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_45400 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GTTGTCTTGGGGGTTCTGCAGGACCATAATAAGAAACCCACACCTGGTTCCCTTCTCAACTTGGAATTTTCAGAGCAAAAACAGGAATCAAGTCTTCCCCACTTCTCCAGTCCCTCAGTGTCTCGCTGTTTTGAACTGTGTGTATCCATGGACAGTCAAGAGCTCAGGAAGTTGAGAGCGGTTTTGTTTCCCACCCTTAGAGTCTGCCAAGCCTCTAGCCCACTGGCCTTGAGAGATGAGTGTGTGCCCAACCAAATGCTGGCTATACCAGTTACAGCCTCCACTCATAAAAGGGAAAAAGCAAAATCTTTATGGTAAAC... | GTTGTCTTGGGGGTTCTGCAGGACCATAATAAGAAACCCACACCTGGTTCCCTTCTCAACTTGGAATTTTCAGAGCAAAAACAGGAATCAAGTCTTCCCCACTTCTCCAGTCCCTCAGTGTCTCGCTGTTTTGAACTGTGTGTATCCATGGACAGTCAAGAGCTCAGGAAGTTGAGAGCGGTTTTGTTTCCCACCCTTAGAGTCTGCCAAGCCTCTAGCCCACTGGCCTTGAGAGATGAGTGTGTGCCCAACCAAATGCTGGCTATACCAGTTACAGCCTCCACTCATAAAAGGGAAAAAGCAAAATCTTTATGGTAAAC... |
Task1_train_45401 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TTGAGGTGGCCTTCTGACACAGACTTGGTGTCCAGGCTGGTTTCTGCAGATGTGGGGAGAGGAGGCCTCTCATGGACTTTCAGGGCATGAGCCATCCTCTCCCATGCCCGGCTTCCCCATCGCACCCCCCTCCCCATCATGAGTATGAGAACCTATGCAACCGAGCAGAGAGAGCCTAGGCTCTTCCAAACGGGCTGGAGAGCCCCCAAATCCCAATAGTGCTGCTGCCAGAGTCCTGGCTGCTCTGTCTTCTGGCCTGGCTTCATTTCAGCCCCTCTGCAAGCCCTGGCCTGGCACCTGGCTTTCTGAAAACCCAGCAC... | TTGAGGTGGCCTTCTGACACAGACTTGGTGTCCAGGCTGGTTTCTGCAGATGTGGGGAGAGGAGGCCTCTCATGGACTTTCAGGGCATGAGCCATCCTCTCCCATGCCCGGCTTCCCCATCGCACCCCCCTCCCCATCATGAGTATGAGAACCTATGCAACCGAGCAGAGAGAGCCTAGGCTCTTCCAAACGGGCTGGAGAGCCCCCAAATCCCAATAGTGCTGCTGCCAGAGTCCTGGCTGCTCTGTCTTCTGGCCTGGCTTCATTTCAGCCCCTCTGCAAGCCCTGGCCTGGCACCTGGCTTTCTGAAAACCCAGCAC... |
Task1_train_45402 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGAGGTGGCCTTCTGACACAGACTTGGTGTCCAGGCTGGTTTCTGCAGATGTGGGGAGAGGAGGCCTCTCATGGACTTTCAGGGCATGAGCCATCCTCTCCCATGCCCGGCTTCCCCATCGCACCCCCCTCCCCATCATGAGTATGAGAACCTATGCAACCGAGCAGAGAGAGCCTAGGCTCTTCCAAACGGGCTGGAGAGCCCCCAAATCCCAATAGTGCTGCTGCCAGAGTCCTGGCTGCTCTGTCTTCTGGCCTGGCTTCATTTCAGCCCCTCTGCAAGCCCTGGCCTGGCACCTGGCTTTCTGAAAACCCAGCACG... | TGAGGTGGCCTTCTGACACAGACTTGGTGTCCAGGCTGGTTTCTGCAGATGTGGGGAGAGGAGGCCTCTCATGGACTTTCAGGGCATGAGCCATCCTCTCCCATGCCCGGCTTCCCCATCGCACCCCCCTCCCCATCATGAGTATGAGAACCTATGCAACCGAGCAGAGAGAGCCTAGGCTCTTCCAAACGGGCTGGAGAGCCCCCAAATCCCAATAGTGCTGCTGCCAGAGTCCTGGCTGCTCTGTCTTCTGGCCTGGCTTCATTTCAGCCCCTCTGCAAGCCCTGGCCTGGCACCTGGCTTTCTGAAAACCCAGCACG... |
Task1_train_45403 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | CTGGAAAATCTAAGATCTACTCAGTACCTAGTGGTCCAAGATTCTAAATTCTAAAATCAAAGGGAAATTATTTTCAACGATCTGGCTGTTAGGACGTTTCCAAACATGGAGATTTGTCACATTTTATTAGTACTTCATCCCCAAGAAGTAGGGAGACCGGGGGCTATGATCCCCAGTCAAGGCCAAGGTTGAAGCAATTTGTTGGAGACCACAAAGCCAGGGCAGAAATAAGGACCCTGGTGTCCTCTCTCCTTATAACAGGGGACCCCTAGCAGAGGGGCCCTGGGTCATCGGTAGGAGCTCATGGTTGTTCCCTGGGA... | CTGGAAAATCTAAGATCTACTCAGTACCTAGTGGTCCAAGATTCTAAATTCTAAAATCAAAGGGAAATTATTTTCAACGATCTGGCTGTTAGGACGTTTCCAAACATGGAGATTTGTCACATTTTATTAGTACTTCATCCCCAAGAAGTAGGGAGACCGGGGGCTATGATCCCCAGTCAAGGCCAAGGTTGAAGCAATTTGTTGGAGACCACAAAGCCAGGGCAGAAATAAGGACCCTGGTGTCCTCTCTCCTTATAACAGGGGACCCCTAGCAGAGGGGCCCTGGGTCATCGGTAGGAGCTCATGGTTGTTCCCTGGGA... |
Task1_train_45404 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AAGAAGAGCTCACCACTGTGCGACAGGCAGAGCATCTCTGGTCAGCCGGGTAGGGCAGCCTGGGGCACAGGAACAGTTCTGGGAGAGATGTGATGGGAGGAGGTGGGGCTGGCAAAGAGGCATCCAGGTCGGCATAGAAGGCAGAGGTAGATTCAGATCCAAGGAAAGAGGAGGGGAGCTGGGGTCCTTTCATCTGAGTGAAATTTTCTTGAGGGCCAGAGGCAGGAGCTGAGGCAGAGGAGCTAGGAAGGTGAGGGAGGGGGCCCTTGGCCTTTCCCACATTTCTGTGCCCCACCTTCCAGGGTGGAAGACTTACTCCT... | AAGAAGAGCTCACCACTGTGCGACAGGCAGAGCATCTCTGGTCAGCCGGGTAGGGCAGCCTGGGGCACAGGAACAGTTCTGGGAGAGATGTGATGGGAGGAGGTGGGGCTGGCAAAGAGGCATCCAGGTCGGCATAGAAGGCAGAGGTAGATTCAGATCCAAGGAAAGAGGAGGGGAGCTGGGGTCCTTTCATCTGAGTGAAATTTTCTTGAGGGCCAGAGGCAGGAGCTGAGGCAGAGGAGCTAGGAAGGTGAGGGAGGGGGCCCTTGGCCTTTCCCACATTTCTGTGCCCCACCTTCCAGGGTGGAAGACTTACTCCT... |
Task1_train_45405 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | CATGTTTGGTTACTTCGAGCCCCTGTACCAGGTGATCCCTGACATGCCGAGGCCCCCAGAGACCTTCCTGAGAAGGGTCACAGGTCAGACTCCCAGGCTGGGAGCTCCAAAAGTGCTGAGTGAACCGTCTTAGGTCTAGGCTGAGGTGGGCTGGGGGCAGAGGGCTCCAGGCGACATCCCTGTTAGGGCCCCCAAGCCCCCGAGAGGTGGATCCCAGGCAGCATCCACGGCTCATCACGAGTAGGGGCTTGATCACACTGGGAGGTGCCAGCCTCTCCCCAGGCCCACCTCTGGGTGCTGTGTCTTGGCAGGTTGGAAAG... | CATGTTTGGTTACTTCGAGCCCCTGTACCAGGTGATCCCTGACATGCCGAGGCCCCCAGAGACCTTCCTGAGAAGGGTCACAGGTCAGACTCCCAGGCTGGGAGCTCCAAAAGTGCTGAGTGAACCGTCTTAGGTCTAGGCTGAGGTGGGCTGGGGGCAGAGGGCTCCAGGCGACATCCCTGTTAGGGCCCCCAAGCCCCCGAGAGGTGGATCCCAGGCAGCATCCACGGCTCATCACGAGTAGGGGCTTGATCACACTGGGAGGTGCCAGCCTCTCCCCAGGCCCACCTCTGGGTGCTGTGTCTTGGCAGGTTGGAAAG... |
Task1_train_45406 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GGCCACCTGGCAGGCGCCCTGGCAGCCGGGGTGATCTGTCTTCTCAGGAGATGTCAGGACCTGGGCAGTCTCCTTCCTCTTTGGTCCTGGGGCCTGGGGTGTTGGCCCTTGCAGACCTACAGAGCCCTGGCTCATAGGTAAAGGGCTGCCGCACCTCTGCGCTTCTCAACACACACTCTCTGTGCACTCTGTTTGAGCCAGACCCTGGGCCAGATGCGAGGTTCAAAGAGCAAGGCCATTCCCCCACCTCCAGGGGCTCTGCTCAGATGGGCAGGCACCCTCCCACCGTCACTAGGACAGAGTGGCAGTGCCCAGCCCCG... | GGCCACCTGGCAGGCGCCCTGGCAGCCGGGGTGATCTGTCTTCTCAGGAGATGTCAGGACCTGGGCAGTCTCCTTCCTCTTTGGTCCTGGGGCCTGGGGTGTTGGCCCTTGCAGACCTACAGAGCCCTGGCTCATAGGTAAAGGGCTGCCGCACCTCTGCGCTTCTCAACACACACTCTCTGTGCACTCTGTTTGAGCCAGACCCTGGGCCAGATGCGAGGTTCAAAGAGCAAGGCCATTCCCCCACCTCCAGGGGCTCTGCTCAGATGGGCAGGCACCCTCCCACCGTCACTAGGACAGAGTGGCAGTGCCCAGCCCCG... |
Task1_train_45407 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CGCCAGGCTGGAGTGCTGTGGCGCGATGTCGGCTCATTGCAACCTCCACCTCCCTGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGCGATTACAGGAATGCACCACCATGCTGGGCTAATTTTTGTATTTTTGGCAGTTAAGTCAGAGCCCGGAACCCAGGGCTTTGGAGCCCAGGCTCCGGAGCACAGGCTCTGCAGCCCAGGCTCTGCTTTGCCCACTGCCAGGTATCTGGCGTGAAACAAAGTTAACGGAGAAAGAATCACTTTCCTTCACCTGTAGCTCCCACCCCGGCCTGGCAAGCTTTGGTTAG... | CGCCAGGCTGGAGTGCTGTGGCGCGATGTCGGCTCATTGCAACCTCCACCTCCCTGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGCGATTACAGGAATGCACCACCATGCTGGGCTAATTTTTGTATTTTTGGCAGTTAAGTCAGAGCCCGGAACCCAGGGCTTTGGAGCCCAGGCTCCGGAGCACAGGCTCTGCAGCCCAGGCTCTGCTTTGCCCACTGCCAGGTATCTGGCGTGAAACAAAGTTAACGGAGAAAGAATCACTTTCCTTCACCTGTAGCTCCCACCCCGGCCTGGCAAGCTTTGGTTAG... |
Task1_train_45408 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | TCAGAGGGTCCCTGCCTGTGCTCTGCCTGGGTGGGGCTGGACAAGCAGGACCCAGCCTCCTTTATCTGCCTTGAGCTTACACAGGAAGCAGCCTGGAGCCAGACTGCCCAGGTTCAAATAGCTGTGTGACCTTGGACAGATTACTGCAGTGTGCCTCAGTTTCCTCATCTGTAAAATGGACATGCTACTGCCTCAAAGGGCTGTTGTGGGGTGATATGAGTCCATCTATATTAAGCATTTACAATAGCTCCTGGCACATAGAGTAAATGCTATATAAATGTGTTCTATTAATATTAAGACATCTTAATAAAAGAGTCCAT... | TCAGAGGGTCCCTGCCTGTGCTCTGCCTGGGTGGGGCTGGACAAGCAGGACCCAGCCTCCTTTATCTGCCTTGAGCTTACACAGGAAGCAGCCTGGAGCCAGACTGCCCAGGTTCAAATAGCTGTGTGACCTTGGACAGATTACTGCAGTGTGCCTCAGTTTCCTCATCTGTAAAATGGACATGCTACTGCCTCAAAGGGCTGTTGTGGGGTGATATGAGTCCATCTATATTAAGCATTTACAATAGCTCCTGGCACATAGAGTAAATGCTATATAAATGTGTTCTATTAATATTAAGACATCTTAATAAAAGAGTCCAT... |
Task1_train_45409 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | GACAGGTGTGGTGCCACTCCCACCAGCAGCCCCCCAGAGGGCATGCTGGGCCTCAGCCACTGCCAGGGGACTGTGAGGAGGAGCCGAGGATGCAGCCTCGTGTTGGGCCCATGCCCGTTCCCAGCCACTCAGTCTTTCCCACTGTCTACCTCCTGCCCCGGTGCTTGCTTCCAACTTTGCATCTCATCACAGAGGATGCTGTCCGTTCTGCAGATGGGACAATTGAGGCATGGCAGTGGGATCAAGTGACTTGACCTTCTGCCAGGGTTGGAATTGGGACATCTACCTCTTGGCCTCCAGCCCCAGTCCTGTCCTGGCCA... | GACAGGTGTGGTGCCACTCCCACCAGCAGCCCCCCAGAGGGCATGCTGGGCCTCAGCCACTGCCAGGGGACTGTGAGGAGGAGCCGAGGATGCAGCCTCGTGTTGGGCCCATGCCCGTTCCCAGCCACTCAGTCTTTCCCACTGTCTACCTCCTGCCCCGGTGCTTGCTTCCAACTTTGCATCTCATCACAGAGGATGCTGTCCGTTCTGCAGATGGGACAATTGAGGCATGGCAGTGGGATCAAGTGACTTGACCTTCTGCCAGGGTTGGAATTGGGACATCTACCTCTTGGCCTCCAGCCCCAGTCCTGTCCTGGCCA... |
Task1_train_45410 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GTGTGTTGTGGGGCTGCCCACAATTGTGCCCCCAAATAGGCATGTTGAAGTCCTAAACCCCAGTACCTGTTAATGCGACCTTATTTGGAAGTAGGGTGTTTGCAGACATAATCAAGTTAAGATGGTGTCATTAGGGTGGGCCCTAATCCATTATAACTATGTCTTTATAAAGAAGAGAAGAGACACAGAGACACACAGGGAGAATGCCATGTGACAACCTATGCAGAGACTGGAGTGACAGGCCAGGCCAGTGGGGAGAACATGAGGACAATGGAACCTGGACTGCCAAGCTCCAGCCCCCAAATCCCTCCCTTCTGGTT... | GTGTGTTGTGGGGCTGCCCACAATTGTGCCCCCAAATAGGCATGTTGAAGTCCTAAACCCCAGTACCTGTTAATGCGACCTTATTTGGAAGTAGGGTGTTTGCAGACATAATCAAGTTAAGATGGTGTCATTAGGGTGGGCCCTAATCCATTATAACTATGTCTTTATAAAGAAGAGAAGAGACACAGAGACACACAGGGAGAATGCCATGTGACAACCTATGCAGAGACTGGAGTGACAGGCCAGGCCAGTGGGGAGAACATGAGGACAATGGAACCTGGACTGCCAAGCTCCAGCCCCCAAATCCCTCCCTTCTGGTT... |
Task1_train_45411 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GAAAGTCTGCCCGGCCTCAGAGTTGCAGCCAGGAGAGTGGCTCAGAATCCAGCATGAAAACATTTGGAAGACATCAAGGTCCATTTAACCAGCACAAGAGCCCCAGCCTTCTTTGCTGTGTCAATGTGGGCTTCTCCAAGCCTCAGTTTTACTTATCCATGAAGTGGGTGTATTAAGGTAACGTTAAGTGGCTATAACAAAGAGACTCATGACAAATCAATGCCTTAAGGAAGATCATGTCTCTCTCTTGTAACAGTCCATAGTGCACATCCTGGGCTACTGTTCCACATGGAATCCAGGGACCTGGTTCCCTTCACTTT... | GAAAGTCTGCCCGGCCTCAGAGTTGCAGCCAGGAGAGTGGCTCAGAATCCAGCATGAAAACATTTGGAAGACATCAAGGTCCATTTAACCAGCACAAGAGCCCCAGCCTTCTTTGCTGTGTCAATGTGGGCTTCTCCAAGCCTCAGTTTTACTTATCCATGAAGTGGGTGTATTAAGGTAACGTTAAGTGGCTATAACAAAGAGACTCATGACAAATCAATGCCTTAAGGAAGATCATGTCTCTCTCTTGTAACAGTCCATAGTGCACATCCTGGGCTACTGTTCCACATGGAATCCAGGGACCTGGTTCCCTTCACTTT... |
Task1_train_45412 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AACCAGCACAAGAGCCCCAGCCTTCTTTGCTGTGTCAATGTGGGCTTCTCCAAGCCTCAGTTTTACTTATCCATGAAGTGGGTGTATTAAGGTAACGTTAAGTGGCTATAACAAAGAGACTCATGACAAATCAATGCCTTAAGGAAGATCATGTCTCTCTCTTGTAACAGTCCATAGTGCACATCCTGGGCTACTGTTCCACATGGAATCCAGGGACCTGGTTCCCTTCACTTTCTTCCTCTCCATTCCTTAGGACATTGTCCTCCTCGTCATAGACAGACACATCACAGGCCCGTCCTTGTTCTGACTCCTGAGAAAGG... | AACCAGCACAAGAGCCCCAGCCTTCTTTGCTGTGTCAATGTGGGCTTCTCCAAGCCTCAGTTTTACTTATCCATGAAGTGGGTGTATTAAGGTAACGTTAAGTGGCTATAACAAAGAGACTCATGACAAATCAATGCCTTAAGGAAGATCATGTCTCTCTCTTGTAACAGTCCATAGTGCACATCCTGGGCTACTGTTCCACATGGAATCCAGGGACCTGGTTCCCTTCACTTTCTTCCTCTCCATTCCTTAGGACATTGTCCTCCTCGTCATAGACAGACACATCACAGGCCCGTCCTTGTTCTGACTCCTGAGAAAGG... |
Task1_train_45413 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | TCCGTTCCCAACTGTAAATGGAGTTGGAGGTGAATTCTGGTCATGTGCCTGGTAGAAATGGGGACCAACTTTGAGGGACAGCCTCAGGCTGTGCAGATATAATGACACCTCCTTGCAACTGTGCAATAGGTACAGCTAGGGTACCTGGCGCCTAGTAAGCCCTCGGTAAAAGTGCTCAATGTTACTGAGCTCAGAGCTCCAAGGGACCTTAGAAACTCTCTGGCCCAACGTCCTCATTTCTTTACAGCTAAAGAAACAGGCCTAGAGAGGAGTGACATTGGCCTGTGTTCCCCATGGGTAAGGAGAAAAGTTGGTTCAGA... | TCCGTTCCCAACTGTAAATGGAGTTGGAGGTGAATTCTGGTCATGTGCCTGGTAGAAATGGGGACCAACTTTGAGGGACAGCCTCAGGCTGTGCAGATATAATGACACCTCCTTGCAACTGTGCAATAGGTACAGCTAGGGTACCTGGCGCCTAGTAAGCCCTCGGTAAAAGTGCTCAATGTTACTGAGCTCAGAGCTCCAAGGGACCTTAGAAACTCTCTGGCCCAACGTCCTCATTTCTTTACAGCTAAAGAAACAGGCCTAGAGAGGAGTGACATTGGCCTGTGTTCCCCATGGGTAAGGAGAAAAGTTGGTTCAGA... |
Task1_train_45414 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCTGGGCAGAGAGCAGGGTCCATATGACCTCTCCCCTGGTCTCCCAGGGTTGGGGGGCATCATTCTAGAGGGACCCTGTGCCCCACAGCAGCGCCCTCGGCTGGGGACCACACAGCTTTATGACTAGGTAGGTGTGGCCCTGGTTTCCAGGACAGGTGGCCAGACTGCTCTGTGACAAAGGGCCACGCCTGCCCCTGGGAGGGGTATTGGGCTGCCGCCCGCAGATGTTGCAGTAGGAACTGAAGAAGATGGCGTGCCTGGGCTTCCTCCTCCCCGTGGGCTTCCTCCTCCTCATCAGCACCGTGGCCGGGGGAAAGTAC... | TCTGGGCAGAGAGCAGGGTCCATATGACCTCTCCCCTGGTCTCCCAGGGTTGGGGGGCATCATTCTAGAGGGACCCTGTGCCCCACAGCAGCGCCCTCGGCTGGGGACCACACAGCTTTATGACTAGGTAGGTGTGGCCCTGGTTTCCAGGACAGGTGGCCAGACTGCTCTGTGACAAAGGGCCACGCCTGCCCCTGGGAGGGGTATTGGGCTGCCGCCCGCAGATGTTGCAGTAGGAACTGAAGAAGATGGCGTGCCTGGGCTTCCTCCTCCCCGTGGGCTTCCTCCTCCTCATCAGCACCGTGGCCGGGGGAAAGTAC... |
Task1_train_45415 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CATCATTCTAGAGGGACCCTGTGCCCCACAGCAGCGCCCTCGGCTGGGGACCACACAGCTTTATGACTAGGTAGGTGTGGCCCTGGTTTCCAGGACAGGTGGCCAGACTGCTCTGTGACAAAGGGCCACGCCTGCCCCTGGGAGGGGTATTGGGCTGCCGCCCGCAGATGTTGCAGTAGGAACTGAAGAAGATGGCGTGCCTGGGCTTCCTCCTCCCCGTGGGCTTCCTCCTCCTCATCAGCACCGTGGCCGGGGGAAAGTACGGCGTGGCCCACGTGGTGTCGGAGAATTGGAGCAAGGACTACTGTATCCTGTTCAGC... | CATCATTCTAGAGGGACCCTGTGCCCCACAGCAGCGCCCTCGGCTGGGGACCACACAGCTTTATGACTAGGTAGGTGTGGCCCTGGTTTCCAGGACAGGTGGCCAGACTGCTCTGTGACAAAGGGCCACGCCTGCCCCTGGGAGGGGTATTGGGCTGCCGCCCGCAGATGTTGCAGTAGGAACTGAAGAAGATGGCGTGCCTGGGCTTCCTCCTCCCCGTGGGCTTCCTCCTCCTCATCAGCACCGTGGCCGGGGGAAAGTACGGCGTGGCCCACGTGGTGTCGGAGAATTGGAGCAAGGACTACTGTATCCTGTTCAGC... |
Task1_train_45416 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | GTTCTTAATATGCGGCCAGGTTAATGAATGTCACGTGAATGAACCAGAAAAAAATGAAGTGTGCCCTTGATCAGCTGGGTTGGTGTGCAGCAAGCTGTGTGACCAGGGGACAGCAGTGGTCCTGAGGGCCGTCACTGTCTGCCGTGCAGAGCCCTTCCTCCCACGGGGGCCTACCTCACCTGTGCCAAGGGCTTGTCTGTGGTCAGTGACCTGGATAGATCTGAATGGGGCTTCTTTTTCGAGGAGTCTTATGGCAGGTCTCTCAGTAAAGACTCCATTCTTGATGATCACACATTTTGGATTTTCCAAATCTGTCAGAG... | GTTCTTAATATGCGGCCAGGTTAATGAATGTCACGTGAATGAACCAGAAAAAAATGAAGTGTGCCCTTGATCAGCTGGGTTGGTGTGCAGCAAGCTGTGTGACCAGGGGACAGCAGTGGTCCTGAGGGCCGTCACTGTCTGCCGTGCAGAGCCCTTCCTCCCACGGGGGCCTACCTCACCTGTGCCAAGGGCTTGTCTGTGGTCAGTGACCTGGATAGATCTGAATGGGGCTTCTTTTTCGAGGAGTCTTATGGCAGGTCTCTCAGTAAAGACTCCATTCTTGATGATCACACATTTTGGATTTTCCAAATCTGTCAGAG... |
Task1_train_45417 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTATGGCAGGTCTCTCAGTAAAGACTCCATTCTTGATGATCACACATTTTGGATTTTCCAAATCTGTCAGAGAATGGGCTTGAGGCGGGGTTTGTGGGCACTAGTTTCACTGGTTTCATTTACCAAAAAGGGGAGCAGAAGTCAAGTATGGTGGCTCATCCCTGTAATCCCAGAGGCAAGAGAATTGCTTGAGCCCAGGAGTTCGAGACCAGCCTGAGCAACATAAGGAGACCCCGTCTCCACAAAAATGAAAAATAACATTTTAGTCAGACGTGGTGGCATGCATCTGTGGTCCCAGCTGCTTGGGAGGGTGAGATGGG... | TTATGGCAGGTCTCTCAGTAAAGACTCCATTCTTGATGATCACACATTTTGGATTTTCCAAATCTGTCAGAGAATGGGCTTGAGGCGGGGTTTGTGGGCACTAGTTTCACTGGTTTCATTTACCAAAAAGGGGAGCAGAAGTCAAGTATGGTGGCTCATCCCTGTAATCCCAGAGGCAAGAGAATTGCTTGAGCCCAGGAGTTCGAGACCAGCCTGAGCAACATAAGGAGACCCCGTCTCCACAAAAATGAAAAATAACATTTTAGTCAGACGTGGTGGCATGCATCTGTGGTCCCAGCTGCTTGGGAGGGTGAGATGGG... |
Task1_train_45418 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | CTCAGTAAAGACTCCATTCTTGATGATCACACATTTTGGATTTTCCAAATCTGTCAGAGAATGGGCTTGAGGCGGGGTTTGTGGGCACTAGTTTCACTGGTTTCATTTACCAAAAAGGGGAGCAGAAGTCAAGTATGGTGGCTCATCCCTGTAATCCCAGAGGCAAGAGAATTGCTTGAGCCCAGGAGTTCGAGACCAGCCTGAGCAACATAAGGAGACCCCGTCTCCACAAAAATGAAAAATAACATTTTAGTCAGACGTGGTGGCATGCATCTGTGGTCCCAGCTGCTTGGGAGGGTGAGATGGGAGGGTTGTTTGAG... | CTCAGTAAAGACTCCATTCTTGATGATCACACATTTTGGATTTTCCAAATCTGTCAGAGAATGGGCTTGAGGCGGGGTTTGTGGGCACTAGTTTCACTGGTTTCATTTACCAAAAAGGGGAGCAGAAGTCAAGTATGGTGGCTCATCCCTGTAATCCCAGAGGCAAGAGAATTGCTTGAGCCCAGGAGTTCGAGACCAGCCTGAGCAACATAAGGAGACCCCGTCTCCACAAAAATGAAAAATAACATTTTAGTCAGACGTGGTGGCATGCATCTGTGGTCCCAGCTGCTTGGGAGGGTGAGATGGGAGGGTTGTTTGAG... |
Task1_train_45419 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | TAACATTTTAGTCAGACGTGGTGGCATGCATCTGTGGTCCCAGCTGCTTGGGAGGGTGAGATGGGAGGGTTGTTTGAGCCCTGGAGTTAAAGTTGCAATGAGCTGTGATTGCACCACTGCACTCTAGCCTGGGTGACAGAACGAGACCCTGTCTCAAAAAAAAAAAAAAAGAAAGAAAGAAAGGAAAAAAAAAACTCATGCCTGTAATCCCAGCACTTTGGGGACCGGGGTGGGCAGATCACGAGGTCAGGAGATCAAGACTATCCTGGCCAACATGGTGAAACCCCGTTTCTACTAAAAATACAAAAATTAGCCAGGTG... | TAACATTTTAGTCAGACGTGGTGGCATGCATCTGTGGTCCCAGCTGCTTGGGAGGGTGAGATGGGAGGGTTGTTTGAGCCCTGGAGTTAAAGTTGCAATGAGCTGTGATTGCACCACTGCACTCTAGCCTGGGTGACAGAACGAGACCCTGTCTCAAAAAAAAAAAAAAAGAAAGAAAGAAAGGAAAAAAAAAACTCATGCCTGTAATCCCAGCACTTTGGGGACCGGGGTGGGCAGATCACGAGGTCAGGAGATCAAGACTATCCTGGCCAACATGGTGAAACCCCGTTTCTACTAAAAATACAAAAATTAGCCAGGTG... |
Task1_train_45420 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TTCAGTACACATGGGTACAACATCCCTGCCCTGGAGTTGCCCAGAGTCTAGGGAGGGGAAAGATCTATTACCCTGGGCCTCGGCCAGCTGGGGAGTGCTGCTGGTGGAGAGGGGCCGTGTGCAGCGAGGGAAGGAGGAGTCGTCAATACCCCCACCCCAGCTTTGCTTTCTTGTCATCAGCCCCAGGGCCCCAGCCTGTGTCCCTCCTCTCCCATTGCTACTTCATCTCCTGGGTCCTCCTTACCAAGCCTGACCACACAGAGGGCCTTGGCCGCTTCCATGGGGAATTGGAAAGCAATAAGATAGCATCCCCTAGAAGC... | TTCAGTACACATGGGTACAACATCCCTGCCCTGGAGTTGCCCAGAGTCTAGGGAGGGGAAAGATCTATTACCCTGGGCCTCGGCCAGCTGGGGAGTGCTGCTGGTGGAGAGGGGCCGTGTGCAGCGAGGGAAGGAGGAGTCGTCAATACCCCCACCCCAGCTTTGCTTTCTTGTCATCAGCCCCAGGGCCCCAGCCTGTGTCCCTCCTCTCCCATTGCTACTTCATCTCCTGGGTCCTCCTTACCAAGCCTGACCACACAGAGGGCCTTGGCCGCTTCCATGGGGAATTGGAAAGCAATAAGATAGCATCCCCTAGAAGC... |
Task1_train_45421 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AACATCCCTGCCCTGGAGTTGCCCAGAGTCTAGGGAGGGGAAAGATCTATTACCCTGGGCCTCGGCCAGCTGGGGAGTGCTGCTGGTGGAGAGGGGCCGTGTGCAGCGAGGGAAGGAGGAGTCGTCAATACCCCCACCCCAGCTTTGCTTTCTTGTCATCAGCCCCAGGGCCCCAGCCTGTGTCCCTCCTCTCCCATTGCTACTTCATCTCCTGGGTCCTCCTTACCAAGCCTGACCACACAGAGGGCCTTGGCCGCTTCCATGGGGAATTGGAAAGCAATAAGATAGCATCCCCTAGAAGCCCAGTGAAGTCTGGGACA... | AACATCCCTGCCCTGGAGTTGCCCAGAGTCTAGGGAGGGGAAAGATCTATTACCCTGGGCCTCGGCCAGCTGGGGAGTGCTGCTGGTGGAGAGGGGCCGTGTGCAGCGAGGGAAGGAGGAGTCGTCAATACCCCCACCCCAGCTTTGCTTTCTTGTCATCAGCCCCAGGGCCCCAGCCTGTGTCCCTCCTCTCCCATTGCTACTTCATCTCCTGGGTCCTCCTTACCAAGCCTGACCACACAGAGGGCCTTGGCCGCTTCCATGGGGAATTGGAAAGCAATAAGATAGCATCCCCTAGAAGCCCAGTGAAGTCTGGGACA... |
Task1_train_45422 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTGTCCCTGTGCCCCTCGTCTGGGTGCGTTAGGGCTGACATACAAAGCACCACAGTGAAAGAACAGCAGTATGCCTCCTCACTAGCCAGGTGTGGGCGGGTGGGTTTCTTCCAAGGCCTCTCTGTGGCCGTGGGTAGCCACCTCTGTCCTGCACCGCTGCAGTCTTCCCTCTGTGTGTGCTCCTGGTAGCTCTGCGCATGCTCATCTTCTTATAAGAACACCATGGCAGCTGGGCGTAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAGATCACGAGGTCAGGAGTTCGAGACCAACCTGACC... | CTGTCCCTGTGCCCCTCGTCTGGGTGCGTTAGGGCTGACATACAAAGCACCACAGTGAAAGAACAGCAGTATGCCTCCTCACTAGCCAGGTGTGGGCGGGTGGGTTTCTTCCAAGGCCTCTCTGTGGCCGTGGGTAGCCACCTCTGTCCTGCACCGCTGCAGTCTTCCCTCTGTGTGTGCTCCTGGTAGCTCTGCGCATGCTCATCTTCTTATAAGAACACCATGGCAGCTGGGCGTAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAGATCACGAGGTCAGGAGTTCGAGACCAACCTGACC... |
Task1_train_45423 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CAATCCAGGCTCTAAGCAAATTATGTATCTCACTGACCCCACCAAACCTCAGAAAAATTTAACAGTGAGAAGCAAAATCTCCTTTAAAGAGCAACTTAGAACAGATAGAAAATATCATACAGCTGACTTCACTAGAGAGAAAGTGCATCAACTGCTTTCACTCAACAAAAAGAAAAAAGAGATGATCAATGCAGATCCCCTCTCCTCCTGGCAGCCCTTACCCTCAGTGAAAAGCCACCACCATTCTCTCTCTGGTGGCCATCAGATCAACCTGCGGCGTTCCCACAAGACAGAATGGAGATTTTCCAAGGTATAGAGCA... | CAATCCAGGCTCTAAGCAAATTATGTATCTCACTGACCCCACCAAACCTCAGAAAAATTTAACAGTGAGAAGCAAAATCTCCTTTAAAGAGCAACTTAGAACAGATAGAAAATATCATACAGCTGACTTCACTAGAGAGAAAGTGCATCAACTGCTTTCACTCAACAAAAAGAAAAAAGAGATGATCAATGCAGATCCCCTCTCCTCCTGGCAGCCCTTACCCTCAGTGAAAAGCCACCACCATTCTCTCTCTGGTGGCCATCAGATCAACCTGCGGCGTTCCCACAAGACAGAATGGAGATTTTCCAAGGTATAGAGCA... |
Task1_train_45424 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CATGTTTCGCTGCCATTACACAGCTCCAAAGCAGGAAAAGAAAATATTTACAAAATACAAGGTTTTTTTTTTCCATTTTTTGTTTTTGTTTTTTTTTTCAATGCTAAAAGGGTTATTCAGAATTTTCAACCTTATAAATAGAAGAAGCACTTTATGCATAGGGATATGGTGCATTATTGTATTTTTTTTTAAAGAAACAATGACAAACCCTTTAACTTGCAAACAGAAAAAAAAATCACTAATGTTGAAAATTGTGAAAAAACCCCAACCATTAAGCAGTTGTCTACTATTTTTATACGATTACAAAATGGCCAAAAAAA... | CATGTTTCGCTGCCATTACACAGCTCCAAAGCAGGAAAAGAAAATATTTACAAAATACAAGGTTTTTTTTTTCCATTTTTTGTTTTTGTTTTTTTTTTCAATGCTAAAAGGGTTATTCAGAATTTTCAACCTTATAAATAGAAGAAGCACTTTATGCATAGGGATATGGTGCATTATTGTATTTTTTTTTAAAGAAACAATGACAAACCCTTTAACTTGCAAACAGAAAAAAAAATCACTAATGTTGAAAATTGTGAAAAAACCCCAACCATTAAGCAGTTGTCTACTATTTTTATACGATTACAAAATGGCCAAAAAAA... |
Task1_train_45425 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | TGGTATGTAGTAAGTGTTCAATAAACATTACAGTTGCAGACTTTTACATTTACCATTACATTACATTGTAATTATTATACAAAAAGGACCCTTTGAGTAGGTCCATAGCAGCTACAGGTATGTATGTTCCAAGAGGGCACACTTGAGGAATTAAAATATTAGAATGAAATTAAAGGAAATGTGTCTGGAATAGCTGTGCAAACTGCTTCCAGATGGAGTGTGGTATCGTAAAATCTGGTGTGTGCATGCCAAATGTCCTGCCATGGGGGCCTGCTGGATCTGTAATTCTGCTCTGTATACCTAAAAAGCATGGACTCTGC... | TGGTATGTAGTAAGTGTTCAATAAACATTACAGTTGCAGACTTTTACATTTACCATTACATTACATTGTAATTATTATACAAAAAGGACCCTTTGAGTAGGTCCATAGCAGCTACAGGTATGTATGTTCCAAGAGGGCACACTTGAGGAATTAAAATATTAGAATGAAATTAAAGGAAATGTGTCTGGAATAGCTGTGCAAACTGCTTCCAGATGGAGTGTGGTATCGTAAAATCTGGTGTGTGCATGCCAAATGTCCTGCCATGGGGGCCTGCTGGATCTGTAATTCTGCTCTGTATACCTAAAAAGCATGGACTCTGC... |
Task1_train_45426 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TACAATATCCATGCAGATAATATAAACAAAATTGGGAAACCAGAAAATTTACTTTTAAAAATCATAGCTGTCTCAACAACCAAACACTCCAGTGAAAATCTTCATCACCTTTTAATACAGTCAAGGAAACACCAATTCTTCCCACATATTCATCTTTTTCAGCCTTCTCTAGTAAGCCAGCCTCTAGCAAAGAGAAAATGAAAGATCTGCTAGTCAATTATCCTGCCCCTCTTTTCCAACTCCTCATGCTCTCTCTCAAATCTGATATTCCTAAGGAGATAAATGCACTTATTTAACATGTATCTTTAAGTATGTTATAA... | TACAATATCCATGCAGATAATATAAACAAAATTGGGAAACCAGAAAATTTACTTTTAAAAATCATAGCTGTCTCAACAACCAAACACTCCAGTGAAAATCTTCATCACCTTTTAATACAGTCAAGGAAACACCAATTCTTCCCACATATTCATCTTTTTCAGCCTTCTCTAGTAAGCCAGCCTCTAGCAAAGAGAAAATGAAAGATCTGCTAGTCAATTATCCTGCCCCTCTTTTCCAACTCCTCATGCTCTCTCTCAAATCTGATATTCCTAAGGAGATAAATGCACTTATTTAACATGTATCTTTAAGTATGTTATAA... |
Task1_train_45427 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | GGGAGTGACAGGAATGAAACGTCTCTGTCTCCACCATGCCAATTTGGAGTGCCACCCATAAAAAGCTTATGTAAAATTTTCTCAAACCAACAGATTTAGAAAAACCAGTAAGATGAGGTGGGCGGATCACGAGGTCAGGAGTTTGAGGCCAGCCTGGTCGACACGGTGAAACTCAGTCTCTACTTAAGAAAAGAAAAAAGAAAAAAATTAGCCTGACTTGGTGGCGGGTACCTGTAATCCCAGCTACTTAGGGAGGCTGAGGCCCGAGAATCACCTGAACCCAGGAGCCAGAGGCTTCAGTGAGCTGAGATCGCACTACT... | GGGAGTGACAGGAATGAAACGTCTCTGTCTCCACCATGCCAATTTGGAGTGCCACCCATAAAAAGCTTATGTAAAATTTTCTCAAACCAACAGATTTAGAAAAACCAGTAAGATGAGGTGGGCGGATCACGAGGTCAGGAGTTTGAGGCCAGCCTGGTCGACACGGTGAAACTCAGTCTCTACTTAAGAAAAGAAAAAAGAAAAAAATTAGCCTGACTTGGTGGCGGGTACCTGTAATCCCAGCTACTTAGGGAGGCTGAGGCCCGAGAATCACCTGAACCCAGGAGCCAGAGGCTTCAGTGAGCTGAGATCGCACTACT... |
Task1_train_45428 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CTGAACTTGCTCCGAATCTCAAACCTTTCTGTTCACAGAACAAACGCTCAAGGGCTTTCAAGAGTGTTTCTGTAGATTAGGCTTATTAGCATCAACTTCATGACTTCTAAAATGTGACTGCTTTCATGTCCAGATAGCTTGAATACAGGTATCTACCAGTGATATGGGGTGGAGAATTAATAATGCTTGGTTACATAAAGTCAGTGTTGCTTATTTTTCAAAACTTTTTTTTTTTTTTTTTTTTTTTACCAATTATGTTATTCCCTTCTCCCCAAGAAGTGGGCAGAAAAGCTTTGTTAACCTCCTTTTACAGATGAGGA... | CTGAACTTGCTCCGAATCTCAAACCTTTCTGTTCACAGAACAAACGCTCAAGGGCTTTCAAGAGTGTTTCTGTAGATTAGGCTTATTAGCATCAACTTCATGACTTCTAAAATGTGACTGCTTTCATGTCCAGATAGCTTGAATACAGGTATCTACCAGTGATATGGGGTGGAGAATTAATAATGCTTGGTTACATAAAGTCAGTGTTGCTTATTTTTCAAAACTTTTTTTTTTTTTTTTTTTTTTTACCAATTATGTTATTCCCTTCTCCCCAAGAAGTGGGCAGAAAAGCTTTGTTAACCTCCTTTTACAGATGAGGA... |
Task1_train_45429 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GCCGGGTTCAGTTTGAGGTTTATCACTTGCTGTGTGATCTTGAACAAGTTACATAACCTTTCTGGGCTTCAGTTTTTATAAAATGAGGATGATAATGGTACTTTCCTCATAGGGTTATTGATTTGGCAGAGTATCTTGGATATGGTAAGCACCCATAATCTGCCTATCAGTGTTATTGTTAGTAGTTAAGATATTAGAAACCATGCCAAAACGTGGGACCTAAAGTGCCACATACAAATTTTACAGTTCAGTGATGCTGTCGATTTAAATCAGTTACATGTTGGCATCAGAAAAATTGTCTTTCCTGACTGAAGCGCTGT... | GCCGGGTTCAGTTTGAGGTTTATCACTTGCTGTGTGATCTTGAACAAGTTACATAACCTTTCTGGGCTTCAGTTTTTATAAAATGAGGATGATAATGGTACTTTCCTCATAGGGTTATTGATTTGGCAGAGTATCTTGGATATGGTAAGCACCCATAATCTGCCTATCAGTGTTATTGTTAGTAGTTAAGATATTAGAAACCATGCCAAAACGTGGGACCTAAAGTGCCACATACAAATTTTACAGTTCAGTGATGCTGTCGATTTAAATCAGTTACATGTTGGCATCAGAAAAATTGTCTTTCCTGACTGAAGCGCTGT... |
Task1_train_45430 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CCTGCAAGTCACACCAAACCATCAACAGAACATTCTCCACATTCGGGGTTTTTCCCCCAGAGACACTTTACAAGGAGTGTCAGTTCCTCCCCTCACTGGCCTGGCCTGAATTCTCCCAGGTCTGAGATTGGGACGACCAGGGTTGGGGGATGGGGCACATCCTGATCATGATAATTCTGACCACACAGGAGCACTTGGGAGCCAGGACGACTCTGGATCCTTCATAGCCAGGGACCATCTGTGCCTTCGAGAAACTCCCCCACCCCACCTGTGCCAAGCCTCTCCCTAATGAAACTAGTGCCAAATACACGGGATCGCAT... | CCTGCAAGTCACACCAAACCATCAACAGAACATTCTCCACATTCGGGGTTTTTCCCCCAGAGACACTTTACAAGGAGTGTCAGTTCCTCCCCTCACTGGCCTGGCCTGAATTCTCCCAGGTCTGAGATTGGGACGACCAGGGTTGGGGGATGGGGCACATCCTGATCATGATAATTCTGACCACACAGGAGCACTTGGGAGCCAGGACGACTCTGGATCCTTCATAGCCAGGGACCATCTGTGCCTTCGAGAAACTCCCCCACCCCACCTGTGCCAAGCCTCTCCCTAATGAAACTAGTGCCAAATACACGGGATCGCAT... |
Task1_train_45431 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGGTTTTCCAGCTTCCTGGCTGGTCCCCTCAACTTGGTAAGGAGCCCTCATAGACATGCACCCACACAGTGTTGGCTAAATTGGCTGAATGTCAGAGCCGGAAGGGACTGAAAACACTGTGTCATCTAAAGGCCTTGTTGAACAGGTGAGGACACAAAATGACGTATCTGAGGTCACATGACTAGTCAGTGGCAGGCCTAGGATTGATCTTCTTTCCTGATTTTCAGTGTTCTTTCCAGGGTGGCGTGGTCCCCTTCAATACTCAGGTTTAAGCACCCAGAGCCCCAGGGGGCCGTGGGTTTTTGGAAGGGTACTCAATT... | GGGTTTTCCAGCTTCCTGGCTGGTCCCCTCAACTTGGTAAGGAGCCCTCATAGACATGCACCCACACAGTGTTGGCTAAATTGGCTGAATGTCAGAGCCGGAAGGGACTGAAAACACTGTGTCATCTAAAGGCCTTGTTGAACAGGTGAGGACACAAAATGACGTATCTGAGGTCACATGACTAGTCAGTGGCAGGCCTAGGATTGATCTTCTTTCCTGATTTTCAGTGTTCTTTCCAGGGTGGCGTGGTCCCCTTCAATACTCAGGTTTAAGCACCCAGAGCCCCAGGGGGCCGTGGGTTTTTGGAAGGGTACTCAATT... |
Task1_train_45432 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAAGGTGGTAGAGAAAACAAACCCTACAGAACTGGTTGGAGTGGTTTGCCGAGTGGATGGATTTTACCAGGTGGTAGAATATAGTGATATTTCCCTGGCAACAGCTCAGAAATGAAGCTCAGATGGATGACTGCTGTTCAATGTGGGGAATATTGCCAACCATTTATTCACTGTACCATTTCTGAGAGATGTTGTCAATGTTTATGAACCTCAGTTGTAGCACCATGTGGCTCAAAAGAAGATTCCTTATGTGGATACCCAACAGCACTTAATTAAGCCAGATAAACCCAGTGGAATAAGTATGGAAAAATTTGTCTTTT... | AAAGGTGGTAGAGAAAACAAACCCTACAGAACTGGTTGGAGTGGTTTGCCGAGTGGATGGATTTTACCAGGTGGTAGAATATAGTGATATTTCCCTGGCAACAGCTCAGAAATGAAGCTCAGATGGATGACTGCTGTTCAATGTGGGGAATATTGCCAACCATTTATTCACTGTACCATTTCTGAGAGATGTTGTCAATGTTTATGAACCTCAGTTGTAGCACCATGTGGCTCAAAAGAAGATTCCTTATGTGGATACCCAACAGCACTTAATTAAGCCAGATAAACCCAGTGGAATAAGTATGGAAAAATTTGTCTTTT... |
Task1_train_45433 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GCACACCACCATTATAGTATTAGTGTATTCTGACTTTGACTGTGTACTTACTTTTACCAGTGAGTTTTACACATTTATTTTTTGTGTTACTAAACAGCATCCTTTTCTTTTGGCTTGAAGAACACTTTTTGAAATTTCATGTAAGACAAATATAGGGGATGAACTCTTTCAACTTTTGTCTGGGAAAGTCTTTATCTTCATTTCTGAAGGACAGTTTTTCTAGGTACAGTATTATTGGTTGGCAGTTTATTTCCTTCAGTACTCTGAATATATAGTCCATTCTCTATGGACCCATAAGGTGTCTGCTGAGAAATTTGCTG... | GCACACCACCATTATAGTATTAGTGTATTCTGACTTTGACTGTGTACTTACTTTTACCAGTGAGTTTTACACATTTATTTTTTGTGTTACTAAACAGCATCCTTTTCTTTTGGCTTGAAGAACACTTTTTGAAATTTCATGTAAGACAAATATAGGGGATGAACTCTTTCAACTTTTGTCTGGGAAAGTCTTTATCTTCATTTCTGAAGGACAGTTTTTCTAGGTACAGTATTATTGGTTGGCAGTTTATTTCCTTCAGTACTCTGAATATATAGTCCATTCTCTATGGACCCATAAGGTGTCTGCTGAGAAATTTGCTG... |
Task1_train_45434 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GTACAGCTCTTTATATTCACTCAGCAGCCACTTTACAATCCCAAGTCTTAGAGGGTTAGGTGAGAATAGAGTTCTTATCAGCCACCTCATGAATTTAGAACCATCTTTCCCCTTGCTGACTCAATACAGTGACCAGGCCCCTCATTTCATCTTTTTTTTTTTTTTTTTTACCCTATCCCTCTCTGACAGATTATGCTAACTTTGAATCTCAAGAATAATAGTTGGAAACTCATTCTCTTCTTTTACCTGGGCTTTTTGTATAAATGGTCCACCCTTTCCCCAGATTTCTGCATTCCATGTGGTATTGGATGTATAGAAGC... | GTACAGCTCTTTATATTCACTCAGCAGCCACTTTACAATCCCAAGTCTTAGAGGGTTAGGTGAGAATAGAGTTCTTATCAGCCACCTCATGAATTTAGAACCATCTTTCCCCTTGCTGACTCAATACAGTGACCAGGCCCCTCATTTCATCTTTTTTTTTTTTTTTTTTACCCTATCCCTCTCTGACAGATTATGCTAACTTTGAATCTCAAGAATAATAGTTGGAAACTCATTCTCTTCTTTTACCTGGGCTTTTTGTATAAATGGTCCACCCTTTCCCCAGATTTCTGCATTCCATGTGGTATTGGATGTATAGAAGC... |
Task1_train_45435 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AAGGGCATGGCAGAGCTTCCCATGAGGTCAGGGAGGGCTCCTGGGGCCGTGCAGGCCACAGTGGGAGAAAGCAGAGAGCAGTGGAGTGATGACCTTCCATGGTTCTGGGTTGCAAGTGACCTAGAGATAAAGGAAGTGGGTGAGGTTCCTTGCCAAGTCTGTTCCAGCTCCATGAGGGTGGGTGCCCAAGATGCCTGAACAGGAAGCAGGGAGGAAGAAAGGGAAGGAGAAAGAAAAATGGAGGGAGAGGCTCAAATGCATTATCCACTTACTGAACATCTGCTGGGTTCCAGGCCCTGGACAAGGTGGTGGGAATATAA... | AAGGGCATGGCAGAGCTTCCCATGAGGTCAGGGAGGGCTCCTGGGGCCGTGCAGGCCACAGTGGGAGAAAGCAGAGAGCAGTGGAGTGATGACCTTCCATGGTTCTGGGTTGCAAGTGACCTAGAGATAAAGGAAGTGGGTGAGGTTCCTTGCCAAGTCTGTTCCAGCTCCATGAGGGTGGGTGCCCAAGATGCCTGAACAGGAAGCAGGGAGGAAGAAAGGGAAGGAGAAAGAAAAATGGAGGGAGAGGCTCAAATGCATTATCCACTTACTGAACATCTGCTGGGTTCCAGGCCCTGGACAAGGTGGTGGGAATATAA... |
Task1_train_45436 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CTTCGTCTCAAAAAAAAAAAAAAAAAAAAGAATCAGGATGAGGTTGGGTACGGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGACCAAGGTCGGTGGATCACCTGAGGTCAGGAGTTTGAGATCAACCTGGCCAACATGGTGAAACCCCGTTTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCAAGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAAGAGAATCGCTTAAACCTGGGAGGCGGAGGTTGCAGTGAGCTGAGATCACGCCATTGCACTCCAGCCTGGGCAACAACTGCGAAACTCCG... | CTTCGTCTCAAAAAAAAAAAAAAAAAAAAGAATCAGGATGAGGTTGGGTACGGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGACCAAGGTCGGTGGATCACCTGAGGTCAGGAGTTTGAGATCAACCTGGCCAACATGGTGAAACCCCGTTTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCAAGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAAGAGAATCGCTTAAACCTGGGAGGCGGAGGTTGCAGTGAGCTGAGATCACGCCATTGCACTCCAGCCTGGGCAACAACTGCGAAACTCCG... |
Task1_train_45437 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATGTTTTCAAGGTTCATCCATGTTGTAGCATGTGTCTGGTGACTGGCTTCCTTCACTTAGCATGTTTCAAGGTTCATCCTGTTGTAGCATGTGTCTGAACTTCATTCCTTATATTTTCCCAACCTCAGCCTTAGGGTCAACCATTTCTTCTCAGATTCCTGGTTCCTCTCATTGAAGGATGTGATTGCCTCTTTTTAATTCTGTCATTGTCTTCCTCCCCCATTTATTTATTTATGTCATTATGGACTCACGGATTGCTGCTTTTTTGTTTTTTTGAGATGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCAC... | ATGTTTTCAAGGTTCATCCATGTTGTAGCATGTGTCTGGTGACTGGCTTCCTTCACTTAGCATGTTTCAAGGTTCATCCTGTTGTAGCATGTGTCTGAACTTCATTCCTTATATTTTCCCAACCTCAGCCTTAGGGTCAACCATTTCTTCTCAGATTCCTGGTTCCTCTCATTGAAGGATGTGATTGCCTCTTTTTAATTCTGTCATTGTCTTCCTCCCCCATTTATTTATTTATGTCATTATGGACTCACGGATTGCTGCTTTTTTGTTTTTTTGAGATGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCAC... |
Task1_train_45438 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CACACTATGCATTTCAATCAAAAATTTACTAAGCCTCAAGTGTTGTGCTGTGGTGAACAGGAGCTGGGGAAGGAATATTTAGAAATGGCATACCCAGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGCTGAAGCGGGAGAATCACGAGGTCAGGAAATCGAGACCATCCTGGCTAACACGGTGAGACCTCGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGCAGAGCTTGC... | CACACTATGCATTTCAATCAAAAATTTACTAAGCCTCAAGTGTTGTGCTGTGGTGAACAGGAGCTGGGGAAGGAATATTTAGAAATGGCATACCCAGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGCTGAAGCGGGAGAATCACGAGGTCAGGAAATCGAGACCATCCTGGCTAACACGGTGAGACCTCGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGCAGAGCTTGC... |
Task1_train_45439 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | CCCAGCGTAAGGAGCCAGCGTTCTTGGACCTTTGTTGTAAGGCTGGGAGGACGGGGTCCTGTCTTTGTTAATCTCTGTATCTGCTCCCTTCCCAGTAGCCTGCTGGTTCGGAGAGCCTCCTGAAAGTTCTGTCCTCACCCAGTTCTCTCCTCTTTCTGCCCAGAGGCTCCTCCCAGCCTCAAGGGGAGAGGACAAAAGATATCTGTGAAGTTTTAACGGCAGAATAGGATTGATAAGTTAATATGGCTGGCTCTTGTATTCTTTTCAGCCTTGCCTTAATCCAGTGCTTCTCAAACATGTATTTCTGTTCCCTGAATCTC... | CCCAGCGTAAGGAGCCAGCGTTCTTGGACCTTTGTTGTAAGGCTGGGAGGACGGGGTCCTGTCTTTGTTAATCTCTGTATCTGCTCCCTTCCCAGTAGCCTGCTGGTTCGGAGAGCCTCCTGAAAGTTCTGTCCTCACCCAGTTCTCTCCTCTTTCTGCCCAGAGGCTCCTCCCAGCCTCAAGGGGAGAGGACAAAAGATATCTGTGAAGTTTTAACGGCAGAATAGGATTGATAAGTTAATATGGCTGGCTCTTGTATTCTTTTCAGCCTTGCCTTAATCCAGTGCTTCTCAAACATGTATTTCTGTTCCCTGAATCTC... |
Task1_train_45440 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CACCCGCCTCGGCCTCCCAAAGTACTGGGATTACAGGCATCAGCCACTGCGCCTGGCCTTACAACACATTTCTTTTCTTTTTCTTTTCTTTTTTTTTTTTTTTTTGAGACAGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGTGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGATTACAGGCGCCCACCACCATGCCTGGCTAATTCTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGTCCAGGCTGGTTTCGAACTCCTGAC... | CACCCGCCTCGGCCTCCCAAAGTACTGGGATTACAGGCATCAGCCACTGCGCCTGGCCTTACAACACATTTCTTTTCTTTTTCTTTTCTTTTTTTTTTTTTTTTTGAGACAGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGTGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGATTACAGGCGCCCACCACCATGCCTGGCTAATTCTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGTCCAGGCTGGTTTCGAACTCCTGAC... |
Task1_train_45441 | A sequence alteration has been identified on Chromosome 17. Is it disease-inducing or harmless? | Benign | ACTTCACCTCTCTTCTGCTTCCCCTTTCCTTCAAGTGGGCTCTAATCTTGGCACAGTGTTCTGAAGTGTGCTTCCCAGTCTCTGCTCTATGCTCCTCCCCCAGGGTAGCTCCCCCAGGGGTGGGTGTAACTGGGTTTGCTCCTGGAAACCCTGCAGGGTAGCTGCATATCTGTTCCTGCTGGGATGGGATGGGATATTTTGGATATTATTGGGTGGGTTGGGGCCGAATGGGATGGGACTTTGACCCTGCTTTCCTCTGTTTCTTGGCCCTCGTGAAGGTTGTGCTTTTCCTCATCTCAGGCCTTTATAACTCCCTTTGG... | ACTTCACCTCTCTTCTGCTTCCCCTTTCCTTCAAGTGGGCTCTAATCTTGGCACAGTGTTCTGAAGTGTGCTTCCCAGTCTCTGCTCTATGCTCCTCCCCCAGGGTAGCTCCCCCAGGGGTGGGTGTAACTGGGTTTGCTCCTGGAAACCCTGCAGGGTAGCTGCATATCTGTTCCTGCTGGGATGGGATGGGATATTTTGGATATTATTGGGTGGGTTGGGGCCGAATGGGATGGGACTTTGACCCTGCTTTCCTCTGTTTCTTGGCCCTCGTGAAGGTTGTGCTTTTCCTCATCTCAGGCCTTTATAACTCCCTTTGG... |
Task1_train_45442 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGAAGCAAACCAACCCACACACATGAAACGGGAACACTAAAAGGAGGCACATTTTGTAACAACCGGATATCAAGAGGAGACAGGGAGCACCTGTTGTTGCCTAGAGTAGGTCAGAGTGGCTTGCTGAAATAATACCATTTTGGCTGGATTTTAAAGAAGAGTTGGTGGAAACTGGTGGACAGAGTTGGACATTTTAGGTAGGCAGGCCTATGTGCAAAAGAACAGGAATGAGAACATGACTTACGGGGAAGCCTGGCAGATCAGCTTGACTGAAGAACAATAACAGATGAAGTTGGAGAGTTGAGGGTCAGAGAAGAGTC... | AGAAGCAAACCAACCCACACACATGAAACGGGAACACTAAAAGGAGGCACATTTTGTAACAACCGGATATCAAGAGGAGACAGGGAGCACCTGTTGTTGCCTAGAGTAGGTCAGAGTGGCTTGCTGAAATAATACCATTTTGGCTGGATTTTAAAGAAGAGTTGGTGGAAACTGGTGGACAGAGTTGGACATTTTAGGTAGGCAGGCCTATGTGCAAAAGAACAGGAATGAGAACATGACTTACGGGGAAGCCTGGCAGATCAGCTTGACTGAAGAACAATAACAGATGAAGTTGGAGAGTTGAGGGTCAGAGAAGAGTC... |
Task1_train_45443 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGGGGAAGGGAAGGAGCTCCAGGCCGGTTCTGACCAGGAAGCCTGGGTACCACCTTCTCTGGCTCCTCTTTTCAGACCTCCAGGTTGCCCCCCAGAGCTCCACAGTCTCTCTCTTCCTCCCCATCCCCTAATCCTCGTTCGCCCTTTCCCATCACAGGTGTGTTAATTTGGGCGCTTCTTGGATTCTACCCTGAGGAGGAGGCGCGTGGTGAGAGGAGAGGTCTGTGTAGGTGGGGTGGGGTTCGCAGGGTCCGTGGTGCTGGCTGGGCGCCATAGGGGGCGCCCCGTTGTAGTCCAGGTTCCCGGAAGGGTGATGGGAA... | GGGGGAAGGGAAGGAGCTCCAGGCCGGTTCTGACCAGGAAGCCTGGGTACCACCTTCTCTGGCTCCTCTTTTCAGACCTCCAGGTTGCCCCCCAGAGCTCCACAGTCTCTCTCTTCCTCCCCATCCCCTAATCCTCGTTCGCCCTTTCCCATCACAGGTGTGTTAATTTGGGCGCTTCTTGGATTCTACCCTGAGGAGGAGGCGCGTGGTGAGAGGAGAGGTCTGTGTAGGTGGGGTGGGGTTCGCAGGGTCCGTGGTGCTGGCTGGGCGCCATAGGGGGCGCCCCGTTGTAGTCCAGGTTCCCGGAAGGGTGATGGGAA... |
Task1_train_45444 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CTCCAGGTCTCTGCTCTCTGCTCTTGGGAAATGTGTAATCTACCTCCCCAGCTCAAGATGCCCCAACAATGCAGCGAGTTTGCATTTCAAGAAACTCCCATTAATATCAATTTACTTCACTGAAACCTCGGGTTCTTCATCAAGTTGATGATTTATGATAAAATCAATTAAATTACGGCCACTTAGGGCCCAGCCGCTTCCTCTCAGATTTCATTGGTGCGGGGCCCAAGTGTCTGGTGGAAAAATGCAAGTTTAGCTGGAGGCGAGGAAAGATAATTCTGCGGCTGAGAAAATTTAATGCAAAACAATTTCCAGGCAAA... | CTCCAGGTCTCTGCTCTCTGCTCTTGGGAAATGTGTAATCTACCTCCCCAGCTCAAGATGCCCCAACAATGCAGCGAGTTTGCATTTCAAGAAACTCCCATTAATATCAATTTACTTCACTGAAACCTCGGGTTCTTCATCAAGTTGATGATTTATGATAAAATCAATTAAATTACGGCCACTTAGGGCCCAGCCGCTTCCTCTCAGATTTCATTGGTGCGGGGCCCAAGTGTCTGGTGGAAAAATGCAAGTTTAGCTGGAGGCGAGGAAAGATAATTCTGCGGCTGAGAAAATTTAATGCAAAACAATTTCCAGGCAAA... |
Task1_train_45445 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCCCACCTCATAGCTGCAAGTAGGGGCGAAAGCTGGAGTGTCTCCTCCCAGCAGCCTCCTCGCCTCCCCGCAAACCTCCGAATCTCCCTGGACCTCCTGGTTGCTGTGGCCCTTCCTCCCCTGATTGGCTTCCTCCCTCTTTCCCAAGGCCAGAGAAGTCCTCTCTTCCCCTCACCTTCCTCCCTCTTCCCATAAAACTTTTAGGAAAATGGGGGCGGGGGCGGTGGAGACCACCAGCCTGGAACTTCAAGTTCAATGGCAAAGTCCCTGACCCTCCCCCCAGGCTGGGCGCCAGCATTATTCTAGGGGCGATTAAACTC... | CCCCACCTCATAGCTGCAAGTAGGGGCGAAAGCTGGAGTGTCTCCTCCCAGCAGCCTCCTCGCCTCCCCGCAAACCTCCGAATCTCCCTGGACCTCCTGGTTGCTGTGGCCCTTCCTCCCCTGATTGGCTTCCTCCCTCTTTCCCAAGGCCAGAGAAGTCCTCTCTTCCCCTCACCTTCCTCCCTCTTCCCATAAAACTTTTAGGAAAATGGGGGCGGGGGCGGTGGAGACCACCAGCCTGGAACTTCAAGTTCAATGGCAAAGTCCCTGACCCTCCCCCCAGGCTGGGCGCCAGCATTATTCTAGGGGCGATTAAACTC... |
Task1_train_45446 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TCAACCCATTATGGTTGACATGGTTCTACTTCTGGGATCTCCATATATGACTATCTCAATTTTAGCCATAAGTGGAAGACAAGGCAAAGTGCCTAGTGGGGGCAGATCAGTTCTACCAGAAATATATTAATACATAGCAAGGGGGTCACTTTTTTTTTTGGAGACAGAGTGCTGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAATCCCGACTCACTGCAACCTTCAGCTCTGGGCTCAATCAATCCTCCTACCTTGGCCTCCCAAGTAGCTAGGACCATAGGCATGCTCCACCACACCCAGCTAATTTTTTAATTAT... | TCAACCCATTATGGTTGACATGGTTCTACTTCTGGGATCTCCATATATGACTATCTCAATTTTAGCCATAAGTGGAAGACAAGGCAAAGTGCCTAGTGGGGGCAGATCAGTTCTACCAGAAATATATTAATACATAGCAAGGGGGTCACTTTTTTTTTTGGAGACAGAGTGCTGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAATCCCGACTCACTGCAACCTTCAGCTCTGGGCTCAATCAATCCTCCTACCTTGGCCTCCCAAGTAGCTAGGACCATAGGCATGCTCCACCACACCCAGCTAATTTTTTAATTAT... |
Task1_train_45447 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TTAGCCAGAGCCAAGCTTAATTAGTATATGGTATATTAAGCATGCATTTTTTTAAGTACACACTGGATTTCAAAACCACATTTGTGATGTCATATCCTTCTTTCTGTTCCTGTCAGGATTAATAAGTAGGAGCTGACTCCAACACAAACTCAAATGCCTTCAAGGGCCTAGAATGGGAGAAGTGCCTGCAGTAACCGGGACAGGACAAGACTACCCTAAAGCATTCAATTCTAATTTAAAATACAGCAACAGGCTGGGCACAGCGGCTCACGCCTGTAATCCCAGCACTTTGGGATGCCAAGGTGGGCGGATCACCTGAG... | TTAGCCAGAGCCAAGCTTAATTAGTATATGGTATATTAAGCATGCATTTTTTTAAGTACACACTGGATTTCAAAACCACATTTGTGATGTCATATCCTTCTTTCTGTTCCTGTCAGGATTAATAAGTAGGAGCTGACTCCAACACAAACTCAAATGCCTTCAAGGGCCTAGAATGGGAGAAGTGCCTGCAGTAACCGGGACAGGACAAGACTACCCTAAAGCATTCAATTCTAATTTAAAATACAGCAACAGGCTGGGCACAGCGGCTCACGCCTGTAATCCCAGCACTTTGGGATGCCAAGGTGGGCGGATCACCTGAG... |
Task1_train_45448 | A sequence alteration has been identified on Chromosome 17. Is it disease-inducing or harmless? | Benign | GGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAAACTCCCAACCTCAGGTTATCAGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGCGCCCAGCAGTTTAGTGATTTCTTTTGCAAAACTGAATGAACACGGGCATCCTATAAATGATAGAAAACAATAATTTGGTGGTTGACTAAGAGAACCCTGGGAGAACATATTTCAAGTTGTAGCCAAGTTTTTTCATCTCTGACCTTCATCACCTGGACTTTTTTTCTAGTCTATAGGAATATATAGAGCACTGAAAGTTTCGCCTATTGTGTCTGTC... | GGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAAACTCCCAACCTCAGGTTATCAGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGCGCCCAGCAGTTTAGTGATTTCTTTTGCAAAACTGAATGAACACGGGCATCCTATAAATGATAGAAAACAATAATTTGGTGGTTGACTAAGAGAACCCTGGGAGAACATATTTCAAGTTGTAGCCAAGTTTTTTCATCTCTGACCTTCATCACCTGGACTTTTTTTCTAGTCTATAGGAATATATAGAGCACTGAAAGTTTCGCCTATTGTGTCTGTC... |
Task1_train_45449 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GCCCCCAACACAGACATTATGAAAAATAATGGGTTTTTTTTTAATGCAGTAGTATATCCAGGTTGGTATATGACAAGGCTTAATTGGACACAATAGAGGACACACCAATAGAGAGGGCAGGTCAGAAGTGATTTCTGATTTAGAAGTCCAAAGAATGCCATTGTAAGAGGATCAGGGTTCATATTCCCGCAACTTTCCCCTTAAATCAGTCTCAGCTCTATCTCTGACTTGTAGATAGAATTTTTGGAGCTTTTTTCCTGGGTGGTGAGGAGCTAGTTTTCAAATCCTTCTAAGACTTGTATTTTGAGCTGTGTATGTGC... | GCCCCCAACACAGACATTATGAAAAATAATGGGTTTTTTTTTAATGCAGTAGTATATCCAGGTTGGTATATGACAAGGCTTAATTGGACACAATAGAGGACACACCAATAGAGAGGGCAGGTCAGAAGTGATTTCTGATTTAGAAGTCCAAAGAATGCCATTGTAAGAGGATCAGGGTTCATATTCCCGCAACTTTCCCCTTAAATCAGTCTCAGCTCTATCTCTGACTTGTAGATAGAATTTTTGGAGCTTTTTTCCTGGGTGGTGAGGAGCTAGTTTTCAAATCCTTCTAAGACTTGTATTTTGAGCTGTGTATGTGC... |
Task1_train_45450 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATAGTATTATTAAAATTAGTCTGTTTCTTTTTACCTTTTTAAAAATGTGCCTCCTAAGATTTTAAAATTATATGTAGCTCTCACTTATTGAACAGCGCTGTTCTAGGAAAAGGGCAGTTCTGTCTATTTTGTCCACTGTTGTGTCTGCAATGCAAGAACAGTGTCTAGTGTGGAATAGGCTCTCAGTAAATATTTGTTTAATGAACAAATTATAAGCTCCAGTGGAATGAGAAATTAAGGTGATGCATTTTTAATATAAAAAGAGCATTTTGTGACCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGC... | ATAGTATTATTAAAATTAGTCTGTTTCTTTTTACCTTTTTAAAAATGTGCCTCCTAAGATTTTAAAATTATATGTAGCTCTCACTTATTGAACAGCGCTGTTCTAGGAAAAGGGCAGTTCTGTCTATTTTGTCCACTGTTGTGTCTGCAATGCAAGAACAGTGTCTAGTGTGGAATAGGCTCTCAGTAAATATTTGTTTAATGAACAAATTATAAGCTCCAGTGGAATGAGAAATTAAGGTGATGCATTTTTAATATAAAAAGAGCATTTTGTGACCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGC... |
Task1_train_45451 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGAAAGCTGAGAACAGGATGGGCTCAGCTCTGTGTGTAGGGACAGGCAGGACACAGGATGGGCTCAGCTCGGTGGGTAGGGACAGGCGGGACACAGGATGGGCTCAGCTCGGTGGGTAGGGACAGGCAGGCCACAGGATGGGCTCAGCTCTGTGTGTAGGGACAGGCAGGCCACAGGATGGGCTCAGCTCGGTGGGTAGGGACAGGCAGGCCACAGGATGGGCTCAGCTCGGTGGGTAGGGACAGGCGGGACACAGGATGGGCTCAGCTCGGTGGGTAGGGACAGGCAGGCCACAGGATGGGCTCAGCTCGGTGGGTAGG... | GGAAAGCTGAGAACAGGATGGGCTCAGCTCTGTGTGTAGGGACAGGCAGGACACAGGATGGGCTCAGCTCGGTGGGTAGGGACAGGCGGGACACAGGATGGGCTCAGCTCGGTGGGTAGGGACAGGCAGGCCACAGGATGGGCTCAGCTCTGTGTGTAGGGACAGGCAGGCCACAGGATGGGCTCAGCTCGGTGGGTAGGGACAGGCAGGCCACAGGATGGGCTCAGCTCGGTGGGTAGGGACAGGCGGGACACAGGATGGGCTCAGCTCGGTGGGTAGGGACAGGCAGGCCACAGGATGGGCTCAGCTCGGTGGGTAGG... |
Task1_train_45452 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCTGAGCCCCCACAAAGTATTGGGTTTACAGGCACCAGCCACCGCGCCTGGCTTCCATACATGTTAGTTTCTAAAATATCAGGAACCCAGTTACGTTTTTTTCCTGGCAAGCAGGAACAGGCTGCACAGTGTAGTGACATTTGCTGGCCAGTGTCACCTTGACCTCTCTGAGCCCGTTTTCTGATCTGCAGAACGGAAGTAGCAATATTCTTAGTCTCCCCTGGTTGTTGAGAGGCTCAACTCAGCCTCTTGTGGTGGTTCCAGGTTCATAGTGTGGGCAAAAAGAAGTACTTTGTGAACTCTAAAGCACTATGCAAAGG... | CCTGAGCCCCCACAAAGTATTGGGTTTACAGGCACCAGCCACCGCGCCTGGCTTCCATACATGTTAGTTTCTAAAATATCAGGAACCCAGTTACGTTTTTTTCCTGGCAAGCAGGAACAGGCTGCACAGTGTAGTGACATTTGCTGGCCAGTGTCACCTTGACCTCTCTGAGCCCGTTTTCTGATCTGCAGAACGGAAGTAGCAATATTCTTAGTCTCCCCTGGTTGTTGAGAGGCTCAACTCAGCCTCTTGTGGTGGTTCCAGGTTCATAGTGTGGGCAAAAAGAAGTACTTTGTGAACTCTAAAGCACTATGCAAAGG... |
Task1_train_45453 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | ACATAAGCTTGAATGAGTCATGAAAGATCTCATAGGCTCAGTCTTCACATCTGAGAAGTGCCTGACAGTGTTATTACAAGAGCTGAATGAAGGACGGGAATGAATATGGAAGCTCTTTGTAAGCAAGGAGGTGTTATACAAATGTCTTTTTTTACCCCCCTACATGCACGTAGTCGGTACAACACTTTTCTGATTGGTCTTGTCAAAGAGGATCTCTTTTCCAGTCTGGAGCTAGAAAATAGTTATCTACATTTGTTACATTAAAACTCCCTTCTGAGAGACTCCCTTTCTCTGCTGGCTGCCAAGGAGCTCAGACCTGA... | ACATAAGCTTGAATGAGTCATGAAAGATCTCATAGGCTCAGTCTTCACATCTGAGAAGTGCCTGACAGTGTTATTACAAGAGCTGAATGAAGGACGGGAATGAATATGGAAGCTCTTTGTAAGCAAGGAGGTGTTATACAAATGTCTTTTTTTACCCCCCTACATGCACGTAGTCGGTACAACACTTTTCTGATTGGTCTTGTCAAAGAGGATCTCTTTTCCAGTCTGGAGCTAGAAAATAGTTATCTACATTTGTTACATTAAAACTCCCTTCTGAGAGACTCCCTTTCTCTGCTGGCTGCCAAGGAGCTCAGACCTGA... |
Task1_train_45454 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TCAGTCTTCACATCTGAGAAGTGCCTGACAGTGTTATTACAAGAGCTGAATGAAGGACGGGAATGAATATGGAAGCTCTTTGTAAGCAAGGAGGTGTTATACAAATGTCTTTTTTTACCCCCCTACATGCACGTAGTCGGTACAACACTTTTCTGATTGGTCTTGTCAAAGAGGATCTCTTTTCCAGTCTGGAGCTAGAAAATAGTTATCTACATTTGTTACATTAAAACTCCCTTCTGAGAGACTCCCTTTCTCTGCTGGCTGCCAAGGAGCTCAGACCTGAACTTGGGACTCACCTGCATCAAAGTTGTAGATCACGC... | TCAGTCTTCACATCTGAGAAGTGCCTGACAGTGTTATTACAAGAGCTGAATGAAGGACGGGAATGAATATGGAAGCTCTTTGTAAGCAAGGAGGTGTTATACAAATGTCTTTTTTTACCCCCCTACATGCACGTAGTCGGTACAACACTTTTCTGATTGGTCTTGTCAAAGAGGATCTCTTTTCCAGTCTGGAGCTAGAAAATAGTTATCTACATTTGTTACATTAAAACTCCCTTCTGAGAGACTCCCTTTCTCTGCTGGCTGCCAAGGAGCTCAGACCTGAACTTGGGACTCACCTGCATCAAAGTTGTAGATCACGC... |
Task1_train_45455 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GTCAGGAGTTGAAGATCAGCCTGACCAGCATGGAGAAACCGCATCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGCGGTGCATGCCTGTAATCCCAGCTACTCGGAAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGGGGTGAGCTGAGATTGTGCCATTGCACTCCAGCCTGGGCAACAAGAGCAAAACTCTGTCTCGAAAAACAAACAAAAAAAACTTCTTGCCTTCAGCCACTGCCTGCTTACTCCTCCTGCACTGACTGGCAGTGTGACCCTGGCCAGTGCCTGGCACAGTGCCTAGAA... | GTCAGGAGTTGAAGATCAGCCTGACCAGCATGGAGAAACCGCATCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGCGGTGCATGCCTGTAATCCCAGCTACTCGGAAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGGGGTGAGCTGAGATTGTGCCATTGCACTCCAGCCTGGGCAACAAGAGCAAAACTCTGTCTCGAAAAACAAACAAAAAAAACTTCTTGCCTTCAGCCACTGCCTGCTTACTCCTCCTGCACTGACTGGCAGTGTGACCCTGGCCAGTGCCTGGCACAGTGCCTAGAA... |
Task1_train_45456 | A sequence alteration has been identified on Chromosome 17. Is it disease-inducing or harmless? | Benign | GGGTCCCTGAGTAGGGAGCAAGGTCAGTCCCTCTCTGGGACATCAGGGTGGAAGGGGAGAGCTCAACCTGGAGACCCTGTGGATGGGGAGGTGAAGGGACTTTTGAGGAGGAGAAGCCCTGTCTCTCCTCTTGGAGGGTCAGGATAGTAGGAAGTCGCAATTTGGCGACCGGACTGGAGGGAGTTCAGCCTAACTGTCAGGTTTTCAGGGTGGGGGGCGGGTCCAGCTCTTCTCTGGGGTTCAGGGTGGTGTGAGGATTCAGCTGGGGCAGGGAGCAGTGCAGGGCCGGGCTCAGCTCACCCTCTCTCCCCAGGACAACC... | GGGTCCCTGAGTAGGGAGCAAGGTCAGTCCCTCTCTGGGACATCAGGGTGGAAGGGGAGAGCTCAACCTGGAGACCCTGTGGATGGGGAGGTGAAGGGACTTTTGAGGAGGAGAAGCCCTGTCTCTCCTCTTGGAGGGTCAGGATAGTAGGAAGTCGCAATTTGGCGACCGGACTGGAGGGAGTTCAGCCTAACTGTCAGGTTTTCAGGGTGGGGGGCGGGTCCAGCTCTTCTCTGGGGTTCAGGGTGGTGTGAGGATTCAGCTGGGGCAGGGAGCAGTGCAGGGCCGGGCTCAGCTCACCCTCTCTCCCCAGGACAACC... |
Task1_train_45457 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GAGCCTCTGCAGCGGACCGCCAGCCTGAGAGGCGCAGAGCTTGTCGGGCAGGGGCCCGCTTGTCCCACTCCCCTGATTTGCAGATGTCAACGGAGGCCCAGCGAAGGGTCAGAGATGAGGCCCCCTCCCTAGTCATTCAACTTACTCTACTTAGCCAGCTGTGTGCCAGATGCTGTACTAAGCGCGGTGGATGCATTATTTTATTTAATTCTCACTACCTTATAAAATGGGTGCTGTTACCATCCCTGTTTTACTAAGGAAGAAACTGAGGCCTAGGCAGGTTACATGTCTCCTTCTGGGTCATACCTACAGTGTTAGTA... | GAGCCTCTGCAGCGGACCGCCAGCCTGAGAGGCGCAGAGCTTGTCGGGCAGGGGCCCGCTTGTCCCACTCCCCTGATTTGCAGATGTCAACGGAGGCCCAGCGAAGGGTCAGAGATGAGGCCCCCTCCCTAGTCATTCAACTTACTCTACTTAGCCAGCTGTGTGCCAGATGCTGTACTAAGCGCGGTGGATGCATTATTTTATTTAATTCTCACTACCTTATAAAATGGGTGCTGTTACCATCCCTGTTTTACTAAGGAAGAAACTGAGGCCTAGGCAGGTTACATGTCTCCTTCTGGGTCATACCTACAGTGTTAGTA... |
Task1_train_45458 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AGCCAGGGGAAAAATACCCTGACTTCACTTTTCTCCTTCCCACTAGTCCTCTCCTCGGGTCCCTGCTGGTGACACCCAGCTGGGAGCCAGAAGACATGTGGGCCCTGTGTTTTTTGTAGAGATTGCAGAGTGTAGCTTGTATTTTTGGTAGAGACGGGGTTTTGCCATGTTGCCCAGGCTGGTCTTCAACTCCTGAGCTCAAGCAATCCACCTGCCTCAGCCTCTCAAAATGCTGCGATTACAGGTGTGAGGCACCTTGCCTAGCACTAAGATTCTTTTTTATCTCACCAGAAGCATCTTGTATAAAATAAGAAAAAAGA... | AGCCAGGGGAAAAATACCCTGACTTCACTTTTCTCCTTCCCACTAGTCCTCTCCTCGGGTCCCTGCTGGTGACACCCAGCTGGGAGCCAGAAGACATGTGGGCCCTGTGTTTTTTGTAGAGATTGCAGAGTGTAGCTTGTATTTTTGGTAGAGACGGGGTTTTGCCATGTTGCCCAGGCTGGTCTTCAACTCCTGAGCTCAAGCAATCCACCTGCCTCAGCCTCTCAAAATGCTGCGATTACAGGTGTGAGGCACCTTGCCTAGCACTAAGATTCTTTTTTATCTCACCAGAAGCATCTTGTATAAAATAAGAAAAAAGA... |
Task1_train_45459 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AAGGCCTTTTAAAATGGCAGTAAAGAGTAATGTTCCTGGGAATAAGAGGAAAAATAAGCCAGTCAACCATGATCTAAGGAAGAATGCAAAGAGAAGGGATGTGGCTGTACAACCTCCAAGAAGGTAAACCTTAGGCGAGGCACAGGGACTCACACCTGTAGTCTCATAGTCTCAGCTACTCAGAAAGCTGAGACAGGAGGATCGCTTGAGCCCAGGAGTTCAGGAGTTTGAGGCCGGCCTGCACAACACAGTGAGACCCCATCTCAAAAAAAAAAAAAAAGAAAGGAAGGCAGGCAGGCAGGCAGGCAAGCAAAATTTAG... | AAGGCCTTTTAAAATGGCAGTAAAGAGTAATGTTCCTGGGAATAAGAGGAAAAATAAGCCAGTCAACCATGATCTAAGGAAGAATGCAAAGAGAAGGGATGTGGCTGTACAACCTCCAAGAAGGTAAACCTTAGGCGAGGCACAGGGACTCACACCTGTAGTCTCATAGTCTCAGCTACTCAGAAAGCTGAGACAGGAGGATCGCTTGAGCCCAGGAGTTCAGGAGTTTGAGGCCGGCCTGCACAACACAGTGAGACCCCATCTCAAAAAAAAAAAAAAAGAAAGGAAGGCAGGCAGGCAGGCAGGCAAGCAAAATTTAG... |
Task1_train_45460 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGCCCTTACTTAGGGGTTGTCTCTTACCTGGCAGGGCTGGGAGGAGATGGGTAGTTCCTGAAAGGCCGATGGAGAAAACTGGGGAGTAGGTTACTACTCCCGTGACTGCCCAGGCCTCTACCCAGACCTGTTTCCACCTGTGCACTGAAATGGATAGGTAGCCACATGTGAGAGGTGAAGAGTCCCGGCCCCAGACTAGAACCCGAGCCAGGTCCCGAGCTGGCTGCTTCCTCCACTCAACATCCCCAGCTCAGTACTCTCAGGCTCTTGGTGCCCCTTGCTTATCTGACATCTGGCCCCTTTGCCTTAACTGGCTGCTT... | TGCCCTTACTTAGGGGTTGTCTCTTACCTGGCAGGGCTGGGAGGAGATGGGTAGTTCCTGAAAGGCCGATGGAGAAAACTGGGGAGTAGGTTACTACTCCCGTGACTGCCCAGGCCTCTACCCAGACCTGTTTCCACCTGTGCACTGAAATGGATAGGTAGCCACATGTGAGAGGTGAAGAGTCCCGGCCCCAGACTAGAACCCGAGCCAGGTCCCGAGCTGGCTGCTTCCTCCACTCAACATCCCCAGCTCAGTACTCTCAGGCTCTTGGTGCCCCTTGCTTATCTGACATCTGGCCCCTTTGCCTTAACTGGCTGCTT... |
Task1_train_45461 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | CTCCCAAAGTGCTGGGATTACAGGCGTCTACAGTTATTCTTGAGAACTACAAGCAAGAAAGGAGGGGAGAACCAGGTCAGTTCAAGGCCACTGGGAGAACTGTCCTGCACCGCCTGCCTCTGAAGCCCATGATGTTTCTGCTTTGTGGGACAGTTGTTCAGGTGCCTGCTTCCCCAGGCCTTCCCCTGCGCCTTCCCCCTCTCTCCTACACACACCATCTGACTGTCCTTCCAGCACGTACACCTCCAGATGCTTGGGTTGGCCTGACCCAAAACAGTCTACTCTCCCGGCCAAGCCAATTGCCCCTGGGATTTTCTGCT... | CTCCCAAAGTGCTGGGATTACAGGCGTCTACAGTTATTCTTGAGAACTACAAGCAAGAAAGGAGGGGAGAACCAGGTCAGTTCAAGGCCACTGGGAGAACTGTCCTGCACCGCCTGCCTCTGAAGCCCATGATGTTTCTGCTTTGTGGGACAGTTGTTCAGGTGCCTGCTTCCCCAGGCCTTCCCCTGCGCCTTCCCCCTCTCTCCTACACACACCATCTGACTGTCCTTCCAGCACGTACACCTCCAGATGCTTGGGTTGGCCTGACCCAAAACAGTCTACTCTCCCGGCCAAGCCAATTGCCCCTGGGATTTTCTGCT... |
Task1_train_45462 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | GGCGTCTACAGTTATTCTTGAGAACTACAAGCAAGAAAGGAGGGGAGAACCAGGTCAGTTCAAGGCCACTGGGAGAACTGTCCTGCACCGCCTGCCTCTGAAGCCCATGATGTTTCTGCTTTGTGGGACAGTTGTTCAGGTGCCTGCTTCCCCAGGCCTTCCCCTGCGCCTTCCCCCTCTCTCCTACACACACCATCTGACTGTCCTTCCAGCACGTACACCTCCAGATGCTTGGGTTGGCCTGACCCAAAACAGTCTACTCTCCCGGCCAAGCCAATTGCCCCTGGGATTTTCTGCTCCTCCAAGATCCCGTGCATAGC... | GGCGTCTACAGTTATTCTTGAGAACTACAAGCAAGAAAGGAGGGGAGAACCAGGTCAGTTCAAGGCCACTGGGAGAACTGTCCTGCACCGCCTGCCTCTGAAGCCCATGATGTTTCTGCTTTGTGGGACAGTTGTTCAGGTGCCTGCTTCCCCAGGCCTTCCCCTGCGCCTTCCCCCTCTCTCCTACACACACCATCTGACTGTCCTTCCAGCACGTACACCTCCAGATGCTTGGGTTGGCCTGACCCAAAACAGTCTACTCTCCCGGCCAAGCCAATTGCCCCTGGGATTTTCTGCTCCTCCAAGATCCCGTGCATAGC... |
Task1_train_45463 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGTTGAAGAGTCCCCCACCTTTTTTTCTGGTAGACCAGTGCAGTACCTGTACCAACCCACACCATCTGGCTGGGGGCAGGTAAAGATGACAACAGGGTGTCCAGAAAACACGGCAGTGGATGCTTCTGTTATGCAATCACGGCAGCAATGAATTCCCCAGAGGAAGCATCTGTAGCCTGTGGTGGTGCTCTTGTCTTCCCACATCTCCACCAGCATCTGGCTGAGGTGTCCTGGTAATCTGACTCACCTTTCCTTCCTTGCCAGAGCTGGGAGAACAGTGGGTTCTGGAGTCGACTGGAATACTTGGGAGATGAGATGAC... | GGTTGAAGAGTCCCCCACCTTTTTTTCTGGTAGACCAGTGCAGTACCTGTACCAACCCACACCATCTGGCTGGGGGCAGGTAAAGATGACAACAGGGTGTCCAGAAAACACGGCAGTGGATGCTTCTGTTATGCAATCACGGCAGCAATGAATTCCCCAGAGGAAGCATCTGTAGCCTGTGGTGGTGCTCTTGTCTTCCCACATCTCCACCAGCATCTGGCTGAGGTGTCCTGGTAATCTGACTCACCTTTCCTTCCTTGCCAGAGCTGGGAGAACAGTGGGTTCTGGAGTCGACTGGAATACTTGGGAGATGAGATGAC... |
Task1_train_45464 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | GTGTTTTGTTCATCGCTGTCTGGTACTACACAGTGGAGTTGCATTTAAGCGACAAGACTTCAAAACCAGGGAGAATAATTAATTAATACATAGCAGCATGAGTCTGCCCACCGTCCCACTCAATCAGCTGACAACTCGAGTGAGTGTGAGGTGGGAGCTTGGAATCTGTCGTCCGCAGTCAGTTTCACAGTGTGGCCATTTGAGCCGTGCATCCTGGGATTTGGTGGAAAGCTGTGCTTTTTTATTCATTGTGGCCCCCAATCACAAGGCCGGCTCCTTCATGTGGGGCTCAGCCAGTGGTGATCAAAGGTAATTTTGAC... | GTGTTTTGTTCATCGCTGTCTGGTACTACACAGTGGAGTTGCATTTAAGCGACAAGACTTCAAAACCAGGGAGAATAATTAATTAATACATAGCAGCATGAGTCTGCCCACCGTCCCACTCAATCAGCTGACAACTCGAGTGAGTGTGAGGTGGGAGCTTGGAATCTGTCGTCCGCAGTCAGTTTCACAGTGTGGCCATTTGAGCCGTGCATCCTGGGATTTGGTGGAAAGCTGTGCTTTTTTATTCATTGTGGCCCCCAATCACAAGGCCGGCTCCTTCATGTGGGGCTCAGCCAGTGGTGATCAAAGGTAATTTTGAC... |
Task1_train_45465 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | GGGTCCCTGGCTCCCACCAAAGGCACCCAGACAGCTCTCCATAGCTGCATCCCCTCCTGGTTCCTGGTCCCCTGCCACCCATCCCCACATCACCATGCCCTTCACTAGAGGACACAGCCTTGGTGTCCTGGTGCAGAATGGTGCCCATGACCCTGCCAGGCAGTGATGGTGCTCCCTGATGAGAACCACAGAGAGGATGCGTTGATGAGGCTCAACAAAGCAGCCCTGGAGCTGTGCCAGAAGCCAAGGCCATTGCAGTCCAACCTCCTGCACCAGATGTGGTAGGTGCCCTGCCAGGAGAGCTGCCCCATCTCCTTCCC... | GGGTCCCTGGCTCCCACCAAAGGCACCCAGACAGCTCTCCATAGCTGCATCCCCTCCTGGTTCCTGGTCCCCTGCCACCCATCCCCACATCACCATGCCCTTCACTAGAGGACACAGCCTTGGTGTCCTGGTGCAGAATGGTGCCCATGACCCTGCCAGGCAGTGATGGTGCTCCCTGATGAGAACCACAGAGAGGATGCGTTGATGAGGCTCAACAAAGCAGCCCTGGAGCTGTGCCAGAAGCCAAGGCCATTGCAGTCCAACCTCCTGCACCAGATGTGGTAGGTGCCCTGCCAGGAGAGCTGCCCCATCTCCTTCCC... |
Task1_train_45466 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | GGCCAGTTTCTCTTGGACACTGACCTAGGGAGGTAGGCTGGTTGAAAAACATCTGCCTTTGGCCTTCCTGCCCCTTTCTGCTGGCCTGGATTCTATCCCAGCTCTGCCTCTCCCTGGCTGTGTGACTTCAGGCAAACCCATTCCACCCTCTGTGCGCTGGCTGGCTCATCCATAAAATGGGTACATCATCTGCCCTACCTACCTCACAGGGTTGTTATGAAAATCAGGTACTCTGTGGATGAAGAAACATTATAAACTGTAAAGCACTGTGCAGAGGTGAGGGATCATGAATAGGTATCTGTGGAATGAATAAAGAGAAT... | GGCCAGTTTCTCTTGGACACTGACCTAGGGAGGTAGGCTGGTTGAAAAACATCTGCCTTTGGCCTTCCTGCCCCTTTCTGCTGGCCTGGATTCTATCCCAGCTCTGCCTCTCCCTGGCTGTGTGACTTCAGGCAAACCCATTCCACCCTCTGTGCGCTGGCTGGCTCATCCATAAAATGGGTACATCATCTGCCCTACCTACCTCACAGGGTTGTTATGAAAATCAGGTACTCTGTGGATGAAGAAACATTATAAACTGTAAAGCACTGTGCAGAGGTGAGGGATCATGAATAGGTATCTGTGGAATGAATAAAGAGAAT... |
Task1_train_45467 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TGGGTGTTTATCGGTATGGCTGTCGAATTAGCATCTGCCGCTCTCAACAGACTGTGAGCCATGTGAGGGCAGGAGCCTTGTTTCTCTCTGCCCACCATTGTATACTCAGTGCCTTGCAGAGTGGCAGGCGGCAGGCACTTAATAAATATTGGCTGAATGTAGCCAATGAGGCCATGTGTAACCTATGAGACATAAAATGGGCTCATCAGTATTATTTAAGGAAGACTTCCTGGAGTGGGTAGGATTTGAGTAGGACCTAGAGACGAGGAGGCTGCAAAAAGCAAACCTTGTTAGCTGGTGGACCTGGCCAAGGTACGCCT... | TGGGTGTTTATCGGTATGGCTGTCGAATTAGCATCTGCCGCTCTCAACAGACTGTGAGCCATGTGAGGGCAGGAGCCTTGTTTCTCTCTGCCCACCATTGTATACTCAGTGCCTTGCAGAGTGGCAGGCGGCAGGCACTTAATAAATATTGGCTGAATGTAGCCAATGAGGCCATGTGTAACCTATGAGACATAAAATGGGCTCATCAGTATTATTTAAGGAAGACTTCCTGGAGTGGGTAGGATTTGAGTAGGACCTAGAGACGAGGAGGCTGCAAAAAGCAAACCTTGTTAGCTGGTGGACCTGGCCAAGGTACGCCT... |
Task1_train_45468 | A sequence alteration has been identified on Chromosome 17. Is it disease-inducing or harmless? | Benign | GGCCAGCCTCCCTCTGACCCGTTGCTGGCCCCCTGACCTCTCCCCATGGCCCTGTTCAGTCGGGTACTCCACCTGCCACTGGTGCCACATGATGGAAGAGGAGTCCTTCCAGAATGAGGAGATTGGCCGCCTGCTCAGTGAGGACTTTGTGAGTGTGAAGGTAGACCGTGAGGAGCGGCCTGACGTGGACAAGGTGTACATGACGTTCGTGCAGGTGAGCAGCCCTCCTCGGGAGTGTATGCGCCACATGGGCTCAGAGCAGCTCCCCTCACCCTCGCCCTCTCTCCGCCAGGCCACCAGCAGCGGCGGGGGCTGGCCCA... | GGCCAGCCTCCCTCTGACCCGTTGCTGGCCCCCTGACCTCTCCCCATGGCCCTGTTCAGTCGGGTACTCCACCTGCCACTGGTGCCACATGATGGAAGAGGAGTCCTTCCAGAATGAGGAGATTGGCCGCCTGCTCAGTGAGGACTTTGTGAGTGTGAAGGTAGACCGTGAGGAGCGGCCTGACGTGGACAAGGTGTACATGACGTTCGTGCAGGTGAGCAGCCCTCCTCGGGAGTGTATGCGCCACATGGGCTCAGAGCAGCTCCCCTCACCCTCGCCCTCTCTCCGCCAGGCCACCAGCAGCGGCGGGGGCTGGCCCA... |
Task1_train_45469 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | GGCTGGCCCATGAATGTGTGGCTGACTCCCAACCTCCAGCCCTTTGTCGGGGGCACCTATTTCCCTCCTGAGGATGGCTTGACCCGAGTCGGCTTCCGCACAGTGTTGCTGAGAATACGAGAACAGGTGGGTGTGCCTCCGGGAGTTGGGGGACCAGGGTGGGGGACTAGGAAACAAGAGCCCCTCCCCCTAGCTGACCTCCAGGTGTGCCCCCACCTCCCGCAGTGGAAACAGAACAAGAACACCCTGCTAGAAAATAGCCAGCGTGTCACCACTGCCCTGCTGGCCCGATCAGAGATCAGCGTGGGTGACCGCCAGCT... | GGCTGGCCCATGAATGTGTGGCTGACTCCCAACCTCCAGCCCTTTGTCGGGGGCACCTATTTCCCTCCTGAGGATGGCTTGACCCGAGTCGGCTTCCGCACAGTGTTGCTGAGAATACGAGAACAGGTGGGTGTGCCTCCGGGAGTTGGGGGACCAGGGTGGGGGACTAGGAAACAAGAGCCCCTCCCCCTAGCTGACCTCCAGGTGTGCCCCCACCTCCCGCAGTGGAAACAGAACAAGAACACCCTGCTAGAAAATAGCCAGCGTGTCACCACTGCCCTGCTGGCCCGATCAGAGATCAGCGTGGGTGACCGCCAGCT... |
Task1_train_45470 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | AGAATACGAGAACAGGTGGGTGTGCCTCCGGGAGTTGGGGGACCAGGGTGGGGGACTAGGAAACAAGAGCCCCTCCCCCTAGCTGACCTCCAGGTGTGCCCCCACCTCCCGCAGTGGAAACAGAACAAGAACACCCTGCTAGAAAATAGCCAGCGTGTCACCACTGCCCTGCTGGCCCGATCAGAGATCAGCGTGGGTGACCGCCAGCTGCCGCCCTCTGCCGCCACCGTGAACAATCGCTGCTTCCAGCAGCTGGATGAGGGCTATGATGAGGAATACGGTGGCTTCGCTGAGGCCCCCAAGTTTCCCACGCCGGGTCA... | AGAATACGAGAACAGGTGGGTGTGCCTCCGGGAGTTGGGGGACCAGGGTGGGGGACTAGGAAACAAGAGCCCCTCCCCCTAGCTGACCTCCAGGTGTGCCCCCACCTCCCGCAGTGGAAACAGAACAAGAACACCCTGCTAGAAAATAGCCAGCGTGTCACCACTGCCCTGCTGGCCCGATCAGAGATCAGCGTGGGTGACCGCCAGCTGCCGCCCTCTGCCGCCACCGTGAACAATCGCTGCTTCCAGCAGCTGGATGAGGGCTATGATGAGGAATACGGTGGCTTCGCTGAGGCCCCCAAGTTTCCCACGCCGGGTCA... |
Task1_train_45471 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CCAGCAGATGGCCTTGCATACCCTGAAAATGATGGCTAACGGGGGCATCCGGGACCATGTGGGGCAGGTGACGGGCACTGGGTGTTCCCTGGAGGGGCAGCAGGGGGCTGTGGGGTGGGGCAGAAGCTGGGACTGGCCTCCAGCTTTGTATCCGCACAGGGCTTTCACCGCTACTCCACAGACCGCCAGTGGCACGTCCCTCACTTTGAGAAGATGCTCTATGACCAGGCACAGCTCGCTGTGGCCTATTCGCAGGCCTTCCAGGTGACCCCTGACCCCAGCCCAGAGAACAGGCATCTCACTCTGGCTGCCCCTCCCAA... | CCAGCAGATGGCCTTGCATACCCTGAAAATGATGGCTAACGGGGGCATCCGGGACCATGTGGGGCAGGTGACGGGCACTGGGTGTTCCCTGGAGGGGCAGCAGGGGGCTGTGGGGTGGGGCAGAAGCTGGGACTGGCCTCCAGCTTTGTATCCGCACAGGGCTTTCACCGCTACTCCACAGACCGCCAGTGGCACGTCCCTCACTTTGAGAAGATGCTCTATGACCAGGCACAGCTCGCTGTGGCCTATTCGCAGGCCTTCCAGGTGACCCCTGACCCCAGCCCAGAGAACAGGCATCTCACTCTGGCTGCCCCTCCCAA... |
Task1_train_45472 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AATATAATCCAAGGCACGCCGTAACAAGGTGTAAAGCTCTGTAAAGTATTTTGCCCAGAGATGAAGGTAGGGGGACAGGAGAGGGAGGGTATGTGTGGATGAGTGGAAAGGAAGAGGGCAGACAAAGAAGGGGCTGAAAGAACTTGCCCAGTGGAGGGGTAGAAGTCCCTGGTCTGACTGCCTGGGAAAGGGGAATCTTCTCCACTCCCACCCCTATCCCATGCCCAGCCAGATCTTGGTTCTGATAGCCTATAGCCAAGGAGACTTCCCTTCTAGTGACCTCCTGGCTGCCCAGAGAGATAGGAGGTGGCTTGCCCCTT... | AATATAATCCAAGGCACGCCGTAACAAGGTGTAAAGCTCTGTAAAGTATTTTGCCCAGAGATGAAGGTAGGGGGACAGGAGAGGGAGGGTATGTGTGGATGAGTGGAAAGGAAGAGGGCAGACAAAGAAGGGGCTGAAAGAACTTGCCCAGTGGAGGGGTAGAAGTCCCTGGTCTGACTGCCTGGGAAAGGGGAATCTTCTCCACTCCCACCCCTATCCCATGCCCAGCCAGATCTTGGTTCTGATAGCCTATAGCCAAGGAGACTTCCCTTCTAGTGACCTCCTGGCTGCCCAGAGAGATAGGAGGTGGCTTGCCCCTT... |
Task1_train_45473 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | ATTGGAGCCAATGTGTGGCTCAGTGCCTGGACAAATGATGCCATGGCAGACAGTAGACAGAACAACACTTCCCTGAGGCTGGGCGTCTATGCTGCTTTAGGAATTCTGCAAGGTGAGCTTGTGGGGGTGTCCAGAAGGGGCTCCAATATCCCTTCTTCTCTGGGCTGCCAGGCCCCCCAAACCGTGCCCTTGCATCCAAGCCTCCCTAACCCACTCTGGTCAACCCGTGTCTCTGATTCTGCCCCTTTGTGCCCGCTCACTAGTCCAGGTGAGCCAGCGCCCTCTGCCTTCTCCAACAGGGTTCTTGGTGATGCTGGCAG... | ATTGGAGCCAATGTGTGGCTCAGTGCCTGGACAAATGATGCCATGGCAGACAGTAGACAGAACAACACTTCCCTGAGGCTGGGCGTCTATGCTGCTTTAGGAATTCTGCAAGGTGAGCTTGTGGGGGTGTCCAGAAGGGGCTCCAATATCCCTTCTTCTCTGGGCTGCCAGGCCCCCCAAACCGTGCCCTTGCATCCAAGCCTCCCTAACCCACTCTGGTCAACCCGTGTCTCTGATTCTGCCCCTTTGTGCCCGCTCACTAGTCCAGGTGAGCCAGCGCCCTCTGCCTTCTCCAACAGGGTTCTTGGTGATGCTGGCAG... |
Task1_train_45474 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTGATGATTGGGGGCCTTTATCCCATAGGTTTATACTGTTAAAACAGTACATAAAATTACATTTAGCTTTGCTTCGGACCGGCGCGGGGGCTCACGCCTGTAATTCAAGCACTTCGGGAGGCCAAGGCGGGTAGATCATCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAATGTGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCAGGGTGGCACACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAACTACTTGAACCTGAGAGGTGGAGGTTGCAGTGAGCTGAGATCGCACCACT... | CTGATGATTGGGGGCCTTTATCCCATAGGTTTATACTGTTAAAACAGTACATAAAATTACATTTAGCTTTGCTTCGGACCGGCGCGGGGGCTCACGCCTGTAATTCAAGCACTTCGGGAGGCCAAGGCGGGTAGATCATCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAATGTGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCAGGGTGGCACACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAACTACTTGAACCTGAGAGGTGGAGGTTGCAGTGAGCTGAGATCGCACCACT... |
Task1_train_45475 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | AAAAAAAGAAAGAAACAAAGAAAGAAAATAGCAAAGCATCCTGACACATGCCTGTAATTCCAGCTACTCAGGAAGCTGAGATGGTAGGATGGCTTTAACCTAGGAGTATGAGGTGGCAGTGAGCTATGATCAGGCCACTGTACTCCAACTTGAATGACAGAGTGCTAATGACAAATACAGTGTATTAAGAATATCTACATCATGGCCTTGAAACCAAGAAAGAACAACTGATTTAAAGCACAACTTTAAGTATTGATAATTTGGGGAAATAAAACATGATATTTTTTAGAAGACAATTGCCTAAAGCCCTTTCTCCTCTC... | AAAAAAAGAAAGAAACAAAGAAAGAAAATAGCAAAGCATCCTGACACATGCCTGTAATTCCAGCTACTCAGGAAGCTGAGATGGTAGGATGGCTTTAACCTAGGAGTATGAGGTGGCAGTGAGCTATGATCAGGCCACTGTACTCCAACTTGAATGACAGAGTGCTAATGACAAATACAGTGTATTAAGAATATCTACATCATGGCCTTGAAACCAAGAAAGAACAACTGATTTAAAGCACAACTTTAAGTATTGATAATTTGGGGAAATAAAACATGATATTTTTTAGAAGACAATTGCCTAAAGCCCTTTCTCCTCTC... |
Task1_train_45476 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ATGAGGTGGCAGTGAGCTATGATCAGGCCACTGTACTCCAACTTGAATGACAGAGTGCTAATGACAAATACAGTGTATTAAGAATATCTACATCATGGCCTTGAAACCAAGAAAGAACAACTGATTTAAAGCACAACTTTAAGTATTGATAATTTGGGGAAATAAAACATGATATTTTTTAGAAGACAATTGCCTAAAGCCCTTTCTCCTCTCCCTCCACCTGCATACAACCTCCTCTTGAAATGAGCACTGCTTACTTATCTAATTTATCCAGTATCCTCCTTCCACCTTCTTTTCAAAATCTAAGCTTTACTAGACTG... | ATGAGGTGGCAGTGAGCTATGATCAGGCCACTGTACTCCAACTTGAATGACAGAGTGCTAATGACAAATACAGTGTATTAAGAATATCTACATCATGGCCTTGAAACCAAGAAAGAACAACTGATTTAAAGCACAACTTTAAGTATTGATAATTTGGGGAAATAAAACATGATATTTTTTAGAAGACAATTGCCTAAAGCCCTTTCTCCTCTCCCTCCACCTGCATACAACCTCCTCTTGAAATGAGCACTGCTTACTTATCTAATTTATCCAGTATCCTCCTTCCACCTTCTTTTCAAAATCTAAGCTTTACTAGACTG... |
Task1_train_45477 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CCACAGCACAACAAAACTCACTTTATAGCTGTCAGAGCCACTTGGAATGTGATACACATGTTGTGTTTGCAAACCCAGGTGCTGTACGAAAGGTAGTTTCATATTAGCAAATTACCACAACGACCTGCTACATTCTACTCATTTTGATTTTGTAATGAGAAAGCCGATTAAACTGTAATAACTTTAAGTTGTGACTCTTAAACAAGTTACACGTTTTGAAGGAGGTGAAAAAACAAAGATGGCGGGTTTGAGGAGCCTTTCTGGGATCCTGTTGAATATCGAGTCCTGAGATTTGCAAATAGCTCTACCTTCATCTATTC... | CCACAGCACAACAAAACTCACTTTATAGCTGTCAGAGCCACTTGGAATGTGATACACATGTTGTGTTTGCAAACCCAGGTGCTGTACGAAAGGTAGTTTCATATTAGCAAATTACCACAACGACCTGCTACATTCTACTCATTTTGATTTTGTAATGAGAAAGCCGATTAAACTGTAATAACTTTAAGTTGTGACTCTTAAACAAGTTACACGTTTTGAAGGAGGTGAAAAAACAAAGATGGCGGGTTTGAGGAGCCTTTCTGGGATCCTGTTGAATATCGAGTCCTGAGATTTGCAAATAGCTCTACCTTCATCTATTC... |
Task1_train_45478 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTGTGTTTGCAAACCCAGGTGCTGTACGAAAGGTAGTTTCATATTAGCAAATTACCACAACGACCTGCTACATTCTACTCATTTTGATTTTGTAATGAGAAAGCCGATTAAACTGTAATAACTTTAAGTTGTGACTCTTAAACAAGTTACACGTTTTGAAGGAGGTGAAAAAACAAAGATGGCGGGTTTGAGGAGCCTTTCTGGGATCCTGTTGAATATCGAGTCCTGAGATTTGCAAATAGCTCTACCTTCATCTATTCCCACTGATCACTGGAGAGTTAAAGTTTAAGGAAACTTCATAGCAATTCTCAAATTAAAGC... | TTGTGTTTGCAAACCCAGGTGCTGTACGAAAGGTAGTTTCATATTAGCAAATTACCACAACGACCTGCTACATTCTACTCATTTTGATTTTGTAATGAGAAAGCCGATTAAACTGTAATAACTTTAAGTTGTGACTCTTAAACAAGTTACACGTTTTGAAGGAGGTGAAAAAACAAAGATGGCGGGTTTGAGGAGCCTTTCTGGGATCCTGTTGAATATCGAGTCCTGAGATTTGCAAATAGCTCTACCTTCATCTATTCCCACTGATCACTGGAGAGTTAAAGTTTAAGGAAACTTCATAGCAATTCTCAAATTAAAGC... |
Task1_train_45479 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AAGAAATTGTTTTCTACTTCTCAGGTTGGCAAAAGTCCCAATATTTCATAACATACTTTGTTGGCTATGGAAAGACAGTTACTATGACAAAATTATGTAACTCTTATAGGGGCAGGTGGCAATATCTATTAAAATTATAAATGCATTTATTTCTTTGAATCTGCAATCTTATCTGTAGAAATTTATACCACACTTACACACAGTTAGGTGTTTACAAAATTATTCTTTACAACATTTTGGGCAATAGCAAGTAATTGGAAACAACTCAAAATATCCCTCAGTTGGGGACTGGTTAAATAAACATCTGTACAACATATTAC... | AAGAAATTGTTTTCTACTTCTCAGGTTGGCAAAAGTCCCAATATTTCATAACATACTTTGTTGGCTATGGAAAGACAGTTACTATGACAAAATTATGTAACTCTTATAGGGGCAGGTGGCAATATCTATTAAAATTATAAATGCATTTATTTCTTTGAATCTGCAATCTTATCTGTAGAAATTTATACCACACTTACACACAGTTAGGTGTTTACAAAATTATTCTTTACAACATTTTGGGCAATAGCAAGTAATTGGAAACAACTCAAAATATCCCTCAGTTGGGGACTGGTTAAATAAACATCTGTACAACATATTAC... |
Task1_train_45480 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTGCTATACTGTATATATGAATGTTGTGCTTTCAGGTATATTTTCCAGCTACAGACATATGTAAGACGCATATAAAGAATTGAATGGGCCTGGCATGGTGGCTTATGCCTCTAATCCCAACATTTTGAGAGGCTGAAGTGGAAGGATCACTTGAACCTGGGAGGTCGAAGCTGCAATAAGCCATGATTGCACCACTGCACTCCAGCCTGGGTGACAGTGACCCTGTCTCAAAAAAAAGAAAAAAGAAAAACGAATGAAGGATGTCATTGAAAAAATACAATATAAAAAAAGTACAGAAATGACAGTGATGAGCTATAGAT... | TTGCTATACTGTATATATGAATGTTGTGCTTTCAGGTATATTTTCCAGCTACAGACATATGTAAGACGCATATAAAGAATTGAATGGGCCTGGCATGGTGGCTTATGCCTCTAATCCCAACATTTTGAGAGGCTGAAGTGGAAGGATCACTTGAACCTGGGAGGTCGAAGCTGCAATAAGCCATGATTGCACCACTGCACTCCAGCCTGGGTGACAGTGACCCTGTCTCAAAAAAAAGAAAAAAGAAAAACGAATGAAGGATGTCATTGAAAAAATACAATATAAAAAAAGTACAGAAATGACAGTGATGAGCTATAGAT... |
Task1_train_45481 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GTACTTTAATACAAGATGGGCTAAATTGCCTTCATGTGAACTTTTTTTCTGTACTAACACTGCATGTTATGTTGTCTGACTTTGCTAACTATGTTTAATCACATATTTACATAAAATCAAAAATTTTTTTTAAATTATATATATAACATAAATATATATAATATAAATATATATATTATATAATATAAATATATATATATTTTATATATTTTATATATATATATATTTTTTTTGAGACAGATTTTTGCTTCATTGCCCAGGCTGGAGAGCAGTGGCGTAGTCATGACCTTGACCTCCTGGGCTCAAGTGATCCTCCCACT... | GTACTTTAATACAAGATGGGCTAAATTGCCTTCATGTGAACTTTTTTTCTGTACTAACACTGCATGTTATGTTGTCTGACTTTGCTAACTATGTTTAATCACATATTTACATAAAATCAAAAATTTTTTTTAAATTATATATATAACATAAATATATATAATATAAATATATATATTATATAATATAAATATATATATATTTTATATATTTTATATATATATATATTTTTTTTGAGACAGATTTTTGCTTCATTGCCCAGGCTGGAGAGCAGTGGCGTAGTCATGACCTTGACCTCCTGGGCTCAAGTGATCCTCCCACT... |
Task1_train_45482 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | ATTTCTCCAAAGAAGATATACAAATGGCCAATAAGTGCATACAGTATGTTCAACATAATTAGCAATCAGGGATGTGCAAACTAAAACTGCAGTGAGATGCCACTTCACACCCATTAGGATGGCTATAATGAAAAAGATGAATAATAACAAGTGTTGGCAAGGATATGAAGAAGTTGGAGTTCTCATACACTGCTAAAAGGAATGTTAGGCAGTGCAGCCACTTTGGAAAATACAAGGCAGTTTTTTAAAATGTTGAACACAGAGGTTTAATGTTCAAAAGGTTAACATTTGACTTTGAAATTCTACTCCTAAGTATAGAT... | ATTTCTCCAAAGAAGATATACAAATGGCCAATAAGTGCATACAGTATGTTCAACATAATTAGCAATCAGGGATGTGCAAACTAAAACTGCAGTGAGATGCCACTTCACACCCATTAGGATGGCTATAATGAAAAAGATGAATAATAACAAGTGTTGGCAAGGATATGAAGAAGTTGGAGTTCTCATACACTGCTAAAAGGAATGTTAGGCAGTGCAGCCACTTTGGAAAATACAAGGCAGTTTTTTAAAATGTTGAACACAGAGGTTTAATGTTCAAAAGGTTAACATTTGACTTTGAAATTCTACTCCTAAGTATAGAT... |
Task1_train_45483 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | CATACAGTATGTTCAACATAATTAGCAATCAGGGATGTGCAAACTAAAACTGCAGTGAGATGCCACTTCACACCCATTAGGATGGCTATAATGAAAAAGATGAATAATAACAAGTGTTGGCAAGGATATGAAGAAGTTGGAGTTCTCATACACTGCTAAAAGGAATGTTAGGCAGTGCAGCCACTTTGGAAAATACAAGGCAGTTTTTTAAAATGTTGAACACAGAGGTTTAATGTTCAAAAGGTTAACATTTGACTTTGAAATTCTACTCCTAAGTATAGATACAGAAGAAATAAAAACACAGGTCAACACACAAACTT... | CATACAGTATGTTCAACATAATTAGCAATCAGGGATGTGCAAACTAAAACTGCAGTGAGATGCCACTTCACACCCATTAGGATGGCTATAATGAAAAAGATGAATAATAACAAGTGTTGGCAAGGATATGAAGAAGTTGGAGTTCTCATACACTGCTAAAAGGAATGTTAGGCAGTGCAGCCACTTTGGAAAATACAAGGCAGTTTTTTAAAATGTTGAACACAGAGGTTTAATGTTCAAAAGGTTAACATTTGACTTTGAAATTCTACTCCTAAGTATAGATACAGAAGAAATAAAAACACAGGTCAACACACAAACTT... |
Task1_train_45484 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | ATATTGATAGGGAAATAAAGATTTAAGAATATTGCTGCAGTGATGTCCTTGAGTAGTCAGAAGGTTTCCTTAGATGAGGAAAGCAACAATTCATTGACAGTAAGTAGAGGAGGCAGAGTCTGCAGGCACAGATGCTGGTAGTTGGGCAAGTGTAGTCATGGAACTTTGTGAACATTCTCTTCTAATTGCTTCAGTTCCTATGCCTCAATTTCCTCATCCATAAAATTGGAATTATAATATCCCTCTCCCATGGTGGTTGTGAGCATTTAATAAGGCAACATATGTAAAATGCTGGTGTGATGCCTGGTACAACTTATGAG... | ATATTGATAGGGAAATAAAGATTTAAGAATATTGCTGCAGTGATGTCCTTGAGTAGTCAGAAGGTTTCCTTAGATGAGGAAAGCAACAATTCATTGACAGTAAGTAGAGGAGGCAGAGTCTGCAGGCACAGATGCTGGTAGTTGGGCAAGTGTAGTCATGGAACTTTGTGAACATTCTCTTCTAATTGCTTCAGTTCCTATGCCTCAATTTCCTCATCCATAAAATTGGAATTATAATATCCCTCTCCCATGGTGGTTGTGAGCATTTAATAAGGCAACATATGTAAAATGCTGGTGTGATGCCTGGTACAACTTATGAG... |
Task1_train_45485 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | CATTAAAACAGTAAACTCCCTAGAGACAGATATAATTTCTTATTAATTTTATATCCACTCAAGCACCAAGTACAGTGCTTCTATTAGAGCAGGATCTCAAGTAATATAGAATCTTCATTGTGAATGAATGGATGAATTAAATATCTCTGCCCCAAGAGTAATTAAATATCTCTGCCCCAACAGCTGGGGCAGCTCCTTCCTAATGGAGGTTATGTTTGAGGAAAACCTTGAACAGATCAGTGGAGCTCAAAAAGGCAGAAGAGGGAATCCTTTTATTGGTAGCCATTATTTAAAGAACATATAAATTTATCTCATCCTTT... | CATTAAAACAGTAAACTCCCTAGAGACAGATATAATTTCTTATTAATTTTATATCCACTCAAGCACCAAGTACAGTGCTTCTATTAGAGCAGGATCTCAAGTAATATAGAATCTTCATTGTGAATGAATGGATGAATTAAATATCTCTGCCCCAAGAGTAATTAAATATCTCTGCCCCAACAGCTGGGGCAGCTCCTTCCTAATGGAGGTTATGTTTGAGGAAAACCTTGAACAGATCAGTGGAGCTCAAAAAGGCAGAAGAGGGAATCCTTTTATTGGTAGCCATTATTTAAAGAACATATAAATTTATCTCATCCTTT... |
Task1_train_45486 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AATCCTTCCTCTGTCTCTCTGGGATGTAATGTCTCCTACACATCAGGAGTATCCTTCTCAAGAACCTGAAAGCCATTCCTCCAACATGCAATCACCAGGAAGCAAAGGGCCTATCTCCCAGTTACTGTGGGAGGATAGGACCCTGACTCCCATAACAGCCATCTAACAGGCACTGTCGCCTAACCTTACTTACACTGACCCACCCTTCACAAGTTTCACTTTCCTGACTACTGAGTTCCTGCTCATCCCCTTCACATTCCCTCCTCCTCCCTCTTAAACACCTAGTCACTTCTGCACAAAGTTCAGTTCCGTTCACGAGG... | AATCCTTCCTCTGTCTCTCTGGGATGTAATGTCTCCTACACATCAGGAGTATCCTTCTCAAGAACCTGAAAGCCATTCCTCCAACATGCAATCACCAGGAAGCAAAGGGCCTATCTCCCAGTTACTGTGGGAGGATAGGACCCTGACTCCCATAACAGCCATCTAACAGGCACTGTCGCCTAACCTTACTTACACTGACCCACCCTTCACAAGTTTCACTTTCCTGACTACTGAGTTCCTGCTCATCCCCTTCACATTCCCTCCTCCTCCCTCTTAAACACCTAGTCACTTCTGCACAAAGTTCAGTTCCGTTCACGAGG... |
Task1_train_45487 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGTGGGAGGATTGCTTGAGGCAAGGAGACTAGCCTGGGCAACATAGTGAGACTCCACTTTTATAAAAAATAAAAATAGCTGAGCATAGTGGCATGTACCTGTGGTCCTAGCTGCTCAGGAGGCTGAGGGAGGCAGATCACTTGAACCCAGCAGGCAGAGGCTACAGTAAGCCATGATTGTACCACTGCACACCAGTCTGGGTGACAGATTGAGACCCTGTCTCCAAGAAGAAACCAAAAAGATATTTAAATCACATTGCAATGCAGTATGAGAAGTTATATAAGAAAAGCATGTGGTCTTACAGGAATAAATAACTGCAA... | GGTGGGAGGATTGCTTGAGGCAAGGAGACTAGCCTGGGCAACATAGTGAGACTCCACTTTTATAAAAAATAAAAATAGCTGAGCATAGTGGCATGTACCTGTGGTCCTAGCTGCTCAGGAGGCTGAGGGAGGCAGATCACTTGAACCCAGCAGGCAGAGGCTACAGTAAGCCATGATTGTACCACTGCACACCAGTCTGGGTGACAGATTGAGACCCTGTCTCCAAGAAGAAACCAAAAAGATATTTAAATCACATTGCAATGCAGTATGAGAAGTTATATAAGAAAAGCATGTGGTCTTACAGGAATAAATAACTGCAA... |
Task1_train_45488 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AATGTAGCAAGGGCCAAGTCTTTTTTCCACCAGCACCCAGCTCTGTGGCCTCTGAGACTTCTCTGAGCTTTGGTTTCTTCGAGCACACAATGGGGATGACTTCACCTTGCTCATGGTTGATGTGACTCCTGAATGAGATCAAGGTCATGTAGCGGAGGCTGGGTCAACACTTGTTCCTTTCCCACTATTCTTTCTCTCCCCTCCTCCCACATACCAGCCACCTATAGCTTTGCCCCCACGCAGCACTTCCACAATGGGGCTGCACCGCCACCGATTTCAGAAGCCCTTCTGCAAGGACACTCGGCAGGCCAAGCTGAGAT... | AATGTAGCAAGGGCCAAGTCTTTTTTCCACCAGCACCCAGCTCTGTGGCCTCTGAGACTTCTCTGAGCTTTGGTTTCTTCGAGCACACAATGGGGATGACTTCACCTTGCTCATGGTTGATGTGACTCCTGAATGAGATCAAGGTCATGTAGCGGAGGCTGGGTCAACACTTGTTCCTTTCCCACTATTCTTTCTCTCCCCTCCTCCCACATACCAGCCACCTATAGCTTTGCCCCCACGCAGCACTTCCACAATGGGGCTGCACCGCCACCGATTTCAGAAGCCCTTCTGCAAGGACACTCGGCAGGCCAAGCTGAGAT... |
Task1_train_45489 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TATTTATGAATTACCTGTGGTTACCTGATAATGCAGAAGAAATCATACTAGATCATAACAACCAGAAGTAATTCACAAATATGTAAAATAGATTCCCATGATGAAAATAATCAAATCTTCTTGCTGAGAACTATTTATTATTTTCTTTCAAAGTTTAGAATCATGAAGGAATGAATACCCAAATAAGTTGGTCTAAACTAATTAGAAAAAAGTAACTAAAAAAATTAAACTGGCTGGGCATAGTGGCTCACACCTGTAATCCCAACACTTTGGGAAGCCAAGATGGGGGGATTGCTTGAGCCAAGGAGTTTGAGACCAAC... | TATTTATGAATTACCTGTGGTTACCTGATAATGCAGAAGAAATCATACTAGATCATAACAACCAGAAGTAATTCACAAATATGTAAAATAGATTCCCATGATGAAAATAATCAAATCTTCTTGCTGAGAACTATTTATTATTTTCTTTCAAAGTTTAGAATCATGAAGGAATGAATACCCAAATAAGTTGGTCTAAACTAATTAGAAAAAAGTAACTAAAAAAATTAAACTGGCTGGGCATAGTGGCTCACACCTGTAATCCCAACACTTTGGGAAGCCAAGATGGGGGGATTGCTTGAGCCAAGGAGTTTGAGACCAAC... |
Task1_train_45490 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CTTTCAGAAGCAGAGTCCTAGAGTAGTGGTTCCCAGCCTTGGCTGGAAAGTAGAACCTCTCAGGGAACTTTTAAAAGTACTGATGTTCTGGTTCTGCCAGAAAACAATATAAGTCAAACCAATATGAGTTGTTAAAACATGTGCATTTGTTATCTCTAAAAGAAAACAAACCCAAATAAGGTGTAATTCAGCTTGTCAGTTGAAGGATTTTTGGTTTTAAAAAGACATTACTTTGGCAGAGAGATTTAAAGTTTGCTGGCATAGGAAGCATTGAATGTAAGTGTTCTAGAATAAGCCCATCATATACCTTTAGTGAGTGT... | CTTTCAGAAGCAGAGTCCTAGAGTAGTGGTTCCCAGCCTTGGCTGGAAAGTAGAACCTCTCAGGGAACTTTTAAAAGTACTGATGTTCTGGTTCTGCCAGAAAACAATATAAGTCAAACCAATATGAGTTGTTAAAACATGTGCATTTGTTATCTCTAAAAGAAAACAAACCCAAATAAGGTGTAATTCAGCTTGTCAGTTGAAGGATTTTTGGTTTTAAAAAGACATTACTTTGGCAGAGAGATTTAAAGTTTGCTGGCATAGGAAGCATTGAATGTAAGTGTTCTAGAATAAGCCCATCATATACCTTTAGTGAGTGT... |
Task1_train_45491 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | ATGTGTGTGCCTTGCAGACCTATGCTGGTTCTCTGTTGTCTGCAGGATAAAGTCCAGACTACGCAGTGGGGCCCTAGGACACCCTCACTGACCCCACGATGGTACAGATGCTCCTCAGCTTACAATGGAGTTACATCCTGGTAGACCCATTGTAAGCTGAAAATAGCATAAATCGAAAATAAATACATCTAATGCACCTAACCTACTGAACACCATAGTTTAGCCTAGGCTACTTTACATGAGCTGAGAAGACTCACAGTCGTCTACAGTGGGGCAAAATCACCTAGCAACACGATCCACTCTGGAGTGCCCGTTGTTCA... | ATGTGTGTGCCTTGCAGACCTATGCTGGTTCTCTGTTGTCTGCAGGATAAAGTCCAGACTACGCAGTGGGGCCCTAGGACACCCTCACTGACCCCACGATGGTACAGATGCTCCTCAGCTTACAATGGAGTTACATCCTGGTAGACCCATTGTAAGCTGAAAATAGCATAAATCGAAAATAAATACATCTAATGCACCTAACCTACTGAACACCATAGTTTAGCCTAGGCTACTTTACATGAGCTGAGAAGACTCACAGTCGTCTACAGTGGGGCAAAATCACCTAGCAACACGATCCACTCTGGAGTGCCCGTTGTTCA... |
Task1_train_45492 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AAAAAGAAAGGCACGGCCAGGGATGGTGGCTCATGCCTGTAATTCCAGCACACTGGAAGGCTAAGGCAGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATCAGCCAGGTGCGGTGGCGTGCGCCTATAATCCCAGCTACTTGAAAAACTGAGGCAGGAGAAACACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGAGCCACTGCACTTCAGCCTGGGTGACAAGAGCGAGACTATGTCTCAAAAAATAAAAAATAAACGGAAA... | AAAAAGAAAGGCACGGCCAGGGATGGTGGCTCATGCCTGTAATTCCAGCACACTGGAAGGCTAAGGCAGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATCAGCCAGGTGCGGTGGCGTGCGCCTATAATCCCAGCTACTTGAAAAACTGAGGCAGGAGAAACACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGAGCCACTGCACTTCAGCCTGGGTGACAAGAGCGAGACTATGTCTCAAAAAATAAAAAATAAACGGAAA... |
Task1_train_45493 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TGGGATAAGCCCATTCTAACCCTGTTTTACCACATCATTTCCTGCTGAAGAGCTTGCCGGGGTTCTCAGTTGCCTATGGGGACATTTTTCAAACAGTCCTAGGCTGGGAGTTGGTGAAGCCACAGAACAAACACAGCACATCTTCCTGGAATATCATTTTTGCACAAATATCTGAGGATAAATGTGAATTTTATGTGAAGAATAATATGACAATATTTTGAGTACTGAAATCCCTCATAAGTTTTGAGATAATCCTGTTACATTTGTCCATAGAGGTTTATAGAGATCTTTCCAAATATATTCATCCAATTCCCACGTAA... | TGGGATAAGCCCATTCTAACCCTGTTTTACCACATCATTTCCTGCTGAAGAGCTTGCCGGGGTTCTCAGTTGCCTATGGGGACATTTTTCAAACAGTCCTAGGCTGGGAGTTGGTGAAGCCACAGAACAAACACAGCACATCTTCCTGGAATATCATTTTTGCACAAATATCTGAGGATAAATGTGAATTTTATGTGAAGAATAATATGACAATATTTTGAGTACTGAAATCCCTCATAAGTTTTGAGATAATCCTGTTACATTTGTCCATAGAGGTTTATAGAGATCTTTCCAAATATATTCATCCAATTCCCACGTAA... |
Task1_train_45494 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GGTGGGAATCAGGGAAAATAGACCTTTTTATGTTCTATTGTCTGTACAGGATGGGGCCTTGGGACAAATTTTTCTGAACAATTAGAGAAAATACTTGTGGAAAGGTATAATCCAAAAGAATGGGTTTTAACACCAAGAACTCAGTTTATTTTTCAAGCTAATGTCTTCTAAAACTTTCACTTACTAAAGAATCATGTCTCCCTTCATGCTCTAATTTTCTTTTTCTTTTTAGAGATAAGATCAGCTGGAGTGCAGTGGCCATAATAGCTCACTGCAGCCTTGATCTCCTGGGCTCAAGCAATCCTTCCACCTCAGCCTCC... | GGTGGGAATCAGGGAAAATAGACCTTTTTATGTTCTATTGTCTGTACAGGATGGGGCCTTGGGACAAATTTTTCTGAACAATTAGAGAAAATACTTGTGGAAAGGTATAATCCAAAAGAATGGGTTTTAACACCAAGAACTCAGTTTATTTTTCAAGCTAATGTCTTCTAAAACTTTCACTTACTAAAGAATCATGTCTCCCTTCATGCTCTAATTTTCTTTTTCTTTTTAGAGATAAGATCAGCTGGAGTGCAGTGGCCATAATAGCTCACTGCAGCCTTGATCTCCTGGGCTCAAGCAATCCTTCCACCTCAGCCTCC... |
Task1_train_45495 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | GGGGTCTCATGGACAGCTGTGTAGAAGGTGTCCTGGAGTGAGGCCAGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCGGAAGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGCTAACACAGTGAAACCGTGTTACAAAAAAAATTAGCCGGGCGAGGTGGTGGGCGCCTGTAGTTCCAGCTACGCGGGAGGCTGAGGTAAAAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGTGAGCCGAGATCGCGCCACTCCAGCCTGGGCGACAGCGAGACTCCGTCACAAAAAAAAAAAA... | GGGGTCTCATGGACAGCTGTGTAGAAGGTGTCCTGGAGTGAGGCCAGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCGGAAGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGCTAACACAGTGAAACCGTGTTACAAAAAAAATTAGCCGGGCGAGGTGGTGGGCGCCTGTAGTTCCAGCTACGCGGGAGGCTGAGGTAAAAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGTGAGCCGAGATCGCGCCACTCCAGCCTGGGCGACAGCGAGACTCCGTCACAAAAAAAAAAAA... |
Task1_train_45496 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GACCCCCTCCCCTGTCACCCTCCATCTTCTTCTTCTTTTTTTTTTGTTTTTGATTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCATGACCTCCACTCACTGCAGCCTCCAACCAGCTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGATTACAGGTGTGTGCCACCACGCCCGGCTAATTTTTTTGTATTTTTAGTACAGATCCGGAGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTTCTGACTTCAAGTGATCCATCCGCCTCCGCCTCCCAAATTTCTGGGACTACAG... | GACCCCCTCCCCTGTCACCCTCCATCTTCTTCTTCTTTTTTTTTTGTTTTTGATTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCATGACCTCCACTCACTGCAGCCTCCAACCAGCTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGATTACAGGTGTGTGCCACCACGCCCGGCTAATTTTTTTGTATTTTTAGTACAGATCCGGAGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTTCTGACTTCAAGTGATCCATCCGCCTCCGCCTCCCAAATTTCTGGGACTACAG... |
Task1_train_45497 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | TACAGGAGGAAGGCTTAGGTGCAGAGAGGGTGGGCCCTGGCAGAAGGCCGACTGGGATGCACTCTGCACTTAAGGTGGAAATGGAGGCGCACTTAAGGTGGAAATGGAGGCTCACCCAAGGTCACGAAGCTAGTGACAGGGCTGGATTCAATCCAGGCCAATCAGACCCTGGTGCAGCACACTGCCTCTAAAGAAGCTACTTCTCACCAAGCCCAATAGGAACTCATAATTGAAATCTACTTCTCAGAGTAAACCTACTACTGATTGGCACCTAAGAAACTCCAAGAGAATAAAGCCCATGGCGGGCGCTTACTTTTAGG... | TACAGGAGGAAGGCTTAGGTGCAGAGAGGGTGGGCCCTGGCAGAAGGCCGACTGGGATGCACTCTGCACTTAAGGTGGAAATGGAGGCGCACTTAAGGTGGAAATGGAGGCTCACCCAAGGTCACGAAGCTAGTGACAGGGCTGGATTCAATCCAGGCCAATCAGACCCTGGTGCAGCACACTGCCTCTAAAGAAGCTACTTCTCACCAAGCCCAATAGGAACTCATAATTGAAATCTACTTCTCAGAGTAAACCTACTACTGATTGGCACCTAAGAAACTCCAAGAGAATAAAGCCCATGGCGGGCGCTTACTTTTAGG... |
Task1_train_45498 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | GACTGTTAGAAAGTCTCCTTATTTTGATCACATATTCACCTATTCCCCTTAATCATGCTTCTGGAACCTCAGAAAAGACACTGTCCCTCTTACACGCAGGAATACCTCAAAGTAGCTGTTAACTCCATCTCCATTTTTTTTCTCTTCTCTGGGATAAATTTCCGTAGTTCCTCCCTGTCCCCAGCTGTTGCTAGACAGTTAATACCCTCTTCTGGAAGCATAATTTGAACTTTCCTCAGGGTCTTTTGTCCCATGTACATGGTTACAATAATAATGGTAGTCATTTCTCATTAAGATATTTATCTTATTATTATTATTAT... | GACTGTTAGAAAGTCTCCTTATTTTGATCACATATTCACCTATTCCCCTTAATCATGCTTCTGGAACCTCAGAAAAGACACTGTCCCTCTTACACGCAGGAATACCTCAAAGTAGCTGTTAACTCCATCTCCATTTTTTTTCTCTTCTCTGGGATAAATTTCCGTAGTTCCTCCCTGTCCCCAGCTGTTGCTAGACAGTTAATACCCTCTTCTGGAAGCATAATTTGAACTTTCCTCAGGGTCTTTTGTCCCATGTACATGGTTACAATAATAATGGTAGTCATTTCTCATTAAGATATTTATCTTATTATTATTATTAT... |
Task1_train_45499 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | TACATGTTGCTCTCTCTACATATATCTATCTCCATCTAGCACTGGACTCTTCTCCTCCTCGTTCTCTGAGGACAGGGAACAAAGAGAGGAGATGGGTTACCGACAGACCCGCACCTTCTCCGCCCGGCCACCAGGTGGCCCTGCGCAGGGGTGGGCCCTACTCTCCAAGGCCTTTGTGTTCACACATGGAAGCCCTGAGTTTTCTGGCTGGGGCTTGGCCTCTTCACCCTCTCTCCCTGCCCTCTGAGAGTGGAGGCTTAGTTGTATTCCACTCACCCCAAGGAGAGGCAAGCTCAAGGAACGAGAACCCAGGAAGCTGG... | TACATGTTGCTCTCTCTACATATATCTATCTCCATCTAGCACTGGACTCTTCTCCTCCTCGTTCTCTGAGGACAGGGAACAAAGAGAGGAGATGGGTTACCGACAGACCCGCACCTTCTCCGCCCGGCCACCAGGTGGCCCTGCGCAGGGGTGGGCCCTACTCTCCAAGGCCTTTGTGTTCACACATGGAAGCCCTGAGTTTTCTGGCTGGGGCTTGGCCTCTTCACCCTCTCTCCCTGCCCTCTGAGAGTGGAGGCTTAGTTGTATTCCACTCACCCCAAGGAGAGGCAAGCTCAAGGAACGAGAACCCAGGAAGCTGG... |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.