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_39000 | Given a variant located on Chromosome 7, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AATAGAATAGAGGGAATGAGTTCTACGACCGAACTGTTTAATGACCTCAGCATCCTATGTCCTGATATTGTGCCTGTGGAGGATAACATTTTTATTTTATTTTTAAAGACAAGATCTTGGTCTGTTGCCTACGCTGGAGTGCAGTGGTGCGATCGTGATTCACTGCAGCCTTGAACTACTGGGTTCAAATGATTCTTCCACCTCAACCTCTTGAGTAGCTGAGACTACAGGTGTGCACCACTACTCCTGGCTCATTTTAATTTTAATTTTAATTTTGTAGAGACAGGGTCTGCCTATTTGCTCAGGTTGGTCTCAAACTC... | AATAGAATAGAGGGAATGAGTTCTACGACCGAACTGTTTAATGACCTCAGCATCCTATGTCCTGATATTGTGCCTGTGGAGGATAACATTTTTATTTTATTTTTAAAGACAAGATCTTGGTCTGTTGCCTACGCTGGAGTGCAGTGGTGCGATCGTGATTCACTGCAGCCTTGAACTACTGGGTTCAAATGATTCTTCCACCTCAACCTCTTGAGTAGCTGAGACTACAGGTGTGCACCACTACTCCTGGCTCATTTTAATTTTAATTTTAATTTTGTAGAGACAGGGTCTGCCTATTTGCTCAGGTTGGTCTCAAACTC... |
Task1_train_39001 | This variant lies on Chromosome 7. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATTATAAGGAAAATGTCAGTAGACTTAGTCACATCATTTCAGTAAATATTTTTTAAGGATTTATTCACCATCCCAGCTGCTAGAGTGCAAAGATGAATGAATTAGGTCTTGTAGGTCCTGCTAAGGAATTTTGTCTTTATTGTGGGGAGCCATTGAAAGTTTTCAAACGGGTGACATGATCAACTATGAAGTCTGGCAGGGATGTGGAAGCAAGATAAGATGTAAGTGACATCTTTTATCATATAGTCCAAAACATTAAATAAAAATAGGTTTAAAAATGAACACTGATACAGGAGTCTCAGAGAATATGCTAAGCATAA... | ATTATAAGGAAAATGTCAGTAGACTTAGTCACATCATTTCAGTAAATATTTTTTAAGGATTTATTCACCATCCCAGCTGCTAGAGTGCAAAGATGAATGAATTAGGTCTTGTAGGTCCTGCTAAGGAATTTTGTCTTTATTGTGGGGAGCCATTGAAAGTTTTCAAACGGGTGACATGATCAACTATGAAGTCTGGCAGGGATGTGGAAGCAAGATAAGATGTAAGTGACATCTTTTATCATATAGTCCAAAACATTAAATAAAAATAGGTTTAAAAATGAACACTGATACAGGAGTCTCAGAGAATATGCTAAGCATAA... |
Task1_train_39002 | This alteration occurs on Chromosome 7. Is it associated with a disease or is it a benign variant? | Benign | ACACTGGGAAGCTATTGAAGAGTTTTAAGCAGGGTACTGAAATGATCTATTTGTGTTTTTAAAAGATTACCAGGCCGGGAGCAGTGGCTCACTGACTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACAAGGTCAGGAGTTTGAGACCAGCCTGGCCAATATGGTGAAAGCCTGTCTCTACTGAAAATATAAAAATCAGCTGGGTGTGGTGGCGGGCGTCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTTGGGAGGTGGAGGTTGCAGTGAGCCGAGATTGCGCC... | ACACTGGGAAGCTATTGAAGAGTTTTAAGCAGGGTACTGAAATGATCTATTTGTGTTTTTAAAAGATTACCAGGCCGGGAGCAGTGGCTCACTGACTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACAAGGTCAGGAGTTTGAGACCAGCCTGGCCAATATGGTGAAAGCCTGTCTCTACTGAAAATATAAAAATCAGCTGGGTGTGGTGGCGGGCGTCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTTGGGAGGTGGAGGTTGCAGTGAGCCGAGATTGCGCC... |
Task1_train_39003 | This variant is present on Chromosome 7. Is the change likely to result in a pathogenic outcome? | Benign | CAGGAGTGTGAACACCTGTCTTAGCCTCCGCAACATCTTGGCTGTGCAGGTCCAAGGAGATGATACTTGTACAGCACCTCAAATGTGGCTGGTACACAGGAGACACTCAGCACACTTTCCTTTCATTCTTTTTTCCTTCCTTAATAATAGTTTGCTGGACAAACTAATTTATTTAAAAAGGGGTCCCCATGGGGAAAAATATGATGACGGAGAGACCACTGATGTCTAGGTCTTTCTCCTCCTCCTTGCCCCAGCAGCTTCTCTGAGAGTGGGGTCTCAATTTACAAGCCATTCTGGCCTGGGCCGCACTGATGTGTGTG... | CAGGAGTGTGAACACCTGTCTTAGCCTCCGCAACATCTTGGCTGTGCAGGTCCAAGGAGATGATACTTGTACAGCACCTCAAATGTGGCTGGTACACAGGAGACACTCAGCACACTTTCCTTTCATTCTTTTTTCCTTCCTTAATAATAGTTTGCTGGACAAACTAATTTATTTAAAAAGGGGTCCCCATGGGGAAAAATATGATGACGGAGAGACCACTGATGTCTAGGTCTTTCTCCTCCTCCTTGCCCCAGCAGCTTCTCTGAGAGTGGGGTCTCAATTTACAAGCCATTCTGGCCTGGGCCGCACTGATGTGTGTG... |
Task1_train_39004 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | TTCCTTAATAATAGTTTGCTGGACAAACTAATTTATTTAAAAAGGGGTCCCCATGGGGAAAAATATGATGACGGAGAGACCACTGATGTCTAGGTCTTTCTCCTCCTCCTTGCCCCAGCAGCTTCTCTGAGAGTGGGGTCTCAATTTACAAGCCATTCTGGCCTGGGCCGCACTGATGTGTGTGGGTATATGAGGGCGTTTGCTTTAATTTGTTGTGATCTCTACAACTCTGTTCTCCTTGCTTGCAACTATTGGCTCTGCTGGGGTTCAGAACTCCCTAAGTTTATGAATGCACTTTGAGCTGGCGTCCAGGCAGCCCC... | TTCCTTAATAATAGTTTGCTGGACAAACTAATTTATTTAAAAAGGGGTCCCCATGGGGAAAAATATGATGACGGAGAGACCACTGATGTCTAGGTCTTTCTCCTCCTCCTTGCCCCAGCAGCTTCTCTGAGAGTGGGGTCTCAATTTACAAGCCATTCTGGCCTGGGCCGCACTGATGTGTGTGGGTATATGAGGGCGTTTGCTTTAATTTGTTGTGATCTCTACAACTCTGTTCTCCTTGCTTGCAACTATTGGCTCTGCTGGGGTTCAGAACTCCCTAAGTTTATGAATGCACTTTGAGCTGGCGTCCAGGCAGCCCC... |
Task1_train_39005 | The following genetic variant occurs on Chromosome 7. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CATTTAGGGGGTGCCAGGAAAGGCAGAGGGCCCAGATGGTGGAAGAAGTGTAGCGGCAGCCCGCCTGGGCATTCCCCTGGGAGGCATGGAGATTAATGAGTAACGTAGAACAGAGGAGCCCTGTTACCCAGGCCCCGCCCCCATGCCCTGGCTGTCCCTTGGCCAGAGCGCCTGGCCTGAGCCCAGGTCCTCTATATCTCATGGGACATGGTGTCTCCTCTGGCTGCTCCTCATGTGGCTGGGAGGATTACGTGAGATGCTGGGTGTGAAAACACGCACGTAGGTGTGAGTGCTGAGCAGCCGCAGGGGTGCGGGGGGGT... | CATTTAGGGGGTGCCAGGAAAGGCAGAGGGCCCAGATGGTGGAAGAAGTGTAGCGGCAGCCCGCCTGGGCATTCCCCTGGGAGGCATGGAGATTAATGAGTAACGTAGAACAGAGGAGCCCTGTTACCCAGGCCCCGCCCCCATGCCCTGGCTGTCCCTTGGCCAGAGCGCCTGGCCTGAGCCCAGGTCCTCTATATCTCATGGGACATGGTGTCTCCTCTGGCTGCTCCTCATGTGGCTGGGAGGATTACGTGAGATGCTGGGTGTGAAAACACGCACGTAGGTGTGAGTGCTGAGCAGCCGCAGGGGTGCGGGGGGGT... |
Task1_train_39006 | A genomic change on Chromosome 7 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCTGGGCCTGGTGGCAGCTCCACCGGGCAGGCCTTGTCTGCATTCTCACGGGTGGGAATCTCAGCCGCCCGGAGACCTGAATGCCTGCCAGCGCTCCCGGTGTCCCGTCAGGACTGCACTGACCCAGGCCCACCTTGCATGTGCCACAGGAATTTCTCCTGGGAACAGCCCCTTGCAAGGCCTCATCAACTGTCTGAAGGAAATCCTTGTGCCTGGGCCCCGGCACCCCGAGACATCCCCAAGCTTCTTGCCACCTCTCCCTAGCCTGGGCACGTCCAGGCTAACCAGAGCAGACCTGGGGCCTGGGAGCCCGCCCTGGG... | CCTGGGCCTGGTGGCAGCTCCACCGGGCAGGCCTTGTCTGCATTCTCACGGGTGGGAATCTCAGCCGCCCGGAGACCTGAATGCCTGCCAGCGCTCCCGGTGTCCCGTCAGGACTGCACTGACCCAGGCCCACCTTGCATGTGCCACAGGAATTTCTCCTGGGAACAGCCCCTTGCAAGGCCTCATCAACTGTCTGAAGGAAATCCTTGTGCCTGGGCCCCGGCACCCCGAGACATCCCCAAGCTTCTTGCCACCTCTCCCTAGCCTGGGCACGTCCAGGCTAACCAGAGCAGACCTGGGGCCTGGGAGCCCGCCCTGGG... |
Task1_train_39007 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | GCCCACACCTGTGGCCAACGCCCTCATGACAGCCGCAGGCCAGGCTTCTATGTGGGTGGCCAGGACAGGCCAGGCTTCTTCCACGGCAGCCAAAGCAGGGCCGCGCCAGAGCCAGGACTGACACGTCCAGTGCTCTGTGCCCAGCACCCCTGTGACCCCCCTTCCCTGGACACAGCAGAAGACAGGGGGCTTCTGCAGTTTGCAGAGATTGAGCTACAGTCCCCCTCATCTGTGAATGTTTGATCTTCACAGGAAGCCCACCAGGAAGCTCCCCACTGCAGGGTCTGGAGAATTGTCTCAAGGAGATACCTGTGCCTGTG... | GCCCACACCTGTGGCCAACGCCCTCATGACAGCCGCAGGCCAGGCTTCTATGTGGGTGGCCAGGACAGGCCAGGCTTCTTCCACGGCAGCCAAAGCAGGGCCGCGCCAGAGCCAGGACTGACACGTCCAGTGCTCTGTGCCCAGCACCCCTGTGACCCCCCTTCCCTGGACACAGCAGAAGACAGGGGGCTTCTGCAGTTTGCAGAGATTGAGCTACAGTCCCCCTCATCTGTGAATGTTTGATCTTCACAGGAAGCCCACCAGGAAGCTCCCCACTGCAGGGTCTGGAGAATTGTCTCAAGGAGATACCTGTGCCTGTG... |
Task1_train_39008 | This variant is present on Chromosome 7. Is the change likely to result in a pathogenic outcome? | Benign | TCCCCAACTCCTGCAGCTGGCTCCATTTACAGGCATTGGCCCTGGTCTGTGTAGACCCAGGCTGCACCACATTCTTCACTCCGCAGTGGGCCTAGTGGAAAATGGCAGAGTGGGCTGGGTGTGGACCACAGGATGCCCCAGCACGCCCTTGGAAGTCTCACTGGGGCAGGACCCGCAGATGAGAGTCCTTTTTCCCAGCTGCCTCCCCAGCCGCCTCCTCCTGCCGGAGCCCCCTGCATACAGGGCAGGAACACCACACACACACGCACCGCGGCGGGCCCTGCCACCAGAATTAGGCTCCCTCATGGGCCAAGTTTCCG... | TCCCCAACTCCTGCAGCTGGCTCCATTTACAGGCATTGGCCCTGGTCTGTGTAGACCCAGGCTGCACCACATTCTTCACTCCGCAGTGGGCCTAGTGGAAAATGGCAGAGTGGGCTGGGTGTGGACCACAGGATGCCCCAGCACGCCCTTGGAAGTCTCACTGGGGCAGGACCCGCAGATGAGAGTCCTTTTTCCCAGCTGCCTCCCCAGCCGCCTCCTCCTGCCGGAGCCCCCTGCATACAGGGCAGGAACACCACACACACACGCACCGCGGCGGGCCCTGCCACCAGAATTAGGCTCCCTCATGGGCCAAGTTTCCG... |
Task1_train_39009 | A genomic variant on Chromosome 7 is under review. What is the biological outcome — benign or pathogenic? | Benign | TCCACCCACACAGCCTCCTTCCTGCTGGGCACACACTGCTCACAACTCAGGAGACCCAGGACTACTCCCCCAGCACAAAGCTGCCCCCAACACCGAGTCTCCCTTCTGGGAGTATGCCACTGTCATCCAGTCAGTGTCAAACAGAAATCGGGCTGAGCTCATTGATTCCCCGACCCACACTAGTCAACAGGTCCTGTATCCTCTGCCTATTAAGTGTCTCTTGAATCCATCACTTCTCTGTCTCCTCTGACACAACTATGGTCCCAGGTCACCACAACCTGTCACCAGGACAACTGATGCGCAGGCCTCCAATTTCGCTC... | TCCACCCACACAGCCTCCTTCCTGCTGGGCACACACTGCTCACAACTCAGGAGACCCAGGACTACTCCCCCAGCACAAAGCTGCCCCCAACACCGAGTCTCCCTTCTGGGAGTATGCCACTGTCATCCAGTCAGTGTCAAACAGAAATCGGGCTGAGCTCATTGATTCCCCGACCCACACTAGTCAACAGGTCCTGTATCCTCTGCCTATTAAGTGTCTCTTGAATCCATCACTTCTCTGTCTCCTCTGACACAACTATGGTCCCAGGTCACCACAACCTGTCACCAGGACAACTGATGCGCAGGCCTCCAATTTCGCTC... |
Task1_train_39010 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGGGGCTGAGTTCCCAGCTTCCCTGGGGCTGCCTCAGACTCCTTCAAGCAGGGCGGCTGCTAAGGGTATGTAATGAGATGGACTACAAGGTTACAAGAGCCACCACTGTGAAGAGTTCCTGGAATATGTGTATGTAAGACAGTGGAAGCAAGGAAGTCCCCTGACCTGATGCCCCTAGGAGAAGGGCTGGGGACTTCCCAGCCCCCAGATGGACCCTGGTTCCAAGCAAATCACTGGGGAGAATCAGGATGTCAAAAGCCAGGCACATTCCTGCCTTAGTGCTCTGTCCTGGCTGTACTCCTGCCTGAAGCACTTTTCCC... | AGGGGCTGAGTTCCCAGCTTCCCTGGGGCTGCCTCAGACTCCTTCAAGCAGGGCGGCTGCTAAGGGTATGTAATGAGATGGACTACAAGGTTACAAGAGCCACCACTGTGAAGAGTTCCTGGAATATGTGTATGTAAGACAGTGGAAGCAAGGAAGTCCCCTGACCTGATGCCCCTAGGAGAAGGGCTGGGGACTTCCCAGCCCCCAGATGGACCCTGGTTCCAAGCAAATCACTGGGGAGAATCAGGATGTCAAAAGCCAGGCACATTCCTGCCTTAGTGCTCTGTCCTGGCTGTACTCCTGCCTGAAGCACTTTTCCC... |
Task1_train_39011 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CCCCTTTACAAGCCACACGGGATGTAGATCTCAGCCCCAAAGCATTGCCTGTTTTCATCATCGACTTCATTCACAGACATAGTTCTAAATGACTTTCAGCTATTTCTAGAAATTAGACACATCTTCCTAAGCGAAGGTTTACCATGTTTAAGGTTCCATGAAAGAATGTGCCCTAAGTTGTTGCCCAGCCCCTGGCTGAGAAGAAACGGGCGTGTGGGAGGCGGGTGAAGAGCACACAGGGAGGGGACGGAGAAGCTCCTGAGCCAGCCTCCTTCATGGCTCAGTTTCATTTCAGTGCGTGGCACTTCCCAGAAGAAACG... | CCCCTTTACAAGCCACACGGGATGTAGATCTCAGCCCCAAAGCATTGCCTGTTTTCATCATCGACTTCATTCACAGACATAGTTCTAAATGACTTTCAGCTATTTCTAGAAATTAGACACATCTTCCTAAGCGAAGGTTTACCATGTTTAAGGTTCCATGAAAGAATGTGCCCTAAGTTGTTGCCCAGCCCCTGGCTGAGAAGAAACGGGCGTGTGGGAGGCGGGTGAAGAGCACACAGGGAGGGGACGGAGAAGCTCCTGAGCCAGCCTCCTTCATGGCTCAGTTTCATTTCAGTGCGTGGCACTTCCCAGAAGAAACG... |
Task1_train_39012 | This sequence variant lies on Chromosome 7. Is it clinically significant, and what condition might it cause if any? | Benign | AGGCAAAGAAGGAAATACATTTCACTTTACAGCTGTCATTTTCTACAGAGGATTTTTTTTTTTCCAGAACAAAATTCAAAAAGTCCGTCTTTTTTGAGCTATAGAACTTTCGTGGTGATTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCTGTCCCCCAGGCTGGAGTGCAGGGGCACAATCTCGGCTCACTGCAAGTGCAAGCTCTGCCTCCCGGGTTCACGCCATTCTCCTTTCAGCCTCCAAAGTAGCTAGGACTACAGGTGCCCGCCACCATGCCCAGCTAATTTTTTTATATTTTTAGTAGAGACGGG... | AGGCAAAGAAGGAAATACATTTCACTTTACAGCTGTCATTTTCTACAGAGGATTTTTTTTTTTCCAGAACAAAATTCAAAAAGTCCGTCTTTTTTGAGCTATAGAACTTTCGTGGTGATTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCTGTCCCCCAGGCTGGAGTGCAGGGGCACAATCTCGGCTCACTGCAAGTGCAAGCTCTGCCTCCCGGGTTCACGCCATTCTCCTTTCAGCCTCCAAAGTAGCTAGGACTACAGGTGCCCGCCACCATGCCCAGCTAATTTTTTTATATTTTTAGTAGAGACGGG... |
Task1_train_39013 | This variant is found on Chromosome 7. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TCATCCACTACAGAACTTTCACCAACACGTCACCTCCAATCATTTCAGTCTCTCATGTTATCGCACCACAGCAACCTACAAGACAAACTCCAAAGCTGCAAACTTTGCAGGCAAACAACAACTTAAGTGTGTTCTTCTTTGAGAAAAGGAACTGAATATTTTTTTTCCTTCTAGCTAATGGATTTCACCATCATCTCACTTTAGGCCATCAAAGATTTTAAAGAACGAAGGATAGGGTATGACTAGAACTGCATGTTGGACAGTGAAGGCAATGTCTAAGTTCATATTGCGGCTCTCCGTTCTCATATTATTGGAACTTA... | TCATCCACTACAGAACTTTCACCAACACGTCACCTCCAATCATTTCAGTCTCTCATGTTATCGCACCACAGCAACCTACAAGACAAACTCCAAAGCTGCAAACTTTGCAGGCAAACAACAACTTAAGTGTGTTCTTCTTTGAGAAAAGGAACTGAATATTTTTTTTCCTTCTAGCTAATGGATTTCACCATCATCTCACTTTAGGCCATCAAAGATTTTAAAGAACGAAGGATAGGGTATGACTAGAACTGCATGTTGGACAGTGAAGGCAATGTCTAAGTTCATATTGCGGCTCTCCGTTCTCATATTATTGGAACTTA... |
Task1_train_39014 | Here is a variant on Chromosome 7. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TCAAAGATTTTAAAGAACGAAGGATAGGGTATGACTAGAACTGCATGTTGGACAGTGAAGGCAATGTCTAAGTTCATATTGCGGCTCTCCGTTCTCATATTATTGGAACTTAATAGGGGTTTACCATGTTTATTAAATGGATGATTGATGACTATTGAATTAATATGATTCATTGGAGCAAGTATTTGTTGGACACCTGATAGGTATGTAAGGTGATCCCTAACTCATGATTAACAGGTTTCCTAGTACCTTTTAAATTGTTGGTGTGTGTTCCAACACTTTCCAGAAAGTTTTATTGGTGGCAATACTCTACAGTCCAA... | TCAAAGATTTTAAAGAACGAAGGATAGGGTATGACTAGAACTGCATGTTGGACAGTGAAGGCAATGTCTAAGTTCATATTGCGGCTCTCCGTTCTCATATTATTGGAACTTAATAGGGGTTTACCATGTTTATTAAATGGATGATTGATGACTATTGAATTAATATGATTCATTGGAGCAAGTATTTGTTGGACACCTGATAGGTATGTAAGGTGATCCCTAACTCATGATTAACAGGTTTCCTAGTACCTTTTAAATTGTTGGTGTGTGTTCCAACACTTTCCAGAAAGTTTTATTGGTGGCAATACTCTACAGTCCAA... |
Task1_train_39015 | Here’s a variant located on Chromosome 7. What is the predicted biological effect — harmless or disease-causing? | Benign | GCAAAGTTGATTGCATCACTCCCTGTTTACAAACCCCAAAAGATTCCATTCCCACTGAGGGAATCCACACTTCTTGGCAGATGCTTCCAGTCTCTTTTGGAAAGTATATATAAATATTTGAGGTATAAATAAAAGAGAATGAGCTGGAATGTTGCAGACTAGAAGGGAGCTAGATAAGGAAATGGGGGCCATAAGCACAAGGACTCCCCTTTCCAGATGGGGTGTAGAGGACATAAGGATGGCAAGACCGTTTACATCCTCGCCAGCTCCCTGGTTGGGAACATAGTAAATATCTTTGTTGATGGTGTGGGAGGAGCTAA... | GCAAAGTTGATTGCATCACTCCCTGTTTACAAACCCCAAAAGATTCCATTCCCACTGAGGGAATCCACACTTCTTGGCAGATGCTTCCAGTCTCTTTTGGAAAGTATATATAAATATTTGAGGTATAAATAAAAGAGAATGAGCTGGAATGTTGCAGACTAGAAGGGAGCTAGATAAGGAAATGGGGGCCATAAGCACAAGGACTCCCCTTTCCAGATGGGGTGTAGAGGACATAAGGATGGCAAGACCGTTTACATCCTCGCCAGCTCCCTGGTTGGGAACATAGTAAATATCTTTGTTGATGGTGTGGGAGGAGCTAA... |
Task1_train_39016 | This mutation occurs on Chromosome 7. Does this change lead to a known medical condition, or is it benign? | Benign | ACTGGTGATGGTGGTTACCTATTGCCTATTCAAAAATAACGGTTTAAAAAACACCCCAAAACTAATAGGGATGGATCGTGAGTGGTTACGGAAAAAGTAAAATAATGTTTTGCCCCTAGTTTGGATTTGACAGGAAGAACTGGTAATATTGGGCCTGAATCCATCCAGCATGGCCCTAACCAGCCAGGGCCAGTCTGGGCTGCTCCCCTTGGGTTGGGCCTGCACCCCATCCCTGTCACTCAGATGGCTTTTGTGGCCTGTGTCCCAGCTTGGTCTTCAGGTCTTGCCTGGCTGAGATTGTTGGTTTTCATGGTAAAAGC... | ACTGGTGATGGTGGTTACCTATTGCCTATTCAAAAATAACGGTTTAAAAAACACCCCAAAACTAATAGGGATGGATCGTGAGTGGTTACGGAAAAAGTAAAATAATGTTTTGCCCCTAGTTTGGATTTGACAGGAAGAACTGGTAATATTGGGCCTGAATCCATCCAGCATGGCCCTAACCAGCCAGGGCCAGTCTGGGCTGCTCCCCTTGGGTTGGGCCTGCACCCCATCCCTGTCACTCAGATGGCTTTTGTGGCCTGTGTCCCAGCTTGGTCTTCAGGTCTTGCCTGGCTGAGATTGTTGGTTTTCATGGTAAAAGC... |
Task1_train_39017 | Given this context: Chromosome 7 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGGATGGATCGTGAGTGGTTACGGAAAAAGTAAAATAATGTTTTGCCCCTAGTTTGGATTTGACAGGAAGAACTGGTAATATTGGGCCTGAATCCATCCAGCATGGCCCTAACCAGCCAGGGCCAGTCTGGGCTGCTCCCCTTGGGTTGGGCCTGCACCCCATCCCTGTCACTCAGATGGCTTTTGTGGCCTGTGTCCCAGCTTGGTCTTCAGGTCTTGCCTGGCTGAGATTGTTGGTTTTCATGGTAAAAGCAGGGTCAGACTCCCTGCCGTCACCTGCTGCGTAAGACACAGAAAGTGCTGCCTGCTGACTGACTGTC... | GGGATGGATCGTGAGTGGTTACGGAAAAAGTAAAATAATGTTTTGCCCCTAGTTTGGATTTGACAGGAAGAACTGGTAATATTGGGCCTGAATCCATCCAGCATGGCCCTAACCAGCCAGGGCCAGTCTGGGCTGCTCCCCTTGGGTTGGGCCTGCACCCCATCCCTGTCACTCAGATGGCTTTTGTGGCCTGTGTCCCAGCTTGGTCTTCAGGTCTTGCCTGGCTGAGATTGTTGGTTTTCATGGTAAAAGCAGGGTCAGACTCCCTGCCGTCACCTGCTGCGTAAGACACAGAAAGTGCTGCCTGCTGACTGACTGTC... |
Task1_train_39018 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | TCTCAAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAATAAAATAAAAATAAAACAAAACTTTCTTATGCTCGCTTCAGCAGCACATAGACTAAAGCAAAACTTTCTCACATCAACAACTGAAAAGGTAGGCCGGATGCAGTGGTTCACATCTGTAATCCCAACACTTTGGGAGGCTGGGGCGGGAGGATCGTTTGAGACCAGCCTGGGCAACACAGTGAGACCCCATCTCTACAGAAGAAAAACATTAAAATAAAATAATTAGCTGGATGTGGTGATGTGATCCTGTAGTCCCAGCTACTCAGAGGCCGA... | TCTCAAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAATAAAATAAAAATAAAACAAAACTTTCTTATGCTCGCTTCAGCAGCACATAGACTAAAGCAAAACTTTCTCACATCAACAACTGAAAAGGTAGGCCGGATGCAGTGGTTCACATCTGTAATCCCAACACTTTGGGAGGCTGGGGCGGGAGGATCGTTTGAGACCAGCCTGGGCAACACAGTGAGACCCCATCTCTACAGAAGAAAAACATTAAAATAAAATAATTAGCTGGATGTGGTGATGTGATCCTGTAGTCCCAGCTACTCAGAGGCCGA... |
Task1_train_39019 | This alteration occurs on Chromosome 7. Is it associated with a disease or is it a benign variant? | Benign | GCAGAATACATCTTCGCAAGGCATTATTCCAATTATGCCAGACATGCCATGGATATACGTAGAGAAAACACCGGAGGCAACATACCAAAATATTAAATGTAATTGACTCTACGAGGTAAAACTGAGTTTTATGTTCCCCTATTTCCTATTTATGCAATAGATTTAAAAAGTATTTTTACGACTAATTATACAATTCAAAAATTGCCTGTGTTGAAAAGCATGAAAGTACATGAAATTGTACTACCCTGGAAACCCCAGGAAGTGTTTAGTTTGGAAAGCCAGGGCCACCTGCTAGTGGGTGAGTCATGGGCACAGGCTCG... | GCAGAATACATCTTCGCAAGGCATTATTCCAATTATGCCAGACATGCCATGGATATACGTAGAGAAAACACCGGAGGCAACATACCAAAATATTAAATGTAATTGACTCTACGAGGTAAAACTGAGTTTTATGTTCCCCTATTTCCTATTTATGCAATAGATTTAAAAAGTATTTTTACGACTAATTATACAATTCAAAAATTGCCTGTGTTGAAAAGCATGAAAGTACATGAAATTGTACTACCCTGGAAACCCCAGGAAGTGTTTAGTTTGGAAAGCCAGGGCCACCTGCTAGTGGGTGAGTCATGGGCACAGGCTCG... |
Task1_train_39020 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | ACAGCAGTGTGCTTCCTTGTTGAAGGGGCACATTCATTTATTAATCCAATGTCCATTAAGGTCACTCTGCCAGGCAGGATGTGGGGCTTATGGCTGGTGCGTGTGGCTTTGTGGGGGGAGGGGTTGTGGCTGGTGAGGACACAAAGCTGACTGCCCTAGAGGAGCTCAGAGCCTCACTTCTGTTTTCTCTTCCCTCCCCACAGGTAAGGCTGGCCTCTCTGCAGTCAGAGGTCTGAGCTCTGCCATGGGGATAGGGGTGTCTTTATTACTGCAGTTTTCTCTAACACCTGGGGGCTACCGGAGTGTGGGCCGAAGCAGGC... | ACAGCAGTGTGCTTCCTTGTTGAAGGGGCACATTCATTTATTAATCCAATGTCCATTAAGGTCACTCTGCCAGGCAGGATGTGGGGCTTATGGCTGGTGCGTGTGGCTTTGTGGGGGGAGGGGTTGTGGCTGGTGAGGACACAAAGCTGACTGCCCTAGAGGAGCTCAGAGCCTCACTTCTGTTTTCTCTTCCCTCCCCACAGGTAAGGCTGGCCTCTCTGCAGTCAGAGGTCTGAGCTCTGCCATGGGGATAGGGGTGTCTTTATTACTGCAGTTTTCTCTAACACCTGGGGGCTACCGGAGTGTGGGCCGAAGCAGGC... |
Task1_train_39021 | Chromosome 7 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTTGTTGAAGGGGCACATTCATTTATTAATCCAATGTCCATTAAGGTCACTCTGCCAGGCAGGATGTGGGGCTTATGGCTGGTGCGTGTGGCTTTGTGGGGGGAGGGGTTGTGGCTGGTGAGGACACAAAGCTGACTGCCCTAGAGGAGCTCAGAGCCTCACTTCTGTTTTCTCTTCCCTCCCCACAGGTAAGGCTGGCCTCTCTGCAGTCAGAGGTCTGAGCTCTGCCATGGGGATAGGGGTGTCTTTATTACTGCAGTTTTCTCTAACACCTGGGGGCTACCGGAGTGTGGGCCGAAGCAGGCGCTGCAGCCGCGGAA... | CTTGTTGAAGGGGCACATTCATTTATTAATCCAATGTCCATTAAGGTCACTCTGCCAGGCAGGATGTGGGGCTTATGGCTGGTGCGTGTGGCTTTGTGGGGGGAGGGGTTGTGGCTGGTGAGGACACAAAGCTGACTGCCCTAGAGGAGCTCAGAGCCTCACTTCTGTTTTCTCTTCCCTCCCCACAGGTAAGGCTGGCCTCTCTGCAGTCAGAGGTCTGAGCTCTGCCATGGGGATAGGGGTGTCTTTATTACTGCAGTTTTCTCTAACACCTGGGGGCTACCGGAGTGTGGGCCGAAGCAGGCGCTGCAGCCGCGGAA... |
Task1_train_39022 | A sequence alteration has been identified on Chromosome 7. Is it disease-inducing or harmless? | Benign | AAGTGCCTCTGTAGACTTGTGCACGGCCCAAGTGTGGGCTGGGAGCAGTGGGTGTGGGACCCCCATGAGTAAAGTGGATTGGATTTAACACAAAGGGAAGGCGACACCTCTTTTGGGTGCTGAGGTCTTTCTGGCCTACTTTCTTGTTCTTGGTTTTGTTGAAGGAAGATGAGTTGCCAGACAGCCAAGGTCCCAGCAGGTGAAGTGCTCCCCCGCCATGGCTTCTGCCTTGGAGCAGGAGCCCCGACAGTATAGACGGTGCTGCAGTGACCCAGGGGTTGGTCTCCCTGACCACTGAGGGACTGAGCATGCCTTTGCTT... | AAGTGCCTCTGTAGACTTGTGCACGGCCCAAGTGTGGGCTGGGAGCAGTGGGTGTGGGACCCCCATGAGTAAAGTGGATTGGATTTAACACAAAGGGAAGGCGACACCTCTTTTGGGTGCTGAGGTCTTTCTGGCCTACTTTCTTGTTCTTGGTTTTGTTGAAGGAAGATGAGTTGCCAGACAGCCAAGGTCCCAGCAGGTGAAGTGCTCCCCCGCCATGGCTTCTGCCTTGGAGCAGGAGCCCCGACAGTATAGACGGTGCTGCAGTGACCCAGGGGTTGGTCTCCCTGACCACTGAGGGACTGAGCATGCCTTTGCTT... |
Task1_train_39023 | This alteration occurs on Chromosome 7. Is it associated with a disease or is it a benign variant? | Benign | AGAAGGGGATGGTACAGGGTGAAATGGTGAAGGAGGGGTACGTGTGTCATTCGGTTGTGAAAGATCTATAGCAGTGACGGTTAAGTGAATTTCCTTTAAGCTAAAAGCATATGTCTAACTACTGAGATAATCTTTAACTTATTGGGCTGCAGCTGGTAGGAGTTGGTTTTACAAAAAGTCAGGATGTCTGGTCACATTCCAGTGCTCAAGGGAGTGTTTCAGCCATGCTCACTGGCATGGGGACACAATGGCAATAAGGAGATGTTTCTCCTCAGGGGCCCCCTATGGTATTCCATAGGTGTCCTACACAGGGGTGACTG... | AGAAGGGGATGGTACAGGGTGAAATGGTGAAGGAGGGGTACGTGTGTCATTCGGTTGTGAAAGATCTATAGCAGTGACGGTTAAGTGAATTTCCTTTAAGCTAAAAGCATATGTCTAACTACTGAGATAATCTTTAACTTATTGGGCTGCAGCTGGTAGGAGTTGGTTTTACAAAAAGTCAGGATGTCTGGTCACATTCCAGTGCTCAAGGGAGTGTTTCAGCCATGCTCACTGGCATGGGGACACAATGGCAATAAGGAGATGTTTCTCCTCAGGGGCCCCCTATGGTATTCCATAGGTGTCCTACACAGGGGTGACTG... |
Task1_train_39024 | Here is a genetic alteration on Chromosome 7. Based on the data, is it a benign variant or a cause of disease? | Benign | CAGCCATGCTCACTGGCATGGGGACACAATGGCAATAAGGAGATGTTTCTCCTCAGGGGCCCCCTATGGTATTCCATAGGTGTCCTACACAGGGGTGACTGGCTAAACTGGCACCCCATAATCCCTTCCACCAGCACTTGCCCCCCGCTTTTTTTAATTAATAACTGCCATTTCTATCATGGCTTGCTTGTGGTGTCTGGCTTCTCTCCCAAGGCATCTTTTGCACCTGTAGACTAAAAATAAGCAGCATAGACAAACAGAAATTAAAGCAAAGTTTGTAGCAGTTGATTCTCCAATGGTTTTAATCCATTTCAGAGGAT... | CAGCCATGCTCACTGGCATGGGGACACAATGGCAATAAGGAGATGTTTCTCCTCAGGGGCCCCCTATGGTATTCCATAGGTGTCCTACACAGGGGTGACTGGCTAAACTGGCACCCCATAATCCCTTCCACCAGCACTTGCCCCCCGCTTTTTTTAATTAATAACTGCCATTTCTATCATGGCTTGCTTGTGGTGTCTGGCTTCTCTCCCAAGGCATCTTTTGCACCTGTAGACTAAAAATAAGCAGCATAGACAAACAGAAATTAAAGCAAAGTTTGTAGCAGTTGATTCTCCAATGGTTTTAATCCATTTCAGAGGAT... |
Task1_train_39025 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GTCCTACACAGGGGTGACTGGCTAAACTGGCACCCCATAATCCCTTCCACCAGCACTTGCCCCCCGCTTTTTTTAATTAATAACTGCCATTTCTATCATGGCTTGCTTGTGGTGTCTGGCTTCTCTCCCAAGGCATCTTTTGCACCTGTAGACTAAAAATAAGCAGCATAGACAAACAGAAATTAAAGCAAAGTTTGTAGCAGTTGATTCTCCAATGGTTTTAATCCATTTCAGAGGATTCAGGTCAGAGAGCCCATCAACAGCTCCATTAAGGGCATCAGCACCAGGTAAGAGAGTTAAGTGGGCTTGAGATGCCTCAA... | GTCCTACACAGGGGTGACTGGCTAAACTGGCACCCCATAATCCCTTCCACCAGCACTTGCCCCCCGCTTTTTTTAATTAATAACTGCCATTTCTATCATGGCTTGCTTGTGGTGTCTGGCTTCTCTCCCAAGGCATCTTTTGCACCTGTAGACTAAAAATAAGCAGCATAGACAAACAGAAATTAAAGCAAAGTTTGTAGCAGTTGATTCTCCAATGGTTTTAATCCATTTCAGAGGATTCAGGTCAGAGAGCCCATCAACAGCTCCATTAAGGGCATCAGCACCAGGTAAGAGAGTTAAGTGGGCTTGAGATGCCTCAA... |
Task1_train_39026 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | CAAGGCATCTTTTGCACCTGTAGACTAAAAATAAGCAGCATAGACAAACAGAAATTAAAGCAAAGTTTGTAGCAGTTGATTCTCCAATGGTTTTAATCCATTTCAGAGGATTCAGGTCAGAGAGCCCATCAACAGCTCCATTAAGGGCATCAGCACCAGGTAAGAGAGTTAAGTGGGCTTGAGATGCCTCAAAAACTTGTTCCTTTAATTTTCTTATGTCCAGTGTTAGATTTTCCTCTCTTCCTTCTAGATAGTGTTTAACCTTTTCCCAATGATGCACAGAGGCATTATAAGATTGAGGAGTAATACAAAAATCAGAA... | CAAGGCATCTTTTGCACCTGTAGACTAAAAATAAGCAGCATAGACAAACAGAAATTAAAGCAAAGTTTGTAGCAGTTGATTCTCCAATGGTTTTAATCCATTTCAGAGGATTCAGGTCAGAGAGCCCATCAACAGCTCCATTAAGGGCATCAGCACCAGGTAAGAGAGTTAAGTGGGCTTGAGATGCCTCAAAAACTTGTTCCTTTAATTTTCTTATGTCCAGTGTTAGATTTTCCTCTCTTCCTTCTAGATAGTGTTTAACCTTTTCCCAATGATGCACAGAGGCATTATAAGATTGAGGAGTAATACAAAAATCAGAA... |
Task1_train_39027 | A mutation is present on Chromosome 7. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ACTATAACCAACAAATTAAACTGGCTGGCTCATTCAGTGTATCACATGACCCTCCATTTTCTTCCTTACCCATAGAAATTGACTATATCAGTTGAGATTTTGCTGGTTTAATAAACTATCCCAAAGTTTCATAGCTTAAAACATCAGCCATTTAGTTGGTTCTTAATTCTGTGGGTTCACTGGGCTGTTCTTGGGTCTGGACCAGCTTGGCTCATCTCAGGCACTCACTCATGCATCTGGGGTAAGCTAGTGCCTGGTATGCAACTGAATGGTCTTGGATAGCCTTATGGACATGTCTGGTAGTTAGCAAGCTCTCAGAC... | ACTATAACCAACAAATTAAACTGGCTGGCTCATTCAGTGTATCACATGACCCTCCATTTTCTTCCTTACCCATAGAAATTGACTATATCAGTTGAGATTTTGCTGGTTTAATAAACTATCCCAAAGTTTCATAGCTTAAAACATCAGCCATTTAGTTGGTTCTTAATTCTGTGGGTTCACTGGGCTGTTCTTGGGTCTGGACCAGCTTGGCTCATCTCAGGCACTCACTCATGCATCTGGGGTAAGCTAGTGCCTGGTATGCAACTGAATGGTCTTGGATAGCCTTATGGACATGTCTGGTAGTTAGCAAGCTCTCAGAC... |
Task1_train_39028 | This genomic variant is located on Chromosome 7. Can you determine its pathogenicity and name any linked disease? | Benign | GTGCTCTGCTTTGAGACACTTTTCTGAATCTGTTAGCAAGAGAAATGCTGAAGCTTTCTCAGATGTCTGCTGTGTCTAGGGAAGATGGGGGATGGCTTCAGAGCAAGAGGCCACAGGTCGGCTGTGAGCATCTGTGTCTAGCTGTTGAGCATCTCCAACAGTGGATGAGTGTCCAGGTAGACCTGAGGCTGTGCCCTGAGATTTCTGATCATCTCCCAGCACTGTCTCCACCAGCTGTACTTCCCGCCCCTCTCGGGAGAAACTAGCTAAAGGCCCCCTGCTACGCAGCTTGAAGAAAGGAAAAGAGGAATATATTGGGG... | GTGCTCTGCTTTGAGACACTTTTCTGAATCTGTTAGCAAGAGAAATGCTGAAGCTTTCTCAGATGTCTGCTGTGTCTAGGGAAGATGGGGGATGGCTTCAGAGCAAGAGGCCACAGGTCGGCTGTGAGCATCTGTGTCTAGCTGTTGAGCATCTCCAACAGTGGATGAGTGTCCAGGTAGACCTGAGGCTGTGCCCTGAGATTTCTGATCATCTCCCAGCACTGTCTCCACCAGCTGTACTTCCCGCCCCTCTCGGGAGAAACTAGCTAAAGGCCCCCTGCTACGCAGCTTGAAGAAAGGAAAAGAGGAATATATTGGGG... |
Task1_train_39029 | Consider a variant on Chromosome 7. Determine its clinical classification and disease relevance. | Benign | TTAACTTATTTAGTCATTAGAACACCACCACATGGAGTAAACCATCATCTTCTCCAGATGAAGAGAAATTAATCAGTTGTCCAAGATCATATGACTAGCAATGGAAAGACAATCTAAACTAAGCAATCCAGCTCCAGATTCTTTTTTTCTTCACCACTGCATGCTGCCTCTCAGAAAGCTCATTTTCTTTGTACAGTCTAAGTTCCTTCTAAGCTCTGATATTCTGTGGTCAATGTAGACTTTCCTTCTCCAACTTTCTCTCTGCAACATGAGAGTAAGGAACAGCTAAACCGCAAAAGGCAATGAGCTTAGCAGGAGAG... | TTAACTTATTTAGTCATTAGAACACCACCACATGGAGTAAACCATCATCTTCTCCAGATGAAGAGAAATTAATCAGTTGTCCAAGATCATATGACTAGCAATGGAAAGACAATCTAAACTAAGCAATCCAGCTCCAGATTCTTTTTTTCTTCACCACTGCATGCTGCCTCTCAGAAAGCTCATTTTCTTTGTACAGTCTAAGTTCCTTCTAAGCTCTGATATTCTGTGGTCAATGTAGACTTTCCTTCTCCAACTTTCTCTCTGCAACATGAGAGTAAGGAACAGCTAAACCGCAAAAGGCAATGAGCTTAGCAGGAGAG... |
Task1_train_39030 | A mutation on Chromosome 7 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGGCCTTTCATGGCGCACGAGGTGTATAAACAAAGGGAAACCATATCTTTCTGGGCAAAACTGCTTTTCTGGATTGTTTATTATGTTTAATCAGCATTGTGGAAAATGCAACAATATCTGTTCATGGACTTGAGAACCCCAGAGTGGGAACAGCAGGTGCGGATGTGGGGAGAAGAAAGGAGGAGGGTCTGGAGAGCGGCCATAGGGGAGGCAAGTGTGAGGAGCCAGGAGTGGGGGCCCTGGGCTGCCCTAGACAGGGACATGCGGGCACCCCGTGGGGTCTTTGGCAGCTCACAGGACAATGGCAGTGGAGGTCTGCT... | AGGCCTTTCATGGCGCACGAGGTGTATAAACAAAGGGAAACCATATCTTTCTGGGCAAAACTGCTTTTCTGGATTGTTTATTATGTTTAATCAGCATTGTGGAAAATGCAACAATATCTGTTCATGGACTTGAGAACCCCAGAGTGGGAACAGCAGGTGCGGATGTGGGGAGAAGAAAGGAGGAGGGTCTGGAGAGCGGCCATAGGGGAGGCAAGTGTGAGGAGCCAGGAGTGGGGGCCCTGGGCTGCCCTAGACAGGGACATGCGGGCACCCCGTGGGGTCTTTGGCAGCTCACAGGACAATGGCAGTGGAGGTCTGCT... |
Task1_train_39031 | This variant is located on Chromosome 7. Evaluate its biological effect and specify any disease association. | Benign | AGTTAAGAGATACAAAAGGGTATATATACCTTTAAAACCTTATCGCTCATCTTTTTCCCTCAACCACCTATTTGCCTTGCAGATGCAAAGTAATATTATCAGTCTCTTATAAATCCTACCATGACATTTTTGCATACAAAAGTGTGAAAAAGTATTTCTGCCCCCTTTTCCCACAAATAGCAGCATACTATACACACTGATTTGCATGATGCTGTGATCACACGATCATATGTTTTTAGAATAATCCTACATGAGTCCATAAAAAGTGTCAACCTAAATAACAGAGAGAGGCTCTCCAAAAGAAAATGAGATTGATTCTG... | AGTTAAGAGATACAAAAGGGTATATATACCTTTAAAACCTTATCGCTCATCTTTTTCCCTCAACCACCTATTTGCCTTGCAGATGCAAAGTAATATTATCAGTCTCTTATAAATCCTACCATGACATTTTTGCATACAAAAGTGTGAAAAAGTATTTCTGCCCCCTTTTCCCACAAATAGCAGCATACTATACACACTGATTTGCATGATGCTGTGATCACACGATCATATGTTTTTAGAATAATCCTACATGAGTCCATAAAAAGTGTCAACCTAAATAACAGAGAGAGGCTCTCCAAAAGAAAATGAGATTGATTCTG... |
Task1_train_39032 | Consider this mutation on Chromosome 7. Is this a benign change or a disease-causing variant? | Benign | TTTGAAGTTTATTTTTTGACCTTGCTTGTATATTCATACAATCCATGTTCTATTTCATTCTATTTATGGTGTCTAGCTCTTACACTTTTAAAGGACTTCCCCGTTTCGAGATTATAAAATAATCTTCCACATTTTCTTCTAAGTGCCTTTATGCTTTCAGTTTTCACTTTTAAATGCCGACCATCTGGAATTTGGGAGCTGGGTGACCAACCTTCGCCGTTGGGAGACACGGATCCAAGTTCTGTTGCTGTCATTCAGATGTTTAACTTCTGAAAGATACGTTCCATTTGCGGAAAATACATCCTCTTTTTCTCAGTGAT... | TTTGAAGTTTATTTTTTGACCTTGCTTGTATATTCATACAATCCATGTTCTATTTCATTCTATTTATGGTGTCTAGCTCTTACACTTTTAAAGGACTTCCCCGTTTCGAGATTATAAAATAATCTTCCACATTTTCTTCTAAGTGCCTTTATGCTTTCAGTTTTCACTTTTAAATGCCGACCATCTGGAATTTGGGAGCTGGGTGACCAACCTTCGCCGTTGGGAGACACGGATCCAAGTTCTGTTGCTGTCATTCAGATGTTTAACTTCTGAAAGATACGTTCCATTTGCGGAAAATACATCCTCTTTTTCTCAGTGAT... |
Task1_train_39033 | A variant found on Chromosome 7 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CAGCACACCCACATCGATGTGCACATCCACCAGGAGTCTGCCCTGGCCAAGCTCCTGCTCACCTGCTGCTCTGCGCTGCGGCCCCGGGCCACCCAGGCCAGGGGCAGCAGCCGGCTGCTGGTGGCCTCGTGGGTGAGTGTGACGGCCTGCCTCGTCGGGCGGCGGGAGGAACTCCCCACCTCCAGCCGCAGCAGCACTCTCTGCCAGCCTCCCTCTGAACAGGACACCGAGCCAGTTATGTCTTCTTACTTAGCGATGTGATTCTCTGGCCTTCTCAGTAAGAGCCTGGGGAGGGGAGGCTCTGGGCTGAAGGGGTGTGG... | CAGCACACCCACATCGATGTGCACATCCACCAGGAGTCTGCCCTGGCCAAGCTCCTGCTCACCTGCTGCTCTGCGCTGCGGCCCCGGGCCACCCAGGCCAGGGGCAGCAGCCGGCTGCTGGTGGCCTCGTGGGTGAGTGTGACGGCCTGCCTCGTCGGGCGGCGGGAGGAACTCCCCACCTCCAGCCGCAGCAGCACTCTCTGCCAGCCTCCCTCTGAACAGGACACCGAGCCAGTTATGTCTTCTTACTTAGCGATGTGATTCTCTGGCCTTCTCAGTAAGAGCCTGGGGAGGGGAGGCTCTGGGCTGAAGGGGTGTGG... |
Task1_train_39034 | A variant found on Chromosome 7 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GGCTGTGGTGAGTAGAGCAGGACAGTGCTTGACTGCCTGTGAGAGGGGTGGGGCATTGCTCTCCTGATTGCCTTCCTCCAACATGGCGCCACAGAATGCTGGCAGTCGGAGAGATCTGATTATCTAGGACCATTCCCTGCCTGTTCAGATGAGCAAACAGCTGAGGGCGGTGGTGGCATGTCCTATTCACACTGTCTGCTCTCCCATACCCTTCCCAGTGCTGTTCCCACCAGGCTGGCTGCCTCTCCCTGCCTTCAACAGTTAATGTCAACTAAGGATCTAAGGACCTGCTCATCTCCAGATACTTGCATTGAGATGGG... | GGCTGTGGTGAGTAGAGCAGGACAGTGCTTGACTGCCTGTGAGAGGGGTGGGGCATTGCTCTCCTGATTGCCTTCCTCCAACATGGCGCCACAGAATGCTGGCAGTCGGAGAGATCTGATTATCTAGGACCATTCCCTGCCTGTTCAGATGAGCAAACAGCTGAGGGCGGTGGTGGCATGTCCTATTCACACTGTCTGCTCTCCCATACCCTTCCCAGTGCTGTTCCCACCAGGCTGGCTGCCTCTCCCTGCCTTCAACAGTTAATGTCAACTAAGGATCTAAGGACCTGCTCATCTCCAGATACTTGCATTGAGATGGG... |
Task1_train_39035 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCCTGATTGCCTTCCTCCAACATGGCGCCACAGAATGCTGGCAGTCGGAGAGATCTGATTATCTAGGACCATTCCCTGCCTGTTCAGATGAGCAAACAGCTGAGGGCGGTGGTGGCATGTCCTATTCACACTGTCTGCTCTCCCATACCCTTCCCAGTGCTGTTCCCACCAGGCTGGCTGCCTCTCCCTGCCTTCAACAGTTAATGTCAACTAAGGATCTAAGGACCTGCTCATCTCCAGATACTTGCATTGAGATGGGGAAGGCAGAGCGTTCCAGATAGTATGTGGTCCCCCAGGAAGCATCACCCCCTGGTTATTCT... | TCCTGATTGCCTTCCTCCAACATGGCGCCACAGAATGCTGGCAGTCGGAGAGATCTGATTATCTAGGACCATTCCCTGCCTGTTCAGATGAGCAAACAGCTGAGGGCGGTGGTGGCATGTCCTATTCACACTGTCTGCTCTCCCATACCCTTCCCAGTGCTGTTCCCACCAGGCTGGCTGCCTCTCCCTGCCTTCAACAGTTAATGTCAACTAAGGATCTAAGGACCTGCTCATCTCCAGATACTTGCATTGAGATGGGGAAGGCAGAGCGTTCCAGATAGTATGTGGTCCCCCAGGAAGCATCACCCCCTGGTTATTCT... |
Task1_train_39036 | A genetic alteration is present on Chromosome 7. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GCTAAGGGGACTAGTGGAGAAGTATGTTAGTTGGGGCCAAAAACAGCATTCCTCGGCAGTGCGGGGTTTCAGCTGACCTCAAAAGGTGGCAAAGGATGTGACACTGGCCCAGAGTCGGGTGGGAAGGGACAATGTGCAGCTGAGCTTCTCTGGAGGAAAAAAGCCACGGGAAAACAGGGCCTCTAGTTAACACATGGGTTGTGTTCCCAACGCTTGTGCTTCGGAAATGTGATGTGTAAATGCATTTTCCAAAAACAAAAGCAAGAAATGAAAAGCGCTCATGATGGTCAGGTTTCCTCAGTGGGTCACTCCACGATACA... | GCTAAGGGGACTAGTGGAGAAGTATGTTAGTTGGGGCCAAAAACAGCATTCCTCGGCAGTGCGGGGTTTCAGCTGACCTCAAAAGGTGGCAAAGGATGTGACACTGGCCCAGAGTCGGGTGGGAAGGGACAATGTGCAGCTGAGCTTCTCTGGAGGAAAAAAGCCACGGGAAAACAGGGCCTCTAGTTAACACATGGGTTGTGTTCCCAACGCTTGTGCTTCGGAAATGTGATGTGTAAATGCATTTTCCAAAAACAAAAGCAAGAAATGAAAAGCGCTCATGATGGTCAGGTTTCCTCAGTGGGTCACTCCACGATACA... |
Task1_train_39037 | This variant is present on Chromosome 7. Is the change likely to result in a pathogenic outcome? | Benign | CCACCACGTCTCCCAGCCCTGCAGGAGGCTCACAGCTACAAGCACAGGATTTTACAGCTGCTTGGGGAATGGGGTTATGAGGTGAAGACCCTGACCCACCCTCCCTGAGAAAGGAAAAGGCATCTTCCTAAGATGAAACCCTCCCTGAGGTCCCCTCCTAGTAGCCTTGGGTGGACAAGAGAGGTGAATGGGGCACAAAGAAGGCTAGGCAGGACTGGGCACCTCTACCTCACCCCCAAAGCCATCAGTCTGCAGCCTAGTCACACCTGAATCACTCTACATTGCGTAAAACTTTAAATGGGCTGGTGTCGATAGCCTGT... | CCACCACGTCTCCCAGCCCTGCAGGAGGCTCACAGCTACAAGCACAGGATTTTACAGCTGCTTGGGGAATGGGGTTATGAGGTGAAGACCCTGACCCACCCTCCCTGAGAAAGGAAAAGGCATCTTCCTAAGATGAAACCCTCCCTGAGGTCCCCTCCTAGTAGCCTTGGGTGGACAAGAGAGGTGAATGGGGCACAAAGAAGGCTAGGCAGGACTGGGCACCTCTACCTCACCCCCAAAGCCATCAGTCTGCAGCCTAGTCACACCTGAATCACTCTACATTGCGTAAAACTTTAAATGGGCTGGTGTCGATAGCCTGT... |
Task1_train_39038 | This sequence variant lies on Chromosome 7. Is it clinically significant, and what condition might it cause if any? | Benign | AGGCCACCAGGACCACACGGGCGGCTCCTACCCCTCAGCCCCAGTCACCTCTCTGGACAGAGCCTCCCATGCCTGGAGAAAAATGGGTGCCCCTGCTCTAGGATTGCAGCCACAGCAGATGGGCATGAGCACAGCTCTTGAGAGGAACTTCCCAGAGTGGTAATGGAATCACCACAGCCGCCCAGGGCATCCCCCAACATCCCGGTTATTCAAGACAGTTGGCTGTTGGATGTGGTGGAGGATGGAGATCCTGGGGTAGAATGAGGAGGTTTCAGTTCTGGCAGCTTGATTCTCGTTCTCCTTCTCCCTGCATACCTCCA... | AGGCCACCAGGACCACACGGGCGGCTCCTACCCCTCAGCCCCAGTCACCTCTCTGGACAGAGCCTCCCATGCCTGGAGAAAAATGGGTGCCCCTGCTCTAGGATTGCAGCCACAGCAGATGGGCATGAGCACAGCTCTTGAGAGGAACTTCCCAGAGTGGTAATGGAATCACCACAGCCGCCCAGGGCATCCCCCAACATCCCGGTTATTCAAGACAGTTGGCTGTTGGATGTGGTGGAGGATGGAGATCCTGGGGTAGAATGAGGAGGTTTCAGTTCTGGCAGCTTGATTCTCGTTCTCCTTCTCCCTGCATACCTCCA... |
Task1_train_39039 | This variant is located on Chromosome 7. Evaluate its biological effect and specify any disease association. | Benign | TGCCCCTGCTCTAGGATTGCAGCCACAGCAGATGGGCATGAGCACAGCTCTTGAGAGGAACTTCCCAGAGTGGTAATGGAATCACCACAGCCGCCCAGGGCATCCCCCAACATCCCGGTTATTCAAGACAGTTGGCTGTTGGATGTGGTGGAGGATGGAGATCCTGGGGTAGAATGAGGAGGTTTCAGTTCTGGCAGCTTGATTCTCGTTCTCCTTCTCCCTGCATACCTCCAGGCACCAAGAACAGCTTCCAGACACTGCAGATGAAGCTAGAAAACATCACCAACCCCTGGAGCCCAAGACACCGCGTGGTCCAGCCA... | TGCCCCTGCTCTAGGATTGCAGCCACAGCAGATGGGCATGAGCACAGCTCTTGAGAGGAACTTCCCAGAGTGGTAATGGAATCACCACAGCCGCCCAGGGCATCCCCCAACATCCCGGTTATTCAAGACAGTTGGCTGTTGGATGTGGTGGAGGATGGAGATCCTGGGGTAGAATGAGGAGGTTTCAGTTCTGGCAGCTTGATTCTCGTTCTCCTTCTCCCTGCATACCTCCAGGCACCAAGAACAGCTTCCAGACACTGCAGATGAAGCTAGAAAACATCACCAACCCCTGGAGCCCAAGACACCGCGTGGTCCAGCCA... |
Task1_train_39040 | A mutation on Chromosome 7 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GACCGGAGTGGTGGAGGAAGAATGGGCGAGGTCTGTGGGTCTGGTTTGAGCCTCTCCCCCTCTCTCTCCCTTCCAGCTAGCCAAAGTCACCATCGTGGACCACCACGCCGCCACGGCCTCTTTCATGAAGCACCTGGAGAATGAGCAGAAGGCCAGGGGGGGCTGCCCTGCAGACTGGGCCTGGATCGTGCCCCCCATCTCGGGCAGCCTCACTCCTGTTTTCCATCAGGAGATGGTCAACTATTTCCTGTCCCCGGCCTTCCGCTACCAGGTGCCCACCCTAACTGGCTCTGCCAGCCTGGGCCCAGCTCTAATTCTAA... | GACCGGAGTGGTGGAGGAAGAATGGGCGAGGTCTGTGGGTCTGGTTTGAGCCTCTCCCCCTCTCTCTCCCTTCCAGCTAGCCAAAGTCACCATCGTGGACCACCACGCCGCCACGGCCTCTTTCATGAAGCACCTGGAGAATGAGCAGAAGGCCAGGGGGGGCTGCCCTGCAGACTGGGCCTGGATCGTGCCCCCCATCTCGGGCAGCCTCACTCCTGTTTTCCATCAGGAGATGGTCAACTATTTCCTGTCCCCGGCCTTCCGCTACCAGGTGCCCACCCTAACTGGCTCTGCCAGCCTGGGCCCAGCTCTAATTCTAA... |
Task1_train_39041 | Chromosome 7 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGGCCTCAGGCTGGGTGCAAGAGGAGAGGGAAAGCCAAAGAGGGAGTCAGAAGAGAGGACAGAAACGGAGTAGGGAGGAAGCAGAGGCCTAAAGAAGGCAGGAGAGCAGGCTGGGGGCGGGGGCTGGTGAGGCAGGTTACTACCTAAGGTGAGCCTAGAGGGGAAGGGTTTGGAGAGGAGTTGTGGGGGTGAAGGCAGAAGGGGAGGCCAGGCTTGGGACTCACCAGGGGCGAGGTGCAGTTGCTGAGCACCCCCGGGGTGGAGGGGCCGCGAGCCGAGGTGGCACCCCAGGCAGCTGCATCTTGTTGTACTCGGCCCCA... | AGGCCTCAGGCTGGGTGCAAGAGGAGAGGGAAAGCCAAAGAGGGAGTCAGAAGAGAGGACAGAAACGGAGTAGGGAGGAAGCAGAGGCCTAAAGAAGGCAGGAGAGCAGGCTGGGGGCGGGGGCTGGTGAGGCAGGTTACTACCTAAGGTGAGCCTAGAGGGGAAGGGTTTGGAGAGGAGTTGTGGGGGTGAAGGCAGAAGGGGAGGCCAGGCTTGGGACTCACCAGGGGCGAGGTGCAGTTGCTGAGCACCCCCGGGGTGGAGGGGCCGCGAGCCGAGGTGGCACCCCAGGCAGCTGCATCTTGTTGTACTCGGCCCCA... |
Task1_train_39042 | This alteration on Chromosome 7 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGCGCCCGGCCATGCTACGATCTTTAAAATGAAAACCTAATCTTGGCACATCTCGGCCTAAAAATCACCATGACCCTTATTGCCCCCCAAGTCCAGGAGCTTTATAAGAACTAGAAAACTGCCCCTCCCGCAAGTCTCATGTCTCTTTTCCCTTCTTGTAGGTCAGGCTTCAGCCATACAATTCCTGAAATTTCTCTCCCATCCTTTCTTACTGGAGATACCTGCACTTGCTTTTCCTCTGCCTAGAGCTCTCCCCTTTACACTCCACCCCCACCTGTGCC... | TCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGCGCCCGGCCATGCTACGATCTTTAAAATGAAAACCTAATCTTGGCACATCTCGGCCTAAAAATCACCATGACCCTTATTGCCCCCCAAGTCCAGGAGCTTTATAAGAACTAGAAAACTGCCCCTCCCGCAAGTCTCATGTCTCTTTTCCCTTCTTGTAGGTCAGGCTTCAGCCATACAATTCCTGAAATTTCTCTCCCATCCTTTCTTACTGGAGATACCTGCACTTGCTTTTCCTCTGCCTAGAGCTCTCCCCTTTACACTCCACCCCCACCTGTGCC... |
Task1_train_39043 | A change on Chromosome 7 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCCACACACTGGCCTAGGCAGTCACTGGTGTACCCCCATGCAGTTCTCTTTGTTCAGTTCCTAGAACAGAAAGAGAAGCAAGCTGGGATTTGTCTAGGGGAAGGATGCCACAGTTCATAGCATTCTCGCTCGGCCCCCTCAGGCCTGCTGCTCGCACCCCAACTGGCCGAGTTAGGGTTACGTACTGTGACCGGTGGACTGCCACTGGGCCTCCCAGGGGCCAAGACCTGGGCCTTGGCCGTGGGAGTGCAGAGCTACAGTCAGCTGACCCTTGGAAAAGTCCTTCCTGTCATGGTGCGGACGCCGTAGCCTCCCGCCTT... | GCCACACACTGGCCTAGGCAGTCACTGGTGTACCCCCATGCAGTTCTCTTTGTTCAGTTCCTAGAACAGAAAGAGAAGCAAGCTGGGATTTGTCTAGGGGAAGGATGCCACAGTTCATAGCATTCTCGCTCGGCCCCCTCAGGCCTGCTGCTCGCACCCCAACTGGCCGAGTTAGGGTTACGTACTGTGACCGGTGGACTGCCACTGGGCCTCCCAGGGGCCAAGACCTGGGCCTTGGCCGTGGGAGTGCAGAGCTACAGTCAGCTGACCCTTGGAAAAGTCCTTCCTGTCATGGTGCGGACGCCGTAGCCTCCCGCCTT... |
Task1_train_39044 | A genomic variant on Chromosome 7 is under review. What is the biological outcome — benign or pathogenic? | Benign | CTTTGCATGATGGTCGTAGGGGGGGATGGGTAGTGGGGGTATCAGACGTCTTCCAGTCCTGGGGAGGGAGTTGAGGCTGTTACCTGAAGACCTAGGTAGCTTAGCCTCAGCGGTTGAGGAACTTTGAGAACCCTGGGTCTCTCACCCAGCAACCCGTCTCAGACCCGGCTGGCCTTAGAGGCGCAGGTCAAGTCTGCACGCGGGCCAGGGTTCTGGGCGGAGCTCGCCTGCCACGACTGGCCACGCCCCCTGCCCACGTGCCACCCAGGCCCGCCCCTCCCTGCCCCCACGTGGCCACCGCTCCACATGGCCCCCTTTGG... | CTTTGCATGATGGTCGTAGGGGGGGATGGGTAGTGGGGGTATCAGACGTCTTCCAGTCCTGGGGAGGGAGTTGAGGCTGTTACCTGAAGACCTAGGTAGCTTAGCCTCAGCGGTTGAGGAACTTTGAGAACCCTGGGTCTCTCACCCAGCAACCCGTCTCAGACCCGGCTGGCCTTAGAGGCGCAGGTCAAGTCTGCACGCGGGCCAGGGTTCTGGGCGGAGCTCGCCTGCCACGACTGGCCACGCCCCCTGCCCACGTGCCACCCAGGCCCGCCCCTCCCTGCCCCCACGTGGCCACCGCTCCACATGGCCCCCTTTGG... |
Task1_train_39045 | This variant is found on Chromosome 7. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTATTAGCAGGAATCTGGGGTGGCACCCTAGCGAGGCCGGAAGGAGTGCGTTCGACTCATGATGTCTGCCGCAGACATAGGACGGGAGCAGGAGCAAGCGTTCCTGGGCAAACGCCTGAGAGGCTGGGTCTCTGTCCGTGGTCCTCTACTGTTCTCCCTATTCTTCATTAACACCTAGCCCCCCAGGCGCCCACCTCAAGCCCCTCCTCACCAAGTAAGACTGCAAGGTGCAGACACACGTGGATGGTGTGAATGTCAAAGGAGGGGCAGTTTCGGATGATGAGCTGACTCAAGTCCTGCAGTGTGACCTGCTCCACAGG... | CTATTAGCAGGAATCTGGGGTGGCACCCTAGCGAGGCCGGAAGGAGTGCGTTCGACTCATGATGTCTGCCGCAGACATAGGACGGGAGCAGGAGCAAGCGTTCCTGGGCAAACGCCTGAGAGGCTGGGTCTCTGTCCGTGGTCCTCTACTGTTCTCCCTATTCTTCATTAACACCTAGCCCCCCAGGCGCCCACCTCAAGCCCCTCCTCACCAAGTAAGACTGCAAGGTGCAGACACACGTGGATGGTGTGAATGTCAAAGGAGGGGCAGTTTCGGATGATGAGCTGACTCAAGTCCTGCAGTGTGACCTGCTCCACAGG... |
Task1_train_39046 | A variant has been detected on Chromosome 7. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AAGGGACGCTGGGAGTTGGGCTGGACTGGGGGTGGAGGAAAGTGGGCAGTATTGTCTTTTTAAAGGAAATGCAAGCCCCTGGTCCCTTGCCACTACTTAAACTGGTTTCTCCTGATCCGTGGCTGGTATTGAGGCAGCCAGTGGTTTCTGACTTTATGGATGACCGGAAACTGGCTGGGCTTCAGAGCCTGGGAGAGGACTGATGTTTACAATGCAGTGTCAATCACAGCCGGGGAGCTCTTGCCTCCAATTCTGGGTGAGCTCTGGGTTTACTGGGTGTCCAGGCAGCCCACAGTCATGAATTGGAAGGGCCTCGGAGC... | AAGGGACGCTGGGAGTTGGGCTGGACTGGGGGTGGAGGAAAGTGGGCAGTATTGTCTTTTTAAAGGAAATGCAAGCCCCTGGTCCCTTGCCACTACTTAAACTGGTTTCTCCTGATCCGTGGCTGGTATTGAGGCAGCCAGTGGTTTCTGACTTTATGGATGACCGGAAACTGGCTGGGCTTCAGAGCCTGGGAGAGGACTGATGTTTACAATGCAGTGTCAATCACAGCCGGGGAGCTCTTGCCTCCAATTCTGGGTGAGCTCTGGGTTTACTGGGTGTCCAGGCAGCCCACAGTCATGAATTGGAAGGGCCTCGGAGC... |
Task1_train_39047 | This mutation on Chromosome 7 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CGGTCGGGGTCCGCCTGGGGTTTCCACAGCGAGGAGCCTCCACCGCTTGCCCACCCGCACCCGCGTCCCAGAGCCGCGCCCTAGTACCTGAAGCCAGACAGACCGGTCAGCCCAAGGTCCGTGAGGCCAGGGTGGGAATCCGGGCCCCCTCACTTCCTCTCCGCTTCTCCTCAGCCGCCTCTCAACGCCTAACCCGGCTTCGGGCTCTGGTCCGCGCGGCCTAAAGCCTCGCGACCTCCAGGCCTCGCCCCCTGCCGCCTCGCGCCCTCCAGGCCCCAACCCCTGTCCCTTCGCGCCCTCCTGGCCCCGCCCTTCGTCGC... | CGGTCGGGGTCCGCCTGGGGTTTCCACAGCGAGGAGCCTCCACCGCTTGCCCACCCGCACCCGCGTCCCAGAGCCGCGCCCTAGTACCTGAAGCCAGACAGACCGGTCAGCCCAAGGTCCGTGAGGCCAGGGTGGGAATCCGGGCCCCCTCACTTCCTCTCCGCTTCTCCTCAGCCGCCTCTCAACGCCTAACCCGGCTTCGGGCTCTGGTCCGCGCGGCCTAAAGCCTCGCGACCTCCAGGCCTCGCCCCCTGCCGCCTCGCGCCCTCCAGGCCCCAACCCCTGTCCCTTCGCGCCCTCCTGGCCCCGCCCTTCGTCGC... |
Task1_train_39048 | A variant affecting Chromosome 7 has been observed. Determine if it's benign or associated with disease. | Benign | AAGCCAGACAGACCGGTCAGCCCAAGGTCCGTGAGGCCAGGGTGGGAATCCGGGCCCCCTCACTTCCTCTCCGCTTCTCCTCAGCCGCCTCTCAACGCCTAACCCGGCTTCGGGCTCTGGTCCGCGCGGCCTAAAGCCTCGCGACCTCCAGGCCTCGCCCCCTGCCGCCTCGCGCCCTCCAGGCCCCAACCCCTGTCCCTTCGCGCCCTCCTGGCCCCGCCCTTCGTCGCCTCGCTAGTGCCGGTTGGCGGGAAAGTCGCGAGCTCCAGCGCTTGCGCACTCCGCCGCCTGGGGGAACTCTGTCCAGCGACCCTTGACGT... | AAGCCAGACAGACCGGTCAGCCCAAGGTCCGTGAGGCCAGGGTGGGAATCCGGGCCCCCTCACTTCCTCTCCGCTTCTCCTCAGCCGCCTCTCAACGCCTAACCCGGCTTCGGGCTCTGGTCCGCGCGGCCTAAAGCCTCGCGACCTCCAGGCCTCGCCCCCTGCCGCCTCGCGCCCTCCAGGCCCCAACCCCTGTCCCTTCGCGCCCTCCTGGCCCCGCCCTTCGTCGCCTCGCTAGTGCCGGTTGGCGGGAAAGTCGCGAGCTCCAGCGCTTGCGCACTCCGCCGCCTGGGGGAACTCTGTCCAGCGACCCTTGACGT... |
Task1_train_39049 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | GTATGGGGCTCCCAAGTTCTCAGAGCCCACCCCACCCTCAGCCTCACCTCAGCCCTAGCGGGATGAGGAGGCTGCCCATCCTGCTTTGAGACAAGGAAACTAGGTGTGAGGAGTAGAGGGGCATGTGCAAGGCCCCAGTGGTTGGGGTTTGGAGCGACTGGAACAAGCCCAGGCCTTCCAGCTTAGCCCCAGCTCACGCTACCTGCCCACACGGCCTTCACATCCATGCTCCCTCACCTCCTTGTCTTCTTTGGGGGTCTTCTTATAGAAATTCTTCTCAGCATTTCCAATCCAAATCACAGAGGGCTGTAGGAGTCGGG... | GTATGGGGCTCCCAAGTTCTCAGAGCCCACCCCACCCTCAGCCTCACCTCAGCCCTAGCGGGATGAGGAGGCTGCCCATCCTGCTTTGAGACAAGGAAACTAGGTGTGAGGAGTAGAGGGGCATGTGCAAGGCCCCAGTGGTTGGGGTTTGGAGCGACTGGAACAAGCCCAGGCCTTCCAGCTTAGCCCCAGCTCACGCTACCTGCCCACACGGCCTTCACATCCATGCTCCCTCACCTCCTTGTCTTCTTTGGGGGTCTTCTTATAGAAATTCTTCTCAGCATTTCCAATCCAAATCACAGAGGGCTGTAGGAGTCGGG... |
Task1_train_39050 | A mutation found on Chromosome 7 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TGCCAGAGGGGCCCACCAGGAGGATGGAGCGGATGAGTGGGGCCATGATGTGGATATCCGGGGAGCCTGAGAGCAAGGAAATGGGCCAGAGCCAGGCAACAGGTCAGCAGCAGGAATCAGGGCTGGAGATGACTGCGTAAGGTCAGGCCAAGGGCCTAGGGCTGGGGGAGGAGGTGCAGATCACAGGGCATACTACCTTCCCCAACACCAGCAGGTCCCCTAGTCCACTAGGTCTGGGAGCCGGGAGTGGCAGCAGGAAATTTTGAATGGCTTATGAGTCTCCAGTATGAGGAGTTGTGCATGGGTCTGGGAGGAGCCTG... | TGCCAGAGGGGCCCACCAGGAGGATGGAGCGGATGAGTGGGGCCATGATGTGGATATCCGGGGAGCCTGAGAGCAAGGAAATGGGCCAGAGCCAGGCAACAGGTCAGCAGCAGGAATCAGGGCTGGAGATGACTGCGTAAGGTCAGGCCAAGGGCCTAGGGCTGGGGGAGGAGGTGCAGATCACAGGGCATACTACCTTCCCCAACACCAGCAGGTCCCCTAGTCCACTAGGTCTGGGAGCCGGGAGTGGCAGCAGGAAATTTTGAATGGCTTATGAGTCTCCAGTATGAGGAGTTGTGCATGGGTCTGGGAGGAGCCTG... |
Task1_train_39051 | Given this variant on Chromosome 7, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCATTCTGGGAGGGGTCTCACCTATGTAGTCTTTCAATGCTACTGACTCACTCTTCCTTAGAAGGCCAGAAATAACAAGCTCTTCGTACAGAGACTCCACAGACCTGGCAGAGGATGGCACAGGAAGACCCCCACCACCACAAGGGACATTAGCAAGTGAGAACACAGGGAAATGGAGGCAGAGATGGGGGCTGTTGTCATGAAGACAGGGTATCAGTGGTTCTCCTGTACAACATTCTGTGGTCAAAAACATCTACAGTGCCTGCAAACAGGCAGAATCAGGTATGGCACCAAATCACTGTCCCAGGAGGCAAGCCTCC... | GCATTCTGGGAGGGGTCTCACCTATGTAGTCTTTCAATGCTACTGACTCACTCTTCCTTAGAAGGCCAGAAATAACAAGCTCTTCGTACAGAGACTCCACAGACCTGGCAGAGGATGGCACAGGAAGACCCCCACCACCACAAGGGACATTAGCAAGTGAGAACACAGGGAAATGGAGGCAGAGATGGGGGCTGTTGTCATGAAGACAGGGTATCAGTGGTTCTCCTGTACAACATTCTGTGGTCAAAAACATCTACAGTGCCTGCAAACAGGCAGAATCAGGTATGGCACCAAATCACTGTCCCAGGAGGCAAGCCTCC... |
Task1_train_39052 | Located on Chromosome 7, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ACCCCATCTGTGCAGAGCTGGACCCGTCCTCTTTCTCCCAGGCCCAAGACCCCATCTGTGCAGAGCTGGACCCGTCCTCTTTCTCCCAGGCCCAAGACCCCATCTGTGCAGAGCTGGACGCGTCCTCTTTCTCCCAGGCCCAGCTACTTTCAGACTCCAGGATCACTGAGTGCTAGTGGGGCCAGAGGGTGGGGACGCTGGGCAGAGGAAGGCAGAGTCAGGGCCCGGGCCAGCCAGTGCTTTCCATCTGCCTCCTGGCACCTCCAGGAGCAGGGACCGGTTCCTGCCCTTCTCATCTGGGCTTCGTCCTCCCACTCCTG... | ACCCCATCTGTGCAGAGCTGGACCCGTCCTCTTTCTCCCAGGCCCAAGACCCCATCTGTGCAGAGCTGGACCCGTCCTCTTTCTCCCAGGCCCAAGACCCCATCTGTGCAGAGCTGGACGCGTCCTCTTTCTCCCAGGCCCAGCTACTTTCAGACTCCAGGATCACTGAGTGCTAGTGGGGCCAGAGGGTGGGGACGCTGGGCAGAGGAAGGCAGAGTCAGGGCCCGGGCCAGCCAGTGCTTTCCATCTGCCTCCTGGCACCTCCAGGAGCAGGGACCGGTTCCTGCCCTTCTCATCTGGGCTTCGTCCTCCCACTCCTG... |
Task1_train_39053 | A variant on Chromosome 7 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TTTTGAAAATAGAGATGTAGATTAAATAATAAATGAGTAAGATACATGCTTGCTGACTGATTAAAGTACTGACTGGTTTAGAATCTAGTTGTGGGGGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTAGATCGCTTGAAGTCAGGAGATCAAGAGCAGCCTGGCCAACATGGTGAAACCCATCTCTACTAAAAATACAAAAATTAGCTGGGCGTATTGTCAAAGGATTGTAGTCCTGGCTACTCAGGAGGCTGAAGCACGAGAATCGCTTGAACCCAGGACACAGAGGCTGCAGT... | TTTTGAAAATAGAGATGTAGATTAAATAATAAATGAGTAAGATACATGCTTGCTGACTGATTAAAGTACTGACTGGTTTAGAATCTAGTTGTGGGGGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTAGATCGCTTGAAGTCAGGAGATCAAGAGCAGCCTGGCCAACATGGTGAAACCCATCTCTACTAAAAATACAAAAATTAGCTGGGCGTATTGTCAAAGGATTGTAGTCCTGGCTACTCAGGAGGCTGAAGCACGAGAATCGCTTGAACCCAGGACACAGAGGCTGCAGT... |
Task1_train_39054 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | GACACAGAGGCTGCAGTGAGCTGAAATCTACAGAATCCAAGCACTTGCACTCCTGTGATCAATTACTGAGCCCAGCAGGCTTCCTGAATGAGGTGACTCTACCCTGACCCTCCTCCTGGGCACCTAGGGTTACCTTCTGTATGGTGACAGCTGCTTGGCCCTGACTGAACTTGTGCCATCCATCCTCCCGAATCCTCCCATCCTGCTCCTCATCTCTTCGAATCTCTCGCATGAAGGTGGCTCGAAGCCGGCCTTGCCTCGCCCGCTCTGCCTTTTGCACTAGAATTATGGCCTCAGTCCGGTGCATTCCTGTAAAGCTC... | GACACAGAGGCTGCAGTGAGCTGAAATCTACAGAATCCAAGCACTTGCACTCCTGTGATCAATTACTGAGCCCAGCAGGCTTCCTGAATGAGGTGACTCTACCCTGACCCTCCTCCTGGGCACCTAGGGTTACCTTCTGTATGGTGACAGCTGCTTGGCCCTGACTGAACTTGTGCCATCCATCCTCCCGAATCCTCCCATCCTGCTCCTCATCTCTTCGAATCTCTCGCATGAAGGTGGCTCGAAGCCGGCCTTGCCTCGCCCGCTCTGCCTTTTGCACTAGAATTATGGCCTCAGTCCGGTGCATTCCTGTAAAGCTC... |
Task1_train_39055 | A genetic alteration is present on Chromosome 7. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GAAGGCAAGGAGGCTCCTCACCAGCCCCTTCCCAGAGGCCAACAGTCATGGAAATAGGGATTTGTGTTTTCTTTGTACTGCTATGGTATATCTAAGTTTTTTAAAAGAAGTTTTCAACTGCAGGAGGTAACATGATTAAGCTCCTTGTATGAGCACACACAAGCATCTGTATTTAACAAATGGGACCAGTTACACATGCATCTTGCTGGTTTCACTGATGCATTTGCATAGTGTTCCACGGTATGGATGTATCATACTTCCTAACACCATTCCTCTCTTCACGAATATTCAGGATTTGGGTTTGGGGTGTTTTTTGTTGT... | GAAGGCAAGGAGGCTCCTCACCAGCCCCTTCCCAGAGGCCAACAGTCATGGAAATAGGGATTTGTGTTTTCTTTGTACTGCTATGGTATATCTAAGTTTTTTAAAAGAAGTTTTCAACTGCAGGAGGTAACATGATTAAGCTCCTTGTATGAGCACACACAAGCATCTGTATTTAACAAATGGGACCAGTTACACATGCATCTTGCTGGTTTCACTGATGCATTTGCATAGTGTTCCACGGTATGGATGTATCATACTTCCTAACACCATTCCTCTCTTCACGAATATTCAGGATTTGGGTTTGGGGTGTTTTTTGTTGT... |
Task1_train_39056 | A variant on Chromosome 7 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CAGAGGCCTTCCATTTACATTTCAGTTTCTTGCCCCATACAAGCCTTGAATTCAGCAATTGTCCTTGGAATTTCCCCCTACATCGCTGTGTTGGTTTTGTGTCCCCAGCAGTGGCCCTCTGTGGTCTCAAAGTCTAAATTCTCAGCCTCATGCTTGTATCCAGAACTGGCAAAAGCCCTCACACACCAATACAAGCCACTGCAGACATTAGCTCACCCCTTGAAGGTTCCTCATTCTCTGGAATATCAAGTCCCCCCATTCTTGCCTCAGCAGCTTTCACTGCCTTCAAACAGATGTTTTCTGACTTCGCTTTCTGGCTT... | CAGAGGCCTTCCATTTACATTTCAGTTTCTTGCCCCATACAAGCCTTGAATTCAGCAATTGTCCTTGGAATTTCCCCCTACATCGCTGTGTTGGTTTTGTGTCCCCAGCAGTGGCCCTCTGTGGTCTCAAAGTCTAAATTCTCAGCCTCATGCTTGTATCCAGAACTGGCAAAAGCCCTCACACACCAATACAAGCCACTGCAGACATTAGCTCACCCCTTGAAGGTTCCTCATTCTCTGGAATATCAAGTCCCCCCATTCTTGCCTCAGCAGCTTTCACTGCCTTCAAACAGATGTTTTCTGACTTCGCTTTCTGGCTT... |
Task1_train_39057 | A variant has been detected on Chromosome 7. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TCTGGCCATCTTTATGTCCTCAACATCTCGCAAAGCTCTCTGTGCAATGGAAGTAGAAATTACCCCAATGTGTGTTGCTATAAAAATGCAAAGTGAGTGCAGCGCCCGTGTTTTGGGTCCATGCCCCACTGGGTTTCTCTGGATGGCTTGATGCATGCTCCATTCTCTGCTGTGGGGAGATAAGGTGGGGACTGGAGCTGACGTGTCAGTGAGGGGCTGCTCAGGCCAGAGCGCAGCATCACCAAGCAGCAGTGTCTTCGGCAAGCAGGAGTCAGTGTGAACGTCTGTGCAGGCTCAGGGCCGGCCGGCAGCACTGCCCG... | TCTGGCCATCTTTATGTCCTCAACATCTCGCAAAGCTCTCTGTGCAATGGAAGTAGAAATTACCCCAATGTGTGTTGCTATAAAAATGCAAAGTGAGTGCAGCGCCCGTGTTTTGGGTCCATGCCCCACTGGGTTTCTCTGGATGGCTTGATGCATGCTCCATTCTCTGCTGTGGGGAGATAAGGTGGGGACTGGAGCTGACGTGTCAGTGAGGGGCTGCTCAGGCCAGAGCGCAGCATCACCAAGCAGCAGTGTCTTCGGCAAGCAGGAGTCAGTGTGAACGTCTGTGCAGGCTCAGGGCCGGCCGGCAGCACTGCCCG... |
Task1_train_39058 | A mutation has occurred on Chromosome 7. What is the medical relevance of this mutation? | Benign | AGTTTTCTGGGATGTCTATATCCAATAGGTCATGATGTGAAGTTCCTCGCCGTGGCTCACTGTCAAAGTCTGAAAGCCGCTGCGGAAGTGGCTCAACGCATGGCAGGCACAGGGGCTCCATGGGGTAAGTAGCCCACAGGACAGCCACTAGGAATGTGGTCCCTCCCTGCATACATGTGCTGTCTCCTGTTGAGTGGGCGAATCTGTTCCTCCATCCTTGAGTTGGGGCAGCTGTGCTCAACAGAAATGCAGCAGAAACCACACCACCTGACTTCTGGGTTAGGTGAGAAGGAACCTCGCAGTTCCTCCTGGATCTCTTG... | AGTTTTCTGGGATGTCTATATCCAATAGGTCATGATGTGAAGTTCCTCGCCGTGGCTCACTGTCAAAGTCTGAAAGCCGCTGCGGAAGTGGCTCAACGCATGGCAGGCACAGGGGCTCCATGGGGTAAGTAGCCCACAGGACAGCCACTAGGAATGTGGTCCCTCCCTGCATACATGTGCTGTCTCCTGTTGAGTGGGCGAATCTGTTCCTCCATCCTTGAGTTGGGGCAGCTGTGCTCAACAGAAATGCAGCAGAAACCACACCACCTGACTTCTGGGTTAGGTGAGAAGGAACCTCGCAGTTCCTCCTGGATCTCTTG... |
Task1_train_39059 | Here is a mutation located on Chromosome 7. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GCGGAAGTGGCTCAACGCATGGCAGGCACAGGGGCTCCATGGGGTAAGTAGCCCACAGGACAGCCACTAGGAATGTGGTCCCTCCCTGCATACATGTGCTGTCTCCTGTTGAGTGGGCGAATCTGTTCCTCCATCCTTGAGTTGGGGCAGCTGTGCTCAACAGAAATGCAGCAGAAACCACACCACCTGACTTCTGGGTTAGGTGAGAAGGAACCTCGCAGTTCCTCCTGGATCTCTTGTAATGTCTGCCGCGGGTGAAACCAGCTGCCACGTTAGGAATCTGCACCAAGACCACCATGTTATGAGGAAGCTCAAGCCAG... | GCGGAAGTGGCTCAACGCATGGCAGGCACAGGGGCTCCATGGGGTAAGTAGCCCACAGGACAGCCACTAGGAATGTGGTCCCTCCCTGCATACATGTGCTGTCTCCTGTTGAGTGGGCGAATCTGTTCCTCCATCCTTGAGTTGGGGCAGCTGTGCTCAACAGAAATGCAGCAGAAACCACACCACCTGACTTCTGGGTTAGGTGAGAAGGAACCTCGCAGTTCCTCCTGGATCTCTTGTAATGTCTGCCGCGGGTGAAACCAGCTGCCACGTTAGGAATCTGCACCAAGACCACCATGTTATGAGGAAGCTCAAGCCAG... |
Task1_train_39060 | This variant is present on Chromosome 7. Is the change likely to result in a pathogenic outcome? | Benign | GGCCAGCCCCAGGGAGTGATGTGAGAGTGAAGGAGCCTCTAGGATGTGCCAGGCTCAGCTGCCACCTGACTTTTCAAATAGGAGGAACCCCCAGTGAGAACTCAGCTGAGCCAGATGACTCCTAAATCCATGAAAGATGATTTCAAATCATATTTTTAAGTTTTGGGGTGGTTTGTTATGTAGCAATAGGTGATCTTGTGACTATGTAACCCTGGGAAAGTTACTTCATTTCTCTGTTTTTTAATCTAAAAACTGGGAATCATGGGAGTTCCTACTGGAAAATGAGTTAACATATAGAAGTATAGAACCACATATGAGTT... | GGCCAGCCCCAGGGAGTGATGTGAGAGTGAAGGAGCCTCTAGGATGTGCCAGGCTCAGCTGCCACCTGACTTTTCAAATAGGAGGAACCCCCAGTGAGAACTCAGCTGAGCCAGATGACTCCTAAATCCATGAAAGATGATTTCAAATCATATTTTTAAGTTTTGGGGTGGTTTGTTATGTAGCAATAGGTGATCTTGTGACTATGTAACCCTGGGAAAGTTACTTCATTTCTCTGTTTTTTAATCTAAAAACTGGGAATCATGGGAGTTCCTACTGGAAAATGAGTTAACATATAGAAGTATAGAACCACATATGAGTT... |
Task1_train_39061 | A sequence alteration has been identified on Chromosome 7. Is it disease-inducing or harmless? | Benign | TAGGATGTGCCAGGCTCAGCTGCCACCTGACTTTTCAAATAGGAGGAACCCCCAGTGAGAACTCAGCTGAGCCAGATGACTCCTAAATCCATGAAAGATGATTTCAAATCATATTTTTAAGTTTTGGGGTGGTTTGTTATGTAGCAATAGGTGATCTTGTGACTATGTAACCCTGGGAAAGTTACTTCATTTCTCTGTTTTTTAATCTAAAAACTGGGAATCATGGGAGTTCCTACTGGAAAATGAGTTAACATATAGAAGTATAGAACCACATATGAGTTAACAAAGACATGGCTGTGATGCCTGGGACTCATTTGGAA... | TAGGATGTGCCAGGCTCAGCTGCCACCTGACTTTTCAAATAGGAGGAACCCCCAGTGAGAACTCAGCTGAGCCAGATGACTCCTAAATCCATGAAAGATGATTTCAAATCATATTTTTAAGTTTTGGGGTGGTTTGTTATGTAGCAATAGGTGATCTTGTGACTATGTAACCCTGGGAAAGTTACTTCATTTCTCTGTTTTTTAATCTAAAAACTGGGAATCATGGGAGTTCCTACTGGAAAATGAGTTAACATATAGAAGTATAGAACCACATATGAGTTAACAAAGACATGGCTGTGATGCCTGGGACTCATTTGGAA... |
Task1_train_39062 | This mutation occurs on Chromosome 7. Does this change lead to a known medical condition, or is it benign? | Benign | GTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCGCCCTCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCGCGCCCGGCCACAATGATTTTTTTATTTCAACTCAATTTTCTGGCCCCAGTTGATTAACCCAGGGATGGGGCACCTATGGCAAGCTGGGCCAGTGAATCTTTTCCAGTCAATATTTGATCTTGGAAAAGGTAAAGTCCCACCAGTTTCTCCTTGGGTCCTTGCCTATAAGAAATGCTGATGTCAATCACATTTCCCACTAAAGAAGTGGAAAAAGCCCAGGTGC... | GTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCGCCCTCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCGCGCCCGGCCACAATGATTTTTTTATTTCAACTCAATTTTCTGGCCCCAGTTGATTAACCCAGGGATGGGGCACCTATGGCAAGCTGGGCCAGTGAATCTTTTCCAGTCAATATTTGATCTTGGAAAAGGTAAAGTCCCACCAGTTTCTCCTTGGGTCCTTGCCTATAAGAAATGCTGATGTCAATCACATTTCCCACTAAAGAAGTGGAAAAAGCCCAGGTGC... |
Task1_train_39063 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | GCCACAATGATTTTTTTATTTCAACTCAATTTTCTGGCCCCAGTTGATTAACCCAGGGATGGGGCACCTATGGCAAGCTGGGCCAGTGAATCTTTTCCAGTCAATATTTGATCTTGGAAAAGGTAAAGTCCCACCAGTTTCTCCTTGGGTCCTTGCCTATAAGAAATGCTGATGTCAATCACATTTCCCACTAAAGAAGTGGAAAAAGCCCAGGTGCAGAGGAAGAATCATAATCATGTAATGCGCCTTCTATCTGAATACTTACTGCGTGCCAGGCACTGCTCTAAGTGTTGTAGGCATGTTAATTCATTGCATCTTCA... | GCCACAATGATTTTTTTATTTCAACTCAATTTTCTGGCCCCAGTTGATTAACCCAGGGATGGGGCACCTATGGCAAGCTGGGCCAGTGAATCTTTTCCAGTCAATATTTGATCTTGGAAAAGGTAAAGTCCCACCAGTTTCTCCTTGGGTCCTTGCCTATAAGAAATGCTGATGTCAATCACATTTCCCACTAAAGAAGTGGAAAAAGCCCAGGTGCAGAGGAAGAATCATAATCATGTAATGCGCCTTCTATCTGAATACTTACTGCGTGCCAGGCACTGCTCTAAGTGTTGTAGGCATGTTAATTCATTGCATCTTCA... |
Task1_train_39064 | This genomic variant is located on Chromosome 7. Can you determine its pathogenicity and name any linked disease? | Benign | AGAGAGCAAGCTAGCTCCATCACCCAGTTATGCCTCTGCAAGGCCCCACCTGCAAATACCATCATACTGAGGGGTACTTTGAATTTTGGTGGGGACACAAACATACCGGCCGTAAGATCTGTCAACGTTCTCATACATTCATCACACATTGTGGTCCCCTTTATGAGAGACTAGGGGGTCGCTGCTGCCAACATGTGGGTGTGCTTCCCAACCAGACACCTCTGCTTCTCCTCCTCTATCTGAGCCTTTGACCCACACAGAGCCTTAAACACAGGACTAGGGTGTTCTAGGCTCTGATGGAGCTCAGGTTGACACCTTCC... | AGAGAGCAAGCTAGCTCCATCACCCAGTTATGCCTCTGCAAGGCCCCACCTGCAAATACCATCATACTGAGGGGTACTTTGAATTTTGGTGGGGACACAAACATACCGGCCGTAAGATCTGTCAACGTTCTCATACATTCATCACACATTGTGGTCCCCTTTATGAGAGACTAGGGGGTCGCTGCTGCCAACATGTGGGTGTGCTTCCCAACCAGACACCTCTGCTTCTCCTCCTCTATCTGAGCCTTTGACCCACACAGAGCCTTAAACACAGGACTAGGGTGTTCTAGGCTCTGATGGAGCTCAGGTTGACACCTTCC... |
Task1_train_39065 | A mutation on Chromosome 7 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TCAGTGTGGACTTGAACCGCTGTGAGTAACACATTTATAAAATCTCTAAGGAGTCAAAATTTCTGTAACACTGTTCCCTCAACAGTAATTTGAGTAAAGAGTTTTATTCTACTAAATGTCAATTTCCAATATAAGCATGAAACATTGTACCACTTATTAGTAAGTTATGAAGACAAAATTAGAAGTCTTTGCACTATGGTAAAAATTTTTTAATTGTCTTTTTCTCTTTTTCTTTAACAACTAGACCTCACAAGAAAGATTATAGAAAATAATTTTAATGAGAGTTATTATACGTAAACTTAATAAATTTCAAAACATCT... | TCAGTGTGGACTTGAACCGCTGTGAGTAACACATTTATAAAATCTCTAAGGAGTCAAAATTTCTGTAACACTGTTCCCTCAACAGTAATTTGAGTAAAGAGTTTTATTCTACTAAATGTCAATTTCCAATATAAGCATGAAACATTGTACCACTTATTAGTAAGTTATGAAGACAAAATTAGAAGTCTTTGCACTATGGTAAAAATTTTTTAATTGTCTTTTTCTCTTTTTCTTTAACAACTAGACCTCACAAGAAAGATTATAGAAAATAATTTTAATGAGAGTTATTATACGTAAACTTAATAAATTTCAAAACATCT... |
Task1_train_39066 | A change on Chromosome 7 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GTTGGACCCCAGTGTGGATGAAGAGGGGCAGAAGGACGGGGTTACACCACACTTGAGTTCCCTTGTGAAAGACGTTCAGATTTCAGACTTTTTCAAAGTAAGTGTGGCAGTTGCATGGCAGTGTTAAGCACACTGACCATGGACGCTCCAAAGGTCCATGTGTATGTGTTCATGTGGGCAACTCCCCAAGATATGGGGCGAGCTGAACCCCCCAGGTACAGAGCAGCCTGCATCGCTGCAGGCTCCATGGGTATCAGGGAGCAGGACCCACCCAGGGACACACATGTGGGCACAGCAAAGGCCTTCACAGACACCCCATG... | GTTGGACCCCAGTGTGGATGAAGAGGGGCAGAAGGACGGGGTTACACCACACTTGAGTTCCCTTGTGAAAGACGTTCAGATTTCAGACTTTTTCAAAGTAAGTGTGGCAGTTGCATGGCAGTGTTAAGCACACTGACCATGGACGCTCCAAAGGTCCATGTGTATGTGTTCATGTGGGCAACTCCCCAAGATATGGGGCGAGCTGAACCCCCCAGGTACAGAGCAGCCTGCATCGCTGCAGGCTCCATGGGTATCAGGGAGCAGGACCCACCCAGGGACACACATGTGGGCACAGCAAAGGCCTTCACAGACACCCCATG... |
Task1_train_39067 | A variant affecting Chromosome 7 has been observed. Determine if it's benign or associated with disease. | Benign | TAAAGCAATTTCTTCTGAAAGTAAATGTAGTGTAGAACAGGCTTTCACAAATACAAACATGAATGTTAGGAAAAAGTCTGGAAAAAATGCAAGAGTACATGTTGTATAAAAACCAAATGCTTATAGCATATCTGTAAAAATTTAACAGGCCTCTTATCATTCCTATCAGTAGCTCCTACAATAATTTTCTAATAGATGGCGGTATGGAATACAGCAAGCTCTGGTATGAATGGTAAGAGCGTTTCTGCACCAAGCCTCATTCCAACTAGACAGGCTATTTATTTATGGCTAAACATGACATTGGATTCTGGGACTGAGGC... | TAAAGCAATTTCTTCTGAAAGTAAATGTAGTGTAGAACAGGCTTTCACAAATACAAACATGAATGTTAGGAAAAAGTCTGGAAAAAATGCAAGAGTACATGTTGTATAAAAACCAAATGCTTATAGCATATCTGTAAAAATTTAACAGGCCTCTTATCATTCCTATCAGTAGCTCCTACAATAATTTTCTAATAGATGGCGGTATGGAATACAGCAAGCTCTGGTATGAATGGTAAGAGCGTTTCTGCACCAAGCCTCATTCCAACTAGACAGGCTATTTATTTATGGCTAAACATGACATTGGATTCTGGGACTGAGGC... |
Task1_train_39068 | With a mutation on Chromosome 7, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AAAACAAAGAAAACGAGATGACCGGTCTGGGAGCTCCTCAATCAGAGTAGAGAAGTTAGAGGGGGGCGGGCGACTTGGTTTTGAAGTCTTAGCTGAACAGTCACCCCTCCTCTCCTTGGCAAAAAGGATTCCTTTAGAACCTCCGAGGCTCCTGGATTTCTCCCTTCGCAAATGGAGCCGCATACTGCATTCCCCCGCTCTTTCGGATCGCTAAGCATGTTTCATGAGGGTCGCTGTCCCCGGGTGGAATGCGGCCGTATGCACGCGCCTCCCTGCACACGCACACACACGCACACTTACAATAAGTGTCTGCAGGAGGA... | AAAACAAAGAAAACGAGATGACCGGTCTGGGAGCTCCTCAATCAGAGTAGAGAAGTTAGAGGGGGGCGGGCGACTTGGTTTTGAAGTCTTAGCTGAACAGTCACCCCTCCTCTCCTTGGCAAAAAGGATTCCTTTAGAACCTCCGAGGCTCCTGGATTTCTCCCTTCGCAAATGGAGCCGCATACTGCATTCCCCCGCTCTTTCGGATCGCTAAGCATGTTTCATGAGGGTCGCTGTCCCCGGGTGGAATGCGGCCGTATGCACGCGCCTCCCTGCACACGCACACACACGCACACTTACAATAAGTGTCTGCAGGAGGA... |
Task1_train_39069 | Given a variant located on Chromosome 7, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGACTCAGTTTCAAAGAACAAGGTGCTATTAAATGAAAATTATTTTGATGATAGTTAATAGTTAATTACTTCTTTTTGGAGCAGTGAAAAAGTGGTGAACATTTCTTTACCTTTATGCTGCTGCCTAGGTCAATACGGTGGTTTAAAAAAATCTCCATGAATACCTGAAAGACCAACTGAAAAAGGAAGTAATTTTAATTTGTCTCTAAAGAGTTCTAGTAACATGTAGTTTTTGAAAAATGTTAATCTGTAAGAATTTGCTTAAAATTTTTTTATCCAGAGGACTCTGTGTACTATTTTTTCTGTAGTAATTTGGTTTC... | TGACTCAGTTTCAAAGAACAAGGTGCTATTAAATGAAAATTATTTTGATGATAGTTAATAGTTAATTACTTCTTTTTGGAGCAGTGAAAAAGTGGTGAACATTTCTTTACCTTTATGCTGCTGCCTAGGTCAATACGGTGGTTTAAAAAAATCTCCATGAATACCTGAAAGACCAACTGAAAAAGGAAGTAATTTTAATTTGTCTCTAAAGAGTTCTAGTAACATGTAGTTTTTGAAAAATGTTAATCTGTAAGAATTTGCTTAAAATTTTTTTATCCAGAGGACTCTGTGTACTATTTTTTCTGTAGTAATTTGGTTTC... |
Task1_train_39070 | Chromosome 7 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGTACTTGAAAGGACAAGCAAGAGGGCAGGAAGTGTGGCTGACAGTCACCATTGGCACAACCTTTTACACACCTTATTCTCCTTTGCTTTACACTCTTCACATGTACTAAAAAGGAGCCGCTGGTGTGGCCCTGAATGAGCCACCTACCCGTGCCTCAGATGACACTGGTGGCCACTCTGTAATGACTCAGACCTTTCTAGTGTAGGATGGCTTGAGCCCGGGAGGCCGAGGCTGAGTGAGCATTGATGGCCCCAAGCACTCCAGTTTGGGTGACAGAGCGAGATGCTGTCTCCACCAAACCAAACAAAAATACCAAAAA... | TGTACTTGAAAGGACAAGCAAGAGGGCAGGAAGTGTGGCTGACAGTCACCATTGGCACAACCTTTTACACACCTTATTCTCCTTTGCTTTACACTCTTCACATGTACTAAAAAGGAGCCGCTGGTGTGGCCCTGAATGAGCCACCTACCCGTGCCTCAGATGACACTGGTGGCCACTCTGTAATGACTCAGACCTTTCTAGTGTAGGATGGCTTGAGCCCGGGAGGCCGAGGCTGAGTGAGCATTGATGGCCCCAAGCACTCCAGTTTGGGTGACAGAGCGAGATGCTGTCTCCACCAAACCAAACAAAAATACCAAAAA... |
Task1_train_39071 | Given a variant located on Chromosome 7, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ACAGATGTGAAATACTGATTAGGACTGGTGGGAAAGTTGTTTACTGAAACCAGAGGCAAGGGGGAGAAGAGAACCAGGAAGTTAAACTTTAAAATGGAGAATCGAAGAAGAAGAGAGCTGAACACACTGACATACTGATTCTTTGAGGAAAAACTTGGGGTTCACTATATTTAACATTAATAAGAGACAAGTTAAGGAGAAAAATTAGCTTGGGGAAGGGAGCTAAGTAAGTAGTTTCGTTTTATATACGTTGAGTTTTCAGCTCCATGGGGTATTCAATTATAGCACTTAAAATGTACTGGAATTTGTTTCCATTGTCT... | ACAGATGTGAAATACTGATTAGGACTGGTGGGAAAGTTGTTTACTGAAACCAGAGGCAAGGGGGAGAAGAGAACCAGGAAGTTAAACTTTAAAATGGAGAATCGAAGAAGAAGAGAGCTGAACACACTGACATACTGATTCTTTGAGGAAAAACTTGGGGTTCACTATATTTAACATTAATAAGAGACAAGTTAAGGAGAAAAATTAGCTTGGGGAAGGGAGCTAAGTAAGTAGTTTCGTTTTATATACGTTGAGTTTTCAGCTCCATGGGGTATTCAATTATAGCACTTAAAATGTACTGGAATTTGTTTCCATTGTCT... |
Task1_train_39072 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | GTGGAGAGACCAGACAGAGGCCTTTGCAATAATCCAGGCAGCTATGATGGTGGCAGGGAAGGTCCATTGGTCCCTCCCTCTGCTGCAGGATGGTCTACAAGATACATTGTTAAATGAAAAAAGCAAGATGTGGAACAGTGTTTTGTAAACTAGCACTCATGAGACACAGCACACACACCTATTTATGCTTCATTGAGTATAGAATCTATTGGGAAGATCACTTCAGAATGATATATTGCTGCTTCATGGAAGGAGAACTGGGTGGCTTGTGGACAGGCACAGCACAGAAATTGACCTTTTCATTTATATCTTTTTGTACC... | GTGGAGAGACCAGACAGAGGCCTTTGCAATAATCCAGGCAGCTATGATGGTGGCAGGGAAGGTCCATTGGTCCCTCCCTCTGCTGCAGGATGGTCTACAAGATACATTGTTAAATGAAAAAAGCAAGATGTGGAACAGTGTTTTGTAAACTAGCACTCATGAGACACAGCACACACACCTATTTATGCTTCATTGAGTATAGAATCTATTGGGAAGATCACTTCAGAATGATATATTGCTGCTTCATGGAAGGAGAACTGGGTGGCTTGTGGACAGGCACAGCACAGAAATTGACCTTTTCATTTATATCTTTTTGTACC... |
Task1_train_39073 | Given this variant on Chromosome 7, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GTCAAGGACGGGCCGGGCGCGGTGGCTTGCCTGTAATCCCAGCACTTTGGTCCGCCATTGCACTCCGGCCTGGGCAACAGAGTGAGACTCGGTCTCAAGAAAAAAAAAAGAAAAAAAATTAAATTAAATTAAATTAAGTCAAGGGTGGGAACTCTGTGGAAATGAAGCTTCTGAAGCTGTCCGGGAAGAGAAGCGGCCCCTGGTCAGGCCGAGAACCCCACAGCAGCAGCCCCGTCTTCCCCCAGCTCACTGCTAGGCGAGGCTGCTCCTGCGCCTCCGGGCTTCCCAAAAATCCAGACGCAAACTGCGCGGCCTCTGCG... | GTCAAGGACGGGCCGGGCGCGGTGGCTTGCCTGTAATCCCAGCACTTTGGTCCGCCATTGCACTCCGGCCTGGGCAACAGAGTGAGACTCGGTCTCAAGAAAAAAAAAAGAAAAAAAATTAAATTAAATTAAATTAAGTCAAGGGTGGGAACTCTGTGGAAATGAAGCTTCTGAAGCTGTCCGGGAAGAGAAGCGGCCCCTGGTCAGGCCGAGAACCCCACAGCAGCAGCCCCGTCTTCCCCCAGCTCACTGCTAGGCGAGGCTGCTCCTGCGCCTCCGGGCTTCCCAAAAATCCAGACGCAAACTGCGCGGCCTCTGCG... |
Task1_train_39074 | Given this variant on Chromosome 7, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCCTTTCCATCTTAAAGGTTCGTGTAACGTGTGAAAATATTGAAAGCAATGGAAATGGGAGTGTAATTGTTTAGTACCTGGTAAATCAGGTCCTGTTTTACCAGCGTATTTTCTTCGATTCTGATTCATCTGAAAAGTGCTTGCATTATCCTAGCCAGGACAGAAAACGGCCAGACTAACATGTGCTACAAATTGATCTGGTAAATGAAGGCACCGCTGCAGTTCTTTTGCTAATCTGAATGAATGTGTTTTGGAGCTTGAGGTTAATTTGCTGGTCCTAATTATAAAATCCTGAACTGGTCACTGTTAGTGAGGAGAAG... | CCCTTTCCATCTTAAAGGTTCGTGTAACGTGTGAAAATATTGAAAGCAATGGAAATGGGAGTGTAATTGTTTAGTACCTGGTAAATCAGGTCCTGTTTTACCAGCGTATTTTCTTCGATTCTGATTCATCTGAAAAGTGCTTGCATTATCCTAGCCAGGACAGAAAACGGCCAGACTAACATGTGCTACAAATTGATCTGGTAAATGAAGGCACCGCTGCAGTTCTTTTGCTAATCTGAATGAATGTGTTTTGGAGCTTGAGGTTAATTTGCTGGTCCTAATTATAAAATCCTGAACTGGTCACTGTTAGTGAGGAGAAG... |
Task1_train_39075 | Given a variant located on Chromosome 7, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCTGCCCTGCTGTGTTTTGGGACTTTGCAGTGGACCATGAAACACAGACATCTTTTTTCTTCCCCCCCCAAGATGGGAGTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAATCTCTGCAACCTCTGCCTCCGGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGATTACAGGCTCATGCCACCACGCCCAGCTAATTTTTGTATTTTTAATAGAGACGGGATTTCACCATGTTGGCCAAGCTGGTCTGGAACCCCTGACCTTGTGATCTGCCCTCCTCAGCCTCCCAAAGTGCTAATATTACAGG... | CCTGCCCTGCTGTGTTTTGGGACTTTGCAGTGGACCATGAAACACAGACATCTTTTTTCTTCCCCCCCCAAGATGGGAGTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAATCTCTGCAACCTCTGCCTCCGGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGATTACAGGCTCATGCCACCACGCCCAGCTAATTTTTGTATTTTTAATAGAGACGGGATTTCACCATGTTGGCCAAGCTGGTCTGGAACCCCTGACCTTGTGATCTGCCCTCCTCAGCCTCCCAAAGTGCTAATATTACAGG... |
Task1_train_39076 | Chromosome 7 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AAGGCCCCAGCGCCAAGGCCTGGCCCTGCAGAGGGCGGGGCTGTTCCCTCACTATCAGTGCCCACTCCCCAAGGAATGCGGACTCAGGACCACCAAGTGGAAATGGATAGTTTGGAGTTAATGAGACCAATTTTTTTTTTTTTTTTTGTCTAGGAGACGTCTGAGTGTCCCTGTTAAACAGGGCCCATCGCAGGAGGCTTCCTCTCCACAGGAGCCGGCTTTGGTAGCAGTGGATTGACCCAGAGGCAAGAGGAGAACTGAGGCCAGTCGGGGGCCAGGAAGGGAGGTTCCGGGAAGCCCAGGAGTTGAAGGCTGCAGTG... | AAGGCCCCAGCGCCAAGGCCTGGCCCTGCAGAGGGCGGGGCTGTTCCCTCACTATCAGTGCCCACTCCCCAAGGAATGCGGACTCAGGACCACCAAGTGGAAATGGATAGTTTGGAGTTAATGAGACCAATTTTTTTTTTTTTTTTTGTCTAGGAGACGTCTGAGTGTCCCTGTTAAACAGGGCCCATCGCAGGAGGCTTCCTCTCCACAGGAGCCGGCTTTGGTAGCAGTGGATTGACCCAGAGGCAAGAGGAGAACTGAGGCCAGTCGGGGGCCAGGAAGGGAGGTTCCGGGAAGCCCAGGAGTTGAAGGCTGCAGTG... |
Task1_train_39077 | A genetic alteration is present on Chromosome 7. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGCTTCCTCTCCACAGGAGCCGGCTTTGGTAGCAGTGGATTGACCCAGAGGCAAGAGGAGAACTGAGGCCAGTCGGGGGCCAGGAAGGGAGGTTCCGGGAAGCCCAGGAGTTGAAGGCTGCAGTGAGCGAGACTGCACCCCTGCACTGTACCCTGGGTGACACAGCAAGACCCCATCTCTCAATAAATAAAAAATAATAAAATAATAAAATAAAGGAGCAGTGAGTGATGAGAACCAAATCTCTCCCCCTCTCCTCACTGCGCCTTCCTAGAGATTCAGGCTCAGATCCAAACAGGTCTGGGAAGAGCTGGTCCTGCTGT... | GGCTTCCTCTCCACAGGAGCCGGCTTTGGTAGCAGTGGATTGACCCAGAGGCAAGAGGAGAACTGAGGCCAGTCGGGGGCCAGGAAGGGAGGTTCCGGGAAGCCCAGGAGTTGAAGGCTGCAGTGAGCGAGACTGCACCCCTGCACTGTACCCTGGGTGACACAGCAAGACCCCATCTCTCAATAAATAAAAAATAATAAAATAATAAAATAAAGGAGCAGTGAGTGATGAGAACCAAATCTCTCCCCCTCTCCTCACTGCGCCTTCCTAGAGATTCAGGCTCAGATCCAAACAGGTCTGGGAAGAGCTGGTCCTGCTGT... |
Task1_train_39078 | A variant has been detected on Chromosome 7. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TTTACCACGACTTTCATATTTCTACCATGGATAAATTAGGTTATAATTTGAAAAGAGATATTTCGTATCCAAATATACACACTTTTGTATGTTCTCTTTATACTGTTTTTCAATTTGGAGATTATGAGGGGTTTCTCCATAATTTTCTGGGAAAAAAACTTTTGTATTTCATAAATGTTCCCACACCATGAACAAAAAGATCACCAACTTCCACATTTAACATGAAACAAACACCAGAGACGTCATCTTACCTCTTGGTAAAGTCTATCATCGTCGTCCTGCACTCCGTCATCTGTAAAAGACACCAGTGTTACCAAGAC... | TTTACCACGACTTTCATATTTCTACCATGGATAAATTAGGTTATAATTTGAAAAGAGATATTTCGTATCCAAATATACACACTTTTGTATGTTCTCTTTATACTGTTTTTCAATTTGGAGATTATGAGGGGTTTCTCCATAATTTTCTGGGAAAAAAACTTTTGTATTTCATAAATGTTCCCACACCATGAACAAAAAGATCACCAACTTCCACATTTAACATGAAACAAACACCAGAGACGTCATCTTACCTCTTGGTAAAGTCTATCATCGTCGTCCTGCACTCCGTCATCTGTAAAAGACACCAGTGTTACCAAGAC... |
Task1_train_39079 | A genetic alteration is present on Chromosome 7. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AGACCCCCGATGGTGTCTAGTACCCACGAAAGTGCAGGAGGCAGTGAAGACCCTGATGGTGTCTAGTACCCACGCAAGTGCAGGAGGCAGGACCATCAAGGAAAGGGGTTTCTCGGAGTAGAGCATGGCTTAGAACAGAGGAGACGTCGTCCCAGAGGGAGAGGTGCTGGAGGGAAAGTGGCCACTCCAGGCGGGCAGCTCCCGTAGCAAACAGCACCATCAATGCTCCAGCAGCACTCACTCAAGTGCAGCATCGGCCTCCTCCGCCGTCCTTCTCCTCCAAGAGAGGAACAAGGAGAAAGCATCGGTAATGGTCACAC... | AGACCCCCGATGGTGTCTAGTACCCACGAAAGTGCAGGAGGCAGTGAAGACCCTGATGGTGTCTAGTACCCACGCAAGTGCAGGAGGCAGGACCATCAAGGAAAGGGGTTTCTCGGAGTAGAGCATGGCTTAGAACAGAGGAGACGTCGTCCCAGAGGGAGAGGTGCTGGAGGGAAAGTGGCCACTCCAGGCGGGCAGCTCCCGTAGCAAACAGCACCATCAATGCTCCAGCAGCACTCACTCAAGTGCAGCATCGGCCTCCTCCGCCGTCCTTCTCCTCCAAGAGAGGAACAAGGAGAAAGCATCGGTAATGGTCACAC... |
Task1_train_39080 | This sequence variant lies on Chromosome 7. Is it clinically significant, and what condition might it cause if any? | Benign | CTAGTACCCACGAAAGTGCAGGAGGCAGTGAAGACCCTGATGGTGTCTAGTACCCACGCAAGTGCAGGAGGCAGGACCATCAAGGAAAGGGGTTTCTCGGAGTAGAGCATGGCTTAGAACAGAGGAGACGTCGTCCCAGAGGGAGAGGTGCTGGAGGGAAAGTGGCCACTCCAGGCGGGCAGCTCCCGTAGCAAACAGCACCATCAATGCTCCAGCAGCACTCACTCAAGTGCAGCATCGGCCTCCTCCGCCGTCCTTCTCCTCCAAGAGAGGAACAAGGAGAAAGCATCGGTAATGGTCACACGTCCTTCCCTCTAATT... | CTAGTACCCACGAAAGTGCAGGAGGCAGTGAAGACCCTGATGGTGTCTAGTACCCACGCAAGTGCAGGAGGCAGGACCATCAAGGAAAGGGGTTTCTCGGAGTAGAGCATGGCTTAGAACAGAGGAGACGTCGTCCCAGAGGGAGAGGTGCTGGAGGGAAAGTGGCCACTCCAGGCGGGCAGCTCCCGTAGCAAACAGCACCATCAATGCTCCAGCAGCACTCACTCAAGTGCAGCATCGGCCTCCTCCGCCGTCCTTCTCCTCCAAGAGAGGAACAAGGAGAAAGCATCGGTAATGGTCACACGTCCTTCCCTCTAATT... |
Task1_train_39081 | This variant lies on Chromosome 7. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGTGGACCAGACCCTCTAGGGTTAGGCCCACACAGAGAGACTCCCACAGGCTCCTGGAAGGCTTTGGGGCATGTTTTTCAGGCCAGCCAGTGGTCCTGATGGGAGGTGGGCCTGGCACAGAGCAGGGCTGGGACTGGCCTTTCATTGTGAGCCTAACCTTAGAGGGAGACCTGGGGCCCACAGAGCCCTGTGACCCTGTACTTCCACGAGGGCTGAAGACCCCCACCCTCCACCATGAGGGGTGATTTCAACCAACCAGGAAACACAGTCCATGATCAGGAAAAACACAAATATGGCCCAGGTGCCACTGGGCCCTCCTG... | AGTGGACCAGACCCTCTAGGGTTAGGCCCACACAGAGAGACTCCCACAGGCTCCTGGAAGGCTTTGGGGCATGTTTTTCAGGCCAGCCAGTGGTCCTGATGGGAGGTGGGCCTGGCACAGAGCAGGGCTGGGACTGGCCTTTCATTGTGAGCCTAACCTTAGAGGGAGACCTGGGGCCCACAGAGCCCTGTGACCCTGTACTTCCACGAGGGCTGAAGACCCCCACCCTCCACCATGAGGGGTGATTTCAACCAACCAGGAAACACAGTCCATGATCAGGAAAAACACAAATATGGCCCAGGTGCCACTGGGCCCTCCTG... |
Task1_train_39082 | Here is a genetic alteration on Chromosome 7. Based on the data, is it a benign variant or a cause of disease? | Benign | CAGCTGCCTCAGCCTTTGCCGCAGCTCCTGGGTGGCGATGGGCAGCGAGATGTCCGAGGCGATGCTGGGGGTCGGCTCCTTGACTGAGATGTGGCCTGGGGAGGCCAGGAGGCTGGAGGAGCTTCTGCCCAGGTCGTGCAGCCCCTGAGGGCCGGCCTCAGGGGGCTGGGCCTTTTCTTCCATACCAGGCTTATCACTGCCCCCAATGACTGGTGTGGATGGAGCTGTGTTGCTGCCACCAGGGCCTGGAGACCCAGACATATGAGATTTGATGGATGTTTTCCTCCCCTCTTTGGACACAGAGGGACGTTTGACTTGAG... | CAGCTGCCTCAGCCTTTGCCGCAGCTCCTGGGTGGCGATGGGCAGCGAGATGTCCGAGGCGATGCTGGGGGTCGGCTCCTTGACTGAGATGTGGCCTGGGGAGGCCAGGAGGCTGGAGGAGCTTCTGCCCAGGTCGTGCAGCCCCTGAGGGCCGGCCTCAGGGGGCTGGGCCTTTTCTTCCATACCAGGCTTATCACTGCCCCCAATGACTGGTGTGGATGGAGCTGTGTTGCTGCCACCAGGGCCTGGAGACCCAGACATATGAGATTTGATGGATGTTTTCCTCCCCTCTTTGGACACAGAGGGACGTTTGACTTGAG... |
Task1_train_39083 | This mutation occurs on Chromosome 7. Does this change lead to a known medical condition, or is it benign? | Benign | CTTGACTGAGATGTGGCCTGGGGAGGCCAGGAGGCTGGAGGAGCTTCTGCCCAGGTCGTGCAGCCCCTGAGGGCCGGCCTCAGGGGGCTGGGCCTTTTCTTCCATACCAGGCTTATCACTGCCCCCAATGACTGGTGTGGATGGAGCTGTGTTGCTGCCACCAGGGCCTGGAGACCCAGACATATGAGATTTGATGGATGTTTTCCTCCCCTCTTTGGACACAGAGGGACGTTTGACTTGAGCTGAGTGTTGGTGGTCTGGAGGCCTTTCTCGCTTTTCGAGATGGAGCACCTAGAGGTGGACATAAACATAAAAATTAA... | CTTGACTGAGATGTGGCCTGGGGAGGCCAGGAGGCTGGAGGAGCTTCTGCCCAGGTCGTGCAGCCCCTGAGGGCCGGCCTCAGGGGGCTGGGCCTTTTCTTCCATACCAGGCTTATCACTGCCCCCAATGACTGGTGTGGATGGAGCTGTGTTGCTGCCACCAGGGCCTGGAGACCCAGACATATGAGATTTGATGGATGTTTTCCTCCCCTCTTTGGACACAGAGGGACGTTTGACTTGAGCTGAGTGTTGGTGGTCTGGAGGCCTTTCTCGCTTTTCGAGATGGAGCACCTAGAGGTGGACATAAACATAAAAATTAA... |
Task1_train_39084 | Chromosome 7 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGGCAGCCGTCAAAGCCTTCACCAGTGACAGCAAGGCTCTCAGCCCTCTGGGGAAAACTGAGAAGCACTGATCTGGCTTCACGTTGAAAACCAATGGGTGGGGGAAAAGTTCACATTTGTTTTACGGAACATCTTAGGTGATGCATATGTTCTAATAAGGAAGTACAGTGTGCAACTTGGATAATGCTGCAGGAAAGCTGATTTTGGTAACGCTCCTGATACAAGGTCAGAGACACTTCCTTTCTGCAAAAGGAAGCAGTTGTAGAATGGGAAAAAGCAACTTGGAAAAGCTATTGGAGATAAACTAACAGTTTACACAG... | TGGCAGCCGTCAAAGCCTTCACCAGTGACAGCAAGGCTCTCAGCCCTCTGGGGAAAACTGAGAAGCACTGATCTGGCTTCACGTTGAAAACCAATGGGTGGGGGAAAAGTTCACATTTGTTTTACGGAACATCTTAGGTGATGCATATGTTCTAATAAGGAAGTACAGTGTGCAACTTGGATAATGCTGCAGGAAAGCTGATTTTGGTAACGCTCCTGATACAAGGTCAGAGACACTTCCTTTCTGCAAAAGGAAGCAGTTGTAGAATGGGAAAAAGCAACTTGGAAAAGCTATTGGAGATAAACTAACAGTTTACACAG... |
Task1_train_39085 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCTGGGGAAAACTGAGAAGCACTGATCTGGCTTCACGTTGAAAACCAATGGGTGGGGGAAAAGTTCACATTTGTTTTACGGAACATCTTAGGTGATGCATATGTTCTAATAAGGAAGTACAGTGTGCAACTTGGATAATGCTGCAGGAAAGCTGATTTTGGTAACGCTCCTGATACAAGGTCAGAGACACTTCCTTTCTGCAAAAGGAAGCAGTTGTAGAATGGGAAAAAGCAACTTGGAAAAGCTATTGGAGATAAACTAACAGTTTACACAGGGGAGCTATCTAGTCAGATTTACACTAGTCTATGATGAAATTTTCT... | TCTGGGGAAAACTGAGAAGCACTGATCTGGCTTCACGTTGAAAACCAATGGGTGGGGGAAAAGTTCACATTTGTTTTACGGAACATCTTAGGTGATGCATATGTTCTAATAAGGAAGTACAGTGTGCAACTTGGATAATGCTGCAGGAAAGCTGATTTTGGTAACGCTCCTGATACAAGGTCAGAGACACTTCCTTTCTGCAAAAGGAAGCAGTTGTAGAATGGGAAAAAGCAACTTGGAAAAGCTATTGGAGATAAACTAACAGTTTACACAGGGGAGCTATCTAGTCAGATTTACACTAGTCTATGATGAAATTTTCT... |
Task1_train_39086 | With a mutation on Chromosome 7, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CAGCCCCCATTATTGTGACACCCTAAACATCCATTTCCAAATCTGTCACTCAGAATGACTACCTACGAAAGAGACCATTCAAGAACAAAGTTTCTAAACTTTAAAGTACAATTTGGGAGATTTTAGACAATAAATGTCAATACTAGAAGCATCCCTATCAAAGTTTCCATTTTAATGATAAACTGGCCTTTATTTTCCTCACCAGTAACACGGGAACAATCCCATCCTGTGAGGACTAAGTCAGACAATGCACAGAGGCCACACGCCAGGCTCCAAGCCCACTGCCTGCGACTGCAGTCATCACCTGAGGGCTTCCTTCC... | CAGCCCCCATTATTGTGACACCCTAAACATCCATTTCCAAATCTGTCACTCAGAATGACTACCTACGAAAGAGACCATTCAAGAACAAAGTTTCTAAACTTTAAAGTACAATTTGGGAGATTTTAGACAATAAATGTCAATACTAGAAGCATCCCTATCAAAGTTTCCATTTTAATGATAAACTGGCCTTTATTTTCCTCACCAGTAACACGGGAACAATCCCATCCTGTGAGGACTAAGTCAGACAATGCACAGAGGCCACACGCCAGGCTCCAAGCCCACTGCCTGCGACTGCAGTCATCACCTGAGGGCTTCCTTCC... |
Task1_train_39087 | Assess the clinical impact of this variant found on Chromosome 7. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AGTAACACGGGAACAATCCCATCCTGTGAGGACTAAGTCAGACAATGCACAGAGGCCACACGCCAGGCTCCAAGCCCACTGCCTGCGACTGCAGTCATCACCTGAGGGCTTCCTTCCCTGGAAATCCCTTTGAGCAATTAAGATCTTTCTCGCCACTATCAAGGACTAGCACATGTGCCACATAAGCATCACAGCGAACATTTACCCTTTTACTTTTGAAGTTCTGTCCCACTTTAATCTCAGATGAGGAACCATCTATAATCAAAGCACAACTGACCAAACATAAACCAAACAAGCAGAGACTATTTCTGACCAATTGT... | AGTAACACGGGAACAATCCCATCCTGTGAGGACTAAGTCAGACAATGCACAGAGGCCACACGCCAGGCTCCAAGCCCACTGCCTGCGACTGCAGTCATCACCTGAGGGCTTCCTTCCCTGGAAATCCCTTTGAGCAATTAAGATCTTTCTCGCCACTATCAAGGACTAGCACATGTGCCACATAAGCATCACAGCGAACATTTACCCTTTTACTTTTGAAGTTCTGTCCCACTTTAATCTCAGATGAGGAACCATCTATAATCAAAGCACAACTGACCAAACATAAACCAAACAAGCAGAGACTATTTCTGACCAATTGT... |
Task1_train_39088 | This variant lies on Chromosome 7. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TAGCCAGCAGCCTGGAGATCATGGGGTGTACACTGGTGCCCACTAACAGGTGGCAAATACACAGTGACCATGCCAGACCCTCCCACAGCCACATCTATCACAACCCTGAACCGCACTGCACGGGGATGTCTGTTTGCTGACTCTGCTGTGTGTGCAACAACGTGTGCAGACTGTGTGTGTGTTTACAAGAACTATCACGTTCTGAGTCTTTAGGCATATAAAACAATGTTACCTTGGACTGTTGCTACTTAAACACTGATTTAAAAATAGAAAAAGAAAAACTTCCCATGATCAACTAAATGTACTCTTGAGGCTTTTAT... | TAGCCAGCAGCCTGGAGATCATGGGGTGTACACTGGTGCCCACTAACAGGTGGCAAATACACAGTGACCATGCCAGACCCTCCCACAGCCACATCTATCACAACCCTGAACCGCACTGCACGGGGATGTCTGTTTGCTGACTCTGCTGTGTGTGCAACAACGTGTGCAGACTGTGTGTGTGTTTACAAGAACTATCACGTTCTGAGTCTTTAGGCATATAAAACAATGTTACCTTGGACTGTTGCTACTTAAACACTGATTTAAAAATAGAAAAAGAAAAACTTCCCATGATCAACTAAATGTACTCTTGAGGCTTTTAT... |
Task1_train_39089 | A mutation has occurred on Chromosome 7. What is the medical relevance of this mutation? | Benign | GGAAAATACAGTCTGACACAAGATATTTTAAACCCACAGAATATTTGTCCTTCCTCTGTTGTTCAACTGCTGTTATAACTTGTTTTCACTTTTATTTTATAATATTTAAGTTTTGAAGTAGCCAAAGGAACACATTTTATAATAATGTGTCATTTTAGACTAGTGAATAATTTTTAAAAATCTGTATTTCTGTTACCTTTTATTCCAGGAGGTAGAGAAGTATTTTCTGGCATGTCAAGAATTAACTGCCATTGATTTAAATGGCATAATGAAAAAGCAGCTCACTACAACACTGAAAATAAATTATTTTAAACATTCTA... | GGAAAATACAGTCTGACACAAGATATTTTAAACCCACAGAATATTTGTCCTTCCTCTGTTGTTCAACTGCTGTTATAACTTGTTTTCACTTTTATTTTATAATATTTAAGTTTTGAAGTAGCCAAAGGAACACATTTTATAATAATGTGTCATTTTAGACTAGTGAATAATTTTTAAAAATCTGTATTTCTGTTACCTTTTATTCCAGGAGGTAGAGAAGTATTTTCTGGCATGTCAAGAATTAACTGCCATTGATTTAAATGGCATAATGAAAAAGCAGCTCACTACAACACTGAAAATAAATTATTTTAAACATTCTA... |
Task1_train_39090 | A variant affecting Chromosome 7 has been observed. Determine if it's benign or associated with disease. | Benign | TTCTGGAACTGCTGCAGGGCAGGGTTAGGACCCGGGGAAGGAGCTGCCCACTGCTTCTGGAGCTGCTGCAGGGCAGGGGTTAGGACCTGGAGAAGGAGCTGCCCACTGCTTCTGGACAGGGCCCAGGGTCCCGCCTGGCACAGAGACACAGGGCGCCAGTGTGCTGGTCACTGTGATGATGCACAGTGCCGGACACACGTGATGATGCCCAGAGGCCACCTGCCTAGCATAGGACAGACAGCCCCCAAACCTCCCACCTGCTGGAAGGATGAGAAATCAAAAGAGAACACAATGTTTCATTAGAATGGTGACTTATTTCT... | TTCTGGAACTGCTGCAGGGCAGGGTTAGGACCCGGGGAAGGAGCTGCCCACTGCTTCTGGAGCTGCTGCAGGGCAGGGGTTAGGACCTGGAGAAGGAGCTGCCCACTGCTTCTGGACAGGGCCCAGGGTCCCGCCTGGCACAGAGACACAGGGCGCCAGTGTGCTGGTCACTGTGATGATGCACAGTGCCGGACACACGTGATGATGCCCAGAGGCCACCTGCCTAGCATAGGACAGACAGCCCCCAAACCTCCCACCTGCTGGAAGGATGAGAAATCAAAAGAGAACACAATGTTTCATTAGAATGGTGACTTATTTCT... |
Task1_train_39091 | Here is a mutation located on Chromosome 9. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CAGGTGGACCCGAAGCTCCTGTTTGATCGGAGAATAACGTTCAATTTACTCCGCCGCTGAACTGATGGTTTAAATATTCATCTTTGGATATGGTTTCACATTAGGCAAAAGTTAGGAGCTTGGAGGCGGTTCCGGGAAGGGGCCTGACCCTCAGTCACCCACGTTCGTAGCCGGGTGATCTGCCCTCGGGCAAGAGAAGGAAGATGATTGGGAGGGTGCCAAGAAAGCCTGGAGAAAGTCCCTTCTGGGTTCAGCGGCTGTAGCCGCTCTCCCAGGACGTTTGTTGGCAATAAATGAAGGAAGGTCGGCCCGGAGACGTT... | CAGGTGGACCCGAAGCTCCTGTTTGATCGGAGAATAACGTTCAATTTACTCCGCCGCTGAACTGATGGTTTAAATATTCATCTTTGGATATGGTTTCACATTAGGCAAAAGTTAGGAGCTTGGAGGCGGTTCCGGGAAGGGGCCTGACCCTCAGTCACCCACGTTCGTAGCCGGGTGATCTGCCCTCGGGCAAGAGAAGGAAGATGATTGGGAGGGTGCCAAGAAAGCCTGGAGAAAGTCCCTTCTGGGTTCAGCGGCTGTAGCCGCTCTCCCAGGACGTTTGTTGGCAATAAATGAAGGAAGGTCGGCCCGGAGACGTT... |
Task1_train_39092 | With a mutation on Chromosome 9, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AAATCTCCCGTAGGGGATCTCAGGTAGGGCATGCCAAGAAATTCCAAGAGACGGGATGGAGAAGAGAAGCCGGAGAAAAATCGGCCAATTAGACTCCTGTAAAAATGTGTCTCCATGTTTGTCCTCCCTCCTGAAATAAGAAATTCATAGCTGGGGGTGGGGAGTAGATGGGGGCTGGGGGAAAAACTTTCTCACATTCACAGAGCAGCTTCCCTCAAAGCGGCACGGAATCGGGAACCCCACTCGGGACAGGGGAAAACGGCCAAGTTCCTAGAAATTTGTTTTCTTTGTGGGGAGCAATTCATGATGGGCGTTCTTGT... | AAATCTCCCGTAGGGGATCTCAGGTAGGGCATGCCAAGAAATTCCAAGAGACGGGATGGAGAAGAGAAGCCGGAGAAAAATCGGCCAATTAGACTCCTGTAAAAATGTGTCTCCATGTTTGTCCTCCCTCCTGAAATAAGAAATTCATAGCTGGGGGTGGGGAGTAGATGGGGGCTGGGGGAAAAACTTTCTCACATTCACAGAGCAGCTTCCCTCAAAGCGGCACGGAATCGGGAACCCCACTCGGGACAGGGGAAAACGGCCAAGTTCCTAGAAATTTGTTTTCTTTGTGGGGAGCAATTCATGATGGGCGTTCTTGT... |
Task1_train_39093 | A genomic variant on Chromosome 9 is under review. What is the biological outcome — benign or pathogenic? | Benign | CCCACTCGGGACAGGGGAAAACGGCCAAGTTCCTAGAAATTTGTTTTCTTTGTGGGGAGCAATTCATGATGGGCGTTCTTGTCTGGTTTCCCCCCACTCCGTCCCCTGACGCCGAGTAACACTTAAACCTTTCTAGTTGCAAAGTCTTTTCAGAGTTTTTTTTTTAGGAAATAAGTTTTGAAAATTCTAGTGCTTAAAAAATGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATTTATAGCCTTTTATTTTCCCTGAGTACATGTTGGCCACTACATTCCAAATTGAT... | CCCACTCGGGACAGGGGAAAACGGCCAAGTTCCTAGAAATTTGTTTTCTTTGTGGGGAGCAATTCATGATGGGCGTTCTTGTCTGGTTTCCCCCCACTCCGTCCCCTGACGCCGAGTAACACTTAAACCTTTCTAGTTGCAAAGTCTTTTCAGAGTTTTTTTTTTAGGAAATAAGTTTTGAAAATTCTAGTGCTTAAAAAATGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATTTATAGCCTTTTATTTTCCCTGAGTACATGTTGGCCACTACATTCCAAATTGAT... |
Task1_train_39094 | With a mutation on Chromosome 9, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTTTGTGGGGAGCAATTCATGATGGGCGTTCTTGTCTGGTTTCCCCCCACTCCGTCCCCTGACGCCGAGTAACACTTAAACCTTTCTAGTTGCAAAGTCTTTTCAGAGTTTTTTTTTTAGGAAATAAGTTTTGAAAATTCTAGTGCTTAAAAAATGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATTTATAGCCTTTTATTTTCCCTGAGTACATGTTGGCCACTACATTCCAAATTGATCTCAAATGGTTTTCCAGCTTGTTGGGGGGTGAGGAAAAATAAATGGA... | CTTTGTGGGGAGCAATTCATGATGGGCGTTCTTGTCTGGTTTCCCCCCACTCCGTCCCCTGACGCCGAGTAACACTTAAACCTTTCTAGTTGCAAAGTCTTTTCAGAGTTTTTTTTTTAGGAAATAAGTTTTGAAAATTCTAGTGCTTAAAAAATGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATTTATAGCCTTTTATTTTCCCTGAGTACATGTTGGCCACTACATTCCAAATTGATCTCAAATGGTTTTCCAGCTTGTTGGGGGGTGAGGAAAAATAAATGGA... |
Task1_train_39095 | A genomic change on Chromosome 9 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCGTCACCCAGGCTGGAGTGCAGTGGAGCAATCTCAGCTCACTGTGACCTCCGCCTCTCGGGTTCAAGCAATTGTCATGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACACGCCACCACACCTGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCATGAACTCCTGACCTCAAGTGATCTGCCCACTTCAGCCCCCCAAAATGCTGGGATTACAGGTGTGAGCCACCACACACTGCCAGAAGTATGTTTTCATTTCTCCTGGGTAAATACCTTTGAGTGGAATTGCTGG... | CCGTCACCCAGGCTGGAGTGCAGTGGAGCAATCTCAGCTCACTGTGACCTCCGCCTCTCGGGTTCAAGCAATTGTCATGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACACGCCACCACACCTGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCATGAACTCCTGACCTCAAGTGATCTGCCCACTTCAGCCCCCCAAAATGCTGGGATTACAGGTGTGAGCCACCACACACTGCCAGAAGTATGTTTTCATTTCTCCTGGGTAAATACCTTTGAGTGGAATTGCTGG... |
Task1_train_39096 | A variant on Chromosome 9 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | ACCGACTCTGTCCCTTCTCATAGCACCTGAAAACCCCGGGAAACGAGGGGAATGCTTTGCTCTCAGCTACTGAGGTTGTCCTGTCACCTTCTCTTCTGCCCTCCTTTGCCATGGCATAGGATAATGTAAGTCAGCAATCTCATTACTCGGTATATAGCCAGAGGAATATAAATCATTCTACCATAAAGACACACGCGTGTGAATGTTTATTGCAACACTATTCACAATAGCAAAGACATGGAATCAACTTAAATGCCCATCAATGACAGATTGGATGCAGAAAATGTGGTACATATACACCATGGAATACTATGCAGCCA... | ACCGACTCTGTCCCTTCTCATAGCACCTGAAAACCCCGGGAAACGAGGGGAATGCTTTGCTCTCAGCTACTGAGGTTGTCCTGTCACCTTCTCTTCTGCCCTCCTTTGCCATGGCATAGGATAATGTAAGTCAGCAATCTCATTACTCGGTATATAGCCAGAGGAATATAAATCATTCTACCATAAAGACACACGCGTGTGAATGTTTATTGCAACACTATTCACAATAGCAAAGACATGGAATCAACTTAAATGCCCATCAATGACAGATTGGATGCAGAAAATGTGGTACATATACACCATGGAATACTATGCAGCCA... |
Task1_train_39097 | The following genetic variant occurs on Chromosome 9. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CCTTTGCCATGGCATAGGATAATGTAAGTCAGCAATCTCATTACTCGGTATATAGCCAGAGGAATATAAATCATTCTACCATAAAGACACACGCGTGTGAATGTTTATTGCAACACTATTCACAATAGCAAAGACATGGAATCAACTTAAATGCCCATCAATGACAGATTGGATGCAGAAAATGTGGTACATATACACCATGGAATACTATGCAGCCATAAAAATAATGAGATCATGCCTTTTGTGGGAACATGGATGGAACTGGAGGCTATTATCCTTTGCAAACTAACGCAGAAATAGAAAACCAAATGCTGCATGTT... | CCTTTGCCATGGCATAGGATAATGTAAGTCAGCAATCTCATTACTCGGTATATAGCCAGAGGAATATAAATCATTCTACCATAAAGACACACGCGTGTGAATGTTTATTGCAACACTATTCACAATAGCAAAGACATGGAATCAACTTAAATGCCCATCAATGACAGATTGGATGCAGAAAATGTGGTACATATACACCATGGAATACTATGCAGCCATAAAAATAATGAGATCATGCCTTTTGTGGGAACATGGATGGAACTGGAGGCTATTATCCTTTGCAAACTAACGCAGAAATAGAAAACCAAATGCTGCATGTT... |
Task1_train_39098 | This is a variant located on Chromosome 9. Is this mutation a likely cause of disease or not? | Benign | GTGTCTCATCTTTAAAAGTTGGGGCTCAGTCTAGGTGCCTCCTGGCCTGAGCACCCCAGAATTCTATGCTGATCCCTTCATTGTGACATGGCCTGTCATCTACTCTTCTGGGAAGACCATCTGCACCTCACTGATACTTGAAGCTCATTGAGTATTGTCACATATCAGCCCAGAAAGTCACAGGGTACAGCAACTCATACTTGCTCCCAGCACCAGGCCAGCCCCATTCTGCCTCCAGGGAGTCACCCAAAATAGAGAGATGAGGGTAAAATAAGACCTAGGAATACTATTTATTTGCCTCCATGGCCTTTGAACTTGCA... | GTGTCTCATCTTTAAAAGTTGGGGCTCAGTCTAGGTGCCTCCTGGCCTGAGCACCCCAGAATTCTATGCTGATCCCTTCATTGTGACATGGCCTGTCATCTACTCTTCTGGGAAGACCATCTGCACCTCACTGATACTTGAAGCTCATTGAGTATTGTCACATATCAGCCCAGAAAGTCACAGGGTACAGCAACTCATACTTGCTCCCAGCACCAGGCCAGCCCCATTCTGCCTCCAGGGAGTCACCCAAAATAGAGAGATGAGGGTAAAATAAGACCTAGGAATACTATTTATTTGCCTCCATGGCCTTTGAACTTGCA... |
Task1_train_39099 | Given this context: Chromosome 9 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | ATATCAGCCCAGAAAGTCACAGGGTACAGCAACTCATACTTGCTCCCAGCACCAGGCCAGCCCCATTCTGCCTCCAGGGAGTCACCCAAAATAGAGAGATGAGGGTAAAATAAGACCTAGGAATACTATTTATTTGCCTCCATGGCCTTTGAACTTGCACATCCAACGTAACGGCTCCTGTGTGTTCTTGATTGTTCCAATTATCATTTTTCCTCTCGAATACCTGAGAGCATTCATTATTTTGCAAGAGATTTGAGAATCCCTGTGCCCTAACTTTTCTTTCCTTGATGTGGGATGTTCTTCTGTGACTAGGTAAGTTT... | ATATCAGCCCAGAAAGTCACAGGGTACAGCAACTCATACTTGCTCCCAGCACCAGGCCAGCCCCATTCTGCCTCCAGGGAGTCACCCAAAATAGAGAGATGAGGGTAAAATAAGACCTAGGAATACTATTTATTTGCCTCCATGGCCTTTGAACTTGCACATCCAACGTAACGGCTCCTGTGTGTTCTTGATTGTTCCAATTATCATTTTTCCTCTCGAATACCTGAGAGCATTCATTATTTTGCAAGAGATTTGAGAATCCCTGTGCCCTAACTTTTCTTTCCTTGATGTGGGATGTTCTTCTGTGACTAGGTAAGTTT... |
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