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_40600 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TTCAAAGACCAGCACAAGCCATGTTTCTGTATCCAAGACAACCCACTCCCAACCAGTCACCAGAGACTGTCATCCCCGGTGCACCTGGACCAAATGGTTTGATGTGGACTTTCCATCCCCTGGACCCCACGGTGGGGACAAGGAAACCTACAACAACATCATCAGGAGTGGGGAAAAAATCTGCCGCCGACCTGAGGAGATCACCAGGCTCCAGTGCCGAGCCAAGAGCCACCCGGAGGTGAGCATCGAACACCTGGGCCAGGTGGTGCAGTGCAGCCGCGAAGAGGGCCTGGTGTGCCGGAACCAGGACCAGCAGGGAC... | TTCAAAGACCAGCACAAGCCATGTTTCTGTATCCAAGACAACCCACTCCCAACCAGTCACCAGAGACTGTCATCCCCGGTGCACCTGGACCAAATGGTTTGATGTGGACTTTCCATCCCCTGGACCCCACGGTGGGGACAAGGAAACCTACAACAACATCATCAGGAGTGGGGAAAAAATCTGCCGCCGACCTGAGGAGATCACCAGGCTCCAGTGCCGAGCCAAGAGCCACCCGGAGGTGAGCATCGAACACCTGGGCCAGGTGGTGCAGTGCAGCCGCGAAGAGGGCCTGGTGTGCCGGAACCAGGACCAGCAGGGAC... |
Task1_train_40601 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GAGGACAGCCAGGGCCAGAGCAGGTGGATGAGGCTGCACAGCCAGGGAGTGTGGCAGAGCCAGGGAGGAGCCACTCCCACACCAGAGGCCCCTGCCCGGGCCAGCTCGGTGTCTGGGGTGGGTGCTGAGGGTGGGGCAGGAAGGAAACTGGGGCACAGCCACCCTCCCCTGTCCCCACACGGGACTCTCGGGACTGTGACCCCGAGAACCAAGGGGTGCCCCGGAGATCGGGAGAGGCCGGACCCTGCAGGTCTCTGTGCTTCTGCAGAAAGGTGAGACCTGGGCCACACCCAACTGCTCCGAGGCCACCTGTGAGGGCA... | GAGGACAGCCAGGGCCAGAGCAGGTGGATGAGGCTGCACAGCCAGGGAGTGTGGCAGAGCCAGGGAGGAGCCACTCCCACACCAGAGGCCCCTGCCCGGGCCAGCTCGGTGTCTGGGGTGGGTGCTGAGGGTGGGGCAGGAAGGAAACTGGGGCACAGCCACCCTCCCCTGTCCCCACACGGGACTCTCGGGACTGTGACCCCGAGAACCAAGGGGTGCCCCGGAGATCGGGAGAGGCCGGACCCTGCAGGTCTCTGTGCTTCTGCAGAAAGGTGAGACCTGGGCCACACCCAACTGCTCCGAGGCCACCTGTGAGGGCA... |
Task1_train_40602 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCTCAAGGGTTGCACAGCCAGCCGCAAGAGCCCCGGCCTCAACCCACGCTCGACTCCCACGGCCCATCTGTGGGCATCTCATGCCGCACGGGCTGCCTGGCTCTCAGCCGAGCGTTTTCCCTCGTCTGCTGTCTCTTGGCCAGAGCCGCAGCATTAATACTTACTGTCAATAGAGAAAGATGCAGCCCCAGGGGCCACCGGGAGACACCCAGCCGGGCTGGCCATGAGGCTGCTGCAGCCCCTCCCTGCCCCGCCCTCCACCCCCTCCCAAGCTTGGGGTCTGGGCTGGGCAGGTGAGGCTCCCTGGGGTCTCTCTCCAT... | CCTCAAGGGTTGCACAGCCAGCCGCAAGAGCCCCGGCCTCAACCCACGCTCGACTCCCACGGCCCATCTGTGGGCATCTCATGCCGCACGGGCTGCCTGGCTCTCAGCCGAGCGTTTTCCCTCGTCTGCTGTCTCTTGGCCAGAGCCGCAGCATTAATACTTACTGTCAATAGAGAAAGATGCAGCCCCAGGGGCCACCGGGAGACACCCAGCCGGGCTGGCCATGAGGCTGCTGCAGCCCCTCCCTGCCCCGCCCTCCACCCCCTCCCAAGCTTGGGGTCTGGGCTGGGCAGGTGAGGCTCCCTGGGGTCTCTCTCCAT... |
Task1_train_40603 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | GGACTCTCAGCCCACCCGTCCTCCTGTCCTCCACGCACGTCCAAGTTGGGGAGATCAAGCCCTTGGCAGGGACTGTGCTTTAGTCACCAGATGCACGTCCTGTGGCCGGGGAAGGCAGCCCTGCACAGAGCAGCTTCATGTTAGGGGACACACCCCAAAGTGATGGGGTGGCTGGTGGTGGGCACTTCTCTGGCTACAAGATGGAGGCCCAGGTGGTCCAGCCCAAGGAGGGCACTGCACGGAGCAGATAACCAAGGGCAGTCAGCCTGGGCAGGGGAGGGGCTGCCTGGGGGGGAGGGGTTGCCTGGGTTGGGGAGGGG... | GGACTCTCAGCCCACCCGTCCTCCTGTCCTCCACGCACGTCCAAGTTGGGGAGATCAAGCCCTTGGCAGGGACTGTGCTTTAGTCACCAGATGCACGTCCTGTGGCCGGGGAAGGCAGCCCTGCACAGAGCAGCTTCATGTTAGGGGACACACCCCAAAGTGATGGGGTGGCTGGTGGTGGGCACTTCTCTGGCTACAAGATGGAGGCCCAGGTGGTCCAGCCCAAGGAGGGCACTGCACGGAGCAGATAACCAAGGGCAGTCAGCCTGGGCAGGGGAGGGGCTGCCTGGGGGGGAGGGGTTGCCTGGGTTGGGGAGGGG... |
Task1_train_40604 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GCTTGGCGCCTGCTTGATCGCCATCTGCGGAAGCAACGGCACCATCATCAGGAAGGCTGTGGCATGTCCTGGAACTCCAGCCACAACGCCATTCACCTTCACCACCGCCTGGGTCCCCCACTCCACGACAAGTAAGCCCTGCCTGGCTCTCCTGAGGCCCAGTACCGTCTGGGTGACAAGGAGGACCCCCTGGGCTCTTAGTGCAGGTGCCCTGTATGGTAGCGACAGTCCCAATCCACTGACCTTCCGGGCTCTGTCTAGGGGTGCACGGCCCCTCAACACCCTGCGTGTCTCCAGGGGCTCCCCACGAAGCCTCAGCA... | GCTTGGCGCCTGCTTGATCGCCATCTGCGGAAGCAACGGCACCATCATCAGGAAGGCTGTGGCATGTCCTGGAACTCCAGCCACAACGCCATTCACCTTCACCACCGCCTGGGTCCCCCACTCCACGACAAGTAAGCCCTGCCTGGCTCTCCTGAGGCCCAGTACCGTCTGGGTGACAAGGAGGACCCCCTGGGCTCTTAGTGCAGGTGCCCTGTATGGTAGCGACAGTCCCAATCCACTGACCTTCCGGGCTCTGTCTAGGGGTGCACGGCCCCTCAACACCCTGCGTGTCTCCAGGGGCTCCCCACGAAGCCTCAGCA... |
Task1_train_40605 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | CTGTCTAGGGGTGCACGGCCCCTCAACACCCTGCGTGTCTCCAGGGGCTCCCCACGAAGCCTCAGCACAATGATTGATGGGATACCCCAAGGAGACAATAAAGCTTTCCTGGACTCCGTCCCATCCCTCAGCACGGCCTATCCCAGCCAGCCAGCTCCCTCAAGGCCAGGCTGCCAGGCCCCAGTCCCTCATGCAGAAACGGCTCTAACCAAGGCTGAGGCAGGCACTGGGGTCCCCAGTATCCCACAGGGGCAGGGCCAGCCCTGGGGAAAGGGTCCTCTGGGGCCCCTCCACCTTGTGAGGCCAGGACTGGAGGATGC... | CTGTCTAGGGGTGCACGGCCCCTCAACACCCTGCGTGTCTCCAGGGGCTCCCCACGAAGCCTCAGCACAATGATTGATGGGATACCCCAAGGAGACAATAAAGCTTTCCTGGACTCCGTCCCATCCCTCAGCACGGCCTATCCCAGCCAGCCAGCTCCCTCAAGGCCAGGCTGCCAGGCCCCAGTCCCTCATGCAGAAACGGCTCTAACCAAGGCTGAGGCAGGCACTGGGGTCCCCAGTATCCCACAGGGGCAGGGCCAGCCCTGGGGAAAGGGTCCTCTGGGGCCCCTCCACCTTGTGAGGCCAGGACTGGAGGATGC... |
Task1_train_40606 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GCTGGTACAATGGGCACCGCCCAGAGCCCGGCCTGGGAGGCGGAGACTTTGAGACGTTTGAAAACCTGAGGCAGAGAGGGTACCAGGTATGCCCTGTGCTGGCTGACATCGAGTGCCGGGCGGCGCAGCTTCCCGACATGCCGCTGGAGGAGCTGGGCCAGCAGGTGGACTGTGACCGCATGCGGGGGCTGATGTGCGCCAACAGCCAACAGAGTCCCCCGCTCTGTCACGACTACGAGCTGCGGGTTCTCTGCTGCGAATACGTGCCCTGTGGCCCCTCCCCGGCCCCAGGCACCAGCCCTCAGCCCTCCCTCAGTGCC... | GCTGGTACAATGGGCACCGCCCAGAGCCCGGCCTGGGAGGCGGAGACTTTGAGACGTTTGAAAACCTGAGGCAGAGAGGGTACCAGGTATGCCCTGTGCTGGCTGACATCGAGTGCCGGGCGGCGCAGCTTCCCGACATGCCGCTGGAGGAGCTGGGCCAGCAGGTGGACTGTGACCGCATGCGGGGGCTGATGTGCGCCAACAGCCAACAGAGTCCCCCGCTCTGTCACGACTACGAGCTGCGGGTTCTCTGCTGCGAATACGTGCCCTGTGGCCCCTCCCCGGCCCCAGGCACCAGCCCTCAGCCCTCCCTCAGTGCC... |
Task1_train_40607 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | GGCCGAGAGCTTCCCCAACTGGACCCTGGCACAGGTGGGGCAGAAGGTGCACTGTGACGTCCACTTCGGCCTGGTGTGCAGGAACTGGGAGCAGGAGGGCGTCTTCAAGATGTGCTACAACTACAGGATCCGGGTCCTCTGCTGCAGTGACGACCACTGCAGGGGACGTGCCACAACCCCGCCACCGACCACAGAGCTGGAGACGGCCACCACCACCACCACCCAGGCCCTGTTCTCAACGCCGCAGCCTACGAGTAGCCCGGGGCTGACCAGGGCTCCCCCGGCCAGCACCACAGCAGTCCCCACCCTCTCAGAAGGAC... | GGCCGAGAGCTTCCCCAACTGGACCCTGGCACAGGTGGGGCAGAAGGTGCACTGTGACGTCCACTTCGGCCTGGTGTGCAGGAACTGGGAGCAGGAGGGCGTCTTCAAGATGTGCTACAACTACAGGATCCGGGTCCTCTGCTGCAGTGACGACCACTGCAGGGGACGTGCCACAACCCCGCCACCGACCACAGAGCTGGAGACGGCCACCACCACCACCACCCAGGCCCTGTTCTCAACGCCGCAGCCTACGAGTAGCCCGGGGCTGACCAGGGCTCCCCCGGCCAGCACCACAGCAGTCCCCACCCTCTCAGAAGGAC... |
Task1_train_40608 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CAACTGGACCCTGGCACAGGTGGGGCAGAAGGTGCACTGTGACGTCCACTTCGGCCTGGTGTGCAGGAACTGGGAGCAGGAGGGCGTCTTCAAGATGTGCTACAACTACAGGATCCGGGTCCTCTGCTGCAGTGACGACCACTGCAGGGGACGTGCCACAACCCCGCCACCGACCACAGAGCTGGAGACGGCCACCACCACCACCACCCAGGCCCTGTTCTCAACGCCGCAGCCTACGAGTAGCCCGGGGCTGACCAGGGCTCCCCCGGCCAGCACCACAGCAGTCCCCACCCTCTCAGAAGGACTGACATCCCCCAGAT... | CAACTGGACCCTGGCACAGGTGGGGCAGAAGGTGCACTGTGACGTCCACTTCGGCCTGGTGTGCAGGAACTGGGAGCAGGAGGGCGTCTTCAAGATGTGCTACAACTACAGGATCCGGGTCCTCTGCTGCAGTGACGACCACTGCAGGGGACGTGCCACAACCCCGCCACCGACCACAGAGCTGGAGACGGCCACCACCACCACCACCCAGGCCCTGTTCTCAACGCCGCAGCCTACGAGTAGCCCGGGGCTGACCAGGGCTCCCCCGGCCAGCACCACAGCAGTCCCCACCCTCTCAGAAGGACTGACATCCCCCAGAT... |
Task1_train_40609 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | CCTCTCAGGCCGAGACCAGCACGCCCAGGACAGAGACGACAATGAGCCCCTTGACTAACACCACCACCAGCCAGGGCACGACCCGCTGTCAACCGAAGTGTGAGTGGACAGAGTGGTTTGACGTGGACTTCCCAACCTCAGGGGTTGCAGGCGGGGACATGGAAACTTTTGAAAACATCAGGGCTGCTGGGGGCAAGATGTGCTGGGCACCAAAGAGCATAGAGTGCCGGGCGGAGAACTACCCCGAGGTAAGCATCGACCAGGTCGGGCAGGTGCTGACCTGCAGCCTGGAGACGGGGCTGACCTGCAAGAACGAAGAC... | CCTCTCAGGCCGAGACCAGCACGCCCAGGACAGAGACGACAATGAGCCCCTTGACTAACACCACCACCAGCCAGGGCACGACCCGCTGTCAACCGAAGTGTGAGTGGACAGAGTGGTTTGACGTGGACTTCCCAACCTCAGGGGTTGCAGGCGGGGACATGGAAACTTTTGAAAACATCAGGGCTGCTGGGGGCAAGATGTGCTGGGCACCAAAGAGCATAGAGTGCCGGGCGGAGAACTACCCCGAGGTAAGCATCGACCAGGTCGGGCAGGTGCTGACCTGCAGCCTGGAGACGGGGCTGACCTGCAAGAACGAAGAC... |
Task1_train_40610 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GAGCACTACAGCCACCGTGACGGTGCCCACCGGATCCACGGCCACCGCCTCCTCCACCCAGGCAACTGCTGGCACCCCACATGTGAGCACCACGGCCACGACACCCACAGTCACCAGCTCCAAAGCCACTCCCTTCTCCAGTCCAGGGACTGCAACCGCCCTTCCAGCACTGAGAAGCACAGCCACCACACCCACAGCTACCAGCTTTACAGCCATCCCCTCCTCCTCCCTGGGCACCACCTGGACCCGCCTATCACAGACCACCACACCCACGGCCACCATGTCCACAGCCACACCCTCCTCCACTCCAGAGACTGTCC... | GAGCACTACAGCCACCGTGACGGTGCCCACCGGATCCACGGCCACCGCCTCCTCCACCCAGGCAACTGCTGGCACCCCACATGTGAGCACCACGGCCACGACACCCACAGTCACCAGCTCCAAAGCCACTCCCTTCTCCAGTCCAGGGACTGCAACCGCCCTTCCAGCACTGAGAAGCACAGCCACCACACCCACAGCTACCAGCTTTACAGCCATCCCCTCCTCCTCCCTGGGCACCACCTGGACCCGCCTATCACAGACCACCACACCCACGGCCACCATGTCCACAGCCACACCCTCCTCCACTCCAGAGACTGTCC... |
Task1_train_40611 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GAACAGCTCACACTACCAAAGTGCTGACTACCACAACCACGGGCTTCACAGCCACCCCCTCCTCCAGCCCAGGGACGGCACGCACGCTTCCAGTGTGGATCAGCACAACCACCACACCCACAACCAGAGGTTCCACGGTGACCCCCTCCTCCATCCCGGGGACCACCCACACCCCCACAGTGCTGACCACCACCACCACAACTGTGGCCACTGGTTCTATGGCAACACCCTCCTCTAGCACACAGACCAGTGGTACTCCCCCATCACTGACCACCACGGCCACTACGATCACGGCCACCGGCTCCACCACCAACCCCTCC... | GAACAGCTCACACTACCAAAGTGCTGACTACCACAACCACGGGCTTCACAGCCACCCCCTCCTCCAGCCCAGGGACGGCACGCACGCTTCCAGTGTGGATCAGCACAACCACCACACCCACAACCAGAGGTTCCACGGTGACCCCCTCCTCCATCCCGGGGACCACCCACACCCCCACAGTGCTGACCACCACCACCACAACTGTGGCCACTGGTTCTATGGCAACACCCTCCTCTAGCACACAGACCAGTGGTACTCCCCCATCACTGACCACCACGGCCACTACGATCACGGCCACCGGCTCCACCACCAACCCCTCC... |
Task1_train_40612 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGACCACCGAGTCACCCCCTTCTCCAGGGACGACCACCCCGGGCCACACCAGGGCCACCTCCAGGACCACGGCCACGGCCACACCCAGCAAGACCCGCACCTCGACCCTGCTGCCCAGCAGCCCCACATCGGCCCCAATAACCACGGTGGTGACCATGGGCTGTGAGCCCCAGTGTGCCTGGTCAGAGTGGCTGGACTACAGCTACCCCATGCCGGGGCCCTCTGGCGGGGACTTTGACACCTACTCCAACATCCGTGCGGCCGGAGGGGCCGTCTGTGAGCAGCCCCTGGGCCTCGAGTGCCGTGCCCAGGCCCAGCCT... | GGACCACCGAGTCACCCCCTTCTCCAGGGACGACCACCCCGGGCCACACCAGGGCCACCTCCAGGACCACGGCCACGGCCACACCCAGCAAGACCCGCACCTCGACCCTGCTGCCCAGCAGCCCCACATCGGCCCCAATAACCACGGTGGTGACCATGGGCTGTGAGCCCCAGTGTGCCTGGTCAGAGTGGCTGGACTACAGCTACCCCATGCCGGGGCCCTCTGGCGGGGACTTTGACACCTACTCCAACATCCGTGCGGCCGGAGGGGCCGTCTGTGAGCAGCCCCTGGGCCTCGAGTGCCGTGCCCAGGCCCAGCCT... |
Task1_train_40613 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CCCAGAACAGACCACCACACCCATGGCCACCATGTCCACAATCCACCCCTCCTCCACTCCGGAGACCACCCACACCTCCACAGTGCTGACCACGAAGGCCACCACGACAAGGGCCACCAGTTCCATGTCCACCCCCTCCTCCACTCCGGGGACGACCTGGATCCTCACAGAGCTGACCACAGCAGCCACTACAACTGCAGCCACTGGCCCCACGGCCACCCCGTCCTCCACCCCAGGGACCACCTGGATCCTCACAGAGCCCAGCACTACAGCCACCGTGACGGTGCCCACCGGATCCACGGCCACCGCCTCCTCCACCC... | CCCAGAACAGACCACCACACCCATGGCCACCATGTCCACAATCCACCCCTCCTCCACTCCGGAGACCACCCACACCTCCACAGTGCTGACCACGAAGGCCACCACGACAAGGGCCACCAGTTCCATGTCCACCCCCTCCTCCACTCCGGGGACGACCTGGATCCTCACAGAGCTGACCACAGCAGCCACTACAACTGCAGCCACTGGCCCCACGGCCACCCCGTCCTCCACCCCAGGGACCACCTGGATCCTCACAGAGCCCAGCACTACAGCCACCGTGACGGTGCCCACCGGATCCACGGCCACCGCCTCCTCCACCC... |
Task1_train_40614 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | CTCCTCCACCCGGGCAACTGCTGGCACCCTCAAAGTGCTGACCAGCACGGCCACCACACCCACAGTCATCAGCTCCAGAGCCACTCCCTCCTCCAGTCCAGGGACTGCAACCGCCCTTCCAGCACTGAGAAGCACAGCCACCACACCCACAGCTACCAGCGTTACAGCCATCCCCTCTTCCTCCCTGGGCACCGCCTGGACCCGCCTATCACAGACCACCACACCCACGGCCACCATGTCCACAGCCACACCCTCCTCTACTCCAGAGACTGTCCACACCTCCACAGTGCTTACCACCACGACCACCACAACCAGGGCCA... | CTCCTCCACCCGGGCAACTGCTGGCACCCTCAAAGTGCTGACCAGCACGGCCACCACACCCACAGTCATCAGCTCCAGAGCCACTCCCTCCTCCAGTCCAGGGACTGCAACCGCCCTTCCAGCACTGAGAAGCACAGCCACCACACCCACAGCTACCAGCGTTACAGCCATCCCCTCTTCCTCCCTGGGCACCGCCTGGACCCGCCTATCACAGACCACCACACCCACGGCCACCATGTCCACAGCCACACCCTCCTCTACTCCAGAGACTGTCCACACCTCCACAGTGCTTACCACCACGACCACCACAACCAGGGCCA... |
Task1_train_40615 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | GAAGCACAGCCACCACACCCACAGCTACCAGCGTTACAGCCATCCCCTCTTCCTCCCTGGGCACCGCCTGGACCCGCCTATCACAGACCACCACACCCACGGCCACCATGTCCACAGCCACACCCTCCTCTACTCCAGAGACTGTCCACACCTCCACAGTGCTTACCACCACGACCACCACAACCAGGGCCACCGGCTCTGTGGCCACCCCCTCCTCCACCCCAGGAACAGCTCACACTACCAAAGTGCCGACTACCACAACCACGGGCTTCACAGCCACCCCCTCCTCCAGCCCAGGGACGGCACTCACGCCTCCAGTG... | GAAGCACAGCCACCACACCCACAGCTACCAGCGTTACAGCCATCCCCTCTTCCTCCCTGGGCACCGCCTGGACCCGCCTATCACAGACCACCACACCCACGGCCACCATGTCCACAGCCACACCCTCCTCTACTCCAGAGACTGTCCACACCTCCACAGTGCTTACCACCACGACCACCACAACCAGGGCCACCGGCTCTGTGGCCACCCCCTCCTCCACCCCAGGAACAGCTCACACTACCAAAGTGCCGACTACCACAACCACGGGCTTCACAGCCACCCCCTCCTCCAGCCCAGGGACGGCACTCACGCCTCCAGTG... |
Task1_train_40616 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCAACCACCAGTACCACCCAGCACTCGACTCCAGCCCTGTCCAGCCCTCACCCTAGCAGCAGGACCACCGAGTCACCCCCTTCTCCAGGGACGACCACCCCGGGCCACACCAGGGGCACCTCCAGGACCACAGCCACAGCCACACCCAGCAAGACCCGCACCTCGACCCTGCTGCCCAGCAGCCCCACATCGGCCCCCATAACCACGGTGGTGACCACGGGCTGTGAGCCCCAGTGTGCCTGGTCAGAGTGGCTGGACTACAGCTACCCCATGCCGGGGCCCTCTGGCGGGGACTTTGACACCTACTCCAACATCCGTGC... | GCAACCACCAGTACCACCCAGCACTCGACTCCAGCCCTGTCCAGCCCTCACCCTAGCAGCAGGACCACCGAGTCACCCCCTTCTCCAGGGACGACCACCCCGGGCCACACCAGGGGCACCTCCAGGACCACAGCCACAGCCACACCCAGCAAGACCCGCACCTCGACCCTGCTGCCCAGCAGCCCCACATCGGCCCCCATAACCACGGTGGTGACCACGGGCTGTGAGCCCCAGTGTGCCTGGTCAGAGTGGCTGGACTACAGCTACCCCATGCCGGGGCCCTCTGGCGGGGACTTTGACACCTACTCCAACATCCGTGC... |
Task1_train_40617 | 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 | TTCGGCCACCTCAGGCACCTTGGGCACCACCCACATCACAGAGCCTTCCACGGGGACTTCCCACACCCCAGCAGCAACCACCGGTACCACCCAGCACTCGACTCCAGCCCTGTCCAGCCCTCACCCTAGCAGCAGGACCACCGAGTCACCCCCTTCCCCAGGGACGACCACCCCGGGCCACACCACGGCCACCTCCAGGACCACGGCCACGGCCACACCCAGCAAGACCCGCACCTCGACCCTGCTGCCCAGCAGCCCCACATCGGCCCCCATAACCACGGTGGTGACCACGGGCTGTGAGCCCCAGTGTGCCTGGTCAG... | TTCGGCCACCTCAGGCACCTTGGGCACCACCCACATCACAGAGCCTTCCACGGGGACTTCCCACACCCCAGCAGCAACCACCGGTACCACCCAGCACTCGACTCCAGCCCTGTCCAGCCCTCACCCTAGCAGCAGGACCACCGAGTCACCCCCTTCCCCAGGGACGACCACCCCGGGCCACACCACGGCCACCTCCAGGACCACGGCCACGGCCACACCCAGCAAGACCCGCACCTCGACCCTGCTGCCCAGCAGCCCCACATCGGCCCCCATAACCACGGTGGTGACCACGGGCTGTGAGCCCCAGTGTGCCTGGTCAG... |
Task1_train_40618 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TGGGGGAGTTGGGCCAGGTCGTGGAATGCAGCCTGGACTTTGGCCTGGTCTGCAGGAACCGTGAGCAGGTGGGGAAGTTCAAGATGTGCTTCAACTATGAAATCCGTGTGTTCTGCTGCAACTACGGCCACTGCCCCAGCACCCCGGCCACCAGCTCTACGGCCATGCCCTCCTCCACTCCGGGGACGACCTGGATCCTCACAGAGCTGACCACAACAGCCACTACGACTGCATCCACTGGATCCACGGCCACCCCGTCCTCCACCCCGGGAACAGCTCCCCCTCCCAAAGTGCTGACCAGCCCGGCCACCACACCCACA... | TGGGGGAGTTGGGCCAGGTCGTGGAATGCAGCCTGGACTTTGGCCTGGTCTGCAGGAACCGTGAGCAGGTGGGGAAGTTCAAGATGTGCTTCAACTATGAAATCCGTGTGTTCTGCTGCAACTACGGCCACTGCCCCAGCACCCCGGCCACCAGCTCTACGGCCATGCCCTCCTCCACTCCGGGGACGACCTGGATCCTCACAGAGCTGACCACAACAGCCACTACGACTGCATCCACTGGATCCACGGCCACCCCGTCCTCCACCCCGGGAACAGCTCCCCCTCCCAAAGTGCTGACCAGCCCGGCCACCACACCCACA... |
Task1_train_40619 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGGTCTGCAGGAACCGTGAGCAGGTGGGGAAGTTCAAGATGTGCTTCAACTATGAAATCCGTGTGTTCTGCTGCAACTACGGCCACTGCCCCAGCACCCCGGCCACCAGCTCTACGGCCATGCCCTCCTCCACTCCGGGGACGACCTGGATCCTCACAGAGCTGACCACAACAGCCACTACGACTGCATCCACTGGATCCACGGCCACCCCGTCCTCCACCCCGGGAACAGCTCCCCCTCCCAAAGTGCTGACCAGCCCGGCCACCACACCCACAGCCACCAGTTCCAAAGCCACTTCCTCCTCCAGTCCAAGGACTGCA... | TGGTCTGCAGGAACCGTGAGCAGGTGGGGAAGTTCAAGATGTGCTTCAACTATGAAATCCGTGTGTTCTGCTGCAACTACGGCCACTGCCCCAGCACCCCGGCCACCAGCTCTACGGCCATGCCCTCCTCCACTCCGGGGACGACCTGGATCCTCACAGAGCTGACCACAACAGCCACTACGACTGCATCCACTGGATCCACGGCCACCCCGTCCTCCACCCCGGGAACAGCTCCCCCTCCCAAAGTGCTGACCAGCCCGGCCACCACACCCACAGCCACCAGTTCCAAAGCCACTTCCTCCTCCAGTCCAAGGACTGCA... |
Task1_train_40620 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GCAACTGTAGCTCAGTGTTCCCAGCAGCTGCCTGGCCGGATAGGACCAGGGCTCGGCCCCTCCACCCCGGGGTTTCCAGCGCCTCTTCTGTCTTCCTCGTGCCCAGTCACGAGCTCTGGGCGGGCTCGACAGGAACCACAGGTCCAGGGCCTCACTGGTGGCTGCTGCCCCCATGAGGGCTGTCCGCGCTCCCAGCTCAGCCCTGAAAGCTCTGGGTCCAGTTCCAGCCCTGGGTGTCATCCTGGCCCAGACAGGCTGGGTTGTGCATGGGGTCCCCGTCGCCTCCCTGCCCCTTGGCTGTGTCTGGTGAGGGAGTTGGA... | GCAACTGTAGCTCAGTGTTCCCAGCAGCTGCCTGGCCGGATAGGACCAGGGCTCGGCCCCTCCACCCCGGGGTTTCCAGCGCCTCTTCTGTCTTCCTCGTGCCCAGTCACGAGCTCTGGGCGGGCTCGACAGGAACCACAGGTCCAGGGCCTCACTGGTGGCTGCTGCCCCCATGAGGGCTGTCCGCGCTCCCAGCTCAGCCCTGAAAGCTCTGGGTCCAGTTCCAGCCCTGGGTGTCATCCTGGCCCAGACAGGCTGGGTTGTGCATGGGGTCCCCGTCGCCTCCCTGCCCCTTGGCTGTGTCTGGTGAGGGAGTTGGA... |
Task1_train_40621 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TCAGTGTTCCCAGCAGCTGCCTGGCCGGATAGGACCAGGGCTCGGCCCCTCCACCCCGGGGTTTCCAGCGCCTCTTCTGTCTTCCTCGTGCCCAGTCACGAGCTCTGGGCGGGCTCGACAGGAACCACAGGTCCAGGGCCTCACTGGTGGCTGCTGCCCCCATGAGGGCTGTCCGCGCTCCCAGCTCAGCCCTGAAAGCTCTGGGTCCAGTTCCAGCCCTGGGTGTCATCCTGGCCCAGACAGGCTGGGTTGTGCATGGGGTCCCCGTCGCCTCCCTGCCCCTTGGCTGTGTCTGGTGAGGGAGTTGGAGGGTCGTCACC... | TCAGTGTTCCCAGCAGCTGCCTGGCCGGATAGGACCAGGGCTCGGCCCCTCCACCCCGGGGTTTCCAGCGCCTCTTCTGTCTTCCTCGTGCCCAGTCACGAGCTCTGGGCGGGCTCGACAGGAACCACAGGTCCAGGGCCTCACTGGTGGCTGCTGCCCCCATGAGGGCTGTCCGCGCTCCCAGCTCAGCCCTGAAAGCTCTGGGTCCAGTTCCAGCCCTGGGTGTCATCCTGGCCCAGACAGGCTGGGTTGTGCATGGGGTCCCCGTCGCCTCCCTGCCCCTTGGCTGTGTCTGGTGAGGGAGTTGGAGGGTCGTCACC... |
Task1_train_40622 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTAGCAGGGAGGAGACGCGCCTCAATCCCAGAGCCCTCACACGACCCAGGCAGACTTGCTGGTCTTTTGGGTGGCAAGTGGCCCTGAGGCCCTCTGAGAAGTCTCCATGTTTCTCTTAGTTTGAGTGGATTTCTGTCCCTTGGTTTGAAAGGATTCCTGGAAAGGCATTACATGCAATTAATTCACACACATCTACTACCACCATGATGCCAGCTCCAGATGAGAAGGACCAAGAGGCAAATCTGGGTGGCCTAGGCCCTCCAAGGGGACATAGGTCTGCCCAACACCACATCCTACACTCCTCCAAGGACCCCTTTTCC... | CTAGCAGGGAGGAGACGCGCCTCAATCCCAGAGCCCTCACACGACCCAGGCAGACTTGCTGGTCTTTTGGGTGGCAAGTGGCCCTGAGGCCCTCTGAGAAGTCTCCATGTTTCTCTTAGTTTGAGTGGATTTCTGTCCCTTGGTTTGAAAGGATTCCTGGAAAGGCATTACATGCAATTAATTCACACACATCTACTACCACCATGATGCCAGCTCCAGATGAGAAGGACCAAGAGGCAAATCTGGGTGGCCTAGGCCCTCCAAGGGGACATAGGTCTGCCCAACACCACATCCTACACTCCTCCAAGGACCCCTTTTCC... |
Task1_train_40623 | 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 | TTCATGTCTGCTGCCACCTTCTGGAGTTTCCCAGTTTGGATTTTTGAGTAAACTGTCTTAAGCAGCATTTCCTTTTAACGTCGTGAAACTAACGATAGCCATGTCCCCTAGCAAGATGCACCTTTGACACACTTTTATTCCCTCTCCTAAAAGTGGCTGAATTAATCTAAGCCTTTATTTCTAGATTATTTCATTTTTCCTTACATTGCATCTCTTTTCTCTCAGAAATTTGTCCTGGAAATTCCCACTCTGCTCTTCCCTGGCATTATCAGCAGTCGCTTAGATCTGTGGGTGTTCTGTGGGAGCTCATTTCTCACCAG... | TTCATGTCTGCTGCCACCTTCTGGAGTTTCCCAGTTTGGATTTTTGAGTAAACTGTCTTAAGCAGCATTTCCTTTTAACGTCGTGAAACTAACGATAGCCATGTCCCCTAGCAAGATGCACCTTTGACACACTTTTATTCCCTCTCCTAAAAGTGGCTGAATTAATCTAAGCCTTTATTTCTAGATTATTTCATTTTTCCTTACATTGCATCTCTTTTCTCTCAGAAATTTGTCCTGGAAATTCCCACTCTGCTCTTCCCTGGCATTATCAGCAGTCGCTTAGATCTGTGGGTGTTCTGTGGGAGCTCATTTCTCACCAG... |
Task1_train_40624 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CCTATGGTATCAGAGTGTTCCAGGCCTGGGGCACTGCACTCACTGCAGACCTGGCCTGAGATTCAGCAGCTGGGCACCCTATGAGATCTAGTTTCTGAATGGCGTCGTCACCTGACTGGGCATACAAGCCACAGGCCCCGTGGTCTGTGGGCGGCCATTGTCCTGTGTGTGGGGTGGGGCACTGGGACCCTCCCACAGCTTTGGCTTTCTCAGAGTTTCTATCCCTGTGTCCTCCTCTGTCAGCAAAGCCCAAAGGTGGGGGGCTCCTGAGCTGCCACCTCCTTTGTTTCTCCAACTCTGCCGGTTCATTGGACTATGCC... | CCTATGGTATCAGAGTGTTCCAGGCCTGGGGCACTGCACTCACTGCAGACCTGGCCTGAGATTCAGCAGCTGGGCACCCTATGAGATCTAGTTTCTGAATGGCGTCGTCACCTGACTGGGCATACAAGCCACAGGCCCCGTGGTCTGTGGGCGGCCATTGTCCTGTGTGTGGGGTGGGGCACTGGGACCCTCCCACAGCTTTGGCTTTCTCAGAGTTTCTATCCCTGTGTCCTCCTCTGTCAGCAAAGCCCAAAGGTGGGGGGCTCCTGAGCTGCCACCTCCTTTGTTTCTCCAACTCTGCCGGTTCATTGGACTATGCC... |
Task1_train_40625 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CCGGGCACACGCTCCCAACCCCTCCCCTCCCAGCGGAACAAGCGCACCGCGTTATCAGCCCGGGGATCCGTGACTGTGGCAGCTGTGGCTGGAGGGGACTTCTGAGTCCAATCCCTGCAACCAGGGACCCTGGGCAGGCTTGCTTGGTGCCAGCTCAGCTCACTGCACACAAAACCGCTTCTAGGGCCTGGGAGGCAAGAAGGCCCAGCTAGGCCAGCCCCCCCACGCCACCTGGGGCCATTTATTTCCCGGGACAAGAGGGCTGAGGAGGGTGACTGGTAGGCCTGCTCTGAGGGTCCCCGAGAGCAGAAATAGCCTCT... | CCGGGCACACGCTCCCAACCCCTCCCCTCCCAGCGGAACAAGCGCACCGCGTTATCAGCCCGGGGATCCGTGACTGTGGCAGCTGTGGCTGGAGGGGACTTCTGAGTCCAATCCCTGCAACCAGGGACCCTGGGCAGGCTTGCTTGGTGCCAGCTCAGCTCACTGCACACAAAACCGCTTCTAGGGCCTGGGAGGCAAGAAGGCCCAGCTAGGCCAGCCCCCCCACGCCACCTGGGGCCATTTATTTCCCGGGACAAGAGGGCTGAGGAGGGTGACTGGTAGGCCTGCTCTGAGGGTCCCCGAGAGCAGAAATAGCCTCT... |
Task1_train_40626 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | AGCCCCAGCCCTGCTGAGAGCAAGACCACAGCTGGTGGTTCACCCAGAAAGTCAGTGGCTGGAGCAGGGTGGAGGGCTGGCCTGGCTCACGGGGCCAAGAGGCAGGAGAATTGCGTTGCCCAAGTGATTCCTGAGGCAGCCCTGCAGCGACATCCCGGAAGGGCAGGACCTGGGCGACGGGGCCAGGGTTCGTGACTCACAGCAAGCGATGTCCAGCAGTTTGCAGTGGATGGAGGGGACCCACAGGTTGGAGGAGCCCGTGTCGAAGACGACTGTGAAGCACTGGGGGGGCGTCCCGATGCCAATCTCCCCGTAGTACT... | AGCCCCAGCCCTGCTGAGAGCAAGACCACAGCTGGTGGTTCACCCAGAAAGTCAGTGGCTGGAGCAGGGTGGAGGGCTGGCCTGGCTCACGGGGCCAAGAGGCAGGAGAATTGCGTTGCCCAAGTGATTCCTGAGGCAGCCCTGCAGCGACATCCCGGAAGGGCAGGACCTGGGCGACGGGGCCAGGGTTCGTGACTCACAGCAAGCGATGTCCAGCAGTTTGCAGTGGATGGAGGGGACCCACAGGTTGGAGGAGCCCGTGTCGAAGACGACTGTGAAGCACTGGGGGGGCGTCCCGATGCCAATCTCCCCGTAGTACT... |
Task1_train_40627 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GCCTCCCAGAGGCTCGGTGATGGGGTGCAGCCTCCACGGAGGCTCGATGATGGGGTGCAGCCTCTCTGGAGGCTCAGGTCATGGGGTACAGCCTCCCCGGAGGCTCAGGTCATGGGATGCAGCCTCCCAGAGGCTCGGTGATGGGGTGCAGCCTCCCCAGAGGCTCAGGTCATGGGGTGCAGCCTCCTCCCAGAGGCTCGGTGATGGGGTGCAGCCTCCCCAGAGGCTCAGGTCATGGGGTGCAGCCTCCCCAGATGCCTGGTTGATGGGGTACAGCCTCCCGGGATGAAGAGGCACAGACAGTATGCATGAAAGGTGAG... | GCCTCCCAGAGGCTCGGTGATGGGGTGCAGCCTCCACGGAGGCTCGATGATGGGGTGCAGCCTCTCTGGAGGCTCAGGTCATGGGGTACAGCCTCCCCGGAGGCTCAGGTCATGGGATGCAGCCTCCCAGAGGCTCGGTGATGGGGTGCAGCCTCCCCAGAGGCTCAGGTCATGGGGTGCAGCCTCCTCCCAGAGGCTCGGTGATGGGGTGCAGCCTCCCCAGAGGCTCAGGTCATGGGGTGCAGCCTCCCCAGATGCCTGGTTGATGGGGTACAGCCTCCCGGGATGAAGAGGCACAGACAGTATGCATGAAAGGTGAG... |
Task1_train_40628 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AAAAGAGAAGTTGCCTTGAAACTCCACGTAGGGAGGAGGCAGTGGCCTGTTTGAATCTGGCCGGCACAGTCCCGCTCCAGGGACCCTGCGGACCCAGCCCATTCCATCAGCCACCACCAGTAGGAGCGCTCCGCCAGCCACGTGTGGGACGCCGGACCCACCTGGGAGTGTCCCCCAGGAGCTGAGGGGCTGCCGAGGCCCGTGAGCTTCACTGCACACCCACACTGCATCTGCAGGGGACTCACCCAAAGGGTCCCCCGAACTCGACAAGCTCCGTCATTTGTGAGGCCCAGTGCAGAATGAAAATGTGCAGCATCTTG... | AAAAGAGAAGTTGCCTTGAAACTCCACGTAGGGAGGAGGCAGTGGCCTGTTTGAATCTGGCCGGCACAGTCCCGCTCCAGGGACCCTGCGGACCCAGCCCATTCCATCAGCCACCACCAGTAGGAGCGCTCCGCCAGCCACGTGTGGGACGCCGGACCCACCTGGGAGTGTCCCCCAGGAGCTGAGGGGCTGCCGAGGCCCGTGAGCTTCACTGCACACCCACACTGCATCTGCAGGGGACTCACCCAAAGGGTCCCCCGAACTCGACAAGCTCCGTCATTTGTGAGGCCCAGTGCAGAATGAAAATGTGCAGCATCTTG... |
Task1_train_40629 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGGGCCCCGCTGGGCTCTCATTGCCGGCGCCCTTGCCGCGGGCGTCCTCCTCGTCTCCTGCCTCCTCTGTGCTGCCTGCTGCTGCTGCCGCCGCCACAGGAAGAAGCCCAGGGACAAGGAGTCCGTGGGTCTGGGCAGTGCCCGCGGCACCACCACCACCCACCTGGTGAGGAGCGGCTCCTTGCTCACTCAGTCCAGAGAGGGCTTGAAATCCAGGCTCCAGAGCCCAGGGCAGCGAGGCGAGTTCAGCCCCAGGGATGGTTTAACCCCCACAGAGGCAGGGCGTTGAGGACCTTCCTGGCAGGGAAAGTGGGTGAACA... | AGGGCCCCGCTGGGCTCTCATTGCCGGCGCCCTTGCCGCGGGCGTCCTCCTCGTCTCCTGCCTCCTCTGTGCTGCCTGCTGCTGCTGCCGCCGCCACAGGAAGAAGCCCAGGGACAAGGAGTCCGTGGGTCTGGGCAGTGCCCGCGGCACCACCACCACCCACCTGGTGAGGAGCGGCTCCTTGCTCACTCAGTCCAGAGAGGGCTTGAAATCCAGGCTCCAGAGCCCAGGGCAGCGAGGCGAGTTCAGCCCCAGGGATGGTTTAACCCCCACAGAGGCAGGGCGTTGAGGACCTTCCTGGCAGGGAAAGTGGGTGAACA... |
Task1_train_40630 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | CAGGGCTCTAAGGCCCCTCAGGCAGGGACCCACCCTGAGCAGCCTGGTCCAGGGACCTCTGGGGCTCCTGATGTGGCCAGTGGGGCAGGAATGGGCTGGCAGCCTGCTGGGCTGGCCCTGAGGGGGCTGGGGGAAGCCAGGCCTCCAACCACAGTGTCCAAAAGGGTGTGGCTGCCTTGGGCCCATCCAGGCCTGAGATCCTGAGGGTGGGGTAGCCCCCGCCCTGGCAGGGCTGGAAGTCGGTCTTCGGACAGAGCCCGTCCTGCCCAGAAGCCCAGGCGAGCCAGCAGCAGGGGTGCAGGGACCGAGTGGCCCAGCCC... | CAGGGCTCTAAGGCCCCTCAGGCAGGGACCCACCCTGAGCAGCCTGGTCCAGGGACCTCTGGGGCTCCTGATGTGGCCAGTGGGGCAGGAATGGGCTGGCAGCCTGCTGGGCTGGCCCTGAGGGGGCTGGGGGAAGCCAGGCCTCCAACCACAGTGTCCAAAAGGGTGTGGCTGCCTTGGGCCCATCCAGGCCTGAGATCCTGAGGGTGGGGTAGCCCCCGCCCTGGCAGGGCTGGAAGTCGGTCTTCGGACAGAGCCCGTCCTGCCCAGAAGCCCAGGCGAGCCAGCAGCAGGGGTGCAGGGACCGAGTGGCCCAGCCC... |
Task1_train_40631 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TCTGTGAGCGGGGCTGGTGGTGGGACAGGAGGTGTCCTGCCTGGACGTGCTCAGGCCCTCCTTTCCTCAGCCTTCGACCTCCCCTTTCTCCAACACGCCCTGCCTTTGGGGTGCAGGAGGGAGCACCCGCAGGTGGGGTGGAGGTGCCGCCTGGCGGTGGGCTGCGGCCAGTCTCCCTGGACTCCAGTATCTTCTTCCTGGGCCCTCCAGGGTCACCTGGGTCTAGGTCCTGGTTCTACTTAGGGAGGGAGGCAGGCTGGGAGAGGGGGACAGAGGGCCTTTTGTCCTGTCCTTGAGTTTCTTCAGGCTTGAATGGGCCT... | TCTGTGAGCGGGGCTGGTGGTGGGACAGGAGGTGTCCTGCCTGGACGTGCTCAGGCCCTCCTTTCCTCAGCCTTCGACCTCCCCTTTCTCCAACACGCCCTGCCTTTGGGGTGCAGGAGGGAGCACCCGCAGGTGGGGTGGAGGTGCCGCCTGGCGGTGGGCTGCGGCCAGTCTCCCTGGACTCCAGTATCTTCTTCCTGGGCCCTCCAGGGTCACCTGGGTCTAGGTCCTGGTTCTACTTAGGGAGGGAGGCAGGCTGGGAGAGGGGGACAGAGGGCCTTTTGTCCTGTCCTTGAGTTTCTTCAGGCTTGAATGGGCCT... |
Task1_train_40632 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CAGGAGGTGTCCTGCCTGGACGTGCTCAGGCCCTCCTTTCCTCAGCCTTCGACCTCCCCTTTCTCCAACACGCCCTGCCTTTGGGGTGCAGGAGGGAGCACCCGCAGGTGGGGTGGAGGTGCCGCCTGGCGGTGGGCTGCGGCCAGTCTCCCTGGACTCCAGTATCTTCTTCCTGGGCCCTCCAGGGTCACCTGGGTCTAGGTCCTGGTTCTACTTAGGGAGGGAGGCAGGCTGGGAGAGGGGGACAGAGGGCCTTTTGTCCTGTCCTTGAGTTTCTTCAGGCTTGAATGGGCCTTGGAGTCCCACCTTCATCCCCACAG... | CAGGAGGTGTCCTGCCTGGACGTGCTCAGGCCCTCCTTTCCTCAGCCTTCGACCTCCCCTTTCTCCAACACGCCCTGCCTTTGGGGTGCAGGAGGGAGCACCCGCAGGTGGGGTGGAGGTGCCGCCTGGCGGTGGGCTGCGGCCAGTCTCCCTGGACTCCAGTATCTTCTTCCTGGGCCCTCCAGGGTCACCTGGGTCTAGGTCCTGGTTCTACTTAGGGAGGGAGGCAGGCTGGGAGAGGGGGACAGAGGGCCTTTTGTCCTGTCCTTGAGTTTCTTCAGGCTTGAATGGGCCTTGGAGTCCCACCTTCATCCCCACAG... |
Task1_train_40633 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | TGTCCTCCTACCATCTTCCCCTGCCAAACCCTGACTCTCAAGCAGCTGTGGCAGAGGCTTTTTCTGGTACCTCTGTGTCCCTCTCCTGTGGTTGGCCACCCCCACCAGAGCCTGGCTGACTGCTGAGTAGGCCCCTCCACTCTCCCCACCAGGGCCACAGCCCCTTCTCTGTCCCGCTTGGCCAAGCTGTTCCCATAGGGTTGGGACTGAGGGCTCCCTCCTCATCCAGCTGTCAAAGCCTGGGCATGGCCAGTGCTGAGACCCTCGCTGTCCCACCAGCGAATCCCTCGAGTTCTGCCCCCTCAGGCTGTCAGCCCAGG... | TGTCCTCCTACCATCTTCCCCTGCCAAACCCTGACTCTCAAGCAGCTGTGGCAGAGGCTTTTTCTGGTACCTCTGTGTCCCTCTCCTGTGGTTGGCCACCCCCACCAGAGCCTGGCTGACTGCTGAGTAGGCCCCTCCACTCTCCCCACCAGGGCCACAGCCCCTTCTCTGTCCCGCTTGGCCAAGCTGTTCCCATAGGGTTGGGACTGAGGGCTCCCTCCTCATCCAGCTGTCAAAGCCTGGGCATGGCCAGTGCTGAGACCCTCGCTGTCCCACCAGCGAATCCCTCGAGTTCTGCCCCCTCAGGCTGTCAGCCCAGG... |
Task1_train_40634 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | TTGGAGGGTGGAAAGAATTCCATCAGGGAAAGAACGAGTGGGCCCCCAGCGTTGGGATGGCAGGAAGTGGGGGTCCTGGGGACGCCTTCCATGGCCCATCCATGGCTCTGCCTCCCAGGGCTACCAGCACTGCCTTTGTGGGCCCTTGGTGCCACCCGGCCAGGCTACAACCTCGCACGTGGGCCTTGGTGCCCCGGCCAGAGGCGCGGACACCCTTCTGGGGGCGCCCCAGGACAGACAGGGGATGGGGGCGAGCAAAGGAAGGCCCAGCCCCAGTACTGAGCCTGCTCCACCAAGGACAAGAGCCACAGCTCCCGGCC... | TTGGAGGGTGGAAAGAATTCCATCAGGGAAAGAACGAGTGGGCCCCCAGCGTTGGGATGGCAGGAAGTGGGGGTCCTGGGGACGCCTTCCATGGCCCATCCATGGCTCTGCCTCCCAGGGCTACCAGCACTGCCTTTGTGGGCCCTTGGTGCCACCCGGCCAGGCTACAACCTCGCACGTGGGCCTTGGTGCCCCGGCCAGAGGCGCGGACACCCTTCTGGGGGCGCCCCAGGACAGACAGGGGATGGGGGCGAGCAAAGGAAGGCCCAGCCCCAGTACTGAGCCTGCTCCACCAAGGACAAGAGCCACAGCTCCCGGCC... |
Task1_train_40635 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | GTTCCCCCTCCCTCGTGGGGCTGCCTGCTGAGTGCTCTCCTTATTTAGTCAGAAGTGACCAGGGCAGGCTGGAGGCTGGGGCAGACGCGGGTCACCCTGAGGCTCGAAAAGCACACCGGCTCCCCTCTAGTCAAGACCAGCATCGGGGTTCTTCCTCAAGACTGGCTCCTCCCCCACTACTTCCAGCCCCCGGAGGTAGGAAGGGTCCCGCCAGCAGTCCAAGGGTGTTGGGAGGGGGCCAGGGTCTCCTCCCACCCAGAGCTTGGCCGGCAGGAACTTTAGCCCCAAGCAGCGTCCGCCCCCCAGCCCTGAACCAGCAC... | GTTCCCCCTCCCTCGTGGGGCTGCCTGCTGAGTGCTCTCCTTATTTAGTCAGAAGTGACCAGGGCAGGCTGGAGGCTGGGGCAGACGCGGGTCACCCTGAGGCTCGAAAAGCACACCGGCTCCCCTCTAGTCAAGACCAGCATCGGGGTTCTTCCTCAAGACTGGCTCCTCCCCCACTACTTCCAGCCCCCGGAGGTAGGAAGGGTCCCGCCAGCAGTCCAAGGGTGTTGGGAGGGGGCCAGGGTCTCCTCCCACCCAGAGCTTGGCCGGCAGGAACTTTAGCCCCAAGCAGCGTCCGCCCCCCAGCCCTGAACCAGCAC... |
Task1_train_40636 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTGGGGGACAGAGTCCTGGGTCTCAACAAGGTGAAAGCTAGCCCCAGCTCTGGCCCAGGGCAGCCGAGGGCACCGCGAACCATGGCTGCATCTCTTTTGGGTGGGCGGCCTTGCCCTCTCCTGAGGCCTCAGGTCAGAGGTCCCCCAGGACAGAAGTCACAGAAAATTTGGCCCCTCAAAAGACACTCCTCAGCCCCCAGCACCAGCCAGTGCCAGCTGCCCTGCAAGTCCTGGAAGGCTGGGGCAGCTCCAGGAGTCCCTGGACACCAAAGGGCTCCTCCTGCTGCCCTCCACTCCAACACACGGTCCCCCACAGAGCA... | TTGGGGGACAGAGTCCTGGGTCTCAACAAGGTGAAAGCTAGCCCCAGCTCTGGCCCAGGGCAGCCGAGGGCACCGCGAACCATGGCTGCATCTCTTTTGGGTGGGCGGCCTTGCCCTCTCCTGAGGCCTCAGGTCAGAGGTCCCCCAGGACAGAAGTCACAGAAAATTTGGCCCCTCAAAAGACACTCCTCAGCCCCCAGCACCAGCCAGTGCCAGCTGCCCTGCAAGTCCTGGAAGGCTGGGGCAGCTCCAGGAGTCCCTGGACACCAAAGGGCTCCTCCTGCTGCCCTCCACTCCAACACACGGTCCCCCACAGAGCA... |
Task1_train_40637 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TCCTGGGTCTCAACAAGGTGAAAGCTAGCCCCAGCTCTGGCCCAGGGCAGCCGAGGGCACCGCGAACCATGGCTGCATCTCTTTTGGGTGGGCGGCCTTGCCCTCTCCTGAGGCCTCAGGTCAGAGGTCCCCCAGGACAGAAGTCACAGAAAATTTGGCCCCTCAAAAGACACTCCTCAGCCCCCAGCACCAGCCAGTGCCAGCTGCCCTGCAAGTCCTGGAAGGCTGGGGCAGCTCCAGGAGTCCCTGGACACCAAAGGGCTCCTCCTGCTGCCCTCCACTCCAACACACGGTCCCCCACAGAGCACTGACCCTCCCCT... | TCCTGGGTCTCAACAAGGTGAAAGCTAGCCCCAGCTCTGGCCCAGGGCAGCCGAGGGCACCGCGAACCATGGCTGCATCTCTTTTGGGTGGGCGGCCTTGCCCTCTCCTGAGGCCTCAGGTCAGAGGTCCCCCAGGACAGAAGTCACAGAAAATTTGGCCCCTCAAAAGACACTCCTCAGCCCCCAGCACCAGCCAGTGCCAGCTGCCCTGCAAGTCCTGGAAGGCTGGGGCAGCTCCAGGAGTCCCTGGACACCAAAGGGCTCCTCCTGCTGCCCTCCACTCCAACACACGGTCCCCCACAGAGCACTGACCCTCCCCT... |
Task1_train_40638 | 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 | CTCTAGCCCCCCTGGGCCTCAGTTTCCCCACTGGGATTTGGGGACATGGAAAGCCCTGGAGCAGAGCTGCCTGGCAGGAGGCACTGATGCTGGTGACAAGATGGGTCCTCCCCTTTGTCCTTCCCTCCCACCCCCCAGGTCCAGCGTCAGCCTGCAGGACGGAGTCTGGGTCCCGAGCGCAGGGGCCCCTCACTGCCTGTACTGGAAGGCGATCTCAGCAATCAGCTTCCTGCGCTGGCGGTACACCTGGTCCGAGAAGCCCTGAGGGCAGAGGGGATGCACGGGTCAGGAGGCTGTGCTGGGGTGGGGGCACAGGCCAC... | CTCTAGCCCCCCTGGGCCTCAGTTTCCCCACTGGGATTTGGGGACATGGAAAGCCCTGGAGCAGAGCTGCCTGGCAGGAGGCACTGATGCTGGTGACAAGATGGGTCCTCCCCTTTGTCCTTCCCTCCCACCCCCCAGGTCCAGCGTCAGCCTGCAGGACGGAGTCTGGGTCCCGAGCGCAGGGGCCCCTCACTGCCTGTACTGGAAGGCGATCTCAGCAATCAGCTTCCTGCGCTGGCGGTACACCTGGTCCGAGAAGCCCTGAGGGCAGAGGGGATGCACGGGTCAGGAGGCTGTGCTGGGGTGGGGGCACAGGCCAC... |
Task1_train_40639 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCTGGGACCCAGGAATTCACAGGAAGGAGAGAGGAAAAAGGAAGTCCCTGGCGGGTAAACACATATGCATGCACACACATCCACGTCTGCACACGCATCCACGCCTGCACACGCATCCATGCCTGCACATGCATCCACGCCCAATCTCTTCCCTGGAAATAAAGCCAGGGGCCCTTAGGCCAGCTTGCAGTGGGGCCCAGCCCTTAGGACAGGCTCCTTGGTGGGGTAGGGGTGGGGGCAGCTGTCCTCCTGGGCCAGCTCCTTGGGGCTGAACCCGCTGCTCGAGGGGTCTTCCAGGCTCCCAGCGGCCGGCACCACCT... | CCTGGGACCCAGGAATTCACAGGAAGGAGAGAGGAAAAAGGAAGTCCCTGGCGGGTAAACACATATGCATGCACACACATCCACGTCTGCACACGCATCCACGCCTGCACACGCATCCATGCCTGCACATGCATCCACGCCCAATCTCTTCCCTGGAAATAAAGCCAGGGGCCCTTAGGCCAGCTTGCAGTGGGGCCCAGCCCTTAGGACAGGCTCCTTGGTGGGGTAGGGGTGGGGGCAGCTGTCCTCCTGGGCCAGCTCCTTGGGGCTGAACCCGCTGCTCGAGGGGTCTTCCAGGCTCCCAGCGGCCGGCACCACCT... |
Task1_train_40640 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CCCAGGAATTCACAGGAAGGAGAGAGGAAAAAGGAAGTCCCTGGCGGGTAAACACATATGCATGCACACACATCCACGTCTGCACACGCATCCACGCCTGCACACGCATCCATGCCTGCACATGCATCCACGCCCAATCTCTTCCCTGGAAATAAAGCCAGGGGCCCTTAGGCCAGCTTGCAGTGGGGCCCAGCCCTTAGGACAGGCTCCTTGGTGGGGTAGGGGTGGGGGCAGCTGTCCTCCTGGGCCAGCTCCTTGGGGCTGAACCCGCTGCTCGAGGGGTCTTCCAGGCTCCCAGCGGCCGGCACCACCTCTAGAGC... | CCCAGGAATTCACAGGAAGGAGAGAGGAAAAAGGAAGTCCCTGGCGGGTAAACACATATGCATGCACACACATCCACGTCTGCACACGCATCCACGCCTGCACACGCATCCATGCCTGCACATGCATCCACGCCCAATCTCTTCCCTGGAAATAAAGCCAGGGGCCCTTAGGCCAGCTTGCAGTGGGGCCCAGCCCTTAGGACAGGCTCCTTGGTGGGGTAGGGGTGGGGGCAGCTGTCCTCCTGGGCCAGCTCCTTGGGGCTGAACCCGCTGCTCGAGGGGTCTTCCAGGCTCCCAGCGGCCGGCACCACCTCTAGAGC... |
Task1_train_40641 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TGTGGGTCTCCGTCTATCCCACGGGCACCCATGCTCCTGGCATCACCCTGAATGGGGCCCCAGGGTTTGAAGGGCCCAGACCCAACCTGCTCCAGCCTGTGGACCACCCAGGCGGGCACAGTGCTGCCTGAGGGGGCTGGCGTTTCACCGGGGCCTCAGGACTCCTGGGGGAGCTGCCCGGTCGGTGGCTAGACTCACCGTCAGGTACTCCAGGTCCTCAGGGCACCAGCATGAAGGCAAAGGCGGCTGCCCAGACCCTGAGTGGGAGGACATCCCCAGGGTTCTTAGCCTGGGTGACCTCTGCCACCATCCATAAAACT... | TGTGGGTCTCCGTCTATCCCACGGGCACCCATGCTCCTGGCATCACCCTGAATGGGGCCCCAGGGTTTGAAGGGCCCAGACCCAACCTGCTCCAGCCTGTGGACCACCCAGGCGGGCACAGTGCTGCCTGAGGGGGCTGGCGTTTCACCGGGGCCTCAGGACTCCTGGGGGAGCTGCCCGGTCGGTGGCTAGACTCACCGTCAGGTACTCCAGGTCCTCAGGGCACCAGCATGAAGGCAAAGGCGGCTGCCCAGACCCTGAGTGGGAGGACATCCCCAGGGTTCTTAGCCTGGGTGACCTCTGCCACCATCCATAAAACT... |
Task1_train_40642 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GAGAACAACGGGCAAGTGCCGGGGGCGGGTGCGCAGACGTTTCCACCAGAGAACGCCCCACTCCACGACTAGGGGCACGGGCATCAGTGAGAGAGAGGGGACAGTGGTTGGCCGGGCCATGGAGACCCAGGCAGAGTATGGAGAGAAAGTGAGGTGAGGGAGGTGGGCTCAACTGCAAAGAGAGAGGCCACAGCATCCTGAGCAGGCACCACACCTGTCCCAAGCCTCACCAGCACTGGGCTAGCTGGTGCCTTGTTTCAGAAAAGAAGGCAAAACAGAAGATCCTACAGCCCCGGCCCTGGAGAGGCTCAGGCTCAGGG... | GAGAACAACGGGCAAGTGCCGGGGGCGGGTGCGCAGACGTTTCCACCAGAGAACGCCCCACTCCACGACTAGGGGCACGGGCATCAGTGAGAGAGAGGGGACAGTGGTTGGCCGGGCCATGGAGACCCAGGCAGAGTATGGAGAGAAAGTGAGGTGAGGGAGGTGGGCTCAACTGCAAAGAGAGAGGCCACAGCATCCTGAGCAGGCACCACACCTGTCCCAAGCCTCACCAGCACTGGGCTAGCTGGTGCCTTGTTTCAGAAAAGAAGGCAAAACAGAAGATCCTACAGCCCCGGCCCTGGAGAGGCTCAGGCTCAGGG... |
Task1_train_40643 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | GCCGCGGCGGCGTTCCGCTGCAGAGGACGGGAGTGCGAATCTGGGAAGCAGGGTTCTGGTTGAACTCCAGCTTCGTCTGCAACATACTGTGTGACTTGGGCAAATTATTTCCCCCGCCCCGTTCCTGCCAGCTTTAAAACGGTCATCAGTGGGGGGTGCTGCGTATCCCCTTTCACTGGGGTGGCTTCTTCACTGAGGAGAGTCGCGCCTCAGAGGAACTGAGGTCCTGCCTGTGTTCGACCTGGTGGGGGGCACTAAGAGCCCCTGATAGTACCCCTGACCCCATCCTTATTGGGTGCACAAGACACAGGTCACTCTGG... | GCCGCGGCGGCGTTCCGCTGCAGAGGACGGGAGTGCGAATCTGGGAAGCAGGGTTCTGGTTGAACTCCAGCTTCGTCTGCAACATACTGTGTGACTTGGGCAAATTATTTCCCCCGCCCCGTTCCTGCCAGCTTTAAAACGGTCATCAGTGGGGGGTGCTGCGTATCCCCTTTCACTGGGGTGGCTTCTTCACTGAGGAGAGTCGCGCCTCAGAGGAACTGAGGTCCTGCCTGTGTTCGACCTGGTGGGGGGCACTAAGAGCCCCTGATAGTACCCCTGACCCCATCCTTATTGGGTGCACAAGACACAGGTCACTCTGG... |
Task1_train_40644 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ATTTCCCCCGCCCCGTTCCTGCCAGCTTTAAAACGGTCATCAGTGGGGGGTGCTGCGTATCCCCTTTCACTGGGGTGGCTTCTTCACTGAGGAGAGTCGCGCCTCAGAGGAACTGAGGTCCTGCCTGTGTTCGACCTGGTGGGGGGCACTAAGAGCCCCTGATAGTACCCCTGACCCCATCCTTATTGGGTGCACAAGACACAGGTCACTCTGGGCGGGCAAGGAGTTTTGGTAGCAGGAGAGGAGTCGGTGGATGGATGGCTGAGGACAGTGCAGAAGGGTGTGGCTGGGCCGTCTTTTTTTGCCTGGAAATTCAAGTT... | ATTTCCCCCGCCCCGTTCCTGCCAGCTTTAAAACGGTCATCAGTGGGGGGTGCTGCGTATCCCCTTTCACTGGGGTGGCTTCTTCACTGAGGAGAGTCGCGCCTCAGAGGAACTGAGGTCCTGCCTGTGTTCGACCTGGTGGGGGGCACTAAGAGCCCCTGATAGTACCCCTGACCCCATCCTTATTGGGTGCACAAGACACAGGTCACTCTGGGCGGGCAAGGAGTTTTGGTAGCAGGAGAGGAGTCGGTGGATGGATGGCTGAGGACAGTGCAGAAGGGTGTGGCTGGGCCGTCTTTTTTTGCCTGGAAATTCAAGTT... |
Task1_train_40645 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCCCACACCCTCCCCGACTCTGTGATTTGGGAAGGCGCCACCAGGCCGGGCTGGAAATTAAATTGTCCCTGGGGCCTGGAGACCCAGAGAACAAGCTCGTCACCACAGCTCAACCCCAGCTCCGGCTCGGCACGAGTGCAGAGTGGGGCAGGGGTCTGTTCTGGGCTCTGAGGAGACCTGCAGGCTGTACAGGAACTGTCTGAGCCTCAGTCTCCCTCTCAGCCCAGCATGTGTTAGTGAATAACTCCCTGCCTAGCAGCATGAGGGGCTGGGTCACAGTGAGTGGCTGGGGTTCAACCTGAAGGGCCCAGATACTTGCT... | CCCCACACCCTCCCCGACTCTGTGATTTGGGAAGGCGCCACCAGGCCGGGCTGGAAATTAAATTGTCCCTGGGGCCTGGAGACCCAGAGAACAAGCTCGTCACCACAGCTCAACCCCAGCTCCGGCTCGGCACGAGTGCAGAGTGGGGCAGGGGTCTGTTCTGGGCTCTGAGGAGACCTGCAGGCTGTACAGGAACTGTCTGAGCCTCAGTCTCCCTCTCAGCCCAGCATGTGTTAGTGAATAACTCCCTGCCTAGCAGCATGAGGGGCTGGGTCACAGTGAGTGGCTGGGGTTCAACCTGAAGGGCCCAGATACTTGCT... |
Task1_train_40646 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | GAGGGCAGGACCCAGCTTAGGTTGCCCAACCTGAAGCTGCAGAGTGGAGGGGACCTAGGCTAGTGTGGCCACCGACCTGCCGGATTTCCTCCAGCACCAGCGTAAAGACCCAGAAGTAGAGGGTGACCTCGGGCCCTGAGGGGCCCTGGGGGGGCGGCCTGAAGTCCACCAGCAGGACGTAGGTGAACAGGAAGAGGAAGGCGAAGTACATGACCACGTTCCCCAGGAACACAGTCACGGGAGCGCCCCAGAATTTCCGCCAGCGTGTGAGCAGGAAGACAGCACGTGGGCCTCGGTCACCCTGAGCCCTCGGCGCCTCC... | GAGGGCAGGACCCAGCTTAGGTTGCCCAACCTGAAGCTGCAGAGTGGAGGGGACCTAGGCTAGTGTGGCCACCGACCTGCCGGATTTCCTCCAGCACCAGCGTAAAGACCCAGAAGTAGAGGGTGACCTCGGGCCCTGAGGGGCCCTGGGGGGGCGGCCTGAAGTCCACCAGCAGGACGTAGGTGAACAGGAAGAGGAAGGCGAAGTACATGACCACGTTCCCCAGGAACACAGTCACGGGAGCGCCCCAGAATTTCCGCCAGCGTGTGAGCAGGAAGACAGCACGTGGGCCTCGGTCACCCTGAGCCCTCGGCGCCTCC... |
Task1_train_40647 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | CCCCCTTGGGCTTTGGGGACAGCCGGCACCCAGCCAGCTCTGCCTGGGCCAGTGAGCGAGGCAGAAGCCCGGGCAGAACCGTGGCCTGGTCTTGCCCCGGACCTTGGGACAGCTGGGCAGAACGGGCTCAGCCAAGCAGCCCACAGGGTGCAGGAGCAGGCAGCGTGGGCAGCTCGGGCAGTGCCATGATGGGGAGGTGGGTAGGCAGGGCTGGGAGGCACCTTCCACTCCACGTCCCCATTGAAGATCTCACTCTTGGCGATGTCCACGCGGTCCCAGGCCACGGCCAGCTTGAGCTCATCCAGATAGTCCTGAGGCTC... | CCCCCTTGGGCTTTGGGGACAGCCGGCACCCAGCCAGCTCTGCCTGGGCCAGTGAGCGAGGCAGAAGCCCGGGCAGAACCGTGGCCTGGTCTTGCCCCGGACCTTGGGACAGCTGGGCAGAACGGGCTCAGCCAAGCAGCCCACAGGGTGCAGGAGCAGGCAGCGTGGGCAGCTCGGGCAGTGCCATGATGGGGAGGTGGGTAGGCAGGGCTGGGAGGCACCTTCCACTCCACGTCCCCATTGAAGATCTCACTCTTGGCGATGTCCACGCGGTCCCAGGCCACGGCCAGCTTGAGCTCATCCAGATAGTCCTGAGGCTC... |
Task1_train_40648 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | GGCAACTTCCTCGGCTGCAACGGGGGTACCCCAGCTAACACCTGGGCCTCGAGGCCACTTCCTGGCACTGAAGGTCCAGGACACCCTTCCTGGATGTTGTCGGGGGAGCAAGCTGGGCCACGTTTCCTCCACGGGCAAGGGCATTTGGCCATGACTTGGTGAGGTCACCAGGGTCACTCAAGGGGGGCCTGCAGCACCTGGGCTGGGTGCGCCTGCTGGAAACCGCTGTCCTCACCAGACTCGCACGTGAGGCTCACCAGCCTCAGCCTCCACAACCATGGACCCCGTAAGACTACGGTGCCTCTCTCAGGCCACTGGGA... | GGCAACTTCCTCGGCTGCAACGGGGGTACCCCAGCTAACACCTGGGCCTCGAGGCCACTTCCTGGCACTGAAGGTCCAGGACACCCTTCCTGGATGTTGTCGGGGGAGCAAGCTGGGCCACGTTTCCTCCACGGGCAAGGGCATTTGGCCATGACTTGGTGAGGTCACCAGGGTCACTCAAGGGGGGCCTGCAGCACCTGGGCTGGGTGCGCCTGCTGGAAACCGCTGTCCTCACCAGACTCGCACGTGAGGCTCACCAGCCTCAGCCTCCACAACCATGGACCCCGTAAGACTACGGTGCCTCTCTCAGGCCACTGGGA... |
Task1_train_40649 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | CTGTCCTCACCAGACTCGCACGTGAGGCTCACCAGCCTCAGCCTCCACAACCATGGACCCCGTAAGACTACGGTGCCTCTCTCAGGCCACTGGGACCAAACTGAGACTGGTGAGAAGAGGCGGGGGAGTTCCTAAACGGGGAGGTTTCTTTGACCTCCTTGTCCTGGTGAGGTTTCTAAACCCAGAGCCACCCGCAGTCCAGACACCCTTCCCAGAGCGTCCCCTCAAGGTGTCCCCAGCCCCTGCTTAGCAGTGCCTCTCCCTGCTGGGGCTGTGTCTGCCTGCCAGCGTCCAGCCCTTCAGCACGCGTTCGTCTCCAG... | CTGTCCTCACCAGACTCGCACGTGAGGCTCACCAGCCTCAGCCTCCACAACCATGGACCCCGTAAGACTACGGTGCCTCTCTCAGGCCACTGGGACCAAACTGAGACTGGTGAGAAGAGGCGGGGGAGTTCCTAAACGGGGAGGTTTCTTTGACCTCCTTGTCCTGGTGAGGTTTCTAAACCCAGAGCCACCCGCAGTCCAGACACCCTTCCCAGAGCGTCCCCTCAAGGTGTCCCCAGCCCCTGCTTAGCAGTGCCTCTCCCTGCTGGGGCTGTGTCTGCCTGCCAGCGTCCAGCCCTTCAGCACGCGTTCGTCTCCAG... |
Task1_train_40650 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | AAGGATACCAGGTCAGGGGGTGAAGGACCTTTGAACCCAGCCTCCCAGACTCTTAACCTGACACCTCCCAGATGAAGCCGAGGCCAGGCACCCAGTGCCCACAGCAGGCTGAAGGCCCCTCATAAGGCTGTGATTCCCAAGACAACACATACAAAGCCTGGGGTGCTGGGACAGAGCCCCAGCAGGGTGTCAGACACAGATCCCACTGTGGGATCCAGGCAGCCCCCATTGACCAAGGTCTGCAACCGCACCTCACCTGGCTGAGAAGGTGTAAGGTGGGCGGGAACCGAGGTTCGGGCGGGCAGGAGTCACATCCAACC... | AAGGATACCAGGTCAGGGGGTGAAGGACCTTTGAACCCAGCCTCCCAGACTCTTAACCTGACACCTCCCAGATGAAGCCGAGGCCAGGCACCCAGTGCCCACAGCAGGCTGAAGGCCCCTCATAAGGCTGTGATTCCCAAGACAACACATACAAAGCCTGGGGTGCTGGGACAGAGCCCCAGCAGGGTGTCAGACACAGATCCCACTGTGGGATCCAGGCAGCCCCCATTGACCAAGGTCTGCAACCGCACCTCACCTGGCTGAGAAGGTGTAAGGTGGGCGGGAACCGAGGTTCGGGCGGGCAGGAGTCACATCCAACC... |
Task1_train_40651 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | CCCCTGCCCACCAGGACTTTGGCCGGCTCTCGCTCGCCTCTGCGATGTCCGTCCCACCCTGTCTCACCCCTGCAGTTTTCTGCTCTGTGGAGCGATGATTGACACATGGCAGGGGGACACTGGTTTTGACATTTGAGCCTGTGCCCAGCCCTTGCCTGGGGAGGAGGTGGGGCAGGAGTCCTGAATGAGCATCTCCCTACTTAGTGACAGTCAGGGGCACGGAGAATGGTGCCCAGGCCAAGGGCAGGGCTTGGGCCAAGTGTGCGCAGCGTGGGGTGTGTGTGCTCCAGCGGCTCCTGCTGCGGAGGGCGGCATGAGGC... | CCCCTGCCCACCAGGACTTTGGCCGGCTCTCGCTCGCCTCTGCGATGTCCGTCCCACCCTGTCTCACCCCTGCAGTTTTCTGCTCTGTGGAGCGATGATTGACACATGGCAGGGGGACACTGGTTTTGACATTTGAGCCTGTGCCCAGCCCTTGCCTGGGGAGGAGGTGGGGCAGGAGTCCTGAATGAGCATCTCCCTACTTAGTGACAGTCAGGGGCACGGAGAATGGTGCCCAGGCCAAGGGCAGGGCTTGGGCCAAGTGTGCGCAGCGTGGGGTGTGTGTGCTCCAGCGGCTCCTGCTGCGGAGGGCGGCATGAGGC... |
Task1_train_40652 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TGGCCGGCTCTCGCTCGCCTCTGCGATGTCCGTCCCACCCTGTCTCACCCCTGCAGTTTTCTGCTCTGTGGAGCGATGATTGACACATGGCAGGGGGACACTGGTTTTGACATTTGAGCCTGTGCCCAGCCCTTGCCTGGGGAGGAGGTGGGGCAGGAGTCCTGAATGAGCATCTCCCTACTTAGTGACAGTCAGGGGCACGGAGAATGGTGCCCAGGCCAAGGGCAGGGCTTGGGCCAAGTGTGCGCAGCGTGGGGTGTGTGTGCTCCAGCGGCTCCTGCTGCGGAGGGCGGCATGAGGCTTGTTTACCTGTGTGCTGG... | TGGCCGGCTCTCGCTCGCCTCTGCGATGTCCGTCCCACCCTGTCTCACCCCTGCAGTTTTCTGCTCTGTGGAGCGATGATTGACACATGGCAGGGGGACACTGGTTTTGACATTTGAGCCTGTGCCCAGCCCTTGCCTGGGGAGGAGGTGGGGCAGGAGTCCTGAATGAGCATCTCCCTACTTAGTGACAGTCAGGGGCACGGAGAATGGTGCCCAGGCCAAGGGCAGGGCTTGGGCCAAGTGTGCGCAGCGTGGGGTGTGTGTGCTCCAGCGGCTCCTGCTGCGGAGGGCGGCATGAGGCTTGTTTACCTGTGTGCTGG... |
Task1_train_40653 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCTCCGCCACTGCATGCCCAGGTTGAGGCCAGTCTACCTGCGTGCAGAGAATGCTTTTCCTAAGTGCCTCTGGGGATTCAGGGGGCCCCTAGGAATGCGTAGAAGTGTGCTGAGGGGCGGTGCCCAACCTGGCAGCTGGGAGCATCACCAGCTCCCATTCCCACAAGTGAGCGGTGCTGAAGCCAAGGAAGGAAGCTTTACCCTGGCGGGCGCAACAGGGCCCTCCGAATGGCGAGGCCTGCAGCCGGGCGAGGGGTGGGCATTGGGACAATGGCCTTTGCAGGCCTGAATGGCCTCTCCGTGCCAGGCGGCCCCCGGGC... | CCTCCGCCACTGCATGCCCAGGTTGAGGCCAGTCTACCTGCGTGCAGAGAATGCTTTTCCTAAGTGCCTCTGGGGATTCAGGGGGCCCCTAGGAATGCGTAGAAGTGTGCTGAGGGGCGGTGCCCAACCTGGCAGCTGGGAGCATCACCAGCTCCCATTCCCACAAGTGAGCGGTGCTGAAGCCAAGGAAGGAAGCTTTACCCTGGCGGGCGCAACAGGGCCCTCCGAATGGCGAGGCCTGCAGCCGGGCGAGGGGTGGGCATTGGGACAATGGCCTTTGCAGGCCTGAATGGCCTCTCCGTGCCAGGCGGCCCCCGGGC... |
Task1_train_40654 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCCAGCTCACTGCGAGGAAGGACGCTTAGCCAGGCCCTGGCTGAAGCCTGCAGCTGGGCTGGACACAGCAGTCATTGGCCTGTGTTGTGGGGGACTTGGGCCTGCCATGGCTGCAGTGGGGACCCTGCCTGAGACAGACAGAGCTGGGGTGGTGACCAACACCGTCGGGGCACCCTCGCAGGAACTGGGCCTGGTGAACTGCCCAGGGACGGGGAAGGAGCAGGGTGAGGCATGGGGACCCCGACACAGGTTGAGCAGCGGGAGAGGAGGCTGAGGAGGGGAAGGAGGGGGCCCGCAGAGTAGCCCCCAGACCCCAAGTC... | CCCAGCTCACTGCGAGGAAGGACGCTTAGCCAGGCCCTGGCTGAAGCCTGCAGCTGGGCTGGACACAGCAGTCATTGGCCTGTGTTGTGGGGGACTTGGGCCTGCCATGGCTGCAGTGGGGACCCTGCCTGAGACAGACAGAGCTGGGGTGGTGACCAACACCGTCGGGGCACCCTCGCAGGAACTGGGCCTGGTGAACTGCCCAGGGACGGGGAAGGAGCAGGGTGAGGCATGGGGACCCCGACACAGGTTGAGCAGCGGGAGAGGAGGCTGAGGAGGGGAAGGAGGGGGCCCGCAGAGTAGCCCCCAGACCCCAAGTC... |
Task1_train_40655 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | TGGGGAGTCAGCCTTTTACATCCTCCCTCCCACCCCTGTGGTTATGGCTGAGTCATGCCTCTGCCACCTTCATATGTTGGAGTCCTAACCCCTTGCACCTTAGATAAGACTGTATTTGGAGATGGGGTCCTTAAAGAGGTATTTATTTAAATGGAGACCATTAGGGTGGGCCCTGGTCCCATGGGACTGGTGTCCTTATATGAAGAAGAGATGAAGACACAGACACAGCGAGAAGCTGGCGTCTGCCAGGCAGGAGAGAGGTCTCGGGATAAACCAGCCCTGTGGCACCGAGATCTTGGACTCCAGCCTCCGGGACCGCG... | TGGGGAGTCAGCCTTTTACATCCTCCCTCCCACCCCTGTGGTTATGGCTGAGTCATGCCTCTGCCACCTTCATATGTTGGAGTCCTAACCCCTTGCACCTTAGATAAGACTGTATTTGGAGATGGGGTCCTTAAAGAGGTATTTATTTAAATGGAGACCATTAGGGTGGGCCCTGGTCCCATGGGACTGGTGTCCTTATATGAAGAAGAGATGAAGACACAGACACAGCGAGAAGCTGGCGTCTGCCAGGCAGGAGAGAGGTCTCGGGATAAACCAGCCCTGTGGCACCGAGATCTTGGACTCCAGCCTCCGGGACCGCG... |
Task1_train_40656 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTGTGGTGGAGAGCTTGCCAAAGTGTTCAGGAAATGGCATTAATGGGGTCCATTATGGCCCGAGTTGCGCAGAGAGGACAGGGAGGGGCTGGATTTTGCTGACCTCCAAGGGGAACCCTTCTATGAACGGAAAGCTCGCACCTCGCTCAATGCATTGCCAAGTTGCGATTCTCATGCATCCCAGTGCTTTGCCGAGGTGCCTACGCCACCCTTGCATGTGTGTCCTCCCCTGGGCACAGGATGCTAAATGGGGTGACAGTAGGAACACCCACCCCCCACCCGCCTCCCACCCAGTGCAGGGACTGGGAGGACTCTACGCC... | CTGTGGTGGAGAGCTTGCCAAAGTGTTCAGGAAATGGCATTAATGGGGTCCATTATGGCCCGAGTTGCGCAGAGAGGACAGGGAGGGGCTGGATTTTGCTGACCTCCAAGGGGAACCCTTCTATGAACGGAAAGCTCGCACCTCGCTCAATGCATTGCCAAGTTGCGATTCTCATGCATCCCAGTGCTTTGCCGAGGTGCCTACGCCACCCTTGCATGTGTGTCCTCCCCTGGGCACAGGATGCTAAATGGGGTGACAGTAGGAACACCCACCCCCCACCCGCCTCCCACCCAGTGCAGGGACTGGGAGGACTCTACGCC... |
Task1_train_40657 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GCTATTTCCTGGGCTGGGAGGATGGGACAGATCCTGTAGGTTTCACCTCTGAAACTGTCCCCACCCTTATCCCATTTCCAGGTCTTTCAGGAAGGAGGCCACACAGCTCCTGGGGTCTTGTGTGAAGTGTCACAAGAATGAACAACCCTTCCCACCCTGCCCTCAAAGCCTAAGCCTCCCCCTGCCACCAGGGCTCAGGCTTTCCCGTCCCCCTGAGCCCCCCAGATGGCCTTTAGACCAACAGTGCTCACACTCCCGTCCCTCTGAGCCCCCCAGATGGCCTTCAGACCAACAGTGCCCACACTCCCATCCTCCTGAGC... | GCTATTTCCTGGGCTGGGAGGATGGGACAGATCCTGTAGGTTTCACCTCTGAAACTGTCCCCACCCTTATCCCATTTCCAGGTCTTTCAGGAAGGAGGCCACACAGCTCCTGGGGTCTTGTGTGAAGTGTCACAAGAATGAACAACCCTTCCCACCCTGCCCTCAAAGCCTAAGCCTCCCCCTGCCACCAGGGCTCAGGCTTTCCCGTCCCCCTGAGCCCCCCAGATGGCCTTTAGACCAACAGTGCTCACACTCCCGTCCCTCTGAGCCCCCCAGATGGCCTTCAGACCAACAGTGCCCACACTCCCATCCTCCTGAGC... |
Task1_train_40658 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTTGTGGACAGGCCACTTCCCTTTCTGTTCTTGTTTCTCCAGCTGAGGAACTGAAGTTGCTAATCACGTCCTGGAGGTGGGGAGAGAGGGCCCTGTGCAGATCCTGGGCTGGAGATAATTTGGGAGGAGGTAAGTCCCCAAGTGGGGGCTGGAGGTGCTCTAGGAGAGGTGGGTCCAGCCCCTGGGGCTCCCAGTCTCAAGGGATACCTGGACCCAGGCCTGCTGGGCACGTGCGGGAGCCTGAGGTGAACGCACTGTGTGGGCTGGGAGGGGCCCGGTGCAGCCGGATTCCAGGGTGCTGACCAGGGATCTGCGACTCA... | TTTGTGGACAGGCCACTTCCCTTTCTGTTCTTGTTTCTCCAGCTGAGGAACTGAAGTTGCTAATCACGTCCTGGAGGTGGGGAGAGAGGGCCCTGTGCAGATCCTGGGCTGGAGATAATTTGGGAGGAGGTAAGTCCCCAAGTGGGGGCTGGAGGTGCTCTAGGAGAGGTGGGTCCAGCCCCTGGGGCTCCCAGTCTCAAGGGATACCTGGACCCAGGCCTGCTGGGCACGTGCGGGAGCCTGAGGTGAACGCACTGTGTGGGCTGGGAGGGGCCCGGTGCAGCCGGATTCCAGGGTGCTGACCAGGGATCTGCGACTCA... |
Task1_train_40659 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TCTGTGGCTAAGAATTGCACTGTGGACTTGGATGTGTGGCGTTGGTGGCAGTAGAATCGACAGACATTTCTCTTGGGCTCACGAGAGGCTGGACAGGCCTCAAAGCACTGGGTTCTCATATTTTACAGACCAGCAAACAGAGGCGTAGGGATGTTCAGAGATGGCCTTGGCAGCACAGTGGGGTGGCTAGCGGGGCTCAGCCCAGGCTGTGGGCTCCAAAGCCCCCACTCTAGCACCCCTGGCACATGCTCCTGGATGGCAGCCAGGCCTGGCACTCAGCGGAAGCTCGGAAACCTGTTGAGGGGTGAAGCCTGGGTTCC... | TCTGTGGCTAAGAATTGCACTGTGGACTTGGATGTGTGGCGTTGGTGGCAGTAGAATCGACAGACATTTCTCTTGGGCTCACGAGAGGCTGGACAGGCCTCAAAGCACTGGGTTCTCATATTTTACAGACCAGCAAACAGAGGCGTAGGGATGTTCAGAGATGGCCTTGGCAGCACAGTGGGGTGGCTAGCGGGGCTCAGCCCAGGCTGTGGGCTCCAAAGCCCCCACTCTAGCACCCCTGGCACATGCTCCTGGATGGCAGCCAGGCCTGGCACTCAGCGGAAGCTCGGAAACCTGTTGAGGGGTGAAGCCTGGGTTCC... |
Task1_train_40660 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TTTTTAGGACCTAGAAGTTGCTAGCTTCGGCCTTCTGAACTGGAATTATATCAGGAGCTGGATCAGTAGGCACCAACTCTTGGGCTTCCCAAGGCCATCTGTCTCCGATAGTGGTTCCTCCGCGTACATAACAAGAAGTAACAGTTATGTAAGTAAGAAAATTACATTTTCTGCTAATTGGAGAAACAAATTTTTTGTCTTTTTCAGAAGTTCTGGTGCTGGCACATTCAGCTCCTCATAAAAGGTTTGAAATACTGGTTTGGGAGAGCACTTGTGGACCTCCCCTCTAATTACAATGGCAACTTGAGGGTTTAACCCTG... | TTTTTAGGACCTAGAAGTTGCTAGCTTCGGCCTTCTGAACTGGAATTATATCAGGAGCTGGATCAGTAGGCACCAACTCTTGGGCTTCCCAAGGCCATCTGTCTCCGATAGTGGTTCCTCCGCGTACATAACAAGAAGTAACAGTTATGTAAGTAAGAAAATTACATTTTCTGCTAATTGGAGAAACAAATTTTTTGTCTTTTTCAGAAGTTCTGGTGCTGGCACATTCAGCTCCTCATAAAAGGTTTGAAATACTGGTTTGGGAGAGCACTTGTGGACCTCCCCTCTAATTACAATGGCAACTTGAGGGTTTAACCCTG... |
Task1_train_40661 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ACCAACTCTTGGGCTTCCCAAGGCCATCTGTCTCCGATAGTGGTTCCTCCGCGTACATAACAAGAAGTAACAGTTATGTAAGTAAGAAAATTACATTTTCTGCTAATTGGAGAAACAAATTTTTTGTCTTTTTCAGAAGTTCTGGTGCTGGCACATTCAGCTCCTCATAAAAGGTTTGAAATACTGGTTTGGGAGAGCACTTGTGGACCTCCCCTCTAATTACAATGGCAACTTGAGGGTTTAACCCTGTCCTATTGATCCCCAGGGTTACACGTTCTCCCTTTTTCCAACGGGGATCTAGGGGATTGGTAATTATTAGT... | ACCAACTCTTGGGCTTCCCAAGGCCATCTGTCTCCGATAGTGGTTCCTCCGCGTACATAACAAGAAGTAACAGTTATGTAAGTAAGAAAATTACATTTTCTGCTAATTGGAGAAACAAATTTTTTGTCTTTTTCAGAAGTTCTGGTGCTGGCACATTCAGCTCCTCATAAAAGGTTTGAAATACTGGTTTGGGAGAGCACTTGTGGACCTCCCCTCTAATTACAATGGCAACTTGAGGGTTTAACCCTGTCCTATTGATCCCCAGGGTTACACGTTCTCCCTTTTTCCAACGGGGATCTAGGGGATTGGTAATTATTAGT... |
Task1_train_40662 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | GGCTTCCCAAGGCCATCTGTCTCCGATAGTGGTTCCTCCGCGTACATAACAAGAAGTAACAGTTATGTAAGTAAGAAAATTACATTTTCTGCTAATTGGAGAAACAAATTTTTTGTCTTTTTCAGAAGTTCTGGTGCTGGCACATTCAGCTCCTCATAAAAGGTTTGAAATACTGGTTTGGGAGAGCACTTGTGGACCTCCCCTCTAATTACAATGGCAACTTGAGGGTTTAACCCTGTCCTATTGATCCCCAGGGTTACACGTTCTCCCTTTTTCCAACGGGGATCTAGGGGATTGGTAATTATTAGTTCTAGTGGGTT... | GGCTTCCCAAGGCCATCTGTCTCCGATAGTGGTTCCTCCGCGTACATAACAAGAAGTAACAGTTATGTAAGTAAGAAAATTACATTTTCTGCTAATTGGAGAAACAAATTTTTTGTCTTTTTCAGAAGTTCTGGTGCTGGCACATTCAGCTCCTCATAAAAGGTTTGAAATACTGGTTTGGGAGAGCACTTGTGGACCTCCCCTCTAATTACAATGGCAACTTGAGGGTTTAACCCTGTCCTATTGATCCCCAGGGTTACACGTTCTCCCTTTTTCCAACGGGGATCTAGGGGATTGGTAATTATTAGTTCTAGTGGGTT... |
Task1_train_40663 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCTGCTTTTCTTGCTTCAATAAAGTTTCTGCTCTGGATGTGAGAGGCCTCCAGGCTGTGTGAGAATCTCTGTCTCTTGATGTTTTGAGGTCCTCCCTCTTCTTTCCCCTGAAATGGACCCTTGTGGGAGCAGGGCAGAGAGAAATGACTTGCTCTGTGTTCCCAAGTATCTTGGGCTTGGGATCCTACTTTGAGTTTCCTCAGATCTTTTATGGACAGAGTTCTGGACCAGGAGGCAGGAGACCGGGGAGGCGGGAGGCCGGGGTTCAATGGGAACCCTCTGACCAGTTGCTTCCTTCCTTGGCTTTGCATTCCTCACCT... | GCTGCTTTTCTTGCTTCAATAAAGTTTCTGCTCTGGATGTGAGAGGCCTCCAGGCTGTGTGAGAATCTCTGTCTCTTGATGTTTTGAGGTCCTCCCTCTTCTTTCCCCTGAAATGGACCCTTGTGGGAGCAGGGCAGAGAGAAATGACTTGCTCTGTGTTCCCAAGTATCTTGGGCTTGGGATCCTACTTTGAGTTTCCTCAGATCTTTTATGGACAGAGTTCTGGACCAGGAGGCAGGAGACCGGGGAGGCGGGAGGCCGGGGTTCAATGGGAACCCTCTGACCAGTTGCTTCCTTCCTTGGCTTTGCATTCCTCACCT... |
Task1_train_40664 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | AAGAATCACTTGAACTCAGGAGGTGGAGGATGCAGTGCGCCGAGATCACGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTTGGTCTCGGAAAAAAAAAAAAAAAGAGAGAGAAAGAAAAAAAAGGAAACTGCCTGCTCCAATCCAGACCCAATGCCTGGACACCCTCTTCCTGGAACCACTTCGGGCACTCCGCCTGTCCCCCAGCAAAGAGGGTGTGGAAGGCTTGTGGTTCCTGCTGCTTCTCTTAGGGAAACTGGTATCCTCTGTCTTCTCCTGCTCTTCTGATCCCCTCTTCCCCCAGCACCCGGGGTTTA... | AAGAATCACTTGAACTCAGGAGGTGGAGGATGCAGTGCGCCGAGATCACGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTTGGTCTCGGAAAAAAAAAAAAAAAGAGAGAGAAAGAAAAAAAAGGAAACTGCCTGCTCCAATCCAGACCCAATGCCTGGACACCCTCTTCCTGGAACCACTTCGGGCACTCCGCCTGTCCCCCAGCAAAGAGGGTGTGGAAGGCTTGTGGTTCCTGCTGCTTCTCTTAGGGAAACTGGTATCCTCTGTCTTCTCCTGCTCTTCTGATCCCCTCTTCCCCCAGCACCCGGGGTTTA... |
Task1_train_40665 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GAATGGCAGAGATGTGGACATGTATATGCATATCCTGCCCTGTCTGTGCACACTCCCCTGCAGGGCTCTGGTCAGCACCCACAAACCTGACTTGTCCATACCGTCCAGTTCCCACCCAGACCTGACCTTGCCATGTGACCTTAGTGGGCTCTTCTCTTTTCTGCCCCTGTTTCCTCAGCAGGAATATGGGGTGAGAATCCCTGCTTAGCAGGGATTCAGTAAGTTCAGGTGAACAAAATATTGGGCACGAGGTAGGCACCCAATACTCAGTACCCAACAGTCAGTACCCAACAGTTTGTAACTGCTACCTTTGTTAATAT... | GAATGGCAGAGATGTGGACATGTATATGCATATCCTGCCCTGTCTGTGCACACTCCCCTGCAGGGCTCTGGTCAGCACCCACAAACCTGACTTGTCCATACCGTCCAGTTCCCACCCAGACCTGACCTTGCCATGTGACCTTAGTGGGCTCTTCTCTTTTCTGCCCCTGTTTCCTCAGCAGGAATATGGGGTGAGAATCCCTGCTTAGCAGGGATTCAGTAAGTTCAGGTGAACAAAATATTGGGCACGAGGTAGGCACCCAATACTCAGTACCCAACAGTCAGTACCCAACAGTTTGTAACTGCTACCTTTGTTAATAT... |
Task1_train_40666 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AGGCATTTACCTACTAGACTGGTGCCAGGAAATTCATCCTCCCGTGAACATACGCTACCACCACTATTATTGGGACATCAAACATTAGAAACATAGTGTGTACTCACTTTGTGCTTCTGGTAAGTCTCCTGATGCTTCTTTAACCCAATCTGCATAGTCATGAATGACAGCAACTCCCAGATTGGGGACAATGAGAGGACACAGTTCATCCACATGGACAGTGCTGTGTTTTAATTTGAGCTCCAGAGGTGTCTGATATAATTTCATGTCTTCATCTGGCTTTCTTTGTCTCAAACTGAGTTTTTCTAAGTGAACTTTGA... | AGGCATTTACCTACTAGACTGGTGCCAGGAAATTCATCCTCCCGTGAACATACGCTACCACCACTATTATTGGGACATCAAACATTAGAAACATAGTGTGTACTCACTTTGTGCTTCTGGTAAGTCTCCTGATGCTTCTTTAACCCAATCTGCATAGTCATGAATGACAGCAACTCCCAGATTGGGGACAATGAGAGGACACAGTTCATCCACATGGACAGTGCTGTGTTTTAATTTGAGCTCCAGAGGTGTCTGATATAATTTCATGTCTTCATCTGGCTTTCTTTGTCTCAAACTGAGTTTTTCTAAGTGAACTTTGA... |
Task1_train_40667 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | CATTGTGAACACAGAAGTCAGGGGTGGAGGGACAGACCAAGAGGATGTGGATGGGATATTCATTAAAGATGCTGCTCTGGGAGTACGACATTCTTGCACAGAGACACTTGGTGAAAGAAAAGCTCCACTTGTAAATTTTGATTGTAGTAACCCACCAACTGAAATGAAGCGGGAATGAAGGGGAGAAAGACTATTACAAAACACAAGCTATTGTTTCTTGAACAATAACAAAAATCAGTAAGGCTGAAATCATTCAATGTTTAATCAAACTACTTATATCAGATGTGGATGACCAGAAGCAGGCTAAGTCAGATTTTGCA... | CATTGTGAACACAGAAGTCAGGGGTGGAGGGACAGACCAAGAGGATGTGGATGGGATATTCATTAAAGATGCTGCTCTGGGAGTACGACATTCTTGCACAGAGACACTTGGTGAAAGAAAAGCTCCACTTGTAAATTTTGATTGTAGTAACCCACCAACTGAAATGAAGCGGGAATGAAGGGGAGAAAGACTATTACAAAACACAAGCTATTGTTTCTTGAACAATAACAAAAATCAGTAAGGCTGAAATCATTCAATGTTTAATCAAACTACTTATATCAGATGTGGATGACCAGAAGCAGGCTAAGTCAGATTTTGCA... |
Task1_train_40668 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AAGTGCTGGGATTACAGATGTGAGCCACCACGCCCCCGCGAGACCTTGTTTTAAATAAATAAATAAAACCATTTTATAGACGAGGAAACAGAGGCTCAGGGCTATATGGAGAATTGCCCATATTTCCCAAATCACCAGAGAATTAAAGAATTAATCTAAATTAGAGCACCTCAAGGTTTGGGCATTGGGGGTAGTCTAGAGGCAGGGAGAGGGGACCCAGCCTCAGGGAATGGTACTTAGGGCCAAGAGAACAGACAAGGTGTCAAGATAGGGAACAATAGCCAGGAGCAGACACCCCTGGTTGGAGCTAGACAAAGAGG... | AAGTGCTGGGATTACAGATGTGAGCCACCACGCCCCCGCGAGACCTTGTTTTAAATAAATAAATAAAACCATTTTATAGACGAGGAAACAGAGGCTCAGGGCTATATGGAGAATTGCCCATATTTCCCAAATCACCAGAGAATTAAAGAATTAATCTAAATTAGAGCACCTCAAGGTTTGGGCATTGGGGGTAGTCTAGAGGCAGGGAGAGGGGACCCAGCCTCAGGGAATGGTACTTAGGGCCAAGAGAACAGACAAGGTGTCAAGATAGGGAACAATAGCCAGGAGCAGACACCCCTGGTTGGAGCTAGACAAAGAGG... |
Task1_train_40669 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | TAAGGAGCTCTTCCTACTACTACACAGTTAAAAACCAACAATGACAGACACGGCAGGCTGATCTATTTTGTACTCTGATCATTATTGTCTTGCATTTGTATGATTACCACATATTTTATGAATTTTTATTTGTCAATAATTTGTATTCATTCATTCATTTTCCAATCCGCTGATTCCTCTTTGGAGTGGCAGGTGGCTGGAGCCTATCTCGGCAGCTCAAGGTGTGAGGAAGGAACCAACGCTGGACAGGACCCCATCTGGGGTTCAGGGCACACCCTCACACTAGGACCATAGAGATGTCACTTCACCTAATGTGCCCA... | TAAGGAGCTCTTCCTACTACTACACAGTTAAAAACCAACAATGACAGACACGGCAGGCTGATCTATTTTGTACTCTGATCATTATTGTCTTGCATTTGTATGATTACCACATATTTTATGAATTTTTATTTGTCAATAATTTGTATTCATTCATTCATTTTCCAATCCGCTGATTCCTCTTTGGAGTGGCAGGTGGCTGGAGCCTATCTCGGCAGCTCAAGGTGTGAGGAAGGAACCAACGCTGGACAGGACCCCATCTGGGGTTCAGGGCACACCCTCACACTAGGACCATAGAGATGTCACTTCACCTAATGTGCCCA... |
Task1_train_40670 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTGGATTTATACTTCTTAGGAAGCAATGAGGTAGAAGCAGAAGAGTGTAGTGATTTAAGACATTGGATTGGGAGGCAGCAAACCAGAGTTCTCGAAGCTCAAGTTTCATCTTTGACGTTTTCCAACTGTTCTGATTGTTAGTGACTTAGTCTTTTGTTTTCTCAATTCATAAGTGTCCACGTTTACTGAGCACTGTTTCAAGATTTGTGCTAAGTGTTTTAAAAGATCTCAAAATCCCCAAAAGAAAGTTTTTAGGCAGGAGCTGAAAAAAAAGGTGGCACAGGTCAAAAATATTGCAAGGAAATGTTTAAACGTTTTCA... | CTGGATTTATACTTCTTAGGAAGCAATGAGGTAGAAGCAGAAGAGTGTAGTGATTTAAGACATTGGATTGGGAGGCAGCAAACCAGAGTTCTCGAAGCTCAAGTTTCATCTTTGACGTTTTCCAACTGTTCTGATTGTTAGTGACTTAGTCTTTTGTTTTCTCAATTCATAAGTGTCCACGTTTACTGAGCACTGTTTCAAGATTTGTGCTAAGTGTTTTAAAAGATCTCAAAATCCCCAAAAGAAAGTTTTTAGGCAGGAGCTGAAAAAAAAGGTGGCACAGGTCAAAAATATTGCAAGGAAATGTTTAAACGTTTTCA... |
Task1_train_40671 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CAGTTGCATGAAGCCAGGTAAGTGATAAGGGCACCATCATCATGGAGGTCATTGATTGTCACAGTAAAAGGAATTTTTGGTTTGTGATGGGAATAAAATCCAGATTGATATGTTTCAAAACCAATTATCCTTGAGAGAGTTGAGATTGTAGACCTTTCTACATGTTTCACTGTAAAGAAAAGCAGAGGTTTGAATAAAGGGAGGAGGATTTAATGTCACGGTAGATTAATCAACATAAATAATTTTTTAAAAAGTAACAGTTCTACAGAAGAGAAATATAAGTGACAAAGCTCTGCACACTAAGGAATTATACAAAATGA... | CAGTTGCATGAAGCCAGGTAAGTGATAAGGGCACCATCATCATGGAGGTCATTGATTGTCACAGTAAAAGGAATTTTTGGTTTGTGATGGGAATAAAATCCAGATTGATATGTTTCAAAACCAATTATCCTTGAGAGAGTTGAGATTGTAGACCTTTCTACATGTTTCACTGTAAAGAAAAGCAGAGGTTTGAATAAAGGGAGGAGGATTTAATGTCACGGTAGATTAATCAACATAAATAATTTTTTAAAAAGTAACAGTTCTACAGAAGAGAAATATAAGTGACAAAGCTCTGCACACTAAGGAATTATACAAAATGA... |
Task1_train_40672 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | AGGAATTATACAAAATGATTTTATACATAATCACACTTAACCTCCCTATACCCCTCAGATAAAGGGAAATAGCACTGAACTACCTTTAACAGAGAAGGAAACAAACTAGTACATAAGTGATTTGTGCAAGGTCTACCACTAGAATATGTGGCAGTCATGATTTCAGCCAATAACTTTAGATTCTAAACATTTTCCAAATGTTATGGAAGGAAGTTAGTTTTCAGTTTGGTTATGCTGGATGCAGGTTGCATATAGGGCATCTAGATGGAAACAATAAGCCTAGTTACTTAAGACATGGGAATCGGTAGAAAGAAGGACTC... | AGGAATTATACAAAATGATTTTATACATAATCACACTTAACCTCCCTATACCCCTCAGATAAAGGGAAATAGCACTGAACTACCTTTAACAGAGAAGGAAACAAACTAGTACATAAGTGATTTGTGCAAGGTCTACCACTAGAATATGTGGCAGTCATGATTTCAGCCAATAACTTTAGATTCTAAACATTTTCCAAATGTTATGGAAGGAAGTTAGTTTTCAGTTTGGTTATGCTGGATGCAGGTTGCATATAGGGCATCTAGATGGAAACAATAAGCCTAGTTACTTAAGACATGGGAATCGGTAGAAAGAAGGACTC... |
Task1_train_40673 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | CTAGGCCATGGCTTTAAGTTTGTTGCAAAGTGTAGTTAGTTGTATTTCACTAATGGGATAAAGCAGTTCACCTAAGCTCTCACTGCCAAGATCTGAAGACAGATCTAGAAAAGTCCTAAGCCCAGATTGCTGACTATTCTGTAATCAACCTAACTAGGCTTAAGATGTACTGCATTAAACTTCTTACACGCTCCTCACCTTTCGTATTCCTCTGATATATAAGGAACACATTCTGGTATAGTCTTTTAGACAAAGATTTAAAAAAAAAAAATCAGACAACACATTGTTTTCATGTATTTGCTTTAAATTGACATCTTTTT... | CTAGGCCATGGCTTTAAGTTTGTTGCAAAGTGTAGTTAGTTGTATTTCACTAATGGGATAAAGCAGTTCACCTAAGCTCTCACTGCCAAGATCTGAAGACAGATCTAGAAAAGTCCTAAGCCCAGATTGCTGACTATTCTGTAATCAACCTAACTAGGCTTAAGATGTACTGCATTAAACTTCTTACACGCTCCTCACCTTTCGTATTCCTCTGATATATAAGGAACACATTCTGGTATAGTCTTTTAGACAAAGATTTAAAAAAAAAAAATCAGACAACACATTGTTTTCATGTATTTGCTTTAAATTGACATCTTTTT... |
Task1_train_40674 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TTGGGGGAGGTACCTAACATGGAGGCTTGGAGTTCATACAGACTTTCGTTATGTTAGGAATTAATTTGGTTTATCTCTTATTCCATCAACTGCTAACCTTGGTTGTCAGGTAAAATTGTTTCCTTATCAGCAGTAAACTTAATCTTATTAGAAAATGTAGAAACAGATCACATGGCTGAAAAGTACTTAGGCTTTGAAAGAAAGCATTTGCTAGTAGACTTTGAAAATAGTAATCCTAGGTCAGGCAGTTCCAATGATGCAATTCTCAAACATCTTATTAAATACAAAGATGCTTGGATAGCAGCACTTCTCTGGTAGGA... | TTGGGGGAGGTACCTAACATGGAGGCTTGGAGTTCATACAGACTTTCGTTATGTTAGGAATTAATTTGGTTTATCTCTTATTCCATCAACTGCTAACCTTGGTTGTCAGGTAAAATTGTTTCCTTATCAGCAGTAAACTTAATCTTATTAGAAAATGTAGAAACAGATCACATGGCTGAAAAGTACTTAGGCTTTGAAAGAAAGCATTTGCTAGTAGACTTTGAAAATAGTAATCCTAGGTCAGGCAGTTCCAATGATGCAATTCTCAAACATCTTATTAAATACAAAGATGCTTGGATAGCAGCACTTCTCTGGTAGGA... |
Task1_train_40675 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | TAGAGAAAAAGTACCTCAAATTCAACCAAATGTTAGCCCCAATTAAGCTGCTCTGCCAGATATGGTATCTCTGCCACAGCACAGTAACACCTGAATCAGCATCTGATTTAATAATCACCATACTGCAGTCATTGATTTGGCAAATGTTTTTCTACATCAGGGCAGGGACTTCAAGTAGTTCACATCCACATGAAGTAGAACACGATCCATACAGTTTTTCCCTGCAAAGACCTGGAGCAGTGCTAGGATGGAATATTCTGATGGAAGTGTTTTGTAATCAGTGCGGTCCAATTCAATGGCCCAGTCACTTGTGGCTATTG... | TAGAGAAAAAGTACCTCAAATTCAACCAAATGTTAGCCCCAATTAAGCTGCTCTGCCAGATATGGTATCTCTGCCACAGCACAGTAACACCTGAATCAGCATCTGATTTAATAATCACCATACTGCAGTCATTGATTTGGCAAATGTTTTTCTACATCAGGGCAGGGACTTCAAGTAGTTCACATCCACATGAAGTAGAACACGATCCATACAGTTTTTCCCTGCAAAGACCTGGAGCAGTGCTAGGATGGAATATTCTGATGGAAGTGTTTTGTAATCAGTGCGGTCCAATTCAATGGCCCAGTCACTTGTGGCTATTG... |
Task1_train_40676 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGTGGCTTTTTACTTTTTAATAGTGGTCTTCAAGTCACACACACCCATTTAAGGATGCTACTTGCAGCAATCTAAAAGTATGGGATTTATGCAGGGAAAACAGTTTCATTTTATATTAGCTACATTTTATTGAGCACCTAAGCACCATGCATCATGCTAAGCATTTTTACAAAGCTTATCACTTAAGTCTCAAAATATCTCTATGATGTATGTACTATTATCTCCTTTTTATGGATGAAGAAACTGGGGCTTGGTGCGTTTACATAATTTGACTAAGGCAAAGCGGCTAGCAAGTGATAGAGTGGATTTTTAAGTCTATG... | AGTGGCTTTTTACTTTTTAATAGTGGTCTTCAAGTCACACACACCCATTTAAGGATGCTACTTGCAGCAATCTAAAAGTATGGGATTTATGCAGGGAAAACAGTTTCATTTTATATTAGCTACATTTTATTGAGCACCTAAGCACCATGCATCATGCTAAGCATTTTTACAAAGCTTATCACTTAAGTCTCAAAATATCTCTATGATGTATGTACTATTATCTCCTTTTTATGGATGAAGAAACTGGGGCTTGGTGCGTTTACATAATTTGACTAAGGCAAAGCGGCTAGCAAGTGATAGAGTGGATTTTTAAGTCTATG... |
Task1_train_40677 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | TTATTGAGCACCTAAGCACCATGCATCATGCTAAGCATTTTTACAAAGCTTATCACTTAAGTCTCAAAATATCTCTATGATGTATGTACTATTATCTCCTTTTTATGGATGAAGAAACTGGGGCTTGGTGCGTTTACATAATTTGACTAAGGCAAAGCGGCTAGCAAGTGATAGAGTGGATTTTTAAGTCTATGGGTATGAATCTAGAACCAATACTTTTCGACTCTTCGCTATCCTGCCTCTTGATGATGTAGGAACAGTACCACATTTTGAGTGTGGTACATGAAAGTATGCAGGATTTGTAGGCTGTATTCTGAAGA... | TTATTGAGCACCTAAGCACCATGCATCATGCTAAGCATTTTTACAAAGCTTATCACTTAAGTCTCAAAATATCTCTATGATGTATGTACTATTATCTCCTTTTTATGGATGAAGAAACTGGGGCTTGGTGCGTTTACATAATTTGACTAAGGCAAAGCGGCTAGCAAGTGATAGAGTGGATTTTTAAGTCTATGGGTATGAATCTAGAACCAATACTTTTCGACTCTTCGCTATCCTGCCTCTTGATGATGTAGGAACAGTACCACATTTTGAGTGTGGTACATGAAAGTATGCAGGATTTGTAGGCTGTATTCTGAAGA... |
Task1_train_40678 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATGCATCATGCTAAGCATTTTTACAAAGCTTATCACTTAAGTCTCAAAATATCTCTATGATGTATGTACTATTATCTCCTTTTTATGGATGAAGAAACTGGGGCTTGGTGCGTTTACATAATTTGACTAAGGCAAAGCGGCTAGCAAGTGATAGAGTGGATTTTTAAGTCTATGGGTATGAATCTAGAACCAATACTTTTCGACTCTTCGCTATCCTGCCTCTTGATGATGTAGGAACAGTACCACATTTTGAGTGTGGTACATGAAAGTATGCAGGATTTGTAGGCTGTATTCTGAAGAAAAAAACCTAGGGGTTCCAT... | ATGCATCATGCTAAGCATTTTTACAAAGCTTATCACTTAAGTCTCAAAATATCTCTATGATGTATGTACTATTATCTCCTTTTTATGGATGAAGAAACTGGGGCTTGGTGCGTTTACATAATTTGACTAAGGCAAAGCGGCTAGCAAGTGATAGAGTGGATTTTTAAGTCTATGGGTATGAATCTAGAACCAATACTTTTCGACTCTTCGCTATCCTGCCTCTTGATGATGTAGGAACAGTACCACATTTTGAGTGTGGTACATGAAAGTATGCAGGATTTGTAGGCTGTATTCTGAAGAAAAAAACCTAGGGGTTCCAT... |
Task1_train_40679 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TGTAGGCTGTATTCTGAAGAAAAAAACCTAGGGGTTCCATGAAGAAGATCAGCCAATGTCTCCCAAAGCTGAATGTTACCACCAGAAGAGGCAGCGCCCCTTGCAAGGAGTATTCTCACATGGCTGGGAAAATGTGTCCGTGACCAAACATCATATGAAATCATTGAAACCAATCATCCTAAGGAGAAAGTAACTAAAGGGCTACCACGCAGGACTGTAATGGCAGTTTAGGCTGACTACTTCTATTTTGGGTTCTCCAGCCAGATTATTCACATTATATGATATGGTAACACCTGAAAGAGGCAATGGATGGTGAATGC... | TGTAGGCTGTATTCTGAAGAAAAAAACCTAGGGGTTCCATGAAGAAGATCAGCCAATGTCTCCCAAAGCTGAATGTTACCACCAGAAGAGGCAGCGCCCCTTGCAAGGAGTATTCTCACATGGCTGGGAAAATGTGTCCGTGACCAAACATCATATGAAATCATTGAAACCAATCATCCTAAGGAGAAAGTAACTAAAGGGCTACCACGCAGGACTGTAATGGCAGTTTAGGCTGACTACTTCTATTTTGGGTTCTCCAGCCAGATTATTCACATTATATGATATGGTAACACCTGAAAGAGGCAATGGATGGTGAATGC... |
Task1_train_40680 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | TTGTGCACAGCCACTGGGTGAGACATCTTCAGTGGCAACTCATGGGAGGACAAGAGAAATTCTTCAGGCAATGCAGGATGAGCTGCTTTTTACTTTGTAAATGTGGTCTTCAAATCACATACACCCATTTAAGGATGTTATTTGGAGCAATCTAGAAGTATAGAATCAGGCAGGGAAAACCGTCTTCTGTTTTACTATATTATAGCTATATTTTATTGAACACCTATGTACCAAGCATTACACTAAGCACTTTTACATAGCTTATCACTTAAATCTCAAAATATCTCTGTGAAGTATTATTAACTCTAATGGGTGAAGAA... | TTGTGCACAGCCACTGGGTGAGACATCTTCAGTGGCAACTCATGGGAGGACAAGAGAAATTCTTCAGGCAATGCAGGATGAGCTGCTTTTTACTTTGTAAATGTGGTCTTCAAATCACATACACCCATTTAAGGATGTTATTTGGAGCAATCTAGAAGTATAGAATCAGGCAGGGAAAACCGTCTTCTGTTTTACTATATTATAGCTATATTTTATTGAACACCTATGTACCAAGCATTACACTAAGCACTTTTACATAGCTTATCACTTAAATCTCAAAATATCTCTGTGAAGTATTATTAACTCTAATGGGTGAAGAA... |
Task1_train_40681 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AATACATCAATAAACAGAGATGAACAAGTGGTAGAGCTCAGCTGCTGGCTGTGCACAGCAGTAGCTATCTTTGTCTCATCAAACGTGGCCAAGTGAAACCCCTAACCTTGTTTTATCCATAGTTGTCTTGTTGACTATTTATGTTGGGCTGGATGGACACCTGGGAGTCATAGCTTAAACCCAAAACTTACCACACACGTACTACATGATCTTGGCTAGAATATTTAATCTAAGTTATACAAACTGTGTTGTATGGAATGGATGTTTGTCTTATATTACAAATGGAGAAATACACTCAGATTATGAATACTACACTTTTA... | AATACATCAATAAACAGAGATGAACAAGTGGTAGAGCTCAGCTGCTGGCTGTGCACAGCAGTAGCTATCTTTGTCTCATCAAACGTGGCCAAGTGAAACCCCTAACCTTGTTTTATCCATAGTTGTCTTGTTGACTATTTATGTTGGGCTGGATGGACACCTGGGAGTCATAGCTTAAACCCAAAACTTACCACACACGTACTACATGATCTTGGCTAGAATATTTAATCTAAGTTATACAAACTGTGTTGTATGGAATGGATGTTTGTCTTATATTACAAATGGAGAAATACACTCAGATTATGAATACTACACTTTTA... |
Task1_train_40682 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | GAATCACTCCTAACTTGCTCAGCAGGAGCCCCAGGTGTCCAGTTTTGCTGTTTAGATGGCAGTGGTGTGGAAGGTGGTTTGGAATAGACTAGGTTTGGAGGCAGGGAGGTAAGTTGGAAGGCTCTTTTTATAATCAGGGCAGAGTGGATAATATAATTAAGTTGGGAGGAGGTGTATTAAGAGGAACGGCCCCAATAATTAATTGGAAAAGTTGAATTGCATGTGGGGGTGAAAGAGGAGACGGGTCAAGATGAGACCAGCTGCCCTGACTTGGGTGATGTGGGTTCTGAGCAGTGGCATTCTCTGAGATCAGGAACAGG... | GAATCACTCCTAACTTGCTCAGCAGGAGCCCCAGGTGTCCAGTTTTGCTGTTTAGATGGCAGTGGTGTGGAAGGTGGTTTGGAATAGACTAGGTTTGGAGGCAGGGAGGTAAGTTGGAAGGCTCTTTTTATAATCAGGGCAGAGTGGATAATATAATTAAGTTGGGAGGAGGTGTATTAAGAGGAACGGCCCCAATAATTAATTGGAAAAGTTGAATTGCATGTGGGGGTGAAAGAGGAGACGGGTCAAGATGAGACCAGCTGCCCTGACTTGGGTGATGTGGGTTCTGAGCAGTGGCATTCTCTGAGATCAGGAACAGG... |
Task1_train_40683 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | TTTTGCTGTTTAGATGGCAGTGGTGTGGAAGGTGGTTTGGAATAGACTAGGTTTGGAGGCAGGGAGGTAAGTTGGAAGGCTCTTTTTATAATCAGGGCAGAGTGGATAATATAATTAAGTTGGGAGGAGGTGTATTAAGAGGAACGGCCCCAATAATTAATTGGAAAAGTTGAATTGCATGTGGGGGTGAAAGAGGAGACGGGTCAAGATGAGACCAGCTGCCCTGACTTGGGTGATGTGGGTTCTGAGCAGTGGCATTCTCTGAGATCAGGAACAGGTTTGGAAGGGGTCCCTGTTAGAGGCAAGATGAGTGGGAGGCC... | TTTTGCTGTTTAGATGGCAGTGGTGTGGAAGGTGGTTTGGAATAGACTAGGTTTGGAGGCAGGGAGGTAAGTTGGAAGGCTCTTTTTATAATCAGGGCAGAGTGGATAATATAATTAAGTTGGGAGGAGGTGTATTAAGAGGAACGGCCCCAATAATTAATTGGAAAAGTTGAATTGCATGTGGGGGTGAAAGAGGAGACGGGTCAAGATGAGACCAGCTGCCCTGACTTGGGTGATGTGGGTTCTGAGCAGTGGCATTCTCTGAGATCAGGAACAGGTTTGGAAGGGGTCCCTGTTAGAGGCAAGATGAGTGGGAGGCC... |
Task1_train_40684 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AAGGGGTCCCTGTTAGAGGCAAGATGAGTGGGAGGCCCATAGGCTATCCAGGTAGAACTATCAAGGAGGCGGTAGGTTATATGGCTGAATCTCAGGACACAGGCTTAGAACAGTGTGGTCTGTAGAGAGAAAGAAGTTGAGCCTGGGACGTTGTGTGATCACCAGGGAGAGTAGGTGGAGGGAGAGGTGTGTGTGCCTGTGAACACTGTGGAGTAACAGCAGCAGCACTGGCTGATTTTCTGTTCATGTCTCAGCTGCATCTGATTTCCATGACATGCTCCTCTTGCTGAGCGCAACCTGGGACTGACTCTCACCTGGGG... | AAGGGGTCCCTGTTAGAGGCAAGATGAGTGGGAGGCCCATAGGCTATCCAGGTAGAACTATCAAGGAGGCGGTAGGTTATATGGCTGAATCTCAGGACACAGGCTTAGAACAGTGTGGTCTGTAGAGAGAAAGAAGTTGAGCCTGGGACGTTGTGTGATCACCAGGGAGAGTAGGTGGAGGGAGAGGTGTGTGTGCCTGTGAACACTGTGGAGTAACAGCAGCAGCACTGGCTGATTTTCTGTTCATGTCTCAGCTGCATCTGATTTCCATGACATGCTCCTCTTGCTGAGCGCAACCTGGGACTGACTCTCACCTGGGG... |
Task1_train_40685 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ATCTGATTTCCATGACATGCTCCTCTTGCTGAGCGCAACCTGGGACTGACTCTCACCTGGGGCTTGAGAGATCTTGATGGCAGATGCTGCTTATTGTTCGTTTGGGAGCTGGAAATGGAAATGATAGTCCCTCTTCATTCACCTCCCTGCCCCCAAGAACACCAGAACAACTTTCCCCAAAGTTCTCTGATTTAAAGCACAAATTTCCTAGGGGAAAGGGGCTTATCGTTTTTTGTTTGTTTATTTGTTTTGTTTTGTTTTTGAGTTGGTGTCTCGCTGTGTCACCCAGGCTGGAATGCAGTGGGGGTGATCTCGTCTCA... | ATCTGATTTCCATGACATGCTCCTCTTGCTGAGCGCAACCTGGGACTGACTCTCACCTGGGGCTTGAGAGATCTTGATGGCAGATGCTGCTTATTGTTCGTTTGGGAGCTGGAAATGGAAATGATAGTCCCTCTTCATTCACCTCCCTGCCCCCAAGAACACCAGAACAACTTTCCCCAAAGTTCTCTGATTTAAAGCACAAATTTCCTAGGGGAAAGGGGCTTATCGTTTTTTGTTTGTTTATTTGTTTTGTTTTGTTTTTGAGTTGGTGTCTCGCTGTGTCACCCAGGCTGGAATGCAGTGGGGGTGATCTCGTCTCA... |
Task1_train_40686 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCTCACCCTCTGTTCTACTATTCATGCTCCCATTGTTTTCCCACTAATTTCTATCTGGTCTGAGGAAACCTCTGGGTGACCGCTTGATGCTGGTACAAAGATTTGTGACACACCCTGAGCCCATGGGACCTCTTCTGATGCTGGCCATGAATTCTGACTTATGCTCAGCTGCTTTCTGGTAACCAGTGCAGAAACCCCTATCCCAGCTCTCAAACATTCAAGGGCCAAATCTATGTAAAAACTACAATACACATGATCTAATAAATACAGGTTGAGTACCCCTAATCCAAACATCCAAAATCTGAAATGCTCCAAAATCT... | TCTCACCCTCTGTTCTACTATTCATGCTCCCATTGTTTTCCCACTAATTTCTATCTGGTCTGAGGAAACCTCTGGGTGACCGCTTGATGCTGGTACAAAGATTTGTGACACACCCTGAGCCCATGGGACCTCTTCTGATGCTGGCCATGAATTCTGACTTATGCTCAGCTGCTTTCTGGTAACCAGTGCAGAAACCCCTATCCCAGCTCTCAAACATTCAAGGGCCAAATCTATGTAAAAACTACAATACACATGATCTAATAAATACAGGTTGAGTACCCCTAATCCAAACATCCAAAATCTGAAATGCTCCAAAATCT... |
Task1_train_40687 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | AGGTGGGGGTTCTTGTCCAAATGACATATTGAGGGAGTACATGGCCATGAGAAGAAGAAGGAGGGAATCCTGGTAGGGCAGGGGAAGAAAGCTAAGCAGGGCTGTGGTCTCAGCTGGAGACAAGCCTCAGGCTGGTTCCTTGGGAAGCTCTGAAGTACAAATTGCATCAAAGTGTTTGTTGCACCCAGAGGCAATGGGGCTCACCTTTGGTACCCCTTATGTCAGGCAGCCACTGGCCTCTAGATGTGCATCATGGGGGCACAGTGTAACCTTCCTGGGTGAGGTGCCTCCCATTTGACCAAGGACAATCCTCTGGAAAG... | AGGTGGGGGTTCTTGTCCAAATGACATATTGAGGGAGTACATGGCCATGAGAAGAAGAAGGAGGGAATCCTGGTAGGGCAGGGGAAGAAAGCTAAGCAGGGCTGTGGTCTCAGCTGGAGACAAGCCTCAGGCTGGTTCCTTGGGAAGCTCTGAAGTACAAATTGCATCAAAGTGTTTGTTGCACCCAGAGGCAATGGGGCTCACCTTTGGTACCCCTTATGTCAGGCAGCCACTGGCCTCTAGATGTGCATCATGGGGGCACAGTGTAACCTTCCTGGGTGAGGTGCCTCCCATTTGACCAAGGACAATCCTCTGGAAAG... |
Task1_train_40688 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GGTACTTAAAGACATGATACTGGATGGGATGACCAAGGAAGGGATTATGACAAAGCAAAAAGGTCTGAGAACAAAGTCCCAGGACATTGCAACATATAAAGATGAAGAGTAACAATAATTGAAACTGAAATGTTGTTGTCAAACAGGCTGAGGATTTGACATAATTCTTACAGTACTATAAATACTATAGTCACTTAATAAATTTCCTACAGGGAATGATGAGGAAACCAGAAAAGAAACAGCCTATATGTAATATGTTGGGGAATAAAAATGCTAAAAATTAAAAATAAGGCAGGTAAGGATGAGAGTGAATACAGGAA... | GGTACTTAAAGACATGATACTGGATGGGATGACCAAGGAAGGGATTATGACAAAGCAAAAAGGTCTGAGAACAAAGTCCCAGGACATTGCAACATATAAAGATGAAGAGTAACAATAATTGAAACTGAAATGTTGTTGTCAAACAGGCTGAGGATTTGACATAATTCTTACAGTACTATAAATACTATAGTCACTTAATAAATTTCCTACAGGGAATGATGAGGAAACCAGAAAAGAAACAGCCTATATGTAATATGTTGGGGAATAAAAATGCTAAAAATTAAAAATAAGGCAGGTAAGGATGAGAGTGAATACAGGAA... |
Task1_train_40689 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TGGGGAAAGCTGAAGAAGAGAGAAAATAGAAGAAAAAAGGGTTTGTGTTTCATAATTTTCATGCCTATGTACAGACAGACCTTAAAACTCAGAAGATAATTCTTCCATGAATAGTAAAATTGTCATATAATATTTCTTCCATTTTTCCACAGAGTTTCTTACAAAATCGTCCTATCCAGCATGCACTTTTGGATACTCTTTCAACTCAGAAGTCAACATAAAGGGTAAAATTTTACTTTTATATTATGAATTATCACCCCAATAAGTCCATTATTTCATGACTTTTTGTTCATGTTGATGTTTTACACACACAAGATTTT... | TGGGGAAAGCTGAAGAAGAGAGAAAATAGAAGAAAAAAGGGTTTGTGTTTCATAATTTTCATGCCTATGTACAGACAGACCTTAAAACTCAGAAGATAATTCTTCCATGAATAGTAAAATTGTCATATAATATTTCTTCCATTTTTCCACAGAGTTTCTTACAAAATCGTCCTATCCAGCATGCACTTTTGGATACTCTTTCAACTCAGAAGTCAACATAAAGGGTAAAATTTTACTTTTATATTATGAATTATCACCCCAATAAGTCCATTATTTCATGACTTTTTGTTCATGTTGATGTTTTACACACACAAGATTTT... |
Task1_train_40690 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | ACCTTAAAACTCAGAAGATAATTCTTCCATGAATAGTAAAATTGTCATATAATATTTCTTCCATTTTTCCACAGAGTTTCTTACAAAATCGTCCTATCCAGCATGCACTTTTGGATACTCTTTCAACTCAGAAGTCAACATAAAGGGTAAAATTTTACTTTTATATTATGAATTATCACCCCAATAAGTCCATTATTTCATGACTTTTTGTTCATGTTGATGTTTTACACACACAAGATTTTAACCTTCGTGAGTGCACAGTAATATTTTTTATTGATCTTTTATTTTTTGTTGTTTCCCACGAGGTCAAACATAAAATA... | ACCTTAAAACTCAGAAGATAATTCTTCCATGAATAGTAAAATTGTCATATAATATTTCTTCCATTTTTCCACAGAGTTTCTTACAAAATCGTCCTATCCAGCATGCACTTTTGGATACTCTTTCAACTCAGAAGTCAACATAAAGGGTAAAATTTTACTTTTATATTATGAATTATCACCCCAATAAGTCCATTATTTCATGACTTTTTGTTCATGTTGATGTTTTACACACACAAGATTTTAACCTTCGTGAGTGCACAGTAATATTTTTTATTGATCTTTTATTTTTTGTTGTTTCCCACGAGGTCAAACATAAAATA... |
Task1_train_40691 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | AAGCTACTAATATGACATCATATAATGCATAGTTAGATATGCAAAAATAGGCTCTTGCAAGCTGGTGTGTGCTCTCTCCAGCACACTGCTGCCCTCAGTATTTGTGGGGTACCTGGTACATTTCTTCCACCTATCACTATTTTTCCAATGGCAATAAAATTGATGTGACTGCCTTTAGGTTTCCATCTCCATTTCCCTCTGATTTTATTCTGCCATTATATGCAATTGACATTTTTAAGCTTCTGTCTGTCTCTTAAATCCAAAGAGTTACCATAAGTTCGTTTTCAGAAACCAAACATTTTGTGTCTGTCTCTGTAAAA... | AAGCTACTAATATGACATCATATAATGCATAGTTAGATATGCAAAAATAGGCTCTTGCAAGCTGGTGTGTGCTCTCTCCAGCACACTGCTGCCCTCAGTATTTGTGGGGTACCTGGTACATTTCTTCCACCTATCACTATTTTTCCAATGGCAATAAAATTGATGTGACTGCCTTTAGGTTTCCATCTCCATTTCCCTCTGATTTTATTCTGCCATTATATGCAATTGACATTTTTAAGCTTCTGTCTGTCTCTTAAATCCAAAGAGTTACCATAAGTTCGTTTTCAGAAACCAAACATTTTGTGTCTGTCTCTGTAAAA... |
Task1_train_40692 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CTACTAATATGACATCATATAATGCATAGTTAGATATGCAAAAATAGGCTCTTGCAAGCTGGTGTGTGCTCTCTCCAGCACACTGCTGCCCTCAGTATTTGTGGGGTACCTGGTACATTTCTTCCACCTATCACTATTTTTCCAATGGCAATAAAATTGATGTGACTGCCTTTAGGTTTCCATCTCCATTTCCCTCTGATTTTATTCTGCCATTATATGCAATTGACATTTTTAAGCTTCTGTCTGTCTCTTAAATCCAAAGAGTTACCATAAGTTCGTTTTCAGAAACCAAACATTTTGTGTCTGTCTCTGTAAAACTG... | CTACTAATATGACATCATATAATGCATAGTTAGATATGCAAAAATAGGCTCTTGCAAGCTGGTGTGTGCTCTCTCCAGCACACTGCTGCCCTCAGTATTTGTGGGGTACCTGGTACATTTCTTCCACCTATCACTATTTTTCCAATGGCAATAAAATTGATGTGACTGCCTTTAGGTTTCCATCTCCATTTCCCTCTGATTTTATTCTGCCATTATATGCAATTGACATTTTTAAGCTTCTGTCTGTCTCTTAAATCCAAAGAGTTACCATAAGTTCGTTTTCAGAAACCAAACATTTTGTGTCTGTCTCTGTAAAACTG... |
Task1_train_40693 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TGGCATGATCTCTGCTCACCGCAACCTCCGCTTCCCCAGTTCAAGCGATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGACTAGAGGCGTGCACCACCATGTCCAGCTAATTTTGTATTTTTAGTTGAGACCGGGTTTCACCATGTTGTCTAGGATGGTCTTGATCTCTTGACCTCGTGATCCGCCTGCCTCGGCTCCCGAAGTGCTGGGATTACAGGTGTGAACCACCGAGCCCAGTTAGGACTCTTTTAAATAACCGGATCTCGCATGATCTAACTGAGAAAGAACTCACTCATCACCAAGGAGATAGTGCTAAGCCA... | TGGCATGATCTCTGCTCACCGCAACCTCCGCTTCCCCAGTTCAAGCGATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGACTAGAGGCGTGCACCACCATGTCCAGCTAATTTTGTATTTTTAGTTGAGACCGGGTTTCACCATGTTGTCTAGGATGGTCTTGATCTCTTGACCTCGTGATCCGCCTGCCTCGGCTCCCGAAGTGCTGGGATTACAGGTGTGAACCACCGAGCCCAGTTAGGACTCTTTTAAATAACCGGATCTCGCATGATCTAACTGAGAAAGAACTCACTCATCACCAAGGAGATAGTGCTAAGCCA... |
Task1_train_40694 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | GGGTTTCACCATGTTGTCTAGGATGGTCTTGATCTCTTGACCTCGTGATCCGCCTGCCTCGGCTCCCGAAGTGCTGGGATTACAGGTGTGAACCACCGAGCCCAGTTAGGACTCTTTTAAATAACCGGATCTCGCATGATCTAACTGAGAAAGAACTCACTCATCACCAAGGAGATAGTGCTAAGCCATTCATGAAGGATCTGTCCCCATGATCCAATCCCTCCCACTAGGCCCCACCTCCAACACTGGGAATCACATTTCAACAGATTTGGAGGGGAGCCAGGTCCAAATCATATCAACTACAGGCACATTTGAGTTAG... | GGGTTTCACCATGTTGTCTAGGATGGTCTTGATCTCTTGACCTCGTGATCCGCCTGCCTCGGCTCCCGAAGTGCTGGGATTACAGGTGTGAACCACCGAGCCCAGTTAGGACTCTTTTAAATAACCGGATCTCGCATGATCTAACTGAGAAAGAACTCACTCATCACCAAGGAGATAGTGCTAAGCCATTCATGAAGGATCTGTCCCCATGATCCAATCCCTCCCACTAGGCCCCACCTCCAACACTGGGAATCACATTTCAACAGATTTGGAGGGGAGCCAGGTCCAAATCATATCAACTACAGGCACATTTGAGTTAG... |
Task1_train_40695 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AATCCCTCCCACTAGGCCCCACCTCCAACACTGGGAATCACATTTCAACAGATTTGGAGGGGAGCCAGGTCCAAATCATATCAACTACAGGCACATTTGAGTTAGTCATATGCTTTATATTTTGGACATAAGGATTCTTCATGTTATAATGAAGTTAGTCATCTATTTTCATTGGTTCAGAATATTTAAGTTTACTTACAATCATGATAGAGTAATACAGCTTAACTAATTAATGTCTATATTTGGGCTGGAATTGCAGGTATTCATTGTTTTGATTTTGGGTGGAAATCATGCAAATTAGATGTTCTGTTTGTCAGTTT... | AATCCCTCCCACTAGGCCCCACCTCCAACACTGGGAATCACATTTCAACAGATTTGGAGGGGAGCCAGGTCCAAATCATATCAACTACAGGCACATTTGAGTTAGTCATATGCTTTATATTTTGGACATAAGGATTCTTCATGTTATAATGAAGTTAGTCATCTATTTTCATTGGTTCAGAATATTTAAGTTTACTTACAATCATGATAGAGTAATACAGCTTAACTAATTAATGTCTATATTTGGGCTGGAATTGCAGGTATTCATTGTTTTGATTTTGGGTGGAAATCATGCAAATTAGATGTTCTGTTTGTCAGTTT... |
Task1_train_40696 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GACATAAGGATTCTTCATGTTATAATGAAGTTAGTCATCTATTTTCATTGGTTCAGAATATTTAAGTTTACTTACAATCATGATAGAGTAATACAGCTTAACTAATTAATGTCTATATTTGGGCTGGAATTGCAGGTATTCATTGTTTTGATTTTGGGTGGAAATCATGCAAATTAGATGTTCTGTTTGTCAGTTTCTTTTGTTCCCTATTCTATCCCCACCTTTTGGCAGAATGCTAGGTGAAGAGTAATTGCTCAATATATTACTTGAATAGAAATTTAAAATGTTACAAATATTTTATTTTTCATTAAAAAAGTGAC... | GACATAAGGATTCTTCATGTTATAATGAAGTTAGTCATCTATTTTCATTGGTTCAGAATATTTAAGTTTACTTACAATCATGATAGAGTAATACAGCTTAACTAATTAATGTCTATATTTGGGCTGGAATTGCAGGTATTCATTGTTTTGATTTTGGGTGGAAATCATGCAAATTAGATGTTCTGTTTGTCAGTTTCTTTTGTTCCCTATTCTATCCCCACCTTTTGGCAGAATGCTAGGTGAAGAGTAATTGCTCAATATATTACTTGAATAGAAATTTAAAATGTTACAAATATTTTATTTTTCATTAAAAAAGTGAC... |
Task1_train_40697 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | TTTTTTTTTGAGACAGTGTTTCTCTCTGTCACTCAGGCTGGAGTACAGTGACACATTCATGACTCACTGCAATCTTGACTTCTGAGCTCAAGAAATTCTCCTACTTCAGCTTACCCAGTAGTTGGGACCTACAGACATGTACCACCATGCCTGGCTAATTTGTAAACGTTTTTGTAGAGATGGGGTTTCCCTATGTTACCCATGCTGGTCTTGAACTCCTGGGCTCAAGTGATCCTCCCGCCTCGACCTCCCAAAGTGTTGGGATAACAGGCATGAACCCTGTGCCTGGCCTCAACTGAATTTGATGGTTCCATTTTGGT... | TTTTTTTTTGAGACAGTGTTTCTCTCTGTCACTCAGGCTGGAGTACAGTGACACATTCATGACTCACTGCAATCTTGACTTCTGAGCTCAAGAAATTCTCCTACTTCAGCTTACCCAGTAGTTGGGACCTACAGACATGTACCACCATGCCTGGCTAATTTGTAAACGTTTTTGTAGAGATGGGGTTTCCCTATGTTACCCATGCTGGTCTTGAACTCCTGGGCTCAAGTGATCCTCCCGCCTCGACCTCCCAAAGTGTTGGGATAACAGGCATGAACCCTGTGCCTGGCCTCAACTGAATTTGATGGTTCCATTTTGGT... |
Task1_train_40698 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | CAAAGAGAATAGGATGTTTACCAGAGGCTGGGAAGGGTAGTGGGAACCTGGGGGAGAGGTGAGCATGGTTAATGGGTATAAAAAATAATAGAAAGAATGAATAAGACCTACTATTTGATAGTGCAATAGAGTGACTCTAGTCAATAATAACTTAATCACACGTTTTAAGATATCTAAAGGAATGTAATTGGATTGTTTATAACACAGAGGATAACTGCTTGAGGGGATAGATACCCCATTCTTCATGATGTGATTATTTCACATTGCATGCCTGTATCAAAACATCTCATGTACCCCATAAATATATAAACCTACTGTGT... | CAAAGAGAATAGGATGTTTACCAGAGGCTGGGAAGGGTAGTGGGAACCTGGGGGAGAGGTGAGCATGGTTAATGGGTATAAAAAATAATAGAAAGAATGAATAAGACCTACTATTTGATAGTGCAATAGAGTGACTCTAGTCAATAATAACTTAATCACACGTTTTAAGATATCTAAAGGAATGTAATTGGATTGTTTATAACACAGAGGATAACTGCTTGAGGGGATAGATACCCCATTCTTCATGATGTGATTATTTCACATTGCATGCCTGTATCAAAACATCTCATGTACCCCATAAATATATAAACCTACTGTGT... |
Task1_train_40699 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ATAATAACTTAATCACACGTTTTAAGATATCTAAAGGAATGTAATTGGATTGTTTATAACACAGAGGATAACTGCTTGAGGGGATAGATACCCCATTCTTCATGATGTGATTATTTCACATTGCATGCCTGTATCAAAACATCTCATGTACCCCATAAATATATAAACCTACTGTGTACCCACAAAAATAAAAAATATATATTTATTAAAGTTAGTCAATTATTGTGCTACAACAATAGTGCTCCTCATAACACACATGTGATTAATTGTATTGGCATCAAAAAAATAGATTAACCATGTTCACAGAATAAGACTGTAAT... | ATAATAACTTAATCACACGTTTTAAGATATCTAAAGGAATGTAATTGGATTGTTTATAACACAGAGGATAACTGCTTGAGGGGATAGATACCCCATTCTTCATGATGTGATTATTTCACATTGCATGCCTGTATCAAAACATCTCATGTACCCCATAAATATATAAACCTACTGTGTACCCACAAAAATAAAAAATATATATTTATTAAAGTTAGTCAATTATTGTGCTACAACAATAGTGCTCCTCATAACACACATGTGATTAATTGTATTGGCATCAAAAAAATAGATTAACCATGTTCACAGAATAAGACTGTAAT... |
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