTGCATATGAGCAGGAGGTAGAAACCAGAGTTTGAGAGGCTACCTGAGGTCAGGCTAGTGGAAAGAAGGTCTGGTGCAGACGGTGGGAGAAGCCGGGCAGAGGAAACTCGGAAATTCACAGCAGGAAGCTC... | GGTTTAGGTTCCCCAGATTTGTGGAACACATGCAGGGTGCTTGAGAGATTCCCAAGCTGTCAAATTAGAAATTACAGATAAACTTTGAATTTTGAAGTACAGGGGACTTTGAGTTAGGGGGTTACAAGAGAGGAGCAAAAACTGCAGGAAGAAAGCTGAGTTCTGGAATTAGTACCATCACAGTAATTGCTGCATATGAGCAGGAGGTAGAAACCAGAGTTTGAGAGGCTACCTGAGGTCAGGCTAGTGGAAAGAAGGTCTGGTGCAGACGGTGGGAGAAGCCGGGCAGAGGAAACTCGGAAATTCACAGCAGGAAGCTC... |
Task1_train_33626 | A mutation is present on Chromosome 1. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GTTTAAGGGTATTTGGCAACTCCCCCATACCACCCTGCTCCTGCTTTTTCCATGTGACTTGCCTGCTCCCCCTTCACCTTCTGCAATAATTGTAAGTTTCCTGAGGCCTCCTTAGAAGCAGAACGGATGCCAGCACTGTGCTCCTGTAAAGCCTGTAGAACCATGAGCCAATCAAATCTCTTTTCTTTATAAATTACCTAGTCTCTGTTATTTCTCTATAGCCATGCAAGAATGGTCTAACACAATGGCTGTCCCTCTTATTTACATTCTGAGCAAGGTCTGAGTGACTAAGGGTGGGGGTGTCAATGCATGGGGTCTGC... | GTTTAAGGGTATTTGGCAACTCCCCCATACCACCCTGCTCCTGCTTTTTCCATGTGACTTGCCTGCTCCCCCTTCACCTTCTGCAATAATTGTAAGTTTCCTGAGGCCTCCTTAGAAGCAGAACGGATGCCAGCACTGTGCTCCTGTAAAGCCTGTAGAACCATGAGCCAATCAAATCTCTTTTCTTTATAAATTACCTAGTCTCTGTTATTTCTCTATAGCCATGCAAGAATGGTCTAACACAATGGCTGTCCCTCTTATTTACATTCTGAGCAAGGTCTGAGTGACTAAGGGTGGGGGTGTCAATGCATGGGGTCTGC... |
Task1_train_33627 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CGGGAAGCTGTGGCAGGAGAATTGCTTAAACCTGGGAGGTGGAGTTTGCAGTGAACCAAGATCACACCGTTGCACTCCAGGCTGGGCAACAGAGCAATACTCCGTTTCAGGGGGAAAAAAAGGAATCATACAATATGTGGTCCTTTCTGACTGGCTTTTCTCACATGGTGTGATGTTTTCCAGGTCCATCCATGCTGTAGCATGTATCAATGTCTCATTCCTTCTTACAGCCAGACAACATTCCATCGTATGGATGGGCCCTGTTCTGTTTATTCATTCATCTATTGGTGGCCACGTGGGTTGTTACCGGTTTTTGGTCA... | CGGGAAGCTGTGGCAGGAGAATTGCTTAAACCTGGGAGGTGGAGTTTGCAGTGAACCAAGATCACACCGTTGCACTCCAGGCTGGGCAACAGAGCAATACTCCGTTTCAGGGGGAAAAAAAGGAATCATACAATATGTGGTCCTTTCTGACTGGCTTTTCTCACATGGTGTGATGTTTTCCAGGTCCATCCATGCTGTAGCATGTATCAATGTCTCATTCCTTCTTACAGCCAGACAACATTCCATCGTATGGATGGGCCCTGTTCTGTTTATTCATTCATCTATTGGTGGCCACGTGGGTTGTTACCGGTTTTTGGTCA... |
Task1_train_33628 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | TTCAATGTTATCAGTGATGATCTCAACTCAACAACAAAATAACCAAAAATTTAAAAATGGGCAAGGGACCATTGGACATTTCTCCAAAGAAGATACACAGATGGCCAATAAGCACATGAAATGAGGCTCAACATCATTCACGATCATGGACAGGCAAGTCTAAACCACGGTGAGACACCACCTCATACCCCTTCGCATGGCACCAGCAAAGACACAGAAAATAACAAGTGTTGCAAGGGAGTGGAGAAACGCGAACCCACATTGATGGGAATGTAAAATGACGCAGCTGCTGTGGCGAACAGTATGCAGGTTCTTCAAAA... | TTCAATGTTATCAGTGATGATCTCAACTCAACAACAAAATAACCAAAAATTTAAAAATGGGCAAGGGACCATTGGACATTTCTCCAAAGAAGATACACAGATGGCCAATAAGCACATGAAATGAGGCTCAACATCATTCACGATCATGGACAGGCAAGTCTAAACCACGGTGAGACACCACCTCATACCCCTTCGCATGGCACCAGCAAAGACACAGAAAATAACAAGTGTTGCAAGGGAGTGGAGAAACGCGAACCCACATTGATGGGAATGTAAAATGACGCAGCTGCTGTGGCGAACAGTATGCAGGTTCTTCAAAA... |
Task1_train_33629 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAATAAGTACTACATGGGAGAGAGAAAAAGAAGGTAGAAACATCTAAATAAATTATGTTTACAGCTTCATGATACAGTGTTCATCCTCCAGGGAAATATCGTAATACAAGTCAGAGCTGGCTTGAACAGGGTTCTTAAATACTGGTGGTTAGCCTGATGCCAAAGAATCAAATAAGCCACCAACATCAATGATACCAATAGATATCATAGTATTAATCGATACATACCTTCTACTGTCTAAACGCTGGGGCTCCTTTAGCCAGTGAGCACCACATGAGCAAAGGAGAAAGGGAAATTTACCCAACATGCACCATATGCAA... | AAATAAGTACTACATGGGAGAGAGAAAAAGAAGGTAGAAACATCTAAATAAATTATGTTTACAGCTTCATGATACAGTGTTCATCCTCCAGGGAAATATCGTAATACAAGTCAGAGCTGGCTTGAACAGGGTTCTTAAATACTGGTGGTTAGCCTGATGCCAAAGAATCAAATAAGCCACCAACATCAATGATACCAATAGATATCATAGTATTAATCGATACATACCTTCTACTGTCTAAACGCTGGGGCTCCTTTAGCCAGTGAGCACCACATGAGCAAAGGAGAAAGGGAAATTTACCCAACATGCACCATATGCAA... |
Task1_train_33630 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | CAAATGTAATAATTCTACAGAAGTAAAAACATGCAAGAATCAAAAGAAGCAAAATAGTTACAGAGAGATAAACAACTTGAAAGACAAATAGTTACAAGAAGAGCAACGGTACCAGGTGCAAGGTTCTAAATCTTTCATTATAATTAGATATAAGGTCTATGCCGGACACGAACTCAAGGTTTTATGTTGTTATCTCTTAGAGAAAAATCCTAAGAACTTCATACATTGTTGGTGTTAGTACCTTATCAGTTAATTGGGCTCTTTTGAAATGCTGAGGATCTGTTTACCCAGGCCAACTCCTTACGGAAGGGGGTTAGGTG... | CAAATGTAATAATTCTACAGAAGTAAAAACATGCAAGAATCAAAAGAAGCAAAATAGTTACAGAGAGATAAACAACTTGAAAGACAAATAGTTACAAGAAGAGCAACGGTACCAGGTGCAAGGTTCTAAATCTTTCATTATAATTAGATATAAGGTCTATGCCGGACACGAACTCAAGGTTTTATGTTGTTATCTCTTAGAGAAAAATCCTAAGAACTTCATACATTGTTGGTGTTAGTACCTTATCAGTTAATTGGGCTCTTTTGAAATGCTGAGGATCTGTTTACCCAGGCCAACTCCTTACGGAAGGGGGTTAGGTG... |
Task1_train_33631 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ATAAGGCTTATTACAGAGACATAAGCACAGAACTTGGAGAATGTGGAGAGTGAGCTTAGCAGAAGCTTCACTGGGTAAGATACTTGTGTTGTTAGCGTCAGTCAGGCATTTATAGGGAGTAATGTAGTCCTTTAGAACCCTTTGCTATTTTTACTTATAGGGAAAACTTCAATTTAGCAGTGGGAATGATTCTTATTTTAGTATGGTATTACATAAAATCTTATCTTTATCCTAATTTTTGATCATTTACAAATTTGATTTCTGAAACTTTTAGTGTTCATGAAGATTTTCTGTGGTTTTGTTTTTAAAAGATTTTTTTG... | ATAAGGCTTATTACAGAGACATAAGCACAGAACTTGGAGAATGTGGAGAGTGAGCTTAGCAGAAGCTTCACTGGGTAAGATACTTGTGTTGTTAGCGTCAGTCAGGCATTTATAGGGAGTAATGTAGTCCTTTAGAACCCTTTGCTATTTTTACTTATAGGGAAAACTTCAATTTAGCAGTGGGAATGATTCTTATTTTAGTATGGTATTACATAAAATCTTATCTTTATCCTAATTTTTGATCATTTACAAATTTGATTTCTGAAACTTTTAGTGTTCATGAAGATTTTCTGTGGTTTTGTTTTTAAAAGATTTTTTTG... |
Task1_train_33632 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | ATACTTTGGTCAGTCTTCACAGCCCTATTGTCTCAAACTAATTTCTTTCCTGCTCTGGAGCTCAGGACTTTATGTTCAGATGTGACAATTTCTTAAAGTTGTGCCCTGACAACTTTCTTAAAAATTTTATCAATGAAAATCTAGTGAAAGACCAACGCTGAAATTTCATCAGATCCCCCTTTTCCTTCCAGTTTAATATTATTCAACTGTTCCTTTTTAAGACTACAAGAAATTAAGACTTGTGCCTTCATCCAGCAATGAAGTGGCAATAGGTAAATTAGACTCCACATTGTATTTTTCCCCACAAAATGTTCACGTTT... | ATACTTTGGTCAGTCTTCACAGCCCTATTGTCTCAAACTAATTTCTTTCCTGCTCTGGAGCTCAGGACTTTATGTTCAGATGTGACAATTTCTTAAAGTTGTGCCCTGACAACTTTCTTAAAAATTTTATCAATGAAAATCTAGTGAAAGACCAACGCTGAAATTTCATCAGATCCCCCTTTTCCTTCCAGTTTAATATTATTCAACTGTTCCTTTTTAAGACTACAAGAAATTAAGACTTGTGCCTTCATCCAGCAATGAAGTGGCAATAGGTAAATTAGACTCCACATTGTATTTTTCCCCACAAAATGTTCACGTTT... |
Task1_train_33633 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATAAGAGCTTCACAGAGTAGACTAAGATGATGTGGAAGAGGATGGAGTCTACTCATTGAGAAGTGAGATTGGACCCAACAGTTCAAAGAGGAGAGGGAGTAGGCCTTGCAGAAATTTCTGCAAGAGGATCCTGCAGGGGGATACCAACATGAAGGCTTAGAGTGGGAGTGGGCCTCCTGTGTTCAGAGGGCAGCTGGAGGCCCATGTGGCTGGAGCAGTGTAAATGAGGGGGAGGATTTGGGGAGGAAGTCAGAGATAAAGGGGCCTTGTAAGGATGTGGACTTTTCTCAGATTGCAACAGGGAACCATTGGATGGTGTT... | ATAAGAGCTTCACAGAGTAGACTAAGATGATGTGGAAGAGGATGGAGTCTACTCATTGAGAAGTGAGATTGGACCCAACAGTTCAAAGAGGAGAGGGAGTAGGCCTTGCAGAAATTTCTGCAAGAGGATCCTGCAGGGGGATACCAACATGAAGGCTTAGAGTGGGAGTGGGCCTCCTGTGTTCAGAGGGCAGCTGGAGGCCCATGTGGCTGGAGCAGTGTAAATGAGGGGGAGGATTTGGGGAGGAAGTCAGAGATAAAGGGGCCTTGTAAGGATGTGGACTTTTCTCAGATTGCAACAGGGAACCATTGGATGGTGTT... |
Task1_train_33634 | A variant on Chromosome 1 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | ATTGTCAAGTTGTAGTATTCAATTCCTTGTCAGTTAAACATAATGCAATGATTTTCTCCAAGTCTGTGACTTGTCGTCTCATTTTTTAGTTGTGTCTTTTGATGAGAAGTTTTTAATTTTGATAAAGCCCATTTATCCTTTTTAAAATAGTGTTTTCTGTATCTTATCTGAAGTTCTTGCCTACTCCAAAGTCAATCAAATATTCATTTTTTTTTTGTAGAAGCTTTATAGTTTTAACTTTTACATGTAGGCCTGTGATCCACCTTTAATTAAATTTTTGTGTGGTTTGAGGTATGAATCAAGGTTAATATTTTTTCCAT... | ATTGTCAAGTTGTAGTATTCAATTCCTTGTCAGTTAAACATAATGCAATGATTTTCTCCAAGTCTGTGACTTGTCGTCTCATTTTTTAGTTGTGTCTTTTGATGAGAAGTTTTTAATTTTGATAAAGCCCATTTATCCTTTTTAAAATAGTGTTTTCTGTATCTTATCTGAAGTTCTTGCCTACTCCAAAGTCAATCAAATATTCATTTTTTTTTTGTAGAAGCTTTATAGTTTTAACTTTTACATGTAGGCCTGTGATCCACCTTTAATTAAATTTTTGTGTGGTTTGAGGTATGAATCAAGGTTAATATTTTTTCCAT... |
Task1_train_33635 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | AAGTTGGGGAGAGAGATGGTGGAGAAGCACTGGTCAGACTGTAAATGATATTGAGTAGAAAGAAGTCAGGGATTTTTGTTTTTAACATGAAAAAGAAATAGAATTGTAACTAAGTTGAAGTTTCTTTACTGTTTCATCTTGTTTCTTTACAAATTTCATCTTGTCATTTACAAGGGTTTATGCCACATAGCTATGGATTTGGGCCCAATATTTGACCTTATAGCAGCTCTAAAATATTAGACTGCAGTTAGGAAATGCCCTCTGGATCTGATTTTTAAACAGAACCAAATGCATTCTACTCTTTTCTGCTTTTAAGAGTA... | AAGTTGGGGAGAGAGATGGTGGAGAAGCACTGGTCAGACTGTAAATGATATTGAGTAGAAAGAAGTCAGGGATTTTTGTTTTTAACATGAAAAAGAAATAGAATTGTAACTAAGTTGAAGTTTCTTTACTGTTTCATCTTGTTTCTTTACAAATTTCATCTTGTCATTTACAAGGGTTTATGCCACATAGCTATGGATTTGGGCCCAATATTTGACCTTATAGCAGCTCTAAAATATTAGACTGCAGTTAGGAAATGCCCTCTGGATCTGATTTTTAAACAGAACCAAATGCATTCTACTCTTTTCTGCTTTTAAGAGTA... |
Task1_train_33636 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GGCATGTCAGAGGTCTTCATGGCAGCCCCTCCCATTACAGGCCTGGAGACCTAGGAGGAAAATATGGTTTTGTAGGCTGTGCCCAGGGCCTTGCAGCTTTGTGCAGTCTCAGGACTTGGTGCCCTCTGTCCCACACATGGCTAAAAGGGGCCAACGTACAGCTCAGCCTGTTGCTTCAGAGGGTCCAAGCCCCAAGCCTTGGAGGCTTACATGTGGTGTTGGACCTGTGAGTGCACAGAAGTCAAGAATTGAGGTTTGGGAACCTCTGCCTAGATTTCAGAGGATGTATGGAAACGCCTGGATTTCCAGGCAGAAGTTTG... | GGCATGTCAGAGGTCTTCATGGCAGCCCCTCCCATTACAGGCCTGGAGACCTAGGAGGAAAATATGGTTTTGTAGGCTGTGCCCAGGGCCTTGCAGCTTTGTGCAGTCTCAGGACTTGGTGCCCTCTGTCCCACACATGGCTAAAAGGGGCCAACGTACAGCTCAGCCTGTTGCTTCAGAGGGTCCAAGCCCCAAGCCTTGGAGGCTTACATGTGGTGTTGGACCTGTGAGTGCACAGAAGTCAAGAATTGAGGTTTGGGAACCTCTGCCTAGATTTCAGAGGATGTATGGAAACGCCTGGATTTCCAGGCAGAAGTTTG... |
Task1_train_33637 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ATTTCAGAGGATGTATGGAAACGCCTGGATTTCCAGGCAGAAGTTTGCTGCAGGGGTGGAGCACTCATGGAGAACCTCTGCTAGAGCAGTGTGGAAGGGAAATGTGGGGTCAGAGCCCCCACACTGAGTCCCCACTGGGGCACTGCCTAGTGGAGCTGTGAGAAGAGGGCCACCAACCTTCAGACCCCAGAATGGTAGATCCACTGATAGCTTGCACCATGCACCTGGAAAAGCTGCAGACACTCAGTGCTAGCCCGTGAAAGCAGCCAGGAGGGGGACTGTACCCTGCAAAGCCATAGGGGTGGAGCTGTCCAAGACCA... | ATTTCAGAGGATGTATGGAAACGCCTGGATTTCCAGGCAGAAGTTTGCTGCAGGGGTGGAGCACTCATGGAGAACCTCTGCTAGAGCAGTGTGGAAGGGAAATGTGGGGTCAGAGCCCCCACACTGAGTCCCCACTGGGGCACTGCCTAGTGGAGCTGTGAGAAGAGGGCCACCAACCTTCAGACCCCAGAATGGTAGATCCACTGATAGCTTGCACCATGCACCTGGAAAAGCTGCAGACACTCAGTGCTAGCCCGTGAAAGCAGCCAGGAGGGGGACTGTACCCTGCAAAGCCATAGGGGTGGAGCTGTCCAAGACCA... |
Task1_train_33638 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGAAACGCCTGGATTTCCAGGCAGAAGTTTGCTGCAGGGGTGGAGCACTCATGGAGAACCTCTGCTAGAGCAGTGTGGAAGGGAAATGTGGGGTCAGAGCCCCCACACTGAGTCCCCACTGGGGCACTGCCTAGTGGAGCTGTGAGAAGAGGGCCACCAACCTTCAGACCCCAGAATGGTAGATCCACTGATAGCTTGCACCATGCACCTGGAAAAGCTGCAGACACTCAGTGCTAGCCCGTGAAAGCAGCCAGGAGGGGGACTGTACCCTGCAAAGCCATAGGGGTGGAGCTGTCCAAGACCATAGGAACCCATCTCTT... | GGAAACGCCTGGATTTCCAGGCAGAAGTTTGCTGCAGGGGTGGAGCACTCATGGAGAACCTCTGCTAGAGCAGTGTGGAAGGGAAATGTGGGGTCAGAGCCCCCACACTGAGTCCCCACTGGGGCACTGCCTAGTGGAGCTGTGAGAAGAGGGCCACCAACCTTCAGACCCCAGAATGGTAGATCCACTGATAGCTTGCACCATGCACCTGGAAAAGCTGCAGACACTCAGTGCTAGCCCGTGAAAGCAGCCAGGAGGGGGACTGTACCCTGCAAAGCCATAGGGGTGGAGCTGTCCAAGACCATAGGAACCCATCTCTT... |
Task1_train_33639 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ACAAAAAATTAGCTGGGCATGGTGATGCACGCCTGTAGTCCCAGCCACTAGGGAGGCTGAGGCAGGAGAATGGCATGAACCTGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGTGCCACTGTACTCCAGCCTGGGCAACAGAGCAAGACTCCGTCTTGGAAAAAAAAAAAGTATCACTTGCCAAAGTCTGTATAATTGTTGAAAATTGAGTTACAATAATGGATCATAACCAGACTTAAATGAACCATTAAAATTATTGTTGTGTTTAATTACAGATAGGGTAAGGAAAATTCTTACTAAGAAATGAGTGGTCAAATACT... | ACAAAAAATTAGCTGGGCATGGTGATGCACGCCTGTAGTCCCAGCCACTAGGGAGGCTGAGGCAGGAGAATGGCATGAACCTGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGTGCCACTGTACTCCAGCCTGGGCAACAGAGCAAGACTCCGTCTTGGAAAAAAAAAAAGTATCACTTGCCAAAGTCTGTATAATTGTTGAAAATTGAGTTACAATAATGGATCATAACCAGACTTAAATGAACCATTAAAATTATTGTTGTGTTTAATTACAGATAGGGTAAGGAAAATTCTTACTAAGAAATGAGTGGTCAAATACT... |
Task1_train_33640 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | GAGAACAATCCCCTTTGGGAGGGTGCTGGCCAGGCTCAGAAACTCACAAAGGACATTTAGGCAGAGGGAACAGCATGAATGGGTGCACAGAAGCCTGAGACAGAACTGCTCATTCGCTGATATTATTTAAAAATGTAAGATGATATTATTAACAAAATTAACAGTAGGGCTTCCACAATATGATTTTGAGAAATAACTGGTCTATGTGAAACTTCTGGAGAGCACAACTGATTTCTTCTTCAGTGCACAATGAGACACTAAAAATATGATGTACTTGGCTGACTGTTTTCTAAGCATATCTTTCAGCAATCCGGTAAAAC... | GAGAACAATCCCCTTTGGGAGGGTGCTGGCCAGGCTCAGAAACTCACAAAGGACATTTAGGCAGAGGGAACAGCATGAATGGGTGCACAGAAGCCTGAGACAGAACTGCTCATTCGCTGATATTATTTAAAAATGTAAGATGATATTATTAACAAAATTAACAGTAGGGCTTCCACAATATGATTTTGAGAAATAACTGGTCTATGTGAAACTTCTGGAGAGCACAACTGATTTCTTCTTCAGTGCACAATGAGACACTAAAAATATGATGTACTTGGCTGACTGTTTTCTAAGCATATCTTTCAGCAATCCGGTAAAAC... |
Task1_train_33641 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCCTACCAAATATCAATAAACGAATGTACTCTGAAGGCAGTCTCCATAGAAATTTTACTTAATAATAATAATACAAAACTCTATTTGTGATGCCAATGACATCTGTCCAAAAAGGTGTCATGAAATCAGCTCTTTTACAAATCATCTCAACTTTGAACTAGATGTTAGCAGGTTGTGCAATCCCGAGATGGTCTCCACAGTATGACCACTATTCCTGAAATTAAGCCAGGAATAATTCAGATGACCAAATTCACTGATAATCCTTAATTATTATATTAGTTATTAGTACTAAACCTATTTTAAGTCAAATTATTAAATAG... | CCCTACCAAATATCAATAAACGAATGTACTCTGAAGGCAGTCTCCATAGAAATTTTACTTAATAATAATAATACAAAACTCTATTTGTGATGCCAATGACATCTGTCCAAAAAGGTGTCATGAAATCAGCTCTTTTACAAATCATCTCAACTTTGAACTAGATGTTAGCAGGTTGTGCAATCCCGAGATGGTCTCCACAGTATGACCACTATTCCTGAAATTAAGCCAGGAATAATTCAGATGACCAAATTCACTGATAATCCTTAATTATTATATTAGTTATTAGTACTAAACCTATTTTAAGTCAAATTATTAAATAG... |
Task1_train_33642 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTACAGGATATCTTCTAAGAGGAATTTTGTCTACTGTATTTCTCTGGCGCACATGGACTCAATACCTCATTGCTTTTCACTTGTGATGATGTCTTTTTTTTATTGCTCTACATCATCTATCCATTGAGGATGTTGCTTGATATGTGTCCTCTGCAAGTATATAGCAAGATTCTCAAAGCCAAGAGAAGTATCTTGTAATTTTTTTTTTTTTTTTTAGATGGAGTCTCGCTTTGTCACCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTCACTGCAACCTCCAACTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCC... | CTACAGGATATCTTCTAAGAGGAATTTTGTCTACTGTATTTCTCTGGCGCACATGGACTCAATACCTCATTGCTTTTCACTTGTGATGATGTCTTTTTTTTATTGCTCTACATCATCTATCCATTGAGGATGTTGCTTGATATGTGTCCTCTGCAAGTATATAGCAAGATTCTCAAAGCCAAGAGAAGTATCTTGTAATTTTTTTTTTTTTTTTTAGATGGAGTCTCGCTTTGTCACCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTCACTGCAACCTCCAACTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCC... |
Task1_train_33643 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCGGCTCACTCACTGCAACCTCCAACTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTACCTGGGATTACAGGCATGCACCACCACACCCAGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCATCATGTTGGCCAGGATGGCCTCGATCTCTTGACCTCGTGTTCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCATCTGGTCCGAGAAGTATCTTGTATTTATATATTGCAATGAGACTTCTCTCTCACGTCTTCACACTAAAGCATCATATCCCTCCAGTTCTGAA... | TCGGCTCACTCACTGCAACCTCCAACTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTACCTGGGATTACAGGCATGCACCACCACACCCAGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCATCATGTTGGCCAGGATGGCCTCGATCTCTTGACCTCGTGTTCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCATCTGGTCCGAGAAGTATCTTGTATTTATATATTGCAATGAGACTTCTCTCTCACGTCTTCACACTAAAGCATCATATCCCTCCAGTTCTGAA... |
Task1_train_33644 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CGGTGTGCCGCTCTGGGCAGCGCTGTGCCTGGCCAGGGAGGTGTGGTGTGGCTTCTTTGTTGCTTTTTTTTGTTTCCCCATCATGTGAGGTTTTTTTGTTGTTGTTGTTTGATTTTTTTTTTTTTTTTTTTTTTTTTTTCAAAAACCTGAGATCAGTTCTGTGTTCTGGAACAGCTCTCCTTTTCCACAGGAGGAGTCCCTCATGGATCGCGGTATTGGTTGGTTGTGGTGATTTGGGGAGCACGAGGGAGAGCAATGCAGGTGGGAGGTGTGGGGGAGCCAGCCTCCCCGCCCGGCCGCACGCCCGTCACTGCTCGTCT... | CGGTGTGCCGCTCTGGGCAGCGCTGTGCCTGGCCAGGGAGGTGTGGTGTGGCTTCTTTGTTGCTTTTTTTTGTTTCCCCATCATGTGAGGTTTTTTTGTTGTTGTTGTTTGATTTTTTTTTTTTTTTTTTTTTTTTTTTCAAAAACCTGAGATCAGTTCTGTGTTCTGGAACAGCTCTCCTTTTCCACAGGAGGAGTCCCTCATGGATCGCGGTATTGGTTGGTTGTGGTGATTTGGGGAGCACGAGGGAGAGCAATGCAGGTGGGAGGTGTGGGGGAGCCAGCCTCCCCGCCCGGCCGCACGCCCGTCACTGCTCGTCT... |
Task1_train_33645 | An alteration has been detected on Chromosome 1. Is it pathogenic, and if so, what disease is involved? | Benign | AGGCCGTGTCGTCCAGGCCCATGTCCTCCTGGCTTGCTCTCCTGCAGACAACCCCGAGAGTGTCCGCCACAGCCTCAGCCAGACATCGGTCATGAAGCTGCCCCTGCTCGGTGGCATCAGGGGGCTCACATGGCTCGGAGAGGTGCTTCCAAAGAGAAGAGAGAAACAGTGAACAGCTCAGCAAACGTTCACTACCCACTTCTAACTGGCATCACCCCCATCCGTGCTGTGGGAGCTAAAGGCTAGCGCTGCCATATCCTTGAGGTCAGGTTCTAAAGTCAGGTCAAATGATAGAGGGCCAGCACAGTGGCCTCTGAGGA... | AGGCCGTGTCGTCCAGGCCCATGTCCTCCTGGCTTGCTCTCCTGCAGACAACCCCGAGAGTGTCCGCCACAGCCTCAGCCAGACATCGGTCATGAAGCTGCCCCTGCTCGGTGGCATCAGGGGGCTCACATGGCTCGGAGAGGTGCTTCCAAAGAGAAGAGAGAAACAGTGAACAGCTCAGCAAACGTTCACTACCCACTTCTAACTGGCATCACCCCCATCCGTGCTGTGGGAGCTAAAGGCTAGCGCTGCCATATCCTTGAGGTCAGGTTCTAAAGTCAGGTCAAATGATAGAGGGCCAGCACAGTGGCCTCTGAGGA... |
Task1_train_33646 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | CACACAAGTCACCTGGAAGTACTGGCAAATGACAGATGCTTAGGCATTTCACCATTTGGAAGCTACTTTGCATTTCCCCACCTGGAAAGTCACTCCCATGATCCTGAAACACATTTTTCATGTGATAAGAAATGTTAACTAAACAATGAGATACTGGAGGCCTGGGAGCTGCATGGGAGGCCTCCAGCAGGTGTCCTGCAGGGCCTCAGAGTAAACAGCATGGGGTGGGTGGGGCAGGGGGAGATCTTTTTTCCTTTCTTTTGAGCAGCGGATACCACCTATTTTGTCTATTTACCTATCTATCTACCTACCTAGCTTTC... | CACACAAGTCACCTGGAAGTACTGGCAAATGACAGATGCTTAGGCATTTCACCATTTGGAAGCTACTTTGCATTTCCCCACCTGGAAAGTCACTCCCATGATCCTGAAACACATTTTTCATGTGATAAGAAATGTTAACTAAACAATGAGATACTGGAGGCCTGGGAGCTGCATGGGAGGCCTCCAGCAGGTGTCCTGCAGGGCCTCAGAGTAAACAGCATGGGGTGGGTGGGGCAGGGGGAGATCTTTTTTCCTTTCTTTTGAGCAGCGGATACCACCTATTTTGTCTATTTACCTATCTATCTACCTACCTAGCTTTC... |
Task1_train_33647 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ACAATTTATCCTGTCATTTTTTGATGTATATGCTATAATACAAATTTTTATATGGATGATAATTTATCATCAATAAAAAACTTATATGTCTGCTCTTTATAAGCCATATGAAATGAGGCATAGACTGGAGAAATGACAATGAATTATGATCAACAAAATATCACAATTTGAATTAAGACTTGATATACAAATACCGATGAGAAAAAATTAAAATTAAGAGTTAAAGAAACAAAGTCAAAATATAACTATGCAGTCTTAGGTATAGTTCTTATTTTCAATTAATCCACTGGCATTCTGTTTTATAAAAATATTTCTCACTT... | ACAATTTATCCTGTCATTTTTTGATGTATATGCTATAATACAAATTTTTATATGGATGATAATTTATCATCAATAAAAAACTTATATGTCTGCTCTTTATAAGCCATATGAAATGAGGCATAGACTGGAGAAATGACAATGAATTATGATCAACAAAATATCACAATTTGAATTAAGACTTGATATACAAATACCGATGAGAAAAAATTAAAATTAAGAGTTAAAGAAACAAAGTCAAAATATAACTATGCAGTCTTAGGTATAGTTCTTATTTTCAATTAATCCACTGGCATTCTGTTTTATAAAAATATTTCTCACTT... |
Task1_train_33648 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | TTAGCAACCACTGCCTTGATCAGTCAGCAGCTATCAACATAGAGGCAAGACCTCTGCCAGCTAAAAGATTATGACTTGCTGAAGGTTCAGATGATCATTAGCACATTTTACCTATAAAGTACTTAAAATTAAGGTATAAACATTCTTTAGACACAATGCTATTGCACACTTTATACGCTACAGTATACTGGAAACATAACTTGTATATATATGCACTGGGAAATCAAAAAATTCATGTCACTTGCTTTATTGCAGTGATCTGGAACCATGCTTGCAGTATCTCCAAAGTATGCCCATACTTTAAATAGTTAGATTACTTA... | TTAGCAACCACTGCCTTGATCAGTCAGCAGCTATCAACATAGAGGCAAGACCTCTGCCAGCTAAAAGATTATGACTTGCTGAAGGTTCAGATGATCATTAGCACATTTTACCTATAAAGTACTTAAAATTAAGGTATAAACATTCTTTAGACACAATGCTATTGCACACTTTATACGCTACAGTATACTGGAAACATAACTTGTATATATATGCACTGGGAAATCAAAAAATTCATGTCACTTGCTTTATTGCAGTGATCTGGAACCATGCTTGCAGTATCTCCAAAGTATGCCCATACTTTAAATAGTTAGATTACTTA... |
Task1_train_33649 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGGAGAGTTTTACACTGGAATTTCTATTTAATTTAAATGAATCATAATGATTTACTTTCAATATTCTATATTTGTATTCAGTATTCAGTATTAAAAGATTGAAGAGATGGAAATCGTTGAAAAACTTCAAGCACGGTTACTAACACAGAAAATAAAATTGGTCTTTATACTTGACCATTTAGGCAGACTCTTTGGTACTTTGATCAAATTAAAGATGCCTTAGCAAGACACAATGTAAATGTATTGAATTTGTTATTGGTACTGTGCTCAATTTCACAAGCACCTTTGCACTCACTACCTGGGTTCAGCTTCTCCTTCTG... | TGGAGAGTTTTACACTGGAATTTCTATTTAATTTAAATGAATCATAATGATTTACTTTCAATATTCTATATTTGTATTCAGTATTCAGTATTAAAAGATTGAAGAGATGGAAATCGTTGAAAAACTTCAAGCACGGTTACTAACACAGAAAATAAAATTGGTCTTTATACTTGACCATTTAGGCAGACTCTTTGGTACTTTGATCAAATTAAAGATGCCTTAGCAAGACACAATGTAAATGTATTGAATTTGTTATTGGTACTGTGCTCAATTTCACAAGCACCTTTGCACTCACTACCTGGGTTCAGCTTCTCCTTCTG... |
Task1_train_33650 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | TCATAATGATTTACTTTCAATATTCTATATTTGTATTCAGTATTCAGTATTAAAAGATTGAAGAGATGGAAATCGTTGAAAAACTTCAAGCACGGTTACTAACACAGAAAATAAAATTGGTCTTTATACTTGACCATTTAGGCAGACTCTTTGGTACTTTGATCAAATTAAAGATGCCTTAGCAAGACACAATGTAAATGTATTGAATTTGTTATTGGTACTGTGCTCAATTTCACAAGCACCTTTGCACTCACTACCTGGGTTCAGCTTCTCCTTCTGAAGGTTCTCCTTTATGAAGGAAAAGGGAGCTTGGGTCAGCA... | TCATAATGATTTACTTTCAATATTCTATATTTGTATTCAGTATTCAGTATTAAAAGATTGAAGAGATGGAAATCGTTGAAAAACTTCAAGCACGGTTACTAACACAGAAAATAAAATTGGTCTTTATACTTGACCATTTAGGCAGACTCTTTGGTACTTTGATCAAATTAAAGATGCCTTAGCAAGACACAATGTAAATGTATTGAATTTGTTATTGGTACTGTGCTCAATTTCACAAGCACCTTTGCACTCACTACCTGGGTTCAGCTTCTCCTTCTGAAGGTTCTCCTTTATGAAGGAAAAGGGAGCTTGGGTCAGCA... |
Task1_train_33651 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | GCTAGTGAGTTAGCTCCAAACATAAAATCCTGGCTTGTTGATTTCCATAGTGTAAACAGTCCCATCATGGTTGACTTCAAGCTACTTATTTGAATTGGCTCCAAACATAAAACAAAATCCTGGCTTGTTTGTTGAGTTCCATAGTGTAAACAGTCCCATCGTGGGTGACTTCAAGCTACTTATTTGATGTTATTGATCATGGAGTTGCCAAGAGGTGTGCACAATTGGCTCTCCTATGCCAGTACAGGCTGGCTCTGGTACACCACTGCTTTTATTTTCCATTTCGTTAATTTCTGCTCTTAACATTATTTCTGTCCTTC... | GCTAGTGAGTTAGCTCCAAACATAAAATCCTGGCTTGTTGATTTCCATAGTGTAAACAGTCCCATCATGGTTGACTTCAAGCTACTTATTTGAATTGGCTCCAAACATAAAACAAAATCCTGGCTTGTTTGTTGAGTTCCATAGTGTAAACAGTCCCATCGTGGGTGACTTCAAGCTACTTATTTGATGTTATTGATCATGGAGTTGCCAAGAGGTGTGCACAATTGGCTCTCCTATGCCAGTACAGGCTGGCTCTGGTACACCACTGCTTTTATTTTCCATTTCGTTAATTTCTGCTCTTAACATTATTTCTGTCCTTC... |
Task1_train_33652 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | CACTCGACGGATCAGCTGGCACCACCCAGATCGATTAACTGGCTCATCTGATCTCGTGGCCCCCACCCTGGAACTGACTTAGCACAAAAGGACACCTCAATTCCTTATGATTTCATCTCCGACCCAACCAATCAACACCCTTGACTCACTGGCCTTCCCCCTCCCACCAAATTATCCTTAAAAACTCTGATCCCCGAATGCTCAGGGAGATCGATTTGAGTACTAATAAGACTCCAGTCTCCTGCACAAGCAGCTCTGTGTACTCTTCCTCTATTGCAATTCCTGTCTTGATAAATCGGCTCTGTGTAGGCGGCGGAAGA... | CACTCGACGGATCAGCTGGCACCACCCAGATCGATTAACTGGCTCATCTGATCTCGTGGCCCCCACCCTGGAACTGACTTAGCACAAAAGGACACCTCAATTCCTTATGATTTCATCTCCGACCCAACCAATCAACACCCTTGACTCACTGGCCTTCCCCCTCCCACCAAATTATCCTTAAAAACTCTGATCCCCGAATGCTCAGGGAGATCGATTTGAGTACTAATAAGACTCCAGTCTCCTGCACAAGCAGCTCTGTGTACTCTTCCTCTATTGCAATTCCTGTCTTGATAAATCGGCTCTGTGTAGGCGGCGGAAGA... |
Task1_train_33653 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CATGATAAGAAAAACTCAACTGTCTATTCAGCAACATACTGTATGTGCCAAATGCATGAAACAATCTGGTCATGTCTCTTAACATGAAATGTATGTATCAAATACTTCATAACATAATGTCTCTTTACCTGCTATACAGAGAGCTCTCTGAAAGCGCATCCATTAATGGTCCAATAATAAACTAAAAAAAAAAAAAAAAAAAGACACGTAATTGAAACTTAGTTGTAAATACAATTTTGAAGTCAGTTTCCCTGATTGAACATCCTACACAGGCTTACAGAAGACCTGCTATAAGCAAAGCTGATCTCTTACGCTGCAGG... | CATGATAAGAAAAACTCAACTGTCTATTCAGCAACATACTGTATGTGCCAAATGCATGAAACAATCTGGTCATGTCTCTTAACATGAAATGTATGTATCAAATACTTCATAACATAATGTCTCTTTACCTGCTATACAGAGAGCTCTCTGAAAGCGCATCCATTAATGGTCCAATAATAAACTAAAAAAAAAAAAAAAAAAAGACACGTAATTGAAACTTAGTTGTAAATACAATTTTGAAGTCAGTTTCCCTGATTGAACATCCTACACAGGCTTACAGAAGACCTGCTATAAGCAAAGCTGATCTCTTACGCTGCAGG... |
Task1_train_33654 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ACATTTTAAAACGTCAAAATCATATGAAAAACTTGCAGGAAGAGAAAAATGATCAGTTTCCTACATAGATCACCTGCAAGCAGCATTTACAGTCATAATTTTATAAATGCTGAACACACATTTAACCAAAATTTTAACTGTGACAATATATTTTATGATATAACTAAGATATACTATGTCAAGACATAGGGGTAAATCCCCTAATATTCCGTTAAGAGGCCACAGGATTTGCTTTCTGTAACAGAGGAAATGGGAGTTGCAGGAAGCATGGAAGCACCATTGCTTATCCCTAAAACTGCAAAATAACTGGCCGAGCGCGG... | ACATTTTAAAACGTCAAAATCATATGAAAAACTTGCAGGAAGAGAAAAATGATCAGTTTCCTACATAGATCACCTGCAAGCAGCATTTACAGTCATAATTTTATAAATGCTGAACACACATTTAACCAAAATTTTAACTGTGACAATATATTTTATGATATAACTAAGATATACTATGTCAAGACATAGGGGTAAATCCCCTAATATTCCGTTAAGAGGCCACAGGATTTGCTTTCTGTAACAGAGGAAATGGGAGTTGCAGGAAGCATGGAAGCACCATTGCTTATCCCTAAAACTGCAAAATAACTGGCCGAGCGCGG... |
Task1_train_33655 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GGCCGAGCGCGGTGGCTCACGCCTGTAATCCCAGCGCTTTGGGAGGCCAAGGCGGGCAGATCACCTGAGGTGAGGAGTTTGAGGCCAGCCTGACCAACACGGTGAAACCCCGTCTCTATTAAAAATACAAAATTAGTGGGGCATGGTGGCGCATGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAACCGCTTGAACCCGGGAAGTGCAGGTTGCGGTGAGCGGAGATTGTGCCATTGCATTCCAGCCTGGGCAACAAGACCGAAACTCCATAAAACAAACAAACAAACAAACAAAACTGCAAAATAACAGAC... | GGCCGAGCGCGGTGGCTCACGCCTGTAATCCCAGCGCTTTGGGAGGCCAAGGCGGGCAGATCACCTGAGGTGAGGAGTTTGAGGCCAGCCTGACCAACACGGTGAAACCCCGTCTCTATTAAAAATACAAAATTAGTGGGGCATGGTGGCGCATGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAACCGCTTGAACCCGGGAAGTGCAGGTTGCGGTGAGCGGAGATTGTGCCATTGCATTCCAGCCTGGGCAACAAGACCGAAACTCCATAAAACAAACAAACAAACAAACAAAACTGCAAAATAACAGAC... |
Task1_train_33656 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CACTTGGCCTCCGGCCTGAGAAAGGGGCCAGCAATAAGGAATGACAGACAGTAAGGCAATCTTACAATGTCAGAAAATGTATTTGGCTTTTTTTTTCTTTTTAAAATAAGTGCATACAAATACAGCTAGAAGCATTTCTGATTTGCCAAGTGCTCTAAAAAAGCAGCGCAAGTCACAGCCTACATAGAACGGTAACTGTCACCAGGATAATAAAGCACAAAGATATGCTAATAACGTTAACAAAAGAAAAAAATGTCTTTATAAGTACATACCTTTTGTCGTCAAAAAAAATATAGAAACACAATGTATTCAAAAAAAAT... | CACTTGGCCTCCGGCCTGAGAAAGGGGCCAGCAATAAGGAATGACAGACAGTAAGGCAATCTTACAATGTCAGAAAATGTATTTGGCTTTTTTTTTCTTTTTAAAATAAGTGCATACAAATACAGCTAGAAGCATTTCTGATTTGCCAAGTGCTCTAAAAAAGCAGCGCAAGTCACAGCCTACATAGAACGGTAACTGTCACCAGGATAATAAAGCACAAAGATATGCTAATAACGTTAACAAAAGAAAAAAATGTCTTTATAAGTACATACCTTTTGTCGTCAAAAAAAATATAGAAACACAATGTATTCAAAAAAAAT... |
Task1_train_33657 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GACATTGGAGCCCACAAGAGGGCATTTTTCCCCACTGGGACAATAGACCTCTCCACTAGCTCCCTGCTGTTTGATGCTTTGTCTGGAGCAAGGGAAGCAGAACTTGTGCGAAGGGACGGACGGGCACTGCACAAAATGGGTGTCCTCCAGCCGCTCGTGGCAGAGGGTGCAGCACAGCGGGGCACTGGTTGCCAGAGAGGAGTCCGGGAGGCTGGCAGGGTGCACTGGCTCCAGTCCTCCTGTGTTGCCTGCTCCCTGGCCCCCCACCTCTCTGGGGCCCAGCCTTCTTTGGTTCATAGAGGACGGAGAGGGCGGACTGT... | GACATTGGAGCCCACAAGAGGGCATTTTTCCCCACTGGGACAATAGACCTCTCCACTAGCTCCCTGCTGTTTGATGCTTTGTCTGGAGCAAGGGAAGCAGAACTTGTGCGAAGGGACGGACGGGCACTGCACAAAATGGGTGTCCTCCAGCCGCTCGTGGCAGAGGGTGCAGCACAGCGGGGCACTGGTTGCCAGAGAGGAGTCCGGGAGGCTGGCAGGGTGCACTGGCTCCAGTCCTCCTGTGTTGCCTGCTCCCTGGCCCCCCACCTCTCTGGGGCCCAGCCTTCTTTGGTTCATAGAGGACGGAGAGGGCGGACTGT... |
Task1_train_33658 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | TCACTTGAACCCAGGAGACGGAGGTTGCAGTGAGCCCAGATCACACCACTGCACTCCAGCCTGGGCAACAGAGCGAGACTCCATCTCAAAAAAAAAACCCCCAAGAAAACCTATAACAATAAAACCTGTTTTTTTCTTTCTTTTCTTGTTTTTTCTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTGTTTTATCACCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAGCCTTTCCGGGATCAAGTGATTCTCCCTCATCAGCCCCCAAGGTAGCTGGGACTACAGGCATGCGCCACCACAGCTGGCTG... | TCACTTGAACCCAGGAGACGGAGGTTGCAGTGAGCCCAGATCACACCACTGCACTCCAGCCTGGGCAACAGAGCGAGACTCCATCTCAAAAAAAAAACCCCCAAGAAAACCTATAACAATAAAACCTGTTTTTTTCTTTCTTTTCTTGTTTTTTCTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTGTTTTATCACCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAGCCTTTCCGGGATCAAGTGATTCTCCCTCATCAGCCCCCAAGGTAGCTGGGACTACAGGCATGCGCCACCACAGCTGGCTG... |
Task1_train_33659 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | CTATCACCTCACATAGTTACCACTTTTTTTTATGTGTGATGAGAACATGATTTATAGTGCTTTGGAGTGTATTTCTTTGAATAGCTTTTTTTAGTGGGTGCTCTAAGTATTACATTTTAAGTTTGTACATATATATTCATTAGCCAATATGGAAATGCAAATTAAAACCACAATGAGATATCACTACACATCTGTCAGAATGGCTAAAATAAAAAATAGTGACAACAACAAACACTAGGTAAGGATGTAAAAAAACTTGGACCACTCATACACTGTTGATGGAAATGTAAAACTACAGCCACTCTGGAAAAGTTTGGCAG... | CTATCACCTCACATAGTTACCACTTTTTTTTATGTGTGATGAGAACATGATTTATAGTGCTTTGGAGTGTATTTCTTTGAATAGCTTTTTTTAGTGGGTGCTCTAAGTATTACATTTTAAGTTTGTACATATATATTCATTAGCCAATATGGAAATGCAAATTAAAACCACAATGAGATATCACTACACATCTGTCAGAATGGCTAAAATAAAAAATAGTGACAACAACAAACACTAGGTAAGGATGTAAAAAAACTTGGACCACTCATACACTGTTGATGGAAATGTAAAACTACAGCCACTCTGGAAAAGTTTGGCAG... |
Task1_train_33660 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TTACAAGGTTGCTTTTTTTTCTTATGAAATTATTGTTTTTCTGGTCTCCCGGCTTGAAATTTTATGTTATATTTGACTCCTCCTGAAGCTCCATTTAAAAAGAATCAAGTCCTATGAATTCTATCCTTATAATCTCTCCCATATTTGCTCCCTACTAAACACTCCCATTTTAATCACCAGGGTTCAGGTTCTTTATGCTGTACTCACAAATGAATGAAACTGCCTTACATCCAATATACTACCAATTTATTAATCTTCCTAAAGTGCACAAACACTCTGAGGTAACTTAAAGGCAAAGACTAAGTTCATTTCTTTATAAA... | TTACAAGGTTGCTTTTTTTTCTTATGAAATTATTGTTTTTCTGGTCTCCCGGCTTGAAATTTTATGTTATATTTGACTCCTCCTGAAGCTCCATTTAAAAAGAATCAAGTCCTATGAATTCTATCCTTATAATCTCTCCCATATTTGCTCCCTACTAAACACTCCCATTTTAATCACCAGGGTTCAGGTTCTTTATGCTGTACTCACAAATGAATGAAACTGCCTTACATCCAATATACTACCAATTTATTAATCTTCCTAAAGTGCACAAACACTCTGAGGTAACTTAAAGGCAAAGACTAAGTTCATTTCTTTATAAA... |
Task1_train_33661 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AAGATTTTCTTTTTTAAAAAAAGTTTATTTTCCACACTATTTGTACAGCTGTAAACTCAAGGAATCATCCAATACTTGTACAAATCTGGGAGAACAGTTAATAAGCACCTTCAGTGGTTTCCACAGTTTAAGAATTTACCATTAAAAAATTTTAGAATAAATCTAATAAAATGAATAAAATAGTTATAAAAATCATACAAAATCATGATGAACATTTGATATAGAGGGTTTAATATGAAACGATAAATACAAAAAGTGAGACTAATTTATGGATTTGGGCTACGTAAAAGACCTACATGGTCCTCGAATCTTGTGATTCT... | AAGATTTTCTTTTTTAAAAAAAGTTTATTTTCCACACTATTTGTACAGCTGTAAACTCAAGGAATCATCCAATACTTGTACAAATCTGGGAGAACAGTTAATAAGCACCTTCAGTGGTTTCCACAGTTTAAGAATTTACCATTAAAAAATTTTAGAATAAATCTAATAAAATGAATAAAATAGTTATAAAAATCATACAAAATCATGATGAACATTTGATATAGAGGGTTTAATATGAAACGATAAATACAAAAAGTGAGACTAATTTATGGATTTGGGCTACGTAAAAGACCTACATGGTCCTCGAATCTTGTGATTCT... |
Task1_train_33662 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | AGTCAACAGAGTTTTCAAGAGGGGACAAAAAGTCAGGTTAAAAAAACAAAAAAACAAAATTGGAAACATCTGCTTCTCTTTAAACTGGAGATGTGAAGCAAGACTGAGGAAATAATGAATATTAGTCATTGTTAATAGTAGCTGGAATGTGTTGACTCAAATGATCATAAACTCTTCTCTATGTAACCTGCCTATTAAAATCTATGAGTAGTGGTATTTGTTCCCATAATTTCAGGAACAAAAGGTTGCCTTGCCTAGGTTTATCGAAGCCAGGAGTCAGCAACTTTTTCTGTCAAGAGCCCACATAGTAGGCTATTTAT... | AGTCAACAGAGTTTTCAAGAGGGGACAAAAAGTCAGGTTAAAAAAACAAAAAAACAAAATTGGAAACATCTGCTTCTCTTTAAACTGGAGATGTGAAGCAAGACTGAGGAAATAATGAATATTAGTCATTGTTAATAGTAGCTGGAATGTGTTGACTCAAATGATCATAAACTCTTCTCTATGTAACCTGCCTATTAAAATCTATGAGTAGTGGTATTTGTTCCCATAATTTCAGGAACAAAAGGTTGCCTTGCCTAGGTTTATCGAAGCCAGGAGTCAGCAACTTTTTCTGTCAAGAGCCCACATAGTAGGCTATTTAT... |
Task1_train_33663 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | GGTTGGTGTGGGAAAAAAAACCCCACCCATTTGGTGTCAGAAGTGTGAGTGAAAACATTGCAGACGTGGTTTTTTAGAAATCCCAACTCCAGGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGGGGCTGAGGAGGGCAGATCATGAGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGCTGCTCGGGACGCTGAAGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTTGCAGTGAG... | GGTTGGTGTGGGAAAAAAAACCCCACCCATTTGGTGTCAGAAGTGTGAGTGAAAACATTGCAGACGTGGTTTTTTAGAAATCCCAACTCCAGGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGGGGCTGAGGAGGGCAGATCATGAGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGCTGCTCGGGACGCTGAAGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTTGCAGTGAG... |
Task1_train_33664 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AAGAATACTTCATTTATTTTCTTAGTTGTGAAAAAATTAGTTAAGAACCTTAAAAAGAACTTTTTACTCTAACCAGATCTTTTAATTTCCTAGAACATACTCTAATATACTAGTTTTCCTAAGCTTGAAACAAATCACAGTACAGAAAAAAACAATAAATGGACATGAGCGAGGATTTTCTCCAGTAAACAGTTTAAATAATAGCCTTTAACTGAGGGAGTGGTGAAATAACACTATCAAAAAGTTCTTTACATTTAGAGTGATAAACAAAGTGCAGATTTTTCACATCTTAAACTCTGAGTGAATACTAAGAATAATTC... | AAGAATACTTCATTTATTTTCTTAGTTGTGAAAAAATTAGTTAAGAACCTTAAAAAGAACTTTTTACTCTAACCAGATCTTTTAATTTCCTAGAACATACTCTAATATACTAGTTTTCCTAAGCTTGAAACAAATCACAGTACAGAAAAAAACAATAAATGGACATGAGCGAGGATTTTCTCCAGTAAACAGTTTAAATAATAGCCTTTAACTGAGGGAGTGGTGAAATAACACTATCAAAAAGTTCTTTACATTTAGAGTGATAAACAAAGTGCAGATTTTTCACATCTTAAACTCTGAGTGAATACTAAGAATAATTC... |
Task1_train_33665 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | CTCATGCCTTCACCTTCTTCGGCAATTTGTTCAAATGTTGTATTATCTTCTCTGACCACCCAATTTAAAACAGTGCCACTCTCTCACTCCTAGCCCTCTTTGTTCTTCCCTGCCTGTCTTCCCTAGCATTCATCATCATTTTACTTACTTATTTCTCATATATTTTACTTGTTTATTGTGTTATTTCCTCTGACAAGGATCAAGTTGCACGAGGGCGGAAATTTTATCCATTACGCTACTGGATTCCTAGTACCCTAGAACAGTGCTTGGCACATTGTAGACATTCATTTGTTGAATGAATAAGAAACTCAAATGTCCAA... | CTCATGCCTTCACCTTCTTCGGCAATTTGTTCAAATGTTGTATTATCTTCTCTGACCACCCAATTTAAAACAGTGCCACTCTCTCACTCCTAGCCCTCTTTGTTCTTCCCTGCCTGTCTTCCCTAGCATTCATCATCATTTTACTTACTTATTTCTCATATATTTTACTTGTTTATTGTGTTATTTCCTCTGACAAGGATCAAGTTGCACGAGGGCGGAAATTTTATCCATTACGCTACTGGATTCCTAGTACCCTAGAACAGTGCTTGGCACATTGTAGACATTCATTTGTTGAATGAATAAGAAACTCAAATGTCCAA... |
Task1_train_33666 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TACTTTCTCACTTATATTACTAACTTGTGTTATTAAATATTCTGCATAAAGATAATTTTAAGATGAAATTTGATGTTATAAAAACTTCTCATTTTATTAAGAGATTAACGCTATGAAACCTGCTGCTATATATTCTTGGAACCAGCTGTGACCCAAAAGATCAATGTAGGGATGTAGGTCCTTCCCCATTCTCTACACACAAAATCAGATACTCTGATGTGCAGCTGTAGCCCCAGTCTACACTGTCTGTTGTATTTTTTGTTTTCTGGTGTCATGTGCCTCCCACCCTGCTCCTAGCAATTGCCATGACAACAAATAGA... | TACTTTCTCACTTATATTACTAACTTGTGTTATTAAATATTCTGCATAAAGATAATTTTAAGATGAAATTTGATGTTATAAAAACTTCTCATTTTATTAAGAGATTAACGCTATGAAACCTGCTGCTATATATTCTTGGAACCAGCTGTGACCCAAAAGATCAATGTAGGGATGTAGGTCCTTCCCCATTCTCTACACACAAAATCAGATACTCTGATGTGCAGCTGTAGCCCCAGTCTACACTGTCTGTTGTATTTTTTGTTTTCTGGTGTCATGTGCCTCCCACCCTGCTCCTAGCAATTGCCATGACAACAAATAGA... |
Task1_train_33667 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GATAATTTTAAGATGAAATTTGATGTTATAAAAACTTCTCATTTTATTAAGAGATTAACGCTATGAAACCTGCTGCTATATATTCTTGGAACCAGCTGTGACCCAAAAGATCAATGTAGGGATGTAGGTCCTTCCCCATTCTCTACACACAAAATCAGATACTCTGATGTGCAGCTGTAGCCCCAGTCTACACTGTCTGTTGTATTTTTTGTTTTCTGGTGTCATGTGCCTCCCACCCTGCTCCTAGCAATTGCCATGACAACAAATAGATAATTGGCTTCCGTAATTTCTCATCTTATTGCCTAAGGCAACAGAGAGCT... | GATAATTTTAAGATGAAATTTGATGTTATAAAAACTTCTCATTTTATTAAGAGATTAACGCTATGAAACCTGCTGCTATATATTCTTGGAACCAGCTGTGACCCAAAAGATCAATGTAGGGATGTAGGTCCTTCCCCATTCTCTACACACAAAATCAGATACTCTGATGTGCAGCTGTAGCCCCAGTCTACACTGTCTGTTGTATTTTTTGTTTTCTGGTGTCATGTGCCTCCCACCCTGCTCCTAGCAATTGCCATGACAACAAATAGATAATTGGCTTCCGTAATTTCTCATCTTATTGCCTAAGGCAACAGAGAGCT... |
Task1_train_33668 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TTTTTTCTGTTAGAATTATCATATTAAGCAGAAGTTTTGCTTCACAAACTCTCAGCCAAATACAAAATACTATGAATAGTATTTACCTTGTGTCTCTTTCCAAAGAACTCATAGTGGTTTGCAGCTATTGCAGATATCCTGGCCATGAGGTATGCAGTTCCTTTTTTTTTTTTTGAGACGGAGCCTTGCTCTGTCGCCCAGGCTGGAGCATAGTGGCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCGTGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCACACCCGGC... | TTTTTTCTGTTAGAATTATCATATTAAGCAGAAGTTTTGCTTCACAAACTCTCAGCCAAATACAAAATACTATGAATAGTATTTACCTTGTGTCTCTTTCCAAAGAACTCATAGTGGTTTGCAGCTATTGCAGATATCCTGGCCATGAGGTATGCAGTTCCTTTTTTTTTTTTTGAGACGGAGCCTTGCTCTGTCGCCCAGGCTGGAGCATAGTGGCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCGTGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCACACCCGGC... |
Task1_train_33669 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | AGCTATTTCCTTTGCATGGGCATAAAATGGAGTATTTCTGTAAGACAGGTTCCTAGGCTGGGAGTGCCTGAGTCAAAGAGCACAGTCATGTGTTGCATAAGGACAGTTCAGTCAAAGATGAACCACATATACAACCGTGGTCCCATAAGATTGTCATATACTGTATTTTTACCATACCTTTTCTATGTTTAGGTAAGTTTATATGCACAAATACTTACCATCCTGCTCTGGTTGCCTACAGTATTTGGTACAGTGCCTGCTGTACAGATTCACTGGCCAGGAGCTATAGGCCACACCCTACAGCCTAGGTGTGTAGTTGG... | AGCTATTTCCTTTGCATGGGCATAAAATGGAGTATTTCTGTAAGACAGGTTCCTAGGCTGGGAGTGCCTGAGTCAAAGAGCACAGTCATGTGTTGCATAAGGACAGTTCAGTCAAAGATGAACCACATATACAACCGTGGTCCCATAAGATTGTCATATACTGTATTTTTACCATACCTTTTCTATGTTTAGGTAAGTTTATATGCACAAATACTTACCATCCTGCTCTGGTTGCCTACAGTATTTGGTACAGTGCCTGCTGTACAGATTCACTGGCCAGGAGCTATAGGCCACACCCTACAGCCTAGGTGTGTAGTTGG... |
Task1_train_33670 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | CAGTGTCAAGTGTATTTTTGGATCATAGTTTTCAAGCATATTTTTAGTACCATTTATAATTTTTTTATATGTCAATATAAAATATTTAGAAAATATTTTCTACTGGATGTTACAAATTAATCTTTATTATCTTTTCTCAGGACTTACAAAGTACCCAAGCATCTAGTCTGGAACTGACAGAGATAAGTAGAGAAAATGTAAATATTAAATCTTTTAATGAGCCACTGGTTTAAAAATGTTGTTTTAGCTGCCATGTTAATGAAATGGCAAGAAGGCTGGGTTTTTGAAAATTATGCTTTTAGAACGCAAGTAATCACTTG... | CAGTGTCAAGTGTATTTTTGGATCATAGTTTTCAAGCATATTTTTAGTACCATTTATAATTTTTTTATATGTCAATATAAAATATTTAGAAAATATTTTCTACTGGATGTTACAAATTAATCTTTATTATCTTTTCTCAGGACTTACAAAGTACCCAAGCATCTAGTCTGGAACTGACAGAGATAAGTAGAGAAAATGTAAATATTAAATCTTTTAATGAGCCACTGGTTTAAAAATGTTGTTTTAGCTGCCATGTTAATGAAATGGCAAGAAGGCTGGGTTTTTGAAAATTATGCTTTTAGAACGCAAGTAATCACTTG... |
Task1_train_33671 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | CTCCCATCTCAGCACTGAATAAAAAACATTCTGTGTCACAATATCCTAGTTTTGGGGCTTTAAAAACGTCTAGGTGTTCCTCACATGCCTTGTCTATAATAAGGAAAGCAAGCAGTAGTTGGGTATTGTTAGCTTTTGAAACAAAAGCCCTACTGGTCTTCTAATTTTGGATATTTTAATTAAAGAATATCTGGACAGTACAAAGTGAATTATTAAAAAACCATTTGTAACTACCTAGATTCAATCAGGATTTCCTTGATTTGTGCAAAGTAAAATATTACAATAAATTTGATACTGCTACTTGTATAAAAACCTATGGT... | CTCCCATCTCAGCACTGAATAAAAAACATTCTGTGTCACAATATCCTAGTTTTGGGGCTTTAAAAACGTCTAGGTGTTCCTCACATGCCTTGTCTATAATAAGGAAAGCAAGCAGTAGTTGGGTATTGTTAGCTTTTGAAACAAAAGCCCTACTGGTCTTCTAATTTTGGATATTTTAATTAAAGAATATCTGGACAGTACAAAGTGAATTATTAAAAAACCATTTGTAACTACCTAGATTCAATCAGGATTTCCTTGATTTGTGCAAAGTAAAATATTACAATAAATTTGATACTGCTACTTGTATAAAAACCTATGGT... |
Task1_train_33672 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AAGGAATTACTTCAAATCTTTGTTATTTAAAAGTATTTAGAAAGTATTTTAGTACTTCTGCCCAACGCACCATTGGGGTGGGGATAGGGCATTGCTATTCTTTACAAATAGCCTGTAAGTAAAAAACAAAATTTTCTTAGGCACAAATTTCTGCCTAATACAAAAGACCGGACCTCTAGTACTGGATGACAAATAGCAATGTTCTTCCCTGCCAGTTTACTAGGGGGCCTACATCTGTGACCACCTGCAGGCTGTTTAGGCTATGCAGTGAAAAGATGCAGTTTCAGTACTTGTCACGCAGTTCCTAACCTTAGGCGAGG... | AAGGAATTACTTCAAATCTTTGTTATTTAAAAGTATTTAGAAAGTATTTTAGTACTTCTGCCCAACGCACCATTGGGGTGGGGATAGGGCATTGCTATTCTTTACAAATAGCCTGTAAGTAAAAAACAAAATTTTCTTAGGCACAAATTTCTGCCTAATACAAAAGACCGGACCTCTAGTACTGGATGACAAATAGCAATGTTCTTCCCTGCCAGTTTACTAGGGGGCCTACATCTGTGACCACCTGCAGGCTGTTTAGGCTATGCAGTGAAAAGATGCAGTTTCAGTACTTGTCACGCAGTTCCTAACCTTAGGCGAGG... |
Task1_train_33673 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGGTTCAAAAACCAGGCATTATTCTAATACTCTCTAGGGCAAATGTATTGCCTTCTAGAACTCAAATGGAATCTCATACCCTTTATCATCGCCCCTTTCTCTCCAGCAGAACATCTCAGAGGAGCTCTTTGCTCCAGAGGACAGCCATGCTCTGACGCGTTCTCAGTGAGGCCCAGTTAAAACAAATGAATACATTAACCATGACAGCTTATATCATGTCTGTCTTTTGAGCAGTTTAAAAAATAAAAAATAAAAAATAACTCAGGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAGCAGTTTGGGAGGCCAAGGTGG... | AGGTTCAAAAACCAGGCATTATTCTAATACTCTCTAGGGCAAATGTATTGCCTTCTAGAACTCAAATGGAATCTCATACCCTTTATCATCGCCCCTTTCTCTCCAGCAGAACATCTCAGAGGAGCTCTTTGCTCCAGAGGACAGCCATGCTCTGACGCGTTCTCAGTGAGGCCCAGTTAAAACAAATGAATACATTAACCATGACAGCTTATATCATGTCTGTCTTTTGAGCAGTTTAAAAAATAAAAAATAAAAAATAACTCAGGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAGCAGTTTGGGAGGCCAAGGTGG... |
Task1_train_33674 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | CACACACTTACAGAGAGGCTTCATGATGAGGTACTAGTGTTTGGAAAATGCTTAGCACTTTTTAACTACACACAGAATTCCTTTTAAAGTCAGCCCTAAACGTCAGTGGATAAAACTGGGCAGACACCTCTTGCCCAACTTGCGATCAGGGACGAAGGCCGATGGTAGACGCAGACGCACACACAGCACCCAGACAGATGATTTTCTTAGAGGACAGGAATGCAAGGGACCACGGCAAGAGTCAAGTTGCTAAAAAACTGAGAAAGCTCCTCAGAGCACAGGCCCCTTTCTCTGAGAAGGCTACTTTTAAACCCTGGCTG... | CACACACTTACAGAGAGGCTTCATGATGAGGTACTAGTGTTTGGAAAATGCTTAGCACTTTTTAACTACACACAGAATTCCTTTTAAAGTCAGCCCTAAACGTCAGTGGATAAAACTGGGCAGACACCTCTTGCCCAACTTGCGATCAGGGACGAAGGCCGATGGTAGACGCAGACGCACACACAGCACCCAGACAGATGATTTTCTTAGAGGACAGGAATGCAAGGGACCACGGCAAGAGTCAAGTTGCTAAAAAACTGAGAAAGCTCCTCAGAGCACAGGCCCCTTTCTCTGAGAAGGCTACTTTTAAACCCTGGCTG... |
Task1_train_33675 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CAGAAGGCAGCTTTGGCCTTGCCTAACTGGGTGGGCCCCTCTGCCAAGAACCTTCACCCACTGCTTTTTGACTATACTAGACAAAAGGAAGGAAGAATGGAGGACGATTAACACTGCAAAGTAGTGCATCTGAAGATAAACGGGAAGGCTGCATCTTTCTGTTTGAAGATTAATTATTTTTATTATTATTTCTTTAAGAGACAGGGTCTCACTCTGTTGCCCAGGCTACAGTGCAGTGGTGCAGTCATAGCTCACTGCAGCCTCAAACTCCTGGGCTCAAACGATCTCCCTGCCTTGGCCTCCCAAAGTGGTGGGATCAC... | CAGAAGGCAGCTTTGGCCTTGCCTAACTGGGTGGGCCCCTCTGCCAAGAACCTTCACCCACTGCTTTTTGACTATACTAGACAAAAGGAAGGAAGAATGGAGGACGATTAACACTGCAAAGTAGTGCATCTGAAGATAAACGGGAAGGCTGCATCTTTCTGTTTGAAGATTAATTATTTTTATTATTATTTCTTTAAGAGACAGGGTCTCACTCTGTTGCCCAGGCTACAGTGCAGTGGTGCAGTCATAGCTCACTGCAGCCTCAAACTCCTGGGCTCAAACGATCTCCCTGCCTTGGCCTCCCAAAGTGGTGGGATCAC... |
Task1_train_33676 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GCATTTCTTCTTGTGATTCACTCTTATTAAATGACACTGCTTTGGGAATGGTTTCTGAAACAGCAATAAAACAAGTGACCTTACTCATTTTCACCTGAATCCTTCATACAGAATTAACAGATATAACCTTTCAAGTAAAGGACAATTAACGGGATAACATTTTCCCAGAGAAATGTGTTCATCTATTACATCCAGTTTCTCCTCTTCTAAATTAGTGAAAAACGTGAGTGTATTTGCCAAGAAAGTACCCAGTGGCCCTGAGAAGCGAGTGTTTAAGACAAAAAACAAAACAGGGAAACTGGACAATCAAATGGAAGAAA... | GCATTTCTTCTTGTGATTCACTCTTATTAAATGACACTGCTTTGGGAATGGTTTCTGAAACAGCAATAAAACAAGTGACCTTACTCATTTTCACCTGAATCCTTCATACAGAATTAACAGATATAACCTTTCAAGTAAAGGACAATTAACGGGATAACATTTTCCCAGAGAAATGTGTTCATCTATTACATCCAGTTTCTCCTCTTCTAAATTAGTGAAAAACGTGAGTGTATTTGCCAAGAAAGTACCCAGTGGCCCTGAGAAGCGAGTGTTTAAGACAAAAAACAAAACAGGGAAACTGGACAATCAAATGGAAGAAA... |
Task1_train_33677 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGCCTATCTGGACTATTTTTCAAAATATGAAGATTTTACTCTTTTTAAAGTTTACACATTTTAGCTAACAATGGCCATGATCAGAACTTATAAAATCCTGCGGGTATACGTAAATGTGAAAAAGATATAATTCATTTAGTAAATCCTATAATGAGAAGCCCTCTAAAATTTGGAGGACAAATAAAAACAAAATCCTTACATATAGCAGATATTAAAAAAAAAGTCTTGCTACCTCAAAACATGTCAAATGTAAACAGCTGAAACATGTCCTTTAGTAATACTATGAAAGACAGTAGTAGGCTGGAGGGATACACATCTAT... | GGCCTATCTGGACTATTTTTCAAAATATGAAGATTTTACTCTTTTTAAAGTTTACACATTTTAGCTAACAATGGCCATGATCAGAACTTATAAAATCCTGCGGGTATACGTAAATGTGAAAAAGATATAATTCATTTAGTAAATCCTATAATGAGAAGCCCTCTAAAATTTGGAGGACAAATAAAAACAAAATCCTTACATATAGCAGATATTAAAAAAAAAGTCTTGCTACCTCAAAACATGTCAAATGTAAACAGCTGAAACATGTCCTTTAGTAATACTATGAAAGACAGTAGTAGGCTGGAGGGATACACATCTAT... |
Task1_train_33678 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCACAACGCCTACATCTTTTCACTGTATCGAGTTGCCCATTAAGAGAAAAAAAAAAAAAAAAAAAAAAAGACTGAATTATCTTTAAAGAAATAATCCTTACTCTATGCTTACCTTCAATATTGTTTCTAAATGACATTTACTGCGTTTTAATTGTGATGTGTTATTTCAGATATTATGGTCCATTTACTAAGAGAAAACTTCAAACGGCCACAAACTGCATTTAGTTATTACCCAAATTTGTCTTAACCACTAACTTTCCATTTTCATCTATAAGCACTAAAGACATGCAAGAAAAATTACTTTTGCTTTTAATGCTGCC... | CCACAACGCCTACATCTTTTCACTGTATCGAGTTGCCCATTAAGAGAAAAAAAAAAAAAAAAAAAAAAAGACTGAATTATCTTTAAAGAAATAATCCTTACTCTATGCTTACCTTCAATATTGTTTCTAAATGACATTTACTGCGTTTTAATTGTGATGTGTTATTTCAGATATTATGGTCCATTTACTAAGAGAAAACTTCAAACGGCCACAAACTGCATTTAGTTATTACCCAAATTTGTCTTAACCACTAACTTTCCATTTTCATCTATAAGCACTAAAGACATGCAAGAAAAATTACTTTTGCTTTTAATGCTGCC... |
Task1_train_33679 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TTTACTCCCTCTTATTGTGTGGCTGTTGCCATGAAATGTTATTTTTAAAAATGAAGGAAAATATAAACTGTGATATGTCCCAGTGGTTGGCATGAAAACACATGATGGATTTGATTTTTTGGTGGAAGGATCATGTAGGTTAGCGCACATATTGACCATGAACTTGTTTCCGTCAAGTAAGTCAGACTGGGCCAGAAGGGGCCTGCCACTGTGGCTCTGGGAGCAGCGGGCTTCATGGGGCTGTGCAAGGTGCCAGCAAACTGCAGCGGTATGTTCTGTCTACACAATAGCACCAGCATCAGGGGGTCGTAGATTCTCTG... | TTTACTCCCTCTTATTGTGTGGCTGTTGCCATGAAATGTTATTTTTAAAAATGAAGGAAAATATAAACTGTGATATGTCCCAGTGGTTGGCATGAAAACACATGATGGATTTGATTTTTTGGTGGAAGGATCATGTAGGTTAGCGCACATATTGACCATGAACTTGTTTCCGTCAAGTAAGTCAGACTGGGCCAGAAGGGGCCTGCCACTGTGGCTCTGGGAGCAGCGGGCTTCATGGGGCTGTGCAAGGTGCCAGCAAACTGCAGCGGTATGTTCTGTCTACACAATAGCACCAGCATCAGGGGGTCGTAGATTCTCTG... |
Task1_train_33680 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TTAACCGAAGAACAAAAATGAGGTAGGGGTGAATTATTGAAGCTTTTACACACAAAGCTAAATATTGCAATTTCTGATCTACATTTGAAAGGATCCGATATGCGTAGCAACTCCAATATCCAGTCTTGTTTTTGGAGAAACAAGGGACAGGAGAGAAAGAAAGAGTCATCATTTGGAGAAAGGAACAAGAAAGTCATTTGTTTTTTACTTTCACATTGGAGAACACAAACACCAATATGAAGGGAAGAAATGTATTTAGGTATTATTCACAGTTTATTCAAATTTCTGAATAAACTACCTACTACAGTTTTCTTGTATGG... | TTAACCGAAGAACAAAAATGAGGTAGGGGTGAATTATTGAAGCTTTTACACACAAAGCTAAATATTGCAATTTCTGATCTACATTTGAAAGGATCCGATATGCGTAGCAACTCCAATATCCAGTCTTGTTTTTGGAGAAACAAGGGACAGGAGAGAAAGAAAGAGTCATCATTTGGAGAAAGGAACAAGAAAGTCATTTGTTTTTTACTTTCACATTGGAGAACACAAACACCAATATGAAGGGAAGAAATGTATTTAGGTATTATTCACAGTTTATTCAAATTTCTGAATAAACTACCTACTACAGTTTTCTTGTATGG... |
Task1_train_33681 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ATACAAAGCAGAACCTAGCTTTGTTTAGGTAGTATCTATCAATTCTCTTGAAATTTATCAGGCTGTAGCTTCTATAGCAGTTCTCGGCTGAGCTGCTCGTCTATTTAAACAAAAATAATATTGAAAGAATATTAACTTCTGAAGACGACTCAGAAATCATAATATAGTGGTCTATTCTTAATGCATGAAGAAAATGTGATATTTTGGCTCTTTTAATACACCTTTGTGAGTTGTAAAATAATAAAGACAGGACTACAAATAAAAATAATCCAAATACTCTATAAAATAAAGACAGATTTGTGCTTCTTGAAGTCTATAAA... | ATACAAAGCAGAACCTAGCTTTGTTTAGGTAGTATCTATCAATTCTCTTGAAATTTATCAGGCTGTAGCTTCTATAGCAGTTCTCGGCTGAGCTGCTCGTCTATTTAAACAAAAATAATATTGAAAGAATATTAACTTCTGAAGACGACTCAGAAATCATAATATAGTGGTCTATTCTTAATGCATGAAGAAAATGTGATATTTTGGCTCTTTTAATACACCTTTGTGAGTTGTAAAATAATAAAGACAGGACTACAAATAAAAATAATCCAAATACTCTATAAAATAAAGACAGATTTGTGCTTCTTGAAGTCTATAAA... |
Task1_train_33682 | This alteration occurs on Chromosome 1. Is it associated with a disease or is it a benign variant? | Benign | TGTCATTATTGCAGATGCGAGCACATGTCAACTCAAGCTGGTTCATTTTTCAGAAGAACATGGAGAGATTTCTTCATGCGATTATGCCATCGACCTTTATCCCTCTCTATACAATGGTAAGGTCTGGACTGAAGACTTTTCCTCATTTTGATTTTCTGTTTAGCTGTTAAAGAATACACAAGAATACTTTTTAAACTTCCCTGCAGGTCACTTTTTCCAGAATAAGATACCATGAGGCTGTGCAGCGTTGGCATTGGCAAAAAAAGGTTGGAACAGTTACATTTTATTTATTTTTTAATGTGGTGTTTTGAAATGTCATA... | TGTCATTATTGCAGATGCGAGCACATGTCAACTCAAGCTGGTTCATTTTTCAGAAGAACATGGAGAGATTTCTTCATGCGATTATGCCATCGACCTTTATCCCTCTCTATACAATGGTAAGGTCTGGACTGAAGACTTTTCCTCATTTTGATTTTCTGTTTAGCTGTTAAAGAATACACAAGAATACTTTTTAAACTTCCCTGCAGGTCACTTTTTCCAGAATAAGATACCATGAGGCTGTGCAGCGTTGGCATTGGCAAAAAAAGGTTGGAACAGTTACATTTTATTTATTTTTTAATGTGGTGTTTTGAAATGTCATA... |
Task1_train_33683 | This variant is located on Chromosome 1. Evaluate its biological effect and specify any disease association. | Benign | TCTTTTTGGTTTTGATTTGCATTTCTCTAACGACCAGTGATGATGAGCTTTTTTTCATGTTTGTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATATCCTTCACCCACTTGTTAATGGGGTTGTTTTTTTCTTGTAAATTTGTTTAAGTTCTTTGTAGATTCTGCATATTACCCCTTTGTCAGATAGATTGCAAAATTTTCTCCCATTCTGTAGATTGCCTGTTCACTCTGATGATAGTTTCTTTTGCTGTGCAGAAGCTCTTTAGTTTAATTAGATCTTATTTGTCAATTTTGGCTTTTGTTGCCATTGC... | TCTTTTTGGTTTTGATTTGCATTTCTCTAACGACCAGTGATGATGAGCTTTTTTTCATGTTTGTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATATCCTTCACCCACTTGTTAATGGGGTTGTTTTTTTCTTGTAAATTTGTTTAAGTTCTTTGTAGATTCTGCATATTACCCCTTTGTCAGATAGATTGCAAAATTTTCTCCCATTCTGTAGATTGCCTGTTCACTCTGATGATAGTTTCTTTTGCTGTGCAGAAGCTCTTTAGTTTAATTAGATCTTATTTGTCAATTTTGGCTTTTGTTGCCATTGC... |
Task1_train_33684 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ATCCTATAACAAATGGAAGGCCATGGAAGGGCTTTAAATGAGAAATGACACGATCAGATTTGTGCTGTGGGCAGCTCATCTTTGATGCTGCCTGGATGACAGATTTGACAGGGACAGGACTAAAGGCAGAAGATTCAGGCAACAGGCTACTTCCTGTTTTAGTTAAAAGATATAAGGATGACCAGGCTCAGTGGCTCACACCTGTAATCTCAGCATTTTGGGAGGCCAAGGTGAGAGGATCACTTGAGGCCAGGAGTTCGAGGCCAGCCTGGGCAACATAGGCCCCATCTCTACAAAAAAATTTTTAAAAATTTAAAAAA... | ATCCTATAACAAATGGAAGGCCATGGAAGGGCTTTAAATGAGAAATGACACGATCAGATTTGTGCTGTGGGCAGCTCATCTTTGATGCTGCCTGGATGACAGATTTGACAGGGACAGGACTAAAGGCAGAAGATTCAGGCAACAGGCTACTTCCTGTTTTAGTTAAAAGATATAAGGATGACCAGGCTCAGTGGCTCACACCTGTAATCTCAGCATTTTGGGAGGCCAAGGTGAGAGGATCACTTGAGGCCAGGAGTTCGAGGCCAGCCTGGGCAACATAGGCCCCATCTCTACAAAAAAATTTTTAAAAATTTAAAAAA... |
Task1_train_33685 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATTATGGAAAGAAGGAGACTGAAAAGTGCTATCTTTACACAGCTGAACTATTGACAGTATTTATCATTTCTTTCTTTCTTTTTTTTTTTTTTTAAATTTGAGACAGGGTCTCTTTCTCTGTCCTCCAGGCTGGAGTGCAGTGGCACCATCAGAGCTCCTGGGCTCAAGCGATCTTCAGTAACTGGCATCAAGCCTCTTGAGTAGCTGGAACTACAGGCACATGCCACCATGCCTGGCTAATTTTGTGTGTGTGGGGGGGGGGTCTCACTATGTTGCCCAGGCTAGTCTTGAACTCCTGGCCTGAAGCAGTCATTCTGCCT... | ATTATGGAAAGAAGGAGACTGAAAAGTGCTATCTTTACACAGCTGAACTATTGACAGTATTTATCATTTCTTTCTTTCTTTTTTTTTTTTTTTAAATTTGAGACAGGGTCTCTTTCTCTGTCCTCCAGGCTGGAGTGCAGTGGCACCATCAGAGCTCCTGGGCTCAAGCGATCTTCAGTAACTGGCATCAAGCCTCTTGAGTAGCTGGAACTACAGGCACATGCCACCATGCCTGGCTAATTTTGTGTGTGTGGGGGGGGGGTCTCACTATGTTGCCCAGGCTAGTCTTGAACTCCTGGCCTGAAGCAGTCATTCTGCCT... |
Task1_train_33686 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | TAAGGCTGTTGTGAAGGTAAATAGAAACTGCGTGTCAAGCACCTGCCATAATGCCTAGTCATTAATATATGTGCAAGCATTCATTACCACTCCTCTCCTTTTAATTGAATGCAACTAAAAGGAGATACTAAACATGTAAAACGTTGTCACCAATTTGCCTGCATTTTGGAAGCCTGTTTTAAGTCTTAATTATTTTTATTATGTAGGTAGTTATCACAGAAACGTGCCAGTTTTATCTTTCGAGATCTGGAAATACAAGTCAATTAAGTAACAGTATGGGCCAGTTGGGAGGAAGTAGCCATGAACTGGGAAGGGTTCTG... | TAAGGCTGTTGTGAAGGTAAATAGAAACTGCGTGTCAAGCACCTGCCATAATGCCTAGTCATTAATATATGTGCAAGCATTCATTACCACTCCTCTCCTTTTAATTGAATGCAACTAAAAGGAGATACTAAACATGTAAAACGTTGTCACCAATTTGCCTGCATTTTGGAAGCCTGTTTTAAGTCTTAATTATTTTTATTATGTAGGTAGTTATCACAGAAACGTGCCAGTTTTATCTTTCGAGATCTGGAAATACAAGTCAATTAAGTAACAGTATGGGCCAGTTGGGAGGAAGTAGCCATGAACTGGGAAGGGTTCTG... |
Task1_train_33687 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ATCTGGAAATACAAGTCAATTAAGTAACAGTATGGGCCAGTTGGGAGGAAGTAGCCATGAACTGGGAAGGGTTCTGAGTTTTACTTCTGTTTGTTGCTAGCCAAGTAATTTTATAACCCTGGGCATTGTCACTATCTCTTCTCTTGCCTGTGAAATGATATGTAGGAGAATACTTGGGCATCATAGGAATTGCCGTTGATTTAAAAATGAATTTGCCGTCCTATCTAGGAGCTCATGTTTTCTGCTTACTGAAAAGCCTAGTAAGAGCTTTTCTTCCACGTACTGCTTCCTGCCCCCTCCCCATACAACTAATCTAGGGA... | ATCTGGAAATACAAGTCAATTAAGTAACAGTATGGGCCAGTTGGGAGGAAGTAGCCATGAACTGGGAAGGGTTCTGAGTTTTACTTCTGTTTGTTGCTAGCCAAGTAATTTTATAACCCTGGGCATTGTCACTATCTCTTCTCTTGCCTGTGAAATGATATGTAGGAGAATACTTGGGCATCATAGGAATTGCCGTTGATTTAAAAATGAATTTGCCGTCCTATCTAGGAGCTCATGTTTTCTGCTTACTGAAAAGCCTAGTAAGAGCTTTTCTTCCACGTACTGCTTCCTGCCCCCTCCCCATACAACTAATCTAGGGA... |
Task1_train_33688 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGAGCCACTGTACTCCAGCCTGGGGGACAGAGCAAGACTGTCTCAAAAAAAAAAAAAGAAAAAAAAAGAGACCTTATAAGGAAATAACCCTGTTAATGCAATGGTATTCATCTTAAGTTTTAGTACTTCAGAAATATATTTTCATTTACTCTTCTTATTCCTTCTAAATTTCTCCTTATGACAAAACAAAACAGTAACACAGGTGTGCATACTGGTCTAGAAGACTGTCTGTTTCTCTTCCTATGAACGTCTTTATCTCGTCTTTTTCATTTCTGCTTCATACT... | TGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGAGCCACTGTACTCCAGCCTGGGGGACAGAGCAAGACTGTCTCAAAAAAAAAAAAAGAAAAAAAAAGAGACCTTATAAGGAAATAACCCTGTTAATGCAATGGTATTCATCTTAAGTTTTAGTACTTCAGAAATATATTTTCATTTACTCTTCTTATTCCTTCTAAATTTCTCCTTATGACAAAACAAAACAGTAACACAGGTGTGCATACTGGTCTAGAAGACTGTCTGTTTCTCTTCCTATGAACGTCTTTATCTCGTCTTTTTCATTTCTGCTTCATACT... |
Task1_train_33689 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CACAGTTCTAGAGGCTGGGAAGTCCAAGGTCTGAGTGAGAGCCCACTTCCTGGTTTGCAGACAGATGCCTTCTCGCTGTGTCCTTACATGGTAGAGGGAGAGAATATCTCTTTTGTACCTCTTCTTAAGGGCACTAATCTCATTCATGAGGGCTCTACTCTCATGATCTAATCACCTCTCAAAAATCCCACCATCACATTAGGAGTTAAGGGGTTAGGACTTCAATATGAATGTGAGGGAGACACAACATTCAGTCCACAGCAAATTCCAGTACATTAAAGATACAAATATGAAATATGTAAATATGAGATTATTTTTTA... | CACAGTTCTAGAGGCTGGGAAGTCCAAGGTCTGAGTGAGAGCCCACTTCCTGGTTTGCAGACAGATGCCTTCTCGCTGTGTCCTTACATGGTAGAGGGAGAGAATATCTCTTTTGTACCTCTTCTTAAGGGCACTAATCTCATTCATGAGGGCTCTACTCTCATGATCTAATCACCTCTCAAAAATCCCACCATCACATTAGGAGTTAAGGGGTTAGGACTTCAATATGAATGTGAGGGAGACACAACATTCAGTCCACAGCAAATTCCAGTACATTAAAGATACAAATATGAAATATGTAAATATGAGATTATTTTTTA... |
Task1_train_33690 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GGTGACAGAGAGAACTCCATCTGAAAAAAAAAAAAAAAGTTTGTCACAAGAGCAGACAGCCTTAAATTGGGGGCCAGGGAAGTTTCTTGGAGAAAATGGCCTCTCTGAAATATTCCTGAATCAATAACAGAAGCATCCTCTGGCAGTTGACTGCAGAACCCCTACCCCTTTTCAGGCCCTTCATTATTCCCTAGAACCTCCAAGTGGGCCAAACATGAGAGGCAACCACAATTGATTAGGAGACAGATCAATCGTTCAAAAAACATAAAACAATAATCTACTGTTCACTGTGGATTTAGCAATTAATCAGCCCTAGAGGA... | GGTGACAGAGAGAACTCCATCTGAAAAAAAAAAAAAAAGTTTGTCACAAGAGCAGACAGCCTTAAATTGGGGGCCAGGGAAGTTTCTTGGAGAAAATGGCCTCTCTGAAATATTCCTGAATCAATAACAGAAGCATCCTCTGGCAGTTGACTGCAGAACCCCTACCCCTTTTCAGGCCCTTCATTATTCCCTAGAACCTCCAAGTGGGCCAAACATGAGAGGCAACCACAATTGATTAGGAGACAGATCAATCGTTCAAAAAACATAAAACAATAATCTACTGTTCACTGTGGATTTAGCAATTAATCAGCCCTAGAGGA... |
Task1_train_33691 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | CAAAAAACATAAAACAATAATCTACTGTTCACTGTGGATTTAGCAATTAATCAGCCCTAGAGGATGAGTGACTTGGCCAGGTGGAGAGGGGAAGGAAGAGTGTTCCAGTTAGAGGGAACAATGTTACATGCTGGAAGAACCGAAATGTAACTAGCATGCATGTAGCTAGTAACACAGAGGAGCCCACGGCTCAGGAGAGCAGGAAATGGGGAGAGAAGAAGCCAGAAAGATGGGCCCCGGCCTTGGTGTTAGGTTAAAATGATTGAACGTTCCCTTTTTTTTTTTTTTGAGACGGAGTTTCTCTCTGTCACCTAGGCTGG... | CAAAAAACATAAAACAATAATCTACTGTTCACTGTGGATTTAGCAATTAATCAGCCCTAGAGGATGAGTGACTTGGCCAGGTGGAGAGGGGAAGGAAGAGTGTTCCAGTTAGAGGGAACAATGTTACATGCTGGAAGAACCGAAATGTAACTAGCATGCATGTAGCTAGTAACACAGAGGAGCCCACGGCTCAGGAGAGCAGGAAATGGGGAGAGAAGAAGCCAGAAAGATGGGCCCCGGCCTTGGTGTTAGGTTAAAATGATTGAACGTTCCCTTTTTTTTTTTTTTGAGACGGAGTTTCTCTCTGTCACCTAGGCTGG... |
Task1_train_33692 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | GTGAGCCACCACGCCCAGCCAATAACCAGTTTTTAACCTAATATTTTTATTCAGTGTTTTGTTGCCCATTACTCATCATCAGCCATTGGTGGTGGCCATTCCTAATAGAGAGAAGACCATCCACAAAACCAAGGCCTCAGCAGTGGTTTTGTTTACATGATTTTACAGCTTCTCACTTTGTGCTTTTCACTGTATCATCCTATCTTGGCATTACACCTCTTATCCTGCCAGGATTATTTACTGTTGCTTGTTCTTTAGTTGACTGAGTTCTTTGAATTGATTCTGTAGGTGCCTTTCATGGTAGCCTGGTTTTAGATCTT... | GTGAGCCACCACGCCCAGCCAATAACCAGTTTTTAACCTAATATTTTTATTCAGTGTTTTGTTGCCCATTACTCATCATCAGCCATTGGTGGTGGCCATTCCTAATAGAGAGAAGACCATCCACAAAACCAAGGCCTCAGCAGTGGTTTTGTTTACATGATTTTACAGCTTCTCACTTTGTGCTTTTCACTGTATCATCCTATCTTGGCATTACACCTCTTATCCTGCCAGGATTATTTACTGTTGCTTGTTCTTTAGTTGACTGAGTTCTTTGAATTGATTCTGTAGGTGCCTTTCATGGTAGCCTGGTTTTAGATCTT... |
Task1_train_33693 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | GGTAATGGGAGTTGCAAAAATAAAAAGACAGGGTACCTTCCCTAGAGGTAAACGTAAACTAGCTTAATTTTGCAACATTTTATTATGGAAAATGGTATACACAGTTCTCAAACAGCCCAGAGGAAAGTAAACTAAGGAAGTTTACTGAGACTGGGAGGGGAAAGGTGAAAAGAAAGGGATACACAAAACGACCAGTGATGAATAGGTAGAAGTTCAGCAGGCAGGTGCAAAAACATTCCAGGAAAAGGCATGGAGGGATGAAATAGTATCAGGGTGTTCAGGTAACTGAACAGTATTATTACTATATTATATATTATATT... | GGTAATGGGAGTTGCAAAAATAAAAAGACAGGGTACCTTCCCTAGAGGTAAACGTAAACTAGCTTAATTTTGCAACATTTTATTATGGAAAATGGTATACACAGTTCTCAAACAGCCCAGAGGAAAGTAAACTAAGGAAGTTTACTGAGACTGGGAGGGGAAAGGTGAAAAGAAAGGGATACACAAAACGACCAGTGATGAATAGGTAGAAGTTCAGCAGGCAGGTGCAAAAACATTCCAGGAAAAGGCATGGAGGGATGAAATAGTATCAGGGTGTTCAGGTAACTGAACAGTATTATTACTATATTATATATTATATT... |
Task1_train_33694 | This variant is located on Chromosome 1. Evaluate its biological effect and specify any disease association. | Benign | AATAAAGAAGCTAGGAGAAATACAAAATGCACCTAACCAACCCCAAGTCACAGAATTACAGAGAATTCTTCCCTATGGGGCGCCGGCTCCTGGCCTCGGCTTTCTAGCGTATACCTTGGTTTTTCTGTTTTTCATCTTCCTAGGTTCACTGTTCAAGTATCAGGCATCATGATCCTCCACCTCCCACCCTTCCCCCAGTGATTTTTTTTTTTTTAAGACAGGGTCTGGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTACAATTACAGCTCACCGCAGCTGAACACTGGGGCCTAAGCGATCCTCCCACCTCAGCTTCCCA... | AATAAAGAAGCTAGGAGAAATACAAAATGCACCTAACCAACCCCAAGTCACAGAATTACAGAGAATTCTTCCCTATGGGGCGCCGGCTCCTGGCCTCGGCTTTCTAGCGTATACCTTGGTTTTTCTGTTTTTCATCTTCCTAGGTTCACTGTTCAAGTATCAGGCATCATGATCCTCCACCTCCCACCCTTCCCCCAGTGATTTTTTTTTTTTTAAGACAGGGTCTGGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTACAATTACAGCTCACCGCAGCTGAACACTGGGGCCTAAGCGATCCTCCCACCTCAGCTTCCCA... |
Task1_train_33695 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | ATGTGGGAGGCTCTATAAGCATGGGGCCACAGAGGAAAAGGCTGAGAGGGAAAGCTTCAATGACTAGGTGACTTCAAAAAGGTCATCCTGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGAACTTTGGGAGGGCCAGGCAGGCGGCAGATCGCTTGAGCTCAGGAGTTTGAGAGCAGCCTGGGCAACATGGGGAAACTCTGTCTCTACAAAAAATACAAAAACTAGCCAGACATGGTGGCGCGCGCCGCTCCTCCCAGCTACTTGGGAGGTTGCGGTGGGAGGGTCACTTGAGACCGGGAGGCGGAAGTTGCAGTGA... | ATGTGGGAGGCTCTATAAGCATGGGGCCACAGAGGAAAAGGCTGAGAGGGAAAGCTTCAATGACTAGGTGACTTCAAAAAGGTCATCCTGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGAACTTTGGGAGGGCCAGGCAGGCGGCAGATCGCTTGAGCTCAGGAGTTTGAGAGCAGCCTGGGCAACATGGGGAAACTCTGTCTCTACAAAAAATACAAAAACTAGCCAGACATGGTGGCGCGCGCCGCTCCTCCCAGCTACTTGGGAGGTTGCGGTGGGAGGGTCACTTGAGACCGGGAGGCGGAAGTTGCAGTGA... |
Task1_train_33696 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CTGTTGTTTCCTGACTTTTTAATGATTGCCATTCTAACTGGTGTGAGATGGTATCTCACTGTGGTTTTGATTTGCATTTCTCTGATGGCCAGTGATGATGAGCATTTTTTCATGTGTGTTTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATATCCTTCGCCCACTTTTTGATGGGGTTGTTTGTTTTTTTCTTGTAAATTTGTTTGAGTTCATTGTAGATTCTGGACATTAGCCCTTTGTCAGATGAGTAGGTTGCAAAAATTTTCTCCCATTCTGTAGTTTTAATGAACTCCTCATTAAAGAAGGAAGA... | CTGTTGTTTCCTGACTTTTTAATGATTGCCATTCTAACTGGTGTGAGATGGTATCTCACTGTGGTTTTGATTTGCATTTCTCTGATGGCCAGTGATGATGAGCATTTTTTCATGTGTGTTTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATATCCTTCGCCCACTTTTTGATGGGGTTGTTTGTTTTTTTCTTGTAAATTTGTTTGAGTTCATTGTAGATTCTGGACATTAGCCCTTTGTCAGATGAGTAGGTTGCAAAAATTTTCTCCCATTCTGTAGTTTTAATGAACTCCTCATTAAAGAAGGAAGA... |
Task1_train_33697 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AGTATGCTGTTACATAATCTCCTGGGCAATAAACATGGCTGCCTTTTGCAAAATTATCAGTTCAAAAATTTAAGCAGCTTTCTCCTAAGATGTTTCAATAAAAACTATCACCTGCACTTTCAACAGTGTTCTCTGACTTTCTAGCAACCCTGAAGTCATTCTCTATTTACAGGACTAGTAATTATTTTTAAACATTTCTTAAATCTGAATACAAGCTATCTCACAAATAGCATTTTGAGTGGTTGTTTTTATTTCTGTATTTAATGTATAGGAGCCTTAATGTGCTAGTTTTCTGGGGACTGGAAAATTGAGACTTTTTC... | AGTATGCTGTTACATAATCTCCTGGGCAATAAACATGGCTGCCTTTTGCAAAATTATCAGTTCAAAAATTTAAGCAGCTTTCTCCTAAGATGTTTCAATAAAAACTATCACCTGCACTTTCAACAGTGTTCTCTGACTTTCTAGCAACCCTGAAGTCATTCTCTATTTACAGGACTAGTAATTATTTTTAAACATTTCTTAAATCTGAATACAAGCTATCTCACAAATAGCATTTTGAGTGGTTGTTTTTATTTCTGTATTTAATGTATAGGAGCCTTAATGTGCTAGTTTTCTGGGGACTGGAAAATTGAGACTTTTTC... |
Task1_train_33698 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGGCAATTGAATCACATTCCAAACAGCAACAAGGAGAAAAATGTGAAGCTAATAGGACAGGGAATGTTATTAAAAACCAGTGTTTTTTAATTCAGAGAAGGCCAACCTGTTCAGGCACTTCTCTCTAAATCTCATGGAGCAGAACACTATCACTCGGCCACCAATGTAAGCAGAAACATTTCTCTGTAGCAGAACACAGGAGACATGATTGGGAGTGGCTGCTGCTACCTGTACTATCATGAGTTCTGACAAAAAGGCTATTTACATTGTGCACTGGAACAGGGTGTTATGAAAAAACCCTCAAATTCAGAATACATTCA... | AGGCAATTGAATCACATTCCAAACAGCAACAAGGAGAAAAATGTGAAGCTAATAGGACAGGGAATGTTATTAAAAACCAGTGTTTTTTAATTCAGAGAAGGCCAACCTGTTCAGGCACTTCTCTCTAAATCTCATGGAGCAGAACACTATCACTCGGCCACCAATGTAAGCAGAAACATTTCTCTGTAGCAGAACACAGGAGACATGATTGGGAGTGGCTGCTGCTACCTGTACTATCATGAGTTCTGACAAAAAGGCTATTTACATTGTGCACTGGAACAGGGTGTTATGAAAAAACCCTCAAATTCAGAATACATTCA... |
Task1_train_33699 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTTGCCAGATGTGGTGGCGGGCACCTGTAATCCCTGCTACTGGGGAGGCTGAGGCAGGATAATCTCTTGAACCCGGGAGGCGGAGGGTGCAGTGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTCAAGAAAAAAAAAAAAGAAAAAAGAACTACCATACAAGACAGCAATCTCACATGTGTGTGTGTGTGTAAAATCAATAGAAATAAAATCAGTATCTCAAATAAATATCTGCATCCCCATGTTCATTA... | GCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTTGCCAGATGTGGTGGCGGGCACCTGTAATCCCTGCTACTGGGGAGGCTGAGGCAGGATAATCTCTTGAACCCGGGAGGCGGAGGGTGCAGTGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTCAAGAAAAAAAAAAAAGAAAAAAGAACTACCATACAAGACAGCAATCTCACATGTGTGTGTGTGTGTAAAATCAATAGAAATAAAATCAGTATCTCAAATAAATATCTGCATCCCCATGTTCATTA... |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.