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_42800 | This sequence variant lies on Chromosome 13. Is it clinically significant, and what condition might it cause if any? | Benign | TTTCTAGCTTATTAATACTCTGTAGCTTTGTGATTGTCTCCTCACTGTCACTTGAAACATCAACAATCAGTGTCTTCATATTGCTGGCAAGAGGTGAATCCTTTTGGTGTTTATGTTTTGAGTTAGGTTCTATGGTATCAGTCCCTTCTAGAGACATAAAGTTCATTGTTTTATGTCTAGAATAGAACCTCCAACTGTTATCTTTTGAAATAGTCCCTTTTGGATAAAAGTTGAACATTTGTAAAGATTTCCTTGCCATCTCTGGTATCAGATTCAGTTGTATTTCAAGTGCTTTTGACTCTAAATGACTAGTAAGCTTA... | TTTCTAGCTTATTAATACTCTGTAGCTTTGTGATTGTCTCCTCACTGTCACTTGAAACATCAACAATCAGTGTCTTCATATTGCTGGCAAGAGGTGAATCCTTTTGGTGTTTATGTTTTGAGTTAGGTTCTATGGTATCAGTCCCTTCTAGAGACATAAAGTTCATTGTTTTATGTCTAGAATAGAACCTCCAACTGTTATCTTTTGAAATAGTCCCTTTTGGATAAAAGTTGAACATTTGTAAAGATTTCCTTGCCATCTCTGGTATCAGATTCAGTTGTATTTCAAGTGCTTTTGACTCTAAATGACTAGTAAGCTTA... |
Task1_train_42801 | A variant was discovered on Chromosome 13. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TGGAGTGTCTTTGTCTGTTTTGTTCCCTGAATCCAGATAAAGAGGAGGTGCTGACGGTATAGAAAGAAAAGTCCTTGACAGAACCACACATGCTTCATCTTTATCTTTGTGTACTTTTTTCTCCAGTTTGTTAATATTCAACACTAATTCCTTTGCATTAAGGATATGTGACATTGGTGAAATCCTTGCCTCTTGGCAGTGTATCCTGAACCTCATATCTATCGTTTTCACTTCATGCCTGTTTTCTTTCTGTGACCTATGTGGTTTTCCTTTTCTTACATCACCACTCCTTGCCTCTGCATCTGCTGTTTTCTCTGTAT... | TGGAGTGTCTTTGTCTGTTTTGTTCCCTGAATCCAGATAAAGAGGAGGTGCTGACGGTATAGAAAGAAAAGTCCTTGACAGAACCACACATGCTTCATCTTTATCTTTGTGTACTTTTTTCTCCAGTTTGTTAATATTCAACACTAATTCCTTTGCATTAAGGATATGTGACATTGGTGAAATCCTTGCCTCTTGGCAGTGTATCCTGAACCTCATATCTATCGTTTTCACTTCATGCCTGTTTTCTTTCTGTGACCTATGTGGTTTTCCTTTTCTTACATCACCACTCCTTGCCTCTGCATCTGCTGTTTTCTCTGTAT... |
Task1_train_42802 | Mutation context: Chromosome 13. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GCTATCCACCCCAAAAGACTTTGTATGTGCTATTTTCCCTGCATCAAATGATTTCTGCTGCCTTAGTTGCAAAGTAGCAGATTTTATTATTCCTTGTAAGTCTTCCTCTCCTTCTTTTCTTGTGTTCAATTCATAACAAGTTAGAGAAGACTCAGAAGGCAAATGTAGGAAGAGAACTGTTTCCTGTTTACTCTTGTGTCCATCCCTTTTCTCTTGCTCTGTGCCTACTCCATCTGCTTGCTGTTGCTCTTCAGTTTCTCCATCCCTGTTCCCTTGCTCCTCACCTTCTCCGTCCTCTTTCCCTTGCTCCTGGCCTTCTC... | GCTATCCACCCCAAAAGACTTTGTATGTGCTATTTTCCCTGCATCAAATGATTTCTGCTGCCTTAGTTGCAAAGTAGCAGATTTTATTATTCCTTGTAAGTCTTCCTCTCCTTCTTTTCTTGTGTTCAATTCATAACAAGTTAGAGAAGACTCAGAAGGCAAATGTAGGAAGAGAACTGTTTCCTGTTTACTCTTGTGTCCATCCCTTTTCTCTTGCTCTGTGCCTACTCCATCTGCTTGCTGTTGCTCTTCAGTTTCTCCATCCCTGTTCCCTTGCTCCTCACCTTCTCCGTCCTCTTTCCCTTGCTCCTGGCCTTCTC... |
Task1_train_42803 | This mutation occurs on Chromosome 13. Does this change lead to a known medical condition, or is it benign? | Benign | TCACCCTCACTGGGCACCCCATTTGCTTTTTTCCCTGTCTCTGATGATTTCTGGTGCCTTGGTTGTAAAATACCAGGTCTGATTATTCCTTGTTGGTCTTCCTCTCCTTCTATTCTTGTGTCCAATATATAATGGGTTAGAGAAGAATTGGAAGGCAAATATAGGAACAGAACTCTTTCCTGTTCATTCTTGTCTCCATCCATTTTCCCTTGCTCTATGCCTACTCCATCTGCTTTCTGTTGCTCTTCAACTTCGTGATCCATTTTCCCTTGCTCTTTGTCTTCTCTATCAACCTTTTCTTGTCCTGCACCTCTTCTGTC... | TCACCCTCACTGGGCACCCCATTTGCTTTTTTCCCTGTCTCTGATGATTTCTGGTGCCTTGGTTGTAAAATACCAGGTCTGATTATTCCTTGTTGGTCTTCCTCTCCTTCTATTCTTGTGTCCAATATATAATGGGTTAGAGAAGAATTGGAAGGCAAATATAGGAACAGAACTCTTTCCTGTTCATTCTTGTCTCCATCCATTTTCCCTTGCTCTATGCCTACTCCATCTGCTTTCTGTTGCTCTTCAACTTCGTGATCCATTTTCCCTTGCTCTTTGTCTTCTCTATCAACCTTTTCTTGTCCTGCACCTCTTCTGTC... |
Task1_train_42804 | This alteration on Chromosome 13 may affect genome function. Does it lead to a disease or is it benign? | Benign | GCTTTCAGACCTTTGTCTTCTGGATGCATTATGTCTTTCTTAGCTGATATTTTTACTTCATCGTCTTCTTTCTGTTGCATGTAATCTTTTGCTTTTTGTACTTTGATTGTGATATCACCCTTACTGGCCACTCCATCTGCTTTTTCCCCTGCCTCTGATGATTTTTGGTGTGATAGTTCTGGAAGATAGTATCTTGTTATTTCAGTGACATACTCTGCTTTTTCTCTCCTTGTATCCAGTTGTAAATGAGAAGGAGAAGGAATGGAAGCGCAGGCATTTGTCAGAAGCACACTTGGTTCACCTTTAATATGTTCTATCCT... | GCTTTCAGACCTTTGTCTTCTGGATGCATTATGTCTTTCTTAGCTGATATTTTTACTTCATCGTCTTCTTTCTGTTGCATGTAATCTTTTGCTTTTTGTACTTTGATTGTGATATCACCCTTACTGGCCACTCCATCTGCTTTTTCCCCTGCCTCTGATGATTTTTGGTGTGATAGTTCTGGAAGATAGTATCTTGTTATTTCAGTGACATACTCTGCTTTTTCTCTCCTTGTATCCAGTTGTAAATGAGAAGGAGAAGGAATGGAAGCGCAGGCATTTGTCAGAAGCACACTTGGTTCACCTTTAATATGTTCTATCCT... |
Task1_train_42805 | Given this context: Chromosome 13 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CCTGCCTCTGATGATTTTTGGTGTGATAGTTCTGGAAGATAGTATCTTGTTATTTCAGTGACATACTCTGCTTTTTCTCTCCTTGTATCCAGTTGTAAATGAGAAGGAGAAGGAATGGAAGCGCAGGCATTTGTCAGAAGCACACTTGGTTCACCTTTAATATGTTCTATCCTTTTCTCTTGCTCTTTAATGTCCAACTGAATTCCCTGTGAAATTGATGATTTCATTTTCTTCAAAGCCCTAATTTTTTCCATTTTTTGCCTCTGTTCTTTTTGCAATATAGATTCTAGGGCCTTTTTTACACTGTTTGAGATATTATC... | CCTGCCTCTGATGATTTTTGGTGTGATAGTTCTGGAAGATAGTATCTTGTTATTTCAGTGACATACTCTGCTTTTTCTCTCCTTGTATCCAGTTGTAAATGAGAAGGAGAAGGAATGGAAGCGCAGGCATTTGTCAGAAGCACACTTGGTTCACCTTTAATATGTTCTATCCTTTTCTCTTGCTCTTTAATGTCCAACTGAATTCCCTGTGAAATTGATGATTTCATTTTCTTCAAAGCCCTAATTTTTTCCATTTTTTGCCTCTGTTCTTTTTGCAATATAGATTCTAGGGCCTTTTTTACACTGTTTGAGATATTATC... |
Task1_train_42806 | A variant on Chromosome 13 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GAAATTCCTTTATACTGAGTATATGTGACAGTGATGACTTCCTTGGCTTCAAAATGATGTTAGGGCTTTTTATTCTTTTCATATCCATTGCTTTTACTCTATCATTCTTTCCCTGTGATATGTGTTGTTTTGTACTTTTAACATTACTTGAGATCACCCCATCAATTGTTTCTTTATTCAATTTGAAGTGAGGTAAAGAAAGAATAGACTCACATATTTTTGCTGCAACCAAATCTATTTCACTCATTCTATGTTTCACATTGACCATTTTGTCTGTCATGTTCCACTGCATTTCTAGTCTGTTACTTGAGGCACCACAG... | GAAATTCCTTTATACTGAGTATATGTGACAGTGATGACTTCCTTGGCTTCAAAATGATGTTAGGGCTTTTTATTCTTTTCATATCCATTGCTTTTACTCTATCATTCTTTCCCTGTGATATGTGTTGTTTTGTACTTTTAACATTACTTGAGATCACCCCATCAATTGTTTCTTTATTCAATTTGAAGTGAGGTAAAGAAAGAATAGACTCACATATTTTTGCTGCAACCAAATCTATTTCACTCATTCTATGTTTCACATTGACCATTTTGTCTGTCATGTTCCACTGCATTTCTAGTCTGTTACTTGAGGCACCACAG... |
Task1_train_42807 | A genomic change on Chromosome 13 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TCCTTTTGGAAATAAGAGACTTGCATATTTTATAGTTTTATGGTATGATCCTAAAGGCAGCATTGAATCTTGTTTTTTCATCTGCCTTGGAGAAATCAAGGGCACAATCCATTCTAGTCTATTCTTAGTTATAGTGCTTAGCTGATCTGCAGAAAACAAGTCTAGTCCTGGTGTCCGGCTTGATAAATTACCTCCTTCTGATAATGCTTCCTTTTCCTGAGGCATTAAATGTTGCAGGAGACAGGGATACTTTTGAGGGCAAGATATATGCTCCCAAAAGTTCTCATAGGAAATTGGTAGGTACTGCCATTTTTGGCCTG... | TCCTTTTGGAAATAAGAGACTTGCATATTTTATAGTTTTATGGTATGATCCTAAAGGCAGCATTGAATCTTGTTTTTTCATCTGCCTTGGAGAAATCAAGGGCACAATCCATTCTAGTCTATTCTTAGTTATAGTGCTTAGCTGATCTGCAGAAAACAAGTCTAGTCCTGGTGTCCGGCTTGATAAATTACCTCCTTCTGATAATGCTTCCTTTTCCTGAGGCATTAAATGTTGCAGGAGACAGGGATACTTTTGAGGGCAAGATATATGCTCCCAAAAGTTCTCATAGGAAATTGGTAGGTACTGCCATTTTTGGCCTG... |
Task1_train_42808 | Here’s a variant located on Chromosome 13. What is the predicted biological effect — harmless or disease-causing? | Benign | TGCTGTCTTTGCCTTATCTTTATGTCTTATGATTTTAGGAGAAATAGATGTGTAGGGATTAGGATAACTCCAGATAGTTCCTGAGACACACAGCTCTTGCTGTTTCTTTGGCAGGGCAAATGTCTTGGGATCTGCCCTTGTTTTCCAGTCTGCAGTTTTAAATTCTTTCTTGTTTTCAATTTGAAGTGGATGTATCTTAGAGAAAAAAACAGATTCTGGATTAAACTCTTCTGCAACATTTATCTTTGCTTCTTGATCTATTAAATCAACTTCTGCTTCTGTCTTCTGGGCTTTAAAGTTCTGTTTCTGCTCCTTATTAT... | TGCTGTCTTTGCCTTATCTTTATGTCTTATGATTTTAGGAGAAATAGATGTGTAGGGATTAGGATAACTCCAGATAGTTCCTGAGACACACAGCTCTTGCTGTTTCTTTGGCAGGGCAAATGTCTTGGGATCTGCCCTTGTTTTCCAGTCTGCAGTTTTAAATTCTTTCTTGTTTTCAATTTGAAGTGGATGTATCTTAGAGAAAAAAACAGATTCTGGATTAAACTCTTCTGCAACATTTATCTTTGCTTCTTGATCTATTAAATCAACTTCTGCTTCTGTCTTCTGGGCTTTAAAGTTCTGTTTCTGCTCCTTATTAT... |
Task1_train_42809 | A variant on Chromosome 13 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CATTTTTTTCTGAATTCCCTTTGTAAATCTGACTTTTTGAGAAAAAAGTTTCTCCCAAAAGCACATCCTCTGATTTACCAAGATGACGATCCTTTCTAAGATATGTGTTTGCCATGAAGTTTTCTGCATAGAATGGATCCATTTCTGTAAGATGTTCTTGCTTCTCTTCCCCACTTTCTCTATCATGTAGTTTTGCTCCCTTTACCAAGTTGGAAGTTCTTCTCTTGTCAATGGGATCAGAATACCTTGCTATCCCTTCAGCTAGTGACTCTATTTGTGTTGGTTGTGTATGACTTAACCCTGATATTCTCATGTCTATC... | CATTTTTTTCTGAATTCCCTTTGTAAATCTGACTTTTTGAGAAAAAAGTTTCTCCCAAAAGCACATCCTCTGATTTACCAAGATGACGATCCTTTCTAAGATATGTGTTTGCCATGAAGTTTTCTGCATAGAATGGATCCATTTCTGTAAGATGTTCTTGCTTCTCTTCCCCACTTTCTCTATCATGTAGTTTTGCTCCCTTTACCAAGTTGGAAGTTCTTCTCTTGTCAATGGGATCAGAATACCTTGCTATCCCTTCAGCTAGTGACTCTATTTGTGTTGGTTGTGTATGACTTAACCCTGATATTCTCATGTCTATC... |
Task1_train_42810 | This sequence variant lies on Chromosome 13. Is it clinically significant, and what condition might it cause if any? | Benign | ACCCCCTTTTTGCCTTGATGCAGTTCTTTCATTTTGGTTGTCAAGTTACAGCTCAGTTCTTTTCTACGTTTCGGACCAGCACCAGCCCTGATATTGAGCATGTATGAAATTGATGGCTTCTTTGCCTTTATAATTCCACATTTGGGATTCACTAAAGTTTTCATGTCTGAAAATTGTTTTAAGTTTCTCGTCGTTTTAGGTGTAGATAAAGCAGGCATGCAGGAACCAAAAATCGCTGTCTCTTTCTTTTCAGTACCACCAGCCTGTTCCTTTTGATGGCTAGAATCAGATGAGATACCACCTTCTCTTGCATAAAATAT... | ACCCCCTTTTTGCCTTGATGCAGTTCTTTCATTTTGGTTGTCAAGTTACAGCTCAGTTCTTTTCTACGTTTCGGACCAGCACCAGCCCTGATATTGAGCATGTATGAAATTGATGGCTTCTTTGCCTTTATAATTCCACATTTGGGATTCACTAAAGTTTTCATGTCTGAAAATTGTTTTAAGTTTCTCGTCGTTTTAGGTGTAGATAAAGCAGGCATGCAGGAACCAAAAATCGCTGTCTCTTTCTTTTCAGTACCACCAGCCTGTTCCTTTTGATGGCTAGAATCAGATGAGATACCACCTTCTCTTGCATAAAATAT... |
Task1_train_42811 | With a mutation on Chromosome 13, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TAGGTGTAGATAAAGCAGGCATGCAGGAACCAAAAATCGCTGTCTCTTTCTTTTCAGTACCACCAGCCTGTTCCTTTTGATGGCTAGAATCAGATGAGATACCACCTTCTCTTGCATAAAATATGATTTCATCAACCTTTGCTTCCCCAGACTTTAGAGGTGAAAACCTAACATGACTCTCTACCTTTTCAAATGGAAATTGATCCAGTGTAGGGCATGAAGTAGACTTCAAAATAGTTTGTGTAAAATGTGTTTGTGGTTGTACCTGAATATTTGTACTTCCTGGTTGGTTCAGTTCCTCATCTGATTTGACAAGCTCA... | TAGGTGTAGATAAAGCAGGCATGCAGGAACCAAAAATCGCTGTCTCTTTCTTTTCAGTACCACCAGCCTGTTCCTTTTGATGGCTAGAATCAGATGAGATACCACCTTCTCTTGCATAAAATATGATTTCATCAACCTTTGCTTCCCCAGACTTTAGAGGTGAAAACCTAACATGACTCTCTACCTTTTCAAATGGAAATTGATCCAGTGTAGGGCATGAAGTAGACTTCAAAATAGTTTGTGTAAAATGTGTTTGTGGTTGTACCTGAATATTTGTACTTCCTGGTTGGTTCAGTTCCTCATCTGATTTGACAAGCTCA... |
Task1_train_42812 | This variant is located on Chromosome 13. Evaluate its biological effect and specify any disease association. | Benign | TGTCATGGGATATGCTATTCTTAGCAAAGACATCAGTGTATGTCTTATCTGCTGTTTCTCCTTGCTTTAATTGAGACGCAGGGAGACAGAACTCTCTCTGCAATCTGCTATGCATTGGAGAGCAAAGGGTATTTAGACATTCAGGTACCAATCCTTTAGTTTGGTTTATCTTTTTAAACTTAGTCTTAAAGTCTAATTCTGATTTCTTTCTGTGGCTTGTGACACTGACTGTCTCTGAGATTGATGGCTTCACAGCCTTTGTATTTACACATTTGGGCTTCGCTGTACTTGTTGTGAGTGCAAATGTTACTCTCTTTTTC... | TGTCATGGGATATGCTATTCTTAGCAAAGACATCAGTGTATGTCTTATCTGCTGTTTCTCCTTGCTTTAATTGAGACGCAGGGAGACAGAACTCTCTCTGCAATCTGCTATGCATTGGAGAGCAAAGGGTATTTAGACATTCAGGTACCAATCCTTTAGTTTGGTTTATCTTTTTAAACTTAGTCTTAAAGTCTAATTCTGATTTCTTTCTGTGGCTTGTGACACTGACTGTCTCTGAGATTGATGGCTTCACAGCCTTTGTATTTACACATTTGGGCTTCGCTGTACTTGTTGTGAGTGCAAATGTTACTCTCTTTTTC... |
Task1_train_42813 | Assess the clinical impact of this variant found on Chromosome 13. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACTACAGGGCCAGGTGCAGTGGCTCACGACTGTAATCCCAGCACTTTGAGAGGCCCAGGTAGGTGGATCACCTGAGGTCAGGGGTTCGAGACCAGCCTGGCCAACATGGTGAAACCGCATCTCTACTAGAAACACAAAAAATTAGCCAGGTGTGATGGTGGGTGCCTGTAATCCCAGCTTCTATGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGGTCATGCCATTGCTCTCCAGCCTGGGCAAAAAGAGCAAAACTCTGTCTAAAAAAAAAAAAAAAAAAAAAACAAAAAAA... | ACTACAGGGCCAGGTGCAGTGGCTCACGACTGTAATCCCAGCACTTTGAGAGGCCCAGGTAGGTGGATCACCTGAGGTCAGGGGTTCGAGACCAGCCTGGCCAACATGGTGAAACCGCATCTCTACTAGAAACACAAAAAATTAGCCAGGTGTGATGGTGGGTGCCTGTAATCCCAGCTTCTATGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGGTCATGCCATTGCTCTCCAGCCTGGGCAAAAAGAGCAAAACTCTGTCTAAAAAAAAAAAAAAAAAAAAAACAAAAAAA... |
Task1_train_42814 | A mutation is present on Chromosome 13. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CACAAAAAATTAGCCAGGTGTGATGGTGGGTGCCTGTAATCCCAGCTTCTATGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGGTCATGCCATTGCTCTCCAGCCTGGGCAAAAAGAGCAAAACTCTGTCTAAAAAAAAAAAAAAAAAAAAAACAAAAAAACAAAAAGAGGCAGAACTATGATATAAAGCTAGACCTTTTTTAACTTCAAAATTTATGTTTTTTCACCATAATATGCTGCTGCCACAGGAGCCATATCTTTTCTCTAATCCTTTTTCTTCAACACCACCCCCT... | CACAAAAAATTAGCCAGGTGTGATGGTGGGTGCCTGTAATCCCAGCTTCTATGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGGTCATGCCATTGCTCTCCAGCCTGGGCAAAAAGAGCAAAACTCTGTCTAAAAAAAAAAAAAAAAAAAAAACAAAAAAACAAAAAGAGGCAGAACTATGATATAAAGCTAGACCTTTTTTAACTTCAAAATTTATGTTTTTTCACCATAATATGCTGCTGCCACAGGAGCCATATCTTTTCTCTAATCCTTTTTCTTCAACACCACCCCCT... |
Task1_train_42815 | Located on Chromosome 13, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAGACAAAAGTGATATGATTTACTATTTTGATGGTCTGTTATACAAACAGGTTCTTAAAGTGTCTAAGGTACTTTTCTCAATAAGTAAATCATCAATAACAGCAAAAATAAACAAGGAACTGCTATTCTTTTTTTTTTTTTTTTTAAGAATTATTAAGGAGGAAAAGTAGGCTGGGTTCTTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGTCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTTGTGGCGCG... | AAGACAAAAGTGATATGATTTACTATTTTGATGGTCTGTTATACAAACAGGTTCTTAAAGTGTCTAAGGTACTTTTCTCAATAAGTAAATCATCAATAACAGCAAAAATAAACAAGGAACTGCTATTCTTTTTTTTTTTTTTTTTAAGAATTATTAAGGAGGAAAAGTAGGCTGGGTTCTTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGTCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTTGTGGCGCG... |
Task1_train_42816 | A variant has been detected on Chromosome 13. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CACACTAAGGTGTTTCTGATTAAATACATTACCCCTTGGGATTTACTTTCATTTTTTAACGAAAGGAAGTCTTCAAAGCAATTCTGATCATTTAAGTTTTTATAAGTACTAATATTTTTAAATTCTATAAACGAATCTTGAAAGGTAGAAGTTCAGTCATTATTGTGTATCAGTAGGAGAGGTTTTTGTGGGAAGGAGCCCTTTTGTATGACCTTTAGTTCCTCTAGGTACCTACTTCTTGCTTTATCTGTGAGTATGTTCTGACTCACACAAAACAAGCTTTCGCCCACACTAGAAACAACCCACAAAACATACATACA... | CACACTAAGGTGTTTCTGATTAAATACATTACCCCTTGGGATTTACTTTCATTTTTTAACGAAAGGAAGTCTTCAAAGCAATTCTGATCATTTAAGTTTTTATAAGTACTAATATTTTTAAATTCTATAAACGAATCTTGAAAGGTAGAAGTTCAGTCATTATTGTGTATCAGTAGGAGAGGTTTTTGTGGGAAGGAGCCCTTTTGTATGACCTTTAGTTCCTCTAGGTACCTACTTCTTGCTTTATCTGTGAGTATGTTCTGACTCACACAAAACAAGCTTTCGCCCACACTAGAAACAACCCACAAAACATACATACA... |
Task1_train_42817 | A genomic variant on Chromosome 13 is under review. What is the biological outcome — benign or pathogenic? | Benign | AAGACTTTGAGCAAAAAAGAGGCAGTCAGTATTTTCTTTCTGGGGACTTGCATGACTTCAGAATGAATGGGCCTATTTAGAATGACATATTCAGAAATAGGATGAATGTGATTGATGAAGGGCTAAGGATTTTGATCCTGTCTTCAGTGTTTGCAGCTGTTATGGATTGATTATGTCTCCCTTTCCCCCAAATTCATATGTTGAAGTCCTAACACTCCGCACCTCAGGATGTGACATTATGTGGGAACAGGGTCATTGCAGATATAATTAGTTAAGATGAGTTCATTAGAGGAGGCCCTTATCCAATGACTGGTGTCCTT... | AAGACTTTGAGCAAAAAAGAGGCAGTCAGTATTTTCTTTCTGGGGACTTGCATGACTTCAGAATGAATGGGCCTATTTAGAATGACATATTCAGAAATAGGATGAATGTGATTGATGAAGGGCTAAGGATTTTGATCCTGTCTTCAGTGTTTGCAGCTGTTATGGATTGATTATGTCTCCCTTTCCCCCAAATTCATATGTTGAAGTCCTAACACTCCGCACCTCAGGATGTGACATTATGTGGGAACAGGGTCATTGCAGATATAATTAGTTAAGATGAGTTCATTAGAGGAGGCCCTTATCCAATGACTGGTGTCCTT... |
Task1_train_42818 | Given a variant located on Chromosome 13, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGTGAAAAATTCCATTAATGACCTCCACGTTTTATGATGTGTAGAGCAAAATCTCAGTCTCCCTGAGTAAGGCCTGCTCCATGTGGACACCTGGCTTTCTCCCTTGTCTACCTCCCTCAGTGGAGAGTCCACCTGCTGGTAGTGCACTCCTTAGGTGCCTGTCTCTGGCTGTCCTGTGCCACCTGCACAGAGTCATGCATGAGCTCCACTGTGGGAAGTCTCTAGAGATGAGCTGAGCTTACCCTACACCAACTGAAAGAGTCTATCTAAGTCCTGAAGATCACAAGTCATCCTCATATTCCCATGAATGTGAATGGAAG... | TGTGAAAAATTCCATTAATGACCTCCACGTTTTATGATGTGTAGAGCAAAATCTCAGTCTCCCTGAGTAAGGCCTGCTCCATGTGGACACCTGGCTTTCTCCCTTGTCTACCTCCCTCAGTGGAGAGTCCACCTGCTGGTAGTGCACTCCTTAGGTGCCTGTCTCTGGCTGTCCTGTGCCACCTGCACAGAGTCATGCATGAGCTCCACTGTGGGAAGTCTCTAGAGATGAGCTGAGCTTACCCTACACCAACTGAAAGAGTCTATCTAAGTCCTGAAGATCACAAGTCATCCTCATATTCCCATGAATGTGAATGGAAG... |
Task1_train_42819 | A sequence alteration has been identified on Chromosome 13. Is it disease-inducing or harmless? | Benign | TTTGTACTATATAACCACCAAATTCTGCAATTCTGTTCTCCAGGTCAGGCTTTGGCTGGCTATCTGTTCCACTCATAACACAAAACTCTACATCTTCAAATATATTAGAAATTTTGTTAACGTTAGTAAGGTTAGGTGCTTTTAAGTGCTCAATAATTCCAATAACTTTCTTCATCTTTGGGGCAGCTTTCCGCTTTTTTTCTTGTGGTTCATCATCACCACCTATATAAAGGTGTTTAGATGCGAGCTTACCAGATGCCTTCCCCCTAAGTTGTTCTAGGTCGTCCAGGGTCATGCACTCATGCCACTCCTTGTCATCT... | TTTGTACTATATAACCACCAAATTCTGCAATTCTGTTCTCCAGGTCAGGCTTTGGCTGGCTATCTGTTCCACTCATAACACAAAACTCTACATCTTCAAATATATTAGAAATTTTGTTAACGTTAGTAAGGTTAGGTGCTTTTAAGTGCTCAATAATTCCAATAACTTTCTTCATCTTTGGGGCAGCTTTCCGCTTTTTTTCTTGTGGTTCATCATCACCACCTATATAAAGGTGTTTAGATGCGAGCTTACCAGATGCCTTCCCCCTAAGTTGTTCTAGGTCGTCCAGGGTCATGCACTCATGCCACTCCTTGTCATCT... |
Task1_train_42820 | A mutation is present on Chromosome 13. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AAAAAAAACCTCTAAGTTTTTAATATGAGCAAAGAACCTGAACAGACATTTTTCCAAAGAAGATATACAATTTTGTCCAACAGGTATATGAAAAGGTACTCAACATCAGAGAAATTTAAATTTAAAGCACAACAAAATACCACCTCACACCTGTAAGGAAGACAATTATCAAAAAGACAAGAGATAACTAGTGTTGGTGAGGGTGTGTAGAAAAGGGACCCCTTGAACACTGTTTGTGGGGATGCAAAGTGGTATAGTTGCTACGGAAACAAGTATGGAGTTTCCTCAAAAAATTAAAAAATAGAACTACCACATGATCC... | AAAAAAAACCTCTAAGTTTTTAATATGAGCAAAGAACCTGAACAGACATTTTTCCAAAGAAGATATACAATTTTGTCCAACAGGTATATGAAAAGGTACTCAACATCAGAGAAATTTAAATTTAAAGCACAACAAAATACCACCTCACACCTGTAAGGAAGACAATTATCAAAAAGACAAGAGATAACTAGTGTTGGTGAGGGTGTGTAGAAAAGGGACCCCTTGAACACTGTTTGTGGGGATGCAAAGTGGTATAGTTGCTACGGAAACAAGTATGGAGTTTCCTCAAAAAATTAAAAAATAGAACTACCACATGATCC... |
Task1_train_42821 | This sequence change occurs on Chromosome 13. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGAGTGTGGTGTCCCGGAGGAGAGGGGAGAAAGTGCTCCATGGAAGAAGAGAAACCGACTCAGTCAAATAACGCCGGGGTGGGGATGGGTCAAGAGAAACAAATGTGAGAGTTGAACATTGGATTTAGAAATGTGCACACTGCTAGCCAGGGGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCACGAGGTCAGGAGATCTAGACCAACCTGTCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCTGGGTGAGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGG... | AGAGTGTGGTGTCCCGGAGGAGAGGGGAGAAAGTGCTCCATGGAAGAAGAGAAACCGACTCAGTCAAATAACGCCGGGGTGGGGATGGGTCAAGAGAAACAAATGTGAGAGTTGAACATTGGATTTAGAAATGTGCACACTGCTAGCCAGGGGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCACGAGGTCAGGAGATCTAGACCAACCTGTCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCTGGGTGAGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGG... |
Task1_train_42822 | A sequence alteration has been identified on Chromosome 13. Is it disease-inducing or harmless? | Benign | CAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGACTACAAGTGCCCGCCACCACTCCCGGCTAATTTTTGTATTTTTGGTGGAGACAGGGTTTCACCATGTTGGCCAGGATGGTCTCTATCTTTTGACCTCATGATCCGACTACCTCGGCTTCCCAAAGAGCTGGGATTACAGGTGTGAGCCACTGCACCCAGCCCATTTCACATCATTTAAATAATCACGCTTACCCATTTCCGACAGTAAGCTTTCATATGCCACTAACTATTAATAGTTAATTGGCCAGGTCTCCTG... | CAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGACTACAAGTGCCCGCCACCACTCCCGGCTAATTTTTGTATTTTTGGTGGAGACAGGGTTTCACCATGTTGGCCAGGATGGTCTCTATCTTTTGACCTCATGATCCGACTACCTCGGCTTCCCAAAGAGCTGGGATTACAGGTGTGAGCCACTGCACCCAGCCCATTTCACATCATTTAAATAATCACGCTTACCCATTTCCGACAGTAAGCTTTCATATGCCACTAACTATTAATAGTTAATTGGCCAGGTCTCCTG... |
Task1_train_42823 | This sequence change occurs on Chromosome 13. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTCCCGAATTGAGCATTCACCTTTCCCTCTCATCTCCCCGACCCCAAACACCATTCAAAGTTTAGACAGCCAGAATGCACCACCAGCTGCATTCTGCATCAGCTCTCTCTCCTCATGGATATTTGATCAGAACGGGAAGAACAATACCAGGCACCCTCCTATCCAATTGTTCTTGAGAAGACCTGTGTTTTTTGTCTTTCCCTTGTTTTCTCCAAAGCACTGATTGTAAATCCTGGCTGCACATTCAAATCACCTGGACAACTCTGAAAAATGTCCGTCCCTGCCTCCTAGCCATCTCATGTTTCACTTCAACGGGTCTG... | CTCCCGAATTGAGCATTCACCTTTCCCTCTCATCTCCCCGACCCCAAACACCATTCAAAGTTTAGACAGCCAGAATGCACCACCAGCTGCATTCTGCATCAGCTCTCTCTCCTCATGGATATTTGATCAGAACGGGAAGAACAATACCAGGCACCCTCCTATCCAATTGTTCTTGAGAAGACCTGTGTTTTTTGTCTTTCCCTTGTTTTCTCCAAAGCACTGATTGTAAATCCTGGCTGCACATTCAAATCACCTGGACAACTCTGAAAAATGTCCGTCCCTGCCTCCTAGCCATCTCATGTTTCACTTCAACGGGTCTG... |
Task1_train_42824 | A variant affecting Chromosome 13 has been observed. Determine if it's benign or associated with disease. | Benign | AAAGAGTCTACACAAAAATATTTGCTTTCATGTGCTTGAGTAAAGAATTTAGTATCTAAGAAGCATAACACCTTTAACGTTTAAAACAATGGTTAATATAATTTATAGGAAAAATTTTTTAATATTCTGTTAAAAACAGCAATAAAAGAAAGAAGATGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACAAGGTCAGGAGATCGAGACCTTCCTGGCTAACAGGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCTGGCATGGTGGCGGGTGCCTGTAGT... | AAAGAGTCTACACAAAAATATTTGCTTTCATGTGCTTGAGTAAAGAATTTAGTATCTAAGAAGCATAACACCTTTAACGTTTAAAACAATGGTTAATATAATTTATAGGAAAAATTTTTTAATATTCTGTTAAAAACAGCAATAAAAGAAAGAAGATGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACAAGGTCAGGAGATCGAGACCTTCCTGGCTAACAGGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCTGGCATGGTGGCGGGTGCCTGTAGT... |
Task1_train_42825 | A variant was discovered on Chromosome 13. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AGGAGATCGAGACCTTCCTGGCTAACAGGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCTGGCATGGTGGCGGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGGAGGAGAATGGCGTGAACCAGTGAACCCGGGAGGTGGAGCTTGCAGTGAGCTGAGATGACGCCACTGCACACCAGCCTGGGCGACAGAGTAAGACTCTGTCTCAAAAAAAAAAAAAAGAAGATATGCAAGAAAGATAATCATACAAGAAGGTAATTATTATTCTTTAATAATTACTGGAGATGCAAATATATTCTACACAGAT... | AGGAGATCGAGACCTTCCTGGCTAACAGGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCTGGCATGGTGGCGGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGGAGGAGAATGGCGTGAACCAGTGAACCCGGGAGGTGGAGCTTGCAGTGAGCTGAGATGACGCCACTGCACACCAGCCTGGGCGACAGAGTAAGACTCTGTCTCAAAAAAAAAAAAAAGAAGATATGCAAGAAAGATAATCATACAAGAAGGTAATTATTATTCTTTAATAATTACTGGAGATGCAAATATATTCTACACAGAT... |
Task1_train_42826 | A mutation on Chromosome 13 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TTGAAGCTATTTCAGTGTTATGGTACATCTAACAGCTGATTTTGGAAGGAGGTAAGCCAAAATGTTATTGATGGCATGAAAAGTGAGACAAATTTTAAAATTAGGCAGATTCAGTTTTTAAGTGATTTTCTTGTATACCCATACATCATCTGCACATTAAGCACTTTTCTCTAATTAAGCCAGGGAAAATACAGAGTAATGATAATATCTGTGAGGTCAGCTGTGATCAGAAGTGCCCACAGGCTGCATCTCTTAAAAACAGTCCATGGCACCTCAAGGGACACTGCAAAGACAGTGGCCGGGAATGTAATTGAGCTTTA... | TTGAAGCTATTTCAGTGTTATGGTACATCTAACAGCTGATTTTGGAAGGAGGTAAGCCAAAATGTTATTGATGGCATGAAAAGTGAGACAAATTTTAAAATTAGGCAGATTCAGTTTTTAAGTGATTTTCTTGTATACCCATACATCATCTGCACATTAAGCACTTTTCTCTAATTAAGCCAGGGAAAATACAGAGTAATGATAATATCTGTGAGGTCAGCTGTGATCAGAAGTGCCCACAGGCTGCATCTCTTAAAAACAGTCCATGGCACCTCAAGGGACACTGCAAAGACAGTGGCCGGGAATGTAATTGAGCTTTA... |
Task1_train_42827 | Here is a variant on Chromosome 13. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CCAGCACGGGCCATAATTTGAAAATCCGCATTAGTGTGTTTCCTGCATTGTGTGTTTAATGTGTGTCTCCACGTCTAAGCTGTAAGCTCCATGAGAGTCCATCGGTTTCATTTCCAGTTGTATACACACAGCACCTCGCACACAGCCTGGCACAGCATAGGCACGGGATAAGTGTTTGATGAGCGAATGAATGAATGAGCTATGGTAAACGTGCAGTGAGCAAACTACATGGGACGGTATCCATGTCCTCATTCTCATAGACATTTATCCTCACCTGGCAGTTCTCTGACTTGCAAACTCCCGTGCTCTTTTCCAAGCAG... | CCAGCACGGGCCATAATTTGAAAATCCGCATTAGTGTGTTTCCTGCATTGTGTGTTTAATGTGTGTCTCCACGTCTAAGCTGTAAGCTCCATGAGAGTCCATCGGTTTCATTTCCAGTTGTATACACACAGCACCTCGCACACAGCCTGGCACAGCATAGGCACGGGATAAGTGTTTGATGAGCGAATGAATGAATGAGCTATGGTAAACGTGCAGTGAGCAAACTACATGGGACGGTATCCATGTCCTCATTCTCATAGACATTTATCCTCACCTGGCAGTTCTCTGACTTGCAAACTCCCGTGCTCTTTTCCAAGCAG... |
Task1_train_42828 | An alteration has been detected on Chromosome 13. Is it pathogenic, and if so, what disease is involved? | Benign | GTCCGTGGGGCTGATGCCCTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTGATGCCGTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTGATGCCCTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTCATGCCCTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTGATGCCCTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTGATGCCCTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTGATGCCGTGCATCTGCGTGGGACCCCAGGCGTCGTGGGGCTGATGCCGTGCGTCTG... | GTCCGTGGGGCTGATGCCCTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTGATGCCGTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTGATGCCCTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTCATGCCCTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTGATGCCCTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTGATGCCCTGCGTCTGCGTGGGACCCCAGGCGTCCGTGGGGCTGATGCCGTGCATCTGCGTGGGACCCCAGGCGTCGTGGGGCTGATGCCGTGCGTCTG... |
Task1_train_42829 | Consider a variant on Chromosome 13. Determine its clinical classification and disease relevance. | Benign | ATCTCTTAAAATAACAGCCATTTTACCGATGCTAAATTATAACAACAAAATCATGTGTTTCTTTCTCCACCCACAGTAGAACACAAAAGCCTGTGCCTTCGCTGTTCTGGAGATGAAGGCCCAGGCTGATGCAGGGGAGCTGGCGGGTGGGAAGAGAGAAATGCTCAAGCATGTACATGTGCCTTCCAGAACCGGCTTCCGTGGCATTGCTTAGACTGCTACACAGTCTGTCACTGGCTCCTGTGACCTGGCTGACCATGGCACTAGGTTCCTGTTCATCTCTGTTGTCTTTCTGTTCTGGATCCATAGCTCAGAATTCC... | ATCTCTTAAAATAACAGCCATTTTACCGATGCTAAATTATAACAACAAAATCATGTGTTTCTTTCTCCACCCACAGTAGAACACAAAAGCCTGTGCCTTCGCTGTTCTGGAGATGAAGGCCCAGGCTGATGCAGGGGAGCTGGCGGGTGGGAAGAGAGAAATGCTCAAGCATGTACATGTGCCTTCCAGAACCGGCTTCCGTGGCATTGCTTAGACTGCTACACAGTCTGTCACTGGCTCCTGTGACCTGGCTGACCATGGCACTAGGTTCCTGTTCATCTCTGTTGTCTTTCTGTTCTGGATCCATAGCTCAGAATTCC... |
Task1_train_42830 | A variant found on Chromosome 13 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CAGCACAAACTGGTCTTGCGCCTACAGGGAGCCCACTGTCATTTGCCACTATAGAAAAAGGAGTCTGGTAGCTGACACTTAGTTGGGGCCAGGCTAGAAGAGAAAATTCAGCCATGGCTGCAGGGGAACGCCCCCAGGGGCAGAGATGGAAGCCTCGTGTTTAGGACTGGAAAGGGGTTGCACTTCTATGTATTTTCTTTTTATGCCTTTCCATCCCAGGATCTAGGGGAAGAACCTACAGGAGAGGATGCTTTCATTTGGGTTTTGATTAACAGGAAACGGGAATAAACAAGGCTAGAGTGTTTTGTCTCTAGCACCTG... | CAGCACAAACTGGTCTTGCGCCTACAGGGAGCCCACTGTCATTTGCCACTATAGAAAAAGGAGTCTGGTAGCTGACACTTAGTTGGGGCCAGGCTAGAAGAGAAAATTCAGCCATGGCTGCAGGGGAACGCCCCCAGGGGCAGAGATGGAAGCCTCGTGTTTAGGACTGGAAAGGGGTTGCACTTCTATGTATTTTCTTTTTATGCCTTTCCATCCCAGGATCTAGGGGAAGAACCTACAGGAGAGGATGCTTTCATTTGGGTTTTGATTAACAGGAAACGGGAATAAACAAGGCTAGAGTGTTTTGTCTCTAGCACCTG... |
Task1_train_42831 | Here’s a variant located on Chromosome 13. What is the predicted biological effect — harmless or disease-causing? | Benign | GCGAATGTGCTCACCTGCTGAGCTGTGGGGCTGGACTAGGTACCAAAATCAGGGTAGAACACTGAGGCGTCTGTGGGCGGGTGTGTGCACATCCACACTTGTACACTCACATTCACATGCACATATGTGCACACGCATGCAATTCATACACATGCACAGTTGTGCTCACAGCCTCGCACGCCCTTGCACACTCGCACTTATACACATGCATGGTCATGCTCACAGCCTCGCACACGCCCTCGCACACTCATCCACACACAGCTGTGCACAAGGAACACAGAGCAGATGTTCTCAGAGGGACTCTGACACCTTTGAGATGA... | GCGAATGTGCTCACCTGCTGAGCTGTGGGGCTGGACTAGGTACCAAAATCAGGGTAGAACACTGAGGCGTCTGTGGGCGGGTGTGTGCACATCCACACTTGTACACTCACATTCACATGCACATATGTGCACACGCATGCAATTCATACACATGCACAGTTGTGCTCACAGCCTCGCACGCCCTTGCACACTCGCACTTATACACATGCATGGTCATGCTCACAGCCTCGCACACGCCCTCGCACACTCATCCACACACAGCTGTGCACAAGGAACACAGAGCAGATGTTCTCAGAGGGACTCTGACACCTTTGAGATGA... |
Task1_train_42832 | A genetic alteration is present on Chromosome 13. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTCAGCCAACACTCTTCATGGCAGTGTCGACCTCGGGTTAGCTTCTGTTGTCTTTGTGGATGGTTTTCCTGGAGCGGCCTGACGTTGACGTGTTCTCTGGTCCCATGTCTTAGCGGGGCATGGTACGGTTTCGTGCCTGACGCGTGCATTAGGGTGTTCTCTTATACTTTCAGTAGCATCTTTCCACAGCAAGGGCCAAACCCTCCTGGTTCCCTTCAGAGTCTTTTTGGCCTGATGATGACTCTTGAGTGATACCCTGTGATGCAGACATGCCCCAGATGGATTCTACTTTCTTTAAAACTAGGGACTTTCAAGATTAA... | TTCAGCCAACACTCTTCATGGCAGTGTCGACCTCGGGTTAGCTTCTGTTGTCTTTGTGGATGGTTTTCCTGGAGCGGCCTGACGTTGACGTGTTCTCTGGTCCCATGTCTTAGCGGGGCATGGTACGGTTTCGTGCCTGACGCGTGCATTAGGGTGTTCTCTTATACTTTCAGTAGCATCTTTCCACAGCAAGGGCCAAACCCTCCTGGTTCCCTTCAGAGTCTTTTTGGCCTGATGATGACTCTTGAGTGATACCCTGTGATGCAGACATGCCCCAGATGGATTCTACTTTCTTTAAAACTAGGGACTTTCAAGATTAA... |
Task1_train_42833 | A mutation on Chromosome 13 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TTCAACTGTGCTGGGTGAAGGAGAACTTCATGGAGAGATGAGGCTGTGGTCAGGGTTTGCAGCCAGGATGGGTGGGATTTAGTTCGGATTTATGGCGATGCTTCATCACCAAAGCAGCAAAACAGCAAGACGCCAGCCTTGCCTGGGGTCCACCAGACAAAGATTAGCATCCGCAAACCAATGAAACCACCTGCAGTAAGCAACATGCAAATCTAAACACAGACTGCTCCACAGGAAAACTGACCTGTCAGAGTCTTGAATCTACATGTGCTTACCCAGAAAAAATGAAAAAAAAAAAAAAAGAGAAAAAAAGAAAAAAA... | TTCAACTGTGCTGGGTGAAGGAGAACTTCATGGAGAGATGAGGCTGTGGTCAGGGTTTGCAGCCAGGATGGGTGGGATTTAGTTCGGATTTATGGCGATGCTTCATCACCAAAGCAGCAAAACAGCAAGACGCCAGCCTTGCCTGGGGTCCACCAGACAAAGATTAGCATCCGCAAACCAATGAAACCACCTGCAGTAAGCAACATGCAAATCTAAACACAGACTGCTCCACAGGAAAACTGACCTGTCAGAGTCTTGAATCTACATGTGCTTACCCAGAAAAAATGAAAAAAAAAAAAAAAGAGAAAAAAAGAAAAAAA... |
Task1_train_42834 | Assess the clinical impact of this variant found on Chromosome 13. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TCATCTACATTAGGTATTTCTCCTAATACTATCCCTCCCCTAGCCCCCCAACCCCTGACAGGCGCCGGGTGTGTGATGTTCCCCTCCCTGTGTCCATGTGCTCTCATTGTTCAACTCCCACTTATGAGTGAGAACCATGCGGTGTTCGGTTTTCTGTTCCTGTGTTAGTTTGCTGAAAATGATGGTTTCCAGCTTCACCCGTGTCCCTGCAGAAGACATGAACCCATCCTTTTCTATGGCTGCACAGTATTCCATGTGCCACATTTTCTTCATCCAGTCTATCACTGATGGGCATCTGGGTTGGTTCCAAGTCTTTGCTA... | TCATCTACATTAGGTATTTCTCCTAATACTATCCCTCCCCTAGCCCCCCAACCCCTGACAGGCGCCGGGTGTGTGATGTTCCCCTCCCTGTGTCCATGTGCTCTCATTGTTCAACTCCCACTTATGAGTGAGAACCATGCGGTGTTCGGTTTTCTGTTCCTGTGTTAGTTTGCTGAAAATGATGGTTTCCAGCTTCACCCGTGTCCCTGCAGAAGACATGAACCCATCCTTTTCTATGGCTGCACAGTATTCCATGTGCCACATTTTCTTCATCCAGTCTATCACTGATGGGCATCTGGGTTGGTTCCAAGTCTTTGCTA... |
Task1_train_42835 | A variant has been detected on Chromosome 13. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CAACAACTTTTAGGATTTCTTCCTCAGTCCTCTTCAAATGCATGTCAATCTTTTAAATGGCTAAATAAACCTCTTGGCAGTTTTACAACTCAAGAAAATTTCAAAACCTGGGACCCACCTCTGAAATGTAATCAAGGAAAATAACGCCCCGTTTCCCAGTGTCCTGGGAGGAGATGGGCCTACCTTGTCATCTGACTCCACACTGTAACTCACCTGAAGCAATGGGTTATGCTATGGTCTGAATGTTTGTCTTCCCTCCAAATTCATGGTTGAAACCCTAACTCCCAAGGTGACGGTTTTAGGAGGTGGAGCCTCTGGGA... | CAACAACTTTTAGGATTTCTTCCTCAGTCCTCTTCAAATGCATGTCAATCTTTTAAATGGCTAAATAAACCTCTTGGCAGTTTTACAACTCAAGAAAATTTCAAAACCTGGGACCCACCTCTGAAATGTAATCAAGGAAAATAACGCCCCGTTTCCCAGTGTCCTGGGAGGAGATGGGCCTACCTTGTCATCTGACTCCACACTGTAACTCACCTGAAGCAATGGGTTATGCTATGGTCTGAATGTTTGTCTTCCCTCCAAATTCATGGTTGAAACCCTAACTCCCAAGGTGACGGTTTTAGGAGGTGGAGCCTCTGGGA... |
Task1_train_42836 | A change on Chromosome 13 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CGGGCGCATCTCCGGTGCCGTTCTCTGAGTGAGGAACACGTTGACAGAAGTGGGTTGTCCAGATATGATCAAGGCAGGGGTCGAAATGGACCTCCTGATGGGAAGTCCCTCTGGGAGGAGTGTCAGCTCCCAGGCAAGGGCTCGCTTTGCCCCTCCATGGCACTGACCTGCTCAGGGCCTCAGCCACCGTGAGTGCTGACTCATGGGAACTTTGATTCTGGGAATGAGGCTGTCAAGGCGCAAGAGCGTTGCTTTTGTTTATGGATTTGGAGAGAGTGCTGGGCTCTGAAACTGTGTACATGAGAGCCTCCTGGAGCATC... | CGGGCGCATCTCCGGTGCCGTTCTCTGAGTGAGGAACACGTTGACAGAAGTGGGTTGTCCAGATATGATCAAGGCAGGGGTCGAAATGGACCTCCTGATGGGAAGTCCCTCTGGGAGGAGTGTCAGCTCCCAGGCAAGGGCTCGCTTTGCCCCTCCATGGCACTGACCTGCTCAGGGCCTCAGCCACCGTGAGTGCTGACTCATGGGAACTTTGATTCTGGGAATGAGGCTGTCAAGGCGCAAGAGCGTTGCTTTTGTTTATGGATTTGGAGAGAGTGCTGGGCTCTGAAACTGTGTACATGAGAGCCTCCTGGAGCATC... |
Task1_train_42837 | This mutation on Chromosome 13 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TAGTTGGGTCTAGCTTTTTGTTATTGCTCGTAGAAAGCCAAATTATACTTTGTTTGAGGAGATAAGATTTCCACCCCAACTTAAAATGTTTTTTCCTTTTAAAAGAAATCATAAGTCATTGTGGCCATACATGCTTGATTTCAATTAAGTGACAATTTTAGGCAGATTTGCTGCCAGAAATAATTGGGCAGTAAAAGAAAAACAACAGGTATCGTGTATAACTGTTGCTCATACTCATAGTTATCATTGACACGTAAAGGTGGCATTCCCCAATTGTCCTCCAAAAATACTTAAAAAGTTTTCCAATGTTTGAGTATCTG... | TAGTTGGGTCTAGCTTTTTGTTATTGCTCGTAGAAAGCCAAATTATACTTTGTTTGAGGAGATAAGATTTCCACCCCAACTTAAAATGTTTTTTCCTTTTAAAAGAAATCATAAGTCATTGTGGCCATACATGCTTGATTTCAATTAAGTGACAATTTTAGGCAGATTTGCTGCCAGAAATAATTGGGCAGTAAAAGAAAAACAACAGGTATCGTGTATAACTGTTGCTCATACTCATAGTTATCATTGACACGTAAAGGTGGCATTCCCCAATTGTCCTCCAAAAATACTTAAAAAGTTTTCCAATGTTTGAGTATCTG... |
Task1_train_42838 | Consider a variant on Chromosome 13. Determine its clinical classification and disease relevance. | Benign | GCTGCCAGAAATAATTGGGCAGTAAAAGAAAAACAACAGGTATCGTGTATAACTGTTGCTCATACTCATAGTTATCATTGACACGTAAAGGTGGCATTCCCCAATTGTCCTCCAAAAATACTTAAAAAGTTTTCCAATGTTTGAGTATCTGCACTTGGCTAGTTTTAAAGTAAGCGTATATCACTAAGCATACATTTGAATATCCACACCAAATACTTCCCTTTTACACAGATTTGTGCAGTTTAAATAAGAAAAAGGCTGGTGGAGATTGGGTGATACTCTGGAATCCAGAGGATTTTTACTGTTTGAGAAAATACAAT... | GCTGCCAGAAATAATTGGGCAGTAAAAGAAAAACAACAGGTATCGTGTATAACTGTTGCTCATACTCATAGTTATCATTGACACGTAAAGGTGGCATTCCCCAATTGTCCTCCAAAAATACTTAAAAAGTTTTCCAATGTTTGAGTATCTGCACTTGGCTAGTTTTAAAGTAAGCGTATATCACTAAGCATACATTTGAATATCCACACCAAATACTTCCCTTTTACACAGATTTGTGCAGTTTAAATAAGAAAAAGGCTGGTGGAGATTGGGTGATACTCTGGAATCCAGAGGATTTTTACTGTTTGAGAAAATACAAT... |
Task1_train_42839 | A mutation found on Chromosome 13 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TCAAAGGAATGTTTATATCACTCAGATAAATATCATAGTGCATTATGGATTGGGAGTGTATTTATTTCATATACAACAGAAAAATGACTGTGTATTATCAAGTAAATACATGCTATATTTAAATAATGTGATAGCAATCACCAATCGCCGAGTTTTTCCTTGGTGTTCTGAAATTAGAATATACAGAAAGGCAAATTAATATTTAAACTCTCTGTATAGTTTTGAGGATCCATAATATGCATAACAAAGAGAGATGACTTTGGGCCATGCGGGGTACGATGGTATCGTGAATGGATTGACTACAGGGGGCCTGCAGAAGT... | TCAAAGGAATGTTTATATCACTCAGATAAATATCATAGTGCATTATGGATTGGGAGTGTATTTATTTCATATACAACAGAAAAATGACTGTGTATTATCAAGTAAATACATGCTATATTTAAATAATGTGATAGCAATCACCAATCGCCGAGTTTTTCCTTGGTGTTCTGAAATTAGAATATACAGAAAGGCAAATTAATATTTAAACTCTCTGTATAGTTTTGAGGATCCATAATATGCATAACAAAGAGAGATGACTTTGGGCCATGCGGGGTACGATGGTATCGTGAATGGATTGACTACAGGGGGCCTGCAGAAGT... |
Task1_train_42840 | Located on Chromosome 13, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TAAATAATGTGATAGCAATCACCAATCGCCGAGTTTTTCCTTGGTGTTCTGAAATTAGAATATACAGAAAGGCAAATTAATATTTAAACTCTCTGTATAGTTTTGAGGATCCATAATATGCATAACAAAGAGAGATGACTTTGGGCCATGCGGGGTACGATGGTATCGTGAATGGATTGACTACAGGGGGCCTGCAGAAGTCACACGCACTCAGGGGCCTGAAGAACTGGGGTAATACCTTGAGCACTAAGATAATTCCATTATTATTGAAAGCGTTTATTGCCTGTGGTTCCTCTGTGGGCACCGTATAAAGTACTTGA... | TAAATAATGTGATAGCAATCACCAATCGCCGAGTTTTTCCTTGGTGTTCTGAAATTAGAATATACAGAAAGGCAAATTAATATTTAAACTCTCTGTATAGTTTTGAGGATCCATAATATGCATAACAAAGAGAGATGACTTTGGGCCATGCGGGGTACGATGGTATCGTGAATGGATTGACTACAGGGGGCCTGCAGAAGTCACACGCACTCAGGGGCCTGAAGAACTGGGGTAATACCTTGAGCACTAAGATAATTCCATTATTATTGAAAGCGTTTATTGCCTGTGGTTCCTCTGTGGGCACCGTATAAAGTACTTGA... |
Task1_train_42841 | A variant on Chromosome 13 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATGGAGGGAAGCCTCAGCCATCCCAAGCCCCAGCATCCTAGCTAAGGCCTCAGACATGTCCATGAGGCCACACTAGGCCAGCAGCCCCCAGAGCCAACCCACAAAGTTGTAAGCAATCACACATGGGCTGTATCAAGTCACCGAGCTTCGGGCAGCCTTGAGAATGACTCCTTCCTCGACCAAATCAGCGAGGCTCCTCTGACCCCTCTTCTCAACGAGGCCTCGCCCCCAGCCCTGATCAAATTCCTCATCCTCCGCCTTGAGGTGGAAGTCCCTGGCCTGCCTTAGCCAGACATCCCTCCTTGGTGCAGTGGGTGTCG... | ATGGAGGGAAGCCTCAGCCATCCCAAGCCCCAGCATCCTAGCTAAGGCCTCAGACATGTCCATGAGGCCACACTAGGCCAGCAGCCCCCAGAGCCAACCCACAAAGTTGTAAGCAATCACACATGGGCTGTATCAAGTCACCGAGCTTCGGGCAGCCTTGAGAATGACTCCTTCCTCGACCAAATCAGCGAGGCTCCTCTGACCCCTCTTCTCAACGAGGCCTCGCCCCCAGCCCTGATCAAATTCCTCATCCTCCGCCTTGAGGTGGAAGTCCCTGGCCTGCCTTAGCCAGACATCCCTCCTTGGTGCAGTGGGTGTCG... |
Task1_train_42842 | A change on Chromosome 13 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ATGAAGCAAAAGTTAAAACCCGCAGCGGAACCCGAGAGCGTTTCTTGGCACCTTGAGGTGCTGGAGGCTTTCTGGCCGCGCAAGTTCTGCCCCACTGAGATTTGATCAGTGAATAAGTGCAATCCTGAAGCAGCAGCATCAGAGAATACGGCTTACGGATTAAGGCCTCTAGTTTTGGATTCAGAAACAGAACATTGCATCCGTGAAGGAATTTGTGAAGTTTAGTTGTGCAGGAAATGTTTTTCATGTCTGCGTTTCTTGACTAGGATCTCCCATTTCTTGTGGGTTATTGTCTGTTTTAATTGAGGTAACCTTTAGAA... | ATGAAGCAAAAGTTAAAACCCGCAGCGGAACCCGAGAGCGTTTCTTGGCACCTTGAGGTGCTGGAGGCTTTCTGGCCGCGCAAGTTCTGCCCCACTGAGATTTGATCAGTGAATAAGTGCAATCCTGAAGCAGCAGCATCAGAGAATACGGCTTACGGATTAAGGCCTCTAGTTTTGGATTCAGAAACAGAACATTGCATCCGTGAAGGAATTTGTGAAGTTTAGTTGTGCAGGAAATGTTTTTCATGTCTGCGTTTCTTGACTAGGATCTCCCATTTCTTGTGGGTTATTGTCTGTTTTAATTGAGGTAACCTTTAGAA... |
Task1_train_42843 | A mutation located on Chromosome 13 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TCGGGGGCAAGACACCGGGGGGTTCCTGCTCCGGTGACTTGCATCTTCCGGGGGAGAAAGACGCTAACTGATAACAGCTTGTGACGAGTTATACGGAGGAACAGACCAGGATTCCGCACCAGGGGACCCATGTCAGATTGAAAGGCCAGAGGTGACTTTTCAGAAACAGTCATTTGAAACCTGGAAGAAGAGCGCCATCATCACAGCAAGTCCCAGCTGGTAACCGCCTCCCACAACGAGGCACTGGCCAGGCATTCGACAGGTCCTGTCTCACTCCATCCTCACGCCCCGCAGCAAGATGGGGCCCAGGCATGGTGGGG... | TCGGGGGCAAGACACCGGGGGGTTCCTGCTCCGGTGACTTGCATCTTCCGGGGGAGAAAGACGCTAACTGATAACAGCTTGTGACGAGTTATACGGAGGAACAGACCAGGATTCCGCACCAGGGGACCCATGTCAGATTGAAAGGCCAGAGGTGACTTTTCAGAAACAGTCATTTGAAACCTGGAAGAAGAGCGCCATCATCACAGCAAGTCCCAGCTGGTAACCGCCTCCCACAACGAGGCACTGGCCAGGCATTCGACAGGTCCTGTCTCACTCCATCCTCACGCCCCGCAGCAAGATGGGGCCCAGGCATGGTGGGG... |
Task1_train_42844 | Chromosome 13 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CAACCCACTCAGGATCCCTCAGGGCCCCTGACCTGGGCGGGACTCTCAGCCCAGGAAGAGTCCCTCCGGATTCTCTCGTTCAGCCAGCGGCCCCTGGTGGCCCCAAGTTGCATTACACAGTCTCAGAGATGACAGCCCAGCTTGGAGGGTGTCAGGCACCCTGTCAGCCCCAGAGAAACCTGCTTAGCTCTAGAGAGCCCAGCCCGGCTCTGGAGAGCCCGGCCATTCTAACAGCCCTGAAGGCGATGGCTCTGTAAGAGGAAGATTCCATCCCAAACCTCTCTGACCAGCTCCTGGGCTTTGTAGCCAAGGAGCCACAG... | CAACCCACTCAGGATCCCTCAGGGCCCCTGACCTGGGCGGGACTCTCAGCCCAGGAAGAGTCCCTCCGGATTCTCTCGTTCAGCCAGCGGCCCCTGGTGGCCCCAAGTTGCATTACACAGTCTCAGAGATGACAGCCCAGCTTGGAGGGTGTCAGGCACCCTGTCAGCCCCAGAGAAACCTGCTTAGCTCTAGAGAGCCCAGCCCGGCTCTGGAGAGCCCGGCCATTCTAACAGCCCTGAAGGCGATGGCTCTGTAAGAGGAAGATTCCATCCCAAACCTCTCTGACCAGCTCCTGGGCTTTGTAGCCAAGGAGCCACAG... |
Task1_train_42845 | This genomic variant is located on Chromosome 13. Can you determine its pathogenicity and name any linked disease? | Benign | GATCAGAAAAATAATATTTAGTGAACCATGTGATTTAAGTCACTGTGTATGTGACATGAAATATTTATACCTAACCCACTAGCAAATGGCTCGTTAAACATATTTGAGATTTAATGTAAGTGAGAATTCTGCCAACCAAGTCAGGATAAACCTTAAACATCGGGAATGCAAAATCAAACAGATCCTTTAACACACATCACAAACAGAGGTGTGGACGCCCCTTTTGTCCCAATGGCAGGGACGGGGCGCTGGCCCCCAGGGTGTCCTGTTTATCCCCTGACCCACACAGTGTCAGGAGCTTGTCTGGAGGGGACGGGGAT... | GATCAGAAAAATAATATTTAGTGAACCATGTGATTTAAGTCACTGTGTATGTGACATGAAATATTTATACCTAACCCACTAGCAAATGGCTCGTTAAACATATTTGAGATTTAATGTAAGTGAGAATTCTGCCAACCAAGTCAGGATAAACCTTAAACATCGGGAATGCAAAATCAAACAGATCCTTTAACACACATCACAAACAGAGGTGTGGACGCCCCTTTTGTCCCAATGGCAGGGACGGGGCGCTGGCCCCCAGGGTGTCCTGTTTATCCCCTGACCCACACAGTGTCAGGAGCTTGTCTGGAGGGGACGGGGAT... |
Task1_train_42846 | Consider this mutation on Chromosome 13. Is this a benign change or a disease-causing variant? | Benign | CCACACACACACACACACACACACAGATGCACGCAGACACGCAGGCACTCATGCACTTACATACACAGATGTGCATGTGTATAACCACACACGTGCGCACACACACACATGCAAGTGCATGCATACCCCCCCACAGACCTGCACATGTACACACCACATGCATGCACAGTTTGTGTGGTGTATGGGGAGGGTGCATGTGGGACGCAACAGAAACACGAATGTAATCATTAGGCTTCCAGTCAAGAGGAGAGTCCTCCTATCTCACTGATTCTAAGATAAGCACCTGGAGCCAACTCGGTTTGTCGTCCCCCTGCGGTGAC... | CCACACACACACACACACACACACAGATGCACGCAGACACGCAGGCACTCATGCACTTACATACACAGATGTGCATGTGTATAACCACACACGTGCGCACACACACACATGCAAGTGCATGCATACCCCCCCACAGACCTGCACATGTACACACCACATGCATGCACAGTTTGTGTGGTGTATGGGGAGGGTGCATGTGGGACGCAACAGAAACACGAATGTAATCATTAGGCTTCCAGTCAAGAGGAGAGTCCTCCTATCTCACTGATTCTAAGATAAGCACCTGGAGCCAACTCGGTTTGTCGTCCCCCTGCGGTGAC... |
Task1_train_42847 | A variant on Chromosome 13 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AGAAAAAAGAAATGCCAGCAAACCCCAAGGCCGAATTGTGGGGGGCAAGGTGTGCCCCAAAGGGGAGTGTCCATGGCAGGTAAGGCTTCCCCTGGCTTCAGGATTCCAAGCCCTGAGGGTCTTGAAGCCTTTTGAATGTGAACAACAGCTCTGGAAGGGAAAATGGGCAGGTCAGCCCCAAGCCCACCAGGCTCCAAGTCAGCACACCTAGCACCTCCAGCTCGCGGCACCCCCATGCTTTTAGTGGGGCAAGGAAGGAGAAAAGAAAACGACACTCACTGAGGGTCTACCCTGTGCAGAGAACCCTGCGAGATGCCCCA... | AGAAAAAAGAAATGCCAGCAAACCCCAAGGCCGAATTGTGGGGGGCAAGGTGTGCCCCAAAGGGGAGTGTCCATGGCAGGTAAGGCTTCCCCTGGCTTCAGGATTCCAAGCCCTGAGGGTCTTGAAGCCTTTTGAATGTGAACAACAGCTCTGGAAGGGAAAATGGGCAGGTCAGCCCCAAGCCCACCAGGCTCCAAGTCAGCACACCTAGCACCTCCAGCTCGCGGCACCCCCATGCTTTTAGTGGGGCAAGGAAGGAGAAAAGAAAACGACACTCACTGAGGGTCTACCCTGTGCAGAGAACCCTGCGAGATGCCCCA... |
Task1_train_42848 | Mutation context: Chromosome 13. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GACAGGACCAGTGGTTCCCTGGGCAGCAAGGCTGACAGGCACTTTTATTTGCTGCTTTGCACTTCCCTCTATTTTTCAAATTTTCAAAAGTGATCACGTGCCATTTTTAATTTAAAAAAATATATATAACTTCCTTAAAAAGCAACGGATGTGCGAGAGCATGTCCCTGGCTGAGCTGAGCACAGTCCCACTCGTCTGTCCCAGGGGACCGGAACACGGAGCAGGAGGAGGGCGGTGAGGCGGTGCACGAGGTGGAGGTGGTCATCAAGCACAACCGGTTCACAAAGGAGACCTATGACTTCGACATCGCCGTGCTCCGG... | GACAGGACCAGTGGTTCCCTGGGCAGCAAGGCTGACAGGCACTTTTATTTGCTGCTTTGCACTTCCCTCTATTTTTCAAATTTTCAAAAGTGATCACGTGCCATTTTTAATTTAAAAAAATATATATAACTTCCTTAAAAAGCAACGGATGTGCGAGAGCATGTCCCTGGCTGAGCTGAGCACAGTCCCACTCGTCTGTCCCAGGGGACCGGAACACGGAGCAGGAGGAGGGCGGTGAGGCGGTGCACGAGGTGGAGGTGGTCATCAAGCACAACCGGTTCACAAAGGAGACCTATGACTTCGACATCGCCGTGCTCCGG... |
Task1_train_42849 | A mutation is present on Chromosome 13. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CTTTTAATTCAGCCGTGAGAAATTGTAAAACTCTGTGCATTGAATGGGGAGCTATTGAGATGGATGGTGTGTGGCATAATTTTGTTGTTCTCCTATGCTTAACAGATGATTAAACTTCAGGAAGTATTTAAGGCATTTTATCTTGGAAAGCACAGTGGTCGAAAACTTCAGTGGCAAACTACTTTGGGACATGCTGTTTTAAAAGCGGAGTTTAAAGAAGTAAGTTGTCTGTTTCATTTATTTTTTATTATTTGTAAATATGTTAATATAATTTTTTTATTGTTACTGGACTTTAGTAGCAAAAAAGGAGTGTTTCACTT... | CTTTTAATTCAGCCGTGAGAAATTGTAAAACTCTGTGCATTGAATGGGGAGCTATTGAGATGGATGGTGTGTGGCATAATTTTGTTGTTCTCCTATGCTTAACAGATGATTAAACTTCAGGAAGTATTTAAGGCATTTTATCTTGGAAAGCACAGTGGTCGAAAACTTCAGTGGCAAACTACTTTGGGACATGCTGTTTTAAAAGCGGAGTTTAAAGAAGTAAGTTGTCTGTTTCATTTATTTTTTATTATTTGTAAATATGTTAATATAATTTTTTTATTGTTACTGGACTTTAGTAGCAAAAAAGGAGTGTTTCACTT... |
Task1_train_42850 | Located on Chromosome 13, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGTGTTTCCAGCTTCTTGTGACCACTCTACAGAAACAGGGTGGGAAATGAATGTGCCACATGGATCACAGGTGAAAAACAATTGTCAAAGCAGCGTAGGTTACACTTTTTCTGTGCGTCGTGTGGCCATCTAGACTAGAATTTGGACAAGACTGGCCGGTTTTGCACATTTAACTTTTGCCTGTTTAACCCTGGTCTGTAACATTTTATAAAGGAACCGTGAAGCTGCTTTTTTTTTTTTTTTTTTGAGACAGGGTCTCCCAGGCTGGAGTGCAGTGGCACAATAACTGCTCACTGCAGCCTCAGCCTCCCAGGCTCCAG... | TGTGTTTCCAGCTTCTTGTGACCACTCTACAGAAACAGGGTGGGAAATGAATGTGCCACATGGATCACAGGTGAAAAACAATTGTCAAAGCAGCGTAGGTTACACTTTTTCTGTGCGTCGTGTGGCCATCTAGACTAGAATTTGGACAAGACTGGCCGGTTTTGCACATTTAACTTTTGCCTGTTTAACCCTGGTCTGTAACATTTTATAAAGGAACCGTGAAGCTGCTTTTTTTTTTTTTTTTTTGAGACAGGGTCTCCCAGGCTGGAGTGCAGTGGCACAATAACTGCTCACTGCAGCCTCAGCCTCCCAGGCTCCAG... |
Task1_train_42851 | A mutation on Chromosome 13 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGTGCTTCGTGAGAGAGGGGACCCTGTCCTCCTAGCAGGGGTCCAGCGGCACCACAGCAAGACTTCTGTGGCCAAGTACACGCCATGCTCAGCTCTGCCCCCACCCGCACCCCCGGACCATCCTGTGTGCAGCTGGGCTGCCCCGGGACCCACACGCGCGAGGGGCACCCGGTGCTCAGGAGCCTCCACACACAGCAGCTCGCACTTAGAACCCACACGCCAAGCAGAAACCCCTCGAAGCGGGCTGGGAGCACGGACCCCTGATTTATAGAGGAGGCCCCGGGGGCCCTGTCGGGGGAGCTGTGGGGACCGGCCCCCCA... | TGTGCTTCGTGAGAGAGGGGACCCTGTCCTCCTAGCAGGGGTCCAGCGGCACCACAGCAAGACTTCTGTGGCCAAGTACACGCCATGCTCAGCTCTGCCCCCACCCGCACCCCCGGACCATCCTGTGTGCAGCTGGGCTGCCCCGGGACCCACACGCGCGAGGGGCACCCGGTGCTCAGGAGCCTCCACACACAGCAGCTCGCACTTAGAACCCACACGCCAAGCAGAAACCCCTCGAAGCGGGCTGGGAGCACGGACCCCTGATTTATAGAGGAGGCCCCGGGGGCCCTGTCGGGGGAGCTGTGGGGACCGGCCCCCCA... |
Task1_train_42852 | This genomic variant is located on Chromosome 13. Can you determine its pathogenicity and name any linked disease? | Benign | AGGTGGCCCTGTGAGAGCTGGGGAGGTGTCCCAAAGTGCCAGCATCCTGCAGATCGAAGGGGACGCACACACCGTGCCACTGCGGGAGGTGTGAGCTCCACGCTGCAGGCTGTGTGAGAGAGGGGTGAGCCGGCGCCCCCGAGTGAAGACACAAAGAATCCCGAGGGCCTGGTGAGGCCACAGGCCCGCACCTCCCACCCCCATGGCCTCGTGGCTCTGTGGGGTGACAGGAACCCGACCCACATGTAGCTCAATCCTCCCAAGGTCAGCTTGTGAAGAAGGGAAAGAAAATTATGGAAACAGGCGTCTCTGTAGGGGAT... | AGGTGGCCCTGTGAGAGCTGGGGAGGTGTCCCAAAGTGCCAGCATCCTGCAGATCGAAGGGGACGCACACACCGTGCCACTGCGGGAGGTGTGAGCTCCACGCTGCAGGCTGTGTGAGAGAGGGGTGAGCCGGCGCCCCCGAGTGAAGACACAAAGAATCCCGAGGGCCTGGTGAGGCCACAGGCCCGCACCTCCCACCCCCATGGCCTCGTGGCTCTGTGGGGTGACAGGAACCCGACCCACATGTAGCTCAATCCTCCCAAGGTCAGCTTGTGAAGAAGGGAAAGAAAATTATGGAAACAGGCGTCTCTGTAGGGGAT... |
Task1_train_42853 | Assess the clinical impact of this variant found on Chromosome 13. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CAGGCCCGCACCTCCCACCCCCATGGCCTCGTGGCTCTGTGGGGTGACAGGAACCCGACCCACATGTAGCTCAATCCTCCCAAGGTCAGCTTGTGAAGAAGGGAAAGAAAATTATGGAAACAGGCGTCTCTGTAGGGGATGCTCCAAGACGCATTTGGAGGCAGGAAAATGCCTGAAGTCCCTCAATGGGCGGATGTCACAGTGCTGGGCGAGCCACGGTGTGTACTCGGGGCCTCACTTTGGGAGCTCAGACGTGTCGCTGGCCCTGACGCTCATTGGTCTGAAGGACAAATCGAAGGCCCTCTGGTCACGGAAGCTCT... | CAGGCCCGCACCTCCCACCCCCATGGCCTCGTGGCTCTGTGGGGTGACAGGAACCCGACCCACATGTAGCTCAATCCTCCCAAGGTCAGCTTGTGAAGAAGGGAAAGAAAATTATGGAAACAGGCGTCTCTGTAGGGGATGCTCCAAGACGCATTTGGAGGCAGGAAAATGCCTGAAGTCCCTCAATGGGCGGATGTCACAGTGCTGGGCGAGCCACGGTGTGTACTCGGGGCCTCACTTTGGGAGCTCAGACGTGTCGCTGGCCCTGACGCTCATTGGTCTGAAGGACAAATCGAAGGCCCTCTGGTCACGGAAGCTCT... |
Task1_train_42854 | A variant was discovered on Chromosome 13. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TTACCTCTTGTGAAAAAGGGAACTGGCATAAAGCTTCTTAGGAAACAAAAAGGCTCGTCAACTAAAAAACTACAGGGGAGAGAAGGAAGCCGAGTCCCTCTAGACAGGACTAAACCCAGATCAAATTTACAAAGGCCCAGACATTGGCAGTAAGCTTTGAGTGCACCAAGAGAGGACTGAACCCAGGTCAAATTAACAAAGGCCCAGACGTTGGCAAGAAGCTTCGAGTGCACCCAGACAGGACTGAACCCAGGTCAATCTAATCAAGGTGGATACACTGGAACTAGGGCCGCCCTTCAAGCTCACAACCTTCACTGAGG... | TTACCTCTTGTGAAAAAGGGAACTGGCATAAAGCTTCTTAGGAAACAAAAAGGCTCGTCAACTAAAAAACTACAGGGGAGAGAAGGAAGCCGAGTCCCTCTAGACAGGACTAAACCCAGATCAAATTTACAAAGGCCCAGACATTGGCAGTAAGCTTTGAGTGCACCAAGAGAGGACTGAACCCAGGTCAAATTAACAAAGGCCCAGACGTTGGCAAGAAGCTTCGAGTGCACCCAGACAGGACTGAACCCAGGTCAATCTAATCAAGGTGGATACACTGGAACTAGGGCCGCCCTTCAAGCTCACAACCTTCACTGAGG... |
Task1_train_42855 | This mutation is located on Chromosome 13. Is it associated with a disease or is it a benign polymorphism? | Benign | ATCAGATGTTGTATTAGCTGTTTACATTTTTTAAAGCCATCATTTCTTGAGTACCTCTACTATACCAAGCATCATGCCAAGCCCTTTAAATATATAAAGTATCACGTCATCTTCATAGAAAAACCTGTGATATTATTACACAGCATAAACGTTAGAGAAAATACAGACATTAAACTTTCTTTACCAAAATATATTTTGGGGGAGAGAAATATGATTATCAGGCAAATGTATAAATCAAGGTTTTCAATAACACTGATTCATTTGTCTTGCCTGTGTGATATGTGCATGAGCTACTGTGACCCTGTGTACAGTGGAGACGT... | ATCAGATGTTGTATTAGCTGTTTACATTTTTTAAAGCCATCATTTCTTGAGTACCTCTACTATACCAAGCATCATGCCAAGCCCTTTAAATATATAAAGTATCACGTCATCTTCATAGAAAAACCTGTGATATTATTACACAGCATAAACGTTAGAGAAAATACAGACATTAAACTTTCTTTACCAAAATATATTTTGGGGGAGAGAAATATGATTATCAGGCAAATGTATAAATCAAGGTTTTCAATAACACTGATTCATTTGTCTTGCCTGTGTGATATGTGCATGAGCTACTGTGACCCTGTGTACAGTGGAGACGT... |
Task1_train_42856 | A change on Chromosome 13 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TGTATTAGCTGTTTACATTTTTTAAAGCCATCATTTCTTGAGTACCTCTACTATACCAAGCATCATGCCAAGCCCTTTAAATATATAAAGTATCACGTCATCTTCATAGAAAAACCTGTGATATTATTACACAGCATAAACGTTAGAGAAAATACAGACATTAAACTTTCTTTACCAAAATATATTTTGGGGGAGAGAAATATGATTATCAGGCAAATGTATAAATCAAGGTTTTCAATAACACTGATTCATTTGTCTTGCCTGTGTGATATGTGCATGAGCTACTGTGACCCTGTGTACAGTGGAGACGTGAAGATACA... | TGTATTAGCTGTTTACATTTTTTAAAGCCATCATTTCTTGAGTACCTCTACTATACCAAGCATCATGCCAAGCCCTTTAAATATATAAAGTATCACGTCATCTTCATAGAAAAACCTGTGATATTATTACACAGCATAAACGTTAGAGAAAATACAGACATTAAACTTTCTTTACCAAAATATATTTTGGGGGAGAGAAATATGATTATCAGGCAAATGTATAAATCAAGGTTTTCAATAACACTGATTCATTTGTCTTGCCTGTGTGATATGTGCATGAGCTACTGTGACCCTGTGTACAGTGGAGACGTGAAGATACA... |
Task1_train_42857 | A mutation located on Chromosome 13 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGCGGTGACCACAAGCCCATGCGAGCCTTAGGGTGAAAATCGCTGATCTGTGAAGCCTCCGCATGGACAATATTAGTTGGGAGGCAATTTTATCATCTCCTGAATCGTGTAACCCTAAAAGGCACAAAGCTGTAGCCACAACAGCTTAACGTCATCGTCTGTTCAGACTGTTTTAAAATTCTAAGCCAAGATATTTTGTTCACCAAAAATTTAATTTTGTACAATAAGTCAATCAAGCCTTCTAAAACAATTACCTGAATCTCTATCCAGAAAGAGATTTTTGCTGGCATCAAGGGGTTTTGTGTGGTTCTGCTGTTTTT... | TGCGGTGACCACAAGCCCATGCGAGCCTTAGGGTGAAAATCGCTGATCTGTGAAGCCTCCGCATGGACAATATTAGTTGGGAGGCAATTTTATCATCTCCTGAATCGTGTAACCCTAAAAGGCACAAAGCTGTAGCCACAACAGCTTAACGTCATCGTCTGTTCAGACTGTTTTAAAATTCTAAGCCAAGATATTTTGTTCACCAAAAATTTAATTTTGTACAATAAGTCAATCAAGCCTTCTAAAACAATTACCTGAATCTCTATCCAGAAAGAGATTTTTGCTGGCATCAAGGGGTTTTGTGTGGTTCTGCTGTTTTT... |
Task1_train_42858 | This variant is found on Chromosome 13. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TTCAGTCTTAGGATTCGTTTCCATTTAGAGCTGCTGCCCATTCTCGTGTTTCTGGAAGGTGCTTTCACTGCTGATGAGCCTAGTAGAGTGCCTGTGGAGGTAGGGTTGCAGGGCCACAGTAAACAGGAGCTCAGCCGTAGCCATGACGTGGGTTTCCCCAAAGTCGCCATGCCAGCCCGTCCTGCTGCTGTGCCGTGAGCACGCCGTGCCCCACAGCCTCCTTGCACTTGCTCCAGGAGTGGAGCATCTCAGGGCTCTGATGGGGGCTCCAGCGTCCACTTCCCGATGGCTGGTCCCTCAAGCCCTTTCCAAAGCTCAGT... | TTCAGTCTTAGGATTCGTTTCCATTTAGAGCTGCTGCCCATTCTCGTGTTTCTGGAAGGTGCTTTCACTGCTGATGAGCCTAGTAGAGTGCCTGTGGAGGTAGGGTTGCAGGGCCACAGTAAACAGGAGCTCAGCCGTAGCCATGACGTGGGTTTCCCCAAAGTCGCCATGCCAGCCCGTCCTGCTGCTGTGCCGTGAGCACGCCGTGCCCCACAGCCTCCTTGCACTTGCTCCAGGAGTGGAGCATCTCAGGGCTCTGATGGGGGCTCCAGCGTCCACTTCCCGATGGCTGGTCCCTCAAGCCCTTTCCAAAGCTCAGT... |
Task1_train_42859 | A change on Chromosome 13 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AGCATGGCATGACCTCGCTGAGGTGACCCTGGTGTCCCACATATCACCCTGAGTGTTCTTAATACACAGTCGAGGGCTGTGTTCATTGGACTATTCTGGTGTCACCGCCCACTTCATTTCTGTGCCTGGCAGCACTTTTACTCCTGGTTGGGAGCATGACCGCCTCCCAGTTCAGCTTCCTCCTGCGTCCCAAGTGAGCGGGGCGGCTGTCCTCGAGGACTCCGGGCTCACAGCCAACCTGCTGGCACGGCTCGAGGACTCCGGGCTCACAGCCAACCTGCTGGCACGGCCGCCCTTTCCCGCCCTGCCTCGGGTGAGCC... | AGCATGGCATGACCTCGCTGAGGTGACCCTGGTGTCCCACATATCACCCTGAGTGTTCTTAATACACAGTCGAGGGCTGTGTTCATTGGACTATTCTGGTGTCACCGCCCACTTCATTTCTGTGCCTGGCAGCACTTTTACTCCTGGTTGGGAGCATGACCGCCTCCCAGTTCAGCTTCCTCCTGCGTCCCAAGTGAGCGGGGCGGCTGTCCTCGAGGACTCCGGGCTCACAGCCAACCTGCTGGCACGGCTCGAGGACTCCGGGCTCACAGCCAACCTGCTGGCACGGCCGCCCTTTCCCGCCCTGCCTCGGGTGAGCC... |
Task1_train_42860 | This mutation is located on Chromosome 13. Is it associated with a disease or is it a benign polymorphism? | Benign | TGTTGCTGCTGGTGGGACTGAGCCCTTGCTCAGACTGTGGGAAGAGCCACTTCAGGCCTCACCCAAGACAGCCCAGAGGCTGGAGTGGCCTCTCCCCACCAGGTCTGTGCAGGTCGGTGCCCCAGAGGCCCCGCTCACACAGGAACAGGGCGGCTGACTCCCTGCACCCCTGGGGGCCCCGTGAGGTGCTTCCTTCGAGGGTCATGGGGTGGAGTGGGCAGAGCACGGCTCCCAGGCGCAGGCCCGTGTGCCTCCCTCCAGCCCCCAAGTGCTCCTGGAAGTTTTCCCGGGGTCTCCACACATCTATTTATGTCTGGCCT... | TGTTGCTGCTGGTGGGACTGAGCCCTTGCTCAGACTGTGGGAAGAGCCACTTCAGGCCTCACCCAAGACAGCCCAGAGGCTGGAGTGGCCTCTCCCCACCAGGTCTGTGCAGGTCGGTGCCCCAGAGGCCCCGCTCACACAGGAACAGGGCGGCTGACTCCCTGCACCCCTGGGGGCCCCGTGAGGTGCTTCCTTCGAGGGTCATGGGGTGGAGTGGGCAGAGCACGGCTCCCAGGCGCAGGCCCGTGTGCCTCCCTCCAGCCCCCAAGTGCTCCTGGAAGTTTTCCCGGGGTCTCCACACATCTATTTATGTCTGGCCT... |
Task1_train_42861 | This mutation is located on Chromosome 13. Is it associated with a disease or is it a benign polymorphism? | Benign | GGACATCGTCCCTGCTGGTCCAGTGCCCTGCCGTCCCCCTGAGTCTTGACTTTATTCTGGATAGTGGAGGTTGGCACAAAAATATCTCCCAGTTAAAGGAATTATAATTCAGTCACCTGACTATTACTGACAAGTCAAAAAAAAATGACTCAGTGGGTTTAGTACCAAGGTAGCAGTGTTCCATTTGATGATTCAGCATATAGCAGGTTCTCTTAGTGAACATTTCTCTTTGTGTATTTGTTTTTCCCCCACATAGCAACGAAGTTAGTTTCTAATGACTTCCATTCTCTACTTTTATCAGAAGCAGATTTCACCTGGAA... | GGACATCGTCCCTGCTGGTCCAGTGCCCTGCCGTCCCCCTGAGTCTTGACTTTATTCTGGATAGTGGAGGTTGGCACAAAAATATCTCCCAGTTAAAGGAATTATAATTCAGTCACCTGACTATTACTGACAAGTCAAAAAAAAATGACTCAGTGGGTTTAGTACCAAGGTAGCAGTGTTCCATTTGATGATTCAGCATATAGCAGGTTCTCTTAGTGAACATTTCTCTTTGTGTATTTGTTTTTCCCCCACATAGCAACGAAGTTAGTTTCTAATGACTTCCATTCTCTACTTTTATCAGAAGCAGATTTCACCTGGAA... |
Task1_train_42862 | A genomic variant on Chromosome 13 is under review. What is the biological outcome — benign or pathogenic? | Benign | TCCTATGGTTCACATTTATTACAGACATGTTACTGTTGCAATTTTTATAAAAGATGGGCAGTTACCAGAAAGGAAATGTTTAAGTTCCCAGATTCCACATAGGCAGAATAAGAGGATGTTCACAGCTGACATGGGGCCCACGCTTGATGAGAAGCGGCTTCCAATGCTCCACCTTGCATGATGCGTTGTGTTCCCAAGTGAACACGTGTGATTGAATGCATCTGTGTATGGTCTTGCTATGCTGCAATTATGAGTGAGAACAGAATTCTCAGATGTACACCTTCCATTTCTGTTCTACAAATGATCTGTCTGTGGTGCTT... | TCCTATGGTTCACATTTATTACAGACATGTTACTGTTGCAATTTTTATAAAAGATGGGCAGTTACCAGAAAGGAAATGTTTAAGTTCCCAGATTCCACATAGGCAGAATAAGAGGATGTTCACAGCTGACATGGGGCCCACGCTTGATGAGAAGCGGCTTCCAATGCTCCACCTTGCATGATGCGTTGTGTTCCCAAGTGAACACGTGTGATTGAATGCATCTGTGTATGGTCTTGCTATGCTGCAATTATGAGTGAGAACAGAATTCTCAGATGTACACCTTCCATTTCTGTTCTACAAATGATCTGTCTGTGGTGCTT... |
Task1_train_42863 | Here is a mutation located on Chromosome 14. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AAAGTGCATTTTTAATTTTGGGGCCGGCCACAATAAAACTCTGTCTAGCTGAAGACATAATATGATTTATAAAATAAATCATTTAGAGATTTGGTTCCTGTCAAAACGATGATGGCTTCACCTTTTGAGCACTGCTGAGAATCATGACACTCCTGTGTCAATCCCTTTTCATTCCATAATTTCTTAATGTTGGTTTATTAATGATTCTGGTTGGAAGCCTATTAAAGAGACATATATTACTAAAAGAAGCACAAACATAACTTCTAACTAGTCATACCAAAAGACTTCCCAGAGCACTGGTGTAGAGAGCAAGTTGGAAG... | AAAGTGCATTTTTAATTTTGGGGCCGGCCACAATAAAACTCTGTCTAGCTGAAGACATAATATGATTTATAAAATAAATCATTTAGAGATTTGGTTCCTGTCAAAACGATGATGGCTTCACCTTTTGAGCACTGCTGAGAATCATGACACTCCTGTGTCAATCCCTTTTCATTCCATAATTTCTTAATGTTGGTTTATTAATGATTCTGGTTGGAAGCCTATTAAAGAGACATATATTACTAAAAGAAGCACAAACATAACTTCTAACTAGTCATACCAAAAGACTTCCCAGAGCACTGGTGTAGAGAGCAAGTTGGAAG... |
Task1_train_42864 | This mutation on Chromosome 14 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GTAACTTAAAAGTCATACACCCTGGAAAGGAGTAAAGAAAGAGGAAAGATCCTCAGCGGCTATACAAGTGAGAGATATGGCAGAGTTCTAATAAGATTGAGTAAAAGCTTGATACTGTCTTACATGAAAGGAGCAAATAATTGTTCTACCTGGAATGTCCGGGCCCCAATTCACAAATGCATTCTTACCTTTTGAACTGAATAATGATCTCTTTCCCAATAAACTGTTCTAAGACAAAAAATCTGAAAGGAAAATTGTTGCACACACATCATATTCTTATATTCTGTATTTTCTGGGACAGTCTGTTTCAGATTAGATGA... | GTAACTTAAAAGTCATACACCCTGGAAAGGAGTAAAGAAAGAGGAAAGATCCTCAGCGGCTATACAAGTGAGAGATATGGCAGAGTTCTAATAAGATTGAGTAAAAGCTTGATACTGTCTTACATGAAAGGAGCAAATAATTGTTCTACCTGGAATGTCCGGGCCCCAATTCACAAATGCATTCTTACCTTTTGAACTGAATAATGATCTCTTTCCCAATAAACTGTTCTAAGACAAAAAATCTGAAAGGAAAATTGTTGCACACACATCATATTCTTATATTCTGTATTTTCTGGGACAGTCTGTTTCAGATTAGATGA... |
Task1_train_42865 | This alteration occurs on Chromosome 14. Is it associated with a disease or is it a benign variant? | Benign | CTGTACATGTAACAGCAAATCGTTCCCTAACTTGTATTTCTTTCTTTGTTTTATTTTCCAATTGACTCTAGAAAGTGAGGTGATTCCTTCTATCAGTTATGAGATTATAGATTTAGATACACCTGTGCACTCGGCTATATAGGCAGATGAAGAGGATGGTCACAATCATGGTGTGACAGAGGCATCCAAAGGTGGCTTGAGTCCCAAATCTCTCTCTCACTGGCTTATCTTGGAATAACATCCTAGAGAAAGTTTTGTTGTCATTAGAGGTTTTCATTTTTAGAATTTAAGTACTTTTCTGCATTGTCTATGTAAATACC... | CTGTACATGTAACAGCAAATCGTTCCCTAACTTGTATTTCTTTCTTTGTTTTATTTTCCAATTGACTCTAGAAAGTGAGGTGATTCCTTCTATCAGTTATGAGATTATAGATTTAGATACACCTGTGCACTCGGCTATATAGGCAGATGAAGAGGATGGTCACAATCATGGTGTGACAGAGGCATCCAAAGGTGGCTTGAGTCCCAAATCTCTCTCTCACTGGCTTATCTTGGAATAACATCCTAGAGAAAGTTTTGTTGTCATTAGAGGTTTTCATTTTTAGAATTTAAGTACTTTTCTGCATTGTCTATGTAAATACC... |
Task1_train_42866 | This variant lies on Chromosome 14. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATGTAAATACCTGATATCTAGTATGAAGGATTTTATTGGATAACATTCTCTGAATGACTTGATAGAACCCAGTGCAACATGGATTACAAAGCTTGGGACACAAAATAAAATTTTGTCTTATTTCATATTTTGTCTATAGCTGGTTTTAGATAAAAAAATATTCTAGACAGGCATCTACTAATTTTTAACTACTTCAATGGAAGAAATGTATCAATGTTCTCTGATTTTCTGTTTGTAATCCAAGGTACTGTCATCAAATGTTGGGGATGAATATGAGTGTAGAGCAGGGGAAAATGGATCTAACAATATCTTAGCAAATC... | ATGTAAATACCTGATATCTAGTATGAAGGATTTTATTGGATAACATTCTCTGAATGACTTGATAGAACCCAGTGCAACATGGATTACAAAGCTTGGGACACAAAATAAAATTTTGTCTTATTTCATATTTTGTCTATAGCTGGTTTTAGATAAAAAAATATTCTAGACAGGCATCTACTAATTTTTAACTACTTCAATGGAAGAAATGTATCAATGTTCTCTGATTTTCTGTTTGTAATCCAAGGTACTGTCATCAAATGTTGGGGATGAATATGAGTGTAGAGCAGGGGAAAATGGATCTAACAATATCTTAGCAAATC... |
Task1_train_42867 | A mutation on Chromosome 14 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TATTTTTACCTTTCTTCCACTTGCTACCAGATTCCTGGAAAACACTGTTTTTGTGCGTGTGTGTGTCTGCTTGTAGTAAGCCATCCCTTCTTCAAAATACAATGCTTCTATAAGATACTGAAAGCCATTTATCTATGTTTGTTAAAATTATGTATAAATTGAGTCAGTAGGTTCCAAAAATGGCGCATTTAATTTCTTTTCTCAGTAGTATACATAGTGCCCATAAGTGTTTGGACACAGCCACATCTGTTTGGTTTTACAGAACCTTAACTTTTTAAAAATTCCTTTTAATATTTAATTTTTTAAGCAATAGGAGAGGC... | TATTTTTACCTTTCTTCCACTTGCTACCAGATTCCTGGAAAACACTGTTTTTGTGCGTGTGTGTGTCTGCTTGTAGTAAGCCATCCCTTCTTCAAAATACAATGCTTCTATAAGATACTGAAAGCCATTTATCTATGTTTGTTAAAATTATGTATAAATTGAGTCAGTAGGTTCCAAAAATGGCGCATTTAATTTCTTTTCTCAGTAGTATACATAGTGCCCATAAGTGTTTGGACACAGCCACATCTGTTTGGTTTTACAGAACCTTAACTTTTTAAAAATTCCTTTTAATATTTAATTTTTTAAGCAATAGGAGAGGC... |
Task1_train_42868 | Given this context: Chromosome 14 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGAAAGCTCTGCCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCAACCACCACCACGTCCAGCTAATTTTTTTGTATTTTTTTAGTAGAGATAGGGTTTCACCGTGTTAGCCAAGATGTTCTCGATCTCCTGAGCTCGTGATCCACCCACCTAGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCATCGTGCCCGGCCGCTAGAGCACTTATTTAAAACAAATACACTGTTT... | TTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGAAAGCTCTGCCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCAACCACCACCACGTCCAGCTAATTTTTTTGTATTTTTTTAGTAGAGATAGGGTTTCACCGTGTTAGCCAAGATGTTCTCGATCTCCTGAGCTCGTGATCCACCCACCTAGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCATCGTGCCCGGCCGCTAGAGCACTTATTTAAAACAAATACACTGTTT... |
Task1_train_42869 | An alteration has been detected on Chromosome 14. Is it pathogenic, and if so, what disease is involved? | Benign | CTCACTGAAAGCTCTGCCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCAACCACCACCACGTCCAGCTAATTTTTTTGTATTTTTTTAGTAGAGATAGGGTTTCACCGTGTTAGCCAAGATGTTCTCGATCTCCTGAGCTCGTGATCCACCCACCTAGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCATCGTGCCCGGCCGCTAGAGCACTTATTTAAAACAAATACACTGTTTAGTTAAATCATATTAAGAATATCCTTTTATATTACAGTTTGTATTTTGTTGTAGG... | CTCACTGAAAGCTCTGCCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCAACCACCACCACGTCCAGCTAATTTTTTTGTATTTTTTTAGTAGAGATAGGGTTTCACCGTGTTAGCCAAGATGTTCTCGATCTCCTGAGCTCGTGATCCACCCACCTAGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCATCGTGCCCGGCCGCTAGAGCACTTATTTAAAACAAATACACTGTTTAGTTAAATCATATTAAGAATATCCTTTTATATTACAGTTTGTATTTTGTTGTAGG... |
Task1_train_42870 | With a mutation on Chromosome 14, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ATCCACCCACCTAGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCATCGTGCCCGGCCGCTAGAGCACTTATTTAAAACAAATACACTGTTTAGTTAAATCATATTAAGAATATCCTTTTATATTACAGTTTGTATTTTGTTGTAGGCCAGTAATTTTCAAACTTAAAAAATCTATTCCCCTAAGACATTTTTTGAATATATAACCTTAAATGTATGCATATTTATTTATAAAGTATATATAAACCATTGTACTATGTTATCCATTATAAATATTAAAAAGTGAATTTAGAAAACAACGAAATGTAGTGATACATAT... | ATCCACCCACCTAGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCATCGTGCCCGGCCGCTAGAGCACTTATTTAAAACAAATACACTGTTTAGTTAAATCATATTAAGAATATCCTTTTATATTACAGTTTGTATTTTGTTGTAGGCCAGTAATTTTCAAACTTAAAAAATCTATTCCCCTAAGACATTTTTTGAATATATAACCTTAAATGTATGCATATTTATTTATAAAGTATATATAAACCATTGTACTATGTTATCCATTATAAATATTAAAAAGTGAATTTAGAAAACAACGAAATGTAGTGATACATAT... |
Task1_train_42871 | Chromosome 14 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CCACCTAGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCATCGTGCCCGGCCGCTAGAGCACTTATTTAAAACAAATACACTGTTTAGTTAAATCATATTAAGAATATCCTTTTATATTACAGTTTGTATTTTGTTGTAGGCCAGTAATTTTCAAACTTAAAAAATCTATTCCCCTAAGACATTTTTTGAATATATAACCTTAAATGTATGCATATTTATTTATAAAGTATATATAAACCATTGTACTATGTTATCCATTATAAATATTAAAAAGTGAATTTAGAAAACAACGAAATGTAGTGATACATATAAAATG... | CCACCTAGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCATCGTGCCCGGCCGCTAGAGCACTTATTTAAAACAAATACACTGTTTAGTTAAATCATATTAAGAATATCCTTTTATATTACAGTTTGTATTTTGTTGTAGGCCAGTAATTTTCAAACTTAAAAAATCTATTCCCCTAAGACATTTTTTGAATATATAACCTTAAATGTATGCATATTTATTTATAAAGTATATATAAACCATTGTACTATGTTATCCATTATAAATATTAAAAAGTGAATTTAGAAAACAACGAAATGTAGTGATACATATAAAATG... |
Task1_train_42872 | A variant was discovered on Chromosome 14. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CTGGCCGCCCAGTCTGGGAAGTGAGGAGCACCTTTGCCCGGCTGCGACCCCGTCTGGGAACTGAGGAGTGTCTCTGCCCCGCCGCCACCCCGTCTGGGAGGTGAGGAGCGTCTCTGACCAGCCGCCCAGTCTGGGAAGTGAGGAGCCCCTCCGCCTGGCAGCCGCCCTATCTGGGAAGTGAGGAGCGTCTCCACCCGGCAGCCGCCCCGTCCAGGAGGTGGGGGGCAGCCCCCGCCCGGCCAGCCGCCCCGTCCGGGAGGTGGGGGGCGCCTCTGCCTGGCCGCCCCATCTGAAAAGTGAGGAGCCCCTCTGCCCGGCCG... | CTGGCCGCCCAGTCTGGGAAGTGAGGAGCACCTTTGCCCGGCTGCGACCCCGTCTGGGAACTGAGGAGTGTCTCTGCCCCGCCGCCACCCCGTCTGGGAGGTGAGGAGCGTCTCTGACCAGCCGCCCAGTCTGGGAAGTGAGGAGCCCCTCCGCCTGGCAGCCGCCCTATCTGGGAAGTGAGGAGCGTCTCCACCCGGCAGCCGCCCCGTCCAGGAGGTGGGGGGCAGCCCCCGCCCGGCCAGCCGCCCCGTCCGGGAGGTGGGGGGCGCCTCTGCCTGGCCGCCCCATCTGAAAAGTGAGGAGCCCCTCTGCCCGGCCG... |
Task1_train_42873 | A variant affecting Chromosome 14 has been observed. Determine if it's benign or associated with disease. | Benign | CTGCCTGGCCGCCCCATCTGAAAAGTGAGGAGCCCCTCTGCCCGGCCGCCGCCCCGTCTGGGAGGTGCACCCAACAGCTCATTGAGAACGGGCCATGATGACGATGGCGGTTTTGTCAAATAGAAAAGGGAGAAATGTGGGGAAAAGAAAGAGAGATCAGATTGTTACTGTGTTTGCTACAAAGAAGTAGACATAGGAGACTCCATTTTGTTCTATACTAAGAAAAATTCTTCTGCCTTGGGATGCTGTTAATCTATAACCTTACCCCCAACCCCGTGCTCTCTGAAACATGTGCTGTGTCCACTCAGGGTTAAATGGAT... | CTGCCTGGCCGCCCCATCTGAAAAGTGAGGAGCCCCTCTGCCCGGCCGCCGCCCCGTCTGGGAGGTGCACCCAACAGCTCATTGAGAACGGGCCATGATGACGATGGCGGTTTTGTCAAATAGAAAAGGGAGAAATGTGGGGAAAAGAAAGAGAGATCAGATTGTTACTGTGTTTGCTACAAAGAAGTAGACATAGGAGACTCCATTTTGTTCTATACTAAGAAAAATTCTTCTGCCTTGGGATGCTGTTAATCTATAACCTTACCCCCAACCCCGTGCTCTCTGAAACATGTGCTGTGTCCACTCAGGGTTAAATGGAT... |
Task1_train_42874 | A mutation has occurred on Chromosome 14. What is the medical relevance of this mutation? | Benign | CATGTCCCTACAACATCCATTTTATCCACAGCTGATACACAACTAATGATTCAACTAGGTCATTTATTTATATTTTAAATTGCCTTCGATGCTCTGTCAGAAGCCTACTTAACACTGAATAATCTAAAGCCCTGGTTCTTCTATAGATCTGATAAGTAAAAGTGTTTTACAAATGAGTTCTACTGAAATATTTTAAATGTTTGCCCTTCCCACTCCCATTTCCTAATCCCTATTCCATGAAGCTTAGGTCAATACAACAGTTTACATATGTTAACATTTACAGAAGAAGAATTCAAACAGAGGTGAAATGAAAGAGACTG... | CATGTCCCTACAACATCCATTTTATCCACAGCTGATACACAACTAATGATTCAACTAGGTCATTTATTTATATTTTAAATTGCCTTCGATGCTCTGTCAGAAGCCTACTTAACACTGAATAATCTAAAGCCCTGGTTCTTCTATAGATCTGATAAGTAAAAGTGTTTTACAAATGAGTTCTACTGAAATATTTTAAATGTTTGCCCTTCCCACTCCCATTTCCTAATCCCTATTCCATGAAGCTTAGGTCAATACAACAGTTTACATATGTTAACATTTACAGAAGAAGAATTCAAACAGAGGTGAAATGAAAGAGACTG... |
Task1_train_42875 | This alteration on Chromosome 14 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTCTTACTATGACTGTTGTCAACAGTTAATTGTCAGAACTAATATGGTTTCCTAAAACAGCACTTCTTTAAAGTTTTTCCAGTTCAACTGAACTAGATTTATACAGTAGGGGTATGTCTTTACAGGGTGAAAAACATACGATGCAAATTTTTAGATATTTTCAAGAGCATGAGAGGTTTATAATCATTTTTACTTCTCTATCCAGAAATTTTTTTTAAACTTCATTTTCCAGCATTAATTATAAAGATGTTTTAAGAAGATCATGGAGAACTCTAGCAGGGAGAATGTAAGTGGGCTGAAATCTAATTCTGATAGGCAAA... | CTCTTACTATGACTGTTGTCAACAGTTAATTGTCAGAACTAATATGGTTTCCTAAAACAGCACTTCTTTAAAGTTTTTCCAGTTCAACTGAACTAGATTTATACAGTAGGGGTATGTCTTTACAGGGTGAAAAACATACGATGCAAATTTTTAGATATTTTCAAGAGCATGAGAGGTTTATAATCATTTTTACTTCTCTATCCAGAAATTTTTTTTAAACTTCATTTTCCAGCATTAATTATAAAGATGTTTTAAGAAGATCATGGAGAACTCTAGCAGGGAGAATGTAAGTGGGCTGAAATCTAATTCTGATAGGCAAA... |
Task1_train_42876 | A variant found on Chromosome 14 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GTCTTTACAGGGTGAAAAACATACGATGCAAATTTTTAGATATTTTCAAGAGCATGAGAGGTTTATAATCATTTTTACTTCTCTATCCAGAAATTTTTTTTAAACTTCATTTTCCAGCATTAATTATAAAGATGTTTTAAGAAGATCATGGAGAACTCTAGCAGGGAGAATGTAAGTGGGCTGAAATCTAATTCTGATAGGCAAAGAAAATGAAAAATTTAGGTTCCACTCTTGGATAATCAACAGAAAATAGGATTTAGATAATTCAGGTAAGCCATAATATGTGTTTTAAGAAATTATTGGATAACTAATTGACAAAC... | GTCTTTACAGGGTGAAAAACATACGATGCAAATTTTTAGATATTTTCAAGAGCATGAGAGGTTTATAATCATTTTTACTTCTCTATCCAGAAATTTTTTTTAAACTTCATTTTCCAGCATTAATTATAAAGATGTTTTAAGAAGATCATGGAGAACTCTAGCAGGGAGAATGTAAGTGGGCTGAAATCTAATTCTGATAGGCAAAGAAAATGAAAAATTTAGGTTCCACTCTTGGATAATCAACAGAAAATAGGATTTAGATAATTCAGGTAAGCCATAATATGTGTTTTAAGAAATTATTGGATAACTAATTGACAAAC... |
Task1_train_42877 | A variant on Chromosome 14 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CTGCATTCTTCTTAAAACCAATTCAATTCTTCATAACCAATGCAAACACGGAAAGCCCTGAAAGTGTAGGATATAGTGCTCCAACATCCAGGTTAAAACTACATAATGAAAGCTTGAAAACAGTTTAAACACTTTTTAATTTGGTTTACCATTACCTATACAATTTTAACTTTTAAAATATAAAATATTTATTATTTTGGTCATGTCTAAATAACCTGGTTCTAACAAACCACTGAAGAACATGGAGGGGTGCAGAGCTTCAGTTAGTATAAGGACAAATAAATATCTGTTGTGTACTGTTGGATACACAGAGCTAAGGT... | CTGCATTCTTCTTAAAACCAATTCAATTCTTCATAACCAATGCAAACACGGAAAGCCCTGAAAGTGTAGGATATAGTGCTCCAACATCCAGGTTAAAACTACATAATGAAAGCTTGAAAACAGTTTAAACACTTTTTAATTTGGTTTACCATTACCTATACAATTTTAACTTTTAAAATATAAAATATTTATTATTTTGGTCATGTCTAAATAACCTGGTTCTAACAAACCACTGAAGAACATGGAGGGGTGCAGAGCTTCAGTTAGTATAAGGACAAATAAATATCTGTTGTGTACTGTTGGATACACAGAGCTAAGGT... |
Task1_train_42878 | With a mutation on Chromosome 14, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TTGACAAATTCAAGTTTGTCAGGTGTGTATAGAAAGATAAAACACAGTCAGAAGAAAGAGACTGAAAACATGTTGTTGGTTATTGTTTCATTTATTGTTAATTGCTTTCTATGTGACAGAAGGTGAACTTTGATTAACTATTTGTTAAAAGGTTGAAAGGAAGTGTTCTTGACCTTCAGAGAAATTTTCAGAGTGTAACCATTGGCTCTTCCTTCTCTATTATAGCAAATTGTTTCTATCATTTTCTTTTCTTTTTTCTTCTTTTAACATTTTTTTTTTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCAGGAGTGCA... | TTGACAAATTCAAGTTTGTCAGGTGTGTATAGAAAGATAAAACACAGTCAGAAGAAAGAGACTGAAAACATGTTGTTGGTTATTGTTTCATTTATTGTTAATTGCTTTCTATGTGACAGAAGGTGAACTTTGATTAACTATTTGTTAAAAGGTTGAAAGGAAGTGTTCTTGACCTTCAGAGAAATTTTCAGAGTGTAACCATTGGCTCTTCCTTCTCTATTATAGCAAATTGTTTCTATCATTTTCTTTTCTTTTTTCTTCTTTTAACATTTTTTTTTTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCAGGAGTGCA... |
Task1_train_42879 | Assess the clinical impact of this variant found on Chromosome 14. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGTGAACTTTGATTAACTATTTGTTAAAAGGTTGAAAGGAAGTGTTCTTGACCTTCAGAGAAATTTTCAGAGTGTAACCATTGGCTCTTCCTTCTCTATTATAGCAAATTGTTTCTATCATTTTCTTTTCTTTTTTCTTCTTTTAACATTTTTTTTTTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCAGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGGGGGGAATACAGGTGCCCACCACCACGCCCGGCTAATTTTTTTGTA... | GGTGAACTTTGATTAACTATTTGTTAAAAGGTTGAAAGGAAGTGTTCTTGACCTTCAGAGAAATTTTCAGAGTGTAACCATTGGCTCTTCCTTCTCTATTATAGCAAATTGTTTCTATCATTTTCTTTTCTTTTTTCTTCTTTTAACATTTTTTTTTTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCAGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGGGGGGAATACAGGTGCCCACCACCACGCCCGGCTAATTTTTTTGTA... |
Task1_train_42880 | A mutation on Chromosome 14 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GTGAACTTTGATTAACTATTTGTTAAAAGGTTGAAAGGAAGTGTTCTTGACCTTCAGAGAAATTTTCAGAGTGTAACCATTGGCTCTTCCTTCTCTATTATAGCAAATTGTTTCTATCATTTTCTTTTCTTTTTTCTTCTTTTAACATTTTTTTTTTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCAGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGGGGGGAATACAGGTGCCCACCACCACGCCCGGCTAATTTTTTTGTAT... | GTGAACTTTGATTAACTATTTGTTAAAAGGTTGAAAGGAAGTGTTCTTGACCTTCAGAGAAATTTTCAGAGTGTAACCATTGGCTCTTCCTTCTCTATTATAGCAAATTGTTTCTATCATTTTCTTTTCTTTTTTCTTCTTTTAACATTTTTTTTTTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCAGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGGGGGGAATACAGGTGCCCACCACCACGCCCGGCTAATTTTTTTGTAT... |
Task1_train_42881 | A mutation located on Chromosome 14 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TTTCAGCAGTTTCAGTTACCTCAGGTCAACTGTGGTCCAAAAATATTAACCTATTTTGAGAGCGAGAGAAAGAAAAAAAAGAAACACATTCACATAAATGCTATTTCAGTATATTGTTATACTTTTTTATTTTATTGTTAGTTATTACTGTTCATCTCTCTCTGTGCCTAATTTATAAATTAAACTTTATCTTAGGTATGCATGTATAGGAAAAATATAGCTTATATAGGGTTCAGTACTATCAGTGGTTTCAAGCATCCACTGGGGTTCTTGGAACACATTATCTGCAAATAAGGGAGAAAATTTGTATTTTTGGGGGG... | TTTCAGCAGTTTCAGTTACCTCAGGTCAACTGTGGTCCAAAAATATTAACCTATTTTGAGAGCGAGAGAAAGAAAAAAAAGAAACACATTCACATAAATGCTATTTCAGTATATTGTTATACTTTTTTATTTTATTGTTAGTTATTACTGTTCATCTCTCTCTGTGCCTAATTTATAAATTAAACTTTATCTTAGGTATGCATGTATAGGAAAAATATAGCTTATATAGGGTTCAGTACTATCAGTGGTTTCAAGCATCCACTGGGGTTCTTGGAACACATTATCTGCAAATAAGGGAGAAAATTTGTATTTTTGGGGGG... |
Task1_train_42882 | Here’s a variant located on Chromosome 14. What is the predicted biological effect — harmless or disease-causing? | Benign | AAGAAAAAAAAGAAACACATTCACATAAATGCTATTTCAGTATATTGTTATACTTTTTTATTTTATTGTTAGTTATTACTGTTCATCTCTCTCTGTGCCTAATTTATAAATTAAACTTTATCTTAGGTATGCATGTATAGGAAAAATATAGCTTATATAGGGTTCAGTACTATCAGTGGTTTCAAGCATCCACTGGGGTTCTTGGAACACATTATCTGCAAATAAGGGAGAAAATTTGTATTTTTGGGGGGAGAATTGGAGATTTGAAATACAGAGGTGACTCCAAATTTGGTTTCTGAGAGTTAAAATTATTTATCACG... | AAGAAAAAAAAGAAACACATTCACATAAATGCTATTTCAGTATATTGTTATACTTTTTTATTTTATTGTTAGTTATTACTGTTCATCTCTCTCTGTGCCTAATTTATAAATTAAACTTTATCTTAGGTATGCATGTATAGGAAAAATATAGCTTATATAGGGTTCAGTACTATCAGTGGTTTCAAGCATCCACTGGGGTTCTTGGAACACATTATCTGCAAATAAGGGAGAAAATTTGTATTTTTGGGGGGAGAATTGGAGATTTGAAATACAGAGGTGACTCCAAATTTGGTTTCTGAGAGTTAAAATTATTTATCACG... |
Task1_train_42883 | A mutation is present on Chromosome 14. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ACACATTCACATAAATGCTATTTCAGTATATTGTTATACTTTTTTATTTTATTGTTAGTTATTACTGTTCATCTCTCTCTGTGCCTAATTTATAAATTAAACTTTATCTTAGGTATGCATGTATAGGAAAAATATAGCTTATATAGGGTTCAGTACTATCAGTGGTTTCAAGCATCCACTGGGGTTCTTGGAACACATTATCTGCAAATAAGGGAGAAAATTTGTATTTTTGGGGGGAGAATTGGAGATTTGAAATACAGAGGTGACTCCAAATTTGGTTTCTGAGAGTTAAAATTATTTATCACGTGTTCTGTTCTTAT... | ACACATTCACATAAATGCTATTTCAGTATATTGTTATACTTTTTTATTTTATTGTTAGTTATTACTGTTCATCTCTCTCTGTGCCTAATTTATAAATTAAACTTTATCTTAGGTATGCATGTATAGGAAAAATATAGCTTATATAGGGTTCAGTACTATCAGTGGTTTCAAGCATCCACTGGGGTTCTTGGAACACATTATCTGCAAATAAGGGAGAAAATTTGTATTTTTGGGGGGAGAATTGGAGATTTGAAATACAGAGGTGACTCCAAATTTGGTTTCTGAGAGTTAAAATTATTTATCACGTGTTCTGTTCTTAT... |
Task1_train_42884 | A genomic change on Chromosome 14 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGATTAAAATAAAAGACATCCTCTCCCAAGACCTGATTAAGATGTAGAGAAAGATTCTTCAAAATCAGATAATGTAATGCTCCTTTAAAATTCACATTTTATTTTTTCCTATTTTCCATAAAACTTTTATAAGTTCTAAATAGCTTCTACAAATAAAAATAACAAAAGGAAGAAAGCTCTGATAACATAGAATATAGAGTAACTGAATAGAAAAGAAAAATCATTTTTTTCCTGGTCTGAATTCCTTAGTAATAAGTAATATAACTTATTAGTTATATTAGTATTTATAGTAAGCAATATAACTTATAAGTTTTTAAGCC... | TGATTAAAATAAAAGACATCCTCTCCCAAGACCTGATTAAGATGTAGAGAAAGATTCTTCAAAATCAGATAATGTAATGCTCCTTTAAAATTCACATTTTATTTTTTCCTATTTTCCATAAAACTTTTATAAGTTCTAAATAGCTTCTACAAATAAAAATAACAAAAGGAAGAAAGCTCTGATAACATAGAATATAGAGTAACTGAATAGAAAAGAAAAATCATTTTTTTCCTGGTCTGAATTCCTTAGTAATAAGTAATATAACTTATTAGTTATATTAGTATTTATAGTAAGCAATATAACTTATAAGTTTTTAAGCC... |
Task1_train_42885 | This mutation is located on Chromosome 14. Is it associated with a disease or is it a benign polymorphism? | Benign | AGGAAGAAAGCTCTGATAACATAGAATATAGAGTAACTGAATAGAAAAGAAAAATCATTTTTTTCCTGGTCTGAATTCCTTAGTAATAAGTAATATAACTTATTAGTTATATTAGTATTTATAGTAAGCAATATAACTTATAAGTTTTTAAGCCACATCACATCAAATGAAATATCAATCATAGCTCAATAAAATGTCTATGGTTAGTAACACCAATGGCTAAGTTTAAAGAAGCTTCATACCTTCAGGGATTAATTGAAAGGAACCAGTGTGCTAGATTTCATGATAAAGTAGAACTCCATGAAGAGCTGAATCATAAA... | AGGAAGAAAGCTCTGATAACATAGAATATAGAGTAACTGAATAGAAAAGAAAAATCATTTTTTTCCTGGTCTGAATTCCTTAGTAATAAGTAATATAACTTATTAGTTATATTAGTATTTATAGTAAGCAATATAACTTATAAGTTTTTAAGCCACATCACATCAAATGAAATATCAATCATAGCTCAATAAAATGTCTATGGTTAGTAACACCAATGGCTAAGTTTAAAGAAGCTTCATACCTTCAGGGATTAATTGAAAGGAACCAGTGTGCTAGATTTCATGATAAAGTAGAACTCCATGAAGAGCTGAATCATAAA... |
Task1_train_42886 | The following genetic variant occurs on Chromosome 14. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GAAATGTTAAGTAATAATTAAGTTGCAGAAAGAGAAAAAATCCATTTTTTGGATTTTTGTATATAAGAATAAAATGTCATAAACCCTACAGATATGCATAGGAACTCTCAGTAGGTAAGAAGAAAGTCTCAATTGTTAAGGTGAATTTTTATAAATATTTTATTGCCTTTACATGTAGTCTAGTGTCTTATATAATTTAACTTTTCTGTATATATAGATTGTATCATATTTTAAGTATAGTTTTGTGTCCTGTTTTTTCTTTTATTATGTGACCATTTTCTAAAGTTAATAAATATTTTTTAAACACCAGTTCAACAAAC... | GAAATGTTAAGTAATAATTAAGTTGCAGAAAGAGAAAAAATCCATTTTTTGGATTTTTGTATATAAGAATAAAATGTCATAAACCCTACAGATATGCATAGGAACTCTCAGTAGGTAAGAAGAAAGTCTCAATTGTTAAGGTGAATTTTTATAAATATTTTATTGCCTTTACATGTAGTCTAGTGTCTTATATAATTTAACTTTTCTGTATATATAGATTGTATCATATTTTAAGTATAGTTTTGTGTCCTGTTTTTTCTTTTATTATGTGACCATTTTCTAAAGTTAATAAATATTTTTTAAACACCAGTTCAACAAAC... |
Task1_train_42887 | Assess the clinical impact of this variant found on Chromosome 14. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CTTTACATGTAGTCTAGTGTCTTATATAATTTAACTTTTCTGTATATATAGATTGTATCATATTTTAAGTATAGTTTTGTGTCCTGTTTTTTCTTTTATTATGTGACCATTTTCTAAAGTTAATAAATATTTTTTAAACACCAGTTCAACAAACTAATATTTAAATTTGGAAGTTTTACCTCATAGTGTCTTGATATTTTTAACTCTTACATATAATTGATGTAATCTTTATATTTACATCATTGCCTTAAATAAGGAATATGTAAATTTTATTATTTTTAAGCTAACTTTTGTTTAGTTTAAAATTATTTTTTTAATAT... | CTTTACATGTAGTCTAGTGTCTTATATAATTTAACTTTTCTGTATATATAGATTGTATCATATTTTAAGTATAGTTTTGTGTCCTGTTTTTTCTTTTATTATGTGACCATTTTCTAAAGTTAATAAATATTTTTTAAACACCAGTTCAACAAACTAATATTTAAATTTGGAAGTTTTACCTCATAGTGTCTTGATATTTTTAACTCTTACATATAATTGATGTAATCTTTATATTTACATCATTGCCTTAAATAAGGAATATGTAAATTTTATTATTTTTAAGCTAACTTTTGTTTAGTTTAAAATTATTTTTTTAATAT... |
Task1_train_42888 | A sequence alteration has been identified on Chromosome 14. Is it disease-inducing or harmless? | Benign | ATATTTATGCATATGTTTGGATTGCAATTACGGGGCAAGTCGTAAGTACCCAGAAGCATGCCTTCCTGGATTGAATATAATATCCAAAGTCATTGGAAGCTCCATTCAATTGCTTAACTAACTCAGTCATTACCCAATTTTCTCCTTTGGTTTGATATCTCAGAGGCAACCTAGGAGAAAATTGCTTGAGTTCCCTGCACATTAATTTAGTAAAAATCAAATTTAACTCTTGTTTATAATTGTCTTCTTAAGATCCATGGACATGTAAAAATTCAGCATAACATCTGAATCTGTGGCATTCAAACGCACACTTCCTAATA... | ATATTTATGCATATGTTTGGATTGCAATTACGGGGCAAGTCGTAAGTACCCAGAAGCATGCCTTCCTGGATTGAATATAATATCCAAAGTCATTGGAAGCTCCATTCAATTGCTTAACTAACTCAGTCATTACCCAATTTTCTCCTTTGGTTTGATATCTCAGAGGCAACCTAGGAGAAAATTGCTTGAGTTCCCTGCACATTAATTTAGTAAAAATCAAATTTAACTCTTGTTTATAATTGTCTTCTTAAGATCCATGGACATGTAAAAATTCAGCATAACATCTGAATCTGTGGCATTCAAACGCACACTTCCTAATA... |
Task1_train_42889 | This variant is found on Chromosome 14. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ATATCCAAAGTCATTGGAAGCTCCATTCAATTGCTTAACTAACTCAGTCATTACCCAATTTTCTCCTTTGGTTTGATATCTCAGAGGCAACCTAGGAGAAAATTGCTTGAGTTCCCTGCACATTAATTTAGTAAAAATCAAATTTAACTCTTGTTTATAATTGTCTTCTTAAGATCCATGGACATGTAAAAATTCAGCATAACATCTGAATCTGTGGCATTCAAACGCACACTTCCTAATAAATGATGCCCCAGGAGACAGAATCAAATCAGAAAGAGATGCAGTGTTTATTGAAAATCTACGTTGGGTGAAAATGTGTT... | ATATCCAAAGTCATTGGAAGCTCCATTCAATTGCTTAACTAACTCAGTCATTACCCAATTTTCTCCTTTGGTTTGATATCTCAGAGGCAACCTAGGAGAAAATTGCTTGAGTTCCCTGCACATTAATTTAGTAAAAATCAAATTTAACTCTTGTTTATAATTGTCTTCTTAAGATCCATGGACATGTAAAAATTCAGCATAACATCTGAATCTGTGGCATTCAAACGCACACTTCCTAATAAATGATGCCCCAGGAGACAGAATCAAATCAGAAAGAGATGCAGTGTTTATTGAAAATCTACGTTGGGTGAAAATGTGTT... |
Task1_train_42890 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | GAAAACAAGTGCAGCAAGGTGTGGTAAAAGGAAAGCAATTTTATTCAAATGCAAGCAGGTGGGGGATGGCCAGGCTCATGCCTTTAACAGACCATTCCCCGTTTGGGGGCTAAGTAAAGGAGTTTAAGACGGAAAAGATATGGGAAATATGTGGGAATAGTGCAGGAACGTGCAGGTCTGCGTGTTTTGTTCTGAAGGTTATCTTGAGTGATGGTCTGTCCTGAGGCCTGATTTGCCTTTTCCTGACTTTGGCCTGGTAGTGGTGGGTTAACTGTAAGTAATTCCCCTCTCAAGGGAGGATTCTGCAGCCAGGTTTCCCT... | GAAAACAAGTGCAGCAAGGTGTGGTAAAAGGAAAGCAATTTTATTCAAATGCAAGCAGGTGGGGGATGGCCAGGCTCATGCCTTTAACAGACCATTCCCCGTTTGGGGGCTAAGTAAAGGAGTTTAAGACGGAAAAGATATGGGAAATATGTGGGAATAGTGCAGGAACGTGCAGGTCTGCGTGTTTTGTTCTGAAGGTTATCTTGAGTGATGGTCTGTCCTGAGGCCTGATTTGCCTTTTCCTGACTTTGGCCTGGTAGTGGTGGGTTAACTGTAAGTAATTCCCCTCTCAAGGGAGGATTCTGCAGCCAGGTTTCCCT... |
Task1_train_42891 | A sequence alteration has been identified on Chromosome 14. Is it disease-inducing or harmless? | Benign | GACAGCGTCTTCTTCCAACAGAAAGCTGTTTCATCTATATTGAAAATCTGTTGTTTAGCATAGCCATCTTTATCAATGATCTTAGTCAGATATTCTGGATAACTTTCGGCAGCTTCTATATCAGCACTTGCTGCTTCACCTTGTAGTTTTATGTAATAAGAATGGCTTCTTTCTTTCAACCTCATGAACTAACCTCTGCTAGCTTCAAACTTTTATTCTGCAACTTTCTCTCCTCTCCCAGATTTCACAGAATTGAAGAGAGTTAGGGTCTTGCCCTGGATTAGGCTTTGGCTTAAGGGAATGTTGTAGCTGATTTGAAC... | GACAGCGTCTTCTTCCAACAGAAAGCTGTTTCATCTATATTGAAAATCTGTTGTTTAGCATAGCCATCTTTATCAATGATCTTAGTCAGATATTCTGGATAACTTTCGGCAGCTTCTATATCAGCACTTGCTGCTTCACCTTGTAGTTTTATGTAATAAGAATGGCTTCTTTCTTTCAACCTCATGAACTAACCTCTGCTAGCTTCAAACTTTTATTCTGCAACTTTCTCTCCTCTCCCAGATTTCACAGAATTGAAGAGAGTTAGGGTCTTGCCCTGGATTAGGCTTTGGCTTAAGGGAATGTTGTAGCTGATTTGAAC... |
Task1_train_42892 | A variant was discovered on Chromosome 14. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ATCAATGATCTTAGTCAGATATTCTGGATAACTTTCGGCAGCTTCTATATCAGCACTTGCTGCTTCACCTTGTAGTTTTATGTAATAAGAATGGCTTCTTTCTTTCAACCTCATGAACTAACCTCTGCTAGCTTCAAACTTTTATTCTGCAACTTTCTCTCCTCTCCCAGATTTCACAGAATTGAAGAGAGTTAGGGTCTTGCCCTGGATTAGGCTTTGGCTTAAGGGAATGTTGTAGCTGATTTGAACTTTTATCCAGATCCCTAAAACTTTCTCCATATCAGCAATAAAGATGGTTCACTTTGTTATCATTCATGAGT... | ATCAATGATCTTAGTCAGATATTCTGGATAACTTTCGGCAGCTTCTATATCAGCACTTGCTGCTTCACCTTGTAGTTTTATGTAATAAGAATGGCTTCTTTCTTTCAACCTCATGAACTAACCTCTGCTAGCTTCAAACTTTTATTCTGCAACTTTCTCTCCTCTCCCAGATTTCACAGAATTGAAGAGAGTTAGGGTCTTGCCCTGGATTAGGCTTTGGCTTAAGGGAATGTTGTAGCTGATTTGAACTTTTATCCAGATCCCTAAAACTTTCTCCATATCAGCAATAAAGATGGTTCACTTTGTTATCATTCATGAGT... |
Task1_train_42893 | Given this variant on Chromosome 14, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AAGAGAGTTAGGGTCTTGCCCTGGATTAGGCTTTGGCTTAAGGGAATGTTGTAGCTGATTTGAACTTTTATCCAGATCCCTAAAACTTTCTCCATATCAGCAATAAAGATGGTTCACTTTGTTATCATTCATGAGTTCACTGGAGTAGCACTTTTAATTTCCTTTGAGAACTTTTTCTTTGCATTCACAATTGACTAATTGTTTGGTGCAAGAGGACTAGCTTTCAGCCTGTCTCAGCTTTAGACATACTTTCCTCACTAAGCTTAATCACTTCTGGCTTAAAAAACTTTTTTACAGACTTTATTGTTTGGGGCAGTTTT... | AAGAGAGTTAGGGTCTTGCCCTGGATTAGGCTTTGGCTTAAGGGAATGTTGTAGCTGATTTGAACTTTTATCCAGATCCCTAAAACTTTCTCCATATCAGCAATAAAGATGGTTCACTTTGTTATCATTCATGAGTTCACTGGAGTAGCACTTTTAATTTCCTTTGAGAACTTTTTCTTTGCATTCACAATTGACTAATTGTTTGGTGCAAGAGGACTAGCTTTCAGCCTGTCTCAGCTTTAGACATACTTTCCTCACTAAGCTTAATCACTTCTGGCTTAAAAAACTTTTTTACAGACTTTATTGTTTGGGGCAGTTTT... |
Task1_train_42894 | A variant was discovered on Chromosome 14. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GATTAGGCTTTGGCTTAAGGGAATGTTGTAGCTGATTTGAACTTTTATCCAGATCCCTAAAACTTTCTCCATATCAGCAATAAAGATGGTTCACTTTGTTATCATTCATGAGTTCACTGGAGTAGCACTTTTAATTTCCTTTGAGAACTTTTTCTTTGCATTCACAATTGACTAATTGTTTGGTGCAAGAGGACTAGCTTTCAGCCTGTCTCAGCTTTAGACATACTTTCCTCACTAAGCTTAATCACTTCTGGCTTAAAAAACTTTTTTACAGACTTTATTGTTTGGGGCAGTTTTAAGTTCACAGCAAAATTGAGCAG... | GATTAGGCTTTGGCTTAAGGGAATGTTGTAGCTGATTTGAACTTTTATCCAGATCCCTAAAACTTTCTCCATATCAGCAATAAAGATGGTTCACTTTGTTATCATTCATGAGTTCACTGGAGTAGCACTTTTAATTTCCTTTGAGAACTTTTTCTTTGCATTCACAATTGACTAATTGTTTGGTGCAAGAGGACTAGCTTTCAGCCTGTCTCAGCTTTAGACATACTTTCCTCACTAAGCTTAATCACTTCTGGCTTAAAAAACTTTTTTACAGACTTTATTGTTTGGGGCAGTTTTAAGTTCACAGCAAAATTGAGCAG... |
Task1_train_42895 | Given this variant on Chromosome 14, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTTGCATTCACAATTGACTAATTGTTTGGTGCAAGAGGACTAGCTTTCAGCCTGTCTCAGCTTTAGACATACTTTCCTCACTAAGCTTAATCACTTCTGGCTTAAAAAACTTTTTTACAGACTTTATTGTTTGGGGCAGTTTTAAGTTCACAGCAAAATTGAGCAGGAAGTACAAGAGTTCCCGTGTGCCCTCTGATGCCACATACAGTCTCCCCCACCCTTAACAACCTGAACCAGAGTGGTACATTCGTTACCGCTGGTGAGCCTACATTGCACATTATTATCTCCCCAAATTTGTAGTTTACATTAGGATTTACTCT... | TTTGCATTCACAATTGACTAATTGTTTGGTGCAAGAGGACTAGCTTTCAGCCTGTCTCAGCTTTAGACATACTTTCCTCACTAAGCTTAATCACTTCTGGCTTAAAAAACTTTTTTACAGACTTTATTGTTTGGGGCAGTTTTAAGTTCACAGCAAAATTGAGCAGGAAGTACAAGAGTTCCCGTGTGCCCTCTGATGCCACATACAGTCTCCCCCACCCTTAACAACCTGAACCAGAGTGGTACATTCGTTACCGCTGGTGAGCCTACATTGCACATTATTATCTCCCCAAATTTGTAGTTTACATTAGGATTTACTCT... |
Task1_train_42896 | A mutation on Chromosome 14 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CAATTTTTAAAAACTTACTAAGAAAGGAGATAAAGATATATCACAGACAAATTTTAGACAACTATTTTTCACACAGCTATACCTGATATTTGTATTTGAGTTGATTCAAAGTTAAAATCAAATTAGCTAACAAGTAATAAAACTCTGAAATGGGGATAGAATAATAGATTCATAAAAGATAATAATAGGCACATTAAAAACAGGCCTATGAAGTATTGGGCCTGAGAAGGAACTCAGGGTTTGAACGCAACCACTTGGTTTTACCAATCGTGAAACTGAGACCCAGAGGGAAAGATAAGGCAGCTGTTGGAGACAAAGGT... | CAATTTTTAAAAACTTACTAAGAAAGGAGATAAAGATATATCACAGACAAATTTTAGACAACTATTTTTCACACAGCTATACCTGATATTTGTATTTGAGTTGATTCAAAGTTAAAATCAAATTAGCTAACAAGTAATAAAACTCTGAAATGGGGATAGAATAATAGATTCATAAAAGATAATAATAGGCACATTAAAAACAGGCCTATGAAGTATTGGGCCTGAGAAGGAACTCAGGGTTTGAACGCAACCACTTGGTTTTACCAATCGTGAAACTGAGACCCAGAGGGAAAGATAAGGCAGCTGTTGGAGACAAAGGT... |
Task1_train_42897 | Consider this mutation on Chromosome 14. Is this a benign change or a disease-causing variant? | Benign | AATAAACATACATGTGCATGTGTCTTTATAGCAGCATGATTTATAGTCCTTTGGGTATATACCCAGTAATGGGATGGCTGGGTCAAATGGTATTTCTAGTTCTAGATCCCTGAGGAATCGCCACACTGACTTCCACAAGGGTTGAACTAGTTTACAGTCCCACCAACAGTGTAAAAGTGTTCCTATTTCTCCACATCCTCTCCAGCACCTGTTGTTTCCTGACTTTTTAATGATCGCCATTCTAACTGCCAACCGTTTTTTTAAATTGCAAGCCCAGTAATTATATTTTCCAAGAATGACATAGCATGTAGTGTGGGAAA... | AATAAACATACATGTGCATGTGTCTTTATAGCAGCATGATTTATAGTCCTTTGGGTATATACCCAGTAATGGGATGGCTGGGTCAAATGGTATTTCTAGTTCTAGATCCCTGAGGAATCGCCACACTGACTTCCACAAGGGTTGAACTAGTTTACAGTCCCACCAACAGTGTAAAAGTGTTCCTATTTCTCCACATCCTCTCCAGCACCTGTTGTTTCCTGACTTTTTAATGATCGCCATTCTAACTGCCAACCGTTTTTTTAAATTGCAAGCCCAGTAATTATATTTTCCAAGAATGACATAGCATGTAGTGTGGGAAA... |
Task1_train_42898 | A sequence alteration has been identified on Chromosome 14. Is it disease-inducing or harmless? | Benign | TTAATGATCGCCATTCTAACTGCCAACCGTTTTTTTAAATTGCAAGCCCAGTAATTATATTTTCCAAGAATGACATAGCATGTAGTGTGGGAAATACAAGCAGTTATGGAGAGTATATTTGAGAGTAATTACAACTGTCCTAAAAATTCTGATGCATGTGATCATGATAATTATTATTCATTAAACTGAACTGCTTGGACAAAATTTACATTTTCCTAAAAATCATGTTTATTAGAGAAATTGTTGTATTATTCTTAAAATATTGTTAACATGAATATCCAAAGTTACCTCGGCAATAAAACATTTATGCTTTTGGGTTT... | TTAATGATCGCCATTCTAACTGCCAACCGTTTTTTTAAATTGCAAGCCCAGTAATTATATTTTCCAAGAATGACATAGCATGTAGTGTGGGAAATACAAGCAGTTATGGAGAGTATATTTGAGAGTAATTACAACTGTCCTAAAAATTCTGATGCATGTGATCATGATAATTATTATTCATTAAACTGAACTGCTTGGACAAAATTTACATTTTCCTAAAAATCATGTTTATTAGAGAAATTGTTGTATTATTCTTAAAATATTGTTAACATGAATATCCAAAGTTACCTCGGCAATAAAACATTTATGCTTTTGGGTTT... |
Task1_train_42899 | An alteration has been detected on Chromosome 14. Is it pathogenic, and if so, what disease is involved? | Benign | TTTGAGAGTAATTACAACTGTCCTAAAAATTCTGATGCATGTGATCATGATAATTATTATTCATTAAACTGAACTGCTTGGACAAAATTTACATTTTCCTAAAAATCATGTTTATTAGAGAAATTGTTGTATTATTCTTAAAATATTGTTAACATGAATATCCAAAGTTACCTCGGCAATAAAACATTTATGCTTTTGGGTTTGCTCCAGGTTTGATCAAGTACTGAAAGGCAGGCCTCTCGCTCTCTGTGGATCATATAAATGATGTAAAGATGGAATTTTGTGAGTATCTTAACAGTGACGCTAATAATACAATAAAT... | TTTGAGAGTAATTACAACTGTCCTAAAAATTCTGATGCATGTGATCATGATAATTATTATTCATTAAACTGAACTGCTTGGACAAAATTTACATTTTCCTAAAAATCATGTTTATTAGAGAAATTGTTGTATTATTCTTAAAATATTGTTAACATGAATATCCAAAGTTACCTCGGCAATAAAACATTTATGCTTTTGGGTTTGCTCCAGGTTTGATCAAGTACTGAAAGGCAGGCCTCTCGCTCTCTGTGGATCATATAAATGATGTAAAGATGGAATTTTGTGAGTATCTTAACAGTGACGCTAATAATACAATAAAT... |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.