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_40500 | This genomic variant is located on Chromosome 10. Can you determine its pathogenicity and name any linked disease? | Benign | GCCCGGCGGCTGCACTCCCCGCGGTGCCCTGCCCACTAGGTCAGGGCCGGGGGCGTTTCCATGAGGGCCGGCGGAGGCCTTGCCGGCGCCCTCACTGGAGCGCAGCTTCCCTCGGAACCAAAGCCTTGACGGGGATTTCCTCTCCTTGAGCCCCCGGTGGGCTCCTCTGCCTCCTTTTGTCACCCCGTTCCTCAGCTGTGTCTTCGTCCCCCACCCCGGCCTGGTGCCGAGGGACCGTCCAAGGGGTCCCCGTCCGCACCTCCCTGCCCTGATTCCGGGCGCTCACTGAAAGTCTCGATGATTTGCCAAGCCCCCCGCCC... | GCCCGGCGGCTGCACTCCCCGCGGTGCCCTGCCCACTAGGTCAGGGCCGGGGGCGTTTCCATGAGGGCCGGCGGAGGCCTTGCCGGCGCCCTCACTGGAGCGCAGCTTCCCTCGGAACCAAAGCCTTGACGGGGATTTCCTCTCCTTGAGCCCCCGGTGGGCTCCTCTGCCTCCTTTTGTCACCCCGTTCCTCAGCTGTGTCTTCGTCCCCCACCCCGGCCTGGTGCCGAGGGACCGTCCAAGGGGTCCCCGTCCGCACCTCCCTGCCCTGATTCCGGGCGCTCACTGAAAGTCTCGATGATTTGCCAAGCCCCCCGCCC... |
Task1_train_40501 | A mutation located on Chromosome 10 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ACCGGGAGGGGCGCCGCGGGCCATTCGCCGCTTCTCCTGGGCCGAGGGCGCAGGCCCCTGCCGCGGGGGCCCCTCGGACTCCACGACTTCGCGGACGCGCGCCCACCGCCATAGCTGAGGTCCCGGGCCAGGCGGCGCGTGGGTGGCTGAGCGGGAGCGCGTCCAGCCAGGCGTGGAGGCCGCGCGGGGCCGGGGTCGAGCCCAGCATGGCGGGGGGGGTGCGGGGCAGTGGCCCGGACAAGGGCATGGGGCCGGAAGAGGCGGGGCCGTTGCCAGGAGACGAGACGGAATGGGCGGGGCGCGGGCGGGGGCCGTTGCCG... | ACCGGGAGGGGCGCCGCGGGCCATTCGCCGCTTCTCCTGGGCCGAGGGCGCAGGCCCCTGCCGCGGGGGCCCCTCGGACTCCACGACTTCGCGGACGCGCGCCCACCGCCATAGCTGAGGTCCCGGGCCAGGCGGCGCGTGGGTGGCTGAGCGGGAGCGCGTCCAGCCAGGCGTGGAGGCCGCGCGGGGCCGGGGTCGAGCCCAGCATGGCGGGGGGGGTGCGGGGCAGTGGCCCGGACAAGGGCATGGGGCCGGAAGAGGCGGGGCCGTTGCCAGGAGACGAGACGGAATGGGCGGGGCGCGGGCGGGGGCCGTTGCCG... |
Task1_train_40502 | A variant has been detected on Chromosome 10. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCTGCCCCCACGGGGTCCAAAAAGGGCTCCAAGGTTAGCCCAGAGGTGGGAGCCAGGGCGCAGGGACAGGACCCCAACCCTGGGGGGACACGGAGGCCTGGGAGTTAACCCTCAGCATGCCAGGGCTCCAGTGATTCGGGTTTTGAGAGATCTTTCCAAAACCCCCAAAGCCCCCAAACCCAAGGGAAGCGCGGAACGTGTCCCTGCCCTGAGCCCACCCACCCATCTGTCCTGCAGGGCCCCAGGGAGTCCTCTTCTCTGCCAGAGCTTCAGCTCTGGGAGGGGCTTGGTGGGCGGAGCAGGTCTGAGTGGAAGGAGAA... | GCTGCCCCCACGGGGTCCAAAAAGGGCTCCAAGGTTAGCCCAGAGGTGGGAGCCAGGGCGCAGGGACAGGACCCCAACCCTGGGGGGACACGGAGGCCTGGGAGTTAACCCTCAGCATGCCAGGGCTCCAGTGATTCGGGTTTTGAGAGATCTTTCCAAAACCCCCAAAGCCCCCAAACCCAAGGGAAGCGCGGAACGTGTCCCTGCCCTGAGCCCACCCACCCATCTGTCCTGCAGGGCCCCAGGGAGTCCTCTTCTCTGCCAGAGCTTCAGCTCTGGGAGGGGCTTGGTGGGCGGAGCAGGTCTGAGTGGAAGGAGAA... |
Task1_train_40503 | Mutation context: Chromosome 10. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GTGCTCTCAGGAACCATGTGGCCAACTCCCCACGCCTGCCACCCTCACCCCACCAGGGCCCAGGACTTGGCACAGCTTCCCGCCAACACCACCTTAAAACATAAAATCAGGCATTAAACCTGGCCTGAGGGGAGGTGGCCTGCTCCAGAGACCTGGACCGAGGCGTCCCCTCCCCTATCCAGCTCTGGCCTCGGCCTGGCAAACCCGGGCAGGAGCCCCCTCACCTGGTTCACAGCCCCTGAGCTGTGGGAGCACATGGCGGACACCCTGGCAAACCCCACGGTAGTCCCGGTGAAGTCGACACCCCTGGAAGTGGGAGT... | GTGCTCTCAGGAACCATGTGGCCAACTCCCCACGCCTGCCACCCTCACCCCACCAGGGCCCAGGACTTGGCACAGCTTCCCGCCAACACCACCTTAAAACATAAAATCAGGCATTAAACCTGGCCTGAGGGGAGGTGGCCTGCTCCAGAGACCTGGACCGAGGCGTCCCCTCCCCTATCCAGCTCTGGCCTCGGCCTGGCAAACCCGGGCAGGAGCCCCCTCACCTGGTTCACAGCCCCTGAGCTGTGGGAGCACATGGCGGACACCCTGGCAAACCCCACGGTAGTCCCGGTGAAGTCGACACCCCTGGAAGTGGGAGT... |
Task1_train_40504 | This alteration occurs on Chromosome 10. Is it associated with a disease or is it a benign variant? | Benign | GTGGCCTGGTCCTGCCCCGAAGGACCAGAGGCTCCAGTTTGTTGCCTACAGCTCCCCCTACCCTGCCACCAGCAGCCCCCCGCAGGTGACTTCAGGCCCCAGGGTACAGGAGGGTGAGCCTCTTGGGCTTGGCGTCCCCTGAGCAGACCCCCATGCAAGACAGCAAAGGCCTGAGTGGGAGGAGGAGGCACCCTCCCTGCCTCCCTTCCCCACCCCCACCACAGGCTTAGGCCTTCCTCTCCACCTGCGGGAGCCCTGGCGTTCGTCCGCCACACCCACCTGAGGCCGGCACAGGTGCTGAGGCTGGCGGCTGAGTCCGG... | GTGGCCTGGTCCTGCCCCGAAGGACCAGAGGCTCCAGTTTGTTGCCTACAGCTCCCCCTACCCTGCCACCAGCAGCCCCCCGCAGGTGACTTCAGGCCCCAGGGTACAGGAGGGTGAGCCTCTTGGGCTTGGCGTCCCCTGAGCAGACCCCCATGCAAGACAGCAAAGGCCTGAGTGGGAGGAGGAGGCACCCTCCCTGCCTCCCTTCCCCACCCCCACCACAGGCTTAGGCCTTCCTCTCCACCTGCGGGAGCCCTGGCGTTCGTCCGCCACACCCACCTGAGGCCGGCACAGGTGCTGAGGCTGGCGGCTGAGTCCGG... |
Task1_train_40505 | With a mutation on Chromosome 10, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GCTGTATTTTAATTCAAACATCGGCCATGCAGAGACTCCCTGCCCCCATATATCCCAGCTGACGCCCCAGGCCCCGGGCCCCCCTCCCTTGCAGGCCATCAGGGCCAATTCAGTTCTGCGTGTGCTTGTTCATCTGGCCAATGCCCTTAGAAGCCCAGCAGTGAAGGGTGTGGTGTGCATGGCCCTGCCTTCCCTGACCCCACCTGGCTGGCTTCCAGCTCACCATGGCTTCCCTGGCAGGCCCAGTTCACAGGCTTCCTGGGCACTGCCGCTGTTCCAAAGCAGGCCAGTCCCACTGAGCTGGGAAGCTGCCTAGACCC... | GCTGTATTTTAATTCAAACATCGGCCATGCAGAGACTCCCTGCCCCCATATATCCCAGCTGACGCCCCAGGCCCCGGGCCCCCCTCCCTTGCAGGCCATCAGGGCCAATTCAGTTCTGCGTGTGCTTGTTCATCTGGCCAATGCCCTTAGAAGCCCAGCAGTGAAGGGTGTGGTGTGCATGGCCCTGCCTTCCCTGACCCCACCTGGCTGGCTTCCAGCTCACCATGGCTTCCCTGGCAGGCCCAGTTCACAGGCTTCCTGGGCACTGCCGCTGTTCCAAAGCAGGCCAGTCCCACTGAGCTGGGAAGCTGCCTAGACCC... |
Task1_train_40506 | This sequence change occurs on Chromosome 10. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTTCCCTCTCTGGCCCCCCCTCAGGCTCCTCCTGGTCACCAGCCTGGTGGTTGTGCTGCTGTGGGAGGCAGGTGCAGTCCCAGCACCCAAGGTAGGTGTGAGCCCCTCCCATCTGGGCAGCAACTCCAGTTGTCACCTTCTGCCCCTACAGCAGGGGATGTGGACAAAGGGCCCCTCTTCTGGCTTCAAACCCCAAGCTGGCTTAGGGGAGAGAGGCATGGGTACGCTCATGACTCTTGATGCCTGTGCAGGCATGAGGAGGGGGCAGGCTTCCCTTCCCTGGGGTCAGATGGACAGGCCTCAAGACACCCAGGTGGTCC... | CTTCCCTCTCTGGCCCCCCCTCAGGCTCCTCCTGGTCACCAGCCTGGTGGTTGTGCTGCTGTGGGAGGCAGGTGCAGTCCCAGCACCCAAGGTAGGTGTGAGCCCCTCCCATCTGGGCAGCAACTCCAGTTGTCACCTTCTGCCCCTACAGCAGGGGATGTGGACAAAGGGCCCCTCTTCTGGCTTCAAACCCCAAGCTGGCTTAGGGGAGAGAGGCATGGGTACGCTCATGACTCTTGATGCCTGTGCAGGCATGAGGAGGGGGCAGGCTTCCCTTCCCTGGGGTCAGATGGACAGGCCTCAAGACACCCAGGTGGTCC... |
Task1_train_40507 | A variant has been detected on Chromosome 10. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GGCAGTGTGCAGAGCTCCCAGTGCCACCCAGGGTCACCATGTTCCCTCTCTGCCATGGACACGAATCACAAGCAAGAACTGTCATGGTTAGAAGCCAGCGTTACCCAGGACCAGCCTCTCCCAACACCATCAGATGTGGGCACAGTCACAGTCCCGGGACTCTAAGGCCCCCCCCAAGCTCTGTCACAACCACTCTAGCCTCCGTGGCTGTCCACAGAGGGACCACTGACCAGCCATGGGGCTGTCCATCCAGGGCCTCTGGTCAGATATGAGCTGTGGGCCCTGAGACACAGGCAGATTTTGAGTAATTACCTAAGGCA... | GGCAGTGTGCAGAGCTCCCAGTGCCACCCAGGGTCACCATGTTCCCTCTCTGCCATGGACACGAATCACAAGCAAGAACTGTCATGGTTAGAAGCCAGCGTTACCCAGGACCAGCCTCTCCCAACACCATCAGATGTGGGCACAGTCACAGTCCCGGGACTCTAAGGCCCCCCCCAAGCTCTGTCACAACCACTCTAGCCTCCGTGGCTGTCCACAGAGGGACCACTGACCAGCCATGGGGCTGTCCATCCAGGGCCTCTGGTCAGATATGAGCTGTGGGCCCTGAGACACAGGCAGATTTTGAGTAATTACCTAAGGCA... |
Task1_train_40508 | Here is a variant on Chromosome 10. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GTGACAGAGTGAGACTCCGTCTCAAAAAAAAAGAAAAGAAAAAAAGAAAAATCCCCAGCACAGAACACAGCCCACAGCCGCTTTCCTTCTCCTAATATGCCTTGGTCAGCTCTTCCCAGGACACCACTCTGGAGACAGCCCTGGACTCTGCTGAGACAAGGCACCAGGAAACACCTTCTTTCAACAAATGCCAACAGGTGAGGGGGTGTAAGGCAGCTCCTTGCACTTGGTACCGCCCCAGTGCCAAGACCTCTGGCCAACTGGACGCAGGGTGGGGGATGTGAAAATCCTGGGTGTTCCTGCAGCATTAAGATCAGGCA... | GTGACAGAGTGAGACTCCGTCTCAAAAAAAAAGAAAAGAAAAAAAGAAAAATCCCCAGCACAGAACACAGCCCACAGCCGCTTTCCTTCTCCTAATATGCCTTGGTCAGCTCTTCCCAGGACACCACTCTGGAGACAGCCCTGGACTCTGCTGAGACAAGGCACCAGGAAACACCTTCTTTCAACAAATGCCAACAGGTGAGGGGGTGTAAGGCAGCTCCTTGCACTTGGTACCGCCCCAGTGCCAAGACCTCTGGCCAACTGGACGCAGGGTGGGGGATGTGAAAATCCTGGGTGTTCCTGCAGCATTAAGATCAGGCA... |
Task1_train_40509 | A sequence alteration has been identified on Chromosome 10. Is it disease-inducing or harmless? | Benign | CCCCCGGGTCCCAGCCCACTGCTCTCGGGTCAGAGGCGGCAGGAAGAGCCTCTCCTGACACACTCTGCTGCTCACTTTTCTTCCTGCATAGCATCTTTCACGTTAAACTGCTCAATCTTTAAAAATGACAAAAACAGTTGCAGACCTGTGGGTGAGAGTTCTCGGTTAACATGCAGTGTCTCTGTGGCTCAGGAAACCCACGGCTCCCCGCGCCCAAGAGCGTCCTGCGGTCTCGCTGGCACAGCGCCCCGTACACTAGGGGGTCCTACAGCTACGTGGCCGTGGGCAGTACTGGGGGCGACCTGGACCTGCTGGCTCAG... | CCCCCGGGTCCCAGCCCACTGCTCTCGGGTCAGAGGCGGCAGGAAGAGCCTCTCCTGACACACTCTGCTGCTCACTTTTCTTCCTGCATAGCATCTTTCACGTTAAACTGCTCAATCTTTAAAAATGACAAAAACAGTTGCAGACCTGTGGGTGAGAGTTCTCGGTTAACATGCAGTGTCTCTGTGGCTCAGGAAACCCACGGCTCCCCGCGCCCAAGAGCGTCCTGCGGTCTCGCTGGCACAGCGCCCCGTACACTAGGGGGTCCTACAGCTACGTGGCCGTGGGCAGTACTGGGGGCGACCTGGACCTGCTGGCTCAG... |
Task1_train_40510 | A mutation on Chromosome 10 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGAGTTTCTGGTGGCCCCACAGAGGTGTCCTGGCTCAGAACCCGCAGGCCATCTAGGGGTCCTGGCTGCCGCTGCAAGTCTGAGCTGCCTCAGCTGTGATCTCTGCATGTCTAACATGGATCGGGGTTGGGTAGAGGTCACTTCTTCCCAGCCCTGCCTCAACTGTGTGTGAGCTGCACTGGCCTCACAGCTCCTGGCCTTGTTGTGCATATGAGGAGCAGCTGAAATGAGGTGGATAGTCTGCCTGCTGCGGTACCCCAGAGAGGGTGGTGCTCAGTGGACCAAGGGGTGCCCTGACCTCGCCTCTGGGATTGCAGAGG... | TGAGTTTCTGGTGGCCCCACAGAGGTGTCCTGGCTCAGAACCCGCAGGCCATCTAGGGGTCCTGGCTGCCGCTGCAAGTCTGAGCTGCCTCAGCTGTGATCTCTGCATGTCTAACATGGATCGGGGTTGGGTAGAGGTCACTTCTTCCCAGCCCTGCCTCAACTGTGTGTGAGCTGCACTGGCCTCACAGCTCCTGGCCTTGTTGTGCATATGAGGAGCAGCTGAAATGAGGTGGATAGTCTGCCTGCTGCGGTACCCCAGAGAGGGTGGTGCTCAGTGGACCAAGGGGTGCCCTGACCTCGCCTCTGGGATTGCAGAGG... |
Task1_train_40511 | A variant was discovered on Chromosome 10. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CGGTCCAGCCCCCGCAGTGACCGCAGCCCCTTTTGCAGAGGAGGGCGCACTGCGCGTGCGCGGGGGCGAGGACCGCTGCTCCGGGCGCGTGGAGCTCTGGCACGCGGGCTCCTGGGGCACCGTGTGCGACGATGGCTGGGACCTGGCGGACGCGGAGGTCGTGTGCCGCCAGCTGGGCTGTGGTCGGGCCGTCGCCGCCCTGGGGGCCGCCGCCTTTGGCCCTGGCTCCGGGCCCGTGTGGCTGGACGAGGTGGGGTGCCGGGGCAGCGAGGCGTCCCTGTGGGGCTGCCCTGCGGAGCGGTGGGGACGCGGAGACCGCG... | CGGTCCAGCCCCCGCAGTGACCGCAGCCCCTTTTGCAGAGGAGGGCGCACTGCGCGTGCGCGGGGGCGAGGACCGCTGCTCCGGGCGCGTGGAGCTCTGGCACGCGGGCTCCTGGGGCACCGTGTGCGACGATGGCTGGGACCTGGCGGACGCGGAGGTCGTGTGCCGCCAGCTGGGCTGTGGTCGGGCCGTCGCCGCCCTGGGGGCCGCCGCCTTTGGCCCTGGCTCCGGGCCCGTGTGGCTGGACGAGGTGGGGTGCCGGGGCAGCGAGGCGTCCCTGTGGGGCTGCCCTGCGGAGCGGTGGGGACGCGGAGACCGCG... |
Task1_train_40512 | Consider a variant on Chromosome 10. Determine its clinical classification and disease relevance. | Benign | TATGACCCGCAGGGCGCAGACTGGCGGAAAATTAGCAGAGCCCTGGGCATGGGCTGCACCTGGCCCTTAAGGGACAATGATGGAAATATTCCTTATTAGCACAATACTGAGCACAGGCTGTGTGATAATGTGTCAAGGGAACTGCAGACATCCTTTCAGAAAAAGTTCATAAAACGGAGAAAGTTTGGTTCCCAACCTAGATTTTTAACCTGTTGAACTCTGTCTAAATGGGTCATCTCGGGATGTCCTCCACTCAACATGACCACGTCTGCCCCTCTGTCCCACCTGTCTCCTCAGTCCTTCCTCCCCACCTTTCAGGA... | TATGACCCGCAGGGCGCAGACTGGCGGAAAATTAGCAGAGCCCTGGGCATGGGCTGCACCTGGCCCTTAAGGGACAATGATGGAAATATTCCTTATTAGCACAATACTGAGCACAGGCTGTGTGATAATGTGTCAAGGGAACTGCAGACATCCTTTCAGAAAAAGTTCATAAAACGGAGAAAGTTTGGTTCCCAACCTAGATTTTTAACCTGTTGAACTCTGTCTAAATGGGTCATCTCGGGATGTCCTCCACTCAACATGACCACGTCTGCCCCTCTGTCCCACCTGTCTCCTCAGTCCTTCCTCCCCACCTTTCAGGA... |
Task1_train_40513 | An alteration has been detected on Chromosome 10. Is it pathogenic, and if so, what disease is involved? | Benign | TATTTTAAAGTTTAGTTTTGCTTTTTGTAGCTGGCTATTAGTTCTAGCAGGTATGCAATGGGCTGAGCTCTTTTGCTGGAATGAGATGTACCTGCATGGCAGTGACCCCTAACTGAGGTGTCAAAAATACAGATTAATAAGTGAATCCAAGCTGAGTTTGGGTGTGGTTGGTCCCATCTCATCACCATTGCTATTGGTAGTAGTAAAACTGATGTTTAAATAGTTCCCACCTGGTCTTGGTGAAAACATAGGAGGGGATCTTCTGTTGGGAGCTGGTTAACCGTGAGAATATGTCTACATGATCAGCAGGGTATATAAGA... | TATTTTAAAGTTTAGTTTTGCTTTTTGTAGCTGGCTATTAGTTCTAGCAGGTATGCAATGGGCTGAGCTCTTTTGCTGGAATGAGATGTACCTGCATGGCAGTGACCCCTAACTGAGGTGTCAAAAATACAGATTAATAAGTGAATCCAAGCTGAGTTTGGGTGTGGTTGGTCCCATCTCATCACCATTGCTATTGGTAGTAGTAAAACTGATGTTTAAATAGTTCCCACCTGGTCTTGGTGAAAACATAGGAGGGGATCTTCTGTTGGGAGCTGGTTAACCGTGAGAATATGTCTACATGATCAGCAGGGTATATAAGA... |
Task1_train_40514 | Here’s a variant located on Chromosome 10. What is the predicted biological effect — harmless or disease-causing? | Benign | TGAACAATCATTGGTTGATTTCTTAAAAAATTGTGGTGAACCAATAAAAGCTAAAGTTCCTTCTAATTGTGGGCTTAACTGAATTACAGTTTTAAAATGTGGTGTCTTCATTGCCACTCAGTTCAATATATTTTCTAACTTCCACTTGATTTAAAAGTCATGTTTGATAGTATATTGCCAGTTTGTTTAAGACAGGTATGATTAACTGCATCTTAGAGAACTCGTCTGTCCTGGACTGACTGAAGAATTTCTGCACTTTGCCATGTTCCATTTTTCCATGGAAACAGTGCTCTGCAGTGAGCCTCTCTCTTCAACTCCAC... | TGAACAATCATTGGTTGATTTCTTAAAAAATTGTGGTGAACCAATAAAAGCTAAAGTTCCTTCTAATTGTGGGCTTAACTGAATTACAGTTTTAAAATGTGGTGTCTTCATTGCCACTCAGTTCAATATATTTTCTAACTTCCACTTGATTTAAAAGTCATGTTTGATAGTATATTGCCAGTTTGTTTAAGACAGGTATGATTAACTGCATCTTAGAGAACTCGTCTGTCCTGGACTGACTGAAGAATTTCTGCACTTTGCCATGTTCCATTTTTCCATGGAAACAGTGCTCTGCAGTGAGCCTCTCTCTTCAACTCCAC... |
Task1_train_40515 | Given this context: Chromosome 10 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GTGCAGCTCCAGGTCTTTCTCCTTTTAGGGGCTTGGGACTGGCCTGCAGGAGGTTAGTGTCCAGGGTGGGAATTTACACCCATCCCCATGGCCACATGGTCCCCTCCTGCCCCATCACCACCTTGGGTGGACCCAGTATGGGAAAGGCCCTCCCCATAGACCATCCTCTGAGGAGTCCCAGGACCCCCTCCCTTGTCCTCCCGCCCCTTCCGCTGTCCCTTCAGTAGCTGTTTCTGTTCCCTGACGCCCACTTCTGGGGCTTACCACATCTCCTGGGCCAGCCTCTTCCTCTTGTGTGCTCTGGGCTTGGGCAGGGACTT... | GTGCAGCTCCAGGTCTTTCTCCTTTTAGGGGCTTGGGACTGGCCTGCAGGAGGTTAGTGTCCAGGGTGGGAATTTACACCCATCCCCATGGCCACATGGTCCCCTCCTGCCCCATCACCACCTTGGGTGGACCCAGTATGGGAAAGGCCCTCCCCATAGACCATCCTCTGAGGAGTCCCAGGACCCCCTCCCTTGTCCTCCCGCCCCTTCCGCTGTCCCTTCAGTAGCTGTTTCTGTTCCCTGACGCCCACTTCTGGGGCTTACCACATCTCCTGGGCCAGCCTCTTCCTCTTGTGTGCTCTGGGCTTGGGCAGGGACTT... |
Task1_train_40516 | Here is a genetic alteration on Chromosome 10. Based on the data, is it a benign variant or a cause of disease? | Benign | CCTGCGCGCGCAGAGGAGCGTAGCCTGCCCCTAGGCCGCGTTCCCGTGAGCTCCATGCCCACAGTGGCCGAGGCCGGCCACAAGCCCACGGTCCCTTCTGCACGGTCCCTGCCGCGCTGGGGCCACCGTGGAGGCCCGGAGGGCCCTGGGAGGAGGGAGGAGGAGCAGAGGCTTTCGGGAGAACCCAGCCCTTCACCGGCCAGGGGAGGCCGCGATGCATCGCGACTGGTTGTGAAGAGCCAGGGGAAGAACTTTACCGTGCAGGTGAGTGGGAGACATCAGAACACCTGCCTGTCCTAAATACGAAGCCTCGAATCCTA... | CCTGCGCGCGCAGAGGAGCGTAGCCTGCCCCTAGGCCGCGTTCCCGTGAGCTCCATGCCCACAGTGGCCGAGGCCGGCCACAAGCCCACGGTCCCTTCTGCACGGTCCCTGCCGCGCTGGGGCCACCGTGGAGGCCCGGAGGGCCCTGGGAGGAGGGAGGAGGAGCAGAGGCTTTCGGGAGAACCCAGCCCTTCACCGGCCAGGGGAGGCCGCGATGCATCGCGACTGGTTGTGAAGAGCCAGGGGAAGAACTTTACCGTGCAGGTGAGTGGGAGACATCAGAACACCTGCCTGTCCTAAATACGAAGCCTCGAATCCTA... |
Task1_train_40517 | A variant was discovered on Chromosome 10. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GAAGCAGAGGTTGCAGTGAGCTAAGATTGTGCCACTGCACTCCAGCCTGGGTAACATAGCAAGACTGTCTCAAAAAAAAAAACAAAAAAGGAGCACATAATTTTATATTTACTTTTCTACAATCTAAAATATGCAAATTCACGATTACATTCTAATGTTTTTCTGATTATATAGAAATGCATGACTGTCATCAGACATCCAAAAGGCATCAAATGTCTAACATGAAATATAAAATTTGTCTATAGTCTTAGCGGTCTGCAAAATTCAGGGCTCTCACCATTCTGAGTATACCGCTCAAGTTTCTTTCCTATGACTTCTTC... | GAAGCAGAGGTTGCAGTGAGCTAAGATTGTGCCACTGCACTCCAGCCTGGGTAACATAGCAAGACTGTCTCAAAAAAAAAAACAAAAAAGGAGCACATAATTTTATATTTACTTTTCTACAATCTAAAATATGCAAATTCACGATTACATTCTAATGTTTTTCTGATTATATAGAAATGCATGACTGTCATCAGACATCCAAAAGGCATCAAATGTCTAACATGAAATATAAAATTTGTCTATAGTCTTAGCGGTCTGCAAAATTCAGGGCTCTCACCATTCTGAGTATACCGCTCAAGTTTCTTTCCTATGACTTCTTC... |
Task1_train_40518 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | CAGGAGCCAGGCGGGCAGGTGGGGGTCCCGGGAAGGGCCTGGGGCTCAATCCCTGACTCCCAGCGGGGAGAAGGGCAGGTCAGGCTCCGGGCTGCTCAGGGCCCATTGCGTCCACAGGCTTCATGAAGCACACGCCCACCAAGCTGCGTGCACCGGCCTACAGCTTCCGTGGGGCCCCCATGCTCCTGGCAGAGAACTGCTCCCCAGGGCCCCGTTACAATGTAAACCCCAAGATACTGAGGACTGGCAAGGACCTTGGCCCTGCCTACTCCATCCTGGGGCGCTACCAAACCAAGACCATGCTGACTCCTGGTCCAGGT... | CAGGAGCCAGGCGGGCAGGTGGGGGTCCCGGGAAGGGCCTGGGGCTCAATCCCTGACTCCCAGCGGGGAGAAGGGCAGGTCAGGCTCCGGGCTGCTCAGGGCCCATTGCGTCCACAGGCTTCATGAAGCACACGCCCACCAAGCTGCGTGCACCGGCCTACAGCTTCCGTGGGGCCCCCATGCTCCTGGCAGAGAACTGCTCCCCAGGGCCCCGTTACAATGTAAACCCCAAGATACTGAGGACTGGCAAGGACCTTGGCCCTGCCTACTCCATCCTGGGGCGCTACCAAACCAAGACCATGCTGACTCCTGGTCCAGGT... |
Task1_train_40519 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | GGAGGCTGAGACAGGAGAATCGCTTGAACCCGGGAGGTGGAAGTTGCAGTGAGCTGAGGTCGTGCCACCGCACTCCAGTTTGGGTAAGAGAGCGAGATTCTGTCTCAAAAAAAAAAAAAAAAATTACACCTAATACCAGGCTGGGTGCAGTGGCTCATGCCTGTAATCCCAGTGCTTTGGAAGGCCAAGGCAGGAGGATCACTTGAGGCCAGGAGTTTGAGACCAGCCTCAGCAACATAGTGAGACTTGTCTTAAAAAATTTTTTTAATTAGCCAGGCATGGTAGTGCATGCCCGTAGTCCCAGCTATTCCAGAGGCTGA... | GGAGGCTGAGACAGGAGAATCGCTTGAACCCGGGAGGTGGAAGTTGCAGTGAGCTGAGGTCGTGCCACCGCACTCCAGTTTGGGTAAGAGAGCGAGATTCTGTCTCAAAAAAAAAAAAAAAAATTACACCTAATACCAGGCTGGGTGCAGTGGCTCATGCCTGTAATCCCAGTGCTTTGGAAGGCCAAGGCAGGAGGATCACTTGAGGCCAGGAGTTTGAGACCAGCCTCAGCAACATAGTGAGACTTGTCTTAAAAAATTTTTTTAATTAGCCAGGCATGGTAGTGCATGCCCGTAGTCCCAGCTATTCCAGAGGCTGA... |
Task1_train_40520 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GCTGTTGAGTGCCTGCTGAGGGCAAGGTATCACGAAGGGTGCCTGAGTACATTCCTCATTTACGTAAATAAAATGTTTGTGAGTCACTGAAAAACACATAAACGGCGTTTTACCAAATGTCTGGAACATACGTAAGATGTATGGCTTAAAGTACATGCTGCATGGTGTGAAATTCACTGGGAGTGGGGGACCCTGAGGGGCAGGCATGGGTGCAACCTGGGAGGGACACTGTGCAAAGGACACAAACAACAAATTCAGAGAGCTCAAAAATCCAAAGCCAAACTGGAGGAAGCCCATGCAATGGACTACTCCTCACACGC... | GCTGTTGAGTGCCTGCTGAGGGCAAGGTATCACGAAGGGTGCCTGAGTACATTCCTCATTTACGTAAATAAAATGTTTGTGAGTCACTGAAAAACACATAAACGGCGTTTTACCAAATGTCTGGAACATACGTAAGATGTATGGCTTAAAGTACATGCTGCATGGTGTGAAATTCACTGGGAGTGGGGGACCCTGAGGGGCAGGCATGGGTGCAACCTGGGAGGGACACTGTGCAAAGGACACAAACAACAAATTCAGAGAGCTCAAAAATCCAAAGCCAAACTGGAGGAAGCCCATGCAATGGACTACTCCTCACACGC... |
Task1_train_40521 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GGCTAATTTTTGTAATTTCAGTAGAAATGGGGTTTCACCATGTTGGCCCAGCTGGTCTCGAACTCCTGACCTCGTTATCCACCCGTCTCATCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCTACCGCGCCCGGCCAACTCTTCAGGATCTATTAAACTTTTTTCTTTTTTTTTTCCCACAGGTAGATAAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCTCAATCATAGCTCACTGCAGCCTTGAACTCCTGGACTCAAGGGATCCTCTTGCCTTAGTCTCAGGAGTAACTGGGACAACAGGCTTGCGCCA... | GGCTAATTTTTGTAATTTCAGTAGAAATGGGGTTTCACCATGTTGGCCCAGCTGGTCTCGAACTCCTGACCTCGTTATCCACCCGTCTCATCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCTACCGCGCCCGGCCAACTCTTCAGGATCTATTAAACTTTTTTCTTTTTTTTTTCCCACAGGTAGATAAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCTCAATCATAGCTCACTGCAGCCTTGAACTCCTGGACTCAAGGGATCCTCTTGCCTTAGTCTCAGGAGTAACTGGGACAACAGGCTTGCGCCA... |
Task1_train_40522 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CCTTGAAACTCAGTATTGCCACTTCTACAGTAACCTTTGAAGCCTCTCCCTTTGGCTGATGCACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAA... | CCTTGAAACTCAGTATTGCCACTTCTACAGTAACCTTTGAAGCCTCTCCCTTTGGCTGATGCACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAA... |
Task1_train_40523 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TTGAAACTCAGTATTGCCACTTCTACAGTAACCTTTGAAGCCTCTCCCTTTGGCTGATGCACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACA... | TTGAAACTCAGTATTGCCACTTCTACAGTAACCTTTGAAGCCTCTCCCTTTGGCTGATGCACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACA... |
Task1_train_40524 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | TCAGTATTGCCACTTCTACAGTAACCTTTGAAGCCTCTCCCTTTGGCTGATGCACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCT... | TCAGTATTGCCACTTCTACAGTAACCTTTGAAGCCTCTCCCTTTGGCTGATGCACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCT... |
Task1_train_40525 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCTACAGTAACCTTTGAAGCCTCTCCCTTTGGCTGATGCACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCTTTTTGTTTTAAATT... | TCTACAGTAACCTTTGAAGCCTCTCCCTTTGGCTGATGCACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCTTTTTGTTTTAAATT... |
Task1_train_40526 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | TTTGAAGCCTCTCCCTTTGGCTGATGCACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCTTTTTGTTTTAAATTTTATTTCATTAA... | TTTGAAGCCTCTCCCTTTGGCTGATGCACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCTTTTTGTTTTAAATTTTATTTCATTAA... |
Task1_train_40527 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCTTTTTGTTTTAAATTTTATTTCATTAACTTAATAGGTGAACAAAATGTGTATT... | CACTTCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCTTTTTGTTTTAAATTTTATTTCATTAACTTAATAGGTGAACAAAATGTGTATT... |
Task1_train_40528 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCTTTTTGTTTTAAATTTTATTTCATTAACTTAATAGGTGAACAAAATGTGTATTTCAA... | TCTGCCCCTTTTTTTTTCTTTCTTTCTTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCTTTTTGTTTTAAATTTTATTTCATTAACTTAATAGGTGAACAAAATGTGTATTTCAA... |
Task1_train_40529 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCTTTTTGTTTTAAATTTTATTTCATTAACTTAATAGGTGAACAAAATGTGTATTTCAAATCTAATTGAAATTCATCTGAAACAT... | TTTTTGCTCTTAAACTCACTGTATTGTCATTTATTTGTTTAAAGACTGTCTTCAGTGGACCAGGAGCTCCTTGAAGACACATCATTTGTCTTACACGTTCTATGTTGTAGTATCTAGTATGGAGTCTGAGGAAGTGCTCAAGTGTGCTGAATGGCTAAGAAATTTGAAAACGGTGCATAATTAGCTTTAATTAAAATCTGAAGGAACTCCATTCTGTTTGATTAGCAAACATTTCTCTTTTTGTTTTAAATTTTATTTCATTAACTTAATAGGTGAACAAAATGTGTATTTCAAATCTAATTGAAATTCATCTGAAACAT... |
Task1_train_40530 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTCCTCACCCCTGCCTTCAGAGTCTAACCTCTCCCCAGGCCTCAGCTGAAGGCCTGGCTCTGAGCCAGCCACCTCCTTCACACAACCCACCTTGCTCTGAAGCTGCCTGCTCACAGCCATGCCCCGATGCCACACCCAGGGGTTCTTGGGGAACATTAATGGGATAAAGGAGTAAGAAAATCAAAGGTCACCAAACGGAGCCCTTAAAGGGCAATGCTCTGCGTGTGCCACGGTGCCCAACAGCATCTCGTGCCAGCTGAGCTGCGGTGTGTGGACCCGGGGAATGGACCGGGCTGGACAACCTCTAAGACTTGGCTCCA... | TTCCTCACCCCTGCCTTCAGAGTCTAACCTCTCCCCAGGCCTCAGCTGAAGGCCTGGCTCTGAGCCAGCCACCTCCTTCACACAACCCACCTTGCTCTGAAGCTGCCTGCTCACAGCCATGCCCCGATGCCACACCCAGGGGTTCTTGGGGAACATTAATGGGATAAAGGAGTAAGAAAATCAAAGGTCACCAAACGGAGCCCTTAAAGGGCAATGCTCTGCGTGTGCCACGGTGCCCAACAGCATCTCGTGCCAGCTGAGCTGCGGTGTGTGGACCCGGGGAATGGACCGGGCTGGACAACCTCTAAGACTTGGCTCCA... |
Task1_train_40531 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CATCTCGTGCCAGCTGAGCTGCGGTGTGTGGACCCGGGGAATGGACCGGGCTGGACAACCTCTAAGACTTGGCTCCAGCTCAGCCTGTGAAGGAATCACCTCTCTGATCCCCACCTCTGCCCCGGAGTGCTAGACCCAGGGAGGAAGAGACCCCATGGACCAGCCAGAGGCCCCCTGCTCCAGGTGAGTGCTGGCCCCAGGGTGGTCACTGGGAACCGGCTGGTCTCAGCCCTCTGGGGCCTCCACCTCACCCGCTGACTTCCTCAGGCTCTCCACCCTTGTCCACATCCTTCCCCCACCCTCACTCCCAGGCTCAGGAG... | CATCTCGTGCCAGCTGAGCTGCGGTGTGTGGACCCGGGGAATGGACCGGGCTGGACAACCTCTAAGACTTGGCTCCAGCTCAGCCTGTGAAGGAATCACCTCTCTGATCCCCACCTCTGCCCCGGAGTGCTAGACCCAGGGAGGAAGAGACCCCATGGACCAGCCAGAGGCCCCCTGCTCCAGGTGAGTGCTGGCCCCAGGGTGGTCACTGGGAACCGGCTGGTCTCAGCCCTCTGGGGCCTCCACCTCACCCGCTGACTTCCTCAGGCTCTCCACCCTTGTCCACATCCTTCCCCCACCCTCACTCCCAGGCTCAGGAG... |
Task1_train_40532 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GGAGTCTGTTCCCCACCAGGGGCTCAGATTCAGGCCCTGGTGCAAGGCCCCAAGCTGGGCCCCACCAAAGTGTGGCAGGGGTGGGGGCCCAGGAATACAGCCTGGGCCTGGCAGTGTCTGCTGCCAAAGAGGCCAGTTCTGCTCCGGGATCGGGAAGAGAGGGAAAAGAAGGAAAGCGAGGAAAGAGAGCTCAGGGTTCCTTGGAAATACCTCCCTCGGGGCATGTGACCTGTCCTGGGGTGTGGAAGGACAGAAGCAGAAAGGGAGGTGCAGGGGAGGAAGGTGCCCCCCAGAGCTCAGATCAGCGGCGGCCAGTGCCC... | GGAGTCTGTTCCCCACCAGGGGCTCAGATTCAGGCCCTGGTGCAAGGCCCCAAGCTGGGCCCCACCAAAGTGTGGCAGGGGTGGGGGCCCAGGAATACAGCCTGGGCCTGGCAGTGTCTGCTGCCAAAGAGGCCAGTTCTGCTCCGGGATCGGGAAGAGAGGGAAAAGAAGGAAAGCGAGGAAAGAGAGCTCAGGGTTCCTTGGAAATACCTCCCTCGGGGCATGTGACCTGTCCTGGGGTGTGGAAGGACAGAAGCAGAAAGGGAGGTGCAGGGGAGGAAGGTGCCCCCCAGAGCTCAGATCAGCGGCGGCCAGTGCCC... |
Task1_train_40533 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | GCAGGGGCTGGGCCTGGGGACCCAAAGACCCATGTAGAGGATGTGGGTGATACCGTCCCACTGACCTCACTCAGACACCCCAGTGGGATGATGCCTGGGCCACAGATGAGTGGTTTTGCTCTGGGTTTGGTTGGGGGAGTGTGAAGGGGGTGGCTCAGCAAGGAGGTGAGGAGGAGGGGCAGCTCTGAGACCCCAGGACTACAGATAGACAGGAGTCCTTTCCGGCAGGCACTGTGAGGAGCAGGGTGGGCTTCACCTTCCTCTCTCTCCCAGCAGTTCTCAAGGCACCACAAAACAACTGCCAGCCTCCCTTCTTCATC... | GCAGGGGCTGGGCCTGGGGACCCAAAGACCCATGTAGAGGATGTGGGTGATACCGTCCCACTGACCTCACTCAGACACCCCAGTGGGATGATGCCTGGGCCACAGATGAGTGGTTTTGCTCTGGGTTTGGTTGGGGGAGTGTGAAGGGGGTGGCTCAGCAAGGAGGTGAGGAGGAGGGGCAGCTCTGAGACCCCAGGACTACAGATAGACAGGAGTCCTTTCCGGCAGGCACTGTGAGGAGCAGGGTGGGCTTCACCTTCCTCTCTCTCCCAGCAGTTCTCAAGGCACCACAAAACAACTGCCAGCCTCCCTTCTTCATC... |
Task1_train_40534 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGTCATGGGGGCAGGGGAGGCTTAGATTTTTATTTTTGGTTTTCAGTCAGCACTCCAGTCCAGTCAGGAGGGCTTCAGACCACGAAGAGGGGAGGTGTCCCCACGGCAGAGCTAGACACAGATCCCAGGACATTCTGTGTGTGGGGGAGACATGGCCCAGAATAGAAGGCCTGTAGAGGCCTGGACATGGCTAAGCCCTTAGAGCTCACCCCAGCCAGCAGAAGGAGGAGGACTTAGGGTGTTCGACGTCGAGAAGCACTGTGAGTCGATGGTAGACACAGCCATTGTTAAAGTTAAATCTTAGGAATCTTAGAAATTAT... | AGTCATGGGGGCAGGGGAGGCTTAGATTTTTATTTTTGGTTTTCAGTCAGCACTCCAGTCCAGTCAGGAGGGCTTCAGACCACGAAGAGGGGAGGTGTCCCCACGGCAGAGCTAGACACAGATCCCAGGACATTCTGTGTGTGGGGGAGACATGGCCCAGAATAGAAGGCCTGTAGAGGCCTGGACATGGCTAAGCCCTTAGAGCTCACCCCAGCCAGCAGAAGGAGGAGGACTTAGGGTGTTCGACGTCGAGAAGCACTGTGAGTCGATGGTAGACACAGCCATTGTTAAAGTTAAATCTTAGGAATCTTAGAAATTAT... |
Task1_train_40535 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | GATTTTTATTTTTGGTTTTCAGTCAGCACTCCAGTCCAGTCAGGAGGGCTTCAGACCACGAAGAGGGGAGGTGTCCCCACGGCAGAGCTAGACACAGATCCCAGGACATTCTGTGTGTGGGGGAGACATGGCCCAGAATAGAAGGCCTGTAGAGGCCTGGACATGGCTAAGCCCTTAGAGCTCACCCCAGCCAGCAGAAGGAGGAGGACTTAGGGTGTTCGACGTCGAGAAGCACTGTGAGTCGATGGTAGACACAGCCATTGTTAAAGTTAAATCTTAGGAATCTTAGAAATTATCAATAAAATTTATCTTATAGAGCC... | GATTTTTATTTTTGGTTTTCAGTCAGCACTCCAGTCCAGTCAGGAGGGCTTCAGACCACGAAGAGGGGAGGTGTCCCCACGGCAGAGCTAGACACAGATCCCAGGACATTCTGTGTGTGGGGGAGACATGGCCCAGAATAGAAGGCCTGTAGAGGCCTGGACATGGCTAAGCCCTTAGAGCTCACCCCAGCCAGCAGAAGGAGGAGGACTTAGGGTGTTCGACGTCGAGAAGCACTGTGAGTCGATGGTAGACACAGCCATTGTTAAAGTTAAATCTTAGGAATCTTAGAAATTATCAATAAAATTTATCTTATAGAGCC... |
Task1_train_40536 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | GTGAGGACCCAGGGAAGAGGCAGAGATGATCAGAACCTGGAAATCTGGAGGGTGCCCCAGGGACCAGCCAGCCAGAGCTCTGGGCAGCGTGGGTGCTGCTGGGCTGTGTGGAGCGGGTCTGGGAGCCGTCACCCAGGTGGGCCTCCAGGGGAAAGGGCCATGGCTTCTAACTCCACCGTCCAGGTCTCTGCTATTGGCATCCCACAGCCCCCTCTTCTGTCAGTGCTCCCAGAGTCCCCTTTCCTGGGCCTGGAGGGCTCCTTTGGGGCAGGCAACATTGGCCGCCAACCCTCTGACCTGCACCAGGAGACACGGGGACC... | GTGAGGACCCAGGGAAGAGGCAGAGATGATCAGAACCTGGAAATCTGGAGGGTGCCCCAGGGACCAGCCAGCCAGAGCTCTGGGCAGCGTGGGTGCTGCTGGGCTGTGTGGAGCGGGTCTGGGAGCCGTCACCCAGGTGGGCCTCCAGGGGAAAGGGCCATGGCTTCTAACTCCACCGTCCAGGTCTCTGCTATTGGCATCCCACAGCCCCCTCTTCTGTCAGTGCTCCCAGAGTCCCCTTTCCTGGGCCTGGAGGGCTCCTTTGGGGCAGGCAACATTGGCCGCCAACCCTCTGACCTGCACCAGGAGACACGGGGACC... |
Task1_train_40537 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ACCCTCCCGGAGACCCCGCCCGCTGTTCTCCGCTCTGCGATTTGGGGGGAGGGGGCGCGGTTCGGCTCGGCCCGGACGCTCGATGACGTCGGCAGTGACGCGCGCGACCCTCCCAGAGAGGGTCCCTGACTCTGGGATCTGGCTTGGATCCGGTAGTGAGGGGCTGACGGTGGGCTCCTGGGGAAGTCTCTGCCCCTAGACCCTGCTGAGGCTTCCAAGAGGCCTTCTCAGGCCTCGCCTCCACCCCCTGCCCGCTTAGCAGGGCCTCAGTTTCCCTGTGTGCTGGGGACCCGGGCCGGGGCTTGCTGAAGTGGCCGGTG... | ACCCTCCCGGAGACCCCGCCCGCTGTTCTCCGCTCTGCGATTTGGGGGGAGGGGGCGCGGTTCGGCTCGGCCCGGACGCTCGATGACGTCGGCAGTGACGCGCGCGACCCTCCCAGAGAGGGTCCCTGACTCTGGGATCTGGCTTGGATCCGGTAGTGAGGGGCTGACGGTGGGCTCCTGGGGAAGTCTCTGCCCCTAGACCCTGCTGAGGCTTCCAAGAGGCCTTCTCAGGCCTCGCCTCCACCCCCTGCCCGCTTAGCAGGGCCTCAGTTTCCCTGTGTGCTGGGGACCCGGGCCGGGGCTTGCTGAAGTGGCCGGTG... |
Task1_train_40538 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGCCCCGCTCACCCCCGGCTCCACTGACCCCGGCCCCGCTCACCCCGGACCCCGCTCACCCCCGACCCCCGGCCCCGCTCACCCCCGGCTCCACTGACCCCGGCCCCGCTCACCCCGACCCCGCTCACCCCCGACCCCCGGCCCCGCTCACCCCCGGCCCCGCTCACCCCGACCCCGCTCACCCCCGACCCCCGGCCCCGCTCACCCCCGACCCGCTCACCCCGACCCCGCTCACCCCCGACCCCCGGCCCCGCTCACCCCCGACCCGCTCACCCCGACCCCGCTCACCCCCGCCCCGCTCACCCCTGCCCCGCTCACCC... | GGCCCCGCTCACCCCCGGCTCCACTGACCCCGGCCCCGCTCACCCCGGACCCCGCTCACCCCCGACCCCCGGCCCCGCTCACCCCCGGCTCCACTGACCCCGGCCCCGCTCACCCCGACCCCGCTCACCCCCGACCCCCGGCCCCGCTCACCCCCGGCCCCGCTCACCCCGACCCCGCTCACCCCCGACCCCCGGCCCCGCTCACCCCCGACCCGCTCACCCCGACCCCGCTCACCCCCGACCCCCGGCCCCGCTCACCCCCGACCCGCTCACCCCGACCCCGCTCACCCCCGCCCCGCTCACCCCTGCCCCGCTCACCC... |
Task1_train_40539 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AAGGGTCCGGGCCACACCCAGCACACTGCAGGAGGGACAGCGGGCAGAGGGCCACATGGGCAGACATGCACCCTGACCTTGGGCCTCTCTCCACTGTAGAAGGGCTATCGGAAGGAGGACTTCCTGGGCCCATAGGTGAAGCCTTCTGGAGGAGAAGGTGACGTGGCCCAGCGTCCAAGGGACAGACTCAGCTCCAGGCTGCTTGGCAGCCCAGCCTGGAGGAGAAGGCTAATGACGGAGGGGCCCCTCGCTGGGGCCCCTGTGTGCATCTTTGAGGGTCCTGGGCCACCAGGAGGGGCAGGGTCTTATAGCTGGGGACT... | AAGGGTCCGGGCCACACCCAGCACACTGCAGGAGGGACAGCGGGCAGAGGGCCACATGGGCAGACATGCACCCTGACCTTGGGCCTCTCTCCACTGTAGAAGGGCTATCGGAAGGAGGACTTCCTGGGCCCATAGGTGAAGCCTTCTGGAGGAGAAGGTGACGTGGCCCAGCGTCCAAGGGACAGACTCAGCTCCAGGCTGCTTGGCAGCCCAGCCTGGAGGAGAAGGCTAATGACGGAGGGGCCCCTCGCTGGGGCCCCTGTGTGCATCTTTGAGGGTCCTGGGCCACCAGGAGGGGCAGGGTCTTATAGCTGGGGACT... |
Task1_train_40540 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | CGAGGCAGGAGGATTGCTTGAGCCCAGGAGTTCGAGACAAGCCTGGGCAACATGGCAAAACCCCATCTCTACAAAAAATAGAAAAAATTAGCCAGGCATGGTGGCACATGCCTGTAGTCCCAGCTATTCGGGAGGCTGAGGCAGGAGGATTGCTGGAACCAGGAGTTTGAGGCTGTAGTGAGCTGTAATGGTACCACTGTACTCCAGCCTGGGGCAATGGATCAAGATACTGTCTCTAAAAGTAAATAAATAAAAATAAAATGACAGGCTGCTGACACCCACTACCAGGCATCACCTTAGAGGTGTAAGGGAATTGGAGA... | CGAGGCAGGAGGATTGCTTGAGCCCAGGAGTTCGAGACAAGCCTGGGCAACATGGCAAAACCCCATCTCTACAAAAAATAGAAAAAATTAGCCAGGCATGGTGGCACATGCCTGTAGTCCCAGCTATTCGGGAGGCTGAGGCAGGAGGATTGCTGGAACCAGGAGTTTGAGGCTGTAGTGAGCTGTAATGGTACCACTGTACTCCAGCCTGGGGCAATGGATCAAGATACTGTCTCTAAAAGTAAATAAATAAAAATAAAATGACAGGCTGCTGACACCCACTACCAGGCATCACCTTAGAGGTGTAAGGGAATTGGAGA... |
Task1_train_40541 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGCCCTCTCCAGGCCAGCCCACCCCTCACCTTGTGCAGGGGGAACCTGGCCTCAAAGACCCCGTCCTTCATCAGATCCTCGAAGGTCTCTGGGTCACAGGGGTTCACGAGTCAGGGGGAGTGAGGTGCTGGGAGAACCCTGCCCGCAGCGCCCCTGTCAGTGCCCCACCCCTGCCCTTACCACCAGCCGAGGTCTTGTTGTTCATGACAACGAAGTTCACGATTCGGATTCTGAGACTCAAGAGCCAGAGCAGGGTGGCCCCGTGTGACCACAGTGGACCCTGCCTCCAGGTCTCAACCTGCCCTCTGGTCTGGCCAGGC... | GGCCCTCTCCAGGCCAGCCCACCCCTCACCTTGTGCAGGGGGAACCTGGCCTCAAAGACCCCGTCCTTCATCAGATCCTCGAAGGTCTCTGGGTCACAGGGGTTCACGAGTCAGGGGGAGTGAGGTGCTGGGAGAACCCTGCCCGCAGCGCCCCTGTCAGTGCCCCACCCCTGCCCTTACCACCAGCCGAGGTCTTGTTGTTCATGACAACGAAGTTCACGATTCGGATTCTGAGACTCAAGAGCCAGAGCAGGGTGGCCCCGTGTGACCACAGTGGACCCTGCCTCCAGGTCTCAACCTGCCCTCTGGTCTGGCCAGGC... |
Task1_train_40542 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | GGGCTGCACGCACCCGTGGGCAGGGCCGGGCGTGGCCTGCGTCCCATACTCTGGCTGCCAGCCGGGTGGGGGCTGCACGCACCCGTGGGCAGGGCCGGGCGTGGCCGGCGTCCCATACTCTGGCTGCCAGCCGGGGTGGGGGCTGCACGCACCCGTGGGCAGGGCCGGGTGTGGCCGGCGTCCCATACTCTGGCTGACCCTGGCGCCCACAGACCCTGATGATCCGAGACTGGTGGATGTGCATGATCATCAGCGTGATGTTCGAGTTCCTGGAGTACAGCCTGGAGCACCAGCTGCCCAACTTCAGCGAGTGCTGGTGG... | GGGCTGCACGCACCCGTGGGCAGGGCCGGGCGTGGCCTGCGTCCCATACTCTGGCTGCCAGCCGGGTGGGGGCTGCACGCACCCGTGGGCAGGGCCGGGCGTGGCCGGCGTCCCATACTCTGGCTGCCAGCCGGGGTGGGGGCTGCACGCACCCGTGGGCAGGGCCGGGTGTGGCCGGCGTCCCATACTCTGGCTGACCCTGGCGCCCACAGACCCTGATGATCCGAGACTGGTGGATGTGCATGATCATCAGCGTGATGTTCGAGTTCCTGGAGTACAGCCTGGAGCACCAGCTGCCCAACTTCAGCGAGTGCTGGTGG... |
Task1_train_40543 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CCCGCCTTTCCCAGTACATGAACATGCACCCTCACTCTCGCCCATGTGCTCACACTCACATGGACACTCGTGCTCACTCTCGCCCATGTGCCACACTCACGTGCTCACTCGCCCATGTGCTCACACTCACATGGACACTCATGCTCACTCTCACCCATGTGCTCACACACGGACACTCGTGCTCACTCTCACCCATGTGCTCACGTACTCTCGCCCATGTGCTCACACACGGACACTCATGCTCACTCTCGCCCATGTGCTCACACACGGACACTCGTGCTCATTCTTGCCCATGTGCTCACACACGGACCCTCGTGCTC... | CCCGCCTTTCCCAGTACATGAACATGCACCCTCACTCTCGCCCATGTGCTCACACTCACATGGACACTCGTGCTCACTCTCGCCCATGTGCCACACTCACGTGCTCACTCGCCCATGTGCTCACACTCACATGGACACTCATGCTCACTCTCACCCATGTGCTCACACACGGACACTCGTGCTCACTCTCACCCATGTGCTCACGTACTCTCGCCCATGTGCTCACACACGGACACTCATGCTCACTCTCGCCCATGTGCTCACACACGGACACTCGTGCTCATTCTTGCCCATGTGCTCACACACGGACCCTCGTGCTC... |
Task1_train_40544 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | GGACACTCGTGCTCACTCTCGCCCATGTGCCACACTCACGTGCTCACTCGCCCATGTGCTCACACTCACATGGACACTCATGCTCACTCTCACCCATGTGCTCACACACGGACACTCGTGCTCACTCTCACCCATGTGCTCACGTACTCTCGCCCATGTGCTCACACACGGACACTCATGCTCACTCTCGCCCATGTGCTCACACACGGACACTCGTGCTCATTCTTGCCCATGTGCTCACACACGGACCCTCGTGCTCACTCTCACGTGCTCACACACGGACACTCATGCTCACTCACCCATGTGCTCACACTCGGACA... | GGACACTCGTGCTCACTCTCGCCCATGTGCCACACTCACGTGCTCACTCGCCCATGTGCTCACACTCACATGGACACTCATGCTCACTCTCACCCATGTGCTCACACACGGACACTCGTGCTCACTCTCACCCATGTGCTCACGTACTCTCGCCCATGTGCTCACACACGGACACTCATGCTCACTCTCGCCCATGTGCTCACACACGGACACTCGTGCTCATTCTTGCCCATGTGCTCACACACGGACCCTCGTGCTCACTCTCACGTGCTCACACACGGACACTCATGCTCACTCACCCATGTGCTCACACTCGGACA... |
Task1_train_40545 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ACCCTCGTGCTCACTCTCACGTGCTCACACACGGACACGTGCTCATTCTTGCCCATGTGCTCACACACTGACCCTCGTGCTCACTCTCACGTGCTCACACACGGACACTCGTGCTCTCACCCATGTGCTCACACACACGTGCTCACCCATGTGCTCACACACGGACACTCGTGCTCATTCTTGCCCATGTGCTCACACACGGACCCTCGTGCTCACTCACGTGCTCACACGGACACGTGCTCACTCTCACATGCTCACGGACACCCATGCTCACACTCATATGCTCACACACGTGCTCACACTCGCCTCACCCATGTGTG... | ACCCTCGTGCTCACTCTCACGTGCTCACACACGGACACGTGCTCATTCTTGCCCATGTGCTCACACACTGACCCTCGTGCTCACTCTCACGTGCTCACACACGGACACTCGTGCTCTCACCCATGTGCTCACACACACGTGCTCACCCATGTGCTCACACACGGACACTCGTGCTCATTCTTGCCCATGTGCTCACACACGGACCCTCGTGCTCACTCACGTGCTCACACGGACACGTGCTCACTCTCACATGCTCACGGACACCCATGCTCACACTCATATGCTCACACACGTGCTCACACTCGCCTCACCCATGTGTG... |
Task1_train_40546 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | AGGTCAGAGGGGAGGAGACGGACCCGACCTTCCTTGGCTGTGCTCTCCAGCCCTGTCCTGTGCTGGACCCAACCTAACCTCTGCAGCCTCCCTGCCCTGGACACAAATCTGGCTGAGACCCCAGACCCTGATGGGGCAGAGCCTGGCACTGGAGGAGCCACCAGGATGGGCCCCTGTGGGTGTGGGCAGAGGGTGATCCTCAGTTCAGGTTTTTGCCAGAAGATGGGTTCCTGCAGGAGGGGGTCTCAGCAGCTCAGACTTCAGATGCGCTCACTGCTGCTCACTGTGGGACAGCCAGACACGGAGCCCTCTGTTCTCCA... | AGGTCAGAGGGGAGGAGACGGACCCGACCTTCCTTGGCTGTGCTCTCCAGCCCTGTCCTGTGCTGGACCCAACCTAACCTCTGCAGCCTCCCTGCCCTGGACACAAATCTGGCTGAGACCCCAGACCCTGATGGGGCAGAGCCTGGCACTGGAGGAGCCACCAGGATGGGCCCCTGTGGGTGTGGGCAGAGGGTGATCCTCAGTTCAGGTTTTTGCCAGAAGATGGGTTCCTGCAGGAGGGGGTCTCAGCAGCTCAGACTTCAGATGCGCTCACTGCTGCTCACTGTGGGACAGCCAGACACGGAGCCCTCTGTTCTCCA... |
Task1_train_40547 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGAGGAGACGGACCCGACCTTCCTTGGCTGTGCTCTCCAGCCCTGTCCTGTGCTGGACCCAACCTAACCTCTGCAGCCTCCCTGCCCTGGACACAAATCTGGCTGAGACCCCAGACCCTGATGGGGCAGAGCCTGGCACTGGAGGAGCCACCAGGATGGGCCCCTGTGGGTGTGGGCAGAGGGTGATCCTCAGTTCAGGTTTTTGCCAGAAGATGGGTTCCTGCAGGAGGGGGTCTCAGCAGCTCAGACTTCAGATGCGCTCACTGCTGCTCACTGTGGGACAGCCAGACACGGAGCCCTCTGTTCTCCAGCAGTTGTGG... | GGAGGAGACGGACCCGACCTTCCTTGGCTGTGCTCTCCAGCCCTGTCCTGTGCTGGACCCAACCTAACCTCTGCAGCCTCCCTGCCCTGGACACAAATCTGGCTGAGACCCCAGACCCTGATGGGGCAGAGCCTGGCACTGGAGGAGCCACCAGGATGGGCCCCTGTGGGTGTGGGCAGAGGGTGATCCTCAGTTCAGGTTTTTGCCAGAAGATGGGTTCCTGCAGGAGGGGGTCTCAGCAGCTCAGACTTCAGATGCGCTCACTGCTGCTCACTGTGGGACAGCCAGACACGGAGCCCTCTGTTCTCCAGCAGTTGTGG... |
Task1_train_40548 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GCCCTCCAGGGCTTGGAGAAGGTGGGGGACACTGTACCCACACCAGAGCCAGAAGGCCAAGGCAGAGAGCCCCTTCCTCAGTCTAGAGGCCACCATAGGTGGTCACACCTGCCCCTACCCCTGAAGACAGCCAAAGGCAGGTGGTGGCTGAGCACAGGGCTGGGCACATGTTGACCACCAAACCCTGCCTTCTGCAGGGACTTGGGCACGTCTCTGGGCCACCTGCAGGTGCTGTGGCTGGCTCGCTGTGGCCTCGCTGACCTGGATGGCATCGCCTCTTTGCCAGCACTTAAGGTGAGTCTGGGCACCCTGGGCTGGGG... | GCCCTCCAGGGCTTGGAGAAGGTGGGGGACACTGTACCCACACCAGAGCCAGAAGGCCAAGGCAGAGAGCCCCTTCCTCAGTCTAGAGGCCACCATAGGTGGTCACACCTGCCCCTACCCCTGAAGACAGCCAAAGGCAGGTGGTGGCTGAGCACAGGGCTGGGCACATGTTGACCACCAAACCCTGCCTTCTGCAGGGACTTGGGCACGTCTCTGGGCCACCTGCAGGTGCTGTGGCTGGCTCGCTGTGGCCTCGCTGACCTGGATGGCATCGCCTCTTTGCCAGCACTTAAGGTGAGTCTGGGCACCCTGGGCTGGGG... |
Task1_train_40549 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | ACCCTGCAGACAGCTCTGACTTCCTGGCCTTGGCTGGGCTCAGGGCCTGGAGGGAACATGGCGTGCGGTGGGTGTCCCTCCAGCTCTTCCACTGGGTGTGTCCTGTCCCGTGGGGAAATCAGGGCTGGGGCTACCTTGGCTGAGTCATCCCCAGTCCCAAGGCTCGTGGACCATCCCTGCATGTCCTGTCCCGTGGGGGGATCAGGGCTGGGGCTACCTTGGCTGAGTCATCGCTGGTCCCAAGGCTCGTGGACCATCCCTGTGTGTCCTGTCCCGTGGGGGGATCAGGGCTGGGGCTACCTTGGCTGAGTCATCCCCAG... | ACCCTGCAGACAGCTCTGACTTCCTGGCCTTGGCTGGGCTCAGGGCCTGGAGGGAACATGGCGTGCGGTGGGTGTCCCTCCAGCTCTTCCACTGGGTGTGTCCTGTCCCGTGGGGAAATCAGGGCTGGGGCTACCTTGGCTGAGTCATCCCCAGTCCCAAGGCTCGTGGACCATCCCTGCATGTCCTGTCCCGTGGGGGGATCAGGGCTGGGGCTACCTTGGCTGAGTCATCGCTGGTCCCAAGGCTCGTGGACCATCCCTGTGTGTCCTGTCCCGTGGGGGGATCAGGGCTGGGGCTACCTTGGCTGAGTCATCCCCAG... |
Task1_train_40550 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TTCTGAGTCCCTGCTGTAGCTGCCGGCCTGCACCAGCGCTTGCTCGGAGGAAGCGCGGTGGTCCCGGGGCGGGTGCCCTATCACCTGCACGAAGGAAGGCAGGCCCGGCCGGCAGCTGCTGGAGTCGGAGTCAGCGCCCCCTGAGCTGCTGGTGTTCAGACAGGGCAGGGAGCCCCACTCCACGGTCTTGTGATGCCGCTCGGAATGCTTTCCAGAGGACTCTGGGCTCCCTGTGTCCAGCTGTGGCCAGGGCCGGGGCTGCCTGTGGACCACGCTCTGCTTGATGGCCACTCCAGCTCCAGACCCCAGCCCTGCCCCCG... | TTCTGAGTCCCTGCTGTAGCTGCCGGCCTGCACCAGCGCTTGCTCGGAGGAAGCGCGGTGGTCCCGGGGCGGGTGCCCTATCACCTGCACGAAGGAAGGCAGGCCCGGCCGGCAGCTGCTGGAGTCGGAGTCAGCGCCCCCTGAGCTGCTGGTGTTCAGACAGGGCAGGGAGCCCCACTCCACGGTCTTGTGATGCCGCTCGGAATGCTTTCCAGAGGACTCTGGGCTCCCTGTGTCCAGCTGTGGCCAGGGCCGGGGCTGCCTGTGGACCACGCTCTGCTTGATGGCCACTCCAGCTCCAGACCCCAGCCCTGCCCCCG... |
Task1_train_40551 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGCGCCCCCTGAGCTGCTGGTGTTCAGACAGGGCAGGGAGCCCCACTCCACGGTCTTGTGATGCCGCTCGGAATGCTTTCCAGAGGACTCTGGGCTCCCTGTGTCCAGCTGTGGCCAGGGCCGGGGCTGCCTGTGGACCACGCTCTGCTTGATGGCCACTCCAGCTCCAGACCCCAGCCCTGCCCCCGTCCAGCCTCACAAGGCAGTGCAGCAGGGAGCCCCTCTTGCCTCCCAGTACCCAGGCTCAGTTCATGGCAGGACAGTGATGGCTGCCTCAACCCCAACGCATTCTACAGATCAGAGAACGCGCATTGGAAGGT... | AGCGCCCCCTGAGCTGCTGGTGTTCAGACAGGGCAGGGAGCCCCACTCCACGGTCTTGTGATGCCGCTCGGAATGCTTTCCAGAGGACTCTGGGCTCCCTGTGTCCAGCTGTGGCCAGGGCCGGGGCTGCCTGTGGACCACGCTCTGCTTGATGGCCACTCCAGCTCCAGACCCCAGCCCTGCCCCCGTCCAGCCTCACAAGGCAGTGCAGCAGGGAGCCCCTCTTGCCTCCCAGTACCCAGGCTCAGTTCATGGCAGGACAGTGATGGCTGCCTCAACCCCAACGCATTCTACAGATCAGAGAACGCGCATTGGAAGGT... |
Task1_train_40552 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | CAGGCGGGCAGGAGGCCCACGCCCACAACTCTTTCTGAGCTGGGCAGAACAATCAATGGCCCACACAGCTGACCGCGAGGCTGCGGGGCCCTGGGCGGGACAGTAGGGTAGGGGGTGAAGGAGCGGCTTCCAGCCAGCTTCACTGTGTGCATGGCCTGGCACTGGGTCCAAAAGGGGCAGGAAGGTGTCGGAGAAGAGCCTCAGCTAGAGTCCGGGCCTTCTGAGCGGGCACCTCCCGCACCAGGACTCTGCGCCCGCCAGCTCCGCAGGGCTCCACCTCCCTCGCCGGGACTGGTGACCCTGCGACCCCGCGACCCCTG... | CAGGCGGGCAGGAGGCCCACGCCCACAACTCTTTCTGAGCTGGGCAGAACAATCAATGGCCCACACAGCTGACCGCGAGGCTGCGGGGCCCTGGGCGGGACAGTAGGGTAGGGGGTGAAGGAGCGGCTTCCAGCCAGCTTCACTGTGTGCATGGCCTGGCACTGGGTCCAAAAGGGGCAGGAAGGTGTCGGAGAAGAGCCTCAGCTAGAGTCCGGGCCTTCTGAGCGGGCACCTCCCGCACCAGGACTCTGCGCCCGCCAGCTCCGCAGGGCTCCACCTCCCTCGCCGGGACTGGTGACCCTGCGACCCCGCGACCCCTG... |
Task1_train_40553 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGGCAGACGGGATGCGGCCCCGGCCCACGGGCAGAGCATTGAGATCCCCAGTGCCTGCATCAGCCGACTGACTGGCAGGGAGGGCACCGGGCAGCCAGGGCGAGGCACACGGGCAGAGAGCGAGGCCAGCAGCAGGGTGCCCCGGGAGCCCGGGGTGCACACGGGCAGCTCCCGGCCCCCAGCCCCCAGCTCCCATGGCAGTTTGGCCCCACTGGGACCATCAAGAGGGAAAGGGGTCGGGTCGACCTTTGAGAGCTTCCGGATCAATATTCCTGGAAACATGGCACATTCCAGCCAGCTCTCCAGCCCTGGCTTCTGTA... | TGGCAGACGGGATGCGGCCCCGGCCCACGGGCAGAGCATTGAGATCCCCAGTGCCTGCATCAGCCGACTGACTGGCAGGGAGGGCACCGGGCAGCCAGGGCGAGGCACACGGGCAGAGAGCGAGGCCAGCAGCAGGGTGCCCCGGGAGCCCGGGGTGCACACGGGCAGCTCCCGGCCCCCAGCCCCCAGCTCCCATGGCAGTTTGGCCCCACTGGGACCATCAAGAGGGAAAGGGGTCGGGTCGACCTTTGAGAGCTTCCGGATCAATATTCCTGGAAACATGGCACATTCCAGCCAGCTCTCCAGCCCTGGCTTCTGTA... |
Task1_train_40554 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGCCAGGGCCTGGCTGCCCGGCTGCGGAGGCCATCCCCCCCAGAGCCCTGGGATGAGGAGGATGGGGCGTCTTGCAGCACCTTCTTTGGCTCTGAGGAGCGGACGGTGACCTGTGTGACTGTCGTGGAGCCGGAAGCCCCACCCAGCCCGGACGTGCTGCAGGCTGCCACCCACAGAGTCGTGGAGCTCAGGCCCCCTTCCCGGTCCCGCTCCACATCCAGCTCCCGCAGCAGGAAGAAGGCCAAGAGGAAGAGGGTGTCCAGGGAGCACGGACGGACGCGCTCTGGGACGCGCTCTGAATCCAGGGACAGGAGCTCGAG... | AGCCAGGGCCTGGCTGCCCGGCTGCGGAGGCCATCCCCCCCAGAGCCCTGGGATGAGGAGGATGGGGCGTCTTGCAGCACCTTCTTTGGCTCTGAGGAGCGGACGGTGACCTGTGTGACTGTCGTGGAGCCGGAAGCCCCACCCAGCCCGGACGTGCTGCAGGCTGCCACCCACAGAGTCGTGGAGCTCAGGCCCCCTTCCCGGTCCCGCTCCACATCCAGCTCCCGCAGCAGGAAGAAGGCCAAGAGGAAGAGGGTGTCCAGGGAGCACGGACGGACGCGCTCTGGGACGCGCTCTGAATCCAGGGACAGGAGCTCGAG... |
Task1_train_40555 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | TGGGGTGGCCATGAGTGCAGGCCCGAGGTCAGCCAGCCAGGTTAGGGGTCAGGGGGCTGTATTGCCACATCCTGTAGGCCTGGGGTCAAGCCTGTTCGCCTGTGGCTGCCCCTGGCAGATGCTTAGGAAGGAGGGTGCCTCAGTGCACCCTGGGTAATTTAAAACTACCCAGCCCACGCCCAGCTTACAGGTGGGAGAACGACCCCCAGAGGTGAGCAGTTGCCTGGTGACGTCTCAGCCCATGCTCCCCCCGCCCACCGACACCGTGGGACCCTCAGTGGCCTTGTGAGCGGCATAGCGAACAGGACGGGGGTCTCACA... | TGGGGTGGCCATGAGTGCAGGCCCGAGGTCAGCCAGCCAGGTTAGGGGTCAGGGGGCTGTATTGCCACATCCTGTAGGCCTGGGGTCAAGCCTGTTCGCCTGTGGCTGCCCCTGGCAGATGCTTAGGAAGGAGGGTGCCTCAGTGCACCCTGGGTAATTTAAAACTACCCAGCCCACGCCCAGCTTACAGGTGGGAGAACGACCCCCAGAGGTGAGCAGTTGCCTGGTGACGTCTCAGCCCATGCTCCCCCCGCCCACCGACACCGTGGGACCCTCAGTGGCCTTGTGAGCGGCATAGCGAACAGGACGGGGGTCTCACA... |
Task1_train_40556 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GTTGCCTCCTGGAGGCAGGGTGCAGCAGTGGCAGCCTGAGGGCTGGCGACAGGTGTCCTGCATGGGGAAATGCTGTCCCTGCCCTTGGCACAGCTGGTGGGAGTGGCTTTGGCGGCCACTGGCCTGTCAAGGGTCTTGTTCTTTGAGTCAAAGCTTGGCTGTGATGTGTGTGGTGAAGACAGAAGTGAGTTGGTGTGCAGGGAGGCCGTGGAGGTCCCCTCCCTCCCTGGGCCTCACCCGTGTTCAGCCTGGACCCAATTCCCCACCAGCCAAGATGCCAGTACGTGTTCTGGAGTTCTTTTTATTAGACTGGGCGGCCG... | GTTGCCTCCTGGAGGCAGGGTGCAGCAGTGGCAGCCTGAGGGCTGGCGACAGGTGTCCTGCATGGGGAAATGCTGTCCCTGCCCTTGGCACAGCTGGTGGGAGTGGCTTTGGCGGCCACTGGCCTGTCAAGGGTCTTGTTCTTTGAGTCAAAGCTTGGCTGTGATGTGTGTGGTGAAGACAGAAGTGAGTTGGTGTGCAGGGAGGCCGTGGAGGTCCCCTCCCTCCCTGGGCCTCACCCGTGTTCAGCCTGGACCCAATTCCCCACCAGCCAAGATGCCAGTACGTGTTCTGGAGTTCTTTTTATTAGACTGGGCGGCCG... |
Task1_train_40557 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGCACATGGCCTCCCCTCCTTGAGGCTCTGGTCTCACCTTCACCAGGACCAGGCTCTTCTCCTTGGGCCTCCCAGCTGACAGGTCCTGCCCGAAGCCCAGGTAGATGGTATAGCGTGGGGAGCCACGGCGCTGCCGTGCCCGGAATTCCACCAGCTCTGAAGAAGGGGACTCTGCTGAGTACCTGGCAGGCAGGTGCTCCCAAGGACCCCTGGAGACAGCCCCCCAGGCAAGGGCCTCACTGACCTTGGAAGAAGACTCTGAAGTCGAAGATGGGGGTGTCACAGTTCCGAGGCAGCAGGCAGGCTGGGGTGGAGGGGCT... | AGCACATGGCCTCCCCTCCTTGAGGCTCTGGTCTCACCTTCACCAGGACCAGGCTCTTCTCCTTGGGCCTCCCAGCTGACAGGTCCTGCCCGAAGCCCAGGTAGATGGTATAGCGTGGGGAGCCACGGCGCTGCCGTGCCCGGAATTCCACCAGCTCTGAAGAAGGGGACTCTGCTGAGTACCTGGCAGGCAGGTGCTCCCAAGGACCCCTGGAGACAGCCCCCCAGGCAAGGGCCTCACTGACCTTGGAAGAAGACTCTGAAGTCGAAGATGGGGGTGTCACAGTTCCGAGGCAGCAGGCAGGCTGGGGTGGAGGGGCT... |
Task1_train_40558 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | GGCCGGCGCTTTTATGGTGGCCAGGCGGGAGTTTCCGGGAAGGGCGCGCGCCGCCTGTTCTTATTATTGGATGCGACCAGCGGAACCCCGCCCCGGCCAGCGCGGAGTAGGGAGGAGTGGAGGGCGTTGGGAGTGGCTGCAGTGAGCCGAGATGGAGCCACTCCACTACAGCCCAGGGGACAGAGCAAGACTCAGTCTCAAAAAAAAAAGGAAGTGGGTAATGGGAGGTGGACGTGCCTCGAAAAAGGGGCAGCTGCACCGTTTGCGTTTCTTTTTTTGAGATGGAGTTTCGCTTTTGTTACCCAGGCTGGAGTGCGGTG... | GGCCGGCGCTTTTATGGTGGCCAGGCGGGAGTTTCCGGGAAGGGCGCGCGCCGCCTGTTCTTATTATTGGATGCGACCAGCGGAACCCCGCCCCGGCCAGCGCGGAGTAGGGAGGAGTGGAGGGCGTTGGGAGTGGCTGCAGTGAGCCGAGATGGAGCCACTCCACTACAGCCCAGGGGACAGAGCAAGACTCAGTCTCAAAAAAAAAAGGAAGTGGGTAATGGGAGGTGGACGTGCCTCGAAAAAGGGGCAGCTGCACCGTTTGCGTTTCTTTTTTTGAGATGGAGTTTCGCTTTTGTTACCCAGGCTGGAGTGCGGTG... |
Task1_train_40559 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTGGTTGTCAAAGCCTTGGGGCTGGGGCTCCTGCAGGCGGGAGTCGAGGCGTCAGCGGGGTCCCTGGGTCTCTGCAGCCTTGGCCCTGCACACCCTCATTCCACGCTGGACACCCCTCCGTCTCCACATCTGTCCCTCTGCCCTCCCCTCTCCTGTCCCCCGTCCCCCACTTCCTGCCTGGTCGCCTGCCCTGTTCTCCATCCTGGGCCTCACCGGAGCTTTGCCACAGCAGCACTTGAGCCGGGGGCCATAGTGCTTGTGGACAAGGACGGCGAGGCCAAGGAGAGCCAGCAGCAGCAGCGCACCCAGCACCCCGCCCA... | CTGGTTGTCAAAGCCTTGGGGCTGGGGCTCCTGCAGGCGGGAGTCGAGGCGTCAGCGGGGTCCCTGGGTCTCTGCAGCCTTGGCCCTGCACACCCTCATTCCACGCTGGACACCCCTCCGTCTCCACATCTGTCCCTCTGCCCTCCCCTCTCCTGTCCCCCGTCCCCCACTTCCTGCCTGGTCGCCTGCCCTGTTCTCCATCCTGGGCCTCACCGGAGCTTTGCCACAGCAGCACTTGAGCCGGGGGCCATAGTGCTTGTGGACAAGGACGGCGAGGCCAAGGAGAGCCAGCAGCAGCAGCGCACCCAGCACCCCGCCCA... |
Task1_train_40560 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | TCCAGGCCTGAGCCCCAGGTAGTGTCGCTGGGAAGGGGCCTCTGTGGAGGGCCCCGGTTTTGGGGACACAGCACCAGCACATCAGGGTCTGTCACCAACACGATCACATGGCCAGGGCGGGGCAGGGAGAGCTTCGGCTCACAGCAGGGATCGCCCGGTGGCAGGGGGGATGGGGCTTCTGAAGTGTGGTCAGGGGCCTTATGCCCGGAGGCGGGAAGGATGGGGCTTCTGCAGTGTACCCAGGGGCCTTATGCAGAGGCTGAAAAAGGAGGGTGGGCCCTGAGAGGACTTGGGGGTGTGGCAGCTCCTGGCCCTCCCTC... | TCCAGGCCTGAGCCCCAGGTAGTGTCGCTGGGAAGGGGCCTCTGTGGAGGGCCCCGGTTTTGGGGACACAGCACCAGCACATCAGGGTCTGTCACCAACACGATCACATGGCCAGGGCGGGGCAGGGAGAGCTTCGGCTCACAGCAGGGATCGCCCGGTGGCAGGGGGGATGGGGCTTCTGAAGTGTGGTCAGGGGCCTTATGCCCGGAGGCGGGAAGGATGGGGCTTCTGCAGTGTACCCAGGGGCCTTATGCAGAGGCTGAAAAAGGAGGGTGGGCCCTGAGAGGACTTGGGGGTGTGGCAGCTCCTGGCCCTCCCTC... |
Task1_train_40561 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ACCTGGCCCCGCACAGCCTGAGCCTCCCGGTCCAGAGTGGTGGTCACGTATACCTCCTTCACATTCTTCAGGTGCGAGTAGAAGACAAAGCAGATTCTGCCCTCCACACAGTCAGGGCGGTCTAGGGGACAGGGGTGGGCTGAGCAAGGAGGGCTCGGGGAGGACGGTAAGGCTCCCCCTCCAGGGCAGGGAGCATCCACCAGCATCCCTACCAGCATCCACGTCGATGCCGCGCTCGAAGGCCGCAAAGAACTCTTCGCCCTCGAACATCTCCACCGTGTCAGAGGGCTCGGGGCCCCGGTACCGCTCCAGCAGCCGCC... | ACCTGGCCCCGCACAGCCTGAGCCTCCCGGTCCAGAGTGGTGGTCACGTATACCTCCTTCACATTCTTCAGGTGCGAGTAGAAGACAAAGCAGATTCTGCCCTCCACACAGTCAGGGCGGTCTAGGGGACAGGGGTGGGCTGAGCAAGGAGGGCTCGGGGAGGACGGTAAGGCTCCCCCTCCAGGGCAGGGAGCATCCACCAGCATCCCTACCAGCATCCACGTCGATGCCGCGCTCGAAGGCCGCAAAGAACTCTTCGCCCTCGAACATCTCCACCGTGTCAGAGGGCTCGGGGCCCCGGTACCGCTCCAGCAGCCGCC... |
Task1_train_40562 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGATGGCCCATCCAACCTCTCTGTCTAGCTGCTCTGTCCAGGCTCCCTGTCCAGTCTCTCTCTCTTTTTTTTTTTTTTTTTTGTTTGAGACGGAGTCTCGCTCTGTTGCCAAGGCTGGAGTGCAGTGGCAGGATCTCAGCTCACTGCAACCTCTGCCTCCAAGGTTCAAGCTATTCTCCTGCCTCAGCCTCCCCATTAGCTGGGATTACAGGCGCCTGCCACCATGCCTGGCTACTTTTTGTATTTTTAGTAAAGAAATAGGGTTTCACCATGTTGGCCAGGCTGGCCTCAAACTATTTTATTTTTTTATTTTTTTTTTG... | AGATGGCCCATCCAACCTCTCTGTCTAGCTGCTCTGTCCAGGCTCCCTGTCCAGTCTCTCTCTCTTTTTTTTTTTTTTTTTTGTTTGAGACGGAGTCTCGCTCTGTTGCCAAGGCTGGAGTGCAGTGGCAGGATCTCAGCTCACTGCAACCTCTGCCTCCAAGGTTCAAGCTATTCTCCTGCCTCAGCCTCCCCATTAGCTGGGATTACAGGCGCCTGCCACCATGCCTGGCTACTTTTTGTATTTTTAGTAAAGAAATAGGGTTTCACCATGTTGGCCAGGCTGGCCTCAAACTATTTTATTTTTTTATTTTTTTTTTG... |
Task1_train_40563 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGAGCACAGGAGGCTGGCCGCCCCACCCCACCAGCCCATCCTCCCACCTCCCTGGGGCCCTGCTGCCGCGCGGCTTCCGGCTGGGGTGGACCTCAGGTCTAGCCGGCAAGCCGGAGGGCGGGCGAGACAACAACGTGGCCTGGAGGCAATGGCCCTGGCCTCTCGTGTCCCCTTCTCTCACCCGCCCAGACTTGCCCTCTTTGGAGGTCGCCCGGGCTAAGGAACATGGAAGGACGCTGGGTGGAGAGTGAGGGGAGAGGATCCCAGCTCCCCGGTGGGGGAAGGCGGGTGTTGGTGGGGAGCAGCTTTGGGAAATCCGG... | GGAGCACAGGAGGCTGGCCGCCCCACCCCACCAGCCCATCCTCCCACCTCCCTGGGGCCCTGCTGCCGCGCGGCTTCCGGCTGGGGTGGACCTCAGGTCTAGCCGGCAAGCCGGAGGGCGGGCGAGACAACAACGTGGCCTGGAGGCAATGGCCCTGGCCTCTCGTGTCCCCTTCTCTCACCCGCCCAGACTTGCCCTCTTTGGAGGTCGCCCGGGCTAAGGAACATGGAAGGACGCTGGGTGGAGAGTGAGGGGAGAGGATCCCAGCTCCCCGGTGGGGGAAGGCGGGTGTTGGTGGGGAGCAGCTTTGGGAAATCCGG... |
Task1_train_40564 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | CAGGGCCCGTGCTTTGTCTGCACGCACTCGCGCCTGGGGGCTCCTAGCTGCGGTGGAGTGTGTGGAGCTGACCTTCCTGGCCCCCAGCTCCTCTCCTGTGCTAAGCTCCGGTAGGGCTGGGAGCTGGCCTGTCACCTCTTGTTTCCAGGCCAATAGGACCAGAATAAGGAAGGAAAACAGGAAACTGGGCCCTGAGAGAGGGCAGGATACTCGTTGGGAGGGTGAACGGGGACACAGCCACGGTGGCGACCCACAGCCCTGGTAATCGCTCGCTCCATGCCCGCAGGGATGTTTGTGGGGGTGGCGTCAGCCCAGGGAGC... | CAGGGCCCGTGCTTTGTCTGCACGCACTCGCGCCTGGGGGCTCCTAGCTGCGGTGGAGTGTGTGGAGCTGACCTTCCTGGCCCCCAGCTCCTCTCCTGTGCTAAGCTCCGGTAGGGCTGGGAGCTGGCCTGTCACCTCTTGTTTCCAGGCCAATAGGACCAGAATAAGGAAGGAAAACAGGAAACTGGGCCCTGAGAGAGGGCAGGATACTCGTTGGGAGGGTGAACGGGGACACAGCCACGGTGGCGACCCACAGCCCTGGTAATCGCTCGCTCCATGCCCGCAGGGATGTTTGTGGGGGTGGCGTCAGCCCAGGGAGC... |
Task1_train_40565 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGCTAATTTTTCTATTTTTAGGGGGTAGAGACGGGGTTTCACCATGTTGCCCAGCGTTCCTCCCGCCACGGCTTTCCAAAGTACTGGGATTACAGGCATGAACCGCCGCACACACCACTTGTATCTCCTATGCCCGTGTCAAGCAGCAGCAGGGCGGTGGGAACGGCTGCACCTGCACTGTGGCAGCTCGCAGGCCTCCCTGACGTCCAGGCGGAGGCTTTCTCAAGTGTGGGTGCCTTGGGTCCGACCCAGGACCCCCTCCCCAGCTCCCGTCCTGTGGAGGAGACCCCACCATGCTTCCTCACCACCGGCTGGAGATG... | TGCTAATTTTTCTATTTTTAGGGGGTAGAGACGGGGTTTCACCATGTTGCCCAGCGTTCCTCCCGCCACGGCTTTCCAAAGTACTGGGATTACAGGCATGAACCGCCGCACACACCACTTGTATCTCCTATGCCCGTGTCAAGCAGCAGCAGGGCGGTGGGAACGGCTGCACCTGCACTGTGGCAGCTCGCAGGCCTCCCTGACGTCCAGGCGGAGGCTTTCTCAAGTGTGGGTGCCTTGGGTCCGACCCAGGACCCCCTCCCCAGCTCCCGTCCTGTGGAGGAGACCCCACCATGCTTCCTCACCACCGGCTGGAGATG... |
Task1_train_40566 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGGGTAGAGACGGGGTTTCACCATGTTGCCCAGCGTTCCTCCCGCCACGGCTTTCCAAAGTACTGGGATTACAGGCATGAACCGCCGCACACACCACTTGTATCTCCTATGCCCGTGTCAAGCAGCAGCAGGGCGGTGGGAACGGCTGCACCTGCACTGTGGCAGCTCGCAGGCCTCCCTGACGTCCAGGCGGAGGCTTTCTCAAGTGTGGGTGCCTTGGGTCCGACCCAGGACCCCCTCCCCAGCTCCCGTCCTGTGGAGGAGACCCCACCATGCTTCCTCACCACCGGCTGGAGATGTCCTGACCCCCTGCCCACTGC... | GGGGTAGAGACGGGGTTTCACCATGTTGCCCAGCGTTCCTCCCGCCACGGCTTTCCAAAGTACTGGGATTACAGGCATGAACCGCCGCACACACCACTTGTATCTCCTATGCCCGTGTCAAGCAGCAGCAGGGCGGTGGGAACGGCTGCACCTGCACTGTGGCAGCTCGCAGGCCTCCCTGACGTCCAGGCGGAGGCTTTCTCAAGTGTGGGTGCCTTGGGTCCGACCCAGGACCCCCTCCCCAGCTCCCGTCCTGTGGAGGAGACCCCACCATGCTTCCTCACCACCGGCTGGAGATGTCCTGACCCCCTGCCCACTGC... |
Task1_train_40567 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | GTGCGCCTCTCGCACAGGCCATTCTGGGTCTGGTGGTGCCAGGTGCCGTGACACGCCGTGCTGGGCTTGTGCTGCAGCTGGGTGGTGTGGCCCTCATTCTCATGTTCCAGCTGCTGGGCAGTGCTCTGCCTGTGTGCTGCGCCTGCAGGCTGCGTGTGCTGCCGTGGATCTCCTGCATCCCTTGACCCCTCCCGCCATCAGAGGAAAGGCTGCTCCCCGAGGCACCGCTTCCCTGTGCGGCGCTGCAGAGGGGCCCTCAGTGTGGCACTCCTCGTCAAAGAAAAATAAAGGCTAGAACTGCACCCCGGATCACGCGCTTT... | GTGCGCCTCTCGCACAGGCCATTCTGGGTCTGGTGGTGCCAGGTGCCGTGACACGCCGTGCTGGGCTTGTGCTGCAGCTGGGTGGTGTGGCCCTCATTCTCATGTTCCAGCTGCTGGGCAGTGCTCTGCCTGTGTGCTGCGCCTGCAGGCTGCGTGTGCTGCCGTGGATCTCCTGCATCCCTTGACCCCTCCCGCCATCAGAGGAAAGGCTGCTCCCCGAGGCACCGCTTCCCTGTGCGGCGCTGCAGAGGGGCCCTCAGTGTGGCACTCCTCGTCAAAGAAAAATAAAGGCTAGAACTGCACCCCGGATCACGCGCTTT... |
Task1_train_40568 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | TACCGCCCGTCCTGCCCTGCCAGAGTCTGCCCGGCTGCTCACCCCCAGGAAGATCTTGATGGCCCGTGAGCATGTGACCCCGGAGTTCCCACAGATGACGTTCTCTGTCAGGATCTTGAAGGTGGGCTGTGAGTCGTTGACACCACAGACGTCCTGCAGGGAGAGGGCGCTGAGGAGGAGCCCTGGAGGCCGTGCCTCTGGGTCCCCGGCCCCTGCGGCCTGGCACCCGATGGTTACCGTGGCCAGGATGTACTCGCAGTTGCCGTCGAATACGAAGCGCTGGCCGTCGAAGGTGATGACGTGGCCCTCCCCGTAGAGGG... | TACCGCCCGTCCTGCCCTGCCAGAGTCTGCCCGGCTGCTCACCCCCAGGAAGATCTTGATGGCCCGTGAGCATGTGACCCCGGAGTTCCCACAGATGACGTTCTCTGTCAGGATCTTGAAGGTGGGCTGTGAGTCGTTGACACCACAGACGTCCTGCAGGGAGAGGGCGCTGAGGAGGAGCCCTGGAGGCCGTGCCTCTGGGTCCCCGGCCCCTGCGGCCTGGCACCCGATGGTTACCGTGGCCAGGATGTACTCGCAGTTGCCGTCGAATACGAAGCGCTGGCCGTCGAAGGTGATGACGTGGCCCTCCCCGTAGAGGG... |
Task1_train_40569 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGATGCCGTTGATGACAGTGGACTGCTCGGCCAGGATGAACTTGTAACCCTCCAGTATGCACGGGCACTGGGCCTTGCGCACACACTCGCCCTTTTGGTTCAGGTAGGTGCCATCGGGGCAGTTGCAACCGTCCACGGGCACGGCGCTGTGGTGGCACTCGGTGGCACGGTCCGACAGCGACAGGCAGGTGCGCTCACAGGCTTGGCTGTTGTAGCTGAAGGTGGTGTTACCCGTGCAGGGGATGGCTGTGGGGGACCCGGGCATCAGACTCTCCGGGAGGGGGCGGCCGGGAGGGCAATCTCGGGTTCCCCTGCCTGCC... | TGATGCCGTTGATGACAGTGGACTGCTCGGCCAGGATGAACTTGTAACCCTCCAGTATGCACGGGCACTGGGCCTTGCGCACACACTCGCCCTTTTGGTTCAGGTAGGTGCCATCGGGGCAGTTGCAACCGTCCACGGGCACGGCGCTGTGGTGGCACTCGGTGGCACGGTCCGACAGCGACAGGCAGGTGCGCTCACAGGCTTGGCTGTTGTAGCTGAAGGTGGTGTTACCCGTGCAGGGGATGGCTGTGGGGGACCCGGGCATCAGACTCTCCGGGAGGGGGCGGCCGGGAGGGCAATCTCGGGTTCCCCTGCCTGCC... |
Task1_train_40570 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | CTGGCGACACAGGGGTGCCTGCCTGTGCCCTCCCGGGCCGGGGCAAGCAGTGGTGGGCCCAGTGGTCTCGTAGTCTGGGGTCGGTGTGAGTTCCGGTTCTCCAGGCTTTTTTCCAGACAACTGCTGGGATTGGTGGGCGAGACCAAGGCTCATCAAAGGCACAGCCTTGGGGGCAGGATCCCCACCATGAGTCAGAGGTAGTTCTGGGGAGCCTGGGCAGGCTGTCACCTCCTCAGCTGTCAGGCCCGAGGTCCTCATGTGGTCCCCAGGAGAAGGGGCAGACGGCCACTTCCGGCCACCAGCCAGCTCCCTGTGTGCCT... | CTGGCGACACAGGGGTGCCTGCCTGTGCCCTCCCGGGCCGGGGCAAGCAGTGGTGGGCCCAGTGGTCTCGTAGTCTGGGGTCGGTGTGAGTTCCGGTTCTCCAGGCTTTTTTCCAGACAACTGCTGGGATTGGTGGGCGAGACCAAGGCTCATCAAAGGCACAGCCTTGGGGGCAGGATCCCCACCATGAGTCAGAGGTAGTTCTGGGGAGCCTGGGCAGGCTGTCACCTCCTCAGCTGTCAGGCCCGAGGTCCTCATGTGGTCCCCAGGAGAAGGGGCAGACGGCCACTTCCGGCCACCAGCCAGCTCCCTGTGTGCCT... |
Task1_train_40571 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACTGAGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGCGCCGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACTGGGAGCTGGGGGGACACTCACCACGGGCACTGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGG... | GGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACTGAGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGCGCCGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACTGGGAGCTGGGGGGACACTCACCACGGGCACTGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGG... |
Task1_train_40572 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGCCGGGCACCGGGAGCTGGGGGGACACTCACTGAGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGAGAGCTGGGGGGACACTCACTGTGCCGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACTG... | GGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGCCGGGCACCGGGAGCTGGGGGGACACTCACTGAGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGAGAGCTGGGGGGACACTCACTGTGCCGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACTG... |
Task1_train_40573 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | GGAGCTGGGGGGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGCCGGGCACCGGGAGCTGGGGGGACACTCACTGAGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGAGAGCTGGGGGGACACTCACTGTGCCGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACTGAGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCAC... | GGAGCTGGGGGGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGCCGGGCACCGGGAGCTGGGGGGACACTCACTGAGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGAGAGCTGGGGGGACACTCACTGTGCCGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCACCGGGAGCTGGGGGGACACTCACCGTGACGGGCACCGGGAGCTGGGGGGACACTCACTGAGGGCACCGGGAGCTGGGGGGACACTCACCACGGGCAC... |
Task1_train_40574 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | TGGACACCTGCTCACACCTGGAGGTGAGCAGCCTGTGCGAGGAGCACCGCATGGACGGCTGTTTCTGCCCAGAAGGTGCGTGTGGAGGATGGCCCCGCCCTGGCACTGCCCACCAGATGAGAGGCAGCCCTGGCCTGGGGTTCTCGCCTGCGCTGAGGGGACGGCTCCGCTGGGTGGTGGGGGCAGCGGCGGCACAGAAGTGCCTCTCCCTCCACCCGATACCGGGGGAGAAGGGGCCTCGGTGTGAGGCCCTTCCCAAAGGGTGGCTTCAGGGAGGCCGGGAAGGGGGCTGCCTTCCTGGTTATCACCCTGGGGACAGA... | TGGACACCTGCTCACACCTGGAGGTGAGCAGCCTGTGCGAGGAGCACCGCATGGACGGCTGTTTCTGCCCAGAAGGTGCGTGTGGAGGATGGCCCCGCCCTGGCACTGCCCACCAGATGAGAGGCAGCCCTGGCCTGGGGTTCTCGCCTGCGCTGAGGGGACGGCTCCGCTGGGTGGTGGGGGCAGCGGCGGCACAGAAGTGCCTCTCCCTCCACCCGATACCGGGGGAGAAGGGGCCTCGGTGTGAGGCCCTTCCCAAAGGGTGGCTTCAGGGAGGCCGGGAAGGGGGCTGCCTTCCTGGTTATCACCCTGGGGACAGA... |
Task1_train_40575 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CAGGGGATCTCACGGGGGTCCCGGGCCCCGCTGAAGTTCCGATCCCCCACTCCCCAGCCAACTACGCCGAGCACTGGTGCTCCCTCCTGAAGAAGACAGAGACCCCCTTTGGCAGGTGCCACTCGGCTGTGGACCCTGCTGAGTATTACAAGGTGGGTGGGACCCACACCCCCAGGCCCCCATGCCATCAAGGTGGACTCAGGGCACCCCCAGCCCCCCATGCCACCCGTGAGGTGGACTCAGAGCACCCGGTTGGGCCCACTGGTTGCTGTGTGTGCGTGTGAGCTTGCGTCTGTGAGCGCCAGGCCACACTCTGCCTC... | CAGGGGATCTCACGGGGGTCCCGGGCCCCGCTGAAGTTCCGATCCCCCACTCCCCAGCCAACTACGCCGAGCACTGGTGCTCCCTCCTGAAGAAGACAGAGACCCCCTTTGGCAGGTGCCACTCGGCTGTGGACCCTGCTGAGTATTACAAGGTGGGTGGGACCCACACCCCCAGGCCCCCATGCCATCAAGGTGGACTCAGGGCACCCCCAGCCCCCCATGCCACCCGTGAGGTGGACTCAGAGCACCCGGTTGGGCCCACTGGTTGCTGTGTGTGCGTGTGAGCTTGCGTCTGTGAGCGCCAGGCCACACTCTGCCTC... |
Task1_train_40576 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TCCTGAAGAAGACAGAGACCCCCTTTGGCAGGTGCCACTCGGCTGTGGACCCTGCTGAGTATTACAAGGTGGGTGGGACCCACACCCCCAGGCCCCCATGCCATCAAGGTGGACTCAGGGCACCCCCAGCCCCCCATGCCACCCGTGAGGTGGACTCAGAGCACCCGGTTGGGCCCACTGGTTGCTGTGTGTGCGTGTGAGCTTGCGTCTGTGAGCGCCAGGCCACACTCTGCCTCCCTGCCTCACTGCCCGTCCACCTTGCTCTGTCGCCCAGAGGTGCAAATATGACACGTGTAACTGTCAGAACAATGAGGACTGCC... | TCCTGAAGAAGACAGAGACCCCCTTTGGCAGGTGCCACTCGGCTGTGGACCCTGCTGAGTATTACAAGGTGGGTGGGACCCACACCCCCAGGCCCCCATGCCATCAAGGTGGACTCAGGGCACCCCCAGCCCCCCATGCCACCCGTGAGGTGGACTCAGAGCACCCGGTTGGGCCCACTGGTTGCTGTGTGTGCGTGTGAGCTTGCGTCTGTGAGCGCCAGGCCACACTCTGCCTCCCTGCCTCACTGCCCGTCCACCTTGCTCTGTCGCCCAGAGGTGCAAATATGACACGTGTAACTGTCAGAACAATGAGGACTGCC... |
Task1_train_40577 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AGGTGGGCTGTGGCTGTGGGCGGGGCCGACTAGGCAGAGCGGGGCTATGGGCTGACTGTGGACGTGGTGAGGGTGCCGTAGAGCATGCTAATGACCAGGGCGTGGTCATAGCAGGGTAGGGTCTTGGGTGCTCCTGGGGCTGGGGGGCTTCTCCACATGCTCCCCACACCTTCAGGAGTCGCCCTGCTGCGTCACGCACCACACGGCGCTTGTCCTCCAGCTTTGGCTCTGGCCGCTGCCTCCTTTGGTCACATGACCGTATAATCGGCCTCCCCTCTGAGACCCTGGGCTGGACCCCCGGCCTCCCTCTGCCTCCCCAG... | AGGTGGGCTGTGGCTGTGGGCGGGGCCGACTAGGCAGAGCGGGGCTATGGGCTGACTGTGGACGTGGTGAGGGTGCCGTAGAGCATGCTAATGACCAGGGCGTGGTCATAGCAGGGTAGGGTCTTGGGTGCTCCTGGGGCTGGGGGGCTTCTCCACATGCTCCCCACACCTTCAGGAGTCGCCCTGCTGCGTCACGCACCACACGGCGCTTGTCCTCCAGCTTTGGCTCTGGCCGCTGCCTCCTTTGGTCACATGACCGTATAATCGGCCTCCCCTCTGAGACCCTGGGCTGGACCCCCGGCCTCCCTCTGCCTCCCCAG... |
Task1_train_40578 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | CCCACCGGCACACAGACCCCAACAACGACACCCATCAGCACCACCACCACGGTGACCCCAACCCCAACACCCACCGGCACACAGACCCCAACATCGACACCCATCACCACCACCACTACGGTGACCCCAACCCCAACACCCACCGGCACACAGACCCCAACCCCGACACCCATCACCACCACCACCACGGTGACCCCAACCCCAACACCCACCGGCACACAGACCCCAACATCGACACCCATCACCACCACCACTACGGTGACCCCAACCCCAACACCCACCGGCACACAGACCCCAACCACGACACCCATCACCACCAC... | CCCACCGGCACACAGACCCCAACAACGACACCCATCAGCACCACCACCACGGTGACCCCAACCCCAACACCCACCGGCACACAGACCCCAACATCGACACCCATCACCACCACCACTACGGTGACCCCAACCCCAACACCCACCGGCACACAGACCCCAACCCCGACACCCATCACCACCACCACCACGGTGACCCCAACCCCAACACCCACCGGCACACAGACCCCAACATCGACACCCATCACCACCACCACTACGGTGACCCCAACCCCAACACCCACCGGCACACAGACCCCAACCACGACACCCATCACCACCAC... |
Task1_train_40579 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | TCGCTAAATGCAACTGGGTGCCCACCACCCAGCTCGGGACAACCTCGAGGGTGGAGGTTGATGCCCAGGCAGCTGGTCACCCTCCTCCGTGTGTGGGGCACTGGGCAGCTGTCACTCAAGGGGGTCCAGGCTCCTCCGCCTGACATGAGGCAGCCCTCTGACCTCTGCCCATGTCCCTCAGTGGTGGAGTGCCCATCTCACAGGGAGTACCAGGCCTGTGGCCCTGCAGAAGAGCCCACGTGCAAATCCAGGTATGTTGTTTGAGGGTCCACCAGGACCGTGGGCTCGCCTTCTGCAGTGCGGAGGGTGGCATCATCTGG... | TCGCTAAATGCAACTGGGTGCCCACCACCCAGCTCGGGACAACCTCGAGGGTGGAGGTTGATGCCCAGGCAGCTGGTCACCCTCCTCCGTGTGTGGGGCACTGGGCAGCTGTCACTCAAGGGGGTCCAGGCTCCTCCGCCTGACATGAGGCAGCCCTCTGACCTCTGCCCATGTCCCTCAGTGGTGGAGTGCCCATCTCACAGGGAGTACCAGGCCTGTGGCCCTGCAGAAGAGCCCACGTGCAAATCCAGGTATGTTGTTTGAGGGTCCACCAGGACCGTGGGCTCGCCTTCTGCAGTGCGGAGGGTGGCATCATCTGG... |
Task1_train_40580 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CCCACTCATTACCTCAGTCTGCAAGACCCCATCTCCCAGTGAGGTGCCATGCATAGGCGCCGGGGTCAGGACTTAGGCGGGTCCTTCGAGGCCACGTCAGCTTCTTTTTCTCCAGGAGGGGCTTGCCTCTGGCTCCGGCCCTCGGTGCTCAGCTGCACTGCCCGGGGCCTCCCCAGGTGTAGCTGGAGGTGGGAAGGAGGAAGCAGCACCTGTGGTCGCTGTTGGCCACCTGGGTGGGAGGAGGCGGCCGCAGGGCAGGGTGGCCCTGGGTGGGAGGAGGCGGCCTAGGGGCAGGGTGGCTCTGGCCTTCTCGGTTTGCT... | CCCACTCATTACCTCAGTCTGCAAGACCCCATCTCCCAGTGAGGTGCCATGCATAGGCGCCGGGGTCAGGACTTAGGCGGGTCCTTCGAGGCCACGTCAGCTTCTTTTTCTCCAGGAGGGGCTTGCCTCTGGCTCCGGCCCTCGGTGCTCAGCTGCACTGCCCGGGGCCTCCCCAGGTGTAGCTGGAGGTGGGAAGGAGGAAGCAGCACCTGTGGTCGCTGTTGGCCACCTGGGTGGGAGGAGGCGGCCGCAGGGCAGGGTGGCCCTGGGTGGGAGGAGGCGGCCTAGGGGCAGGGTGGCTCTGGCCTTCTCGGTTTGCT... |
Task1_train_40581 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | GGGGAGCAGGCTCGAGGGGCTCAGGGGGCGGCAGGGGGAAGCTGGGCCGAGATGGAGCCCTAGGGTCCCCACCGGAAGGATGCCCATTAAAATCACCCCTGGAAAGTAATGGCTCCACTCTGGCACCCACCTCCCCTGACCCCCGACTGGAGGGGCCCCACGAGGGAGGGACCTTGGGCTGACGCTGGAGAGACAACTGCTGGGACCCAGGTGGGGCCGGCCTCCTGTCCCCCAGTCTGGGGGTGCAATGCAGTTCCCAGGGAACTCCACCCCTGTCGGAGCTGCTCCCTGCCCGCCGTTGGTAGCATGGGATGCCCGTG... | GGGGAGCAGGCTCGAGGGGCTCAGGGGGCGGCAGGGGGAAGCTGGGCCGAGATGGAGCCCTAGGGTCCCCACCGGAAGGATGCCCATTAAAATCACCCCTGGAAAGTAATGGCTCCACTCTGGCACCCACCTCCCCTGACCCCCGACTGGAGGGGCCCCACGAGGGAGGGACCTTGGGCTGACGCTGGAGAGACAACTGCTGGGACCCAGGTGGGGCCGGCCTCCTGTCCCCCAGTCTGGGGGTGCAATGCAGTTCCCAGGGAACTCCACCCCTGTCGGAGCTGCTCCCTGCCCGCCGTTGGTAGCATGGGATGCCCGTG... |
Task1_train_40582 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | GAAGCTGGGCCGAGATGGAGCCCTAGGGTCCCCACCGGAAGGATGCCCATTAAAATCACCCCTGGAAAGTAATGGCTCCACTCTGGCACCCACCTCCCCTGACCCCCGACTGGAGGGGCCCCACGAGGGAGGGACCTTGGGCTGACGCTGGAGAGACAACTGCTGGGACCCAGGTGGGGCCGGCCTCCTGTCCCCCAGTCTGGGGGTGCAATGCAGTTCCCAGGGAACTCCACCCCTGTCGGAGCTGCTCCCTGCCCGCCGTTGGTAGCATGGGATGCCCGTGGAAGGCACACGGCCGCCCCCACGCATCGGCCTGCCCT... | GAAGCTGGGCCGAGATGGAGCCCTAGGGTCCCCACCGGAAGGATGCCCATTAAAATCACCCCTGGAAAGTAATGGCTCCACTCTGGCACCCACCTCCCCTGACCCCCGACTGGAGGGGCCCCACGAGGGAGGGACCTTGGGCTGACGCTGGAGAGACAACTGCTGGGACCCAGGTGGGGCCGGCCTCCTGTCCCCCAGTCTGGGGGTGCAATGCAGTTCCCAGGGAACTCCACCCCTGTCGGAGCTGCTCCCTGCCCGCCGTTGGTAGCATGGGATGCCCGTGGAAGGCACACGGCCGCCCCCACGCATCGGCCTGCCCT... |
Task1_train_40583 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | CATGGGCGGCAGCCCCTGAGGATCAAGAAGGGATCGAGGAGCAGGGAGTCGGGCTCGGGGATGACCTGCTGTTTCCCCACCAGCCACCTGCAGTGGGGAGGGCCTGGCCTCCAAGTCACCCCAGCAGGCCTGGCGTCCAAGTCCTGCCCTCAGCAGCCCCCGGGCCTGGCCTCATTGGGGTGTCAGGGGTCTGGCAGCCCAGGCTGGCCCCGGGGATGCATGGCTATCACTTGCCTCACAATGCTCAGGGCTCAGGTACCCCCATGTCCTCGCCCTCTTCTGGGGGATGTCTCAGGGCCCCAAGGCATCATCTGAGCTTC... | CATGGGCGGCAGCCCCTGAGGATCAAGAAGGGATCGAGGAGCAGGGAGTCGGGCTCGGGGATGACCTGCTGTTTCCCCACCAGCCACCTGCAGTGGGGAGGGCCTGGCCTCCAAGTCACCCCAGCAGGCCTGGCGTCCAAGTCCTGCCCTCAGCAGCCCCCGGGCCTGGCCTCATTGGGGTGTCAGGGGTCTGGCAGCCCAGGCTGGCCCCGGGGATGCATGGCTATCACTTGCCTCACAATGCTCAGGGCTCAGGTACCCCCATGTCCTCGCCCTCTTCTGGGGGATGTCTCAGGGCCCCAAGGCATCATCTGAGCTTC... |
Task1_train_40584 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | CTGGCCTCATTGGGGTGTCAGGGGTCTGGCAGCCCAGGCTGGCCCCGGGGATGCATGGCTATCACTTGCCTCACAATGCTCAGGGCTCAGGTACCCCCATGTCCTCGCCCTCTTCTGGGGGATGTCTCAGGGCCCCAAGGCATCATCTGAGCTTCTCTGAGAGTAGAAAGCTCTGGAACTCACGTGTTCTGGGGCACAGATGTGTGGACCCTGCTCAGGGCATGGCCTGGGAGCCACTTCCCTAAAACTCAGTCGGTTCGCCTGGCTCTTCAGAACCTGTGCCGCTCATGTGGGTTCTGAGCAGGGACCGCGGGTGGGGA... | CTGGCCTCATTGGGGTGTCAGGGGTCTGGCAGCCCAGGCTGGCCCCGGGGATGCATGGCTATCACTTGCCTCACAATGCTCAGGGCTCAGGTACCCCCATGTCCTCGCCCTCTTCTGGGGGATGTCTCAGGGCCCCAAGGCATCATCTGAGCTTCTCTGAGAGTAGAAAGCTCTGGAACTCACGTGTTCTGGGGCACAGATGTGTGGACCCTGCTCAGGGCATGGCCTGGGAGCCACTTCCCTAAAACTCAGTCGGTTCGCCTGGCTCTTCAGAACCTGTGCCGCTCATGTGGGTTCTGAGCAGGGACCGCGGGTGGGGA... |
Task1_train_40585 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | CCTCACAATGCTCAGGGCTCAGGTACCCCCATGTCCTCGCCCTCTTCTGGGGGATGTCTCAGGGCCCCAAGGCATCATCTGAGCTTCTCTGAGAGTAGAAAGCTCTGGAACTCACGTGTTCTGGGGCACAGATGTGTGGACCCTGCTCAGGGCATGGCCTGGGAGCCACTTCCCTAAAACTCAGTCGGTTCGCCTGGCTCTTCAGAACCTGTGCCGCTCATGTGGGTTCTGAGCAGGGACCGCGGGTGGGGACAGGAAGACAGACCTGCTGGCGCAGCTCCAGACCGGTGACAGAGCCGCAGGGAGGGGCGGGCGGCCCC... | CCTCACAATGCTCAGGGCTCAGGTACCCCCATGTCCTCGCCCTCTTCTGGGGGATGTCTCAGGGCCCCAAGGCATCATCTGAGCTTCTCTGAGAGTAGAAAGCTCTGGAACTCACGTGTTCTGGGGCACAGATGTGTGGACCCTGCTCAGGGCATGGCCTGGGAGCCACTTCCCTAAAACTCAGTCGGTTCGCCTGGCTCTTCAGAACCTGTGCCGCTCATGTGGGTTCTGAGCAGGGACCGCGGGTGGGGACAGGAAGACAGACCTGCTGGCGCAGCTCCAGACCGGTGACAGAGCCGCAGGGAGGGGCGGGCGGCCCC... |
Task1_train_40586 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CCCCAAGGCATCATCTGAGCTTCTCTGAGAGTAGAAAGCTCTGGAACTCACGTGTTCTGGGGCACAGATGTGTGGACCCTGCTCAGGGCATGGCCTGGGAGCCACTTCCCTAAAACTCAGTCGGTTCGCCTGGCTCTTCAGAACCTGTGCCGCTCATGTGGGTTCTGAGCAGGGACCGCGGGTGGGGACAGGAAGACAGACCTGCTGGCGCAGCTCCAGACCGGTGACAGAGCCGCAGGGAGGGGCGGGCGGCCCCCAAGTGCGGGCCTCTCATGCTCAGCTGCCTTCTCTTCTGCCCACAGTCGTGAGCTCCACGCACA... | CCCCAAGGCATCATCTGAGCTTCTCTGAGAGTAGAAAGCTCTGGAACTCACGTGTTCTGGGGCACAGATGTGTGGACCCTGCTCAGGGCATGGCCTGGGAGCCACTTCCCTAAAACTCAGTCGGTTCGCCTGGCTCTTCAGAACCTGTGCCGCTCATGTGGGTTCTGAGCAGGGACCGCGGGTGGGGACAGGAAGACAGACCTGCTGGCGCAGCTCCAGACCGGTGACAGAGCCGCAGGGAGGGGCGGGCGGCCCCCAAGTGCGGGCCTCTCATGCTCAGCTGCCTTCTCTTCTGCCCACAGTCGTGAGCTCCACGCACA... |
Task1_train_40587 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CAGCACACCTGGCACCGTGTCTCTCTCTACAGCCAGGACGACACCTGCCCCAGGTACCGCTACCTCTGTCAAAAAAACTTTCTCAACTCCCAGCCCTCCGCCAGTGCCGGCAACATCAACATCATCCATGTCGACCACGGCCCCGGGGACCTCTGTGGTCTCCAGCAAGCCCACCCCCACGGAGCCCAGCACATCCTCCTGCCTGCAGGAGCTTTGCACCTGGACCGAGTGGATCGATGGCAGCTACCCTGCTCCTGGAATAAATGGTGGAGATTTTGACACATTTCAAAATTTGAGAGACGAAGGATACACATTCTGTG... | CAGCACACCTGGCACCGTGTCTCTCTCTACAGCCAGGACGACACCTGCCCCAGGTACCGCTACCTCTGTCAAAAAAACTTTCTCAACTCCCAGCCCTCCGCCAGTGCCGGCAACATCAACATCATCCATGTCGACCACGGCCCCGGGGACCTCTGTGGTCTCCAGCAAGCCCACCCCCACGGAGCCCAGCACATCCTCCTGCCTGCAGGAGCTTTGCACCTGGACCGAGTGGATCGATGGCAGCTACCCTGCTCCTGGAATAAATGGTGGAGATTTTGACACATTTCAAAATTTGAGAGACGAAGGATACACATTCTGTG... |
Task1_train_40588 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AACTTTCTCAACTCCCAGCCCTCCGCCAGTGCCGGCAACATCAACATCATCCATGTCGACCACGGCCCCGGGGACCTCTGTGGTCTCCAGCAAGCCCACCCCCACGGAGCCCAGCACATCCTCCTGCCTGCAGGAGCTTTGCACCTGGACCGAGTGGATCGATGGCAGCTACCCTGCTCCTGGAATAAATGGTGGAGATTTTGACACATTTCAAAATTTGAGAGACGAAGGATACACATTCTGTGAAAGTCCTCGAAGCGTGCAGTGCCGGGCAGAGAGCTTCCCCAACACGCCGCTGGCAGACCTGGGGCAGGACGTCA... | AACTTTCTCAACTCCCAGCCCTCCGCCAGTGCCGGCAACATCAACATCATCCATGTCGACCACGGCCCCGGGGACCTCTGTGGTCTCCAGCAAGCCCACCCCCACGGAGCCCAGCACATCCTCCTGCCTGCAGGAGCTTTGCACCTGGACCGAGTGGATCGATGGCAGCTACCCTGCTCCTGGAATAAATGGTGGAGATTTTGACACATTTCAAAATTTGAGAGACGAAGGATACACATTCTGTGAAAGTCCTCGAAGCGTGCAGTGCCGGGCAGAGAGCTTCCCCAACACGCCGCTGGCAGACCTGGGGCAGGACGTCA... |
Task1_train_40589 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | CAGTCCAGCCCAGACCACTCCTTCAACAACCTCCAAGACCACTGAAACCCAGGCCTCAGGCTCCTCAGCCCCCAGCAGCACACCTGGCACCGTGTCTCTCTCTACAGCCAGGACGACACCTGCCCCAGGTACCGCTACCTCTGTCAAAAAAACTTTCTCAACTCCCAGCCCTCCGCCAGTGCCGGCAACATCAACATCATCCATGTCGACCACGGCCCCGGGGACCTCTGTGGTCTCCAGCAAGCCCACCCCCACGGAGCCCAGCACATCCTCCTGCCTGCAGGAGCTTTGCACCTGGACCGAGTGGATTGATGGCAGCT... | CAGTCCAGCCCAGACCACTCCTTCAACAACCTCCAAGACCACTGAAACCCAGGCCTCAGGCTCCTCAGCCCCCAGCAGCACACCTGGCACCGTGTCTCTCTCTACAGCCAGGACGACACCTGCCCCAGGTACCGCTACCTCTGTCAAAAAAACTTTCTCAACTCCCAGCCCTCCGCCAGTGCCGGCAACATCAACATCATCCATGTCGACCACGGCCCCGGGGACCTCTGTGGTCTCCAGCAAGCCCACCCCCACGGAGCCCAGCACATCCTCCTGCCTGCAGGAGCTTTGCACCTGGACCGAGTGGATTGATGGCAGCT... |
Task1_train_40590 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GTACAAGCAGCACAACCTCTGCCACTACCACCAGCAGAATCTCTGGTCCTGAAACTACTCCCAGCCCTGTTCCTACCACCAGCACAACCTCTGCCACTACAACCAGCACAACCTCAGCTCCTACAACCAGCACAACCTCTGCCCCTACAAGCAGCACAACCTCCAGTCCACAGACCAGCACAACCTCGGCTCCTACAACCAGCACAACTTCTGGTCCTGGAACTACCCCAAGCCCTGTTCCCACGACCAGCACAACCTCTGCCCCTACAACAAGAACAACTTCTGCTCCTAAAAGCAGCACAACCTCTGCCGCTACAACC... | GTACAAGCAGCACAACCTCTGCCACTACCACCAGCAGAATCTCTGGTCCTGAAACTACTCCCAGCCCTGTTCCTACCACCAGCACAACCTCTGCCACTACAACCAGCACAACCTCAGCTCCTACAACCAGCACAACCTCTGCCCCTACAAGCAGCACAACCTCCAGTCCACAGACCAGCACAACCTCGGCTCCTACAACCAGCACAACTTCTGGTCCTGGAACTACCCCAAGCCCTGTTCCCACGACCAGCACAACCTCTGCCCCTACAACAAGAACAACTTCTGCTCCTAAAAGCAGCACAACCTCTGCCGCTACAACC... |
Task1_train_40591 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | CTCTGCTCCTACAACCAGCACAACCTCTGCCCCTATAAGCAGCACAACCTCTGCCACTACAACCAGCACAACCTCTGGTCCTGGAACTACTCCCAGCCCTGTTCCTACCACGAGCACAACCTCTGCTCCTACAACCAGCACAACCTCTGGTCCTGGAACTACTCCCAGTGCTGTTCCCACCACCAGCATAACCTCTGCACCTACAACCAGCACAAACTCTGCCCCTATAAGCAGCACAACCTCTGCCACTACAACCAGCAGAATCTCTGGTCCTGAAACTACTCCCAGCCCTGTTCCTACCGCCAGCACAACCTCTGCTT... | CTCTGCTCCTACAACCAGCACAACCTCTGCCCCTATAAGCAGCACAACCTCTGCCACTACAACCAGCACAACCTCTGGTCCTGGAACTACTCCCAGCCCTGTTCCTACCACGAGCACAACCTCTGCTCCTACAACCAGCACAACCTCTGGTCCTGGAACTACTCCCAGTGCTGTTCCCACCACCAGCATAACCTCTGCACCTACAACCAGCACAAACTCTGCCCCTATAAGCAGCACAACCTCTGCCACTACAACCAGCAGAATCTCTGGTCCTGAAACTACTCCCAGCCCTGTTCCTACCGCCAGCACAACCTCTGCTT... |
Task1_train_40592 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | GTCCTGGAACTACTCCCAGTGCTGTTCCCACCACCAGCATAACCTCTGCACCTACAACCAGCACAAACTCTGCCCCTATAAGCAGCACAACCTCTGCCACTACAACCAGCAGAATCTCTGGTCCTGAAACTACTCCCAGCCCTGTTCCTACCGCCAGCACAACCTCTGCTTCTACAACTAGCACAACCTCTGGTCCTGGAACTACTCCCAGCCCTGTTCCTACCACCAGCACAATCTCTGTTCCTACCACCAGCACAACTTCTGCTTCTACAACCAGCACAACCTCTGCTTCTACAACCAGCACAACCTCTGGTCCTGGA... | GTCCTGGAACTACTCCCAGTGCTGTTCCCACCACCAGCATAACCTCTGCACCTACAACCAGCACAAACTCTGCCCCTATAAGCAGCACAACCTCTGCCACTACAACCAGCAGAATCTCTGGTCCTGAAACTACTCCCAGCCCTGTTCCTACCGCCAGCACAACCTCTGCTTCTACAACTAGCACAACCTCTGGTCCTGGAACTACTCCCAGCCCTGTTCCTACCACCAGCACAATCTCTGTTCCTACCACCAGCACAACTTCTGCTTCTACAACCAGCACAACCTCTGCTTCTACAACCAGCACAACCTCTGGTCCTGGA... |
Task1_train_40593 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | AACCAGCACAAACTCTGCCCCTATAAGCAGCACAACCTCTGCCACTACAACCAGCAGAATCTCTGGTCCTGAAACTACTCCCAGCCCTGTTCCTACCGCCAGCACAACCTCTGCTTCTACAACTAGCACAACCTCTGGTCCTGGAACTACTCCCAGCCCTGTTCCTACCACCAGCACAATCTCTGTTCCTACCACCAGCACAACTTCTGCTTCTACAACCAGCACAACCTCTGCTTCTACAACCAGCACAACCTCTGGTCCTGGAACTACTCCCAGCCCTGTTCCCACCACCAGCACAACCTCTGCTCCCACAACAAGCA... | AACCAGCACAAACTCTGCCCCTATAAGCAGCACAACCTCTGCCACTACAACCAGCAGAATCTCTGGTCCTGAAACTACTCCCAGCCCTGTTCCTACCGCCAGCACAACCTCTGCTTCTACAACTAGCACAACCTCTGGTCCTGGAACTACTCCCAGCCCTGTTCCTACCACCAGCACAATCTCTGTTCCTACCACCAGCACAACTTCTGCTTCTACAACCAGCACAACCTCTGCTTCTACAACCAGCACAACCTCTGGTCCTGGAACTACTCCCAGCCCTGTTCCCACCACCAGCACAACCTCTGCTCCCACAACAAGCA... |
Task1_train_40594 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | CCCTACAACCAGCACAATCTCTGCCTCTACCACCAGCACAACCTCTGCGACTACAACCAGCACAACCTCTGCTACTACAACCAGCACAATCTCTGCCCCTACAACCAGCACAACTTTGTCTCCTACAACCAGCACAACCTCTACTACTATAACCAGCACAACTTCTGCCCCTATAAGCAGCACAACTTCCACACCACAGACCAGCACAACTTCGGCTCCTACAACCAGCACAACTTCTGGTCCTGGAACTACTTCAAGCCCTGTTCCCACCACCAGCACAACCTCTGCCCCTACAACCAGCACAACCTCTGCCCCTACAA... | CCCTACAACCAGCACAATCTCTGCCTCTACCACCAGCACAACCTCTGCGACTACAACCAGCACAACCTCTGCTACTACAACCAGCACAATCTCTGCCCCTACAACCAGCACAACTTTGTCTCCTACAACCAGCACAACCTCTACTACTATAACCAGCACAACTTCTGCCCCTATAAGCAGCACAACTTCCACACCACAGACCAGCACAACTTCGGCTCCTACAACCAGCACAACTTCTGGTCCTGGAACTACTTCAAGCCCTGTTCCCACCACCAGCACAACCTCTGCCCCTACAACCAGCACAACCTCTGCCCCTACAA... |
Task1_train_40595 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | CTACTACTATAACCAGCACAACTTCTGCCCCTATAAGCAGCACAACTTCCACACCACAGACCAGCACAACTTCGGCTCCTACAACCAGCACAACTTCTGGTCCTGGAACTACTTCAAGCCCTGTTCCCACCACCAGCACAACCTCTGCCCCTACAACCAGCACAACCTCTGCCCCTACAACCAGAACAACCTCTGTCCCTACAAGCAGCACAACCTCCACTGCTACAACCAGCACAACCTCTGGCCCTGGAACTACTCCCAGCCCTGTTCCCACCACCAGTACAACCTCTGCTCCTACAACCAGAACAACCTCTGCTCCT... | CTACTACTATAACCAGCACAACTTCTGCCCCTATAAGCAGCACAACTTCCACACCACAGACCAGCACAACTTCGGCTCCTACAACCAGCACAACTTCTGGTCCTGGAACTACTTCAAGCCCTGTTCCCACCACCAGCACAACCTCTGCCCCTACAACCAGCACAACCTCTGCCCCTACAACCAGAACAACCTCTGTCCCTACAAGCAGCACAACCTCCACTGCTACAACCAGCACAACCTCTGGCCCTGGAACTACTCCCAGCCCTGTTCCCACCACCAGTACAACCTCTGCTCCTACAACCAGAACAACCTCTGCTCCT... |
Task1_train_40596 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AACTTCGGCTCCTACAACCAGCACAACTTCTGGTCCTGGAACTACTTCAAGCCCTGTTCCCACCACCAGCACAACCTCTGCCCCTACAACCAGCACAACCTCTGCCCCTACAACCAGAACAACCTCTGTCCCTACAAGCAGCACAACCTCCACTGCTACAACCAGCACAACCTCTGGCCCTGGAACTACTCCCAGCCCTGTTCCCACCACCAGTACAACCTCTGCTCCTACAACCAGAACAACCTCTGCTCCTACAACCAGCACAACCTCTGCCCCTACAACCAGCACAACCTCTGCCCCTACAAGCAGCACAACCTCAG... | AACTTCGGCTCCTACAACCAGCACAACTTCTGGTCCTGGAACTACTTCAAGCCCTGTTCCCACCACCAGCACAACCTCTGCCCCTACAACCAGCACAACCTCTGCCCCTACAACCAGAACAACCTCTGTCCCTACAAGCAGCACAACCTCCACTGCTACAACCAGCACAACCTCTGGCCCTGGAACTACTCCCAGCCCTGTTCCCACCACCAGTACAACCTCTGCTCCTACAACCAGAACAACCTCTGCTCCTACAACCAGCACAACCTCTGCCCCTACAACCAGCACAACCTCTGCCCCTACAAGCAGCACAACCTCAG... |
Task1_train_40597 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | CCACCAGCACAACCTCTGCTCCCACAACAAGCACAACCTCTGCCCCTACAACCAGCACAATCTCGGCCCCAACAACCAGCACACCCTCTGCCCCTACAACCAGCACAACCTTAGCTCCTACAACCAGCACAACCTCTGCCCCTACAACCAGCACAACCTCTACCCCTACAAGCAGCACAACCTCCTCTCCACAGACCAGCACAACCTCGGCTTCTACCACCAGCATAACTTCTGGTCCTGGAACTACCCCAAGCCCTGTTCCCACCACCAGCACAACCTCTGCTCCTACAACCAGCACAACCTCTGCCGCTACAACCAGC... | CCACCAGCACAACCTCTGCTCCCACAACAAGCACAACCTCTGCCCCTACAACCAGCACAATCTCGGCCCCAACAACCAGCACACCCTCTGCCCCTACAACCAGCACAACCTTAGCTCCTACAACCAGCACAACCTCTGCCCCTACAACCAGCACAACCTCTACCCCTACAAGCAGCACAACCTCCTCTCCACAGACCAGCACAACCTCGGCTTCTACCACCAGCATAACTTCTGGTCCTGGAACTACCCCAAGCCCTGTTCCCACCACCAGCACAACCTCTGCTCCTACAACCAGCACAACCTCTGCCGCTACAACCAGC... |
Task1_train_40598 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TCAGAGCACTTCCTCTTGGCAGAAATCCAGGACAACCACTTTGGTGACAACCAGCACAACCTCCACTCCACAGACCAGCACAACCTCTGCTCCTACAACCAGCACAACCTCTGCTCCCACAACCAGCACAACTTCTGCCCCTACAACCAGCACAACCTCCACTCCACAGACCAGCATATCCTCTGCCCCTACAAGCAGCACAACCTCGGCTCCTACAAGCAGCACAATCTCTGCTCGTACAACCAGCATAATCTCTGCCCCTACAACCAGCACAACCTCTTCCCCTACAACCAGCACAACCTCTGCTACTACAACCAGCA... | TCAGAGCACTTCCTCTTGGCAGAAATCCAGGACAACCACTTTGGTGACAACCAGCACAACCTCCACTCCACAGACCAGCACAACCTCTGCTCCTACAACCAGCACAACCTCTGCTCCCACAACCAGCACAACTTCTGCCCCTACAACCAGCACAACCTCCACTCCACAGACCAGCATATCCTCTGCCCCTACAAGCAGCACAACCTCGGCTCCTACAAGCAGCACAATCTCTGCTCGTACAACCAGCATAATCTCTGCCCCTACAACCAGCACAACCTCTTCCCCTACAACCAGCACAACCTCTGCTACTACAACCAGCA... |
Task1_train_40599 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | CACCAGCACAGCCTCTGTTTCAAAGACCAGCACAAGCCATGTTTCTGTATCCAAGACAACCCACTCCCAACCAGTCACCAGAGACTGTCATCCCCGGTGCACCTGGACCAAATGGTTTGATGTGGACTTTCCATCCCCTGGACCCCACGGTGGGGACAAGGAAACCTACAACAACATCATCAGGAGTGGGGAAAAAATCTGCCGCCGACCTGAGGAGATCACCAGGCTCCAGTGCCGAGCCAAGAGCCACCCGGAGGTGAGCATCGAACACCTGGGCCAGGTGGTGCAGTGCAGCCGCGAAGAGGGCCTGGTGTGCCGGA... | CACCAGCACAGCCTCTGTTTCAAAGACCAGCACAAGCCATGTTTCTGTATCCAAGACAACCCACTCCCAACCAGTCACCAGAGACTGTCATCCCCGGTGCACCTGGACCAAATGGTTTGATGTGGACTTTCCATCCCCTGGACCCCACGGTGGGGACAAGGAAACCTACAACAACATCATCAGGAGTGGGGAAAAAATCTGCCGCCGACCTGAGGAGATCACCAGGCTCCAGTGCCGAGCCAAGAGCCACCCGGAGGTGAGCATCGAACACCTGGGCCAGGTGGTGCAGTGCAGCCGCGAAGAGGGCCTGGTGTGCCGGA... |
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