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_32500 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTTCACTGAACACCTACCGTATGCCTTATCCTGTTATGAATGCTGGGGCTGCTGACACTAGTAACACCCAGTGCCTGAGCTCAAGAAGTTCCTAATCTAGGGTGTGGTCCCTATAGTCCCACCTACTCAGGAGGCTGAGGCAGAAGGAATGCTTGAAACCAAGAACTCCAGGCTGTAATGCACTATGATCATACCTATGAATAGCTGCTACACGCAAGCCCAGGCAACATAGACAAACCCCCATTTCTAAAAAAAAAAAAAGAAGTTCTTAATCTAGTGGTGAAAACACACATAAGTAGATCAGTGCATACCATGGGGTA... | TTTCACTGAACACCTACCGTATGCCTTATCCTGTTATGAATGCTGGGGCTGCTGACACTAGTAACACCCAGTGCCTGAGCTCAAGAAGTTCCTAATCTAGGGTGTGGTCCCTATAGTCCCACCTACTCAGGAGGCTGAGGCAGAAGGAATGCTTGAAACCAAGAACTCCAGGCTGTAATGCACTATGATCATACCTATGAATAGCTGCTACACGCAAGCCCAGGCAACATAGACAAACCCCCATTTCTAAAAAAAAAAAAAGAAGTTCTTAATCTAGTGGTGAAAACACACATAAGTAGATCAGTGCATACCATGGGGTA... |
Task1_train_32501 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | TTGGCAGCCTCAAGTAAAATAGGAGGAGAGAGAGGCTCAGAGTGGGTTGCAGAGGAACTGGTGAATAAATTCTTGAGCCTTCTTCTTCTCTGTCATATCAAGCTTTTGGTGACCAGCTGGGTTTCGAAGCAATAAGCTGCCAAATATGCTAGCTGCAAGAAAAAACACAGAAAAGAAATGATTCAGCAAAAGAAGGTACTAAAGACACACATCACTTAACGACAGGGATATGTTCTGAGAAATGTGTCATTAGGTGATTTCATCATTGTGCAAACATCATAGCGTGTACTTAAACTTTCACAAACCTGTACTTACACAAT... | TTGGCAGCCTCAAGTAAAATAGGAGGAGAGAGAGGCTCAGAGTGGGTTGCAGAGGAACTGGTGAATAAATTCTTGAGCCTTCTTCTTCTCTGTCATATCAAGCTTTTGGTGACCAGCTGGGTTTCGAAGCAATAAGCTGCCAAATATGCTAGCTGCAAGAAAAAACACAGAAAAGAAATGATTCAGCAAAAGAAGGTACTAAAGACACACATCACTTAACGACAGGGATATGTTCTGAGAAATGTGTCATTAGGTGATTTCATCATTGTGCAAACATCATAGCGTGTACTTAAACTTTCACAAACCTGTACTTACACAAT... |
Task1_train_32502 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGCAACCTGGACGGCAGAGGTTGCAGTGAGCCCAGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGTAAGACTGTCTCAAAAAAAAAAAAAAAAAAAAGGCCGGGCGCAGTGGCTCATGCTTGTAATCCCAACACTTTGGGAAGCTGGGGCGGGCAGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGCAAAACCCCGTCTCTATAGAAAATACAAAAATTAGCCGGGTATGGTGGCGGGCACCTGTAATGCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGTTTGAACCTGGGAGGCAGAGG... | TGCAACCTGGACGGCAGAGGTTGCAGTGAGCCCAGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGTAAGACTGTCTCAAAAAAAAAAAAAAAAAAAAGGCCGGGCGCAGTGGCTCATGCTTGTAATCCCAACACTTTGGGAAGCTGGGGCGGGCAGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGCAAAACCCCGTCTCTATAGAAAATACAAAAATTAGCCGGGTATGGTGGCGGGCACCTGTAATGCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGTTTGAACCTGGGAGGCAGAGG... |
Task1_train_32503 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AAACAGATGACCCAAATAGAACTGAGGGGCTTGATACCATTTCTTACCAATTTTAGCAGGAGCAACTTAGCAATTAATAGTGTCACCCCACTTACTGTAGGTATTTTAAGAGAAAAATTTTTTTTTTTTTCGAGATGGAGTCTTGCTCCGTCTCCCAGGCTGGAATGCAATGGCACGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTACCTCAGCCTCCAGAGTACATGGGATTACAGGCACCTGCCACCACGCCCATCTAATTTTTGTATTTTTAGTAGTGACGGAGTTTCGCCATGTTGG... | AAACAGATGACCCAAATAGAACTGAGGGGCTTGATACCATTTCTTACCAATTTTAGCAGGAGCAACTTAGCAATTAATAGTGTCACCCCACTTACTGTAGGTATTTTAAGAGAAAAATTTTTTTTTTTTTCGAGATGGAGTCTTGCTCCGTCTCCCAGGCTGGAATGCAATGGCACGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTACCTCAGCCTCCAGAGTACATGGGATTACAGGCACCTGCCACCACGCCCATCTAATTTTTGTATTTTTAGTAGTGACGGAGTTTCGCCATGTTGG... |
Task1_train_32504 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCTTGATACCATTTCTTACCAATTTTAGCAGGAGCAACTTAGCAATTAATAGTGTCACCCCACTTACTGTAGGTATTTTAAGAGAAAAATTTTTTTTTTTTTCGAGATGGAGTCTTGCTCCGTCTCCCAGGCTGGAATGCAATGGCACGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTACCTCAGCCTCCAGAGTACATGGGATTACAGGCACCTGCCACCACGCCCATCTAATTTTTGTATTTTTAGTAGTGACGGAGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCA... | GCTTGATACCATTTCTTACCAATTTTAGCAGGAGCAACTTAGCAATTAATAGTGTCACCCCACTTACTGTAGGTATTTTAAGAGAAAAATTTTTTTTTTTTTCGAGATGGAGTCTTGCTCCGTCTCCCAGGCTGGAATGCAATGGCACGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTACCTCAGCCTCCAGAGTACATGGGATTACAGGCACCTGCCACCACGCCCATCTAATTTTTGTATTTTTAGTAGTGACGGAGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCA... |
Task1_train_32505 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CCCCATCAAGGACAAAGATGAGCTGGGGGGCCCATAGGAGAGGATTCATACCACCCAGCCCCCTGTGGCACCTTCTTCCAGCGTAAAATCCCGCGAGACTGGCACTATCTGGTCCAGAGAGACATCGTCCCCGGTAATGGCCATCCTCCGGTGCGTATAGAGGAAGAGACTAAGGGCAGGAAGCAGAGGTGAGGATGGGGGCCCGCTGGCTGTCCCTCAGCCCTATCTTGGAGGTCTCGGGGTGCTCACACTCGCTCGTTGGTCCCTAACACTGTGCTGGTGGTGCCCTGGCTAGGCACACTCCTCATGCCATCTCTGTC... | CCCCATCAAGGACAAAGATGAGCTGGGGGGCCCATAGGAGAGGATTCATACCACCCAGCCCCCTGTGGCACCTTCTTCCAGCGTAAAATCCCGCGAGACTGGCACTATCTGGTCCAGAGAGACATCGTCCCCGGTAATGGCCATCCTCCGGTGCGTATAGAGGAAGAGACTAAGGGCAGGAAGCAGAGGTGAGGATGGGGGCCCGCTGGCTGTCCCTCAGCCCTATCTTGGAGGTCTCGGGGTGCTCACACTCGCTCGTTGGTCCCTAACACTGTGCTGGTGGTGCCCTGGCTAGGCACACTCCTCATGCCATCTCTGTC... |
Task1_train_32506 | This variant is located on Chromosome 1. Evaluate its biological effect and specify any disease association. | Benign | TAGCCACAGTACACATAATTCTAGCTTCCAATAGGGATAAGAGTGATGTGGCCGCTCCTATCAGGAAGCTGTCAGTTCCTGGACGCTCCTGTGGGGGATCTTGGGGAAGGAAGCTTATTCTTCCAGCCAGGATCAAGCTGATAAATGGGACCATCTCCCCATTCTCTGTTCACACTGGATCAGCCTCCTTATTCCTCTCCTTCTCCCTAGCTTAATGCAGCCCAGCTTTGGAGTAGTAATTACCTTCACATGACCCAGTAATCATATTCCCTGGGTGTTGAGCAGAGCATGTGTGTACGGGGATGAGGTCACAGGACTTT... | TAGCCACAGTACACATAATTCTAGCTTCCAATAGGGATAAGAGTGATGTGGCCGCTCCTATCAGGAAGCTGTCAGTTCCTGGACGCTCCTGTGGGGGATCTTGGGGAAGGAAGCTTATTCTTCCAGCCAGGATCAAGCTGATAAATGGGACCATCTCCCCATTCTCTGTTCACACTGGATCAGCCTCCTTATTCCTCTCCTTCTCCCTAGCTTAATGCAGCCCAGCTTTGGAGTAGTAATTACCTTCACATGACCCAGTAATCATATTCCCTGGGTGTTGAGCAGAGCATGTGTGTACGGGGATGAGGTCACAGGACTTT... |
Task1_train_32507 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | TCCCTAACTTTGCTGTATTTTTATCTGTACCACTTACCACTAGCTGACACTACATATTTATTTATGTATTTCTCTCCCTCAACTAGGATATAAGCTTATGAGAGCCGAGACTTTTATCCTCCCCTGCTTATCTCCAGTGTGCAGAACAGACACCTGAGTAAAATTATTAAATGAAAGAAATGAACGTAAGGAGTTTTTAGACGGAATGACATTCAAAGCATCTGTGACACTTTCAGAGACAACATAGCACAGTACTTTCACAGAGTAGTCCCTTAAGACTTGCTGAAGTTTATTTGCAAAGAGGTAAACTATTATCTGAA... | TCCCTAACTTTGCTGTATTTTTATCTGTACCACTTACCACTAGCTGACACTACATATTTATTTATGTATTTCTCTCCCTCAACTAGGATATAAGCTTATGAGAGCCGAGACTTTTATCCTCCCCTGCTTATCTCCAGTGTGCAGAACAGACACCTGAGTAAAATTATTAAATGAAAGAAATGAACGTAAGGAGTTTTTAGACGGAATGACATTCAAAGCATCTGTGACACTTTCAGAGACAACATAGCACAGTACTTTCACAGAGTAGTCCCTTAAGACTTGCTGAAGTTTATTTGCAAAGAGGTAAACTATTATCTGAA... |
Task1_train_32508 | This alteration occurs on Chromosome 1. Is it associated with a disease or is it a benign variant? | Benign | GAATCTCCTACTTTGGGGATTAGGCTCACTCAGCTACTTCATAGCCCACTTGGAAATTCGGTCATTTTTCCAGTTGCTCTTTGTTGGAGGGAAACTTTCTTAACAAGATTCTGAGGACTCCATAAAAACCGTAAGGTGGGAGGAATTGGGATCTGAAGGTCCTTGGCAAACATGTCCACTGCGGCTGCTGGAGGCAAAGCAACGGAAGTTGAAGAGACTTTGCAACAGCTGCAAGAGTTTCACTCCCGGTGCGGAGAAGGGTAGCGGAGCTAGGCTACCCCACCCGGGCGGCGTCCAGCAGCCAGGTCCCTGCTGAACCC... | GAATCTCCTACTTTGGGGATTAGGCTCACTCAGCTACTTCATAGCCCACTTGGAAATTCGGTCATTTTTCCAGTTGCTCTTTGTTGGAGGGAAACTTTCTTAACAAGATTCTGAGGACTCCATAAAAACCGTAAGGTGGGAGGAATTGGGATCTGAAGGTCCTTGGCAAACATGTCCACTGCGGCTGCTGGAGGCAAAGCAACGGAAGTTGAAGAGACTTTGCAACAGCTGCAAGAGTTTCACTCCCGGTGCGGAGAAGGGTAGCGGAGCTAGGCTACCCCACCCGGGCGGCGTCCAGCAGCCAGGTCCCTGCTGAACCC... |
Task1_train_32509 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | TGGTGAAACCCCGTCTCTACTAAAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATTAGTCAGGTTTGGTGGCGGCCACCTGTAATCCCAGCTACTCAGGAAGCTGAGATAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTTCAGTGAACCAAGATCCGGCCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCGGTCTCAAAAAAAAAAAAATAATAATTAGCCAGATGTGGTGGCGCATGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGTAGGAGAATTGCTTGAACCCAGGA... | TGGTGAAACCCCGTCTCTACTAAAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATTAGTCAGGTTTGGTGGCGGCCACCTGTAATCCCAGCTACTCAGGAAGCTGAGATAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTTCAGTGAACCAAGATCCGGCCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCGGTCTCAAAAAAAAAAAAATAATAATTAGCCAGATGTGGTGGCGCATGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGTAGGAGAATTGCTTGAACCCAGGA... |
Task1_train_32510 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTGAATCCGACTTTTACAGTCTGAAATTCAGACTTCCTGCCCTACTGCAATGGGAGTAAAAACCACCTGAACCTCTTTTTGGCAGCTTCTTCTCTTACTCCCAAATGGCAACAAGTGTTATCTCTTTGATTGAGCTCTTGGTCCATGCAGTCTAATTACCAATTCAGAACAGTGGGGGAACTTCTTATTTTACACAACTGGCAACTGAGTACAGATTTCCACTACTGCAGTAGTTAGAAGAGAGTAGTTGGGGTTGAAATTAAAAGTCTTAAAGTTAACAGAAGTTCATGTTCTGGCTTTGTCACTTACTAGCTGTGTAA... | TTGAATCCGACTTTTACAGTCTGAAATTCAGACTTCCTGCCCTACTGCAATGGGAGTAAAAACCACCTGAACCTCTTTTTGGCAGCTTCTTCTCTTACTCCCAAATGGCAACAAGTGTTATCTCTTTGATTGAGCTCTTGGTCCATGCAGTCTAATTACCAATTCAGAACAGTGGGGGAACTTCTTATTTTACACAACTGGCAACTGAGTACAGATTTCCACTACTGCAGTAGTTAGAAGAGAGTAGTTGGGGTTGAAATTAAAAGTCTTAAAGTTAACAGAAGTTCATGTTCTGGCTTTGTCACTTACTAGCTGTGTAA... |
Task1_train_32511 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AAGCTTGAAATCCTCAGTGCGTGTTTCTAACACCTGAGGGGAAATGGCTTAATGATTTTAAGGGTTTCCTTATTATTTATCCATATTCATCCCATATTTATTAAATGACAGCTACTGTTCCTAGACCTTCATGGACAATGGATCAGCTCTTACAGAACTTACTCACTGAGATAAAATGAAATGCCATTATTTAGGAGGCAGGGAAATAATTGGAAATTGCTTCCACAAGATCCTCTATCAATAAGATAGAGAGTTAAATAAGTAATCAGAAAGTAGCACTGACCAAAGAGGGACAGATAAAATTATATACAGAAAATGAA... | AAGCTTGAAATCCTCAGTGCGTGTTTCTAACACCTGAGGGGAAATGGCTTAATGATTTTAAGGGTTTCCTTATTATTTATCCATATTCATCCCATATTTATTAAATGACAGCTACTGTTCCTAGACCTTCATGGACAATGGATCAGCTCTTACAGAACTTACTCACTGAGATAAAATGAAATGCCATTATTTAGGAGGCAGGGAAATAATTGGAAATTGCTTCCACAAGATCCTCTATCAATAAGATAGAGAGTTAAATAAGTAATCAGAAAGTAGCACTGACCAAAGAGGGACAGATAAAATTATATACAGAAAATGAA... |
Task1_train_32512 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGGTATTGTGTCTACTGAACTAGCACATAAAATCCTTAGTAACCGACAGCATATTAAGGCTCTGTTTCTACCAGCAACCACAGAGATTTTGTCCTGGAAGAAAGCAATAGAAAGTGGTATCCTGGATAGAGATCTTGCCAATAACTTAAAATCGATTTGTATACCTGATGTGATGCCCCACATGCAACTAGCAGACTCTGCAGAACAAAATATTAATCCTGGAGCAGCAGTTCTACCGTGCAGCAAGAGCCACCCTAAGGCCACAGCAAGCCAGAGTGAGAATCTGTTGTTCCAGCTGATGACTCACAGCTATATTAATG... | AGGTATTGTGTCTACTGAACTAGCACATAAAATCCTTAGTAACCGACAGCATATTAAGGCTCTGTTTCTACCAGCAACCACAGAGATTTTGTCCTGGAAGAAAGCAATAGAAAGTGGTATCCTGGATAGAGATCTTGCCAATAACTTAAAATCGATTTGTATACCTGATGTGATGCCCCACATGCAACTAGCAGACTCTGCAGAACAAAATATTAATCCTGGAGCAGCAGTTCTACCGTGCAGCAAGAGCCACCCTAAGGCCACAGCAAGCCAGAGTGAGAATCTGTTGTTCCAGCTGATGACTCACAGCTATATTAATG... |
Task1_train_32513 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GTAGATGGAGGTATCATTCACCATATATCTGGGATGAGACTTTCTGTTGATAATGCCTTCAGACATGGCTTAATTGGTGAAGATTTAGCCGAGAAACTCAAAAGAGTTGAGAACTTAAACATCCATCAGATTTTTAATCCTGAAACGAAGGAAAATATTTCCCTCCCTAAAGCCATAAAATTAGATCTTATTACCTCAGACCTGAAAAGAGAAATCCAGGAGGTTCAGGCCTTTACTGGAAACTTTGTGGATCTCATTTCTGGTCAGAGATTGACCTTGGCAGAAGCTAAAAAAGAAGGACTGTTAACTAATGAAGCAGT... | GTAGATGGAGGTATCATTCACCATATATCTGGGATGAGACTTTCTGTTGATAATGCCTTCAGACATGGCTTAATTGGTGAAGATTTAGCCGAGAAACTCAAAAGAGTTGAGAACTTAAACATCCATCAGATTTTTAATCCTGAAACGAAGGAAAATATTTCCCTCCCTAAAGCCATAAAATTAGATCTTATTACCTCAGACCTGAAAAGAGAAATCCAGGAGGTTCAGGCCTTTACTGGAAACTTTGTGGATCTCATTTCTGGTCAGAGATTGACCTTGGCAGAAGCTAAAAAAGAAGGACTGTTAACTAATGAAGCAGT... |
Task1_train_32514 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | TATATTTATAAGGATTAGAGGATTTAATACATTTCCTTGTTTGCTTGACAGGAGCTCAATTTGGAAATGGAAGACCAACAGGAGAACCTAGATACTCTTGAGCACCTGGTCACTGAACTGAGCTCTTGTGGCTTTGCGCTGGACTTGTGCCAGCATCAGGACAGGGTACAGAATCTAAGAAAAGACTTCACAGAGCTACAGAAGACAGTTAAAGAGAGGTGAGTTATCACTTGTGTTGGTCAGCATTGGGGAACTATTTTTTCTTGTTATGGAGTGAAATGATCTTTTCTCTTTTCTTCCTTTACCAGAACAGATGGCAT... | TATATTTATAAGGATTAGAGGATTTAATACATTTCCTTGTTTGCTTGACAGGAGCTCAATTTGGAAATGGAAGACCAACAGGAGAACCTAGATACTCTTGAGCACCTGGTCACTGAACTGAGCTCTTGTGGCTTTGCGCTGGACTTGTGCCAGCATCAGGACAGGGTACAGAATCTAAGAAAAGACTTCACAGAGCTACAGAAGACAGTTAAAGAGAGGTGAGTTATCACTTGTGTTGGTCAGCATTGGGGAACTATTTTTTCTTGTTATGGAGTGAAATGATCTTTTCTCTTTTCTTCCTTTACCAGAACAGATGGCAT... |
Task1_train_32515 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | CCCTTGGGGACACAGCCTGCACTGTGGAAATGCCACCTCTCTCCCCTTGCCTGAGTGAAGAGCTGTTAGATCCAGAATTGCATGTTCTCATAACCCCCAGCCTGAGAGAGAAAACAGAGTCTGAGCTAAAGTTTGAGGAGGATGAGCGATGGATTATGATGGAGGCTGAGGGAGAGTGGGAGGAAGAGAAACTGTCAGACAGGGAAAAGACTTTTCTGATGGCAGATGAGAAGAACAGCCTGGCAGATATTTTTGAAGAAAGAGAACAAGCAAACACAGCAGTGGTGGAGGATGGATCCGATTGCTTAGCTGCTGTCTTG... | CCCTTGGGGACACAGCCTGCACTGTGGAAATGCCACCTCTCTCCCCTTGCCTGAGTGAAGAGCTGTTAGATCCAGAATTGCATGTTCTCATAACCCCCAGCCTGAGAGAGAAAACAGAGTCTGAGCTAAAGTTTGAGGAGGATGAGCGATGGATTATGATGGAGGCTGAGGGAGAGTGGGAGGAAGAGAAACTGTCAGACAGGGAAAAGACTTTTCTGATGGCAGATGAGAAGAACAGCCTGGCAGATATTTTTGAAGAAAGAGAACAAGCAAACACAGCAGTGGTGGAGGATGGATCCGATTGCTTAGCTGCTGTCTTG... |
Task1_train_32516 | Given this context: Chromosome 1 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TCTATAGTATTTTATATATACATATACCTATATGTAATATATATTTTGTATATATGAAAAATAACCATGTAGAGTCTGAAGCTTTAGTGTCCAGATAAGTGAAACTGACAGTTATGTTGAGCATCTGCTATTGATGGGGTATAAATCACATTTGCAAAGTTTGGTAAGTTCTGTTCTGTTTTCTATTTTGGCTTATATTCTATTCGTTTACATGTAGACTATTAAGGAAGAGACAGATGGTCTGCATGAAGAGCTGGAGTTTATTCGGATCCTTGGAGCAGATTTGATTTTTGCCTGTGGAGAAACTGAGAAGCCTGAAG... | TCTATAGTATTTTATATATACATATACCTATATGTAATATATATTTTGTATATATGAAAAATAACCATGTAGAGTCTGAAGCTTTAGTGTCCAGATAAGTGAAACTGACAGTTATGTTGAGCATCTGCTATTGATGGGGTATAAATCACATTTGCAAAGTTTGGTAAGTTCTGTTCTGTTTTCTATTTTGGCTTATATTCTATTCGTTTACATGTAGACTATTAAGGAAGAGACAGATGGTCTGCATGAAGAGCTGGAGTTTATTCGGATCCTTGGAGCAGATTTGATTTTTGCCTGTGGAGAAACTGAGAAGCCTGAAG... |
Task1_train_32517 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAATACCCAGATTAAAAGGAATTTGGAGCCTAATGGATTCTGAAGGAAGTGCTTACTCTGTTCTCCATGGAACTGGGGAACTTCAGGCTGCCAGGACTTTGTATAGGATAGTGTTTTCACCCTAATTTGCTTCCCCTTCTAGGCCTCTTGGCAGCAGAAGCATGTGAGACCAGCTTGACCTCCATCTTCCCAGATTGTGGGTTATGGTCCAGAATCTTACCAAGTAATTAAGGTTTTCTGGGGTTTTGTGGCAAAGTTCAGCTGGCAGCGGCACCAACGAAAAGTGCATTTCTTTTTTTTTCTTTTTTTTTTTTTCTTTT... | AAATACCCAGATTAAAAGGAATTTGGAGCCTAATGGATTCTGAAGGAAGTGCTTACTCTGTTCTCCATGGAACTGGGGAACTTCAGGCTGCCAGGACTTTGTATAGGATAGTGTTTTCACCCTAATTTGCTTCCCCTTCTAGGCCTCTTGGCAGCAGAAGCATGTGAGACCAGCTTGACCTCCATCTTCCCAGATTGTGGGTTATGGTCCAGAATCTTACCAAGTAATTAAGGTTTTCTGGGGTTTTGTGGCAAAGTTCAGCTGGCAGCGGCACCAACGAAAAGTGCATTTCTTTTTTTTTCTTTTTTTTTTTTTCTTTT... |
Task1_train_32518 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | CAGCTTGCAGTCTAGCTGGGAGCCCAGAATTGCACAAAACAAACCTGAGAATTGTACAGGCTGGATCTAGGGCCTCAAGTGATGTGCAGTGGATTCAAAAGGGGCGTGCAGAGAGGACAGTGAAGGGGGTGTGGGCAGGAGATTCCGAGACTCTGACCAAGATGACATGGGGACAAAGCCCTGTGGATTCAGCCTCCTAAACAGCTTTCTCCTCTGCCCCTCCACCCCATCACCATTAGAGACTCATGGTCATTGTACCCACCCCCACATCTGATTGCTGTACCTGCCTCCAACTGCAGGGCCCTGACTCCTGTCTCCCT... | CAGCTTGCAGTCTAGCTGGGAGCCCAGAATTGCACAAAACAAACCTGAGAATTGTACAGGCTGGATCTAGGGCCTCAAGTGATGTGCAGTGGATTCAAAAGGGGCGTGCAGAGAGGACAGTGAAGGGGGTGTGGGCAGGAGATTCCGAGACTCTGACCAAGATGACATGGGGACAAAGCCCTGTGGATTCAGCCTCCTAAACAGCTTTCTCCTCTGCCCCTCCACCCCATCACCATTAGAGACTCATGGTCATTGTACCCACCCCCACATCTGATTGCTGTACCTGCCTCCAACTGCAGGGCCCTGACTCCTGTCTCCCT... |
Task1_train_32519 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | GCGTAAGTGTCCCACAGGAGTTTGTTCGGTGCATAGAACAGGCATGTGTACACGACTGTTCACGTATGTCCGTGTTTGGGTGCGAGTCTACGTGTAGTGTGGCTGTATAAGGACCAGTTCCTGCAGAGCTGTGGGAAGTTAGCGACGTTACTGACTGTGCAGACAAAGCCCCCTGAGACGCGGAGCAGGTGGCCTCACTGCCCTCCCAGCCAGCTGGACCAGACCCCTCTCCACAGGGCCCCCCACCCCAGGGGGCTGGGCAGGATGGGCATGGTACTGACCAGGGACTGCAGGATGGCGTGGTTGGTGGCATTCATGCA... | GCGTAAGTGTCCCACAGGAGTTTGTTCGGTGCATAGAACAGGCATGTGTACACGACTGTTCACGTATGTCCGTGTTTGGGTGCGAGTCTACGTGTAGTGTGGCTGTATAAGGACCAGTTCCTGCAGAGCTGTGGGAAGTTAGCGACGTTACTGACTGTGCAGACAAAGCCCCCTGAGACGCGGAGCAGGTGGCCTCACTGCCCTCCCAGCCAGCTGGACCAGACCCCTCTCCACAGGGCCCCCCACCCCAGGGGGCTGGGCAGGATGGGCATGGTACTGACCAGGGACTGCAGGATGGCGTGGTTGGTGGCATTCATGCA... |
Task1_train_32520 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AACAGGTGGTCACAAAAAAAGAGAATTTGTCCAAACGGAAGAAAGAATTCAGATTCCAAAGATTATTATAATAATTCATACGTTACTCACATTTAAGACTTTGCAACTCCAAATAAAAATGAAGCATAGTCAGAATGAAGCACATGCCTCCTCATTATATAGAGAAAGCATACAATTACAGCAACTGTGAAGGACAAATATTTTATTCTCATATGGAATGTGTTTTAGAGGTGGCTGAGGATCCCCTGGTTTACCTTTCTTATTTTTAATTTAATATGTCATTATACTGCAACTTAGTGTTACTTTATGTTTAAGAACCC... | AACAGGTGGTCACAAAAAAAGAGAATTTGTCCAAACGGAAGAAAGAATTCAGATTCCAAAGATTATTATAATAATTCATACGTTACTCACATTTAAGACTTTGCAACTCCAAATAAAAATGAAGCATAGTCAGAATGAAGCACATGCCTCCTCATTATATAGAGAAAGCATACAATTACAGCAACTGTGAAGGACAAATATTTTATTCTCATATGGAATGTGTTTTAGAGGTGGCTGAGGATCCCCTGGTTTACCTTTCTTATTTTTAATTTAATATGTCATTATACTGCAACTTAGTGTTACTTTATGTTTAAGAACCC... |
Task1_train_32521 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CAAAATCAAAATTAAACCTGTAATCTCAGCTACTTGGAAGGTGAAGTGGGACGACTGCTTGAGCCCAGGAGTTTGAAACCAGCCTGGGTAACACAGTAAGACCGTGTCTCAATCAATCAATCAATAAAAAATTATAAAAACAATAATATAGGACAGTTTCTTAACTTTAGTACAATTAATATTTGGGGCCAAATAATTCTGTTATGGGAAGTTGTCCTGTGCCTACTAGAATGTTAGCAATGTCTCTGGCCTCTACCCATTAGATGCCAGGAACCCACCTCCCCAGTTATTAGAACCAAAAATGTCTCCAGGGATTGCCA... | CAAAATCAAAATTAAACCTGTAATCTCAGCTACTTGGAAGGTGAAGTGGGACGACTGCTTGAGCCCAGGAGTTTGAAACCAGCCTGGGTAACACAGTAAGACCGTGTCTCAATCAATCAATCAATAAAAAATTATAAAAACAATAATATAGGACAGTTTCTTAACTTTAGTACAATTAATATTTGGGGCCAAATAATTCTGTTATGGGAAGTTGTCCTGTGCCTACTAGAATGTTAGCAATGTCTCTGGCCTCTACCCATTAGATGCCAGGAACCCACCTCCCCAGTTATTAGAACCAAAAATGTCTCCAGGGATTGCCA... |
Task1_train_32522 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GGAGGAGTGGATTTATCTGAATAAAAGAAACAAAAATCAATTCCATATAAGTGGTACAATATAACAAAAAGGAACGTACAGAAATTGGCCTCCCTGGGAGAATCCCATAGCATTGTAGCCTTGCTGCAATTTAGGATCCTTAGCAAGTGCCTGACACACTGTTGTTACTTGGGAATTGACATTCAAGAAGAAGCTGTTCTCCACGTCCTAAAAAAGAAGCCAGAGAGAAGTGAGAGGATGGGACTGAAAACAACCACTGACATCTTCTCTAAGAGGTAAACTCATTTAGGTTGGTATCCTCACATGAGCCACTCAAGGGT... | GGAGGAGTGGATTTATCTGAATAAAAGAAACAAAAATCAATTCCATATAAGTGGTACAATATAACAAAAAGGAACGTACAGAAATTGGCCTCCCTGGGAGAATCCCATAGCATTGTAGCCTTGCTGCAATTTAGGATCCTTAGCAAGTGCCTGACACACTGTTGTTACTTGGGAATTGACATTCAAGAAGAAGCTGTTCTCCACGTCCTAAAAAAGAAGCCAGAGAGAAGTGAGAGGATGGGACTGAAAACAACCACTGACATCTTCTCTAAGAGGTAAACTCATTTAGGTTGGTATCCTCACATGAGCCACTCAAGGGT... |
Task1_train_32523 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | ATCTCAGACCTTAATTTTCAGAATCAAGATGAAAACATGCCAAGTCAGTACCTTGCACAGTTGGCGGCTAAGCCGTTTTTCTGTGAGCTTCAAGGATGCAAATATGAATTTGTGACCAGAGAGGCTCTGTTAATGCATTATCTTAAAAAGCATAATTATTCAAAAGAAAAAGTCCTTCAGTTAACCATGTTCCAACATCGGTATTCCCCATTTCAGTGTCATATTTGCCAAAGGTCATTTACAAGAAAAACACACCTTAGGATTCATTATAAAAATAAACATCAAATTGGCAGTGACAGAGCAACTCACAAACTATTAGA... | ATCTCAGACCTTAATTTTCAGAATCAAGATGAAAACATGCCAAGTCAGTACCTTGCACAGTTGGCGGCTAAGCCGTTTTTCTGTGAGCTTCAAGGATGCAAATATGAATTTGTGACCAGAGAGGCTCTGTTAATGCATTATCTTAAAAAGCATAATTATTCAAAAGAAAAAGTCCTTCAGTTAACCATGTTCCAACATCGGTATTCCCCATTTCAGTGTCATATTTGCCAAAGGTCATTTACAAGAAAAACACACCTTAGGATTCATTATAAAAATAAACATCAAATTGGCAGTGACAGAGCAACTCACAAACTATTAGA... |
Task1_train_32524 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGTTTAAATACTGAGCTGGGAGGCAGGGAAGGAAGTAGTGGGGCTGGCTTAAGGGTATAGCCGCCTCAGGGGAGTCACCCAGCAGCAGTCACCTGGTAGGTCCAGAGAGTGAGATGGGATCAGGAACTGGCATAGACCTCAGTCATTGGTCCTCAAGCTGAGGGGTGGAACTGTAGCTGGGCAGGGCCCGGGCCTCCCGAGGTGCCCATGTCCCACTGACCCAAGGACAAGATGGCCAGTGGAGAAAGGTGCAGATTAAGATGTTTGTTTTGGTAACAGCCGAATGATGCTCGCTGGAAGGAAAGCCGCCCTATTCCTTC... | TGTTTAAATACTGAGCTGGGAGGCAGGGAAGGAAGTAGTGGGGCTGGCTTAAGGGTATAGCCGCCTCAGGGGAGTCACCCAGCAGCAGTCACCTGGTAGGTCCAGAGAGTGAGATGGGATCAGGAACTGGCATAGACCTCAGTCATTGGTCCTCAAGCTGAGGGGTGGAACTGTAGCTGGGCAGGGCCCGGGCCTCCCGAGGTGCCCATGTCCCACTGACCCAAGGACAAGATGGCCAGTGGAGAAAGGTGCAGATTAAGATGTTTGTTTTGGTAACAGCCGAATGATGCTCGCTGGAAGGAAAGCCGCCCTATTCCTTC... |
Task1_train_32525 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ATGAAGAGGAGACTCATAGTTGCAAGTGTTTAGTGAATGTTTATGCAATGAATAAATGAACGAACAACTCTGCCTGTTGGATTCCCAGCCCATCAACTTGGCCATCTAGGAAAGTCACACTCCAGAACAGAGCCAGTCCCCACCCTCCCTGCAATGTACATAGGGAAACAGGCCCAGGGAGGAGAAAGAGCTTCCCTGAATCATTGGGTCAGGGCAGAGCCAGACTAACTCGGAGCTCTCCCTAGGTTAGGGCTCCACCCCATGGCCTCACCCTAAAGCAGGAACCCTTGTGTCAGTGCAGGGGGCATTTACCTCTTTCC... | ATGAAGAGGAGACTCATAGTTGCAAGTGTTTAGTGAATGTTTATGCAATGAATAAATGAACGAACAACTCTGCCTGTTGGATTCCCAGCCCATCAACTTGGCCATCTAGGAAAGTCACACTCCAGAACAGAGCCAGTCCCCACCCTCCCTGCAATGTACATAGGGAAACAGGCCCAGGGAGGAGAAAGAGCTTCCCTGAATCATTGGGTCAGGGCAGAGCCAGACTAACTCGGAGCTCTCCCTAGGTTAGGGCTCCACCCCATGGCCTCACCCTAAAGCAGGAACCCTTGTGTCAGTGCAGGGGGCATTTACCTCTTTCC... |
Task1_train_32526 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGTTTAGTGAATGTTTATGCAATGAATAAATGAACGAACAACTCTGCCTGTTGGATTCCCAGCCCATCAACTTGGCCATCTAGGAAAGTCACACTCCAGAACAGAGCCAGTCCCCACCCTCCCTGCAATGTACATAGGGAAACAGGCCCAGGGAGGAGAAAGAGCTTCCCTGAATCATTGGGTCAGGGCAGAGCCAGACTAACTCGGAGCTCTCCCTAGGTTAGGGCTCCACCCCATGGCCTCACCCTAAAGCAGGAACCCTTGTGTCAGTGCAGGGGGCATTTACCTCTTTCCCAGGGGGACCAGAGAATCCAGGAAGG... | TGTTTAGTGAATGTTTATGCAATGAATAAATGAACGAACAACTCTGCCTGTTGGATTCCCAGCCCATCAACTTGGCCATCTAGGAAAGTCACACTCCAGAACAGAGCCAGTCCCCACCCTCCCTGCAATGTACATAGGGAAACAGGCCCAGGGAGGAGAAAGAGCTTCCCTGAATCATTGGGTCAGGGCAGAGCCAGACTAACTCGGAGCTCTCCCTAGGTTAGGGCTCCACCCCATGGCCTCACCCTAAAGCAGGAACCCTTGTGTCAGTGCAGGGGGCATTTACCTCTTTCCCAGGGGGACCAGAGAATCCAGGAAGG... |
Task1_train_32527 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | TAAGAGGGTATTATTAGAGAACAGAAGAGTTTAGAGTGATCTTGGCTCCCAAAATCACATGGTTTAATCATGTGTTTAAATCATAGGGTTTAATCCTATGTCTTCAACTTTTCTCAAATTCAGCTTTCTCATAGGTTAAATGTGGATGCTAACATCAGCCTAATAGGCCTGAAGGGCATTTCAGAATTATTTACAATACGAAACATTAAAATATTCTCTATACTTAGGGGATTTGTTGTTATTTCAGCCTTCCAGCTTCTGAATTCTCTTAGCTTTTGGGAGGTTTTTGTTTGTTTGTTTTTTGTTTGTTTGTTTGTTTT... | TAAGAGGGTATTATTAGAGAACAGAAGAGTTTAGAGTGATCTTGGCTCCCAAAATCACATGGTTTAATCATGTGTTTAAATCATAGGGTTTAATCCTATGTCTTCAACTTTTCTCAAATTCAGCTTTCTCATAGGTTAAATGTGGATGCTAACATCAGCCTAATAGGCCTGAAGGGCATTTCAGAATTATTTACAATACGAAACATTAAAATATTCTCTATACTTAGGGGATTTGTTGTTATTTCAGCCTTCCAGCTTCTGAATTCTCTTAGCTTTTGGGAGGTTTTTGTTTGTTTGTTTTTTGTTTGTTTGTTTGTTTT... |
Task1_train_32528 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CCTCAGTCGTGAACAGGTATATTTTTAAAGAAAGATTATGTTGCTGGCCAGGTGCGGTGGCTCATGCCTATAATCCCAGCATTTTGGGATGCTGAGGCGGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACTCCATCTGTACTAAAAATACAAAATTAGCCAGGTGTGGCGGTGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCAAGATCACGCCGTTGCACTCCAGCCTGGGCAACAAGAGTGAAACT... | CCTCAGTCGTGAACAGGTATATTTTTAAAGAAAGATTATGTTGCTGGCCAGGTGCGGTGGCTCATGCCTATAATCCCAGCATTTTGGGATGCTGAGGCGGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACTCCATCTGTACTAAAAATACAAAATTAGCCAGGTGTGGCGGTGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCAAGATCACGCCGTTGCACTCCAGCCTGGGCAACAAGAGTGAAACT... |
Task1_train_32529 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | CTCCCGACCCCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCCGAGATTACAGGCTTTAGCCACTGTACCCGGCCTTGAAAATCTTTATAGTAAAAAGTTGAAAGAAAAAAGGAGTACAGTACCCATCCCCATCCCACAGTAGGGTAGTGAGATATTGGATGTAAAACACGTGGCTCAGTGTCTGGCACACAAAAAATAACCGCACAATAAATATTCTCTATTATAGCAGTAAATTTTGAGTTTTTAATAATGCTGTAATAGGCAGATTTTTTTCCCATTATAAGCTAGTTTCTTGTGGAGGGAGAAAATAAACTTAA... | CTCCCGACCCCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCCGAGATTACAGGCTTTAGCCACTGTACCCGGCCTTGAAAATCTTTATAGTAAAAAGTTGAAAGAAAAAAGGAGTACAGTACCCATCCCCATCCCACAGTAGGGTAGTGAGATATTGGATGTAAAACACGTGGCTCAGTGTCTGGCACACAAAAAATAACCGCACAATAAATATTCTCTATTATAGCAGTAAATTTTGAGTTTTTAATAATGCTGTAATAGGCAGATTTTTTTCCCATTATAAGCTAGTTTCTTGTGGAGGGAGAAAATAAACTTAA... |
Task1_train_32530 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GTGGCTCAGTGTCTGGCACACAAAAAATAACCGCACAATAAATATTCTCTATTATAGCAGTAAATTTTGAGTTTTTAATAATGCTGTAATAGGCAGATTTTTTTCCCATTATAAGCTAGTTTCTTGTGGAGGGAGAAAATAAACTTAATGGGAAACTCCAGTTTAGTGACAGACACCAATTTCTATAATATTAAGAGGATAATTTATGAAGTCAAGCTACTAATTTCCATGTGTCGCTGTAACATCCTCTTATTATTTCATGCATTAATTTGTGTTAGACTATATTTATTTGTATCTATATATAGTTGATCTTTGAATTT... | GTGGCTCAGTGTCTGGCACACAAAAAATAACCGCACAATAAATATTCTCTATTATAGCAGTAAATTTTGAGTTTTTAATAATGCTGTAATAGGCAGATTTTTTTCCCATTATAAGCTAGTTTCTTGTGGAGGGAGAAAATAAACTTAATGGGAAACTCCAGTTTAGTGACAGACACCAATTTCTATAATATTAAGAGGATAATTTATGAAGTCAAGCTACTAATTTCCATGTGTCGCTGTAACATCCTCTTATTATTTCATGCATTAATTTGTGTTAGACTATATTTATTTGTATCTATATATAGTTGATCTTTGAATTT... |
Task1_train_32531 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | CCTGGAATGAGTCTCTTTTTTCTTGTATTTTTTATTATTATAATTTTTTTGAGGCAGGGTCTCCCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTGATCATAGCTCACTGTAGCCTCAAACTCCTGGGCCCAGGAGATCCTTCTGCCTCAGCCTCCTGAGTAGCTAAGACTTACACGTGTGTGCCACAATGCCTATTTAAAAATTTTTTTTTTATTCTTCTTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGTTGTGCAGTGGCATTATCTTGACTCACTGCAACCTCCGCTTCCCAGGTTCCAGTGAAACTGTTG... | CCTGGAATGAGTCTCTTTTTTCTTGTATTTTTTATTATTATAATTTTTTTGAGGCAGGGTCTCCCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTGATCATAGCTCACTGTAGCCTCAAACTCCTGGGCCCAGGAGATCCTTCTGCCTCAGCCTCCTGAGTAGCTAAGACTTACACGTGTGTGCCACAATGCCTATTTAAAAATTTTTTTTTTATTCTTCTTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGTTGTGCAGTGGCATTATCTTGACTCACTGCAACCTCCGCTTCCCAGGTTCCAGTGAAACTGTTG... |
Task1_train_32532 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGGAGCCTTATGTGGTGGGCGCAGTGATGTGGAGTTCCAGGCCCTTGGCCAAAGTGTCAGGGCCTTCTCCACTCTCCTCTCTTCCTCTCCCTCTTGGAGGAGTGGAGGACAGGAGAAGGGGTTGCACGGACCGGGCAGGGTGGAGGGTGCTTGCCAGCATGAGGGAGCCTGCAGGAATGGCTCTGCAGAGGAAAGTTTGGGAGAGCCAACCTCAAACTTTGATTGGAATCTTTGGGATGTGTCGATGGAGTCCTGGGCCAGTGGAGAGCATGCTGGATAGTGGGAACTGGGAACTGTCCCTGTCCTTTTGATACCCTCAG... | TGGAGCCTTATGTGGTGGGCGCAGTGATGTGGAGTTCCAGGCCCTTGGCCAAAGTGTCAGGGCCTTCTCCACTCTCCTCTCTTCCTCTCCCTCTTGGAGGAGTGGAGGACAGGAGAAGGGGTTGCACGGACCGGGCAGGGTGGAGGGTGCTTGCCAGCATGAGGGAGCCTGCAGGAATGGCTCTGCAGAGGAAAGTTTGGGAGAGCCAACCTCAAACTTTGATTGGAATCTTTGGGATGTGTCGATGGAGTCCTGGGCCAGTGGAGAGCATGCTGGATAGTGGGAACTGGGAACTGTCCCTGTCCTTTTGATACCCTCAG... |
Task1_train_32533 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTTTCTTGTACCTTCTAGACACCCCACACCTTCCCCAAACATTCATCGTACTTGTGTGCCTTCCTGCCTTGAAACAGGCTCCTCTCCTAAAAACATATTCATCACTCAAGGCTCTGTTCATCACGTCAAATGTCACCGCTTCCCTGAAGCCTGAACTGACCCCAACCTCAACTATTAATAGCTGAAACTGCTCCCTTCTCTGGGTGTGCCCGCTTGGCCGGTCTATTGTCCTGGCTGTACAATCCCCCCCAGAACTATTTTCTTTTTTCTTGAGGAGTCTCGCTCTGTTGCCAGGCTGGAGTGCAGTGGCATGATCTCGG... | CTTTCTTGTACCTTCTAGACACCCCACACCTTCCCCAAACATTCATCGTACTTGTGTGCCTTCCTGCCTTGAAACAGGCTCCTCTCCTAAAAACATATTCATCACTCAAGGCTCTGTTCATCACGTCAAATGTCACCGCTTCCCTGAAGCCTGAACTGACCCCAACCTCAACTATTAATAGCTGAAACTGCTCCCTTCTCTGGGTGTGCCCGCTTGGCCGGTCTATTGTCCTGGCTGTACAATCCCCCCCAGAACTATTTTCTTTTTTCTTGAGGAGTCTCGCTCTGTTGCCAGGCTGGAGTGCAGTGGCATGATCTCGG... |
Task1_train_32534 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | AGGCTCCTCTCCTAAAAACATATTCATCACTCAAGGCTCTGTTCATCACGTCAAATGTCACCGCTTCCCTGAAGCCTGAACTGACCCCAACCTCAACTATTAATAGCTGAAACTGCTCCCTTCTCTGGGTGTGCCCGCTTGGCCGGTCTATTGTCCTGGCTGTACAATCCCCCCCAGAACTATTTTCTTTTTTCTTGAGGAGTCTCGCTCTGTTGCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACTTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTATAGGCG... | AGGCTCCTCTCCTAAAAACATATTCATCACTCAAGGCTCTGTTCATCACGTCAAATGTCACCGCTTCCCTGAAGCCTGAACTGACCCCAACCTCAACTATTAATAGCTGAAACTGCTCCCTTCTCTGGGTGTGCCCGCTTGGCCGGTCTATTGTCCTGGCTGTACAATCCCCCCCAGAACTATTTTCTTTTTTCTTGAGGAGTCTCGCTCTGTTGCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACTTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTATAGGCG... |
Task1_train_32535 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | GATCATTCCAGCAGGTATCTCAGCACCCTGTGACAGAGCTGCAGTACCCTGAATGGAGAGGGACTCCCAGGTACCCCACCCACTTCCTGATTTCAAACCTTTGCCCACTACTTGCTGGGCTATTGACAAGTCCGCCCTAATCCCCACTTTCTTCTGCGCCTCCTGAATCTCCTTTCATGGTTTGGGCTCTGCTCGAGGGCTTGGTGTGAGCCTCCTCGGGGCCACTTCCTAGTCTGGGCCTCCCCAGCGAGCCCCTCCCTGACCTCCCTGCTTCCAGGCTCACCCTTTCATGTCAACCCTCCTGTTTTTTTTTTTTTTTT... | GATCATTCCAGCAGGTATCTCAGCACCCTGTGACAGAGCTGCAGTACCCTGAATGGAGAGGGACTCCCAGGTACCCCACCCACTTCCTGATTTCAAACCTTTGCCCACTACTTGCTGGGCTATTGACAAGTCCGCCCTAATCCCCACTTTCTTCTGCGCCTCCTGAATCTCCTTTCATGGTTTGGGCTCTGCTCGAGGGCTTGGTGTGAGCCTCCTCGGGGCCACTTCCTAGTCTGGGCCTCCCCAGCGAGCCCCTCCCTGACCTCCCTGCTTCCAGGCTCACCCTTTCATGTCAACCCTCCTGTTTTTTTTTTTTTTTT... |
Task1_train_32536 | Given this context: Chromosome 1 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGTTGAGGCCACCAGGTGGGAGGCCCCAGAGGTGGGGTGCCGCAGGCCCAGCAGAAGTTCTACTCCAGATTCCAGTGGGGCCAGTGGACTTCCTGCCTTCCTCTGTCCTCAGAACAGGCCTGGCAAAAGCAGGCAGTGACATGGGGAGCACTGGAGACTGGCACAGCAGAATTAAAAAGAGGATGTATGGAGAGATGGCAGAGGTGAAGCCCAGGGAGGAACCGAGGGACAGCAGAAAAGGCCACCTTGGGCAAGCCATTCCTCTCTCTGAGCCTAGGTCTTCTGGCGTGTGAATGGGGACTTTGCCACACACTGTGGGG... | AGTTGAGGCCACCAGGTGGGAGGCCCCAGAGGTGGGGTGCCGCAGGCCCAGCAGAAGTTCTACTCCAGATTCCAGTGGGGCCAGTGGACTTCCTGCCTTCCTCTGTCCTCAGAACAGGCCTGGCAAAAGCAGGCAGTGACATGGGGAGCACTGGAGACTGGCACAGCAGAATTAAAAAGAGGATGTATGGAGAGATGGCAGAGGTGAAGCCCAGGGAGGAACCGAGGGACAGCAGAAAAGGCCACCTTGGGCAAGCCATTCCTCTCTCTGAGCCTAGGTCTTCTGGCGTGTGAATGGGGACTTTGCCACACACTGTGGGG... |
Task1_train_32537 | An alteration has been detected on Chromosome 1. Is it pathogenic, and if so, what disease is involved? | Benign | TTTCCTCCTCTTCCTCAGTGGAGTGAGTTCCAGGGTGGTTCCCAGTTTGTAATGCATCATTTGGGACCACGGCTCATGCTCAATCTGACTCTTTTCAGCTTCTGGAGATGTGTGGGTGCCTGCAGAGATGGGCTTTGCGATCTGAAGCTCTGAGCAGTAGTATTTTTTGTGGGCTTCGTAGTTATCCCTTTTCTTGTACCGAGCACCACATATGTTACATTCGTAGATCACCCCTTTTGTTTTCAAACCCTTCTTGGTCTTTTTGGTAAGCTCGCTTTCCTTGGGTTCCACTTCGTCCGAGGGCTTGGAGGCTGTGTCTT... | TTTCCTCCTCTTCCTCAGTGGAGTGAGTTCCAGGGTGGTTCCCAGTTTGTAATGCATCATTTGGGACCACGGCTCATGCTCAATCTGACTCTTTTCAGCTTCTGGAGATGTGTGGGTGCCTGCAGAGATGGGCTTTGCGATCTGAAGCTCTGAGCAGTAGTATTTTTTGTGGGCTTCGTAGTTATCCCTTTTCTTGTACCGAGCACCACATATGTTACATTCGTAGATCACCCCTTTTGTTTTCAAACCCTTCTTGGTCTTTTTGGTAAGCTCGCTTTCCTTGGGTTCCACTTCGTCCGAGGGCTTGGAGGCTGTGTCTT... |
Task1_train_32538 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TTGTCATGGGAGTTACATAAGGAGAGGCAGGGAAACCCCCCTTCATGACGCATCCCCCATAAGCCAGGCACATGCTGGGGAAATGGTTGGTTTTAGGGAGAGTCACAGGCTCTCCTGGGACAGGTATCGTTCAGTTTTTCCTTACAACAACCACTATGAGGTCTTTTTAAAAATTATTATTACTATTTTCTCTACTTTACTGATGAAGAAGCGGAGGCTCAGAGAAGCTAAGTAATGTACCAAAGATCACACAGCTGGTAAGTGCTGTCATTCGGGTTTGAACCCAGCTCTCCTCATCTCTAAGTCCTCAGTTCCTTTTT... | TTGTCATGGGAGTTACATAAGGAGAGGCAGGGAAACCCCCCTTCATGACGCATCCCCCATAAGCCAGGCACATGCTGGGGAAATGGTTGGTTTTAGGGAGAGTCACAGGCTCTCCTGGGACAGGTATCGTTCAGTTTTTCCTTACAACAACCACTATGAGGTCTTTTTAAAAATTATTATTACTATTTTCTCTACTTTACTGATGAAGAAGCGGAGGCTCAGAGAAGCTAAGTAATGTACCAAAGATCACACAGCTGGTAAGTGCTGTCATTCGGGTTTGAACCCAGCTCTCCTCATCTCTAAGTCCTCAGTTCCTTTTT... |
Task1_train_32539 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | GGATAGACTAGGGGATGAAGGAAGGAAGGAAGGCAACACCCAGAGTACTCTGGAATCTGGTTTATTAGCTGGGGGTTGAAGTGGCAGGGAAGGACAGTGTTGGGGCGAGGCCTCCAGTCACCCAGTTCCTCCCCGGGCTGCTCCTCCCGACTGGACCAGGGTAGGTTGAGCTGCTGGGAGTGGAGTATCATGGGTGGCCCTTTCTGCAGGAGAAAAGAGCTTCCCTGCTGCGGAGGGGAGGCAGGCAGTGGGCAAGCCCCCCTAGCATCCGGTACAGGCAGCGTAGGCACAGATTTCACATGTGCCCGGGTCCTCAGCGA... | GGATAGACTAGGGGATGAAGGAAGGAAGGAAGGCAACACCCAGAGTACTCTGGAATCTGGTTTATTAGCTGGGGGTTGAAGTGGCAGGGAAGGACAGTGTTGGGGCGAGGCCTCCAGTCACCCAGTTCCTCCCCGGGCTGCTCCTCCCGACTGGACCAGGGTAGGTTGAGCTGCTGGGAGTGGAGTATCATGGGTGGCCCTTTCTGCAGGAGAAAAGAGCTTCCCTGCTGCGGAGGGGAGGCAGGCAGTGGGCAAGCCCCCCTAGCATCCGGTACAGGCAGCGTAGGCACAGATTTCACATGTGCCCGGGTCCTCAGCGA... |
Task1_train_32540 | This alteration occurs on Chromosome 1. Is it associated with a disease or is it a benign variant? | Benign | TGCCCTTATTCCTGAAATTGGCTGATTCTTGTCCCGTCTTACAAGGGGATTTGTACCCATTATATCACGTGTTGGGCAATCTGCTCTGTGAGACAGGCAGAAAGGTATTATTTCTCTCCATTTTACAAATAAAAGAAACTGAACCAGAGAAGTGACATAACTTAGCAAGGTTATCATGATGAATCTAAGACTTGAACCCAGGTCTTCTAACCTCCAGTCTAGCAGTTTCCAAATTGCCACATCACCTAGTAATATCAAACTTGATACTGCTCTTTACATTACAGTACCAATAAATGAACAGATAGGAAATGCCACACAAA... | TGCCCTTATTCCTGAAATTGGCTGATTCTTGTCCCGTCTTACAAGGGGATTTGTACCCATTATATCACGTGTTGGGCAATCTGCTCTGTGAGACAGGCAGAAAGGTATTATTTCTCTCCATTTTACAAATAAAAGAAACTGAACCAGAGAAGTGACATAACTTAGCAAGGTTATCATGATGAATCTAAGACTTGAACCCAGGTCTTCTAACCTCCAGTCTAGCAGTTTCCAAATTGCCACATCACCTAGTAATATCAAACTTGATACTGCTCTTTACATTACAGTACCAATAAATGAACAGATAGGAAATGCCACACAAA... |
Task1_train_32541 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | GGGAGGGATTGCTTTAATAAAACAAGGTAACAAGAATAAAAGGCAAGCTTAATATCCAAAAGACACGGACAGTTGTTCGCCCAATTCCAACTTCCAAAAATAACTGAAATTCCAGGAACTTCAGAAGAAAAAAGCAAATAGAGAAGAACGCAATTCTTCAGCTCTTCAATCTTTTCCAAATTGTTTAACAATGCTATGTGTTTTTTAAAATGTGAATTTTTCTCCCCTTCCTTCAAATTCTGGCAACAGATGCTAAATGTTTTATACTCCACACATTCATATAATGTCCATGCATTAAGCCTACTTTAAAAGGCAAAGGC... | GGGAGGGATTGCTTTAATAAAACAAGGTAACAAGAATAAAAGGCAAGCTTAATATCCAAAAGACACGGACAGTTGTTCGCCCAATTCCAACTTCCAAAAATAACTGAAATTCCAGGAACTTCAGAAGAAAAAAGCAAATAGAGAAGAACGCAATTCTTCAGCTCTTCAATCTTTTCCAAATTGTTTAACAATGCTATGTGTTTTTTAAAATGTGAATTTTTCTCCCCTTCCTTCAAATTCTGGCAACAGATGCTAAATGTTTTATACTCCACACATTCATATAATGTCCATGCATTAAGCCTACTTTAAAAGGCAAAGGC... |
Task1_train_32542 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CAATAGCAAAGACTTGGAACCAACCCAAATGTCCAACAATGATAGACTGGATTAAGAAAATGTGGCACATGTACACCATGGAATACTATGCAGCCATAAAAAATGATGAGTTCATGTCCTTTGTAGGGACATGGATGAAATTGGAAATCATCATTCTCAGTAAACTATTGCAAGAACAAAAAACCAAACACCACATATTCTCACTCATAGGTGGGAATTGAACAGTGAGAACACATGGACACAGGAAGGGGAACATGACACTCTGGGGACTGTTGTGGGGTGGGGAGAGAGGGGAGGGATAGCATTGGGAGATATACCTA... | CAATAGCAAAGACTTGGAACCAACCCAAATGTCCAACAATGATAGACTGGATTAAGAAAATGTGGCACATGTACACCATGGAATACTATGCAGCCATAAAAAATGATGAGTTCATGTCCTTTGTAGGGACATGGATGAAATTGGAAATCATCATTCTCAGTAAACTATTGCAAGAACAAAAAACCAAACACCACATATTCTCACTCATAGGTGGGAATTGAACAGTGAGAACACATGGACACAGGAAGGGGAACATGACACTCTGGGGACTGTTGTGGGGTGGGGAGAGAGGGGAGGGATAGCATTGGGAGATATACCTA... |
Task1_train_32543 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | AGCTATTATTCCTGCTATAAGGATAATAATTAAGCAAAATACTACAGCAGTGGAAACTCTCTGTCCAATATTTCAGTTAGAAGGTGCTACCATGTATAACTCTACCACAAATAGTAGAGTGTGTGTAGCGATTCCCACAAGGGTGGTGTAGTAGATCATTTCCATCTAAAATTTTAGTTGCCAAGATATAGAATTTCCCTTTTGGAAGGTCTATGAAGTTCCTTGGTTTTATTTTCCTAAAGAAATTTCTGCGTTATGAGCAACCTACTCACTTTTATTACATGGCAGGATTTGCAGGATAATTGGCCAGAACTATCTGG... | AGCTATTATTCCTGCTATAAGGATAATAATTAAGCAAAATACTACAGCAGTGGAAACTCTCTGTCCAATATTTCAGTTAGAAGGTGCTACCATGTATAACTCTACCACAAATAGTAGAGTGTGTGTAGCGATTCCCACAAGGGTGGTGTAGTAGATCATTTCCATCTAAAATTTTAGTTGCCAAGATATAGAATTTCCCTTTTGGAAGGTCTATGAAGTTCCTTGGTTTTATTTTCCTAAAGAAATTTCTGCGTTATGAGCAACCTACTCACTTTTATTACATGGCAGGATTTGCAGGATAATTGGCCAGAACTATCTGG... |
Task1_train_32544 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TAACATTTTCTTTAGAATTACTGAAGGAAACTATTGTACACATGTAACACTACAGTTTTTAAAAGGTCAAATTTTTCAAACAAAACATAAAGAAAAGCAGACTGAATCTCTTATGCAAATCTCACTAACCTCCCATTCTTCCTTCCCACATTCTAGGAAAAAGATTAATGATGTTGAGTATTGCTCCTTCCTGTGGTGTCTGGGAAGGAGGGTAGTTGTGTTTTCTAATCTTTTAACCTCATCTTCTCTACTCTTTCTTTTTTTTTCTTTTTCTTTCTTTCTTTCTTTTTTTATTTTTTTGAAACCGAGTTTTGCTCTTG... | TAACATTTTCTTTAGAATTACTGAAGGAAACTATTGTACACATGTAACACTACAGTTTTTAAAAGGTCAAATTTTTCAAACAAAACATAAAGAAAAGCAGACTGAATCTCTTATGCAAATCTCACTAACCTCCCATTCTTCCTTCCCACATTCTAGGAAAAAGATTAATGATGTTGAGTATTGCTCCTTCCTGTGGTGTCTGGGAAGGAGGGTAGTTGTGTTTTCTAATCTTTTAACCTCATCTTCTCTACTCTTTCTTTTTTTTTCTTTTTCTTTCTTTCTTTCTTTTTTTATTTTTTTGAAACCGAGTTTTGCTCTTG... |
Task1_train_32545 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTGTTTGGAATATAAATTAGTACAGCAATTATGGAAAACTGTGGAGTTTCCCCAACAAAGTGAAAATAGAACTACCATATGATCCAGCAATCTTACTTCTGGGTATACATCCAAAGGATTTGAAGTCAGTATGTGATATACACTATGGTGTGTGAAAATGTGGTATATATATATGATACAATACTATTTAACCTTAAAAAGGAGGGAAATTCTGTCATTGGCAACAACATTGGTGAACCTGGAGGATATTATGCTAAGTGAAAAAAGCCTGGCACAGAAAAACAAATACCACATCTTCTCACTTAAATGTGGAATCTAAA... | TTGTTTGGAATATAAATTAGTACAGCAATTATGGAAAACTGTGGAGTTTCCCCAACAAAGTGAAAATAGAACTACCATATGATCCAGCAATCTTACTTCTGGGTATACATCCAAAGGATTTGAAGTCAGTATGTGATATACACTATGGTGTGTGAAAATGTGGTATATATATATGATACAATACTATTTAACCTTAAAAAGGAGGGAAATTCTGTCATTGGCAACAACATTGGTGAACCTGGAGGATATTATGCTAAGTGAAAAAAGCCTGGCACAGAAAAACAAATACCACATCTTCTCACTTAAATGTGGAATCTAAA... |
Task1_train_32546 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | TCATTCCTCCCCTCCCTGCCCTTGACTGCAGTGTACATGGCAGTCATCTCATCTGACTTGGTTTCCGTCACTTTCCCTCTCAGAGTCAAGCTCGAAGGAGAAGCTGAGCTGCGTTCTTGAGATCTGGGGACGTGGTGGGAGATGTGGTCACAAGGCAGGTGGTGGAGGAGGCCAGAATGGAGCTGGCCAAGGAAGGTGCGTGGCAGGGAAGGGGAGGTTCTGTGATGGATGCTTTCCCCAGAAGCCTGATACGCAGTGGCCAGGGAGACTGAGTCCCGGGAGAGGGTTTGGGGTGGGAGAGGTCTGAGCATGAGGGGCAG... | TCATTCCTCCCCTCCCTGCCCTTGACTGCAGTGTACATGGCAGTCATCTCATCTGACTTGGTTTCCGTCACTTTCCCTCTCAGAGTCAAGCTCGAAGGAGAAGCTGAGCTGCGTTCTTGAGATCTGGGGACGTGGTGGGAGATGTGGTCACAAGGCAGGTGGTGGAGGAGGCCAGAATGGAGCTGGCCAAGGAAGGTGCGTGGCAGGGAAGGGGAGGTTCTGTGATGGATGCTTTCCCCAGAAGCCTGATACGCAGTGGCCAGGGAGACTGAGTCCCGGGAGAGGGTTTGGGGTGGGAGAGGTCTGAGCATGAGGGGCAG... |
Task1_train_32547 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ATAGGGTCACCCTATGTTGACCAGGCTGGTCTTAAACTTCTGAACTCAAGTGATCCACTGGCCTTCGCCTCCCAAACTGCTGGGATTACAAGCGGAGCTACTGAGCCTGGCCTAGCTTCTTCTTGATGCCTTTTCTCACACCTCACATCCAATCCATCAGCAATGCCTGTTGGCTCTACTTTAAAAATAGGCCCCCAGACACCCCTGACAATCCACCACTTTCCTTTTTATTTGTTTTTAGAGTTGGGATCTTGCTTTCTTGTGAAGGCTGGAGTGCAGTCGGGCGATCATAGCTCACTGCAGCCTCGAACTTCCAGGCT... | ATAGGGTCACCCTATGTTGACCAGGCTGGTCTTAAACTTCTGAACTCAAGTGATCCACTGGCCTTCGCCTCCCAAACTGCTGGGATTACAAGCGGAGCTACTGAGCCTGGCCTAGCTTCTTCTTGATGCCTTTTCTCACACCTCACATCCAATCCATCAGCAATGCCTGTTGGCTCTACTTTAAAAATAGGCCCCCAGACACCCCTGACAATCCACCACTTTCCTTTTTATTTGTTTTTAGAGTTGGGATCTTGCTTTCTTGTGAAGGCTGGAGTGCAGTCGGGCGATCATAGCTCACTGCAGCCTCGAACTTCCAGGCT... |
Task1_train_32548 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CTGGCCTTCGCCTCCCAAACTGCTGGGATTACAAGCGGAGCTACTGAGCCTGGCCTAGCTTCTTCTTGATGCCTTTTCTCACACCTCACATCCAATCCATCAGCAATGCCTGTTGGCTCTACTTTAAAAATAGGCCCCCAGACACCCCTGACAATCCACCACTTTCCTTTTTATTTGTTTTTAGAGTTGGGATCTTGCTTTCTTGTGAAGGCTGGAGTGCAGTCGGGCGATCATAGCTCACTGCAGCCTCGAACTTCCAGGCTCAAGCGATCTTCCTGCCTCAGCGTCCAGCTGGGACTACAGGCACGTGACACGTCTCC... | CTGGCCTTCGCCTCCCAAACTGCTGGGATTACAAGCGGAGCTACTGAGCCTGGCCTAGCTTCTTCTTGATGCCTTTTCTCACACCTCACATCCAATCCATCAGCAATGCCTGTTGGCTCTACTTTAAAAATAGGCCCCCAGACACCCCTGACAATCCACCACTTTCCTTTTTATTTGTTTTTAGAGTTGGGATCTTGCTTTCTTGTGAAGGCTGGAGTGCAGTCGGGCGATCATAGCTCACTGCAGCCTCGAACTTCCAGGCTCAAGCGATCTTCCTGCCTCAGCGTCCAGCTGGGACTACAGGCACGTGACACGTCTCC... |
Task1_train_32549 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GAAGGTGTAGGCTGGGGGCTCTTTGACACACACGAGGGTCTCGGCATTCAGGATGCAGTTGTCCACGTGGACTGGATGACTATCATCCTTCCTCTCTGCCTGGACCTCTGGGGCCAATGTCACACATGTTAGCAAGGGAGCACCTCGGGAGACGGCATAGCTCTCTTCTTGGCAGGGGAGGTGCTTCCCAAAATGTGTTTGAGTCTACGGAATGCCCAATGAACTAGGGGGGTGTCTTTGGCTAAGCCACAAGCCTAGGGGTCAGGACAAGTCTGCAGGCTTCCTAGGACAGTTCTTGGCAGAAGTGAGCAGGGTGTGGC... | GAAGGTGTAGGCTGGGGGCTCTTTGACACACACGAGGGTCTCGGCATTCAGGATGCAGTTGTCCACGTGGACTGGATGACTATCATCCTTCCTCTCTGCCTGGACCTCTGGGGCCAATGTCACACATGTTAGCAAGGGAGCACCTCGGGAGACGGCATAGCTCTCTTCTTGGCAGGGGAGGTGCTTCCCAAAATGTGTTTGAGTCTACGGAATGCCCAATGAACTAGGGGGGTGTCTTTGGCTAAGCCACAAGCCTAGGGGTCAGGACAAGTCTGCAGGCTTCCTAGGACAGTTCTTGGCAGAAGTGAGCAGGGTGTGGC... |
Task1_train_32550 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | GTCTGTTCCCCAGTTTGAGACAAAAGTCTAATTTCTGTGTCCTCTGCCTGGCACAAGCAACAGTACCTCTGAGGTACTGGAATAACCAGGCTTTCCTTAAGGGAAAAAGCCCTGCTCCTCCCCCATCCCAACCCCCATTAGTCTCTAGGACAGATAATCTGATGATTCTCAAAAGTGGAAATATTCTTCAAAGAAGGAGAATTCCTTCTTGACTTCTACAGGAGTCCACAAAGCAGGAAAAGGAATCAGGCATTAGGCAACTGACATGTTATTCATTTGATCTTTTATAGCCACATCTGAGGTTGATACTAGTATGCTCA... | GTCTGTTCCCCAGTTTGAGACAAAAGTCTAATTTCTGTGTCCTCTGCCTGGCACAAGCAACAGTACCTCTGAGGTACTGGAATAACCAGGCTTTCCTTAAGGGAAAAAGCCCTGCTCCTCCCCCATCCCAACCCCCATTAGTCTCTAGGACAGATAATCTGATGATTCTCAAAAGTGGAAATATTCTTCAAAGAAGGAGAATTCCTTCTTGACTTCTACAGGAGTCCACAAAGCAGGAAAAGGAATCAGGCATTAGGCAACTGACATGTTATTCATTTGATCTTTTATAGCCACATCTGAGGTTGATACTAGTATGCTCA... |
Task1_train_32551 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGCTCATTCTTTTTTTAAAAAAATTTTTTTTTTTTTTTGAGACAAGGTCTTGCTTTGTTACCCAGGTTGGAGTGCAGTGGTGCAATCACAGTTCACTGCAGCCTCAACCTCCCAGGCTCAAGAAATCCTCCCACCTCAACCTCCTGAGTAGCTAGGACTACAGGTGCGTGCCACCATGCCAAGCTAATTTTCTTTTATTTTTTGTAGAGATGGAGTCTCACTATGTTGCCCAGGCTAGTCTCTAACTCCTGAGCTCAAGTGATCCTCCTGCCTTGGCCTCCCGAAAGTGCAGGGTTATAGGCATGAGCTACCATGCCCAG... | AGCTCATTCTTTTTTTAAAAAAATTTTTTTTTTTTTTTGAGACAAGGTCTTGCTTTGTTACCCAGGTTGGAGTGCAGTGGTGCAATCACAGTTCACTGCAGCCTCAACCTCCCAGGCTCAAGAAATCCTCCCACCTCAACCTCCTGAGTAGCTAGGACTACAGGTGCGTGCCACCATGCCAAGCTAATTTTCTTTTATTTTTTGTAGAGATGGAGTCTCACTATGTTGCCCAGGCTAGTCTCTAACTCCTGAGCTCAAGTGATCCTCCTGCCTTGGCCTCCCGAAAGTGCAGGGTTATAGGCATGAGCTACCATGCCCAG... |
Task1_train_32552 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGGTCCTAGACATCACTACAGCACTGTAAAGCCTGATGAACCTGATGGCCCAGCAATGCTCTCAGTTTCCTTTCTATAAGCAAAGCCCCTTAGGCACGTCTGTAACCCAGAATCTCATCCTTGGCCCCACAATCCTATGCTACAGCCTCTCTAGACAAACTCATCTAGCTCACCTATTTACAGTTTTGACCACCAGGGCAGGAAAATAAAGCAAGAAGCAGGGAAGGCTCTACATATATTACATGGCTTCCTGCTGTCTTTAGAAAGCTTTCTATTTTAACCAAATCTTATTAAATCACCCTCAGTTGTGTCTATTCCTC... | TGGTCCTAGACATCACTACAGCACTGTAAAGCCTGATGAACCTGATGGCCCAGCAATGCTCTCAGTTTCCTTTCTATAAGCAAAGCCCCTTAGGCACGTCTGTAACCCAGAATCTCATCCTTGGCCCCACAATCCTATGCTACAGCCTCTCTAGACAAACTCATCTAGCTCACCTATTTACAGTTTTGACCACCAGGGCAGGAAAATAAAGCAAGAAGCAGGGAAGGCTCTACATATATTACATGGCTTCCTGCTGTCTTTAGAAAGCTTTCTATTTTAACCAAATCTTATTAAATCACCCTCAGTTGTGTCTATTCCTC... |
Task1_train_32553 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGGAAAAACAGAAAGTAATGGCCATTGTTAGAATCGACACTCAGAACAACCCTGTCTACCAGGTACCTAGTAGTGTGACAAGTATCGTGAAAATTATAAAAAATAGAACTACTTTTTATTGAATGTTTTCTGTGTACCACAGTTCTAATTTCCTCCATGCATTTTAAAATTTATTCTTACAACAACCGTATAAGGTATGCACAATCATTATCCCCATTTTACAGATGAGAGAACTGAGGATCCAAGAGGTTAAGTAACTCACTCAAGATCACAGAGGTAGTGAATAGCAGAGCTAGGAGTTCCCCAACTCCAGCTCCTGT... | GGGAAAAACAGAAAGTAATGGCCATTGTTAGAATCGACACTCAGAACAACCCTGTCTACCAGGTACCTAGTAGTGTGACAAGTATCGTGAAAATTATAAAAAATAGAACTACTTTTTATTGAATGTTTTCTGTGTACCACAGTTCTAATTTCCTCCATGCATTTTAAAATTTATTCTTACAACAACCGTATAAGGTATGCACAATCATTATCCCCATTTTACAGATGAGAGAACTGAGGATCCAAGAGGTTAAGTAACTCACTCAAGATCACAGAGGTAGTGAATAGCAGAGCTAGGAGTTCCCCAACTCCAGCTCCTGT... |
Task1_train_32554 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CATGCCAATGGCATATCCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTGAGTATGTAGGAGCTTCCTGAAAAGTCTCTATAACCTTCTCCAGGAGCTGTGTTCACAGTCCTTCAGCTCTGGGGTCCAGGCCTCCCAGAACAAAGCCCAGACTTCTTGGTTTGGCCCAAGCATACCTGCGACTGTTTTCCTCTACAACTCTCGCCTCTGTCTACTCCACACGCCCCAAGCACTCTCTTGCTTCTAGGCTTGGCCATGTGCAGTTTGTGTACGGTTCCCAAGCCAAAGGGTAGTATTTGACTGTGGAAAAGGGGATCATTG... | CATGCCAATGGCATATCCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTGAGTATGTAGGAGCTTCCTGAAAAGTCTCTATAACCTTCTCCAGGAGCTGTGTTCACAGTCCTTCAGCTCTGGGGTCCAGGCCTCCCAGAACAAAGCCCAGACTTCTTGGTTTGGCCCAAGCATACCTGCGACTGTTTTCCTCTACAACTCTCGCCTCTGTCTACTCCACACGCCCCAAGCACTCTCTTGCTTCTAGGCTTGGCCATGTGCAGTTTGTGTACGGTTCCCAAGCCAAAGGGTAGTATTTGACTGTGGAAAAGGGGATCATTG... |
Task1_train_32555 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | GACAATGTGGATAGATTTGGAGAGAGCAGAGGTTCAAGGCCTGGCAGTCTCAGTGAGGTCAAAGAGCAGCAGCAGGAGGAGGGTGGGAGGAAGCTAAGGGAATAGTGTTGTATGTAATCAGTGGGTTATGGCAATTTGAAATTGCAAAGATGAATTTGTTCCACATGAAGCCAAGAGCCAGCGTGTAGCCTATAGGCAGGTGAATGGAATAGAGTAAGTTACTGGAGATGAGAGTTAAGGAACTGAGAGGGCAGGGACTTGAATGAGTAATCTGGAGCAGGTCTGCAAACACTTTCTGCAAAGGCCAGTCAGTCTTTAAG... | GACAATGTGGATAGATTTGGAGAGAGCAGAGGTTCAAGGCCTGGCAGTCTCAGTGAGGTCAAAGAGCAGCAGCAGGAGGAGGGTGGGAGGAAGCTAAGGGAATAGTGTTGTATGTAATCAGTGGGTTATGGCAATTTGAAATTGCAAAGATGAATTTGTTCCACATGAAGCCAAGAGCCAGCGTGTAGCCTATAGGCAGGTGAATGGAATAGAGTAAGTTACTGGAGATGAGAGTTAAGGAACTGAGAGGGCAGGGACTTGAATGAGTAATCTGGAGCAGGTCTGCAAACACTTTCTGCAAAGGCCAGTCAGTCTTTAAG... |
Task1_train_32556 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | GAGAGAGCAAGTGTAGACTGGGACACTAGCAAAAAGCCTATAGCACACACTTCTCCTCTCTAATTCCCAGTCTGAAGTATAGAGCAGCATCTGCTACTGCCCTCCCTGTCTCCTCCCATCACCCGATTTGTTTTGTCCTCTCTCATCCTCACTGGATTTGTTATACCCTGAGGGACCGCCAGTCTAAGCAGGGCCAGCAGCAGACTTGGCTCCTTGAGGACTGCTGGGAGGTGGGTGTATGTGGGGAGAGCTTGTAGTCTCAGTGTCTCTTCTTCCCTTATCCTGGCCTTGCCCCGGCCTTTATGGGGCTTCAGAGTCCG... | GAGAGAGCAAGTGTAGACTGGGACACTAGCAAAAAGCCTATAGCACACACTTCTCCTCTCTAATTCCCAGTCTGAAGTATAGAGCAGCATCTGCTACTGCCCTCCCTGTCTCCTCCCATCACCCGATTTGTTTTGTCCTCTCTCATCCTCACTGGATTTGTTATACCCTGAGGGACCGCCAGTCTAAGCAGGGCCAGCAGCAGACTTGGCTCCTTGAGGACTGCTGGGAGGTGGGTGTATGTGGGGAGAGCTTGTAGTCTCAGTGTCTCTTCTTCCCTTATCCTGGCCTTGCCCCGGCCTTTATGGGGCTTCAGAGTCCG... |
Task1_train_32557 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CATGATCTGCCAGTGGAATATGTCCTAGGGAAGAGGATACTACATTCCGAGACCCCGCAGGCCCCGCCCTCCTTCCGATCTGCGAAGTACCCCCTTCCACTTACCATTTGTAATTGGAGGTTGGGTCTTCCTACCTTCTGTAAGATGGCTGCCGCTGTAAGAGAAGCCAGGGAGGGGACCGTGAGCCTCAAGAGCACAGGAATCAAAAGGGACAGAAGGAGAGACAGGGCTGGGGTCGTACCCTGCTGGGGCGTGTCCAGGAAGTACTGGGGGTCAGTGATGCGGGTGTTGATGGGCTCCAGCAGTCCCACGAGGTCCTC... | CATGATCTGCCAGTGGAATATGTCCTAGGGAAGAGGATACTACATTCCGAGACCCCGCAGGCCCCGCCCTCCTTCCGATCTGCGAAGTACCCCCTTCCACTTACCATTTGTAATTGGAGGTTGGGTCTTCCTACCTTCTGTAAGATGGCTGCCGCTGTAAGAGAAGCCAGGGAGGGGACCGTGAGCCTCAAGAGCACAGGAATCAAAAGGGACAGAAGGAGAGACAGGGCTGGGGTCGTACCCTGCTGGGGCGTGTCCAGGAAGTACTGGGGGTCAGTGATGCGGGTGTTGATGGGCTCCAGCAGTCCCACGAGGTCCTC... |
Task1_train_32558 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAGGTGACTCTTACAAGGTAAGTAGGACCTTCCCAGGCGGACAGAGAGAGAGGAGGGATGTAGAAAGGGAGTCCCAGATGGGAGGAGCAGGGCACAGGCATGGAGATGGGAATTTTTTTTTTTTTTTTTGAAATGGAGTCTTGCTCTGTCATGCAGGCTGGAGTGCAGGGGCGCAATCTTGGCTCACTGCAACTTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTTCCAACTAGCTAGGACTACAGGTGCCTGCCACCATGCCTGGCTAATTTTTTTTTGTATTTTTAGTAGCGATGGGGTTTCACCGTGTT... | AAGGTGACTCTTACAAGGTAAGTAGGACCTTCCCAGGCGGACAGAGAGAGAGGAGGGATGTAGAAAGGGAGTCCCAGATGGGAGGAGCAGGGCACAGGCATGGAGATGGGAATTTTTTTTTTTTTTTTTGAAATGGAGTCTTGCTCTGTCATGCAGGCTGGAGTGCAGGGGCGCAATCTTGGCTCACTGCAACTTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTTCCAACTAGCTAGGACTACAGGTGCCTGCCACCATGCCTGGCTAATTTTTTTTTGTATTTTTAGTAGCGATGGGGTTTCACCGTGTT... |
Task1_train_32559 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCCACACTCCAGACTCATTTACCCAATTGCTTCCTTCATTTGGATATGTATTAGGCATCTCACACTTAACATGTCCAGAACCAAACTCCAGATTCACACCCCTGCCTCCCAGAATCTTTTCTACCCCAGGAAATGGCAGCTAACTACATCCTTCCAATTGCTCACATCAAATACTGTAGCATCATTTCTTTGACACTCAAATCTGATATCAGCAAACCTTATTAGCTTTACCTTAATATCCTCAGATCCAGCCACTTCTCACTACCTCTGTATCATCACTCTGTCCAAACCACCATCTCTCACCTAATTTTTGCACTCCT... | CCCACACTCCAGACTCATTTACCCAATTGCTTCCTTCATTTGGATATGTATTAGGCATCTCACACTTAACATGTCCAGAACCAAACTCCAGATTCACACCCCTGCCTCCCAGAATCTTTTCTACCCCAGGAAATGGCAGCTAACTACATCCTTCCAATTGCTCACATCAAATACTGTAGCATCATTTCTTTGACACTCAAATCTGATATCAGCAAACCTTATTAGCTTTACCTTAATATCCTCAGATCCAGCCACTTCTCACTACCTCTGTATCATCACTCTGTCCAAACCACCATCTCTCACCTAATTTTTGCACTCCT... |
Task1_train_32560 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGAGGGGTGGACGCACTGAACAGTAAGGGCTGGGGAGCTAAAGGCCTCTGTGTTGTGGAGAGGGAGGAAGAGAGAGACTTGAAAGGAGGGGAAGCTGTGCCCCAGAATGGACACTGGGATGTCGGATTTCAGAGGTGATGCCTTTCTAGTACAGTGCAGAGACCCTCCGGTAAGAATGATCCCGTTTTATGGTTAAAGAAACAGGCTTGGAGAGCTTGTTGCCCAGTCACCCAACTCTAGTCAACAGCAGTGTTGGTCTGCTATACTCTACTTGCTCACGCTCTGTCTCCATTTTTCAGGTCCACTCTAGAACAGTCGAT... | GGAGGGGTGGACGCACTGAACAGTAAGGGCTGGGGAGCTAAAGGCCTCTGTGTTGTGGAGAGGGAGGAAGAGAGAGACTTGAAAGGAGGGGAAGCTGTGCCCCAGAATGGACACTGGGATGTCGGATTTCAGAGGTGATGCCTTTCTAGTACAGTGCAGAGACCCTCCGGTAAGAATGATCCCGTTTTATGGTTAAAGAAACAGGCTTGGAGAGCTTGTTGCCCAGTCACCCAACTCTAGTCAACAGCAGTGTTGGTCTGCTATACTCTACTTGCTCACGCTCTGTCTCCATTTTTCAGGTCCACTCTAGAACAGTCGAT... |
Task1_train_32561 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TCTCCGCCCGCGTCCAGCCGGCCTCCCTCATTGTCCTCGCTCGCCCCGGCCTCGTGGCGCGGGGAGGCGTTCCATACACGTTTCCCCTTGGCCTTTGCCTCATCCGCTGCCCTCCACCCACTCCCCCTGCCCCCAGGCTCCACACCCACCCGGTCTGTGCGGCCTGCCCGTCCGCGGGTGCCACGTGTTCAGCCTGCCAGCCCCGCCCAAACGCACCCCTCAGCCTGGCCGCCAGCCTGACCCAGAACCCCTGCGCCGGAGGGAGGGTGGGAATGTCTGCACGTGGGTCTGGGTGTGAGCTGTCTGAGAGTCTGGATGTA... | TCTCCGCCCGCGTCCAGCCGGCCTCCCTCATTGTCCTCGCTCGCCCCGGCCTCGTGGCGCGGGGAGGCGTTCCATACACGTTTCCCCTTGGCCTTTGCCTCATCCGCTGCCCTCCACCCACTCCCCCTGCCCCCAGGCTCCACACCCACCCGGTCTGTGCGGCCTGCCCGTCCGCGGGTGCCACGTGTTCAGCCTGCCAGCCCCGCCCAAACGCACCCCTCAGCCTGGCCGCCAGCCTGACCCAGAACCCCTGCGCCGGAGGGAGGGTGGGAATGTCTGCACGTGGGTCTGGGTGTGAGCTGTCTGAGAGTCTGGATGTA... |
Task1_train_32562 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | GTCACCGAGTAGGCTCTGGCTTCTGCCACAGCGCACCTGTCTGCCGCTGCCGCCTCAGCTGCTTTGGCCCAGCCAGCTTCAGATCTGGTCTTGGCGAGCTCTCGCCAGGACCCCAAGGCTGTTGGTCTGTCTGGCCCTTGCCCCACCCCCTTGCCAGATCCCTGGTGTCTGGAGCTGAGTGGCCGGGCATCGGTCCCAAGCATCAAAGCCTTTGGCCTTTCTCCTCCCAGGCCTCCACAAAGGCCTGGCAGACAGAGGTCTCATTCCAGCCTGACTCTTGTCCCCTGGGGGACCCAGACAAAGCACAGCAGCCGCTCAGA... | GTCACCGAGTAGGCTCTGGCTTCTGCCACAGCGCACCTGTCTGCCGCTGCCGCCTCAGCTGCTTTGGCCCAGCCAGCTTCAGATCTGGTCTTGGCGAGCTCTCGCCAGGACCCCAAGGCTGTTGGTCTGTCTGGCCCTTGCCCCACCCCCTTGCCAGATCCCTGGTGTCTGGAGCTGAGTGGCCGGGCATCGGTCCCAAGCATCAAAGCCTTTGGCCTTTCTCCTCCCAGGCCTCCACAAAGGCCTGGCAGACAGAGGTCTCATTCCAGCCTGACTCTTGTCCCCTGGGGGACCCAGACAAAGCACAGCAGCCGCTCAGA... |
Task1_train_32563 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGGAAATAAAACTTGTGGCTGCAGTAACAAAAGGAGTGAAAGGAGGCAGAAACACAGGCAGTGGCTGGCGGGCCACCCAGAGGGCCTGGCGGGGGAAGGGGGGGGGCAGTCCCAGCACCCTCCTCCTGAGCCTCCAGCCACATCCTGGAGCACAGGGCCATATTCTAGAATGCAAGACCCACATCCAAATTGGGGGACCCTCCGGAGACACTGCACACGATGGGAGCTTATAACAGGTTTCCTGAATGGAACAGATCCTGACCTACGTGTGGACAAATCCCTCATTTGAGCTGACAGAAGGGTGGAGTTTGTCAAAAAGA... | TGGAAATAAAACTTGTGGCTGCAGTAACAAAAGGAGTGAAAGGAGGCAGAAACACAGGCAGTGGCTGGCGGGCCACCCAGAGGGCCTGGCGGGGGAAGGGGGGGGGCAGTCCCAGCACCCTCCTCCTGAGCCTCCAGCCACATCCTGGAGCACAGGGCCATATTCTAGAATGCAAGACCCACATCCAAATTGGGGGACCCTCCGGAGACACTGCACACGATGGGAGCTTATAACAGGTTTCCTGAATGGAACAGATCCTGACCTACGTGTGGACAAATCCCTCATTTGAGCTGACAGAAGGGTGGAGTTTGTCAAAAAGA... |
Task1_train_32564 | Given this context: Chromosome 1 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CACTCAGGTCAAGAAATAGAAGCCCGTCCAGTGTCCCTTTCTTATCTTTCCCCATTCCCTACTCTCTAATATAACCCCATCCTGTTGTCTGGATGTAACTTTTTTGAATTTCCCTATTTCTGACCTGTGATGTTCCTATAACTGCTGCAAAATTTGTAATTGCTTCAAGTTTTTACTTCCTTCCTTCCTTCCCTCCCTCCCTCCTTCCCTCCTTCCTTCCTTCCTTCCTTGAACTCCTGACCTCAAGTGATCCACCCGCCTCGGTGGATCTTTCCCTTTCTTTCTTTCTTTTCTTTTCTTTTCTTTTCTTTCCTTCTTTC... | CACTCAGGTCAAGAAATAGAAGCCCGTCCAGTGTCCCTTTCTTATCTTTCCCCATTCCCTACTCTCTAATATAACCCCATCCTGTTGTCTGGATGTAACTTTTTTGAATTTCCCTATTTCTGACCTGTGATGTTCCTATAACTGCTGCAAAATTTGTAATTGCTTCAAGTTTTTACTTCCTTCCTTCCTTCCCTCCCTCCCTCCTTCCCTCCTTCCTTCCTTCCTTCCTTGAACTCCTGACCTCAAGTGATCCACCCGCCTCGGTGGATCTTTCCCTTTCTTTCTTTCTTTTCTTTTCTTTTCTTTTCTTTCCTTCTTTC... |
Task1_train_32565 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ATCCCAATTGAAGAGTGAATAGGAGATGATAGGATAGCTTTATTCGTTTCTCAACTCAAGAGCTCCCTCTTCTATTGCTACAGTAATGGACTTTTTTGTTGCTGTTGTCTTGAGACAGAGTCTCACTCTGTCAGCACAGGCTGGAGTGCAATGGCACAATCTCAGCTTACTGCAACCTCTGGCTCCTGGACTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACACGCCACCACACCTAGCTGATTTTGTTTTTCTTTTTGAAATTTCTGAGCTCAAGCAATCCACCTGCCTCGGCCTCCCAA... | ATCCCAATTGAAGAGTGAATAGGAGATGATAGGATAGCTTTATTCGTTTCTCAACTCAAGAGCTCCCTCTTCTATTGCTACAGTAATGGACTTTTTTGTTGCTGTTGTCTTGAGACAGAGTCTCACTCTGTCAGCACAGGCTGGAGTGCAATGGCACAATCTCAGCTTACTGCAACCTCTGGCTCCTGGACTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACACGCCACCACACCTAGCTGATTTTGTTTTTCTTTTTGAAATTTCTGAGCTCAAGCAATCCACCTGCCTCGGCCTCCCAA... |
Task1_train_32566 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | GGTCAGAGGAAAGGTCAGATGGCTTAGAGTATGGGCCATCAGCTTGCTTCTGGTTAGTCGGCCCAGTGATCCCCCAACACCCATCCCACTGCCAGTTTGCTAGGAGTATTTCAGATTTGTAAAGTGGGGTTGGGGTCAGGTGGGACCACTGAGGCAGGAGAGGAGTGCTATTCTTAGAAGGAGGAATCGACCCTAGAACTCTGCAGTGGAAGGGTGGCAGGACATGTTCCAGGGAGCACAGTTTGGGAACAGATACAAATACTCTACCCCTCTTCTAGGTTCACAGCAAGGCCACTGGTACAGACAATCTTTGAAGGTGG... | GGTCAGAGGAAAGGTCAGATGGCTTAGAGTATGGGCCATCAGCTTGCTTCTGGTTAGTCGGCCCAGTGATCCCCCAACACCCATCCCACTGCCAGTTTGCTAGGAGTATTTCAGATTTGTAAAGTGGGGTTGGGGTCAGGTGGGACCACTGAGGCAGGAGAGGAGTGCTATTCTTAGAAGGAGGAATCGACCCTAGAACTCTGCAGTGGAAGGGTGGCAGGACATGTTCCAGGGAGCACAGTTTGGGAACAGATACAAATACTCTACCCCTCTTCTAGGTTCACAGCAAGGCCACTGGTACAGACAATCTTTGAAGGTGG... |
Task1_train_32567 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | GGGTGCTACTGTCTCCACATTATAGATTTGGAAACTGAGGCTTAGAAATATTCACTATTGGCTAGACGCGGTGGCTTACGCCTGTAATTCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACCTGAGGTAAGGAGTTAAAGACCAGCCTGGACAACGTGGTGACACCCCGGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGTGGACACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGCGGTGGAGGTTGCAGTGAGCCGAGATCAGGCCATTGCACTCCAGCCTGG... | GGGTGCTACTGTCTCCACATTATAGATTTGGAAACTGAGGCTTAGAAATATTCACTATTGGCTAGACGCGGTGGCTTACGCCTGTAATTCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACCTGAGGTAAGGAGTTAAAGACCAGCCTGGACAACGTGGTGACACCCCGGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGTGGACACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGCGGTGGAGGTTGCAGTGAGCCGAGATCAGGCCATTGCACTCCAGCCTGG... |
Task1_train_32568 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GTCTTCGTCTTTGAAATCCAAAGTCAATCAGAAAACATGTTTGTTTATATGTGTCTTTTCTCAAGTCAATCAGAAAACATGTTTGTTTATATGTGTCTTCTGAAACTACCATAAGAGAGCCTATAACTCCAGAACCACATTAACTTTCATATTATAAAGGGGAAATATCTGATTTAAACATGATCTAGATTACCCAAAATATCCTATTTCATTTGGAAAGTGACACTTTAGTTACTTTAAAAATAGACACCTCTTTAAAACTCTTCCTCTCTTTTATTTGTTCCCTCAAGTTTGAAAATTCTTCCTCATCCATCTCTTAC... | GTCTTCGTCTTTGAAATCCAAAGTCAATCAGAAAACATGTTTGTTTATATGTGTCTTTTCTCAAGTCAATCAGAAAACATGTTTGTTTATATGTGTCTTCTGAAACTACCATAAGAGAGCCTATAACTCCAGAACCACATTAACTTTCATATTATAAAGGGGAAATATCTGATTTAAACATGATCTAGATTACCCAAAATATCCTATTTCATTTGGAAAGTGACACTTTAGTTACTTTAAAAATAGACACCTCTTTAAAACTCTTCCTCTCTTTTATTTGTTCCCTCAAGTTTGAAAATTCTTCCTCATCCATCTCTTAC... |
Task1_train_32569 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GACACTGATGAGGCTGCGGCAGAGGACAAGCGGCGACGGCGACGACGTAGGGAAAAACGGAAGAGGGCTTTATTGAACCTACCGGGGACACAGACCTCTGGGGAAGCTAAGGATGGTCCTCCCAAGAAGCAGGTCTGTGGGGATAGCATCAAGCCTGAAGAAACCGAGCAGGAGGTGGCTGCCGATGAAACTAGGAACCTGCCTCACTCCAAGCAAGGCAACAAAAATGACTTAGAGATGGGGATTAAGGCAGCAAGGCCTGAAATAGCTGATAGAGCTACCTCAGAAGTGCCAGGGAGCCAAGCCAGTCCTAACCCAGT... | GACACTGATGAGGCTGCGGCAGAGGACAAGCGGCGACGGCGACGACGTAGGGAAAAACGGAAGAGGGCTTTATTGAACCTACCGGGGACACAGACCTCTGGGGAAGCTAAGGATGGTCCTCCCAAGAAGCAGGTCTGTGGGGATAGCATCAAGCCTGAAGAAACCGAGCAGGAGGTGGCTGCCGATGAAACTAGGAACCTGCCTCACTCCAAGCAAGGCAACAAAAATGACTTAGAGATGGGGATTAAGGCAGCAAGGCCTGAAATAGCTGATAGAGCTACCTCAGAAGTGCCAGGGAGCCAAGCCAGTCCTAACCCAGT... |
Task1_train_32570 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GTGTTCCTGATCCTAATTCCTATCTGTCTAACGTGGAGGTGATCAAGTGTGGCTGTAGGCCTTTGTTTTCCAATGGTGCTATATTCTGTTTTCAAACACTTCACTGAACCCAGCTGTCTTGCAAACTTTCAGTGGTGCTGTCCCTGGATGGGGGCTACAAAAACAAGAATTGGTGAAGATCTTGCTCTTCAGTGCTGAAAATGGATGATGGACTTTGGCTGTGAGCCAGGCCTAGGATGGTTCTTGTCCTATATCCACCTAGTCTTCACCTGGGGCTATAATTCTGTCCTGGAAAAAGAACTCTGAAAACCTGGGTCAGG... | GTGTTCCTGATCCTAATTCCTATCTGTCTAACGTGGAGGTGATCAAGTGTGGCTGTAGGCCTTTGTTTTCCAATGGTGCTATATTCTGTTTTCAAACACTTCACTGAACCCAGCTGTCTTGCAAACTTTCAGTGGTGCTGTCCCTGGATGGGGGCTACAAAAACAAGAATTGGTGAAGATCTTGCTCTTCAGTGCTGAAAATGGATGATGGACTTTGGCTGTGAGCCAGGCCTAGGATGGTTCTTGTCCTATATCCACCTAGTCTTCACCTGGGGCTATAATTCTGTCCTGGAAAAAGAACTCTGAAAACCTGGGTCAGG... |
Task1_train_32571 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GGTACATTGAGAACCTGAAAGGTTTCCTGGCAGAAATACTGAGGAAACGGATTTAAGTTTGGCAATAAAACTGGCTTTACCAAAAAAAGCAGTGGGAACTAGTGGGAATTTAAAGTTGCTTTAGTGGGAATTAATGCCCCCTAGTCACCTTTCGGAGAACTTCATAAGTGCCAGACAATATCACAAATACCTGACAAACTCATTTAATCCTTAATCTGTTTTACAAAAACAGAAGAGGTACAGAAAAGTTAAGGACTTAACGGGAGGTGGTAAAGCTGTGGTTGGAACTGGTTTTCTGTACTCAACTGCTAGATGCTTCT... | GGTACATTGAGAACCTGAAAGGTTTCCTGGCAGAAATACTGAGGAAACGGATTTAAGTTTGGCAATAAAACTGGCTTTACCAAAAAAAGCAGTGGGAACTAGTGGGAATTTAAAGTTGCTTTAGTGGGAATTAATGCCCCCTAGTCACCTTTCGGAGAACTTCATAAGTGCCAGACAATATCACAAATACCTGACAAACTCATTTAATCCTTAATCTGTTTTACAAAAACAGAAGAGGTACAGAAAAGTTAAGGACTTAACGGGAGGTGGTAAAGCTGTGGTTGGAACTGGTTTTCTGTACTCAACTGCTAGATGCTTCT... |
Task1_train_32572 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CCAGAACTGTTACTCCCAGCCCACTTCGAGCCTGATGAAGTGAAGACACAGTGGTCCAGTACTGGCTAAAGGTGTCAAAACGTTCTACACAGCTGAGGGCTCTGCTATCACTCCAGCGACCCCCCTGCAACCGAGTATATCCACCTAAACAAAAGAAGAAAAGGTAGTAATGAAAATCTACTGTTCTACATCTAAACATTTAGTATAACTACTATATAACAAGAAATAAATGGTTTAGAAATTACTTTCTCTATATACATATAATGTAATATTCTTAAATTTGCCAATTCCTGAAAGATTGTGGCTTAAATACAGTAAGA... | CCAGAACTGTTACTCCCAGCCCACTTCGAGCCTGATGAAGTGAAGACACAGTGGTCCAGTACTGGCTAAAGGTGTCAAAACGTTCTACACAGCTGAGGGCTCTGCTATCACTCCAGCGACCCCCCTGCAACCGAGTATATCCACCTAAACAAAAGAAGAAAAGGTAGTAATGAAAATCTACTGTTCTACATCTAAACATTTAGTATAACTACTATATAACAAGAAATAAATGGTTTAGAAATTACTTTCTCTATATACATATAATGTAATATTCTTAAATTTGCCAATTCCTGAAAGATTGTGGCTTAAATACAGTAAGA... |
Task1_train_32573 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AATAGTTAAGCACTTAATAAATGTTGGTTGCTGTTATGTCATTATTATTATTGTTATATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATGTAGCCTGGTCTCGGGTATTAGAGAATTGGAGAATATTGAGTAGAAACTTAGGATTCAGCCATAACTGCAAGCCTTAGCTGGGGATGGGAGGATAGACCCAAGGTTGGGGCTTTTGGCAACTGACCCTGATATCATCACAAGGCTTTCCAAAGTAGGAGCCAGTACTTGTTGAGAACTGTTAGATTTCTAAGGTGTTCTAGTTATCTTTAGGACCT... | AATAGTTAAGCACTTAATAAATGTTGGTTGCTGTTATGTCATTATTATTATTGTTATATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATGTAGCCTGGTCTCGGGTATTAGAGAATTGGAGAATATTGAGTAGAAACTTAGGATTCAGCCATAACTGCAAGCCTTAGCTGGGGATGGGAGGATAGACCCAAGGTTGGGGCTTTTGGCAACTGACCCTGATATCATCACAAGGCTTTCCAAAGTAGGAGCCAGTACTTGTTGAGAACTGTTAGATTTCTAAGGTGTTCTAGTTATCTTTAGGACCT... |
Task1_train_32574 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | GCACCCACCACCACGCCTGGCTAATTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATCTTGGCCAGGCTGATCTTGAACTCCTGACCTCATGATCTACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCGCGCCTGGCCTGTTTTTTGTTTTTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTATCTTATGTGAAGGGAATCAGTTTCCTGTCCTGGGAAATTGAGATAGATGCATTCATTCATTCATTCATTCATACATTCAACTGCATACTAGGCCCTCTGAGCAGGAGAAG... | GCACCCACCACCACGCCTGGCTAATTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATCTTGGCCAGGCTGATCTTGAACTCCTGACCTCATGATCTACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCGCGCCTGGCCTGTTTTTTGTTTTTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTATCTTATGTGAAGGGAATCAGTTTCCTGTCCTGGGAAATTGAGATAGATGCATTCATTCATTCATTCATTCATACATTCAACTGCATACTAGGCCCTCTGAGCAGGAGAAG... |
Task1_train_32575 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GCAGTAGGAGTGGGAGACAGATCTCAGAGTTGCTTGCTAACATCTGAATTTTCATTTTCAAGCAGGAAAATGCTGAGGAAGGAAAGTAGGTTGTTATCCTGAGATAGCTGAGAAGTAGCATTCGTAACTCTGCTGCTTGGCTGTGAACCTCCTTGTATATGGAACTAGGATCTTGTTTCCCATTTGCATGTCTCTTTTTTTGTTAAGAGATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAATGGCACCATCTCGGCTCACTGCACCCTCTGCCTCCGGGGTTCAGACAATTCTCCTGCCTCAGCCTCCCGAGATGC... | GCAGTAGGAGTGGGAGACAGATCTCAGAGTTGCTTGCTAACATCTGAATTTTCATTTTCAAGCAGGAAAATGCTGAGGAAGGAAAGTAGGTTGTTATCCTGAGATAGCTGAGAAGTAGCATTCGTAACTCTGCTGCTTGGCTGTGAACCTCCTTGTATATGGAACTAGGATCTTGTTTCCCATTTGCATGTCTCTTTTTTTGTTAAGAGATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAATGGCACCATCTCGGCTCACTGCACCCTCTGCCTCCGGGGTTCAGACAATTCTCCTGCCTCAGCCTCCCGAGATGC... |
Task1_train_32576 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACTTTGCGGAAACTGTGCTGGCCCTGGAGTACTTACACAACTATGGCATCGTGCACCGTGACCTCAAGCCTGACAAGTATGTCCACAGTCTGTGTCCCTTGTCCAGGGTCTCCCTCTTGGGTCTCCAGATAAAATGTTGGCAAGCACAGTAGCTCTAAATCTATCCAGATGGCTACCGGGAAAACATGCTCCTGTGTGTGTCCATCTGGGCCTAGTTCTCTAGCCCCCCGACCACCCCAGATGCAGATCATTGCCTCAAGGTCTGGCTGGAACACTATAAGGCTTCGGTGACATGGAAGAGTCATTGAGGAGCCCCACTG... | ACTTTGCGGAAACTGTGCTGGCCCTGGAGTACTTACACAACTATGGCATCGTGCACCGTGACCTCAAGCCTGACAAGTATGTCCACAGTCTGTGTCCCTTGTCCAGGGTCTCCCTCTTGGGTCTCCAGATAAAATGTTGGCAAGCACAGTAGCTCTAAATCTATCCAGATGGCTACCGGGAAAACATGCTCCTGTGTGTGTCCATCTGGGCCTAGTTCTCTAGCCCCCCGACCACCCCAGATGCAGATCATTGCCTCAAGGTCTGGCTGGAACACTATAAGGCTTCGGTGACATGGAAGAGTCATTGAGGAGCCCCACTG... |
Task1_train_32577 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ACTCAAATCCTGGCTCCATCACTAACAGGCTCTTGACCTTGAGCAAGTTGCTTAACTTCTCTAAGCCTCAAGTTTCTTATCCAAAAATGTGGATATAATAGAGGCCAGCTGATAGGTTGTGACATTTAAATATATATGACAAGCTTATATAGTCCCTGATACACACATAAATGCTAGCTGCCATTTCTCATCACCACCACCGTCTCTTGGGGTCTGGACACGGGAGAGGGCTTCACAGGTCAGGGGCTGTGGGGAAAATGGACCTAGGCTCAGGCTCTGTCTGTGACTAGAGTTGTGCTGACATCAACAGACTGGACCAG... | ACTCAAATCCTGGCTCCATCACTAACAGGCTCTTGACCTTGAGCAAGTTGCTTAACTTCTCTAAGCCTCAAGTTTCTTATCCAAAAATGTGGATATAATAGAGGCCAGCTGATAGGTTGTGACATTTAAATATATATGACAAGCTTATATAGTCCCTGATACACACATAAATGCTAGCTGCCATTTCTCATCACCACCACCGTCTCTTGGGGTCTGGACACGGGAGAGGGCTTCACAGGTCAGGGGCTGTGGGGAAAATGGACCTAGGCTCAGGCTCTGTCTGTGACTAGAGTTGTGCTGACATCAACAGACTGGACCAG... |
Task1_train_32578 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCAGAACCAGGCCCCATACTTCGTGTTCAGGCTCCAGTCTGAGTACTGTTCTCTTCCTGGCACAGCACGTGGAGGATGGAGGTCCGGCCAGTGAGGCAGGGCTTCGTCAAGGTGACCTCATCACCCATGTCAATGGGGAACCTGTGCATGGCCTGGTGCACACGGAGGTGGTAGAGCTGATCCTGAAGGTTAGTGCTGGGCGTGCTGCCTGCATGGTCCCTGAATGACCTCAGCCTGTGAGTCTGTGATGGCAGTTAGGGGAGTGGGTGAGTTGGGTGCACACACATCTACACCGAGTATGGATGTAGGTACACACAGGC... | CCAGAACCAGGCCCCATACTTCGTGTTCAGGCTCCAGTCTGAGTACTGTTCTCTTCCTGGCACAGCACGTGGAGGATGGAGGTCCGGCCAGTGAGGCAGGGCTTCGTCAAGGTGACCTCATCACCCATGTCAATGGGGAACCTGTGCATGGCCTGGTGCACACGGAGGTGGTAGAGCTGATCCTGAAGGTTAGTGCTGGGCGTGCTGCCTGCATGGTCCCTGAATGACCTCAGCCTGTGAGTCTGTGATGGCAGTTAGGGGAGTGGGTGAGTTGGGTGCACACACATCTACACCGAGTATGGATGTAGGTACACACAGGC... |
Task1_train_32579 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | AAAAAAAAAAAAAAAAATTAGCCGAGTGTGGTAGCACATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAAGTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTTAAAAAAAAAAAAAAAAGATGTAGGTACACACAGAACTTGAATGTGGCACAACAGAGAGTTTTCTCCACAAGGCAGTACCCTCCCTGACTAAGGCCCAGGGATCCTTCTGAGCTGTGGGTAGGGCTGCAGAATGGGACGGATTAGCCTGTTTTCT... | AAAAAAAAAAAAAAAAATTAGCCGAGTGTGGTAGCACATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAAGTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTTAAAAAAAAAAAAAAAAGATGTAGGTACACACAGAACTTGAATGTGGCACAACAGAGAGTTTTCTCCACAAGGCAGTACCCTCCCTGACTAAGGCCCAGGGATCCTTCTGAGCTGTGGGTAGGGCTGCAGAATGGGACGGATTAGCCTGTTTTCT... |
Task1_train_32580 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | TCATTGTTTTGGTGTATAGCATAGCCTTTTTGAGCCTTTCTTCAGCTTCATGATGTGACCAGAACCACGTGAGCATTCCAAGAGCAGACACACCCCATTTACAGATAAGAGCACCCTCCTTGCCTTGTTTACAAAGCTCTTCAGTATGCTATATACACTTGGCTTGACTTTTGGCCACAATAGCAAACTAAAATGATCTCTTGAGAGAGCTGGTATTAAAAACTACTCAGCATGGTGTAGTTGTAATTGTTTACCCCAAGAAATATCACCTTAGGCTGGGTACAGTAGCTCATGCCTATAATCCCAGTACTTTAGGAGGC... | TCATTGTTTTGGTGTATAGCATAGCCTTTTTGAGCCTTTCTTCAGCTTCATGATGTGACCAGAACCACGTGAGCATTCCAAGAGCAGACACACCCCATTTACAGATAAGAGCACCCTCCTTGCCTTGTTTACAAAGCTCTTCAGTATGCTATATACACTTGGCTTGACTTTTGGCCACAATAGCAAACTAAAATGATCTCTTGAGAGAGCTGGTATTAAAAACTACTCAGCATGGTGTAGTTGTAATTGTTTACCCCAAGAAATATCACCTTAGGCTGGGTACAGTAGCTCATGCCTATAATCCCAGTACTTTAGGAGGC... |
Task1_train_32581 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GGATTGGCTCAGGAAACTGAGAGAGGCAGGGTCAAAGAGTTCAGGGAGGGACAAGGATAAATCTAGTCACACAGAGATGCTAGAATTGCTGGAGCTGGGTCTCAGGAGCACCTCCTTCCTGGAGTACCTCCTTCCCCCAAATCCCCACTGTCTCCATTCATCCACTGTACCTTCAACAGCAGCCCCAACACCTGCCATCCTACCTTTGCCCAGGCTTCGCCCCCACTTGTGAGCTCATGTCCTCCAGAAAGCTCTCTAGGACACCTCACTGACTCTTTCCCTGCAGACTGAGGGACCTCAACTGAAACCTAGAGACTCCC... | GGATTGGCTCAGGAAACTGAGAGAGGCAGGGTCAAAGAGTTCAGGGAGGGACAAGGATAAATCTAGTCACACAGAGATGCTAGAATTGCTGGAGCTGGGTCTCAGGAGCACCTCCTTCCTGGAGTACCTCCTTCCCCCAAATCCCCACTGTCTCCATTCATCCACTGTACCTTCAACAGCAGCCCCAACACCTGCCATCCTACCTTTGCCCAGGCTTCGCCCCCACTTGTGAGCTCATGTCCTCCAGAAAGCTCTCTAGGACACCTCACTGACTCTTTCCCTGCAGACTGAGGGACCTCAACTGAAACCTAGAGACTCCC... |
Task1_train_32582 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TAAAAAAAAGAATAAAGGTATGAAAGGGTTTGAGGCCTGAGAGCAGTGTGGTAAGCCCAGCAGGGAAGAAGCCCCCTATACTTCTCTAAAGCCTGGGTGCCTGCTTGAGGAGGGAAGGCAGGAACCCAGGGGCAGGGGAGGGGATCTCTTCAGCAATTATGATGACCACTGTAACCTCCTGGCCCAGGGTTCCCAGGATACTGAGTAAGGGGCCCAAAGACTATAAACCCAGCTGTGAGAATGCCTGTTTGCTGGGCCTCATCAAGGCCTCCAGGACCTCAGTGCAAGGGAAGAAGGAAAAAAGAGAAAAAAGGTGACAG... | TAAAAAAAAGAATAAAGGTATGAAAGGGTTTGAGGCCTGAGAGCAGTGTGGTAAGCCCAGCAGGGAAGAAGCCCCCTATACTTCTCTAAAGCCTGGGTGCCTGCTTGAGGAGGGAAGGCAGGAACCCAGGGGCAGGGGAGGGGATCTCTTCAGCAATTATGATGACCACTGTAACCTCCTGGCCCAGGGTTCCCAGGATACTGAGTAAGGGGCCCAAAGACTATAAACCCAGCTGTGAGAATGCCTGTTTGCTGGGCCTCATCAAGGCCTCCAGGACCTCAGTGCAAGGGAAGAAGGAAAAAAGAGAAAAAAGGTGACAG... |
Task1_train_32583 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | TTTGAGACGGAGTCTCTCTGTCGCCCAGGCTGGAGTGCAGGGGTAGGATCTTGGCTCCTGCAACCTCTGCCTCCTGGTTTCAGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTTCAGGCGCGTGCCACCATGCCCAGGTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGGTGGCCGGGCTGATTGAGAACTCCTGACCTCAGGTGATCTGGCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAACCACTATGCCCAGCCTGTTTTTAATTTTTTTAGAGATGGGGTCTTGTCATGTT... | TTTGAGACGGAGTCTCTCTGTCGCCCAGGCTGGAGTGCAGGGGTAGGATCTTGGCTCCTGCAACCTCTGCCTCCTGGTTTCAGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTTCAGGCGCGTGCCACCATGCCCAGGTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGGTGGCCGGGCTGATTGAGAACTCCTGACCTCAGGTGATCTGGCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAACCACTATGCCCAGCCTGTTTTTAATTTTTTTAGAGATGGGGTCTTGTCATGTT... |
Task1_train_32584 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GCAGGTACACGCACACACAAAACTACAGCTAACATCATATATAATGGTGAAGTACTAAATGCTTTCTTCTTAAGAATGGGAACAAGGCAAGGATGCCTACCATCACCACTTACATTCAACTGTGTACTGGAAGTCCTAGCCAGTGGAATAAAGCAAAGAAAAAAAAAAGGGATATAGATAGAAAAGAAAGAAGTTAAAGTGTCTTTATTTACAAAAGACATGACCATATGCATAGAAAACCTGAACAGATTTCCAAAAAGTTACCAAAAGTAATAATTGAGTTTAGGAAGGTCTCAGGATACAAGGTCAACAGAAAAAAT... | GCAGGTACACGCACACACAAAACTACAGCTAACATCATATATAATGGTGAAGTACTAAATGCTTTCTTCTTAAGAATGGGAACAAGGCAAGGATGCCTACCATCACCACTTACATTCAACTGTGTACTGGAAGTCCTAGCCAGTGGAATAAAGCAAAGAAAAAAAAAAGGGATATAGATAGAAAAGAAAGAAGTTAAAGTGTCTTTATTTACAAAAGACATGACCATATGCATAGAAAACCTGAACAGATTTCCAAAAAGTTACCAAAAGTAATAATTGAGTTTAGGAAGGTCTCAGGATACAAGGTCAACAGAAAAAAT... |
Task1_train_32585 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | ATGGATCTCGCACAAGAAAGAATTCAGGGCGAGTCCGCAATGCAAAGTGAGAGCAAGTTTATTAAAGTACAAGAATAAAAGAATGGATAGTCCATAGATAGAGCAGCTCCAAGGGCTGCTTGCCCATTTTTATGGTTATTTCTTGATGGTACGCTAAACAAGGGGTGGGTTATTCACGCCTCCACTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTTTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTGGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATCCCTCAGCTTCCCGAGTAGCTG... | ATGGATCTCGCACAAGAAAGAATTCAGGGCGAGTCCGCAATGCAAAGTGAGAGCAAGTTTATTAAAGTACAAGAATAAAAGAATGGATAGTCCATAGATAGAGCAGCTCCAAGGGCTGCTTGCCCATTTTTATGGTTATTTCTTGATGGTACGCTAAACAAGGGGTGGGTTATTCACGCCTCCACTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTTTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTGGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATCCCTCAGCTTCCCGAGTAGCTG... |
Task1_train_32586 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GAGCAGCTCCAAGGGCTGCTTGCCCATTTTTATGGTTATTTCTTGATGGTACGCTAAACAAGGGGTGGGTTATTCACGCCTCCACTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTTTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTGGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATCCCTCAGCTTCCCGAGTAGCTGGGACTGCAGGCGCCAGCAACCTCGCCCGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGAGGGTCTCGATCTCCTGACCT... | GAGCAGCTCCAAGGGCTGCTTGCCCATTTTTATGGTTATTTCTTGATGGTACGCTAAACAAGGGGTGGGTTATTCACGCCTCCACTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTTTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTGGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATCCCTCAGCTTCCCGAGTAGCTGGGACTGCAGGCGCCAGCAACCTCGCCCGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGAGGGTCTCGATCTCCTGACCT... |
Task1_train_32587 | Given this context: Chromosome 1 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GCTGCTTGCCCATTTTTATGGTTATTTCTTGATGGTACGCTAAACAAGGGGTGGGTTATTCACGCCTCCACTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTTTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTGGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATCCCTCAGCTTCCCGAGTAGCTGGGACTGCAGGCGCCAGCAACCTCGCCCGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGAGGGTCTCGATCTCCTGACCTCGTGATCTGCTCGC... | GCTGCTTGCCCATTTTTATGGTTATTTCTTGATGGTACGCTAAACAAGGGGTGGGTTATTCACGCCTCCACTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTTTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTGGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATCCCTCAGCTTCCCGAGTAGCTGGGACTGCAGGCGCCAGCAACCTCGCCCGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGAGGGTCTCGATCTCCTGACCTCGTGATCTGCTCGC... |
Task1_train_32588 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTCTTTCGGTACTCAACCACCAACTCCTAATCCTCCCTGGTCCCCCAAGTGGGCTAGGGGCTTCTTGGGAGTCCCTCGCACTGCTCTAAGCATCCAGGCAGAGTCATTATTCCGGGTGCCAGGTTGCTCTTTTTCCAGCAGCCTTCAGGGGACTCCTGGCTGGGCGGAGTCTGTAGAGGCGCGCGGAGTCCTGGGAGAGCGTCAGATGTATTTCCTTTCCCTTTTTTCGCTCGTGTCCCGCCGGGTGGCGCTCACCACCTCCCCGGAACACGCGAGTCTCCTGTCGCGGTTCCGGTCGGAATTACCCCGTGGAGCACGCC... | CTCTTTCGGTACTCAACCACCAACTCCTAATCCTCCCTGGTCCCCCAAGTGGGCTAGGGGCTTCTTGGGAGTCCCTCGCACTGCTCTAAGCATCCAGGCAGAGTCATTATTCCGGGTGCCAGGTTGCTCTTTTTCCAGCAGCCTTCAGGGGACTCCTGGCTGGGCGGAGTCTGTAGAGGCGCGCGGAGTCCTGGGAGAGCGTCAGATGTATTTCCTTTCCCTTTTTTCGCTCGTGTCCCGCCGGGTGGCGCTCACCACCTCCCCGGAACACGCGAGTCTCCTGTCGCGGTTCCGGTCGGAATTACCCCGTGGAGCACGCC... |
Task1_train_32589 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CGCCGGGTGGCGCTCACCACCTCCCCGGAACACGCGAGTCTCCTGTCGCGGTTCCGGTCGGAATTACCCCGTGGAGCACGCCGATATGGCTGCGCTGACACTGAGGGGTGTCCGGGAGCTGCTGAAGCGTGTGGACCTCGCGACGGTCCCGCGGAGACATCGATATAAGAAGAAATGGGTAAGGTCCGGCTGGGGGCGCAGGAGGGAAAAGTGAGGGTGGAAACTTCTCCAGTCTTTCCGTTTCCCGGCCCTCTAGAACGCCTAGCGTCTTTCCCAAGCACTCCACGGAACGTCCTTAGGCACCTCCCTCTCTCGTCTTT... | CGCCGGGTGGCGCTCACCACCTCCCCGGAACACGCGAGTCTCCTGTCGCGGTTCCGGTCGGAATTACCCCGTGGAGCACGCCGATATGGCTGCGCTGACACTGAGGGGTGTCCGGGAGCTGCTGAAGCGTGTGGACCTCGCGACGGTCCCGCGGAGACATCGATATAAGAAGAAATGGGTAAGGTCCGGCTGGGGGCGCAGGAGGGAAAAGTGAGGGTGGAAACTTCTCCAGTCTTTCCGTTTCCCGGCCCTCTAGAACGCCTAGCGTCTTTCCCAAGCACTCCACGGAACGTCCTTAGGCACCTCCCTCTCTCGTCTTT... |
Task1_train_32590 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AAAAGTGAGGGTGGAAACTTCTCCAGTCTTTCCGTTTCCCGGCCCTCTAGAACGCCTAGCGTCTTTCCCAAGCACTCCACGGAACGTCCTTAGGCACCTCCCTCTCTCGTCTTTTCCGTCACCGCCTCTGTCCGCACTCTATGTCCCGAGCGTTAGTGTCTTCCACTTGTTACGTCTGCAGTCTCCTGACTCCGCCCAAGTTGCGTCATCACCTTCGCCTTCATTCTTTTAGTGATGTCACTGTCTCTTGTTCCCCAGCTGTGTCCACCTACCTTTCTGTCCCCCACTCCCCCTTTTACTTCCCTCCCTCCCCTCCCCCT... | AAAAGTGAGGGTGGAAACTTCTCCAGTCTTTCCGTTTCCCGGCCCTCTAGAACGCCTAGCGTCTTTCCCAAGCACTCCACGGAACGTCCTTAGGCACCTCCCTCTCTCGTCTTTTCCGTCACCGCCTCTGTCCGCACTCTATGTCCCGAGCGTTAGTGTCTTCCACTTGTTACGTCTGCAGTCTCCTGACTCCGCCCAAGTTGCGTCATCACCTTCGCCTTCATTCTTTTAGTGATGTCACTGTCTCTTGTTCCCCAGCTGTGTCCACCTACCTTTCTGTCCCCCACTCCCCCTTTTACTTCCCTCCCTCCCCTCCCCCT... |
Task1_train_32591 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | CTTTCCGTTTCCCGGCCCTCTAGAACGCCTAGCGTCTTTCCCAAGCACTCCACGGAACGTCCTTAGGCACCTCCCTCTCTCGTCTTTTCCGTCACCGCCTCTGTCCGCACTCTATGTCCCGAGCGTTAGTGTCTTCCACTTGTTACGTCTGCAGTCTCCTGACTCCGCCCAAGTTGCGTCATCACCTTCGCCTTCATTCTTTTAGTGATGTCACTGTCTCTTGTTCCCCAGCTGTGTCCACCTACCTTTCTGTCCCCCACTCCCCCTTTTACTTCCCTCCCTCCCCTCCCCCTTTCCCTTGCCCATTCTTCCCCCACATG... | CTTTCCGTTTCCCGGCCCTCTAGAACGCCTAGCGTCTTTCCCAAGCACTCCACGGAACGTCCTTAGGCACCTCCCTCTCTCGTCTTTTCCGTCACCGCCTCTGTCCGCACTCTATGTCCCGAGCGTTAGTGTCTTCCACTTGTTACGTCTGCAGTCTCCTGACTCCGCCCAAGTTGCGTCATCACCTTCGCCTTCATTCTTTTAGTGATGTCACTGTCTCTTGTTCCCCAGCTGTGTCCACCTACCTTTCTGTCCCCCACTCCCCCTTTTACTTCCCTCCCTCCCCTCCCCCTTTCCCTTGCCCATTCTTCCCCCACATG... |
Task1_train_32592 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | TCCTCATTGATTTTCCAGCCCGGTCGCCCTCACCCCTCGGAAAATACCATAGCGACCTTGCCTGCACTCCTGGGTCTCCGCCGCCTTGCAGGAAAGGATTCAGCCCCTTCCTCAACCTCGAGCTGCCTCTGGCGACCGGGCAAGGTTACAGCGACCACCCTGTCCATACTGCCGGCCCAAACCCTGGCAAAAGGTGCAACGAATCCTCTCATCCTCTGGACTCTCCTTGCTTCTCCAGAGACCCTTTTTCTTGCCTCACTGGAAGCCCTGGAATTTCTTCTATGACCGGCACGCCCCCCTGCCCACCCCAGCCGATTCCC... | TCCTCATTGATTTTCCAGCCCGGTCGCCCTCACCCCTCGGAAAATACCATAGCGACCTTGCCTGCACTCCTGGGTCTCCGCCGCCTTGCAGGAAAGGATTCAGCCCCTTCCTCAACCTCGAGCTGCCTCTGGCGACCGGGCAAGGTTACAGCGACCACCCTGTCCATACTGCCGGCCCAAACCCTGGCAAAAGGTGCAACGAATCCTCTCATCCTCTGGACTCTCCTTGCTTCTCCAGAGACCCTTTTTCTTGCCTCACTGGAAGCCCTGGAATTTCTTCTATGACCGGCACGCCCCCCTGCCCACCCCAGCCGATTCCC... |
Task1_train_32593 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CCCTGCCCACCCCAGCCGATTCCCTCGCCACCTCCACCATCTCTTCCACCCCCACAACCTTCCTCGCACTCAGGGAGATGGTCTTTTGAGTCCTCTTCCCCACTCCTGGAAAGGACCTACTGCCGCTAGCCCTGCCACTCGGGTTCCCCACTCTCCAGCCCTTATTTTGAGCAGTTCAGCATTCCGGGGTCACCCCCTCTCTGTCAGCGGACACCTTATTGCAGCTGGATGAGTCCCTCCAGAATGCGGCGTCCCTGTCTTCAAGGCACGTACTGTGACCAGCACACTAATCTCTGTTACTCTAGCGGATGGCCTTCAGC... | CCCTGCCCACCCCAGCCGATTCCCTCGCCACCTCCACCATCTCTTCCACCCCCACAACCTTCCTCGCACTCAGGGAGATGGTCTTTTGAGTCCTCTTCCCCACTCCTGGAAAGGACCTACTGCCGCTAGCCCTGCCACTCGGGTTCCCCACTCTCCAGCCCTTATTTTGAGCAGTTCAGCATTCCGGGGTCACCCCCTCTCTGTCAGCGGACACCTTATTGCAGCTGGATGAGTCCCTCCAGAATGCGGCGTCCCTGTCTTCAAGGCACGTACTGTGACCAGCACACTAATCTCTGTTACTCTAGCGGATGGCCTTCAGC... |
Task1_train_32594 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | CCCACTCCTGGAAAGGACCTACTGCCGCTAGCCCTGCCACTCGGGTTCCCCACTCTCCAGCCCTTATTTTGAGCAGTTCAGCATTCCGGGGTCACCCCCTCTCTGTCAGCGGACACCTTATTGCAGCTGGATGAGTCCCTCCAGAATGCGGCGTCCCTGTCTTCAAGGCACGTACTGTGACCAGCACACTAATCTCTGTTACTCTAGCGGATGGCCTTCAGCTTTTGGAACCAGCCCGGCAACCTCCTTTCCCCTTGCTCATCAGTCCCCGGGAACGAGCCCAGTGACCTCCCCTCAGCTCACTCATGTACCCTTGGAAA... | CCCACTCCTGGAAAGGACCTACTGCCGCTAGCCCTGCCACTCGGGTTCCCCACTCTCCAGCCCTTATTTTGAGCAGTTCAGCATTCCGGGGTCACCCCCTCTCTGTCAGCGGACACCTTATTGCAGCTGGATGAGTCCCTCCAGAATGCGGCGTCCCTGTCTTCAAGGCACGTACTGTGACCAGCACACTAATCTCTGTTACTCTAGCGGATGGCCTTCAGCTTTTGGAACCAGCCCGGCAACCTCCTTTCCCCTTGCTCATCAGTCCCCGGGAACGAGCCCAGTGACCTCCCCTCAGCTCACTCATGTACCCTTGGAAA... |
Task1_train_32595 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | TCCCTAGTCAACACTCCCCAGCACACCCCTTCTGGCCAGCCCAAGCCCGCTAAGGCCCACACCTGTCCCCCACCTCCCTCCTGCCTCTCTGGTCCTTCTTGTATGCAGCCATACATCACAACTCCTTCAAATTCCAGCCCCAAAGAACTTCCCCCAGGGACTACCTTACTGACTGTGGTCCCTAGAGCTCTCAAAAGTGTTATCCCCACTTCTTTTCCCCTCTGCCTTCCTTGTGATCCTGTCTCGGCCAATAGTTATGCTCAGAGCAGCCGCCATGGACCCTCCATAGGGCCCCCCTGCAATACCCATATATGCTCTGT... | TCCCTAGTCAACACTCCCCAGCACACCCCTTCTGGCCAGCCCAAGCCCGCTAAGGCCCACACCTGTCCCCCACCTCCCTCCTGCCTCTCTGGTCCTTCTTGTATGCAGCCATACATCACAACTCCTTCAAATTCCAGCCCCAAAGAACTTCCCCCAGGGACTACCTTACTGACTGTGGTCCCTAGAGCTCTCAAAAGTGTTATCCCCACTTCTTTTCCCCTCTGCCTTCCTTGTGATCCTGTCTCGGCCAATAGTTATGCTCAGAGCAGCCGCCATGGACCCTCCATAGGGCCCCCCTGCAATACCCATATATGCTCTGT... |
Task1_train_32596 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTGGGACTACAGGTGCATGCCACCACGCCCGGCTAATTAAAAAATTTTTTTTGTGCAGGTGGGGTCTCACTATGTTTTCCAGACTGTAATAACTTTCCTATTGGAGTATAATACAGAAGTGACCAAATCATAAGTGTACTGTTTAAAGAATTATCTTATAGTTAGTCTGGGCAACATAGCAAAATGCTGTCCCTACAAAAATACAAAAATTAGGCCGGGCATGGTGGCTCATGCCTGTAATCCTAGCATTTCAGGAGGCCAAGGCGGGCAGATCATGAGGTCAGGAGATCGAGACCATCCTGGCTAGCACGGTGAAACCC... | CTGGGACTACAGGTGCATGCCACCACGCCCGGCTAATTAAAAAATTTTTTTTGTGCAGGTGGGGTCTCACTATGTTTTCCAGACTGTAATAACTTTCCTATTGGAGTATAATACAGAAGTGACCAAATCATAAGTGTACTGTTTAAAGAATTATCTTATAGTTAGTCTGGGCAACATAGCAAAATGCTGTCCCTACAAAAATACAAAAATTAGGCCGGGCATGGTGGCTCATGCCTGTAATCCTAGCATTTCAGGAGGCCAAGGCGGGCAGATCATGAGGTCAGGAGATCGAGACCATCCTGGCTAGCACGGTGAAACCC... |
Task1_train_32597 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCCGCCTCGGCCTTCCAAAGTGCTAGGATTACAGGCGTGAGCCACCATGCCCGACCCCGTCTTTTTTTTTGAGATGGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTACAACCTCCACCTCCCGGGTTCAAGTGATTCTCATACCTCAGCCTCCCGAGTAGCTGGGATTATAGACATGCACCCCCATGCTTGGCTAATTTTTGTATTTTTATTTGGCCGGGCTGGTCTGGAACTCCCAACCTCAGGTGATCCTCTGAAAG... | TCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCCGCCTCGGCCTTCCAAAGTGCTAGGATTACAGGCGTGAGCCACCATGCCCGACCCCGTCTTTTTTTTTGAGATGGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTACAACCTCCACCTCCCGGGTTCAAGTGATTCTCATACCTCAGCCTCCCGAGTAGCTGGGATTATAGACATGCACCCCCATGCTTGGCTAATTTTTGTATTTTTATTTGGCCGGGCTGGTCTGGAACTCCCAACCTCAGGTGATCCTCTGAAAG... |
Task1_train_32598 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | TCGATCCAGTCCATGAGCAATGCCATATAGCGCGGCGCAGAGAGCTTGGCGGGCCGCCGGTACTGGCGCTCGTCCTGCCAGCGGTACTCGTAGCGGGGCCCGCCGGCCATGACCGGGCAGCTGGTCTCACTGCAGCGCTCCGCCATAGTGCCGTAGATGAGGTTGATGCGGTTGAAGAAGTCCACCACGTGCACGGCGATCCAGTCGTCGATGTTCTCCCCGGGTGGTAGCCTCACCACACTGCGCAGGTCCAGGCCCGACTTGAGAGAGGCCTGTGCCTTCTTGTACAGCTCAAAGCGCTGTGTGCCCGGCTCAAAGCG... | TCGATCCAGTCCATGAGCAATGCCATATAGCGCGGCGCAGAGAGCTTGGCGGGCCGCCGGTACTGGCGCTCGTCCTGCCAGCGGTACTCGTAGCGGGGCCCGCCGGCCATGACCGGGCAGCTGGTCTCACTGCAGCGCTCCGCCATAGTGCCGTAGATGAGGTTGATGCGGTTGAAGAAGTCCACCACGTGCACGGCGATCCAGTCGTCGATGTTCTCCCCGGGTGGTAGCCTCACCACACTGCGCAGGTCCAGGCCCGACTTGAGAGAGGCCTGTGCCTTCTTGTACAGCTCAAAGCGCTGTGTGCCCGGCTCAAAGCG... |
Task1_train_32599 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GGGTGAGGTCTGGAGGACCCAGGGACATCTTGGCTATCCCTCTGGTGGACTTTCCTGGTCAATGCATTATAGGGGGCCCCTTCTTCCATAAAATTCCTTTCTGGAGGTGACATAAAACACCACTCCCTTCACTGTCATGTAGATGGGATGTTTTTCTTCTCTCTGTAGTGGGCCGGCTCCTCCTCAATAAAGAGCCTCACCAGGGGTTTCTGCTTAGTCGGGCATGGCACCTGCCTGGCCAGAGCTGCAAGCAGCCCTGGGGGCTGTACCAGGACCAGGGTCAACCCTGCTAGTGGCTACAGCTGCAACTGGGCCTGCCA... | GGGTGAGGTCTGGAGGACCCAGGGACATCTTGGCTATCCCTCTGGTGGACTTTCCTGGTCAATGCATTATAGGGGGCCCCTTCTTCCATAAAATTCCTTTCTGGAGGTGACATAAAACACCACTCCCTTCACTGTCATGTAGATGGGATGTTTTTCTTCTCTCTGTAGTGGGCCGGCTCCTCCTCAATAAAGAGCCTCACCAGGGGTTTCTGCTTAGTCGGGCATGGCACCTGCCTGGCCAGAGCTGCAAGCAGCCCTGGGGGCTGTACCAGGACCAGGGTCAACCCTGCTAGTGGCTACAGCTGCAACTGGGCCTGCCA... |
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