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_42300 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AGAGGAAGTACAGGGTGCTGGAGAGTAATAGATGGGGCGGCTACTCCAGACATGGGCCAAATTGAGGCCATGGACTGAGGAATGCTGACAGGACCTGGAAGTCCCTTGTGCTGGGTGGAGCATGGTTCATGGAAAAGAAAGGGAAAAAAGTAAGGAGAGGAGCAGGGCCAAGCTGGCTCTTGAAGGGCTTTACAAACACATTAAGGGGTTAGGACTTTATTTGGAGTCCCTGCGAGCCATTAGAGGTTTTAAGCAGCATCTAATATGATTGGGTTTGCATTTTACAAATATCACTGTGGCTGCCATGAGGATGATGGATT... | AGAGGAAGTACAGGGTGCTGGAGAGTAATAGATGGGGCGGCTACTCCAGACATGGGCCAAATTGAGGCCATGGACTGAGGAATGCTGACAGGACCTGGAAGTCCCTTGTGCTGGGTGGAGCATGGTTCATGGAAAAGAAAGGGAAAAAAGTAAGGAGAGGAGCAGGGCCAAGCTGGCTCTTGAAGGGCTTTACAAACACATTAAGGGGTTAGGACTTTATTTGGAGTCCCTGCGAGCCATTAGAGGTTTTAAGCAGCATCTAATATGATTGGGTTTGCATTTTACAAATATCACTGTGGCTGCCATGAGGATGATGGATT... |
Task1_train_42301 | This mutation on Chromosome 12 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CCCATGTTCGTCACAAGAATTAATGGGGATTAGTTATGTGAAAGTGCTTTGTAAACTCTAGAGTGTTCTATATATATAAAGGGTTATTACTATTTTTTCATTACCTTGGAGTACTTCGATTCTATCCTGATTGCCATTGTCTCTACTTATCCCTCAGTTCCCTTCAACCTCATAAAAATGTCTAAATTATAAATGCAAAATGTAATATTATGACTATGATTCAAAATTTCAAAATGCTTCACAAATAGTAAATGGTTTTTCATCTTTTACTAGTGAGGGGCAGGTCCTATATTCAGTTTGCTTCTCATGGTCCTGTGTCT... | CCCATGTTCGTCACAAGAATTAATGGGGATTAGTTATGTGAAAGTGCTTTGTAAACTCTAGAGTGTTCTATATATATAAAGGGTTATTACTATTTTTTCATTACCTTGGAGTACTTCGATTCTATCCTGATTGCCATTGTCTCTACTTATCCCTCAGTTCCCTTCAACCTCATAAAAATGTCTAAATTATAAATGCAAAATGTAATATTATGACTATGATTCAAAATTTCAAAATGCTTCACAAATAGTAAATGGTTTTTCATCTTTTACTAGTGAGGGGCAGGTCCTATATTCAGTTTGCTTCTCATGGTCCTGTGTCT... |
Task1_train_42302 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CAGGCTGGTCTTGAACTCCTGGGCTCAAGCAGTCCTCCTGCCTCATCCTTCCAAAGTGCTGGGATTACAGGCATGAGCCACTATGCCTGGCCTGGTTTCTGCTTTATCCTTACGTATTTTCTGAAATTGTCTTGCCATATGTATTAGTCCATTTTCACACTGCTGATAAAGACATACCAGAGACTGGGAAGAAAAAGATGTTTAATTGGACTTACGGTCCCATATGGCTGGGGAGGCCTTAGAATCATGGTGGGAGGCGAAAGGTACTTCTTACACGGCAGCGGCAAGAGAAAATGAGGAAGATGTAAAAGCAGAAACCC... | CAGGCTGGTCTTGAACTCCTGGGCTCAAGCAGTCCTCCTGCCTCATCCTTCCAAAGTGCTGGGATTACAGGCATGAGCCACTATGCCTGGCCTGGTTTCTGCTTTATCCTTACGTATTTTCTGAAATTGTCTTGCCATATGTATTAGTCCATTTTCACACTGCTGATAAAGACATACCAGAGACTGGGAAGAAAAAGATGTTTAATTGGACTTACGGTCCCATATGGCTGGGGAGGCCTTAGAATCATGGTGGGAGGCGAAAGGTACTTCTTACACGGCAGCGGCAAGAGAAAATGAGGAAGATGTAAAAGCAGAAACCC... |
Task1_train_42303 | This variant lies on Chromosome 12. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AACTCGCGCGCCAGGGCCCCACTTAACTTTGCAGCTGCCCGCGCCCCGCCCGTGGGTGTGCGCTGGGGAGCCGTGACCCGAACGCCCGTTTTTACTGCCCCGGTCTCTTCCTCCGTCTTTCTTTGGAAGAGGGTTGTCGCTGCCCAGCGGGGTTGGAGGGGGGGTCTGGGTGACTTTCTCCCCCCTGACCCTCTTTTGTCTCCTCCCGCACGTGGCTTCCAGGCCGAGGTGGGGACAGCGCCGTTCGTCAGCTTCAGGCTTCCCCGGGGCTCGGTGCAGGGGCCACCCGGAGCGGAGTGGGGACTGGCCCGCCCTCCCCC... | AACTCGCGCGCCAGGGCCCCACTTAACTTTGCAGCTGCCCGCGCCCCGCCCGTGGGTGTGCGCTGGGGAGCCGTGACCCGAACGCCCGTTTTTACTGCCCCGGTCTCTTCCTCCGTCTTTCTTTGGAAGAGGGTTGTCGCTGCCCAGCGGGGTTGGAGGGGGGGTCTGGGTGACTTTCTCCCCCCTGACCCTCTTTTGTCTCCTCCCGCACGTGGCTTCCAGGCCGAGGTGGGGACAGCGCCGTTCGTCAGCTTCAGGCTTCCCCGGGGCTCGGTGCAGGGGCCACCCGGAGCGGAGTGGGGACTGGCCCGCCCTCCCCC... |
Task1_train_42304 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AGAGGTCTTCCAAAAGCTGCCATCACATCTTCCTACATTCATCAGCAGTGCCTGCCCATGAATTCTGCTTTCCCTCTTTTAACAATAAAGAAACAATCAGTGTCTAAAGCCAACCCTTCCATATCTCCACCAGATCCTAAGCCCTTTCTCCTACTCAAGAGCATCTTTCCAACAACTTTCCCCTCACTCCTGCATCATCAACTTTTCTCTCTCCAAAATTATTCTTGTCAACATACAAACATGCTGTTGTGTCTTCCATCTTGTTCTCACTTCTCTCAACTACTCCTGCATTACTCTGCTTCCCTTCTTGGAAAAGAAAC... | AGAGGTCTTCCAAAAGCTGCCATCACATCTTCCTACATTCATCAGCAGTGCCTGCCCATGAATTCTGCTTTCCCTCTTTTAACAATAAAGAAACAATCAGTGTCTAAAGCCAACCCTTCCATATCTCCACCAGATCCTAAGCCCTTTCTCCTACTCAAGAGCATCTTTCCAACAACTTTCCCCTCACTCCTGCATCATCAACTTTTCTCTCTCCAAAATTATTCTTGTCAACATACAAACATGCTGTTGTGTCTTCCATCTTGTTCTCACTTCTCTCAACTACTCCTGCATTACTCTGCTTCCCTTCTTGGAAAAGAAAC... |
Task1_train_42305 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AAGGCGGAGCTTGCAGTGAGCCGATATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGCGAAACTCCGTCTCAAAAAAAAAAAAAAAAAACTTGTAAGAGAAGGCCATTTTGTTTCTGAAAAAAATAACCACCAAATCCACATGCAGTTAAAAGCGACTGAAATTTCCAATAATGAATAGAACTAAGCACAAGATCAAAAATAAAACAGAACACTGAAAAAATAATATAAGCTATATCAACTATATCAATAGAAGAAAAACAACCCACAAAGAAAAAAGTGACTGAATACTGGATAATGGGGAAAATCACTGCCAAGTC... | AAGGCGGAGCTTGCAGTGAGCCGATATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGCGAAACTCCGTCTCAAAAAAAAAAAAAAAAAACTTGTAAGAGAAGGCCATTTTGTTTCTGAAAAAAATAACCACCAAATCCACATGCAGTTAAAAGCGACTGAAATTTCCAATAATGAATAGAACTAAGCACAAGATCAAAAATAAAACAGAACACTGAAAAAATAATATAAGCTATATCAACTATATCAATAGAAGAAAAACAACCCACAAAGAAAAAAGTGACTGAATACTGGATAATGGGGAAAATCACTGCCAAGTC... |
Task1_train_42306 | Chromosome 12 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GTTTAAAGCCTAAGAACTCCCTAAAGGATGAAGGTAGTAAAACAACAGACTATCTATTAGTAATGGTATCTCAATACTAAAATTGTGCAGGAGTATAATGAAATCTAATACCACATCATTACAGCTTTTGAATTTTACAAATATAGTTATACTGACAATGCCTATTACTATTTGTCTGATACAAGGACAAAATTACGTATCTTGTGTTACTGTCAACATATTTTGTATTTATTAAATATTCAAAGCAGTTACGCCTTTCTTAGAATACAGGAAACACGCAATATATTAGTCAACAAAACACAACATTTTAGAATAAAATC... | GTTTAAAGCCTAAGAACTCCCTAAAGGATGAAGGTAGTAAAACAACAGACTATCTATTAGTAATGGTATCTCAATACTAAAATTGTGCAGGAGTATAATGAAATCTAATACCACATCATTACAGCTTTTGAATTTTACAAATATAGTTATACTGACAATGCCTATTACTATTTGTCTGATACAAGGACAAAATTACGTATCTTGTGTTACTGTCAACATATTTTGTATTTATTAAATATTCAAAGCAGTTACGCCTTTCTTAGAATACAGGAAACACGCAATATATTAGTCAACAAAACACAACATTTTAGAATAAAATC... |
Task1_train_42307 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | AAATTAAGCCTGCTGACTTTCACTGTGATTGTGGTTTGATATCATGCAGGATAGATCACAACTGCTGATTCATATTAGGAAAGAGAGCCCCCAACTGTCACAAGCACATTGTGTTTGAAAATACAAAACCTTACCAAATCACTTAGTACTTAAAATTAACAACATCCTCATCATCTTGTGGTTGAAATGATGACTGAACAATAACTCAAGCTAGTTGTGTTCTATATATTTTTAATTAATATAATTAGTATTCCTAGATCTTTTTAAATTGCTCTACTCTAGCCCTAGGGAAAAATGATTTCAGAAGGCTGAATACGTAT... | AAATTAAGCCTGCTGACTTTCACTGTGATTGTGGTTTGATATCATGCAGGATAGATCACAACTGCTGATTCATATTAGGAAAGAGAGCCCCCAACTGTCACAAGCACATTGTGTTTGAAAATACAAAACCTTACCAAATCACTTAGTACTTAAAATTAACAACATCCTCATCATCTTGTGGTTGAAATGATGACTGAACAATAACTCAAGCTAGTTGTGTTCTATATATTTTTAATTAATATAATTAGTATTCCTAGATCTTTTTAAATTGCTCTACTCTAGCCCTAGGGAAAAATGATTTCAGAAGGCTGAATACGTAT... |
Task1_train_42308 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AGAGAACTGCACTGGTGGCTGGGGGGCCATACCCCATCGACCTTGATGGAACAGCTGAAGGACACGGTTGTTTCCACTCTGACGCTGGCTTTCTGCTCTTTGCTCTCAAACGCCTCAGTGCTCCTTCCACAGGCTCTCTGAGTATCACTTGAAATATTCAGAGGAAAGTGGCTCTAAACTTTATGTTGGCCAAACACAAAGCCAGTGCCCATCACGGAAAGAACTCAAGAACATGGGCATATTCTTGCCTCTTATATTTGACGTTTTGCCTAACTCCAGTCTTTTATCAACTTTTGGACTTATAACTTTTAGAAGTTTTA... | AGAGAACTGCACTGGTGGCTGGGGGGCCATACCCCATCGACCTTGATGGAACAGCTGAAGGACACGGTTGTTTCCACTCTGACGCTGGCTTTCTGCTCTTTGCTCTCAAACGCCTCAGTGCTCCTTCCACAGGCTCTCTGAGTATCACTTGAAATATTCAGAGGAAAGTGGCTCTAAACTTTATGTTGGCCAAACACAAAGCCAGTGCCCATCACGGAAAGAACTCAAGAACATGGGCATATTCTTGCCTCTTATATTTGACGTTTTGCCTAACTCCAGTCTTTTATCAACTTTTGGACTTATAACTTTTAGAAGTTTTA... |
Task1_train_42309 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | GGATTTAAATGTGGAAAGCATGGACCTTTTTTAAGGTCAGACAAAGCCAGATTTTAATTCCAAGTCTGACACTTATGAATTTGGACTTTGAGCATATTTTTGAACTCTCTGAGTCTCAGTTTTCTCATCTGTAAGTGGGGATAAAAATATCTATATATAAGAGGCATTGTAAAGATTAAATAATATATGTATACATATATATAACCACTTAACAAATTGCCTCATACTTAGTTAATAATAAAATGGTTCATATTAATAGTTGGCCAAAGAAAAAATATTTGGCTAATAGATGTAGAAATTTTAATAGCTAGAAAGTATTT... | GGATTTAAATGTGGAAAGCATGGACCTTTTTTAAGGTCAGACAAAGCCAGATTTTAATTCCAAGTCTGACACTTATGAATTTGGACTTTGAGCATATTTTTGAACTCTCTGAGTCTCAGTTTTCTCATCTGTAAGTGGGGATAAAAATATCTATATATAAGAGGCATTGTAAAGATTAAATAATATATGTATACATATATATAACCACTTAACAAATTGCCTCATACTTAGTTAATAATAAAATGGTTCATATTAATAGTTGGCCAAAGAAAAAATATTTGGCTAATAGATGTAGAAATTTTAATAGCTAGAAAGTATTT... |
Task1_train_42310 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | GAGGCGCCCCCCATCTCCCGGACGGGGCAGCTGCCGGGCAGGGGCTGCCCCCTACCTCCCTCCCGGACGGGGCGGCTGGCCGGGCAGGGGCTGCCCCCCATCTCCTGGACAGGGCGGCTGCCGGGCAGAGACGCTCCTCACTTCCCGGACGGGGTGGCTGCTGGGCGGAGGGGCTCCTCACTTCCCAGATGAAGCGGCTGCCGGGCGGAGGGGCTCCTCACTTCTCAGACGGGGCGGCCGGGCAGAGACGCTCCTCACCTCCCAGACGGGGTGGTGGTCGGGCAGAGACACTCCTCAGTTCCCAGACGGAGTCGCGGCCA... | GAGGCGCCCCCCATCTCCCGGACGGGGCAGCTGCCGGGCAGGGGCTGCCCCCTACCTCCCTCCCGGACGGGGCGGCTGGCCGGGCAGGGGCTGCCCCCCATCTCCTGGACAGGGCGGCTGCCGGGCAGAGACGCTCCTCACTTCCCGGACGGGGTGGCTGCTGGGCGGAGGGGCTCCTCACTTCCCAGATGAAGCGGCTGCCGGGCGGAGGGGCTCCTCACTTCTCAGACGGGGCGGCCGGGCAGAGACGCTCCTCACCTCCCAGACGGGGTGGTGGTCGGGCAGAGACACTCCTCAGTTCCCAGACGGAGTCGCGGCCA... |
Task1_train_42311 | Given this context: Chromosome 12 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AAAAAAGGAACCAGAGTTTGGAATTGGACAGACCAGGGTCCAAGGATTCTGTCACTTACTAATTCTGTGATCTTGGACAAGCCACTTATCTTCTTTGAGCTACTGTTTCTTTATCTGTAATATAAGTATTACATGACACCATAGCACATAGAGCTGCTGTGAGAATTATTAATAATGGTGAAATTAATAACTGCCATTTGCTGAGCACAGACTATATGCCAGACTTTAATACTGGGTCATAAAATCCTCACAGCAACCCTCCCAGGTTGGTTTTTTTTTCTTAGTTTATATTTTTGAGATTGGGACACTTGGGTTTAGAG... | AAAAAAGGAACCAGAGTTTGGAATTGGACAGACCAGGGTCCAAGGATTCTGTCACTTACTAATTCTGTGATCTTGGACAAGCCACTTATCTTCTTTGAGCTACTGTTTCTTTATCTGTAATATAAGTATTACATGACACCATAGCACATAGAGCTGCTGTGAGAATTATTAATAATGGTGAAATTAATAACTGCCATTTGCTGAGCACAGACTATATGCCAGACTTTAATACTGGGTCATAAAATCCTCACAGCAACCCTCCCAGGTTGGTTTTTTTTTCTTAGTTTATATTTTTGAGATTGGGACACTTGGGTTTAGAG... |
Task1_train_42312 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | TTTGTGATTTGGTCTCTCTACTTACCTGGCCACATGCCTCACATTTTTTATTCTAGTATACTTTTGCTTTTTATACTTTTAGTAGAGATGGGGTTTTGCCACGTTGCCCAGGCTGGTCTCGAACTCCTGGACTTAGGCTATCCACTCACCTCAGCTTCCCAAAATGTGGGATTACAGGCATGAGCCACCGTGCCCGGCCTTTATTCTAGTATACTAAAAAAGGTGTAGGTTCCCAAATGTGCCATCCTTTCTCTCACCTCCAGGGCTTTGTTTTCTCTGTTGGAACGAAGACAACTTACACTTCACCTGGATGACTTCTT... | TTTGTGATTTGGTCTCTCTACTTACCTGGCCACATGCCTCACATTTTTTATTCTAGTATACTTTTGCTTTTTATACTTTTAGTAGAGATGGGGTTTTGCCACGTTGCCCAGGCTGGTCTCGAACTCCTGGACTTAGGCTATCCACTCACCTCAGCTTCCCAAAATGTGGGATTACAGGCATGAGCCACCGTGCCCGGCCTTTATTCTAGTATACTAAAAAAGGTGTAGGTTCCCAAATGTGCCATCCTTTCTCTCACCTCCAGGGCTTTGTTTTCTCTGTTGGAACGAAGACAACTTACACTTCACCTGGATGACTTCTT... |
Task1_train_42313 | A mutation on Chromosome 12 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GCCTAGGCAACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAAAGAAAAGAAAAGAAAAGAAAAGAATAAAGTGTTGCTGCCTTAAATTATGAAAGAATCAAGTATTAAAAATTTTCTTGTAAATTTTGCATCCATAAATTTTCTATAAATCCATTCTAATTGAGTCCCTAACTCTCCATCTTCCTTCTTCGGTATAGAGAAATAATTTGATTATTTACATCGAGGCCTACTTCAAGTTACCTGAATAAGGTGAACCAGAGACACAGTTTAAGAAAAGTTTGGGCCGGGTGCAGTGCCTCATGCCAGTAATCCCAGC... | GCCTAGGCAACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAAAGAAAAGAAAAGAAAAGAAAAGAATAAAGTGTTGCTGCCTTAAATTATGAAAGAATCAAGTATTAAAAATTTTCTTGTAAATTTTGCATCCATAAATTTTCTATAAATCCATTCTAATTGAGTCCCTAACTCTCCATCTTCCTTCTTCGGTATAGAGAAATAATTTGATTATTTACATCGAGGCCTACTTCAAGTTACCTGAATAAGGTGAACCAGAGACACAGTTTAAGAAAAGTTTGGGCCGGGTGCAGTGCCTCATGCCAGTAATCCCAGC... |
Task1_train_42314 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AATGCAAGTATTTCTTACATTTCAGAAATGCCTCTGGACTTGAATACCTACTTGCATAATTAAACTCAAAGCCTATTCTAACTAATTACACCCACAGTAAGTCCTTTTCCATTACTGTTTTTCCAAAAAGTAAATCCTCTGGTTTAAACAACCATATTCTGGCTTCTTAAAGGTCTTAATCTTTTCTCCAACAAACTTCTGAAAGCTCAGCCTGCTTTTACAAATTGCTCTGCTCCACTGAACACATACACTAGTTGGCCAGATGCCTTTCTAAACACAATTAACACATCTGTAAGTTCTATGTTATGTATTTCACAGTA... | AATGCAAGTATTTCTTACATTTCAGAAATGCCTCTGGACTTGAATACCTACTTGCATAATTAAACTCAAAGCCTATTCTAACTAATTACACCCACAGTAAGTCCTTTTCCATTACTGTTTTTCCAAAAAGTAAATCCTCTGGTTTAAACAACCATATTCTGGCTTCTTAAAGGTCTTAATCTTTTCTCCAACAAACTTCTGAAAGCTCAGCCTGCTTTTACAAATTGCTCTGCTCCACTGAACACATACACTAGTTGGCCAGATGCCTTTCTAAACACAATTAACACATCTGTAAGTTCTATGTTATGTATTTCACAGTA... |
Task1_train_42315 | This genomic variant is located on Chromosome 12. Can you determine its pathogenicity and name any linked disease? | Benign | CACTTCTTGTGTAAAACAGTAAAAATGGAACAGTTATAATGTTTCTATATTATTTAGGAGAGGCCTTGATAGATGAACCACAGGAAAGGTATTGTACAAATTGGTGCTATATGCTGAATATTTTCTGATAAAGTTGAATTTTTGAGTAGGTTTTTTTCTCATAGGCAGAAATGATATAAGAACAGAAACTATAACTCTCAACTTTTATTGTAGCAAAGCATACCACTTATTGTAGAAAAGCATAACACATTCAAATGGCATCTAGTTAAATGCTTGTTTTAACTTACAGAATGAATGAGTGAGAAAAAATTGTCCAAAGA... | CACTTCTTGTGTAAAACAGTAAAAATGGAACAGTTATAATGTTTCTATATTATTTAGGAGAGGCCTTGATAGATGAACCACAGGAAAGGTATTGTACAAATTGGTGCTATATGCTGAATATTTTCTGATAAAGTTGAATTTTTGAGTAGGTTTTTTTCTCATAGGCAGAAATGATATAAGAACAGAAACTATAACTCTCAACTTTTATTGTAGCAAAGCATACCACTTATTGTAGAAAAGCATAACACATTCAAATGGCATCTAGTTAAATGCTTGTTTTAACTTACAGAATGAATGAGTGAGAAAAAATTGTCCAAAGA... |
Task1_train_42316 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AACAAACATTTGTTTAAAGATTTGATTATACAAAATAGTATGTTCTCTAACTTTGATAAGATTAACATGAACAAAATAACTTTTATGTTATTTAATGACTGATAAACATTAAATATTTGATCAAATAAGATATTTTTACTACTTAAACTTTCTCCAGTAGAAAATTTAACTTAACAGTCTAATATTGATTGAAATAGAAGAAATCATCTTTAAATTCATTCAAATTATCCTAGTTTTCAGTCATTCTGAAAATTTGAGAAAAGCTGGACTATACTATGAATTTGAGGCTTGTTCTACAGAGAGAAACAGCTATTCGTTTA... | AACAAACATTTGTTTAAAGATTTGATTATACAAAATAGTATGTTCTCTAACTTTGATAAGATTAACATGAACAAAATAACTTTTATGTTATTTAATGACTGATAAACATTAAATATTTGATCAAATAAGATATTTTTACTACTTAAACTTTCTCCAGTAGAAAATTTAACTTAACAGTCTAATATTGATTGAAATAGAAGAAATCATCTTTAAATTCATTCAAATTATCCTAGTTTTCAGTCATTCTGAAAATTTGAGAAAAGCTGGACTATACTATGAATTTGAGGCTTGTTCTACAGAGAGAAACAGCTATTCGTTTA... |
Task1_train_42317 | This is a variant located on Chromosome 12. Is this mutation a likely cause of disease or not? | Benign | TATAGACTGGGTGTCAGAAGACTTTTCCAATCTACTTTTTGAATAAAGGAAGATGGAATATAAAATGATTTGTTTCCCTTAAAAAGAGGGAGGGCAGGTTATAGACTGAGGAACTGAACAATTTTAAAAAGTTCAAACAATTATTTGAACCAACTATTTACCATATCTGCAGAGAGTCTAGAAATCACAATTAATTTGACTTCTCGAATTCAAAAACGGTTCTGTTTTATGATAGTAACGCAAAAACTTCATACCTATAAATTACTGTATAGAATGTTTGTATTAAGCTATTTTTCTCTGAATATGTCTTTAGAAGAACA... | TATAGACTGGGTGTCAGAAGACTTTTCCAATCTACTTTTTGAATAAAGGAAGATGGAATATAAAATGATTTGTTTCCCTTAAAAAGAGGGAGGGCAGGTTATAGACTGAGGAACTGAACAATTTTAAAAAGTTCAAACAATTATTTGAACCAACTATTTACCATATCTGCAGAGAGTCTAGAAATCACAATTAATTTGACTTCTCGAATTCAAAAACGGTTCTGTTTTATGATAGTAACGCAAAAACTTCATACCTATAAATTACTGTATAGAATGTTTGTATTAAGCTATTTTTCTCTGAATATGTCTTTAGAAGAACA... |
Task1_train_42318 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | TTCGAGGCTTAACCTGTCATAAATGTATCTTCTTAATTTCTCTCCTTCAAAACTGCTTCAGAACTTTGTATGAAGCGAGAAAGTAATTACAAATATCTTAGATTTTTCTTATTGCATGGTGACAGAATAATCAATCAAAATCTGCAAAATGGAGACATTTTTCAATCTTTAAGGAAGATGTTAAAAACTAAACAAACACAGAAGAACTATGTCCAACTCTTTAAAATGAACAATGAATTCTAATTACCTCTTCTTGAAACACAATTATGGCTTCCTGGAATTGTTTTTCACTTTCCCCTGTGGCGCTCAAAAGCTTTGTG... | TTCGAGGCTTAACCTGTCATAAATGTATCTTCTTAATTTCTCTCCTTCAAAACTGCTTCAGAACTTTGTATGAAGCGAGAAAGTAATTACAAATATCTTAGATTTTTCTTATTGCATGGTGACAGAATAATCAATCAAAATCTGCAAAATGGAGACATTTTTCAATCTTTAAGGAAGATGTTAAAAACTAAACAAACACAGAAGAACTATGTCCAACTCTTTAAAATGAACAATGAATTCTAATTACCTCTTCTTGAAACACAATTATGGCTTCCTGGAATTGTTTTTCACTTTCCCCTGTGGCGCTCAAAAGCTTTGTG... |
Task1_train_42319 | This alteration occurs on Chromosome 12. Is it associated with a disease or is it a benign variant? | Benign | TAAACCAAGCACCAAGTAGTTATTTGTTTTGTCCTCTGTTACACAGAATTCCCCAGGGAAGACTGAAACTTACTGTGTCTGATTCTCTGGTGTTCAGAGAACACAGCCTAGAACATTTGCAGTATAGCTTTTATAGTGTTAGAAATTTGGATAAAGCGGTTCCTACTCTGAACGAAGAGGCCCATAGCCTCCTCTAATTTAGCTCTGCAATGTGGGGACATCATGAGCTGCAGGGAACACGAGCAGAATGAGAGTTTAGATGTTACACCCGGCGTCTTGGGTCACTCTCCCTCACCCCCAGTTGTACTAGAATAGTATGT... | TAAACCAAGCACCAAGTAGTTATTTGTTTTGTCCTCTGTTACACAGAATTCCCCAGGGAAGACTGAAACTTACTGTGTCTGATTCTCTGGTGTTCAGAGAACACAGCCTAGAACATTTGCAGTATAGCTTTTATAGTGTTAGAAATTTGGATAAAGCGGTTCCTACTCTGAACGAAGAGGCCCATAGCCTCCTCTAATTTAGCTCTGCAATGTGGGGACATCATGAGCTGCAGGGAACACGAGCAGAATGAGAGTTTAGATGTTACACCCGGCGTCTTGGGTCACTCTCCCTCACCCCCAGTTGTACTAGAATAGTATGT... |
Task1_train_42320 | This variant is located on Chromosome 12. Evaluate its biological effect and specify any disease association. | Benign | TCAGAAAATGATGACAATAACCCTTTAAATTTGTTGTGAAAAACAAACTAGTCAATGTAAGTAAAATATTTACAACAGTCCTTGATATGCAGAAATAAATGTTAGCTATTATACTTATTATGACTAATAGCAAGATATGTCACACAAAAAGAGATTTCTGTAATATGTGCAGTTTTCTTTAAATGTCATTAGAATTTTTTAAAGCCTCATACATTACCTTTTCATCTATCTTGTTTCTTGGAGACTGTTTATGTGTAACATTTGATTTTGTATTTTCTGCATTTCTCTGACTATACTGCTTATAGCCCTCTTTAATTTCA... | TCAGAAAATGATGACAATAACCCTTTAAATTTGTTGTGAAAAACAAACTAGTCAATGTAAGTAAAATATTTACAACAGTCCTTGATATGCAGAAATAAATGTTAGCTATTATACTTATTATGACTAATAGCAAGATATGTCACACAAAAAGAGATTTCTGTAATATGTGCAGTTTTCTTTAAATGTCATTAGAATTTTTTAAAGCCTCATACATTACCTTTTCATCTATCTTGTTTCTTGGAGACTGTTTATGTGTAACATTTGATTTTGTATTTTCTGCATTTCTCTGACTATACTGCTTATAGCCCTCTTTAATTTCA... |
Task1_train_42321 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ACTTGGGAGCCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAATAAGCCGAGATTGCACCATTGCACTCCAGCCTGGGCAACAAGAGCAAAACTCCGTCTCAAAAACAAACAAACAAAAAAACAAAACCACAACAAAAAAACACAACACCAAGATGGAGTTGCTCTAGTTCAAACACCTGATACAGGGAGTAAATTTCATTTATTTTTAAAGTAAACTTCTTCATTTTCTGCAGCCACACTGGCTTTTCTTTGAGTTCTGTGAATGGGTCAGTCCCACCCAGGGATCACACAGGATGTTGCCCTCTGCT... | ACTTGGGAGCCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAATAAGCCGAGATTGCACCATTGCACTCCAGCCTGGGCAACAAGAGCAAAACTCCGTCTCAAAAACAAACAAACAAAAAAACAAAACCACAACAAAAAAACACAACACCAAGATGGAGTTGCTCTAGTTCAAACACCTGATACAGGGAGTAAATTTCATTTATTTTTAAAGTAAACTTCTTCATTTTCTGCAGCCACACTGGCTTTTCTTTGAGTTCTGTGAATGGGTCAGTCCCACCCAGGGATCACACAGGATGTTGCCCTCTGCT... |
Task1_train_42322 | Located on Chromosome 12, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ATACCTATTAAATGCTTATCATATGCAAAGCACTGGGCATGTCTGGAAGTCATTAAATGCTTACAGTAATGGAGGAGTGTTTTAAACAACCACAAAAAAAGCAAAGTGACCAAATGACCTGAAAGGCAATTAAAAAAAAAATGAAAAAAATTATGCAGCAGTTTTAAAGTTCATTCATCCATGAATTCAGCAAAAGAGCTAATTTATTCTCTCCATATTCACAGAAACAAAATAATGCATCATATAGCATAAATGTTTAAAAAATCAGAATTACATTTAATATAAAAAATTTTGATATTATAGTTTTTAAAATACATTAG... | ATACCTATTAAATGCTTATCATATGCAAAGCACTGGGCATGTCTGGAAGTCATTAAATGCTTACAGTAATGGAGGAGTGTTTTAAACAACCACAAAAAAAGCAAAGTGACCAAATGACCTGAAAGGCAATTAAAAAAAAAATGAAAAAAATTATGCAGCAGTTTTAAAGTTCATTCATCCATGAATTCAGCAAAAGAGCTAATTTATTCTCTCCATATTCACAGAAACAAAATAATGCATCATATAGCATAAATGTTTAAAAAATCAGAATTACATTTAATATAAAAAATTTTGATATTATAGTTTTTAAAATACATTAG... |
Task1_train_42323 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | TTGAGCACTTTGGCGAGGCCGAATAGCATAGGTCATATGAGTCTGAGTTTTAATACTTGCTCTACCTCTAACTCACTCTGTAATCTTGGACAGTGTAGCTTCTGCTTCAGTCGTATCATCTGTAAAGTGGGGATAATAGCAGGATTTATCATAGGGTTCTTGTGCTGCTTAAATGGCACATAGTTGGTGATTAATATATTATTTTGTTAATAATTAGATACATTATGATACCAGTCATAATTAAAAATGCAGAATACCAAAATTAAAAGAAGTTTAATTCTGGGTTGTAGAGTTCTTGTTTCTGTCTTTATGCTTTTTTT... | TTGAGCACTTTGGCGAGGCCGAATAGCATAGGTCATATGAGTCTGAGTTTTAATACTTGCTCTACCTCTAACTCACTCTGTAATCTTGGACAGTGTAGCTTCTGCTTCAGTCGTATCATCTGTAAAGTGGGGATAATAGCAGGATTTATCATAGGGTTCTTGTGCTGCTTAAATGGCACATAGTTGGTGATTAATATATTATTTTGTTAATAATTAGATACATTATGATACCAGTCATAATTAAAAATGCAGAATACCAAAATTAAAAGAAGTTTAATTCTGGGTTGTAGAGTTCTTGTTTCTGTCTTTATGCTTTTTTT... |
Task1_train_42324 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AAATAGGTAAGTTAACTTTGGTCTGTAACTAAGAAATTTAAGCATGTTTTATAGATTACTTAGTCTCCCAGTATATCTTGAATAAAGGAAAGTGTGAATAGCCAACTTTCTTCATGGAAAAATATTTTATAAATTTTGATTATTACTATGCAATCTGTTTATCTTTCATTTTTCTCTGGTAAGGGTGGTATTTTTGTCACTATTTACAGATCACTGAGTAAACCATATTTCTTGCTATCAGTAGGAACTGTTTCCATTCAGTAAGGTGTACCTAGTATGTGCAGAACATTCTCGGGCTTTGAGAAGACTTTTTTTTTTTT... | AAATAGGTAAGTTAACTTTGGTCTGTAACTAAGAAATTTAAGCATGTTTTATAGATTACTTAGTCTCCCAGTATATCTTGAATAAAGGAAAGTGTGAATAGCCAACTTTCTTCATGGAAAAATATTTTATAAATTTTGATTATTACTATGCAATCTGTTTATCTTTCATTTTTCTCTGGTAAGGGTGGTATTTTTGTCACTATTTACAGATCACTGAGTAAACCATATTTCTTGCTATCAGTAGGAACTGTTTCCATTCAGTAAGGTGTACCTAGTATGTGCAGAACATTCTCGGGCTTTGAGAAGACTTTTTTTTTTTT... |
Task1_train_42325 | Chromosome 12 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AATCCCATTTCAGGAACAAAATAAATAACACCATAGGATTCACAACTGAAGGTGGCTTCCTGATGAAGCCTAAGGAAGCAGTAGCTTTTTTAAACTGCAGAAAGGAAGCTTCTCTCACCACAGATTTACTCAGGGCAAGTGGAAATACATGTTAAGAATGCTTACCCTAGTTAAGTGCTAGACAGCGCCCCCCTTTAGAAAAACAAGGCTCCGGTAGCCTATTCAGATCTACTTCCAGAATAAGACGATTCTTGAATCAAAACCATAAGTCAGTCGGCGCTTTCACTGTGACACCATGCAGAGTCGGAACTCTAACTGGT... | AATCCCATTTCAGGAACAAAATAAATAACACCATAGGATTCACAACTGAAGGTGGCTTCCTGATGAAGCCTAAGGAAGCAGTAGCTTTTTTAAACTGCAGAAAGGAAGCTTCTCTCACCACAGATTTACTCAGGGCAAGTGGAAATACATGTTAAGAATGCTTACCCTAGTTAAGTGCTAGACAGCGCCCCCCTTTAGAAAAACAAGGCTCCGGTAGCCTATTCAGATCTACTTCCAGAATAAGACGATTCTTGAATCAAAACCATAAGTCAGTCGGCGCTTTCACTGTGACACCATGCAGAGTCGGAACTCTAACTGGT... |
Task1_train_42326 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | AGTCTATCAAAAGGTAATAAAGACTAGTTTTAAAAAGGTATAAAAAAGTCTGTTTTAACACTGAGTACCCCAAGACAGTAAGAAGGGAACAATAGACACCAGGGCCTACTTGAGGGTAGAGGGTGAGAGGAGGGTGAGAATTGAAAAACTACCTATTGGGTATTATGCTGATTACCTGGGTGACCAAATTATCTGTACACCAAACACTCGCAAAATGCAACTTACCCATGTAACAAACCTGCACATGTACCCACTGAACTTAAAAGTTAGAAAGAAAAAAAAAAACTACTTAAAACACTTGACTTTGATCTAATAAATCA... | AGTCTATCAAAAGGTAATAAAGACTAGTTTTAAAAAGGTATAAAAAAGTCTGTTTTAACACTGAGTACCCCAAGACAGTAAGAAGGGAACAATAGACACCAGGGCCTACTTGAGGGTAGAGGGTGAGAGGAGGGTGAGAATTGAAAAACTACCTATTGGGTATTATGCTGATTACCTGGGTGACCAAATTATCTGTACACCAAACACTCGCAAAATGCAACTTACCCATGTAACAAACCTGCACATGTACCCACTGAACTTAAAAGTTAGAAAGAAAAAAAAAAACTACTTAAAACACTTGACTTTGATCTAATAAATCA... |
Task1_train_42327 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | CCTATTCAATAAAAAGGTTCAAACTCTACAGACAAAAAAAAAGGTACCCTTGGTTTGTTTGTTTTCAGGGAAGATTAAATTTAGGAGTTGCCAACACCCAAACGAAAAACATTCCAGAGTATTAGACTCCATTGTAGTGGGAAGTCATCTACATTCTCAGCACTATGTTCTCTTACTCAAAGCAGGGGTATTAACAAAAGATGTTTCTTAGGATCTCACAAGATACACTCTACTTACTTCCCCCAGTAAACATTACCCTTGTTTAAAAAAAAAAAAAGTACTTGAAAAATAATTTTAGCACATGCAGCCAGAAAAAAAGT... | CCTATTCAATAAAAAGGTTCAAACTCTACAGACAAAAAAAAAGGTACCCTTGGTTTGTTTGTTTTCAGGGAAGATTAAATTTAGGAGTTGCCAACACCCAAACGAAAAACATTCCAGAGTATTAGACTCCATTGTAGTGGGAAGTCATCTACATTCTCAGCACTATGTTCTCTTACTCAAAGCAGGGGTATTAACAAAAGATGTTTCTTAGGATCTCACAAGATACACTCTACTTACTTCCCCCAGTAAACATTACCCTTGTTTAAAAAAAAAAAAAGTACTTGAAAAATAATTTTAGCACATGCAGCCAGAAAAAAAGT... |
Task1_train_42328 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CATTGTGGAAGGCAAAGGGGAAGCAATCAACTTCTTCAAAAGGTGGCTGGAAAGACAGAAAGAATGAGGGGGAAATGCCACACTTTTTAACCATCAGGTGTCATGAGAACTCCCTCACTATCACAAGAACAGCTTGGGAGAAACCACCCCCATGATCCAATCACCTCTCACCAGGTCCTTCCCTCAACATATGGGGATTGTAATTCGAGGTGAGATTTGGGTGGGGACACAGAGCCAAGCCATGTTATGCATGGAGCCTTGTATCCATCACAACAGTTCTACATAGAACATACCTGTCAACCTCCAAATATACTTCATGT... | CATTGTGGAAGGCAAAGGGGAAGCAATCAACTTCTTCAAAAGGTGGCTGGAAAGACAGAAAGAATGAGGGGGAAATGCCACACTTTTTAACCATCAGGTGTCATGAGAACTCCCTCACTATCACAAGAACAGCTTGGGAGAAACCACCCCCATGATCCAATCACCTCTCACCAGGTCCTTCCCTCAACATATGGGGATTGTAATTCGAGGTGAGATTTGGGTGGGGACACAGAGCCAAGCCATGTTATGCATGGAGCCTTGTATCCATCACAACAGTTCTACATAGAACATACCTGTCAACCTCCAAATATACTTCATGT... |
Task1_train_42329 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCTCGGCTCACTGCAAGCTCTGCCTCCCGGGTTCAAGAGATTCTCCTGCCTCAGCCTCTGGAGTAGCTGGGATTACAGGCACGCGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGAGTTTCACCATGTTGGCCAGGATGGTGTCAATCTCTTGACCTCGTGATCCACCTGCCTCAGCCTCCCAAGCCATTGGTTTTTATAGATACAGACCCTGAAGAAAAATAGATGGACTATGAAAAAATACTATTTTTATCGGATACTTTGGCCTGTGTCAGAATTTGGCATCTGAATTTAGATACTTAGTATGAGC... | TCTCGGCTCACTGCAAGCTCTGCCTCCCGGGTTCAAGAGATTCTCCTGCCTCAGCCTCTGGAGTAGCTGGGATTACAGGCACGCGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGAGTTTCACCATGTTGGCCAGGATGGTGTCAATCTCTTGACCTCGTGATCCACCTGCCTCAGCCTCCCAAGCCATTGGTTTTTATAGATACAGACCCTGAAGAAAAATAGATGGACTATGAAAAAATACTATTTTTATCGGATACTTTGGCCTGTGTCAGAATTTGGCATCTGAATTTAGATACTTAGTATGAGC... |
Task1_train_42330 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CAAGAGATTCTCCTGCCTCAGCCTCTGGAGTAGCTGGGATTACAGGCACGCGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGAGTTTCACCATGTTGGCCAGGATGGTGTCAATCTCTTGACCTCGTGATCCACCTGCCTCAGCCTCCCAAGCCATTGGTTTTTATAGATACAGACCCTGAAGAAAAATAGATGGACTATGAAAAAATACTATTTTTATCGGATACTTTGGCCTGTGTCAGAATTTGGCATCTGAATTTAGATACTTAGTATGAGCCTGTTGAATAATGAGTTGAGAGAAAAATGGAAT... | CAAGAGATTCTCCTGCCTCAGCCTCTGGAGTAGCTGGGATTACAGGCACGCGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGAGTTTCACCATGTTGGCCAGGATGGTGTCAATCTCTTGACCTCGTGATCCACCTGCCTCAGCCTCCCAAGCCATTGGTTTTTATAGATACAGACCCTGAAGAAAAATAGATGGACTATGAAAAAATACTATTTTTATCGGATACTTTGGCCTGTGTCAGAATTTGGCATCTGAATTTAGATACTTAGTATGAGCCTGTTGAATAATGAGTTGAGAGAAAAATGGAAT... |
Task1_train_42331 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | TATTTCAACACCAGAATGCAGAGAAGATCAATTCATGATTCAAGTTCGACAGGAAGAACCTTGTTGTTTTTCCCCTTTTTGTGGTGAGTATTGTAGAGATAATTTCTTGGAAGAAGAGAAAGGATCTAGGAAAAAAATCTCTTATTTGATGTGAATTTTATGAGACTGATGGCAAGCAATATTCTGATGTTATAAGAATTCAACTGAATGAGAACTCTTGTAAAGAAAGTATGACATTTTAAATGACTAGACAATAATAATAAATACCTTCCCCCATCAACAAAAACTACATACATCAGTCCAAATATGACCAAGATATT... | TATTTCAACACCAGAATGCAGAGAAGATCAATTCATGATTCAAGTTCGACAGGAAGAACCTTGTTGTTTTTCCCCTTTTTGTGGTGAGTATTGTAGAGATAATTTCTTGGAAGAAGAGAAAGGATCTAGGAAAAAAATCTCTTATTTGATGTGAATTTTATGAGACTGATGGCAAGCAATATTCTGATGTTATAAGAATTCAACTGAATGAGAACTCTTGTAAAGAAAGTATGACATTTTAAATGACTAGACAATAATAATAAATACCTTCCCCCATCAACAAAAACTACATACATCAGTCCAAATATGACCAAGATATT... |
Task1_train_42332 | A variant was discovered on Chromosome 12. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CATGCACTGGAAGAATTCGATTTATTATTATTTTTAGCTCCATTATTCTAACATTTATTTCCAGTCCCATTGGAATTGTCTAATGACTAAAGTCCTGAAATATCAAATGAATTAGTGTCCATAAGACTACTTTACAACTTACAAGGCACTATAAAAAGCAAGACATTATTAGCTTATGAGGAAAAATGCCTTTTATGTGAATGTATTGGAATCATTTATTTATGTCAAGAATAAAATTCATTTTATTACTGATGTCATATGAAAACTAAATGCATCCAGGAAAAGTTGATGCTTTAGACACAATTCTTGAAACTTTAAGC... | CATGCACTGGAAGAATTCGATTTATTATTATTTTTAGCTCCATTATTCTAACATTTATTTCCAGTCCCATTGGAATTGTCTAATGACTAAAGTCCTGAAATATCAAATGAATTAGTGTCCATAAGACTACTTTACAACTTACAAGGCACTATAAAAAGCAAGACATTATTAGCTTATGAGGAAAAATGCCTTTTATGTGAATGTATTGGAATCATTTATTTATGTCAAGAATAAAATTCATTTTATTACTGATGTCATATGAAAACTAAATGCATCCAGGAAAAGTTGATGCTTTAGACACAATTCTTGAAACTTTAAGC... |
Task1_train_42333 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATTTATTATTATTTTTAGCTCCATTATTCTAACATTTATTTCCAGTCCCATTGGAATTGTCTAATGACTAAAGTCCTGAAATATCAAATGAATTAGTGTCCATAAGACTACTTTACAACTTACAAGGCACTATAAAAAGCAAGACATTATTAGCTTATGAGGAAAAATGCCTTTTATGTGAATGTATTGGAATCATTTATTTATGTCAAGAATAAAATTCATTTTATTACTGATGTCATATGAAAACTAAATGCATCCAGGAAAAGTTGATGCTTTAGACACAATTCTTGAAACTTTAAGCCTGGTCCTGTATTTGGTGG... | ATTTATTATTATTTTTAGCTCCATTATTCTAACATTTATTTCCAGTCCCATTGGAATTGTCTAATGACTAAAGTCCTGAAATATCAAATGAATTAGTGTCCATAAGACTACTTTACAACTTACAAGGCACTATAAAAAGCAAGACATTATTAGCTTATGAGGAAAAATGCCTTTTATGTGAATGTATTGGAATCATTTATTTATGTCAAGAATAAAATTCATTTTATTACTGATGTCATATGAAAACTAAATGCATCCAGGAAAAGTTGATGCTTTAGACACAATTCTTGAAACTTTAAGCCTGGTCCTGTATTTGGTGG... |
Task1_train_42334 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTGCTAACATAAAAGAAATACAGACAGGTTACCGCCTATGTAGGCACCTTAGGAGTTTCTTTCATGTTCAGATATTTCCTTGGTCCTTTAAGGGAAGATTAGTAAGTACTTCATTCCTCCCAGGTTTTCTTTATGGGCATTGTCTCTTGTATCTTTTTCTTTTTCCTTGGTATGGGTTATCACAACATCCTTTTAAGTATGTATTGTCAGATGGTAGCATTGCTAACTGCTTATGGTCTGGCCAGAGTTTCCATTTGTGATTTAATTACCCCATTTTCCAATGAAGTGCCACCTTGCCAGTGTAAACATTTTATTCCCAA... | CTGCTAACATAAAAGAAATACAGACAGGTTACCGCCTATGTAGGCACCTTAGGAGTTTCTTTCATGTTCAGATATTTCCTTGGTCCTTTAAGGGAAGATTAGTAAGTACTTCATTCCTCCCAGGTTTTCTTTATGGGCATTGTCTCTTGTATCTTTTTCTTTTTCCTTGGTATGGGTTATCACAACATCCTTTTAAGTATGTATTGTCAGATGGTAGCATTGCTAACTGCTTATGGTCTGGCCAGAGTTTCCATTTGTGATTTAATTACCCCATTTTCCAATGAAGTGCCACCTTGCCAGTGTAAACATTTTATTCCCAA... |
Task1_train_42335 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAAGTGGAAATAAAACACAAATTACATTTCTATTAGGCATGTGTATTCTACATAATTTTTGGAGGGGATAATCCTCTATTTTTTGAATTACATATTAAAAAATTAGTCAAACACTATTATCATTAGATCACTACAGTTTCTTTTCCTTCTACCCTTCGGTAATGTCTTAATGTGACTATGCCTGAACTTAGCACTTCATTAAGATTATATTCTACTATAATTGCATGATATTTTCTCCTACCATCCTTTTTCATACCAGAAGTTCTTAGCATTCTACTCACTCCATATGTCAGACAAGTAAGGTAATTATCAGTGACACC... | AAAGTGGAAATAAAACACAAATTACATTTCTATTAGGCATGTGTATTCTACATAATTTTTGGAGGGGATAATCCTCTATTTTTTGAATTACATATTAAAAAATTAGTCAAACACTATTATCATTAGATCACTACAGTTTCTTTTCCTTCTACCCTTCGGTAATGTCTTAATGTGACTATGCCTGAACTTAGCACTTCATTAAGATTATATTCTACTATAATTGCATGATATTTTCTCCTACCATCCTTTTTCATACCAGAAGTTCTTAGCATTCTACTCACTCCATATGTCAGACAAGTAAGGTAATTATCAGTGACACC... |
Task1_train_42336 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | AGTTGGTTAGACGGATCAGTCATGGTAGATTTTTGTGTATTTTAATGTAGCAGATAGGAGATTCAAGCTTTTTTTCTCTCAAGCTTGAGAATACAGAGGGCATAGGTCTGGCTTACCTTGTAAAAAATGCCAGCAGCTAACAATGAAATTCTACCCAACACAGGCTGGGTATTTCTCTGATTTTTTGCCTTGGGTTTACAGTATTCCTAGAGTTACCAGAAAACTATAGTGGACAATTAGCGGTGGATGCCAAGAGAATGCTTGGAACTTTGAGAATGTTGGGGTGGACATTAATCAATTGATATAAGCTTTGGGTATGG... | AGTTGGTTAGACGGATCAGTCATGGTAGATTTTTGTGTATTTTAATGTAGCAGATAGGAGATTCAAGCTTTTTTTCTCTCAAGCTTGAGAATACAGAGGGCATAGGTCTGGCTTACCTTGTAAAAAATGCCAGCAGCTAACAATGAAATTCTACCCAACACAGGCTGGGTATTTCTCTGATTTTTTGCCTTGGGTTTACAGTATTCCTAGAGTTACCAGAAAACTATAGTGGACAATTAGCGGTGGATGCCAAGAGAATGCTTGGAACTTTGAGAATGTTGGGGTGGACATTAATCAATTGATATAAGCTTTGGGTATGG... |
Task1_train_42337 | A variant on Chromosome 12 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GATTTTGAAAATGTAAAATACAATAATTACAACCAATTGCAGGGTATCCACTTGATATTAGGCACTAGACATTTATAAACATTCCAGAAATCTGCTTTTTGGTGAAAATGGTTGTATAATTGATTCAGTTTGCTATGTTTTTCATATCTAATGAAACTACATATTCCAAAATAGTTAAGGAAATAAGAAATTTATCCCAACTTGTTTGTATATTCACAACTATTGATTGAATTTTTTTCATACTTATTTGAAACGTTTCATCAATGCATGTATTAGCCCAGTTATCCTAAAGTAAAGTTGACTTGCCCCAACTCCAGTTT... | GATTTTGAAAATGTAAAATACAATAATTACAACCAATTGCAGGGTATCCACTTGATATTAGGCACTAGACATTTATAAACATTCCAGAAATCTGCTTTTTGGTGAAAATGGTTGTATAATTGATTCAGTTTGCTATGTTTTTCATATCTAATGAAACTACATATTCCAAAATAGTTAAGGAAATAAGAAATTTATCCCAACTTGTTTGTATATTCACAACTATTGATTGAATTTTTTTCATACTTATTTGAAACGTTTCATCAATGCATGTATTAGCCCAGTTATCCTAAAGTAAAGTTGACTTGCCCCAACTCCAGTTT... |
Task1_train_42338 | A mutation located on Chromosome 12 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AAAAGCAATGGCAACAAAAGACAAAATTGACAAATGGGATCTAATTAAACTAAAGAGCTTCTGTACAGCAAAAGAAACTACCATCAGAGCGAACAGGCAACCTACAAAATGGGAGAAAATTGTCACAACCTACTCATCTGACAAAGGGCTAATATCCAGAATCTGCAATGAACTCAAACAAATTTACAAGAGAAAAACAAACAACCCCATCAAAAAGTGGGCGAAGGACATGAACAGACACTTCTCAAAAGAAGACATTTATGCAGCCAAAAGACACATGAAAAAATGCTTATCATCACTGGCCATCAGAGAAATGCAAA... | AAAAGCAATGGCAACAAAAGACAAAATTGACAAATGGGATCTAATTAAACTAAAGAGCTTCTGTACAGCAAAAGAAACTACCATCAGAGCGAACAGGCAACCTACAAAATGGGAGAAAATTGTCACAACCTACTCATCTGACAAAGGGCTAATATCCAGAATCTGCAATGAACTCAAACAAATTTACAAGAGAAAAACAAACAACCCCATCAAAAAGTGGGCGAAGGACATGAACAGACACTTCTCAAAAGAAGACATTTATGCAGCCAAAAGACACATGAAAAAATGCTTATCATCACTGGCCATCAGAGAAATGCAAA... |
Task1_train_42339 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TCGTTGAATAATTTTGATGAGCCTCAGCCATTATCCCTTTAAATATTTCTTCATTTTCTCTACTATTTTAGACCCCCTCCGGATATCATCTATGTCTCAACTGCCATTTTATATTTTCCATAACTGTCTTCTTTGATCTACATTCTTGATAATTTCTTCAATACTATCATCCTTTTCACTAAAGTTCTCTTCTTCTTTATCTAATCTGCTCTTTAATACCTCAAGAGATTTTTAATTTTAGTTATTTTGTTCTGTTCCAGAAGGTCTATCTTGTTCTCTTTCAAACTTGCTTGGTTATTTAATATTATTTACCATTATTT... | TCGTTGAATAATTTTGATGAGCCTCAGCCATTATCCCTTTAAATATTTCTTCATTTTCTCTACTATTTTAGACCCCCTCCGGATATCATCTATGTCTCAACTGCCATTTTATATTTTCCATAACTGTCTTCTTTGATCTACATTCTTGATAATTTCTTCAATACTATCATCCTTTTCACTAAAGTTCTCTTCTTCTTTATCTAATCTGCTCTTTAATACCTCAAGAGATTTTTAATTTTAGTTATTTTGTTCTGTTCCAGAAGGTCTATCTTGTTCTCTTTCAAACTTGCTTGGTTATTTAATATTATTTACCATTATTT... |
Task1_train_42340 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | ATTGTTGGCTTGGAGTTTTTATTCTTTGCTATTTTTTTGTATTGGCTTTGCAATAAAAACCACCATCTATTTCTCTTTTAGTACAAACATATTTCCAGTTTAATTGTTGCAATAAAAAATGTTCTATGTCGATTTTCCTAAAACAACATATTAAAATAATGATAAATAGTAAAATCGATCCATTGATAACAATTAGTTTGAAGTGTTCATGCATACTAAAAAAATACATTCTGAACAATGAATGTGTTTATTTTTCAGAATTTTACACTCCATGAAGTAACCAATGACTTTGACAATATGACTGTATCCACAATTATAGA... | ATTGTTGGCTTGGAGTTTTTATTCTTTGCTATTTTTTTGTATTGGCTTTGCAATAAAAACCACCATCTATTTCTCTTTTAGTACAAACATATTTCCAGTTTAATTGTTGCAATAAAAAATGTTCTATGTCGATTTTCCTAAAACAACATATTAAAATAATGATAAATAGTAAAATCGATCCATTGATAACAATTAGTTTGAAGTGTTCATGCATACTAAAAAAATACATTCTGAACAATGAATGTGTTTATTTTTCAGAATTTTACACTCCATGAAGTAACCAATGACTTTGACAATATGACTGTATCCACAATTATAGA... |
Task1_train_42341 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CTATTTCTCTTTTAGTACAAACATATTTCCAGTTTAATTGTTGCAATAAAAAATGTTCTATGTCGATTTTCCTAAAACAACATATTAAAATAATGATAAATAGTAAAATCGATCCATTGATAACAATTAGTTTGAAGTGTTCATGCATACTAAAAAAATACATTCTGAACAATGAATGTGTTTATTTTTCAGAATTTTACACTCCATGAAGTAACCAATGACTTTGACAATATGACTGTATCCACAATTATAGATAAACTGACAATATTCAGCTACTATACATTTTGGTTAACAGCAAGTACTTCAGTTGGAAATGGGAA... | CTATTTCTCTTTTAGTACAAACATATTTCCAGTTTAATTGTTGCAATAAAAAATGTTCTATGTCGATTTTCCTAAAACAACATATTAAAATAATGATAAATAGTAAAATCGATCCATTGATAACAATTAGTTTGAAGTGTTCATGCATACTAAAAAAATACATTCTGAACAATGAATGTGTTTATTTTTCAGAATTTTACACTCCATGAAGTAACCAATGACTTTGACAATATGACTGTATCCACAATTATAGATAAACTGACAATATTCAGCTACTATACATTTTGGTTAACAGCAAGTACTTCAGTTGGAAATGGGAA... |
Task1_train_42342 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTATGTGTATAACCAAAAATCTGGGTACTAGGAAATTTTTTACAACATTGAGAGAATTCCTTGGTTTATCTGACTTAAAATCACATCCTAAATTTAGAGAAACATCTCATAAGAAAATATATTTATGACACAGCATAAAAACGTGTAGTAACAAATGCAAAAATATCTCTCTTGAACCAACTTAACCTTTATTTTAGCTTTGCATTTTTCCATTTAAAATGAAATATTTGACACAATAGTACGTTTATCTGCTTCTCTCTCTTTTATTCTTTGCTGTTAATTTATTTACATTTTTTGCAAGATAATGAAGCTTGAATATC... | TTATGTGTATAACCAAAAATCTGGGTACTAGGAAATTTTTTACAACATTGAGAGAATTCCTTGGTTTATCTGACTTAAAATCACATCCTAAATTTAGAGAAACATCTCATAAGAAAATATATTTATGACACAGCATAAAAACGTGTAGTAACAAATGCAAAAATATCTCTCTTGAACCAACTTAACCTTTATTTTAGCTTTGCATTTTTCCATTTAAAATGAAATATTTGACACAATAGTACGTTTATCTGCTTCTCTCTCTTTTATTCTTTGCTGTTAATTTATTTACATTTTTTGCAAGATAATGAAGCTTGAATATC... |
Task1_train_42343 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GAGGAAGAAACCCAAATTCCAGAGCTCTTAATTCCCATTACGTTACTTTGTCAATTAGGCTAAACCAGCCTAATTCAGTTATTGAAGCTAAAAATAGAGCCTCCATGAAAATGTTTCCCTAATTAAACCGTGACTTCTAAAATGTGTTAAATAAGAAAAAATACAATTCCTATATAAATTATCCTATAGTACTTTTAAATAATAAAACAACACTTAAAGGATTTCAAATGAAGAAAATACATACTTTACTGTTTTAATACATTGTTCTTCTGGCTGAGGCTGGTCAAAGCTACACTGATCTTCAAATAAAGGCTCGTCAA... | GAGGAAGAAACCCAAATTCCAGAGCTCTTAATTCCCATTACGTTACTTTGTCAATTAGGCTAAACCAGCCTAATTCAGTTATTGAAGCTAAAAATAGAGCCTCCATGAAAATGTTTCCCTAATTAAACCGTGACTTCTAAAATGTGTTAAATAAGAAAAAATACAATTCCTATATAAATTATCCTATAGTACTTTTAAATAATAAAACAACACTTAAAGGATTTCAAATGAAGAAAATACATACTTTACTGTTTTAATACATTGTTCTTCTGGCTGAGGCTGGTCAAAGCTACACTGATCTTCAAATAAAGGCTCGTCAA... |
Task1_train_42344 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTCCAGAGCTCTTAATTCCCATTACGTTACTTTGTCAATTAGGCTAAACCAGCCTAATTCAGTTATTGAAGCTAAAAATAGAGCCTCCATGAAAATGTTTCCCTAATTAAACCGTGACTTCTAAAATGTGTTAAATAAGAAAAAATACAATTCCTATATAAATTATCCTATAGTACTTTTAAATAATAAAACAACACTTAAAGGATTTCAAATGAAGAAAATACATACTTTACTGTTTTAATACATTGTTCTTCTGGCTGAGGCTGGTCAAAGCTACACTGATCTTCAAATAAAGGCTCGTCAATGCTACACTGTTCTTC... | TTCCAGAGCTCTTAATTCCCATTACGTTACTTTGTCAATTAGGCTAAACCAGCCTAATTCAGTTATTGAAGCTAAAAATAGAGCCTCCATGAAAATGTTTCCCTAATTAAACCGTGACTTCTAAAATGTGTTAAATAAGAAAAAATACAATTCCTATATAAATTATCCTATAGTACTTTTAAATAATAAAACAACACTTAAAGGATTTCAAATGAAGAAAATACATACTTTACTGTTTTAATACATTGTTCTTCTGGCTGAGGCTGGTCAAAGCTACACTGATCTTCAAATAAAGGCTCGTCAATGCTACACTGTTCTTC... |
Task1_train_42345 | The following genetic variant occurs on Chromosome 12. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ATTATTATTCTTCCTGTTACCTCAGTTCATAATCCGCCAATTCCTCTTCCTCCATTACTCTTGCATTTGCTCTTTTTCATTCCCATAGAAAATAGTTCAGTGTCACCTCTCCTTTTTAAATCTTGCAACAGAATTTTTGTAATGGCTTCCAACCTGTTGTTCTTGCCTTTAGACTGTATTTCATTCATGTTGCCACTCAACAGCTTTCAGATTTATTGTCCAAAACCGTAGTTCTGATCTTGTCATTCTTCTGCTCAAAACCCATCAGTAGTTCTTCATTTCCTACAAAATAAAGTTCTTCACCTTTGGCCTTATCTTGT... | ATTATTATTCTTCCTGTTACCTCAGTTCATAATCCGCCAATTCCTCTTCCTCCATTACTCTTGCATTTGCTCTTTTTCATTCCCATAGAAAATAGTTCAGTGTCACCTCTCCTTTTTAAATCTTGCAACAGAATTTTTGTAATGGCTTCCAACCTGTTGTTCTTGCCTTTAGACTGTATTTCATTCATGTTGCCACTCAACAGCTTTCAGATTTATTGTCCAAAACCGTAGTTCTGATCTTGTCATTCTTCTGCTCAAAACCCATCAGTAGTTCTTCATTTCCTACAAAATAAAGTTCTTCACCTTTGGCCTTATCTTGT... |
Task1_train_42346 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ACTTGTGACACTGTTTATTTGGAGGCATTTTCTGTTTAGTAGGTAAACACAAAGCTTAACCTTTAATTCCTCATAAAGTCATTGTTATTATATTTAACTCATTGTTTCAGATTGAGGAATTGTGACAATTTTGGCTTCCACATCTTTGCTCACATTACCTACAGCTAGCTTTCTCCCCATCAGTGCCTGTTAAATTCTTTCTTCAAATATTGCCCAAATACTAGTCTTTTCCTGAGGCATTCTCATTAAAATAATAAATGTATGTACTAAATAAATTGTATTACATTTTCTATATAAATTTACACTACATGACATGAGAA... | ACTTGTGACACTGTTTATTTGGAGGCATTTTCTGTTTAGTAGGTAAACACAAAGCTTAACCTTTAATTCCTCATAAAGTCATTGTTATTATATTTAACTCATTGTTTCAGATTGAGGAATTGTGACAATTTTGGCTTCCACATCTTTGCTCACATTACCTACAGCTAGCTTTCTCCCCATCAGTGCCTGTTAAATTCTTTCTTCAAATATTGCCCAAATACTAGTCTTTTCCTGAGGCATTCTCATTAAAATAATAAATGTATGTACTAAATAAATTGTATTACATTTTCTATATAAATTTACACTACATGACATGAGAA... |
Task1_train_42347 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | ATTAAATTAATGATTTTTCAAGAAAACAAATTATCAAAATTATTTGAAAAAGTGAAAAACAAATCAATAATATGGCAAAGAGGTGGAAAGAGATTTTTCAAATGTTGCTAAACTAGGAAAGATGTTATAACTAAATTCTTACAACCTATTAAGGAGCAAAAATACTTTATTTCTAAAAGCTATATATTTCAGATCAAAATTGTACAAGCATAGCACAGATAAAAGAAACTAGAAGCTAGTTGCACTTATGAATATAGATGATTGGGGTTCTCAGTTGTAGAAAACAGACACTCTAGCTACTTTAGGCAGTAAGTTTTTTT... | ATTAAATTAATGATTTTTCAAGAAAACAAATTATCAAAATTATTTGAAAAAGTGAAAAACAAATCAATAATATGGCAAAGAGGTGGAAAGAGATTTTTCAAATGTTGCTAAACTAGGAAAGATGTTATAACTAAATTCTTACAACCTATTAAGGAGCAAAAATACTTTATTTCTAAAAGCTATATATTTCAGATCAAAATTGTACAAGCATAGCACAGATAAAAGAAACTAGAAGCTAGTTGCACTTATGAATATAGATGATTGGGGTTCTCAGTTGTAGAAAACAGACACTCTAGCTACTTTAGGCAGTAAGTTTTTTT... |
Task1_train_42348 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ATTTATTTACATTTTTTGTCCTTGCACTATCCCAAACAGATATGATTAAAATAGTATGTTATAAAATCATTTGAAATAGTTTATCTTTGGGATTAGATTATAAATTGATAATTTAGTTTGCTAAATTAATTTGATAAATTAATTCACTTTTCCCATTTGATTGTGTTTAACTTTTATATGTAACACAGATTCATGATTCCAAGATGAAAACTACATTAAAAAAGCATACTCAAGATATTGTGCATTAGTCCATCCTTTTCACTCTTCTCTCGCATTTACTCTTATATGTGGAATTTTTGTATAATATGTACATATATAAT... | ATTTATTTACATTTTTTGTCCTTGCACTATCCCAAACAGATATGATTAAAATAGTATGTTATAAAATCATTTGAAATAGTTTATCTTTGGGATTAGATTATAAATTGATAATTTAGTTTGCTAAATTAATTTGATAAATTAATTCACTTTTCCCATTTGATTGTGTTTAACTTTTATATGTAACACAGATTCATGATTCCAAGATGAAAACTACATTAAAAAAGCATACTCAAGATATTGTGCATTAGTCCATCCTTTTCACTCTTCTCTCGCATTTACTCTTATATGTGGAATTTTTGTATAATATGTACATATATAAT... |
Task1_train_42349 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | TATGTTAAGAAGATTTAAGGAGCAATATATTTTTTTAAATGAGTTAACAATAAAGTTGCTTTAAAAAATTAAATACTTTTCAAATTTTGAAAGTAAAACAATAAGAAAACTGAGTTAAAACCTGCACTAAAAGTATGCAAAAGAATAAAAGAGAAGAAATGAGAAGGATTGGGACCCTTAACCAATGTCCACATATTAAAACTAAGTAAAATAATATTTCTACTTACATGTGCAGTGACACACAGGAAAGATATCAGCTAAATAAAAATAAACTGCAGCAGTACTCAGTTAACAGTACAATAAAAAATAATTATTTCATT... | TATGTTAAGAAGATTTAAGGAGCAATATATTTTTTTAAATGAGTTAACAATAAAGTTGCTTTAAAAAATTAAATACTTTTCAAATTTTGAAAGTAAAACAATAAGAAAACTGAGTTAAAACCTGCACTAAAAGTATGCAAAAGAATAAAAGAGAAGAAATGAGAAGGATTGGGACCCTTAACCAATGTCCACATATTAAAACTAAGTAAAATAATATTTCTACTTACATGTGCAGTGACACACAGGAAAGATATCAGCTAAATAAAAATAAACTGCAGCAGTACTCAGTTAACAGTACAATAAAAAATAATTATTTCATT... |
Task1_train_42350 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AGAACATTTTTAGGTGTCTGGCAAGTATCCTCTAAATCAAGGTAAAGATAATAATTTAGTGGCAGTGTTCATATTTTCCTATGACTGTAAGATTTAGGTGCCTCACAAAATATTAATATTTAGCCTCTTATGAAAGGTTCGTTTTTCTTCTAACACTTTAGTAGCTGAATACAAAGAAAATACACAACAGCTGTTTATAAATGAAATAAAAAGTTTCCATTTTTTATCTGAGTTTCTCATTTATTTGCAGAGAACGAATAAAATAAAAATATCCTAGTGTTGTTTGCACCACAGCATACCAGTAAATCTTAAGGATTGTG... | AGAACATTTTTAGGTGTCTGGCAAGTATCCTCTAAATCAAGGTAAAGATAATAATTTAGTGGCAGTGTTCATATTTTCCTATGACTGTAAGATTTAGGTGCCTCACAAAATATTAATATTTAGCCTCTTATGAAAGGTTCGTTTTTCTTCTAACACTTTAGTAGCTGAATACAAAGAAAATACACAACAGCTGTTTATAAATGAAATAAAAAGTTTCCATTTTTTATCTGAGTTTCTCATTTATTTGCAGAGAACGAATAAAATAAAAATATCCTAGTGTTGTTTGCACCACAGCATACCAGTAAATCTTAAGGATTGTG... |
Task1_train_42351 | Chromosome 12 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CACTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGGTTGCATGGTGACAGATTCTTAATTGGCTGTTCAATGCTTCAAATAAGGGTAAGCTACAGGAGGGTATGATATCTAAATGTAATAAAAATTTTGACTGCATCACTTCATCATAGTTTTGCATAAATTCTGCTAATGTTTATTAGAGCTTTTATTTAAAAACTGTGAAACTATGAGGTACAGCCCAAGTCCCATGTCCTTCCATGAAGTGACTTCCATGTTCGCAGTAATTGGTGTGATGCAATACCGACCTCACTGCCCCAGATAGCCGAAGCATTTAT... | CACTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGGTTGCATGGTGACAGATTCTTAATTGGCTGTTCAATGCTTCAAATAAGGGTAAGCTACAGGAGGGTATGATATCTAAATGTAATAAAAATTTTGACTGCATCACTTCATCATAGTTTTGCATAAATTCTGCTAATGTTTATTAGAGCTTTTATTTAAAAACTGTGAAACTATGAGGTACAGCCCAAGTCCCATGTCCTTCCATGAAGTGACTTCCATGTTCGCAGTAATTGGTGTGATGCAATACCGACCTCACTGCCCCAGATAGCCGAAGCATTTAT... |
Task1_train_42352 | A variant has been detected on Chromosome 12. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GGTATATGACATCATGAAGTGGCTGTAAAAGTTGAGGCTAGAAGTGTGGTGGGCTCAGATCGGAAAGGCCCTTTTATTCCATCTAAAGGAGTTTGAAGTTTATCCTGAAGATAATGGTTTTTAATCAGTGGTACAGCAAAAGCAAATTTAAGTTTTAGAAATAGAACTATGATAAAAGTGGGTTGGATTTCACTGGAGGCTAGGTGACCAGCAAAGAAGTTATTACAGTAATCTAGTGTGAGTAATGAAGGAATTCTGGCAATAAGAATGAGAAGGGTAATAGCAATAACATTCAATAAACGTGGCATCAGTAAATTGTT... | GGTATATGACATCATGAAGTGGCTGTAAAAGTTGAGGCTAGAAGTGTGGTGGGCTCAGATCGGAAAGGCCCTTTTATTCCATCTAAAGGAGTTTGAAGTTTATCCTGAAGATAATGGTTTTTAATCAGTGGTACAGCAAAAGCAAATTTAAGTTTTAGAAATAGAACTATGATAAAAGTGGGTTGGATTTCACTGGAGGCTAGGTGACCAGCAAAGAAGTTATTACAGTAATCTAGTGTGAGTAATGAAGGAATTCTGGCAATAAGAATGAGAAGGGTAATAGCAATAACATTCAATAAACGTGGCATCAGTAAATTGTT... |
Task1_train_42353 | A mutation located on Chromosome 12 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CTAGTGGCAATGATACTCTGAGAGCAATGATGCCCAGTGGCCAGTTTTTGGTATCTAAATGCCTTCCCCACTAAAAGGAACCTGGGCTCTTTAAAGAAATGGTTTATTCCAAGTATGGGCATGAAGTATGTAGGTAAGTCTAAGACATCTTATGCTAGAAAACAAGTCAAGCTTTGAGGCTTCGTTCAAAAGACTAATGAATTTTTGTCAAGACAATATAAGAGTCAACTTTAAAGGACTCTCTTTGGCTAAAGTTGAGACAAAAGAATATGACTCCAACTAAAACACATGGAATATTTAAAAATCTGTGAGTCTAATCT... | CTAGTGGCAATGATACTCTGAGAGCAATGATGCCCAGTGGCCAGTTTTTGGTATCTAAATGCCTTCCCCACTAAAAGGAACCTGGGCTCTTTAAAGAAATGGTTTATTCCAAGTATGGGCATGAAGTATGTAGGTAAGTCTAAGACATCTTATGCTAGAAAACAAGTCAAGCTTTGAGGCTTCGTTCAAAAGACTAATGAATTTTTGTCAAGACAATATAAGAGTCAACTTTAAAGGACTCTCTTTGGCTAAAGTTGAGACAAAAGAATATGACTCCAACTAAAACACATGGAATATTTAAAAATCTGTGAGTCTAATCT... |
Task1_train_42354 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | ACTTCTGATATATTTCTTATACAAAGATTAAAAATCATGAATTTTATCTCAAAAAATACGACAATGCCATACTACCAATATTTGCTGATAGTGTTCCTATACCTCAGGTAAATAAGAGAAATAATAATGTTAAAATTATACATTTAAAAATAATAATATCACATACAAAGCAATATTCTAATAAGTAGTTAAGGCTGTCCTTAGACAACATAAAATAATAATAAAAATCCCAATATTGAGAAAAAGATGAATTACTGTAATTTCCAAAATAAAAATGAGTACTTAATAATTATAACTCAAGTATACTCACAAATGGATCA... | ACTTCTGATATATTTCTTATACAAAGATTAAAAATCATGAATTTTATCTCAAAAAATACGACAATGCCATACTACCAATATTTGCTGATAGTGTTCCTATACCTCAGGTAAATAAGAGAAATAATAATGTTAAAATTATACATTTAAAAATAATAATATCACATACAAAGCAATATTCTAATAAGTAGTTAAGGCTGTCCTTAGACAACATAAAATAATAATAAAAATCCCAATATTGAGAAAAAGATGAATTACTGTAATTTCCAAAATAAAAATGAGTACTTAATAATTATAACTCAAGTATACTCACAAATGGATCA... |
Task1_train_42355 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTTGGTTCTACCCTATGCGCCTGGAAGTCCTCGAATCCCAGTCCCTGCATGGGTAGGCTGTACACATGGGTACAGAGCAAACCTACTGCCTGTATCTATACAGCATGTCCTGTTATTCCAAAGAGAATGGAGCAAATCTCTCTGTTAGTATTAACCAATTCCGCACTTGGTAACCTTGTCTAGTACAGACAGCTGGTGTCATTTTGACACCTGGGGCCACACACAAAGAAAGCAGCCCAGCTGATGCTGCCAAGAGAAACTGCTGAAGGGCCAGACACATTCCAGCAAGGAGGGGTGTGGGGTCTTTCACGTAGATTGCA... | TTTGGTTCTACCCTATGCGCCTGGAAGTCCTCGAATCCCAGTCCCTGCATGGGTAGGCTGTACACATGGGTACAGAGCAAACCTACTGCCTGTATCTATACAGCATGTCCTGTTATTCCAAAGAGAATGGAGCAAATCTCTCTGTTAGTATTAACCAATTCCGCACTTGGTAACCTTGTCTAGTACAGACAGCTGGTGTCATTTTGACACCTGGGGCCACACACAAAGAAAGCAGCCCAGCTGATGCTGCCAAGAGAAACTGCTGAAGGGCCAGACACATTCCAGCAAGGAGGGGTGTGGGGTCTTTCACGTAGATTGCA... |
Task1_train_42356 | Located on Chromosome 12, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TTCATTCATTCAGTCATTCATTCACCCACTTACTGAAAGCTGCCTAAGTGCCAGGCTCGGTGCTAGGAGATTGAAAGCACCATTCACAATTGCCAAGGCAGTCTTTTTTCCTTGCATTTTTAAGATAAATTCTTAAATTTCCTGATCAGCAGAACTCGTAGGAGAGTTCCACAGCCTTGGTAGAACCTAGCCCACTTTCAGTTTCACACATTTTAATAAACATAGTTGGGTTTAACTTCAGAGAGGCTTCAATTGTGTTTACTTTAAATGATTAAGCATTAACAAAGGGAGGCATAGTATTCTGGATGAGTCCCTTTCTA... | TTCATTCATTCAGTCATTCATTCACCCACTTACTGAAAGCTGCCTAAGTGCCAGGCTCGGTGCTAGGAGATTGAAAGCACCATTCACAATTGCCAAGGCAGTCTTTTTTCCTTGCATTTTTAAGATAAATTCTTAAATTTCCTGATCAGCAGAACTCGTAGGAGAGTTCCACAGCCTTGGTAGAACCTAGCCCACTTTCAGTTTCACACATTTTAATAAACATAGTTGGGTTTAACTTCAGAGAGGCTTCAATTGTGTTTACTTTAAATGATTAAGCATTAACAAAGGGAGGCATAGTATTCTGGATGAGTCCCTTTCTA... |
Task1_train_42357 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GAAACTATGACACGGTCTCCTTTCAGCACACAGGGAGCCCCCTACCTGCAACAGCAGATAACCTGTGCCTTCTCTTGCTCCTGAAAAAAACATTGATTAACTTTCACAAAACTGTTTAGATCCATGCCAATATCGTGCACTCTGAGGCAATAGAACAAGTTGAAAAATTGTGATAAACATTCATTTGAAATGCAGCCAAGCTGACTTTTAAAAGCCTTGCACATTGTTATTTGATAGCTTCTTCCTGCTTTGGTTGGTAAAATGAACTCTTTAAGTGGGCAATTCATGATGTCGCAATAGAATAGTGAATGAACTAAAAA... | GAAACTATGACACGGTCTCCTTTCAGCACACAGGGAGCCCCCTACCTGCAACAGCAGATAACCTGTGCCTTCTCTTGCTCCTGAAAAAAACATTGATTAACTTTCACAAAACTGTTTAGATCCATGCCAATATCGTGCACTCTGAGGCAATAGAACAAGTTGAAAAATTGTGATAAACATTCATTTGAAATGCAGCCAAGCTGACTTTTAAAAGCCTTGCACATTGTTATTTGATAGCTTCTTCCTGCTTTGGTTGGTAAAATGAACTCTTTAAGTGGGCAATTCATGATGTCGCAATAGAATAGTGAATGAACTAAAAA... |
Task1_train_42358 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ATATGATATAACCAATGATAAAATAATAACTAGCATGAGCATTTACTTTATTATAGTCAGTGTACTGAGTACTTTAAAGATATTAACCCATTTATTTCTCACAATAACTCTATCACATAGATTCATATAGACTCTATCATATAGAAACTAGAGCACAGAGATTAAGTATTTGGTCTAAAAGATGGCGAAATGGCATAGCTAATAAATGGCATAGCCAGGATATAAATTTGAACAATCTTGATTCAGAACTTGGGCATGAAGCAATTATAATTTTGCTACTTACATGGCTGGCATCTACAACACAAGTCTGCTTTCAATCA... | ATATGATATAACCAATGATAAAATAATAACTAGCATGAGCATTTACTTTATTATAGTCAGTGTACTGAGTACTTTAAAGATATTAACCCATTTATTTCTCACAATAACTCTATCACATAGATTCATATAGACTCTATCATATAGAAACTAGAGCACAGAGATTAAGTATTTGGTCTAAAAGATGGCGAAATGGCATAGCTAATAAATGGCATAGCCAGGATATAAATTTGAACAATCTTGATTCAGAACTTGGGCATGAAGCAATTATAATTTTGCTACTTACATGGCTGGCATCTACAACACAAGTCTGCTTTCAATCA... |
Task1_train_42359 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTTGTATTTATCAAAGCAAGCATGATGCTGGGATGCTTAAATAACAGTACAGTACATTGCAAAGGAACTAGGGAATAATGTTCCTATTATTTTTGTCCATGGTCAGCCTATTACTAGAAAAGAGTGACCACATTGATTTCTAAAGTCCTTATATTCAAAACTTTCTGTGCTGACCACCATCATTTATGTTTTTCCCATCTCTACTTAAAAACGTCAACTAGCCCCAACTTTTCCTCTAGTTATTTCTTTTATTAGATTTATTCTGTTCTCCACAATAAAATCTATCTTCTGTTCCCATCCATGACAATTCAAGTAGTTAT... | TTTGTATTTATCAAAGCAAGCATGATGCTGGGATGCTTAAATAACAGTACAGTACATTGCAAAGGAACTAGGGAATAATGTTCCTATTATTTTTGTCCATGGTCAGCCTATTACTAGAAAAGAGTGACCACATTGATTTCTAAAGTCCTTATATTCAAAACTTTCTGTGCTGACCACCATCATTTATGTTTTTCCCATCTCTACTTAAAAACGTCAACTAGCCCCAACTTTTCCTCTAGTTATTTCTTTTATTAGATTTATTCTGTTCTCCACAATAAAATCTATCTTCTGTTCCCATCCATGACAATTCAAGTAGTTAT... |
Task1_train_42360 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ACATTGATTTCTAAAGTCCTTATATTCAAAACTTTCTGTGCTGACCACCATCATTTATGTTTTTCCCATCTCTACTTAAAAACGTCAACTAGCCCCAACTTTTCCTCTAGTTATTTCTTTTATTAGATTTATTCTGTTCTCCACAATAAAATCTATCTTCTGTTCCCATCCATGACAATTCAAGTAGTTATAATGGGTGGATATAGGGTATGATAAATGTTGGTAAATCCACTGAGTTCCTTGAGTTCCACATTGATGTCTTTTAGGATGTGACTAGGGGTAGGCTAAATATTTTCTAGTTTCTCAGATCCTACCCCTGG... | ACATTGATTTCTAAAGTCCTTATATTCAAAACTTTCTGTGCTGACCACCATCATTTATGTTTTTCCCATCTCTACTTAAAAACGTCAACTAGCCCCAACTTTTCCTCTAGTTATTTCTTTTATTAGATTTATTCTGTTCTCCACAATAAAATCTATCTTCTGTTCCCATCCATGACAATTCAAGTAGTTATAATGGGTGGATATAGGGTATGATAAATGTTGGTAAATCCACTGAGTTCCTTGAGTTCCACATTGATGTCTTTTAGGATGTGACTAGGGGTAGGCTAAATATTTTCTAGTTTCTCAGATCCTACCCCTGG... |
Task1_train_42361 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | AAGAAGAAGGGACAAGCCAGGTGTGGTGGCTCACATCTGGAATCCCAGCACTTTAGGAGGCTGAGGTGGGCAGATCGCTTGAGCCCAGGAGAGTTTGAGACCAGCCTGGGCAATATAGTGAGACGCCATCGCTACAAAAAAACACAAAAGTTAGCCAAGCATGGTGGTATGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGGATCACCTGAGCCTAGGAGATGGAGGTTGCAGTGAGCCGGGATGGCGCCCCGCATTCCAGTCTGAGTGACAGAGTGAGATTGTCTCAACAAAAAGAAGGAGCGCTGCTAG... | AAGAAGAAGGGACAAGCCAGGTGTGGTGGCTCACATCTGGAATCCCAGCACTTTAGGAGGCTGAGGTGGGCAGATCGCTTGAGCCCAGGAGAGTTTGAGACCAGCCTGGGCAATATAGTGAGACGCCATCGCTACAAAAAAACACAAAAGTTAGCCAAGCATGGTGGTATGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGGATCACCTGAGCCTAGGAGATGGAGGTTGCAGTGAGCCGGGATGGCGCCCCGCATTCCAGTCTGAGTGACAGAGTGAGATTGTCTCAACAAAAAGAAGGAGCGCTGCTAG... |
Task1_train_42362 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTTGTAGAGACAGGGTTTCACCCGTGTTGTTCAGGCTCATCTCAAACTCCTGAGCTCAGGTGATCCAGCTACCTCAGCCTCCCAAACTGCTGGGATTACAGGCATAAGCGACCACACCTGACCTCAACATAATTAAAATGAAGACATTTTGGCATTTAAAGGATAAATTTCAGTTTTATAACATCTCATTTCGTACATATAGATGCTGTTCGACTTATGATGGGGTTACATCCTGATAAACCCATCACAAATTGAAAATACCTAAGTCCATAACTTAGACTAGCCTAACTTAAGCATCCTCAACACACGTGCATTAGCCT... | TTTGTAGAGACAGGGTTTCACCCGTGTTGTTCAGGCTCATCTCAAACTCCTGAGCTCAGGTGATCCAGCTACCTCAGCCTCCCAAACTGCTGGGATTACAGGCATAAGCGACCACACCTGACCTCAACATAATTAAAATGAAGACATTTTGGCATTTAAAGGATAAATTTCAGTTTTATAACATCTCATTTCGTACATATAGATGCTGTTCGACTTATGATGGGGTTACATCCTGATAAACCCATCACAAATTGAAAATACCTAAGTCCATAACTTAGACTAGCCTAACTTAAGCATCCTCAACACACGTGCATTAGCCT... |
Task1_train_42363 | The following genetic variant occurs on Chromosome 12. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CAGACTTCTTATACCTAGCAAATAAATGTCATTGAATTGGCCAATTTCCTGCCCCAGGTTTCCTGATATGACTTCTGAGCTGGTGTCTGGAGGCCCAGGACCTCTCTGTTCCACGCCTTCCTTGCAGCAGCACCTACATTGCCACTGGTTCAAATTCTTTGAATCGGTTACTAAAATAAATTAACTACTTCAAGCTTGTATTGCAAATACCCATTCCAACTGTATGCTAAAAGGAGGCTGCACTTGAGAATAATTACACATTTTCTAAACTATTCCTTCAACCACGTGTTTTTTTTCCCCCTGCATTCCTAACTCACCAG... | CAGACTTCTTATACCTAGCAAATAAATGTCATTGAATTGGCCAATTTCCTGCCCCAGGTTTCCTGATATGACTTCTGAGCTGGTGTCTGGAGGCCCAGGACCTCTCTGTTCCACGCCTTCCTTGCAGCAGCACCTACATTGCCACTGGTTCAAATTCTTTGAATCGGTTACTAAAATAAATTAACTACTTCAAGCTTGTATTGCAAATACCCATTCCAACTGTATGCTAAAAGGAGGCTGCACTTGAGAATAATTACACATTTTCTAAACTATTCCTTCAACCACGTGTTTTTTTTCCCCCTGCATTCCTAACTCACCAG... |
Task1_train_42364 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | TATATGATGAGATTTTGCTTTATGGTATTGCCAGTATTATCTGAAAAGTAAAGGATTCTAAAGGAAATTAGGGCAAATATTTATTTATTTACTTATTTTTTGAGACAGGGTCTCTGTTGCTCAGGCTGGAGTACAGTGGTGTGACCTCAGCTCACTGCAGCCTCAGCCTCCTAGACTCAAGTGATCCTCCTGCCCTAGCCTCCCAAATACCTGGGACTATAGGAGCATGCCACCATACCTGGCTAATTTTTGTATTTTTTTCAGAGACAGGGTTTTGCCATGTTGCCCAGGCTGGTCTTGAATTCCTGAACTCAAGTGAT... | TATATGATGAGATTTTGCTTTATGGTATTGCCAGTATTATCTGAAAAGTAAAGGATTCTAAAGGAAATTAGGGCAAATATTTATTTATTTACTTATTTTTTGAGACAGGGTCTCTGTTGCTCAGGCTGGAGTACAGTGGTGTGACCTCAGCTCACTGCAGCCTCAGCCTCCTAGACTCAAGTGATCCTCCTGCCCTAGCCTCCCAAATACCTGGGACTATAGGAGCATGCCACCATACCTGGCTAATTTTTGTATTTTTTTCAGAGACAGGGTTTTGCCATGTTGCCCAGGCTGGTCTTGAATTCCTGAACTCAAGTGAT... |
Task1_train_42365 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CAAAAAATAATAATAATAATAATAATAATAATAATTCATGCTTACCCCTTTACCAAGAATTCTGCCTTCTCCACCAAGCTGTCCTCTCTACTAGTCTCTCCTTCTCCATGAATCCTTCTCTGAGTGCTCCAGCTCTGCCGCCTCTCCTAACACTACAGACCCTCACACTAGAGGAACATTGTGATAAAATATAAAGGAAGTCTTGAACCCCAAAGCATATAGCAGAGAAGGGAAATGATTAACAGATTGATTTCCTGCAATCTGTTCATTCATATACTGGGCCTACATACATCAGAGATTAATTTTAGGCACTGTTGTTT... | CAAAAAATAATAATAATAATAATAATAATAATAATTCATGCTTACCCCTTTACCAAGAATTCTGCCTTCTCCACCAAGCTGTCCTCTCTACTAGTCTCTCCTTCTCCATGAATCCTTCTCTGAGTGCTCCAGCTCTGCCGCCTCTCCTAACACTACAGACCCTCACACTAGAGGAACATTGTGATAAAATATAAAGGAAGTCTTGAACCCCAAAGCATATAGCAGAGAAGGGAAATGATTAACAGATTGATTTCCTGCAATCTGTTCATTCATATACTGGGCCTACATACATCAGAGATTAATTTTAGGCACTGTTGTTT... |
Task1_train_42366 | This mutation on Chromosome 12 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TAGAGGAACATTGTGATAAAATATAAAGGAAGTCTTGAACCCCAAAGCATATAGCAGAGAAGGGAAATGATTAACAGATTGATTTCCTGCAATCTGTTCATTCATATACTGGGCCTACATACATCAGAGATTAATTTTAGGCACTGTTGTTTTCTATATGTTCAGGGTTTTGTTTTGTTTTGTTTTGTTTGTCTCTGTAACAAAATTACAGTCTTCTTAAATAGGGGCCTTATTATCCCACAGCATTCATTCAGCAAATTACTCATTCAACAAGTAGTTATTAGGTACTTGTTATATGTCAGGCACTGTTTACTGCTGTA... | TAGAGGAACATTGTGATAAAATATAAAGGAAGTCTTGAACCCCAAAGCATATAGCAGAGAAGGGAAATGATTAACAGATTGATTTCCTGCAATCTGTTCATTCATATACTGGGCCTACATACATCAGAGATTAATTTTAGGCACTGTTGTTTTCTATATGTTCAGGGTTTTGTTTTGTTTTGTTTTGTTTGTCTCTGTAACAAAATTACAGTCTTCTTAAATAGGGGCCTTATTATCCCACAGCATTCATTCAGCAAATTACTCATTCAACAAGTAGTTATTAGGTACTTGTTATATGTCAGGCACTGTTTACTGCTGTA... |
Task1_train_42367 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGTACTTGTTATATGTCAGGCACTGTTTACTGCTGTATCCCTAGCGCAAAGATCAAGAGACAAAATGTAAAGCCTCCTACCTGCCTCAAGGCTTAAATTCTAACACACTCGTCAATTGATCCTCTCATTACTCAGATTATATCCACCCCATTTAATTAGTAATAATTGTGAACTATCAACCAACTTCTAATATATGTTGCTTCCTTTAAGAGCTAACAGATTTATAAACTAAGAATGTACATATATTGAAAATAGCATTGTATATAAACTTATATCCTTTTTTATTGTTTAGTGTTTCTTCATATAGCTTTAAAATTATG... | GGTACTTGTTATATGTCAGGCACTGTTTACTGCTGTATCCCTAGCGCAAAGATCAAGAGACAAAATGTAAAGCCTCCTACCTGCCTCAAGGCTTAAATTCTAACACACTCGTCAATTGATCCTCTCATTACTCAGATTATATCCACCCCATTTAATTAGTAATAATTGTGAACTATCAACCAACTTCTAATATATGTTGCTTCCTTTAAGAGCTAACAGATTTATAAACTAAGAATGTACATATATTGAAAATAGCATTGTATATAAACTTATATCCTTTTTTATTGTTTAGTGTTTCTTCATATAGCTTTAAAATTATG... |
Task1_train_42368 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AAAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCCAATAGTGTACAATTAACTTGGTAGTTTTTGGTAGCTCAGTGTTGAGTTACCCTGGTGGATTATTGGGCTTCTTGTCCTCACCTCTCTTTTTCTGTTTGGGCTGTGTTGGGTGGGGGTGGGGAGTTGGAGTTTCATTCTTTGTTCAACAGTAAGTATCAAAAGGGGAAGTAAGGCTGGGTGTGGTGGCTCATGCCTGTAATCCCACCACTTTGGGAGGCCGAGGCAGGCGCATCACAAGGTCAGGAGATTGAGACCATCCTGGCTAACA... | AAAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCCAATAGTGTACAATTAACTTGGTAGTTTTTGGTAGCTCAGTGTTGAGTTACCCTGGTGGATTATTGGGCTTCTTGTCCTCACCTCTCTTTTTCTGTTTGGGCTGTGTTGGGTGGGGGTGGGGAGTTGGAGTTTCATTCTTTGTTCAACAGTAAGTATCAAAAGGGGAAGTAAGGCTGGGTGTGGTGGCTCATGCCTGTAATCCCACCACTTTGGGAGGCCGAGGCAGGCGCATCACAAGGTCAGGAGATTGAGACCATCCTGGCTAACA... |
Task1_train_42369 | This variant is located on Chromosome 12. Evaluate its biological effect and specify any disease association. | Benign | TTTATAGTCCACCTTATCATGACAAAGGAAACTTTTGAGTAGTAATTAAAATAAAGGAAAATCATATAAGATTATTCTAGATGAAATCACATTTGTTTACCTTAAAATTTCCCTACCTACTTGTTAAAGCTCTCAGACCATGACCCTTTGATTTTATAGGAAGTCCTCCAGGGCTACTCCTTGGTCCCTGAAATTGCTCAAGTGTGCACCATTTTCTTTCTTTCTTTGGGTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGTGATTTCAGCTCATTGCAACCTCCACCT... | TTTATAGTCCACCTTATCATGACAAAGGAAACTTTTGAGTAGTAATTAAAATAAAGGAAAATCATATAAGATTATTCTAGATGAAATCACATTTGTTTACCTTAAAATTTCCCTACCTACTTGTTAAAGCTCTCAGACCATGACCCTTTGATTTTATAGGAAGTCCTCCAGGGCTACTCCTTGGTCCCTGAAATTGCTCAAGTGTGCACCATTTTCTTTCTTTCTTTGGGTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGTGATTTCAGCTCATTGCAACCTCCACCT... |
Task1_train_42370 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GCAGGGAATACAGGCGCCCACCACTATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTGCTGTGTTGGCCAGGCTGGTCTGGAACTCCTGACCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCGGCCACCTGAAGTTTTTATAAGGCCCTTGAGAACTCTGGCACTTTGTTGTGGTTGATCAGAGCCATGCAGGTAGTCTCATAGGTCCTTCAGTCCACAAATATTGAGGGTCCACCCTGTGCCATGTTATGGGGGCCTCTGTCATTTTGCTCAGGA... | GCAGGGAATACAGGCGCCCACCACTATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTGCTGTGTTGGCCAGGCTGGTCTGGAACTCCTGACCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCGGCCACCTGAAGTTTTTATAAGGCCCTTGAGAACTCTGGCACTTTGTTGTGGTTGATCAGAGCCATGCAGGTAGTCTCATAGGTCCTTCAGTCCACAAATATTGAGGGTCCACCCTGTGCCATGTTATGGGGGCCTCTGTCATTTTGCTCAGGA... |
Task1_train_42371 | Chromosome 12 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TATCTTTCTAGATGAACCTTTGGATCATTGTGCAAAGTTCTCCCCAACCAAGACCCAATTCTCTGATACATTTTTGGTAACATTTTAATTATAATTCCATAAAACTTATACATTAGTTTTAGAATATTTGGCAACTTTACAATATCAATCTTTCTATCTGAAAACATGACGTAGCTTTCTATTTCTCAAAACTCCAGCTCACACACATTAAGGTTATTGTTGTTTTCTTAGACTTAATTTCCTCATATATTTTCTTTCTTTTCTTCCTTCTTTCCTTCCTTTTCCCTTCCTTTGCCCTTCCCTTCCCTTCCCTTCCATTC... | TATCTTTCTAGATGAACCTTTGGATCATTGTGCAAAGTTCTCCCCAACCAAGACCCAATTCTCTGATACATTTTTGGTAACATTTTAATTATAATTCCATAAAACTTATACATTAGTTTTAGAATATTTGGCAACTTTACAATATCAATCTTTCTATCTGAAAACATGACGTAGCTTTCTATTTCTCAAAACTCCAGCTCACACACATTAAGGTTATTGTTGTTTTCTTAGACTTAATTTCCTCATATATTTTCTTTCTTTTCTTCCTTCTTTCCTTCCTTTTCCCTTCCTTTGCCCTTCCCTTCCCTTCCCTTCCATTC... |
Task1_train_42372 | Chromosome 12 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TAGTAATTACATTACAAAGTGGACAAAGAGGGATGTTAAAATAACAAAAGAAGGCCCACTTGAAAGGGAGCTTCCAAACCTTTATCTGAAAGATATCAATATTACTTTGTATCAATGTTTTCAGCTTTAATACTTCTATCTGTCAGAGCCTTCCTTCAGCCCTGGTGCAAGAGTGATATTCAAGGGTCAGTAAATGGCTGCTTCACGTATCACCAGTTGGAAGATTGATGGGAGACCTTCATTCTACTGCTGCCTCCGTTTTAGATTGAAATCCTCCCAGATATGCTACAAAGAACACGAGGTGACAATTGGCTGGAAAG... | TAGTAATTACATTACAAAGTGGACAAAGAGGGATGTTAAAATAACAAAAGAAGGCCCACTTGAAAGGGAGCTTCCAAACCTTTATCTGAAAGATATCAATATTACTTTGTATCAATGTTTTCAGCTTTAATACTTCTATCTGTCAGAGCCTTCCTTCAGCCCTGGTGCAAGAGTGATATTCAAGGGTCAGTAAATGGCTGCTTCACGTATCACCAGTTGGAAGATTGATGGGAGACCTTCATTCTACTGCTGCCTCCGTTTTAGATTGAAATCCTCCCAGATATGCTACAAAGAACACGAGGTGACAATTGGCTGGAAAG... |
Task1_train_42373 | Consider a variant on Chromosome 12. Determine its clinical classification and disease relevance. | Benign | CGCTTTTGCAAACTTTAATACTACATTCTTTTGGCAGTAACTGTCCTCCTGGGAGGACGGTTATGAAAATGAGTAACAGTCATCTTGGAAAAGTATGTTTTCTTATTTAACATAGAATTTCTCCTAACTCTCAATCCCCATGTACTAAGACTCCCTACCATTATAAGAGAGCATACTGTCTGTTTTAATCACCCTCCAACAAAGCTCCCAAACCTGACATTAATAGTAAATATTCAAAATGATGTTCTTAAAGAGTAATTTAGACTCACCTTCTATTAATCTAGGAATCGGAGCAGGACCTGGCCCAAACTTTTCAAATG... | CGCTTTTGCAAACTTTAATACTACATTCTTTTGGCAGTAACTGTCCTCCTGGGAGGACGGTTATGAAAATGAGTAACAGTCATCTTGGAAAAGTATGTTTTCTTATTTAACATAGAATTTCTCCTAACTCTCAATCCCCATGTACTAAGACTCCCTACCATTATAAGAGAGCATACTGTCTGTTTTAATCACCCTCCAACAAAGCTCCCAAACCTGACATTAATAGTAAATATTCAAAATGATGTTCTTAAAGAGTAATTTAGACTCACCTTCTATTAATCTAGGAATCGGAGCAGGACCTGGCCCAAACTTTTCAAATG... |
Task1_train_42374 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TACTTGTTTAGAGCTGGGCACTGGGCTAAGTGATTTATGTTTTATTTTATTTAAAACTCAGACAAGCCCATAAAGTAGAAACAGCTCTCCCTATGATGAGGATGAGAAAACGAGGCTTCGAGAAATTACTGTAAAGAAATTCCCCAAGGTCAAACAGCTTATAGGAAACAGAACTCAGACTAAGACAAGTTTATTGAACCCTATTTTTCTATAATTTTAACCCATCCTTTATACATACAATTGCATAGTTCTGCAAATATGCCTAAAATTGCAAAATGTAACTGATTAAAGTCTTCAGCAGAAATTTTATAATAGAAAAT... | TACTTGTTTAGAGCTGGGCACTGGGCTAAGTGATTTATGTTTTATTTTATTTAAAACTCAGACAAGCCCATAAAGTAGAAACAGCTCTCCCTATGATGAGGATGAGAAAACGAGGCTTCGAGAAATTACTGTAAAGAAATTCCCCAAGGTCAAACAGCTTATAGGAAACAGAACTCAGACTAAGACAAGTTTATTGAACCCTATTTTTCTATAATTTTAACCCATCCTTTATACATACAATTGCATAGTTCTGCAAATATGCCTAAAATTGCAAAATGTAACTGATTAAAGTCTTCAGCAGAAATTTTATAATAGAAAAT... |
Task1_train_42375 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCCTAGCTTAGAAGTCAGGAAAGGTCAGACTCAAAGTCTCTTCTCCTCTTTCTCTGGCTTTAAGAGTGGTCATGGGTGAGGCTTCAGTTGTTTTCTATGCTGCATGGGATCGCATCCTAAGATGATCTCGCTTTAAACTAGGGTCATGCTACTTTGTCAAGGTCATGTTGGTTGGCCAAGGACTTTCCAGGTTTCAGCACTGTAAGTCCCAAGTCCTTGGACCCTAAACTGTGGACTATACAGATAAGTAAACTGTGGTAAGGCTTGTTCGGAAAGATAACTTACAAGGGCCAAAAAAAGAAAAACACTAATTTTACTAC... | CCCTAGCTTAGAAGTCAGGAAAGGTCAGACTCAAAGTCTCTTCTCCTCTTTCTCTGGCTTTAAGAGTGGTCATGGGTGAGGCTTCAGTTGTTTTCTATGCTGCATGGGATCGCATCCTAAGATGATCTCGCTTTAAACTAGGGTCATGCTACTTTGTCAAGGTCATGTTGGTTGGCCAAGGACTTTCCAGGTTTCAGCACTGTAAGTCCCAAGTCCTTGGACCCTAAACTGTGGACTATACAGATAAGTAAACTGTGGTAAGGCTTGTTCGGAAAGATAACTTACAAGGGCCAAAAAAAGAAAAACACTAATTTTACTAC... |
Task1_train_42376 | This is a variant located on Chromosome 12. Is this mutation a likely cause of disease or not? | Benign | AATTTTATCCTGCTGTTTCACTTTCATCAATATAATAGATAGCACTCAGTGGCAAATTACACCAGTTTTTGATCTGCAATGGACAAGTCTGCCATGTTAGAGCAAGAAAAAGATGAGAAAAAAGAGAATTTACCAAGCCGACTTTTAAAAATGTCTATTAATATTTTTGTAAATGCCCAGTGATTATTTCTCTAGGACTACATTCTTTAAAGCCTTACAATTTTTGTTGTTCACTTAGAGAACAAGATAAAATCTTTGTTGATCAAAGGATGATATCTACATCCTGATTAGAGAATTGGACTCCTACAGTGAGGTGTCAT... | AATTTTATCCTGCTGTTTCACTTTCATCAATATAATAGATAGCACTCAGTGGCAAATTACACCAGTTTTTGATCTGCAATGGACAAGTCTGCCATGTTAGAGCAAGAAAAAGATGAGAAAAAAGAGAATTTACCAAGCCGACTTTTAAAAATGTCTATTAATATTTTTGTAAATGCCCAGTGATTATTTCTCTAGGACTACATTCTTTAAAGCCTTACAATTTTTGTTGTTCACTTAGAGAACAAGATAAAATCTTTGTTGATCAAAGGATGATATCTACATCCTGATTAGAGAATTGGACTCCTACAGTGAGGTGTCAT... |
Task1_train_42377 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | CATCATTTTTTTGAGCTACTTCTTACCACAAGATGTTCATCTTGTACACACCTTGTACAGCCCTCGAGTCAATTGATTTCTTTTAGTGAGAAGTGGTATTTATTTAGAATCTAAGTTGTGAGGGCTACTGATGTGGCTTTGCTTCCAGGTCCTCTCAAAAGGCTGAGCTGGGAAATGTATTTGTTCAGATAAATTTATCTATCTAAATCTATCTTATTGTCTATCTAAACATATCTATCTAAATATAGCTATATAAATCTCTGTATCTCTCTATCTCTCTGTATCTAAAACCATAAATTCATTCTAATAACTGGAATTCC... | CATCATTTTTTTGAGCTACTTCTTACCACAAGATGTTCATCTTGTACACACCTTGTACAGCCCTCGAGTCAATTGATTTCTTTTAGTGAGAAGTGGTATTTATTTAGAATCTAAGTTGTGAGGGCTACTGATGTGGCTTTGCTTCCAGGTCCTCTCAAAAGGCTGAGCTGGGAAATGTATTTGTTCAGATAAATTTATCTATCTAAATCTATCTTATTGTCTATCTAAACATATCTATCTAAATATAGCTATATAAATCTCTGTATCTCTCTATCTCTCTGTATCTAAAACCATAAATTCATTCTAATAACTGGAATTCC... |
Task1_train_42378 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | AATGACGTTCTCTGTATTTCCCCATATAGCTAAATGATGCCCATTCTTTAAGACCCAAATACCTCCTTCTCTAGAAACTTTCCCTGGTTCATTGTATCTCTGATAGTCTTGTCCTTTCTCCAAGTTTATGTAGCATTTGTTATCTGAATTACTCACTTGATCCTTATCACCTACTGTGTTTTCTGGAACTTAATTCTATGTTTTTAATCATGTCATATCTTATTTTTGTACTGTAGATGCTGAAGAATTTTCTACATTTATTAATTCCATAATGAGTGATGAAAATATGTCCAAGACACAAACAGTTTATGACTCAGACT... | AATGACGTTCTCTGTATTTCCCCATATAGCTAAATGATGCCCATTCTTTAAGACCCAAATACCTCCTTCTCTAGAAACTTTCCCTGGTTCATTGTATCTCTGATAGTCTTGTCCTTTCTCCAAGTTTATGTAGCATTTGTTATCTGAATTACTCACTTGATCCTTATCACCTACTGTGTTTTCTGGAACTTAATTCTATGTTTTTAATCATGTCATATCTTATTTTTGTACTGTAGATGCTGAAGAATTTTCTACATTTATTAATTCCATAATGAGTGATGAAAATATGTCCAAGACACAAACAGTTTATGACTCAGACT... |
Task1_train_42379 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | GTTGGGAATTTCAAAAGTGTAATTAAAAGAGGAAGTGTGTTCAGGATTTATAATTAAAATAGGTGCCAATGTTATTAAGCTGCAGGCTAGTTATTTAAAGAAGGGATTAATGAATTAAGTTTCACTTGTAAAAGAAGTAACTGAAAAAGTCCTACAGATTACTATTGAACTTTTCACAGGCCTTTAAAAAAATTCTGTATTTTAACATTATACTCATATTGGTATTCTGCTCTTATCATCAAATCTAAAGTCCCATTATTAAACTCTCTTTAATGTATACCACCAAGAATTTCCCCTTGGATTCAGTTACTCACTTTTCA... | GTTGGGAATTTCAAAAGTGTAATTAAAAGAGGAAGTGTGTTCAGGATTTATAATTAAAATAGGTGCCAATGTTATTAAGCTGCAGGCTAGTTATTTAAAGAAGGGATTAATGAATTAAGTTTCACTTGTAAAAGAAGTAACTGAAAAAGTCCTACAGATTACTATTGAACTTTTCACAGGCCTTTAAAAAAATTCTGTATTTTAACATTATACTCATATTGGTATTCTGCTCTTATCATCAAATCTAAAGTCCCATTATTAAACTCTCTTTAATGTATACCACCAAGAATTTCCCCTTGGATTCAGTTACTCACTTTTCA... |
Task1_train_42380 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AATTCCCAAACCTCAAAGCACTTACATTGTGTGTGTATGTGTGTGTGTGTGTGTGTTTGTGTGCGCACGTGTGTGTGTGCTGGAGATACTGAGTTTAGAGATGTTGAGTTTGAGATATCTGTTAGACATCCAAGTGGAGGAATTGAGTCAGAAGTTGATTCTGTGAATTTGGAGTTCAGAAGAGAGGTTGGAGCTACAGCGAAAAAGTTGTGATTTCATCAGCATTCAGATGAAATTAAAACCATGAGCCTGATTAAGATCACCTAAGGGGAGGGAGTGAGGAGAAGGAAGAGCACTGAGTTCCAGGACAGTCCAATATT... | AATTCCCAAACCTCAAAGCACTTACATTGTGTGTGTATGTGTGTGTGTGTGTGTGTTTGTGTGCGCACGTGTGTGTGTGCTGGAGATACTGAGTTTAGAGATGTTGAGTTTGAGATATCTGTTAGACATCCAAGTGGAGGAATTGAGTCAGAAGTTGATTCTGTGAATTTGGAGTTCAGAAGAGAGGTTGGAGCTACAGCGAAAAAGTTGTGATTTCATCAGCATTCAGATGAAATTAAAACCATGAGCCTGATTAAGATCACCTAAGGGGAGGGAGTGAGGAGAAGGAAGAGCACTGAGTTCCAGGACAGTCCAATATT... |
Task1_train_42381 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GATATCCTTGGTCCTTCCAAAATTTTGTGTCTTTATAGAGATATATTCAAAGGATGATGGAAGTTCATTTTATAATCTTACAAAACTTAAAGATGAGATCACTCTTAGCATGCTAAAGGTAAGTTTGAAACTGTTTTCAAACCATTAAGTTAGTTACCAAAAATCCACTATTAGGCCCTGGATGGGCCTGCTTTCAGAGTTATGCTTGCTCTTGTGAGAGCAGTTACCTTTTCTTGTGTAAGAATGGGTTGGAGCCAGAGGTGGAGTTTACTCCTCATGAGAAAAGTAGATGTCCAGTGGTGTCCAGCTTTGACTTCACA... | GATATCCTTGGTCCTTCCAAAATTTTGTGTCTTTATAGAGATATATTCAAAGGATGATGGAAGTTCATTTTATAATCTTACAAAACTTAAAGATGAGATCACTCTTAGCATGCTAAAGGTAAGTTTGAAACTGTTTTCAAACCATTAAGTTAGTTACCAAAAATCCACTATTAGGCCCTGGATGGGCCTGCTTTCAGAGTTATGCTTGCTCTTGTGAGAGCAGTTACCTTTTCTTGTGTAAGAATGGGTTGGAGCCAGAGGTGGAGTTTACTCCTCATGAGAAAAGTAGATGTCCAGTGGTGTCCAGCTTTGACTTCACA... |
Task1_train_42382 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GCTCCTCATTCCGCTTTTGAATCTATTGCCTTAGCATTGCCAGTCAGATACCTGGGCTGTTTCCTGCTTTGGATTCCTCATAGTTAGAATCTTGCATTCAAGCTCTCAAATCTGACAACTAATGTCACATATTCTCTGATTAGGCTTTGATAAGACCAAGTAATTTAACAATACAGGATTGTTTAGGACTGAATTATAAAGATTCATCATATAGAACCCTTGCTCATTATTTCAAGTATTACTAATAAAATCGCTAATATCTAGCATCATTACAAATTAGCAAAACTAATTGTCCTCAATAGAGACTCATTTCTTACTAT... | GCTCCTCATTCCGCTTTTGAATCTATTGCCTTAGCATTGCCAGTCAGATACCTGGGCTGTTTCCTGCTTTGGATTCCTCATAGTTAGAATCTTGCATTCAAGCTCTCAAATCTGACAACTAATGTCACATATTCTCTGATTAGGCTTTGATAAGACCAAGTAATTTAACAATACAGGATTGTTTAGGACTGAATTATAAAGATTCATCATATAGAACCCTTGCTCATTATTTCAAGTATTACTAATAAAATCGCTAATATCTAGCATCATTACAAATTAGCAAAACTAATTGTCCTCAATAGAGACTCATTTCTTACTAT... |
Task1_train_42383 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCTATTGCCTTAGCATTGCCAGTCAGATACCTGGGCTGTTTCCTGCTTTGGATTCCTCATAGTTAGAATCTTGCATTCAAGCTCTCAAATCTGACAACTAATGTCACATATTCTCTGATTAGGCTTTGATAAGACCAAGTAATTTAACAATACAGGATTGTTTAGGACTGAATTATAAAGATTCATCATATAGAACCCTTGCTCATTATTTCAAGTATTACTAATAAAATCGCTAATATCTAGCATCATTACAAATTAGCAAAACTAATTGTCCTCAATAGAGACTCATTTCTTACTATATTGAAAGCAATAAAAATGCT... | TCTATTGCCTTAGCATTGCCAGTCAGATACCTGGGCTGTTTCCTGCTTTGGATTCCTCATAGTTAGAATCTTGCATTCAAGCTCTCAAATCTGACAACTAATGTCACATATTCTCTGATTAGGCTTTGATAAGACCAAGTAATTTAACAATACAGGATTGTTTAGGACTGAATTATAAAGATTCATCATATAGAACCCTTGCTCATTATTTCAAGTATTACTAATAAAATCGCTAATATCTAGCATCATTACAAATTAGCAAAACTAATTGTCCTCAATAGAGACTCATTTCTTACTATATTGAAAGCAATAAAAATGCT... |
Task1_train_42384 | A mutation found on Chromosome 12 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TTCTAAGAAGCAACATAGTACAAATTCATAATTTTCCATCACCTGAAATTGCAAGTTAACTTTGTCTTTTTTGCTACAAATCTCATTTTTCTGAGAGAATAAAGTATTACAAGTAAAGGCAAAGTTTCTCGTACTTACCTGTACCTATCACCTCCACAGAAGTAACTACTATTATTAATTCAATGCCTGTCTTTCAAGTTTTATATTTCACATACACATCTGTCTAATACATGGTATTATTTTATACTTTAAGAATAAAAAATTTATATAAACAGTATGCTAAATCTTATCACTTGCTTTTTCTTACTCCATTATTTTTG... | TTCTAAGAAGCAACATAGTACAAATTCATAATTTTCCATCACCTGAAATTGCAAGTTAACTTTGTCTTTTTTGCTACAAATCTCATTTTTCTGAGAGAATAAAGTATTACAAGTAAAGGCAAAGTTTCTCGTACTTACCTGTACCTATCACCTCCACAGAAGTAACTACTATTATTAATTCAATGCCTGTCTTTCAAGTTTTATATTTCACATACACATCTGTCTAATACATGGTATTATTTTATACTTTAAGAATAAAAAATTTATATAAACAGTATGCTAAATCTTATCACTTGCTTTTTCTTACTCCATTATTTTTG... |
Task1_train_42385 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTGGGCCTTTGGTCTTTCACGAGGGCTTAGGCCATCACTTCCTTTGGTTGTCAGGCCTTCAGACTCACTCTGAATTAAACCACTGGCTTTCCTAGTTTTCCAGTTTGCAGATGAAAGATTGTGTGATTCTTGGCCTCCATAATCATGTGAGCCAATTCCTAGAATCTATCTATCTATCTATCTATCTATCTATCTATCTAATCTATCCACCCATCCATCCACCACCCACCTACCTACCTACCTACCTACCTATCAATCATCTGTCTATCCATCCATCCTATTGGCTCTGTTTCTCTGGAGAATCCTAATGCAACAGGCAA... | TTGGGCCTTTGGTCTTTCACGAGGGCTTAGGCCATCACTTCCTTTGGTTGTCAGGCCTTCAGACTCACTCTGAATTAAACCACTGGCTTTCCTAGTTTTCCAGTTTGCAGATGAAAGATTGTGTGATTCTTGGCCTCCATAATCATGTGAGCCAATTCCTAGAATCTATCTATCTATCTATCTATCTATCTATCTATCTAATCTATCCACCCATCCATCCACCACCCACCTACCTACCTACCTACCTACCTATCAATCATCTGTCTATCCATCCATCCTATTGGCTCTGTTTCTCTGGAGAATCCTAATGCAACAGGCAA... |
Task1_train_42386 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | ATTATGTTTGCATTGACTTATGCAACTAAAGACTCAAGTGGGCTGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTGGGGGGCCAAGGCGGGCGAATCACGAGGTCAGGAGTTCGAGACCAGCCTGAGCAATATGGTGAAACCCCATCTCTACTAAAAATACAAATTAGCCGGGCGTGGTGGCACACGCCTGTAGTCCCAGCTACTAGGAAAGCTGATGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCACGCCACTGATTCCAGCCCGGGTGACAGAGTGAGACTCCATCTCAAAA... | ATTATGTTTGCATTGACTTATGCAACTAAAGACTCAAGTGGGCTGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTGGGGGGCCAAGGCGGGCGAATCACGAGGTCAGGAGTTCGAGACCAGCCTGAGCAATATGGTGAAACCCCATCTCTACTAAAAATACAAATTAGCCGGGCGTGGTGGCACACGCCTGTAGTCCCAGCTACTAGGAAAGCTGATGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCACGCCACTGATTCCAGCCCGGGTGACAGAGTGAGACTCCATCTCAAAA... |
Task1_train_42387 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GCACTTCAAAAGAAGACATACATGCAGCCAACAAGCATATGAAAAAAATGTGCAACATCACTGATCATTAGAGAAACACAAACCAAAACCACAATGAGATGCCATCTCACCCAAATGGCTATTAAAATGTAAAAAACATAACAGACGCTGGCAAGGTTATGGAAAAAAAAGCAATGTTTATACACTGTTGGTGGGAGTGTAAATTAGTTCAACCATTATAGAAGACAGTACGGTGATTCCTCAAAGATCTAAAGACAGAAATACCATTCAACACAGCAATCCCATTACTGGGTATATACCCAATGGAATAAAAATCATTC... | GCACTTCAAAAGAAGACATACATGCAGCCAACAAGCATATGAAAAAAATGTGCAACATCACTGATCATTAGAGAAACACAAACCAAAACCACAATGAGATGCCATCTCACCCAAATGGCTATTAAAATGTAAAAAACATAACAGACGCTGGCAAGGTTATGGAAAAAAAAGCAATGTTTATACACTGTTGGTGGGAGTGTAAATTAGTTCAACCATTATAGAAGACAGTACGGTGATTCCTCAAAGATCTAAAGACAGAAATACCATTCAACACAGCAATCCCATTACTGGGTATATACCCAATGGAATAAAAATCATTC... |
Task1_train_42388 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTTAAATTCCTATACCAAAAGGTGGACCAAAAATGAGCTCCCTAGCAAAAAAGATAAAAATATGATCAGTTTTGCAACTCATATAACCTTTAAGATAAAAACAAACTCGTCCTGGAAAGGCGAAGCTGTTTCAGTTTCTGAGGTATGAAAGTTATTTATCCCACAGGTCCTCATAAGAAGACTGCTATATCAATTCATGATGGAGTTTTAAAAATTCATAATGAGAAGGTATTTTATTTTTCTTCAGCATGGGTGTGACTAGTCTTAAACAGGTCAAATATATGCATGTGTGTGAAAGGGAGAGATTTGCAAGAAATTAA... | TTTAAATTCCTATACCAAAAGGTGGACCAAAAATGAGCTCCCTAGCAAAAAAGATAAAAATATGATCAGTTTTGCAACTCATATAACCTTTAAGATAAAAACAAACTCGTCCTGGAAAGGCGAAGCTGTTTCAGTTTCTGAGGTATGAAAGTTATTTATCCCACAGGTCCTCATAAGAAGACTGCTATATCAATTCATGATGGAGTTTTAAAAATTCATAATGAGAAGGTATTTTATTTTTCTTCAGCATGGGTGTGACTAGTCTTAAACAGGTCAAATATATGCATGTGTGTGAAAGGGAGAGATTTGCAAGAAATTAA... |
Task1_train_42389 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | GCAGTGAGCCGAGATCATGTCATTACACTCCAGCCTGGGCAGCAAGAAAAAAACTACATCTCAAAAAAAAAAAAAAAAAAAGAATAACAAGAAAGACAATCCCAGTTCTGCGTACAATAATGTGACTATGGGAAAACTACTTAAACTTCAGGAGCCTCAGTTTCCTTATCTGTAAAAGAAGGATAAGAATAAGCACTTATACCTCACAGGGTTGAGGCAATCAGGTACATAGTAGACAATAGGCTCTATGTCTGAATTTAAACCACTAATTAGCTGTGTTACTTTGGATTCGTTATTTAACCACTCTCTGAAGATAACAG... | GCAGTGAGCCGAGATCATGTCATTACACTCCAGCCTGGGCAGCAAGAAAAAAACTACATCTCAAAAAAAAAAAAAAAAAAAGAATAACAAGAAAGACAATCCCAGTTCTGCGTACAATAATGTGACTATGGGAAAACTACTTAAACTTCAGGAGCCTCAGTTTCCTTATCTGTAAAAGAAGGATAAGAATAAGCACTTATACCTCACAGGGTTGAGGCAATCAGGTACATAGTAGACAATAGGCTCTATGTCTGAATTTAAACCACTAATTAGCTGTGTTACTTTGGATTCGTTATTTAACCACTCTCTGAAGATAACAG... |
Task1_train_42390 | This alteration occurs on Chromosome 12. Is it associated with a disease or is it a benign variant? | Benign | GGGATTAAGACCCTTAAAAAAGAGGCTTCAGGTAGCTTCTCTTGACCTCCAGAGGACTGCAAAATGCAACGCTTACAATTTGATGAGGTTTGATCTTGGACTTCCCAGCCTCCAGAACTGTGAGAAATAAATTTCTGTTCTTTATAAATTACCCAGTCTGTGGTATTCTGTGATAGAACAAAACAGACATTGCTTGGCAATAAATGGTAGCTACCACTATGGTACTTACATCAATAATACATATTATATTATTACTTATTATATACTTGTTATATTTATTATGTTACTAATTATCTAATCTAAGCTTTTCATCTAAATCA... | GGGATTAAGACCCTTAAAAAAGAGGCTTCAGGTAGCTTCTCTTGACCTCCAGAGGACTGCAAAATGCAACGCTTACAATTTGATGAGGTTTGATCTTGGACTTCCCAGCCTCCAGAACTGTGAGAAATAAATTTCTGTTCTTTATAAATTACCCAGTCTGTGGTATTCTGTGATAGAACAAAACAGACATTGCTTGGCAATAAATGGTAGCTACCACTATGGTACTTACATCAATAATACATATTATATTATTACTTATTATATACTTGTTATATTTATTATGTTACTAATTATCTAATCTAAGCTTTTCATCTAAATCA... |
Task1_train_42391 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CTCTTGCAGTGCAGACTATAGCACCTCCAGTTAATCTGGTCACAGTCATTGTAAAAAATGAATTAAGTGTTATTAGATGTATATTGCCTCACCTGTCTTATCTGATGTAATTGCTGTGTAGAAGGAAACTCCTACAGGGAAGAGAAGGAGGGAGTCAACACACTAATACACTACTTAAATCACATTTAAAACGTCAGTTCTTGGAAACAGTAAAAATATTAGTGGTTGCCTAAGGTTAGAGAGAAGGGAGGAATGAGTAGGTAAAGCACAGAGAATTTTTAGGGCACTGAAACTATTCTGTATGATACTATAATGACAGA... | CTCTTGCAGTGCAGACTATAGCACCTCCAGTTAATCTGGTCACAGTCATTGTAAAAAATGAATTAAGTGTTATTAGATGTATATTGCCTCACCTGTCTTATCTGATGTAATTGCTGTGTAGAAGGAAACTCCTACAGGGAAGAGAAGGAGGGAGTCAACACACTAATACACTACTTAAATCACATTTAAAACGTCAGTTCTTGGAAACAGTAAAAATATTAGTGGTTGCCTAAGGTTAGAGAGAAGGGAGGAATGAGTAGGTAAAGCACAGAGAATTTTTAGGGCACTGAAACTATTCTGTATGATACTATAATGACAGA... |
Task1_train_42392 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | GTGATATGTATTCTTTAGGAACTGTTATGTATGCTGTATTTAATAAAGGGAAACCTATATTTGAAGTCAACAAGCAAGATATTTACAAGAGTTTCAGTAGGCAGTTGGATCAGGTATTTGCCTATAAATAATTTGCTTGCATTAAAAAATTTATTAAATGTGTCTTTGATTTTTTTCCAAAATGTGTTCAGGAAATTCTTTAAATGACATGAGTATCTCATTTTAAGTTTGCATAAGATCAGCTTAATAATTTATTATATTTTTATTTTAACAAATTTATAAGTAACGCAGACTAGGCCAGGTGCTCTGGCTCACGCCTG... | GTGATATGTATTCTTTAGGAACTGTTATGTATGCTGTATTTAATAAAGGGAAACCTATATTTGAAGTCAACAAGCAAGATATTTACAAGAGTTTCAGTAGGCAGTTGGATCAGGTATTTGCCTATAAATAATTTGCTTGCATTAAAAAATTTATTAAATGTGTCTTTGATTTTTTTCCAAAATGTGTTCAGGAAATTCTTTAAATGACATGAGTATCTCATTTTAAGTTTGCATAAGATCAGCTTAATAATTTATTATATTTTTATTTTAACAAATTTATAAGTAACGCAGACTAGGCCAGGTGCTCTGGCTCACGCCTG... |
Task1_train_42393 | Consider this mutation on Chromosome 12. Is this a benign change or a disease-causing variant? | Benign | GTTCCTAGATGAACCTATGTCTTGCCCAAAGCAGGGGGGTCAAAAAATCCAGGGAACAGAAGAAAGACTCCTCCTAAAACTATTCTGTTTATCCATGAGATACTCGATTAGCTCCTTATTTTCTAGATAAATTCCCATTTTAGCCATGTATGAGAGATTTAAGAACCACATAGTTAACATTATTTTTTCTCAAGACAGCTTACAATTTGGGGTGTTCTTTCTCTTTCTTCACAATTTTGGGTTCAGTGGGAATTGAGACCCCTATTCCTGCCTCCCTCCCCAAGAGGGGACATGATGGTGGGTGAGGGAGGATGAGCAGG... | GTTCCTAGATGAACCTATGTCTTGCCCAAAGCAGGGGGGTCAAAAAATCCAGGGAACAGAAGAAAGACTCCTCCTAAAACTATTCTGTTTATCCATGAGATACTCGATTAGCTCCTTATTTTCTAGATAAATTCCCATTTTAGCCATGTATGAGAGATTTAAGAACCACATAGTTAACATTATTTTTTCTCAAGACAGCTTACAATTTGGGGTGTTCTTTCTCTTTCTTCACAATTTTGGGTTCAGTGGGAATTGAGACCCCTATTCCTGCCTCCCTCCCCAAGAGGGGACATGATGGTGGGTGAGGGAGGATGAGCAGG... |
Task1_train_42394 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AACCTTCAGCTGGGTGGCTCACAACCCTTGTGCTCCAGCCCTATGGAACTAGGATGATTTCCTAAGATGCCCTGATTCTTCAGTCCTTCATGCTTTTGCACCGGTCGTTTCTTCATTCTGCGACACACACTCCTCCTTCCTTGCGATACAGATTGTGTCCCTGTGCTCAATCCTGCTACCTGACTAACTCCAGCCCATGCAATTCTCCTCTAAGAAGGTTTCCTTGACTCCAGTCAGGCAGACTTCCTCCTTCTGGCTCCCATGATATCCTGTGAATATTACTTACCACAATGCATGTTTTAATTTATTTTCTTGTCCAA... | AACCTTCAGCTGGGTGGCTCACAACCCTTGTGCTCCAGCCCTATGGAACTAGGATGATTTCCTAAGATGCCCTGATTCTTCAGTCCTTCATGCTTTTGCACCGGTCGTTTCTTCATTCTGCGACACACACTCCTCCTTCCTTGCGATACAGATTGTGTCCCTGTGCTCAATCCTGCTACCTGACTAACTCCAGCCCATGCAATTCTCCTCTAAGAAGGTTTCCTTGACTCCAGTCAGGCAGACTTCCTCCTTCTGGCTCCCATGATATCCTGTGAATATTACTTACCACAATGCATGTTTTAATTTATTTTCTTGTCCAA... |
Task1_train_42395 | Located on Chromosome 12, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AGAAAATACCAATACAATATCCTTCTTCTCTTCATTTATCTTAACTTGAGCAATACTTTGTCTATCATATTCTCAAAACATATCAGAATAACAAGGGATACTCTTGAAAAGTATGAAACACAAATAAGGCTTTTTATTGTTACTTAATGACTTTCAAAACTAAGGTCATAAAAATGTTTAATCTTTTTTTAAAAATCTCTTACTAATGTGTATAAGCTATCACTTCTGTGCTCCAATATATGTATCCTTCATATAAAGTGACAGCTATCTTGCAGAAAAATGATTGGTTCCATACCCTCTCTCCTCAGCCTGGCCTACCA... | AGAAAATACCAATACAATATCCTTCTTCTCTTCATTTATCTTAACTTGAGCAATACTTTGTCTATCATATTCTCAAAACATATCAGAATAACAAGGGATACTCTTGAAAAGTATGAAACACAAATAAGGCTTTTTATTGTTACTTAATGACTTTCAAAACTAAGGTCATAAAAATGTTTAATCTTTTTTTAAAAATCTCTTACTAATGTGTATAAGCTATCACTTCTGTGCTCCAATATATGTATCCTTCATATAAAGTGACAGCTATCTTGCAGAAAAATGATTGGTTCCATACCCTCTCTCCTCAGCCTGGCCTACCA... |
Task1_train_42396 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGATCATAGAGGGAGCAACAAAGGCTGATGCTGCAGAATATTCAGTAATGACAACAGGAGGACAATCATCTGCTAAACTTAGTGTTGACTGTAAGTGAGACTTCTTTAGATGTCTTCTCAGTGGGCTTATTAATGATGGTTGTGTTAATTCGGTTTCAGAAAAGTTTCTATTTGATTTCTATTTGCGATGATTTTTAAGTATGTAAAATGGATTTCATTCCAGCTAAGTGTCTATGTCAGATCAATCAGGATATTTAAGGAAGGAACCACGACTCAATTTAATAGTAGAGCGCCAATATTAGGAAGGAAGTATAAAAATC... | TGATCATAGAGGGAGCAACAAAGGCTGATGCTGCAGAATATTCAGTAATGACAACAGGAGGACAATCATCTGCTAAACTTAGTGTTGACTGTAAGTGAGACTTCTTTAGATGTCTTCTCAGTGGGCTTATTAATGATGGTTGTGTTAATTCGGTTTCAGAAAAGTTTCTATTTGATTTCTATTTGCGATGATTTTTAAGTATGTAAAATGGATTTCATTCCAGCTAAGTGTCTATGTCAGATCAATCAGGATATTTAAGGAAGGAACCACGACTCAATTTAATAGTAGAGCGCCAATATTAGGAAGGAAGTATAAAAATC... |
Task1_train_42397 | Chromosome 12 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AAGACTCTAGTTACATATGTGCTAGACTGCTTTCTGTTGTCCCACCACTCGCCGATGCACAGTTCAATTATTTTTAGTCGTTTTTCTTTCGTCATTTTGGATAGTTTCCATTGGTACATGCTTATTGATCTTTTCTTCTGTGGTGTTTAATATGCTGTTAATCTCACCCAGTTTATTTTACAATTCAAATATTGTAATTTTCATTTCTGGAGATTTCACTTGAGTCTTTTCTTCCATTTCTGTTTATAATTTTCCTGTTTTCCTCTACTTTCTTGAACATGTGGAGCATATTTATAATAACTATTTTGATATCCTCATCT... | AAGACTCTAGTTACATATGTGCTAGACTGCTTTCTGTTGTCCCACCACTCGCCGATGCACAGTTCAATTATTTTTAGTCGTTTTTCTTTCGTCATTTTGGATAGTTTCCATTGGTACATGCTTATTGATCTTTTCTTCTGTGGTGTTTAATATGCTGTTAATCTCACCCAGTTTATTTTACAATTCAAATATTGTAATTTTCATTTCTGGAGATTTCACTTGAGTCTTTTCTTCCATTTCTGTTTATAATTTTCCTGTTTTCCTCTACTTTCTTGAACATGTGGAGCATATTTATAATAACTATTTTGATATCCTCATCT... |
Task1_train_42398 | A mutation found on Chromosome 12 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GCCCAGGCAACAAGATACACCAAGCTTTGTATATTAGTTCTGCTCTTTTGGCTTCCAAGTGAACCTTCTAAGTCATGGGCATTAAGGCTGGGTCTTAAGTAATGGTTTTGTACTCAAGTGTTTCTTGGGAAAACTAGGATATGCTAACTAGTGGCAAAGAGTACAAAGTGACCTAGCAAATTAAAAATTATTAACAACAAGAATAAACCACAAGAGCCCAAGTTAAAACATCCAGAAGATTAATTTGCTGAATATCATGTTGTTTTCACTGAATGTGGCCAAAAAGATCTTCAGAGCGATGGCAAAATAGGAAACTGACA... | GCCCAGGCAACAAGATACACCAAGCTTTGTATATTAGTTCTGCTCTTTTGGCTTCCAAGTGAACCTTCTAAGTCATGGGCATTAAGGCTGGGTCTTAAGTAATGGTTTTGTACTCAAGTGTTTCTTGGGAAAACTAGGATATGCTAACTAGTGGCAAAGAGTACAAAGTGACCTAGCAAATTAAAAATTATTAACAACAAGAATAAACCACAAGAGCCCAAGTTAAAACATCCAGAAGATTAATTTGCTGAATATCATGTTGTTTTCACTGAATGTGGCCAAAAAGATCTTCAGAGCGATGGCAAAATAGGAAACTGACA... |
Task1_train_42399 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | TATCTATGGACTCTCCATCTCACAAACTATCTTTCTTATACCAGTGTTTCACAAAACACACTTTGGGAAACTTCTTTAGAATACCACATATTTTATGTCTTTAGCCTGTATTCCTTTTCTGAATTCTGAACAGGATCTCTCCTTCTGTTTTGCATTTTTAATAAATTCAGGAATTTGCACTTCTACAGCTGAAGGAATCCATCTACTATATCAAGTACATTTTCTATTCTTGAAATTGACCATTACAAATTTTTGGTTAATTGTTTTAAAATAACTTAAAGTAATGATGTCTTAAACTAAAAAAATCAGTTGTGTTAACT... | TATCTATGGACTCTCCATCTCACAAACTATCTTTCTTATACCAGTGTTTCACAAAACACACTTTGGGAAACTTCTTTAGAATACCACATATTTTATGTCTTTAGCCTGTATTCCTTTTCTGAATTCTGAACAGGATCTCTCCTTCTGTTTTGCATTTTTAATAAATTCAGGAATTTGCACTTCTACAGCTGAAGGAATCCATCTACTATATCAAGTACATTTTCTATTCTTGAAATTGACCATTACAAATTTTTGGTTAATTGTTTTAAAATAACTTAAAGTAATGATGTCTTAAACTAAAAAAATCAGTTGTGTTAACT... |
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