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_34600 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GGAAGACATAATCATTGACCTTGTTCACAAATTTTGTTCTCTCCTCATTATTACTGAAGATTCTAAGAAAAATGAAATGGCAGAGCTAGATATTATGGGCTTGGCTCTAAAACTTGCAAATTCTCTGATAAGGGAATTTAAGAAAAGTGATATTAAAGTTTTACCAAATGCTGAAAAAATGTTTTCTTTTCCACCAATTGATAAAGAGACAGTTGATAAAATATCCAATTTTGTATATGAACAGTTCATAGAAAAATGCACATCTCATGATATTCAAAAAGGTGATGAAAGTAACATTGCTATAGGGATGATTGCTGCTC... | GGAAGACATAATCATTGACCTTGTTCACAAATTTTGTTCTCTCCTCATTATTACTGAAGATTCTAAGAAAAATGAAATGGCAGAGCTAGATATTATGGGCTTGGCTCTAAAACTTGCAAATTCTCTGATAAGGGAATTTAAGAAAAGTGATATTAAAGTTTTACCAAATGCTGAAAAAATGTTTTCTTTTCCACCAATTGATAAAGAGACAGTTGATAAAATATCCAATTTTGTATATGAACAGTTCATAGAAAAATGCACATCTCATGATATTCAAAAAGGTGATGAAAGTAACATTGCTATAGGGATGATTGCTGCTC... |
Task1_train_34601 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | GAAAAAAGGTGACATCCAAAATCCAGTACTTAGCTCTATAAATGCAATTATGAAAAGCGGCATGATTAACCTAACATCAGGGTTGGCTACAGGTGTGACAAATAAAAAGGAAGTGGATGAAAATAAAGTGGGAATTTGTACTCAAAAACATAGTGAGAATGTATCAAAAGTTACTTCAACTACCACTGTGAAAAGTAAAGATACTCAGGAGCCAAATTTGAGTGAAACATTTAATAATAATGAAATTGAGAAGAAAAGAAATTTAATTCCAACAGATAAAAAAGGGAAAGATGATGAGATATACACACATTTTTCATTAA... | GAAAAAAGGTGACATCCAAAATCCAGTACTTAGCTCTATAAATGCAATTATGAAAAGCGGCATGATTAACCTAACATCAGGGTTGGCTACAGGTGTGACAAATAAAAAGGAAGTGGATGAAAATAAAGTGGGAATTTGTACTCAAAAACATAGTGAGAATGTATCAAAAGTTACTTCAACTACCACTGTGAAAAGTAAAGATACTCAGGAGCCAAATTTGAGTGAAACATTTAATAATAATGAAATTGAGAAGAAAAGAAATTTAATTCCAACAGATAAAAAAGGGAAAGATGATGAGATATACACACATTTTTCATTAA... |
Task1_train_34602 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | TAGTTCAACCATTGTGGAAGATACTGTGGCGATTCCTCAAAGATCTAGCAGCAAAAATACCATTTGACTCAGCAATTCCATTACTGGGTATATATGCAAAGGAATACAAGCCATTCTATTATAAAGATACATGCACATGAATGTTCATTGCAGCACTATTCACAATCGCAATTGGTTGATTTGGGAATCAACTCGAATGCCCATCAATGATAGACTGGATAAAGAAAATGTGGTACGTATACACCATAGAACACTATGCAGCCATAAAAAGGAATGAGATCATGTCCTTTGCAGGGACATGAATGGAGCCAGAAGCCATT... | TAGTTCAACCATTGTGGAAGATACTGTGGCGATTCCTCAAAGATCTAGCAGCAAAAATACCATTTGACTCAGCAATTCCATTACTGGGTATATATGCAAAGGAATACAAGCCATTCTATTATAAAGATACATGCACATGAATGTTCATTGCAGCACTATTCACAATCGCAATTGGTTGATTTGGGAATCAACTCGAATGCCCATCAATGATAGACTGGATAAAGAAAATGTGGTACGTATACACCATAGAACACTATGCAGCCATAAAAAGGAATGAGATCATGTCCTTTGCAGGGACATGAATGGAGCCAGAAGCCATT... |
Task1_train_34603 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ATACTGTGGCGATTCCTCAAAGATCTAGCAGCAAAAATACCATTTGACTCAGCAATTCCATTACTGGGTATATATGCAAAGGAATACAAGCCATTCTATTATAAAGATACATGCACATGAATGTTCATTGCAGCACTATTCACAATCGCAATTGGTTGATTTGGGAATCAACTCGAATGCCCATCAATGATAGACTGGATAAAGAAAATGTGGTACGTATACACCATAGAACACTATGCAGCCATAAAAAGGAATGAGATCATGTCCTTTGCAGGGACATGAATGGAGCCAGAAGCCATTATCCTCAGGAAATTAACACA... | ATACTGTGGCGATTCCTCAAAGATCTAGCAGCAAAAATACCATTTGACTCAGCAATTCCATTACTGGGTATATATGCAAAGGAATACAAGCCATTCTATTATAAAGATACATGCACATGAATGTTCATTGCAGCACTATTCACAATCGCAATTGGTTGATTTGGGAATCAACTCGAATGCCCATCAATGATAGACTGGATAAAGAAAATGTGGTACGTATACACCATAGAACACTATGCAGCCATAAAAAGGAATGAGATCATGTCCTTTGCAGGGACATGAATGGAGCCAGAAGCCATTATCCTCAGGAAATTAACACA... |
Task1_train_34604 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TGGTTGATTTGGGAATCAACTCGAATGCCCATCAATGATAGACTGGATAAAGAAAATGTGGTACGTATACACCATAGAACACTATGCAGCCATAAAAAGGAATGAGATCATGTCCTTTGCAGGGACATGAATGGAGCCAGAAGCCATTATCCTCAGGAAATTAACACAGGAACAGAAAACCAAGCACTGCATGTTCTCATTTATAAGTGAGAGCTGAATGATGAGAAGACATGGACACCTGGTGGGGAACAACCCACACTGGGGCCTGTCTTGGGGGCAGAGGGAAGAAGAGCATCAGGAAGAATAGCTAATGGATGCTG... | TGGTTGATTTGGGAATCAACTCGAATGCCCATCAATGATAGACTGGATAAAGAAAATGTGGTACGTATACACCATAGAACACTATGCAGCCATAAAAAGGAATGAGATCATGTCCTTTGCAGGGACATGAATGGAGCCAGAAGCCATTATCCTCAGGAAATTAACACAGGAACAGAAAACCAAGCACTGCATGTTCTCATTTATAAGTGAGAGCTGAATGATGAGAAGACATGGACACCTGGTGGGGAACAACCCACACTGGGGCCTGTCTTGGGGGCAGAGGGAAGAAGAGCATCAGGAAGAATAGCTAATGGATGCTG... |
Task1_train_34605 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | TGTTCTCCTTCTCAACTCCCTGTCCCCCAATATCTCCTAAGTCCAACCGTTAGTTATACAACTTAGCATTCTAACAGGATGAAGTATGATGCTTGTGCAGGGAAAATGGAGTTGCAAAGCCTTTGTATAGGCTCATTTTACGCCCCACAAGAGCTCTGGTTTCCAATGTGTGTGGAGTACCCATGGGCATGGGCTATATATCAACTGAAGTCTGGATACAAACTTACATATACATGTGTATGTATACGTGTGTGGGGGTACAGGTGTATTATAGGCATGTGTATAAATATATATTATATATATATATTTAATGAGAACAA... | TGTTCTCCTTCTCAACTCCCTGTCCCCCAATATCTCCTAAGTCCAACCGTTAGTTATACAACTTAGCATTCTAACAGGATGAAGTATGATGCTTGTGCAGGGAAAATGGAGTTGCAAAGCCTTTGTATAGGCTCATTTTACGCCCCACAAGAGCTCTGGTTTCCAATGTGTGTGGAGTACCCATGGGCATGGGCTATATATCAACTGAAGTCTGGATACAAACTTACATATACATGTGTATGTATACGTGTGTGGGGGTACAGGTGTATTATAGGCATGTGTATAAATATATATTATATATATATATTTAATGAGAACAA... |
Task1_train_34606 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | AGTTAATGGGTGCAGCACACCAACATGGCACATGTATACATATGTAACAAACCTGCACGTTGTGCACATGTACCCTACAACTTAAAGTATAATAATAAAAAAAAGTTGTCTCTTTTCTATGTGTTTCATAATGTACACAATCTTTTAACATTATACAACATGCTATATTTTCTTTTTTTCTTTCTTTTCTATTTTTTTTTTGAGATGGAGTCTCATTCTGTTGCCTCGGTTGGAGTACAGAATTGCCATTTTGGCTCACTGCAACCTCCGGCTTCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA... | AGTTAATGGGTGCAGCACACCAACATGGCACATGTATACATATGTAACAAACCTGCACGTTGTGCACATGTACCCTACAACTTAAAGTATAATAATAAAAAAAAGTTGTCTCTTTTCTATGTGTTTCATAATGTACACAATCTTTTAACATTATACAACATGCTATATTTTCTTTTTTTCTTTCTTTTCTATTTTTTTTTTGAGATGGAGTCTCATTCTGTTGCCTCGGTTGGAGTACAGAATTGCCATTTTGGCTCACTGCAACCTCCGGCTTCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA... |
Task1_train_34607 | Located on Chromosome 2, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TTCTACTTCCCTAACTGTTCTTGTTTTTAGGGTCCTCCTGGAAAGAATGGTGAAACTGGACCTCAGGGACCCCCAGGGCCTACTGTAAGTTCACTCATATAAAATTGGAGATGAAAATAGGGTGGAGGTGGGGCAGGAAGAATGCTTCAAAAATTACATAATCTCTGACACCATGTTGTTACAGTTTACCAAAGCAATGATGAAACTTGCTGACCTAGTTATCTAGCTAAATGCTAGCATTGAGTTTAGAGTGTACATGTGTGCTTTGGGTCCAGGTCCTCCCTTTTCTTCACATCACTACTTTTATAATTAAGCAACAG... | TTCTACTTCCCTAACTGTTCTTGTTTTTAGGGTCCTCCTGGAAAGAATGGTGAAACTGGACCTCAGGGACCCCCAGGGCCTACTGTAAGTTCACTCATATAAAATTGGAGATGAAAATAGGGTGGAGGTGGGGCAGGAAGAATGCTTCAAAAATTACATAATCTCTGACACCATGTTGTTACAGTTTACCAAAGCAATGATGAAACTTGCTGACCTAGTTATCTAGCTAAATGCTAGCATTGAGTTTAGAGTGTACATGTGTGCTTTGGGTCCAGGTCCTCCCTTTTCTTCACATCACTACTTTTATAATTAAGCAACAG... |
Task1_train_34608 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | GAACACAACATATTAACCACTGGACATATTATCAATTTTGATCATTAAAATTCTACCTATAAAAAGGAACACTTTCTTAAATAATTGACAGTAGTTTTTAACCCATATCTAAATGAAAATAGCTCTGGCAGTGTTATTTAAGACTGTCAAAAATAATAATATCATTTTGGGAGTCATTAACATTTAAAGTAGCATATATAAAGGAAACTAGATCATTTAGAAAATTGTATAGTCTTTTAGACACCTGCACACGTATGTTTATCGCAGCATAATTCACAGTTGTAAAGATATGGAACCAGCCTAAGTGCCCATCAGCGGAT... | GAACACAACATATTAACCACTGGACATATTATCAATTTTGATCATTAAAATTCTACCTATAAAAAGGAACACTTTCTTAAATAATTGACAGTAGTTTTTAACCCATATCTAAATGAAAATAGCTCTGGCAGTGTTATTTAAGACTGTCAAAAATAATAATATCATTTTGGGAGTCATTAACATTTAAAGTAGCATATATAAAGGAAACTAGATCATTTAGAAAATTGTATAGTCTTTTAGACACCTGCACACGTATGTTTATCGCAGCATAATTCACAGTTGTAAAGATATGGAACCAGCCTAAGTGCCCATCAGCGGAT... |
Task1_train_34609 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ACACTATGAAAAATCATAACATGCTGATGATTAACAACCAAGACAGTCCCCATCTTCAGTTCAGGCTAGTAAACAAGACAGACACCACACATAACTTGTTTCCCTTTTAAAATTAACATCTCTGAAGTATGCAGCGTGAAGCAGGGCATACAGAACTAAAGGTAATTAAAAGCAGAAGACTGCCTTTCCTTTCTTACCCTCATATCACTCTTATTAGGGGTAGGAACAGATGTAGTATTATGAGAAACTGGGTAGAATTTATAGAATAATATATGGTGGTAGACCTGGCAAACATCACCTCCTCTGGACATCCTTAATTA... | ACACTATGAAAAATCATAACATGCTGATGATTAACAACCAAGACAGTCCCCATCTTCAGTTCAGGCTAGTAAACAAGACAGACACCACACATAACTTGTTTCCCTTTTAAAATTAACATCTCTGAAGTATGCAGCGTGAAGCAGGGCATACAGAACTAAAGGTAATTAAAAGCAGAAGACTGCCTTTCCTTTCTTACCCTCATATCACTCTTATTAGGGGTAGGAACAGATGTAGTATTATGAGAAACTGGGTAGAATTTATAGAATAATATATGGTGGTAGACCTGGCAAACATCACCTCCTCTGGACATCCTTAATTA... |
Task1_train_34610 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | AAAAATGTTGCTAGATGAGTACACTGTGTGATCCAAATTTCAAGATGGCACCTGAAATCTTTGCCATAACTTTGATACCAAGATGAACAAATAAGGGCATAATAATAATATGTTACATAAACGTATAAATTTGGAGAACAAATCAACCCAAAGACTGCTGATAAATATAGCAATAACCTTTCTACTGTGCTGATACAGGGCTCTCTTACTCTTAATACGTAAGTAACATAGTGAAACCACTTATAATATAAAAAATCCAAGTCCTTTGGGATTGGTAAAGACAGCTAATAAATAAGTAGGATGAAAGAATCAAGAGCCGA... | AAAAATGTTGCTAGATGAGTACACTGTGTGATCCAAATTTCAAGATGGCACCTGAAATCTTTGCCATAACTTTGATACCAAGATGAACAAATAAGGGCATAATAATAATATGTTACATAAACGTATAAATTTGGAGAACAAATCAACCCAAAGACTGCTGATAAATATAGCAATAACCTTTCTACTGTGCTGATACAGGGCTCTCTTACTCTTAATACGTAAGTAACATAGTGAAACCACTTATAATATAAAAAATCCAAGTCCTTTGGGATTGGTAAAGACAGCTAATAAATAAGTAGGATGAAAGAATCAAGAGCCGA... |
Task1_train_34611 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CAAATATTTGAATGCCTGTTATATACAAATTGCTATGCCACAGGAACTATAGACACATCCTCTCCCTTCAAGAGTTCTCACAGTCAGGAAAATGAAACACAAGCAATTTAAAAGTAAAGTACAAGAGGCCAAATAACAATTCAATACAGTGACATCCAAAGGTAAAAAATTATTGGTTACCAAATCAGTAGAAGAGAGAAGTCATATGGAACAGAGTCTTCTAAATGATCTTTACCTGAATCCAAACACATTTGTTTCCTTTTTCAGATTCAACTTATCAGTATATAAAAGGTTCTGCTGACATTAAATCCAACCAGGGA... | CAAATATTTGAATGCCTGTTATATACAAATTGCTATGCCACAGGAACTATAGACACATCCTCTCCCTTCAAGAGTTCTCACAGTCAGGAAAATGAAACACAAGCAATTTAAAAGTAAAGTACAAGAGGCCAAATAACAATTCAATACAGTGACATCCAAAGGTAAAAAATTATTGGTTACCAAATCAGTAGAAGAGAGAAGTCATATGGAACAGAGTCTTCTAAATGATCTTTACCTGAATCCAAACACATTTGTTTCCTTTTTCAGATTCAACTTATCAGTATATAAAAGGTTCTGCTGACATTAAATCCAACCAGGGA... |
Task1_train_34612 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CAGCTAATTCTTGTACTTTTAGTAGAAACGGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCTCCTGAACTCATGATCCGCCCCCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCCGGCCAAAACACTGTTTTTCAAAAAAGTTTACTGGCATCTTATCTAAAATGTGTTATTTTTCAGTTTAGTGTGTCTTAGAGCAGGGTTCCCCAACCCCTGGACCATGGACCGCTACCACTCTGTGGCCTGTTAGGAATTGGGCTGCACAGCAAGAGCGGGCCAGCAAGCATTATCACATGAGCTCTT... | CAGCTAATTCTTGTACTTTTAGTAGAAACGGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCTCCTGAACTCATGATCCGCCCCCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCCGGCCAAAACACTGTTTTTCAAAAAAGTTTACTGGCATCTTATCTAAAATGTGTTATTTTTCAGTTTAGTGTGTCTTAGAGCAGGGTTCCCCAACCCCTGGACCATGGACCGCTACCACTCTGTGGCCTGTTAGGAATTGGGCTGCACAGCAAGAGCGGGCCAGCAAGCATTATCACATGAGCTCTT... |
Task1_train_34613 | This genomic variant is located on Chromosome 2. Can you determine its pathogenicity and name any linked disease? | Benign | AGCTGGGGTTGGTCTGAATGTTCTCCATTCCATTGAAGTGTGTGTTATTCAAGACAAAATTTTAGAACAGGAAGGCACCTTAGGTATCACTAATCCAAGCCCCTCGCTTAAAGGAAGTACCAGCTGTTTCCTCTCAGGGTCCTCAAGAAACCATAGACTTTTAAAGAGCAGCTATGGTTCTTAAGCCTAGTCTAATCCAGGGCTGCCAACAGTGTCACTGGCACACTACCAGATGCTGGGCGCTTCACAGTCCGTATTGGAAAGCCTACCGGAATGGCAGGCATCCCTCTAAGGCTACAAAAGTTGCCATTCTTCTTAGC... | AGCTGGGGTTGGTCTGAATGTTCTCCATTCCATTGAAGTGTGTGTTATTCAAGACAAAATTTTAGAACAGGAAGGCACCTTAGGTATCACTAATCCAAGCCCCTCGCTTAAAGGAAGTACCAGCTGTTTCCTCTCAGGGTCCTCAAGAAACCATAGACTTTTAAAGAGCAGCTATGGTTCTTAAGCCTAGTCTAATCCAGGGCTGCCAACAGTGTCACTGGCACACTACCAGATGCTGGGCGCTTCACAGTCCGTATTGGAAAGCCTACCGGAATGGCAGGCATCCCTCTAAGGCTACAAAAGTTGCCATTCTTCTTAGC... |
Task1_train_34614 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ACCAGTGCCGTGCCTATATTATGAACTCTTTTTCTTTTCTTTTCTTTTTTTTTTTTTATATTATAGCCTCTTTTAGCTCTTTAAGTCTTCTATGGGTTTAATGGGAGGCTTTAGTGGTGTATAGAGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAAATGGATTTATTTTATTCTACAAATGAAATGAATAAAATCACCTGAAATGGAACGGAATGGCTACAGCGAGTGTCCAAAGACCACAAAACTGTTTCCTGACATGTGCTTAGCATATTTAAATTGTTCTCACAGTATCATCCTGAGAGCAGAGAGA... | ACCAGTGCCGTGCCTATATTATGAACTCTTTTTCTTTTCTTTTCTTTTTTTTTTTTTATATTATAGCCTCTTTTAGCTCTTTAAGTCTTCTATGGGTTTAATGGGAGGCTTTAGTGGTGTATAGAGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAAATGGATTTATTTTATTCTACAAATGAAATGAATAAAATCACCTGAAATGGAACGGAATGGCTACAGCGAGTGTCCAAAGACCACAAAACTGTTTCCTGACATGTGCTTAGCATATTTAAATTGTTCTCACAGTATCATCCTGAGAGCAGAGAGA... |
Task1_train_34615 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GGGGTCTCACTATATTGCCCAGACTGGTCTCAAACTCCTCGCCTCAAGTAGTTCTCCAGCCTTAACTTCCCAAAGTGCTGGGATTACAGTGCATTAATTATTATGACTTAGGATAATTAATTATTATGACTTAGGATAATATCCTAGAATATTTTGTTGATAATTACAAGATTTTATTGTTCATTTCCTCTTTGTATCACATCCGTGAGGTTTGCATTATTAGACTTGTTAATGCTATTCTGATAGGTCTGATGTATACTGGGAATCTCATGATTCTGAAATGTTCAATACTTTTAATAGAGTAGTACCTTATGGTAGTT... | GGGGTCTCACTATATTGCCCAGACTGGTCTCAAACTCCTCGCCTCAAGTAGTTCTCCAGCCTTAACTTCCCAAAGTGCTGGGATTACAGTGCATTAATTATTATGACTTAGGATAATTAATTATTATGACTTAGGATAATATCCTAGAATATTTTGTTGATAATTACAAGATTTTATTGTTCATTTCCTCTTTGTATCACATCCGTGAGGTTTGCATTATTAGACTTGTTAATGCTATTCTGATAGGTCTGATGTATACTGGGAATCTCATGATTCTGAAATGTTCAATACTTTTAATAGAGTAGTACCTTATGGTAGTT... |
Task1_train_34616 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AAGGTTAAGTGTTTAAAGGTTTTAATAATTTATGATTATTTACAAAGCACAATTTTCAGGTTGTTAAATTGTGTCAAACTACTCAGGCACTTGCAATTCAGCTTAAATTAGGACACCAATCAATAGCTGAGAGCCTATTTGGTGCATAAGACTGTCAACCAAATGTGATTATATGTAATTAAGCAATATGATAACAAAAGAGAGATAATTACAAAGGTGGCAAACTTGGTGAAAAGTTATTTCAGTTCACACAATAGCAATATTCCAGCAGAATATGTGAATTATTTTGATTAAATTTTTAAGTACCTTAACATCATTAT... | AAGGTTAAGTGTTTAAAGGTTTTAATAATTTATGATTATTTACAAAGCACAATTTTCAGGTTGTTAAATTGTGTCAAACTACTCAGGCACTTGCAATTCAGCTTAAATTAGGACACCAATCAATAGCTGAGAGCCTATTTGGTGCATAAGACTGTCAACCAAATGTGATTATATGTAATTAAGCAATATGATAACAAAAGAGAGATAATTACAAAGGTGGCAAACTTGGTGAAAAGTTATTTCAGTTCACACAATAGCAATATTCCAGCAGAATATGTGAATTATTTTGATTAAATTTTTAAGTACCTTAACATCATTAT... |
Task1_train_34617 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GCAGAATAAAATCTAAATTCTTGGTCATTCAAAGTACATCAGAATTCGGACCCATCCTTCCTTCACAACCAGGCCTCACTGATGCACATGCTGGTCCCCCCACCCCGCTTCCCTGGGCCCGAGCTTTGATGCATGGCACTCCTTGGGCCAGAACGGCACATGACTGTCATCTGAAGAGGTTATGAACTCACTGAGGCTAGCACTGTGCTTTATTCATTCTTGTATCTTCAGGTACAAGGCTGTGCGTACAGCAGAGAATTTTTTTTTCGGGGTGTTAAATTCACATCACTCTGAAAATTGTATTATAAAGAAATATTTCT... | GCAGAATAAAATCTAAATTCTTGGTCATTCAAAGTACATCAGAATTCGGACCCATCCTTCCTTCACAACCAGGCCTCACTGATGCACATGCTGGTCCCCCCACCCCGCTTCCCTGGGCCCGAGCTTTGATGCATGGCACTCCTTGGGCCAGAACGGCACATGACTGTCATCTGAAGAGGTTATGAACTCACTGAGGCTAGCACTGTGCTTTATTCATTCTTGTATCTTCAGGTACAAGGCTGTGCGTACAGCAGAGAATTTTTTTTTCGGGGTGTTAAATTCACATCACTCTGAAAATTGTATTATAAAGAAATATTTCT... |
Task1_train_34618 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | TTTCTACATATGGCTAGCCAGTTTTCCCAGCACCATTTATTAAATAGGGAATCCTTTCCCCATTTCTTGTTTTTGTCAGGTTTGTCAAAGATCAGATGGTTGTAGACGTGTGGTATTATTTCTGAGGGCTCTCTTCTGTTCCATTGGTCTATATCTCTGTTTTGGTACCAGTACCATGCTGTTTTGGTTACTGTAGCCTTGTAGTATAGTTTGAAGTCAGGTAGCATGATGCCTCCAGCTTTGTTCTTTTGGCTTAGGATTAAGACAATCAAGTCTTAAGCAAAAGTAAATGAAGTGTTACTCTCCCCTCCCCAACAGAA... | TTTCTACATATGGCTAGCCAGTTTTCCCAGCACCATTTATTAAATAGGGAATCCTTTCCCCATTTCTTGTTTTTGTCAGGTTTGTCAAAGATCAGATGGTTGTAGACGTGTGGTATTATTTCTGAGGGCTCTCTTCTGTTCCATTGGTCTATATCTCTGTTTTGGTACCAGTACCATGCTGTTTTGGTTACTGTAGCCTTGTAGTATAGTTTGAAGTCAGGTAGCATGATGCCTCCAGCTTTGTTCTTTTGGCTTAGGATTAAGACAATCAAGTCTTAAGCAAAAGTAAATGAAGTGTTACTCTCCCCTCCCCAACAGAA... |
Task1_train_34619 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TTAAATTTACAATAGGTTATCAGTTTGTTTCTAAGTATAGAGAATATAGATAATGATTTAATTTCCTCAAGAATAAATATAATTACTCCATAAACTAATAATTTTACAAGTACATTTCTAAGGTCTCTATGTGTTTAGTCCATTATCATGTCAACCCTATGAGGTAAGGTCCATTGTAACATCTATTTATCAATGGAGAGACTAAGGCACATAGAGGCAAGTGCCAGGCTCAAGTTTAGCCAGATAATAAACAATAGAGCCAAGATTTGAACCCAGACAGTTGTAATTACTCTGCTATCAGAGATAACATAGTCATAAGG... | TTAAATTTACAATAGGTTATCAGTTTGTTTCTAAGTATAGAGAATATAGATAATGATTTAATTTCCTCAAGAATAAATATAATTACTCCATAAACTAATAATTTTACAAGTACATTTCTAAGGTCTCTATGTGTTTAGTCCATTATCATGTCAACCCTATGAGGTAAGGTCCATTGTAACATCTATTTATCAATGGAGAGACTAAGGCACATAGAGGCAAGTGCCAGGCTCAAGTTTAGCCAGATAATAAACAATAGAGCCAAGATTTGAACCCAGACAGTTGTAATTACTCTGCTATCAGAGATAACATAGTCATAAGG... |
Task1_train_34620 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | ATAAAAATGTTAGACAATGGTGATCTTTAATATGCTGAAGAATTTATGCAAACAAATAATTTATCAGCATTTGAAAAATCTCTTAATAATCAAGAATGGGACTAAAAGAAAATTTCAATTTTTACCTATGCTATTTTTATAAACTGAAAAAAACGGAATTTCTTTAATTGTACTCTGATATCATTTCAATCAGCAATACTAAAGCAAGATATTCCAAGGTTATTTTTCTTGTCCAATGGGCTCTCTTCACAAGAAACACGTAAGGTAAATAAATCCAGATTTAAACACTTAAAAACTATAGTGTTCTAATATAAGATAGG... | ATAAAAATGTTAGACAATGGTGATCTTTAATATGCTGAAGAATTTATGCAAACAAATAATTTATCAGCATTTGAAAAATCTCTTAATAATCAAGAATGGGACTAAAAGAAAATTTCAATTTTTACCTATGCTATTTTTATAAACTGAAAAAAACGGAATTTCTTTAATTGTACTCTGATATCATTTCAATCAGCAATACTAAAGCAAGATATTCCAAGGTTATTTTTCTTGTCCAATGGGCTCTCTTCACAAGAAACACGTAAGGTAAATAAATCCAGATTTAAACACTTAAAAACTATAGTGTTCTAATATAAGATAGG... |
Task1_train_34621 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGTCTTGTTAGTACCATGAGAGCAGTAAGACAGTAGCCACGCTCTCTAGATGCAGCTGAAAATATTAGGGTGTTAGATGCATGTTCCAGTTCCTTCTATCCTCAGGGTGAAGCTGAGAGCAGGTATTTATCCCTTACTGCGCTAAAGCAGGCATTATTTATCTGCACTAAGGCAGGCATTTATCTCTCTCTACTCTAAGCCAGGGAGAAGCTCTGTGGCAAATACCTATACTACTGTCATTCAGACTACATCCTCTGAGGGTATGGCCACTGGGAGTGGGCCCGTTTTATATCTACCTCTTTGTTTTCTGTGGTCTAGAG... | AGTCTTGTTAGTACCATGAGAGCAGTAAGACAGTAGCCACGCTCTCTAGATGCAGCTGAAAATATTAGGGTGTTAGATGCATGTTCCAGTTCCTTCTATCCTCAGGGTGAAGCTGAGAGCAGGTATTTATCCCTTACTGCGCTAAAGCAGGCATTATTTATCTGCACTAAGGCAGGCATTTATCTCTCTCTACTCTAAGCCAGGGAGAAGCTCTGTGGCAAATACCTATACTACTGTCATTCAGACTACATCCTCTGAGGGTATGGCCACTGGGAGTGGGCCCGTTTTATATCTACCTCTTTGTTTTCTGTGGTCTAGAG... |
Task1_train_34622 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GTCATTGGAACTTGAACTTGTACTGGCCGAAATACAAAACAGTTATTTTTATAGGGGTGCACATAGTATCTCTTATATGTGAAAAAGAGAGTAATTTTTTTTCTTATAGAACCTGCAGATATCTTTCAACAAGGAACATGAAGAAAATGCATATTTGAGGTCCGAAATAATGTCTCTTCATGAAGCATCAGAAAAAGCACAAGTAAATGCTCATGATTTTGTTAGTTTTTAGATGTTATTTAATTTTGTTCAATTAAATAACCAAGAAACAAAATTAGTCTTGATTATATAAATTCATACCATCTCCATCACCCAACTTT... | GTCATTGGAACTTGAACTTGTACTGGCCGAAATACAAAACAGTTATTTTTATAGGGGTGCACATAGTATCTCTTATATGTGAAAAAGAGAGTAATTTTTTTTCTTATAGAACCTGCAGATATCTTTCAACAAGGAACATGAAGAAAATGCATATTTGAGGTCCGAAATAATGTCTCTTCATGAAGCATCAGAAAAAGCACAAGTAAATGCTCATGATTTTGTTAGTTTTTAGATGTTATTTAATTTTGTTCAATTAAATAACCAAGAAACAAAATTAGTCTTGATTATATAAATTCATACCATCTCCATCACCCAACTTT... |
Task1_train_34623 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | CTGCCACCACTTCTGTTCAACATTTTACTGGAGGTCCTAGCCAATGTAATAAGAAACAAAAGGCATAAAGATGGCAAGGAAAAAATAAAATTATTAAGTCACAGATGACATGATTATATACATAGAAGACCCAAAATAAATCTACATACAAACTATAAGAATAATTTAGCAAGGTTGCTGAACACAAAGTCAATATATAAAAATTATAGTTTAATATATCAGCAAATGAATTGAAAATGAAATTAAAAGATGATCCTATCTTCAGTGTGTAAGAACGGTGTGAACAGCAAGAATTTAGTGGTGTATTTAGTACTGTCCAG... | CTGCCACCACTTCTGTTCAACATTTTACTGGAGGTCCTAGCCAATGTAATAAGAAACAAAAGGCATAAAGATGGCAAGGAAAAAATAAAATTATTAAGTCACAGATGACATGATTATATACATAGAAGACCCAAAATAAATCTACATACAAACTATAAGAATAATTTAGCAAGGTTGCTGAACACAAAGTCAATATATAAAAATTATAGTTTAATATATCAGCAAATGAATTGAAAATGAAATTAAAAGATGATCCTATCTTCAGTGTGTAAGAACGGTGTGAACAGCAAGAATTTAGTGGTGTATTTAGTACTGTCCAG... |
Task1_train_34624 | Located on Chromosome 2, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAATGCCCATCAATGATAGACTAGATAAAGAAAATGTGGCACATACACACCATGGAATACTATGCAGCCATAAAAAAGAATGAGTTCATGTCCTTTGCAGGGACATGGATGAAGCTGGAAACCAGCATTCTCAGCAAACTAACACAGGAACAGAAAACCAAACACTGCATGTTCTCACTCATAAGTGGGAGTTGAACAATGAGAACACATGGACATAGGGAGGGGAATATCACACACCAGGGCCTGTCAGGGGGTCGGGGGCACGGGGAGGGATAGCATTAGGAGAAATACCTAATGTAGATGATGGGCTGATGGGTGCA... | AAATGCCCATCAATGATAGACTAGATAAAGAAAATGTGGCACATACACACCATGGAATACTATGCAGCCATAAAAAAGAATGAGTTCATGTCCTTTGCAGGGACATGGATGAAGCTGGAAACCAGCATTCTCAGCAAACTAACACAGGAACAGAAAACCAAACACTGCATGTTCTCACTCATAAGTGGGAGTTGAACAATGAGAACACATGGACATAGGGAGGGGAATATCACACACCAGGGCCTGTCAGGGGGTCGGGGGCACGGGGAGGGATAGCATTAGGAGAAATACCTAATGTAGATGATGGGCTGATGGGTGCA... |
Task1_train_34625 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | AATGCCCATCAATGATAGACTAGATAAAGAAAATGTGGCACATACACACCATGGAATACTATGCAGCCATAAAAAAGAATGAGTTCATGTCCTTTGCAGGGACATGGATGAAGCTGGAAACCAGCATTCTCAGCAAACTAACACAGGAACAGAAAACCAAACACTGCATGTTCTCACTCATAAGTGGGAGTTGAACAATGAGAACACATGGACATAGGGAGGGGAATATCACACACCAGGGCCTGTCAGGGGGTCGGGGGCACGGGGAGGGATAGCATTAGGAGAAATACCTAATGTAGATGATGGGCTGATGGGTGCAG... | AATGCCCATCAATGATAGACTAGATAAAGAAAATGTGGCACATACACACCATGGAATACTATGCAGCCATAAAAAAGAATGAGTTCATGTCCTTTGCAGGGACATGGATGAAGCTGGAAACCAGCATTCTCAGCAAACTAACACAGGAACAGAAAACCAAACACTGCATGTTCTCACTCATAAGTGGGAGTTGAACAATGAGAACACATGGACATAGGGAGGGGAATATCACACACCAGGGCCTGTCAGGGGGTCGGGGGCACGGGGAGGGATAGCATTAGGAGAAATACCTAATGTAGATGATGGGCTGATGGGTGCAG... |
Task1_train_34626 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GTTCTTAAGAAATCTGCTTTAATGAACAAATCAGAGTGATTTGTACTTAATACTTGATTTTGTTTCAAAGGCCACATAGGCATTTGAAAAATAAGTTTTTGCCTGAATCCTGTAATTTCAGCTTTCTTAGCAATTTCTCTTTTCTGAAACAGTGAAAATGTAAACTTTAGGGTAGCCTCTGTTCAAATAATCACAATATGTGAATTGAAGTTTGAGGAGTTCATAGAGTGTTACTGAATTTGTCTGTTTTCTAAAGGAAATTGATTCATTTTTTTCAAATTATTTTACAGGATCCTTCAAACCAAAAATGTGGTGGAAGA... | GTTCTTAAGAAATCTGCTTTAATGAACAAATCAGAGTGATTTGTACTTAATACTTGATTTTGTTTCAAAGGCCACATAGGCATTTGAAAAATAAGTTTTTGCCTGAATCCTGTAATTTCAGCTTTCTTAGCAATTTCTCTTTTCTGAAACAGTGAAAATGTAAACTTTAGGGTAGCCTCTGTTCAAATAATCACAATATGTGAATTGAAGTTTGAGGAGTTCATAGAGTGTTACTGAATTTGTCTGTTTTCTAAAGGAAATTGATTCATTTTTTTCAAATTATTTTACAGGATCCTTCAAACCAAAAATGTGGTGGAAGA... |
Task1_train_34627 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | GCTTGTAATACCAGCATTTTGACAGGCCGAGGCAGGCAGATTACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAATGTGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCTGGGGTGGTGGTGCACACTTGTAATCCCAACTATTCAGGAGGCTGAGGTAGGAGAATCACTTGAACCAGGGAGGCAGAAGTTGCAATGAGCCGAGATCGTGCCATTTGCATATCAGCCTGGGCAACAAGAGCAAAACTTCGTCTTAAAAAAAAAAAAAAAAAAAGAATAAAGAAAGAAAGAAGAGAACGGCCGGGCGCGG... | GCTTGTAATACCAGCATTTTGACAGGCCGAGGCAGGCAGATTACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAATGTGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCTGGGGTGGTGGTGCACACTTGTAATCCCAACTATTCAGGAGGCTGAGGTAGGAGAATCACTTGAACCAGGGAGGCAGAAGTTGCAATGAGCCGAGATCGTGCCATTTGCATATCAGCCTGGGCAACAAGAGCAAAACTTCGTCTTAAAAAAAAAAAAAAAAAAAGAATAAAGAAAGAAAGAAGAGAACGGCCGGGCGCGG... |
Task1_train_34628 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTAGGTTGGTACAAAAGTATTTGGGGCCTTAGCCTTACTTTCAATGGCAAAAATCACAATTACTTTTGCACCAACTGACTCTCCTATATGCCAAGTCCAGGGATATAGAACTTACCATTTGGAGGGTGTTTTCAATAGATGGGGCACTTTTATGGAGCATTTGGGAAAGCGCTGCTTTACTGGAAGCAAGTATGCAGGGTCTCTCCTGCTAGCATGTCCAAATGCTTGTGTCAGTGGCAGTATTATTTGGGAACTTATAAAAATAAAATGTTACTGTTTCTAATATTTGATAATTTGTCTCTCTGGATTCCTAGTTGAGA... | TTAGGTTGGTACAAAAGTATTTGGGGCCTTAGCCTTACTTTCAATGGCAAAAATCACAATTACTTTTGCACCAACTGACTCTCCTATATGCCAAGTCCAGGGATATAGAACTTACCATTTGGAGGGTGTTTTCAATAGATGGGGCACTTTTATGGAGCATTTGGGAAAGCGCTGCTTTACTGGAAGCAAGTATGCAGGGTCTCTCCTGCTAGCATGTCCAAATGCTTGTGTCAGTGGCAGTATTATTTGGGAACTTATAAAAATAAAATGTTACTGTTTCTAATATTTGATAATTTGTCTCTCTGGATTCCTAGTTGAGA... |
Task1_train_34629 | Located on Chromosome 2, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ACACCCAAGTAATGTTTATGTTACTCGAGCATGCTGAATTTGACTTTGACTCCTGATATCCATAAGGGTGCATCTTCCCCTTCCCTATCGCAGCTGCCCCGGCCTTCAGTAGTTATCCAAAGTCACTCCTCTTACAAAGACTAAGTGTGCTAAATGGATTTCCCTTAAACTACTTGATGCAAAGAAATGGAGGATGTCAACGGAATCACCCATGATTAATTGTCAACATGTTTCCTGTCCAGCAACTCAAAATGTCCTAAATCAAGCAATACTAATAATGTCCACATTGGTAGTTCTGAAAATTCACTATGGTCTTTGAT... | ACACCCAAGTAATGTTTATGTTACTCGAGCATGCTGAATTTGACTTTGACTCCTGATATCCATAAGGGTGCATCTTCCCCTTCCCTATCGCAGCTGCCCCGGCCTTCAGTAGTTATCCAAAGTCACTCCTCTTACAAAGACTAAGTGTGCTAAATGGATTTCCCTTAAACTACTTGATGCAAAGAAATGGAGGATGTCAACGGAATCACCCATGATTAATTGTCAACATGTTTCCTGTCCAGCAACTCAAAATGTCCTAAATCAAGCAATACTAATAATGTCCACATTGGTAGTTCTGAAAATTCACTATGGTCTTTGAT... |
Task1_train_34630 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | AGAGAATTGGAGTGGTAGTCTGAGTATGAAGTGGGAACAAAAGAGGGTTCTTTAAGGTGAGGAAATAGCAGTGTGTTTGTATATTGATGAGAATGGTCCAGTGGAAAAGGAAAAAAATTGATGATATCGGGAAAGAATTGTTGGAGTGATGTCTTTAAGGAGGCAGGAAGGCATGGGATCCAGTGCATGGATCCGTATCTAGGAACACAGTTGATCCCTAACAACAGGAGAGAAAACAGATACACAGATACAGGTATGGTATGTAGGTAATTGCAATGGAAGTTTTGAGAAAGTTCTCCACAGGTTGCTTCAGTGTTCTG... | AGAGAATTGGAGTGGTAGTCTGAGTATGAAGTGGGAACAAAAGAGGGTTCTTTAAGGTGAGGAAATAGCAGTGTGTTTGTATATTGATGAGAATGGTCCAGTGGAAAAGGAAAAAAATTGATGATATCGGGAAAGAATTGTTGGAGTGATGTCTTTAAGGAGGCAGGAAGGCATGGGATCCAGTGCATGGATCCGTATCTAGGAACACAGTTGATCCCTAACAACAGGAGAGAAAACAGATACACAGATACAGGTATGGTATGTAGGTAATTGCAATGGAAGTTTTGAGAAAGTTCTCCACAGGTTGCTTCAGTGTTCTG... |
Task1_train_34631 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TCAACTCAGGATAATTCGGAAGTGTTATTTCTTAAAGAAAATAATCAAAATGTATATGGTTTAGATGATTCAGAACATATTTCTTCTATAGTTGATGTACCTCCCAGAGGTGAGATTGTTTTAAAAATTCATTTTGAGTATTTGTATTAGTTACATTCATCAGATGTTCTTCCTGAGGGCAATTATGTATAACAGTTAATAAGTTAGCTCTCTTATGTTACCGATTTGCTAACTTCTGCCATTTAAAACTGCTGGTGATAGATTTAATTTTAAAGTAAATATGCTGACAAACATCACACCCACAGTGGCCTAATACTGTT... | TCAACTCAGGATAATTCGGAAGTGTTATTTCTTAAAGAAAATAATCAAAATGTATATGGTTTAGATGATTCAGAACATATTTCTTCTATAGTTGATGTACCTCCCAGAGGTGAGATTGTTTTAAAAATTCATTTTGAGTATTTGTATTAGTTACATTCATCAGATGTTCTTCCTGAGGGCAATTATGTATAACAGTTAATAAGTTAGCTCTCTTATGTTACCGATTTGCTAACTTCTGCCATTTAAAACTGCTGGTGATAGATTTAATTTTAAAGTAAATATGCTGACAAACATCACACCCACAGTGGCCTAATACTGTT... |
Task1_train_34632 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | TAATGGTAAAGCAAAAACTTGAGTCTGGGTAATGGTTGAGCAAGAAAAAAGATGGCATTTACATTTTATTTACATAGTATTCCTAAATGATAATCTGTGGTGTAGTCTGGTGCTTACAGATTTGCCATAGATTTTCAGACTGGGATATGGAACTATAACAATTTTGAATTTAGAGCTTAGAATTGTTTTTCCTTTCTGAAAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGGCATATGTATATGTATATAATATATACACACACACATATATACACACATATATATGGTATACATATAATGTATACAGTATACATA... | TAATGGTAAAGCAAAAACTTGAGTCTGGGTAATGGTTGAGCAAGAAAAAAGATGGCATTTACATTTTATTTACATAGTATTCCTAAATGATAATCTGTGGTGTAGTCTGGTGCTTACAGATTTGCCATAGATTTTCAGACTGGGATATGGAACTATAACAATTTTGAATTTAGAGCTTAGAATTGTTTTTCCTTTCTGAAAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGGCATATGTATATGTATATAATATATACACACACACATATATACACACATATATATGGTATACATATAATGTATACAGTATACATA... |
Task1_train_34633 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GTATCACTTTAAGACAGGCTCGCGCCTCTCCCCAGGGCCGATGCAGGACTTCTGTCTCTCCACCACAACTTCATTGCCTTTTGCTCTAGCTTTCTGCTGCCGGAGTGAATTTTCTCACAAAATAAATGTGGCCATGCCATGTCTGAAAGCAATGGCTGGTGGTTTTCCAAGAGGTTTTTTATTAAGTCTTGACTTTTTAGCATGGCTTACAAGGCCAGTTCTCTCTCTCACACACACACACACACACACACACACACACACACACACGTGCACACACTCATATGAAACCTTTCATATCACCTTCATACAGGGTTGGTGTC... | GTATCACTTTAAGACAGGCTCGCGCCTCTCCCCAGGGCCGATGCAGGACTTCTGTCTCTCCACCACAACTTCATTGCCTTTTGCTCTAGCTTTCTGCTGCCGGAGTGAATTTTCTCACAAAATAAATGTGGCCATGCCATGTCTGAAAGCAATGGCTGGTGGTTTTCCAAGAGGTTTTTTATTAAGTCTTGACTTTTTAGCATGGCTTACAAGGCCAGTTCTCTCTCTCACACACACACACACACACACACACACACACACACACACGTGCACACACTCATATGAAACCTTTCATATCACCTTCATACAGGGTTGGTGTC... |
Task1_train_34634 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CAGAAACACATGGAATTTAGCATGCCTGTTCATGGCTGCTAATCAGGCCAGGGCAGATGACTATGGGGAAGGCCTGTGTGGGAGGGGTGGGCCATGAGGAGGGAGTCAGAGAGCAGAAGAGGGCTGGGGACTGCCAGGGGTGGGTGGAGGGCTTTTAGAGACAAGACTTCACTTAGTGGGGATGGACTGAAGTGTTTGGAAGACTGATCTAAAATCAGAGTCCAGAGATGTGAGGCTAGCCACTTTGTGGGCAAGGAGGTGGGATGAGACAATGGGATTGTAGCATTCACTAGCACCCTGGGGTCTCTGGACACATCAGT... | CAGAAACACATGGAATTTAGCATGCCTGTTCATGGCTGCTAATCAGGCCAGGGCAGATGACTATGGGGAAGGCCTGTGTGGGAGGGGTGGGCCATGAGGAGGGAGTCAGAGAGCAGAAGAGGGCTGGGGACTGCCAGGGGTGGGTGGAGGGCTTTTAGAGACAAGACTTCACTTAGTGGGGATGGACTGAAGTGTTTGGAAGACTGATCTAAAATCAGAGTCCAGAGATGTGAGGCTAGCCACTTTGTGGGCAAGGAGGTGGGATGAGACAATGGGATTGTAGCATTCACTAGCACCCTGGGGTCTCTGGACACATCAGT... |
Task1_train_34635 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TCACTTTCCTTTTCCTGCATCTCCTCCTTGTTGTTGACTTTGCAAGTGGCGTGCAGCCCAGCCTGCATTCAGTTACAATAAATGGGAGCTAAATCTTGGATTCACATGGACAAAAAGATGGGAACAGTGGACACTGGGGACTCCAAAAAAGGAGGAAGGGGCAGGGGCAAGGGCTGAAAAGCTTCCTTTTGGGCACTATGTTCACTGTCTGGGTGACAGGATCAGTAGAAGCCCAAACCTCAGCACCATGCATTATACACTTGTAACAAACCTGCACATGTACCTGCTGAATCTAAAATTAAAAAAAAAAAAGATATGCC... | TCACTTTCCTTTTCCTGCATCTCCTCCTTGTTGTTGACTTTGCAAGTGGCGTGCAGCCCAGCCTGCATTCAGTTACAATAAATGGGAGCTAAATCTTGGATTCACATGGACAAAAAGATGGGAACAGTGGACACTGGGGACTCCAAAAAAGGAGGAAGGGGCAGGGGCAAGGGCTGAAAAGCTTCCTTTTGGGCACTATGTTCACTGTCTGGGTGACAGGATCAGTAGAAGCCCAAACCTCAGCACCATGCATTATACACTTGTAACAAACCTGCACATGTACCTGCTGAATCTAAAATTAAAAAAAAAAAAGATATGCC... |
Task1_train_34636 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GATGCCTCCAGTTTTGTTCTTTTTGCTCAGCATTGCTTTCACTATTTGGGGTCTTTTGTGGTTCCATATACATTTTAGGGTTTTTTTCCCTATTTATGTGAAGAATGTAATTTTTTTGTTTGTTTTTGTTTTGTTTTGTTTTAGAGATGGGGTCTTGTTATGTTGTCCAGGCTAGACTTGAACTCCTGGGCTCAAGCAATCCTCCCACCTCAGACTCCTGAGTAGCTAGGACTACAGGCATTTGCCACTGCACTTGGCTTGTCACTGGTATTTTGATAGGGACTGCATTAAATCTGTAGGTCACCTTGGGTAGTATGGTC... | GATGCCTCCAGTTTTGTTCTTTTTGCTCAGCATTGCTTTCACTATTTGGGGTCTTTTGTGGTTCCATATACATTTTAGGGTTTTTTTCCCTATTTATGTGAAGAATGTAATTTTTTTGTTTGTTTTTGTTTTGTTTTGTTTTAGAGATGGGGTCTTGTTATGTTGTCCAGGCTAGACTTGAACTCCTGGGCTCAAGCAATCCTCCCACCTCAGACTCCTGAGTAGCTAGGACTACAGGCATTTGCCACTGCACTTGGCTTGTCACTGGTATTTTGATAGGGACTGCATTAAATCTGTAGGTCACCTTGGGTAGTATGGTC... |
Task1_train_34637 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | CTATGCATTAATGTTTAGGTGGTGACTAACCACTCAGGGTTTTAGAGACAAACAGACCTTATTCTGTCACTCACTGACTGAGCGTGGCCAAGTCTTTCAGCCTCTCTAAGCCTCAGTGTCCTCATCCATAAAATGGGACCAATCGTAGCATCCACTTCTGAGAACTGTTCAGAAGTGGAAATGAGCTAGTTTAGGTGGCTGTGTCTGGCATACGCCAATGGTTTGATAAGTATTAGCTTGTGCCTTTATTAGGCCAACTCCTTTTTGTTAGGTGACTGAGAAACCAAGGACCTTCTGCCCTTTATGCACCAGTCACTATT... | CTATGCATTAATGTTTAGGTGGTGACTAACCACTCAGGGTTTTAGAGACAAACAGACCTTATTCTGTCACTCACTGACTGAGCGTGGCCAAGTCTTTCAGCCTCTCTAAGCCTCAGTGTCCTCATCCATAAAATGGGACCAATCGTAGCATCCACTTCTGAGAACTGTTCAGAAGTGGAAATGAGCTAGTTTAGGTGGCTGTGTCTGGCATACGCCAATGGTTTGATAAGTATTAGCTTGTGCCTTTATTAGGCCAACTCCTTTTTGTTAGGTGACTGAGAAACCAAGGACCTTCTGCCCTTTATGCACCAGTCACTATT... |
Task1_train_34638 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | ACTTATATTCACATATAAACCTGCTGGAATCCTTTCTGAAACTCTACACTCTATTGACCTCAGCACAACTGAGTGAAGGGGAACGAAAGGGAGAGACCATCTTCACCCTTTGTTTTTGTGGAATTTATTTAGAAAAATTTTATTGAGAGATTCTAAAAAGTATAAGAAACTAACAAATTTTTACCACTGCATTCATGTTGGCTTTTTGAGCACATAGCTCTAAGTGGGGGGATGGCGGGGATGCCTCAAAAGGGGAGAGGAAGGACTCTCCTTGGCCTGGGAATAGGTGTGCCTATGGGAACCATAGGAGCAAGAGTCAA... | ACTTATATTCACATATAAACCTGCTGGAATCCTTTCTGAAACTCTACACTCTATTGACCTCAGCACAACTGAGTGAAGGGGAACGAAAGGGAGAGACCATCTTCACCCTTTGTTTTTGTGGAATTTATTTAGAAAAATTTTATTGAGAGATTCTAAAAAGTATAAGAAACTAACAAATTTTTACCACTGCATTCATGTTGGCTTTTTGAGCACATAGCTCTAAGTGGGGGGATGGCGGGGATGCCTCAAAAGGGGAGAGGAAGGACTCTCCTTGGCCTGGGAATAGGTGTGCCTATGGGAACCATAGGAGCAAGAGTCAA... |
Task1_train_34639 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGAACAACTGTTTTTCTCACTATGTAAAAAAATTAGCTATTTTTCATTAAACATATTTGTGTAACACAATTATTTTAAATGAGTTAATACATATTTTTATGGTTTTTCAGTTTTGATTTATGATATATTAAATGTCAATAGATATAACCTGCACAGATAGGCTCTCTGGAATTCTCAATGATTTTTTAGAGTATAAAGAGTTTCTGAGCCCAAAAGGTTTGTGAACCACTGACTTGAATTCATCCAGCTCTCTACCCAATCTACTAACGCAGGCTGGCTAAGATAAAGTGGAGAGAATTAGGAATGCCACTAATGCTATA... | TGAACAACTGTTTTTCTCACTATGTAAAAAAATTAGCTATTTTTCATTAAACATATTTGTGTAACACAATTATTTTAAATGAGTTAATACATATTTTTATGGTTTTTCAGTTTTGATTTATGATATATTAAATGTCAATAGATATAACCTGCACAGATAGGCTCTCTGGAATTCTCAATGATTTTTTAGAGTATAAAGAGTTTCTGAGCCCAAAAGGTTTGTGAACCACTGACTTGAATTCATCCAGCTCTCTACCCAATCTACTAACGCAGGCTGGCTAAGATAAAGTGGAGAGAATTAGGAATGCCACTAATGCTATA... |
Task1_train_34640 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | ATTTAAAATTGTTTCTTGAGATGCTTCTACTGAAACCAGTGATCTAACTTCCGAGGTGGAGATACCCTACCAAAGAATTGTCCAAAAAGGTACAAAAGAGAATATGTTAATACTCACGAAGTTCTTTAACACAGTCGCTGACAAGCTGTTGTTCCTTTTCTTCATAGGTAACAGTTTCTGTCTTTATGTGACAAGCCTTCAAGAAAAAAATCAGTATGTGACAATACCTTCTAGTGATTTTATAGAAATAACTACAAAAACCTTTAATTCTCATTTGAAGACTAAATTTCATCACTTACAAAGGAAAAAACCCAACAACC... | ATTTAAAATTGTTTCTTGAGATGCTTCTACTGAAACCAGTGATCTAACTTCCGAGGTGGAGATACCCTACCAAAGAATTGTCCAAAAAGGTACAAAAGAGAATATGTTAATACTCACGAAGTTCTTTAACACAGTCGCTGACAAGCTGTTGTTCCTTTTCTTCATAGGTAACAGTTTCTGTCTTTATGTGACAAGCCTTCAAGAAAAAAATCAGTATGTGACAATACCTTCTAGTGATTTTATAGAAATAACTACAAAAACCTTTAATTCTCATTTGAAGACTAAATTTCATCACTTACAAAGGAAAAAACCCAACAACC... |
Task1_train_34641 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AAGGGAAAGTGATTCTGTTTAAGTACTCATCTTCCCTTGGCATTCTGGCATTAGGAATTCTTGGATACGATGTTAATACTGCTTCAGGTTTTTCCTGAACAGTCCATTTATAGATGTTTACATGCTCCTTTCTATCAAGGGACTTCATTTTCAGTGTCTTTTCACACCAAGCTTTTGATTGAGTTATTTTTGATTTACCACCCCAACTATATGGGTCTTGAATCTCTGTTTTATGAACAGAATTTTCTGCTTGAGGAAGCTGCGTGAATACATGTTCTTTCCTTAGTTTCTTAAGCAGTATATCTGTAAGTATTTCTGAT... | AAGGGAAAGTGATTCTGTTTAAGTACTCATCTTCCCTTGGCATTCTGGCATTAGGAATTCTTGGATACGATGTTAATACTGCTTCAGGTTTTTCCTGAACAGTCCATTTATAGATGTTTACATGCTCCTTTCTATCAAGGGACTTCATTTTCAGTGTCTTTTCACACCAAGCTTTTGATTGAGTTATTTTTGATTTACCACCCCAACTATATGGGTCTTGAATCTCTGTTTTATGAACAGAATTTTCTGCTTGAGGAAGCTGCGTGAATACATGTTCTTTCCTTAGTTTCTTAAGCAGTATATCTGTAAGTATTTCTGAT... |
Task1_train_34642 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | AATGTTTTTTAGTTTTCAGAGTGCAAGGTCTTTGACCTCCTTTGAAAAGTTTATTCCTAATTATTTTATTCTTTTTGATGCTATTGTAAACTGGAATTATTTTCTTGATTTCTTTTTTGGATAGTTCATTGTTAGTGTATAGAAACAAAACTGATTTTTCTGTGTTGGTTTTATCTCCTGCAACTTTACTGAATTCATGTATTGGTTCTAACAGGTCTTTTTGTGTGGAGTCTACAGAATTTTCTATATGTAAGATCCTGCCATCCGCAAACAAAGATAAAGAAATATTATTATGTATTTTAAAGTGTAGTACTATACTT... | AATGTTTTTTAGTTTTCAGAGTGCAAGGTCTTTGACCTCCTTTGAAAAGTTTATTCCTAATTATTTTATTCTTTTTGATGCTATTGTAAACTGGAATTATTTTCTTGATTTCTTTTTTGGATAGTTCATTGTTAGTGTATAGAAACAAAACTGATTTTTCTGTGTTGGTTTTATCTCCTGCAACTTTACTGAATTCATGTATTGGTTCTAACAGGTCTTTTTGTGTGGAGTCTACAGAATTTTCTATATGTAAGATCCTGCCATCCGCAAACAAAGATAAAGAAATATTATTATGTATTTTAAAGTGTAGTACTATACTT... |
Task1_train_34643 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | AAATCGTGTTGGAAAGAATCAGTGAGTTATAAAGACAGCAAGGATTTGCACACCCAAGATTCCAGACAGAAAGGAAGTCCAGAGACATGGAGCCCATCATTTGGTGCCATTTTTCCTTCAAGGCATTTATGCCTTGAGATGGCCAAGAAGTTAAAAAGCTGAGCAGAGCTTTGAGATAGAAATACAACGATGTGAGAACAAAAACCAGAGTCCAGGGCTTGTTGGGATGAGAAGTCCTGGAAAACACCCGGTTGGGACCCCAAAAGAGAATGAGTGTCTCTTCAAATGTTATGACCTAAGTTACCTCATGTGCCTCACAC... | AAATCGTGTTGGAAAGAATCAGTGAGTTATAAAGACAGCAAGGATTTGCACACCCAAGATTCCAGACAGAAAGGAAGTCCAGAGACATGGAGCCCATCATTTGGTGCCATTTTTCCTTCAAGGCATTTATGCCTTGAGATGGCCAAGAAGTTAAAAAGCTGAGCAGAGCTTTGAGATAGAAATACAACGATGTGAGAACAAAAACCAGAGTCCAGGGCTTGTTGGGATGAGAAGTCCTGGAAAACACCCGGTTGGGACCCCAAAAGAGAATGAGTGTCTCTTCAAATGTTATGACCTAAGTTACCTCATGTGCCTCACAC... |
Task1_train_34644 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CCTTTGTCATTAAGATGATAATGCTAGACAAATTAATGTTTAGACATAAACAGCAAACACAATTTTAACATTTTTCATAATATTGAGAGATGTTTCAGTATTATATAATCAAAAAATCTATTACAAATACACATGTATACATCTTATAAAAATACATTTAAAAACAAAAATGGGACAAATACTGGGTCATTATTCCTCCAAAGGTGAGCTGGTATTATGAAGAGGCTTTGATTTCTTTCTCTTTATCAGGATATTCTTCCACCTCTGAGGAGAACATTAACTCTGGAGAAGAAAATGAACAGATCATACTTAAAATTGTT... | CCTTTGTCATTAAGATGATAATGCTAGACAAATTAATGTTTAGACATAAACAGCAAACACAATTTTAACATTTTTCATAATATTGAGAGATGTTTCAGTATTATATAATCAAAAAATCTATTACAAATACACATGTATACATCTTATAAAAATACATTTAAAAACAAAAATGGGACAAATACTGGGTCATTATTCCTCCAAAGGTGAGCTGGTATTATGAAGAGGCTTTGATTTCTTTCTCTTTATCAGGATATTCTTCCACCTCTGAGGAGAACATTAACTCTGGAGAAGAAAATGAACAGATCATACTTAAAATTGTT... |
Task1_train_34645 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TAGCGAAGTGCCTGACATGTAAGTACTCAAAACATTTTGTTGAATTAAACGCTAAATTCAAAAGAGCTATTTCCATGCAAATTAGTCTGTAAATAGTCAATAAACAAATATACTTAATAAAACGAAAAAGAAATACAAAGCCTATTACTTCTTTGGTGATACAGCTCCCACGATAGCTTGTTCAGAAGAACTAGTGTCACTATGTCCACTTTTTGTTTACAAAGGCTCCTTACATAAGCAGTGATGGTATTTAGAGGTAACTATTTTAGGGGGTTCTTAACCACTAGGTACAGCAAAGTCACAAAACTCTACCTTATATA... | TAGCGAAGTGCCTGACATGTAAGTACTCAAAACATTTTGTTGAATTAAACGCTAAATTCAAAAGAGCTATTTCCATGCAAATTAGTCTGTAAATAGTCAATAAACAAATATACTTAATAAAACGAAAAAGAAATACAAAGCCTATTACTTCTTTGGTGATACAGCTCCCACGATAGCTTGTTCAGAAGAACTAGTGTCACTATGTCCACTTTTTGTTTACAAAGGCTCCTTACATAAGCAGTGATGGTATTTAGAGGTAACTATTTTAGGGGGTTCTTAACCACTAGGTACAGCAAAGTCACAAAACTCTACCTTATATA... |
Task1_train_34646 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | CTCGTGTCCAGTTGAGGGGATGATGGAGCTCAGCCAAGGAAAAAGTCACAGGTGGTTTTAGGTGACCTAGATTACACCCTGGCTCTGTTAATGGTTAGTTGACAGTGACAGGCTCACATATCAGGAGAGAGGGGAAGACGCTCTCTAAAAACAAGATGAGAACAATAACAGAAAAAGTACCCCAACAAGTCCCCCACCCCATGCAACTGGGACTTGCAACCTGAGCCTGGTCCCTTCAGTGTCCATTTGACCCCCACCCCCATCCCCGGGGAATGCACACTGCACCCGGCACCCGTCTCTGCCTTGCCTGGGTTAGTTTA... | CTCGTGTCCAGTTGAGGGGATGATGGAGCTCAGCCAAGGAAAAAGTCACAGGTGGTTTTAGGTGACCTAGATTACACCCTGGCTCTGTTAATGGTTAGTTGACAGTGACAGGCTCACATATCAGGAGAGAGGGGAAGACGCTCTCTAAAAACAAGATGAGAACAATAACAGAAAAAGTACCCCAACAAGTCCCCCACCCCATGCAACTGGGACTTGCAACCTGAGCCTGGTCCCTTCAGTGTCCATTTGACCCCCACCCCCATCCCCGGGGAATGCACACTGCACCCGGCACCCGTCTCTGCCTTGCCTGGGTTAGTTTA... |
Task1_train_34647 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGCCTGGCTAATTTTTTGTATTTTAGTGGAGATGGGGTTTCACAATGTTACCCAGGCTGGTCTCAAACCCCTGAGCTCGGGCAATCTGCTGGCTTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGAGCCTAGCCAGAGGTACCACTTCTAATGGGCTCTCTTCTGTCATTGTTCTTGACTACAGAGAGGATTCTCTCTCCCTTTGCCATTTCTTGAGACTTCCAGAGAAGGGAAGAGTACTTTGACCTTTTTGACCACCATTTCCCCAAAGTGTCACCTATAGAACTGTAGCATTGCAAGATGCTCCATT... | GGCCTGGCTAATTTTTTGTATTTTAGTGGAGATGGGGTTTCACAATGTTACCCAGGCTGGTCTCAAACCCCTGAGCTCGGGCAATCTGCTGGCTTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGAGCCTAGCCAGAGGTACCACTTCTAATGGGCTCTCTTCTGTCATTGTTCTTGACTACAGAGAGGATTCTCTCTCCCTTTGCCATTTCTTGAGACTTCCAGAGAAGGGAAGAGTACTTTGACCTTTTTGACCACCATTTCCCCAAAGTGTCACCTATAGAACTGTAGCATTGCAAGATGCTCCATT... |
Task1_train_34648 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GAACTGAGTACCAGAACTTGTCCCTCCTCTGCCACTCTGCCAGGAGGAAACTGGTTTAAGAAGCCCCTTGGTATAAATTATGCATGCGACTGAACCTGGGAGTAAATGCAGAAAGAAAGGGACCTAAAGAGGCAGTTCCAGCTGGGCGCAGTGGCTCACACTTGTAATCCCAGCACTTCGGGAGGCCAAGGCGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACGTGGTGAAACCCCATCTCAACTAAAAATACAAAAATTAGCCGGGTGTGGTGGCACACACCTGTAATCCCAGCTACTCTGGAGGC... | GAACTGAGTACCAGAACTTGTCCCTCCTCTGCCACTCTGCCAGGAGGAAACTGGTTTAAGAAGCCCCTTGGTATAAATTATGCATGCGACTGAACCTGGGAGTAAATGCAGAAAGAAAGGGACCTAAAGAGGCAGTTCCAGCTGGGCGCAGTGGCTCACACTTGTAATCCCAGCACTTCGGGAGGCCAAGGCGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACGTGGTGAAACCCCATCTCAACTAAAAATACAAAAATTAGCCGGGTGTGGTGGCACACACCTGTAATCCCAGCTACTCTGGAGGC... |
Task1_train_34649 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GCACATGACCTTTTAGTGGCTGAATTTGATCAAGGATAGAATTCAGAGGGCATATTGCCAGGCGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCTGGTGGATCATCTAAGGTCAGGAGTTTGAGACCAGCCTGACTAACATGGTGAAACCCCATCTCTACTAAAATACAAAAATTAGCCGGACGTGGTGGTGGGCGCCTGTAATCCCAGCTATTGGGGAGGCTGAGGCAGGAGAATCGCTAGAACCCGGGAGGTGGAGGTTGCAGTGAGCCCAGATCGCACCATTGCACTCCAGCCTGGGCGACAG... | GCACATGACCTTTTAGTGGCTGAATTTGATCAAGGATAGAATTCAGAGGGCATATTGCCAGGCGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCTGGTGGATCATCTAAGGTCAGGAGTTTGAGACCAGCCTGACTAACATGGTGAAACCCCATCTCTACTAAAATACAAAAATTAGCCGGACGTGGTGGTGGGCGCCTGTAATCCCAGCTATTGGGGAGGCTGAGGCAGGAGAATCGCTAGAACCCGGGAGGTGGAGGTTGCAGTGAGCCCAGATCGCACCATTGCACTCCAGCCTGGGCGACAG... |
Task1_train_34650 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CATATTGAACAGAACAGAAAAAGAGTACCTATTAATAAATACCTGTGGTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCATTCTGTTGCCCAGGCTTGAGTGCAGTGGGGCCATCTCAGCTCACTGCAAGCTCCACCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCGGGGACTACAGGCGCCCACCACCACGCCCGGCTAATTTTTTGTACTTTTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCCAACCTCGTAATCCACCCTCCTCGGCCTCCCA... | CATATTGAACAGAACAGAAAAAGAGTACCTATTAATAAATACCTGTGGTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCATTCTGTTGCCCAGGCTTGAGTGCAGTGGGGCCATCTCAGCTCACTGCAAGCTCCACCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCGGGGACTACAGGCGCCCACCACCACGCCCGGCTAATTTTTTGTACTTTTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCCAACCTCGTAATCCACCCTCCTCGGCCTCCCA... |
Task1_train_34651 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CTCCTGGGCTCCAGTGATCCTCCCACCTTAGCCCCCCAAGTAGCTGGGACTACAGGCACATGCCACCACGCCTGGCTAATTTGTGTATTTTTACTAGAGGCAAGGTTTCACCGTGTTGCCCAGGCTGGTCTCAAACTCCTGGTCTCAAGTTATCCATCTGCTCTGGCCTCCTAAAGTGCTGAGATTACAAGCGTGAGCCACTTCGCCTGGCCGATAATTAGTTCTTCACTGACTTAAAGAGATGAATATATTTGGGTTAACGTATAAGAATTACATGAGAATGATTCAAATTCCCTACAATTAGTTTAAATTTGAGATAC... | CTCCTGGGCTCCAGTGATCCTCCCACCTTAGCCCCCCAAGTAGCTGGGACTACAGGCACATGCCACCACGCCTGGCTAATTTGTGTATTTTTACTAGAGGCAAGGTTTCACCGTGTTGCCCAGGCTGGTCTCAAACTCCTGGTCTCAAGTTATCCATCTGCTCTGGCCTCCTAAAGTGCTGAGATTACAAGCGTGAGCCACTTCGCCTGGCCGATAATTAGTTCTTCACTGACTTAAAGAGATGAATATATTTGGGTTAACGTATAAGAATTACATGAGAATGATTCAAATTCCCTACAATTAGTTTAAATTTGAGATAC... |
Task1_train_34652 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | GGGTACACCACTGTATTTTGGTACATGCTTTCACGTGTTTGTGAAAGCACTTCAAAATTAATCTGTCACTCTTTTCCTAAATCCATGTTTACTGAAATAGTTATTTAGTGTTGCAATACAAACTCTACAAACTTGGTTGTTTCCAAAAGTATCTAAGTTAGTTGCATAGAACTCAGAACACAAAAAAACAATGCTCAGAAATTATGACTAATTCCCAGGATGTGTTGGGAGTCTCCAAGACTACCCCCAGGTTCAGTGATTTGCCAGAAAGACTCACGGAATTTAACATGTAGTTGTAGTCATGGCTAAGATTTATTACA... | GGGTACACCACTGTATTTTGGTACATGCTTTCACGTGTTTGTGAAAGCACTTCAAAATTAATCTGTCACTCTTTTCCTAAATCCATGTTTACTGAAATAGTTATTTAGTGTTGCAATACAAACTCTACAAACTTGGTTGTTTCCAAAAGTATCTAAGTTAGTTGCATAGAACTCAGAACACAAAAAAACAATGCTCAGAAATTATGACTAATTCCCAGGATGTGTTGGGAGTCTCCAAGACTACCCCCAGGTTCAGTGATTTGCCAGAAAGACTCACGGAATTTAACATGTAGTTGTAGTCATGGCTAAGATTTATTACA... |
Task1_train_34653 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AGATTTCAGCCTCACTAATACTCAGCTGGGTACAAATAAAAATGAGAAATTTTACTTATCTCCCTAGAAGAGATGAAGAATACTGGCAGAACACACTGTTGATGAGGGAATGGGAAATCATGTGGTGTACATGTACTATACAAGCTCTCTGGAGAAAAAGTTGACAGTAACCATTGACCTAACAATAATATCTTAAGGAGTTGATCCATAAATTGATCATCACAGATGTGAGAAAATATTTATATTAGCATTGTTTATAAAAAAAAATTTGAAGCAACCTAAATATCAATGGCTGAATAAATGAATACTTTCAGGCCTGA... | AGATTTCAGCCTCACTAATACTCAGCTGGGTACAAATAAAAATGAGAAATTTTACTTATCTCCCTAGAAGAGATGAAGAATACTGGCAGAACACACTGTTGATGAGGGAATGGGAAATCATGTGGTGTACATGTACTATACAAGCTCTCTGGAGAAAAAGTTGACAGTAACCATTGACCTAACAATAATATCTTAAGGAGTTGATCCATAAATTGATCATCACAGATGTGAGAAAATATTTATATTAGCATTGTTTATAAAAAAAAATTTGAAGCAACCTAAATATCAATGGCTGAATAAATGAATACTTTCAGGCCTGA... |
Task1_train_34654 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GTGTACTCCCACCTTATCCTCACTTGTGCCTCTTCATAGCTTTCAGTTTAGCTCTACTCAAAGTCTTTAGTTTCTTATCTCCTGTCCTGGCTTTTGCACAAACTACTCCTCTGTATAGATTCTCTTTTCGTCTCTTCTTTAGTTAAGTCCGGGTTTTGGTTTTTGGTTTTGGGGTGGAGTGTTTTTTTATCGTCGGTGGTGGTTTGAGTTTTTCTTTTCTTTTTTTTTTAATGTTGTTGTTGTTGTTTGCAGGTTTCAGCCTGTGTTTATTTCTCTCTCTCTTTTTTTTTTTTTTTTTTTTTTCAGATGCAGTCCCTTTC... | GTGTACTCCCACCTTATCCTCACTTGTGCCTCTTCATAGCTTTCAGTTTAGCTCTACTCAAAGTCTTTAGTTTCTTATCTCCTGTCCTGGCTTTTGCACAAACTACTCCTCTGTATAGATTCTCTTTTCGTCTCTTCTTTAGTTAAGTCCGGGTTTTGGTTTTTGGTTTTGGGGTGGAGTGTTTTTTTATCGTCGGTGGTGGTTTGAGTTTTTCTTTTCTTTTTTTTTTAATGTTGTTGTTGTTGTTTGCAGGTTTCAGCCTGTGTTTATTTCTCTCTCTCTTTTTTTTTTTTTTTTTTTTTTCAGATGCAGTCCCTTTC... |
Task1_train_34655 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TGCTGCTAAGAGCATCCGCTTGCACCTTCTGCTCATCCCCAGACAAGCTTTGTCCTGTGACCATAATGAACTCTTCATGCCGTTTCCAACTTTAGCCCATGTTATTCTTCTTGTCTGAATATCCACCCTTTTCTCTGTTCTCAATAATAAGTTCAGGCTTTTCGTCTTCTGAGAAGCCCTTTCTGACTTCCACAGGCTGAACCACTGGCTTCTGCTCCTCTACATAATACTTCAATTCCAGCATTGATCTCACTCTATCATGATCATGGGTTTAGCTGTCTGTCCCTGCCACTGCTGTGTGTTCCTCTTGAGGGCAGGAA... | TGCTGCTAAGAGCATCCGCTTGCACCTTCTGCTCATCCCCAGACAAGCTTTGTCCTGTGACCATAATGAACTCTTCATGCCGTTTCCAACTTTAGCCCATGTTATTCTTCTTGTCTGAATATCCACCCTTTTCTCTGTTCTCAATAATAAGTTCAGGCTTTTCGTCTTCTGAGAAGCCCTTTCTGACTTCCACAGGCTGAACCACTGGCTTCTGCTCCTCTACATAATACTTCAATTCCAGCATTGATCTCACTCTATCATGATCATGGGTTTAGCTGTCTGTCCCTGCCACTGCTGTGTGTTCCTCTTGAGGGCAGGAA... |
Task1_train_34656 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | TCATAGGCATGTGTCTTTAAATTTGAAGAAAAATTACCTACTGTGGCTTTTTTAAAGAAAATGTATTTATTACCTAAGAAAAACCATGTCTCTCTCTCTCTCTCACACACGCACACATACACTCTCTCTCTCCATATATACACACACACACACACATACATATATATACATATACATATATAAACATATATATATGACTCAGCTGCATAAAACAATGTAACTAAATTGTTGATCGCTAAAATGTTCACTTCTGTGCCTCTAAATCAAGTTGATTTTGACAATGAGGAAATGCCTTGGTGAACCATGTTGGTTTTACTTTT... | TCATAGGCATGTGTCTTTAAATTTGAAGAAAAATTACCTACTGTGGCTTTTTTAAAGAAAATGTATTTATTACCTAAGAAAAACCATGTCTCTCTCTCTCTCTCACACACGCACACATACACTCTCTCTCTCCATATATACACACACACACACACATACATATATATACATATACATATATAAACATATATATATGACTCAGCTGCATAAAACAATGTAACTAAATTGTTGATCGCTAAAATGTTCACTTCTGTGCCTCTAAATCAAGTTGATTTTGACAATGAGGAAATGCCTTGGTGAACCATGTTGGTTTTACTTTT... |
Task1_train_34657 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GCCCAACCCTGTCTCCACTTATCTGTAAGCATATATCAAGCCCTTCATAATAATATGAATGTTTGAGAGCTTTCAAAAACAATCGTCTTTTAAAATTTGGTACCTTAAACCATGAAGTGTTCTTTAGCCTTATGGAAATTCTTTCTTATCTACATGAAAAGGAGAAAATTAATTTTTTAAAAGTCTAGAGTAGACCAAGTGTTTCACAAAACTACCAACCCCTGCATGAAATGTTGCTACTCAATCTAAAAGTGAGAGACATTTTTTTTAACTCATTTCACTACAACAAAGTGCTTCTGTTGCAGTTATGTCTTACTTTC... | GCCCAACCCTGTCTCCACTTATCTGTAAGCATATATCAAGCCCTTCATAATAATATGAATGTTTGAGAGCTTTCAAAAACAATCGTCTTTTAAAATTTGGTACCTTAAACCATGAAGTGTTCTTTAGCCTTATGGAAATTCTTTCTTATCTACATGAAAAGGAGAAAATTAATTTTTTAAAAGTCTAGAGTAGACCAAGTGTTTCACAAAACTACCAACCCCTGCATGAAATGTTGCTACTCAATCTAAAAGTGAGAGACATTTTTTTTAACTCATTTCACTACAACAAAGTGCTTCTGTTGCAGTTATGTCTTACTTTC... |
Task1_train_34658 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GCAAGAAGTAAGGATAAATACCTGTTAAAAAAAAAAAAAAAAAAAGGAGGAAAACAGAGTAAAGGAAAAGAACCAGGGGAGCAGAGTATCGTAGTAATCAAAGAGGAAGCAAGTTATGAAAGTGGCCAAGAAAGTAACATGCTACAGAGATAAAGAAAAATGAGGATGGCCACAAATCTGAAACAACAAAAGAAGTATTTTGATAACTCTGCAAGAATAGAAGGCAGAATAGAATACACATTGTTCCTAATCAATAGCATATACTCCCTATACTGATGTCAAGGTTACCTTAAGAATTAAATTAAGAATGATAACTACCA... | GCAAGAAGTAAGGATAAATACCTGTTAAAAAAAAAAAAAAAAAAAGGAGGAAAACAGAGTAAAGGAAAAGAACCAGGGGAGCAGAGTATCGTAGTAATCAAAGAGGAAGCAAGTTATGAAAGTGGCCAAGAAAGTAACATGCTACAGAGATAAAGAAAAATGAGGATGGCCACAAATCTGAAACAACAAAAGAAGTATTTTGATAACTCTGCAAGAATAGAAGGCAGAATAGAATACACATTGTTCCTAATCAATAGCATATACTCCCTATACTGATGTCAAGGTTACCTTAAGAATTAAATTAAGAATGATAACTACCA... |
Task1_train_34659 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCTTGTTGACCAGGCTGGTCTTGAACTCCTGACTTCAGGTGACCCGCCTATCTTGGCCTCCCAAAGTGCGGGGATTACAGGCATTAGCCACCGAGCCCAGCCTCAGCTCCCACTTACAAGTGAGAACATGCAGTATTTGGTTTTCTGTCCTGCACTAATTTACTTAGGATAATGGCCTCCAGTTCCATCCATGTTGCTGCAAAGGACACGATTTCATTCTTTTTTATGGCTGTGCAGTAGTCCATGATGTATATGTACCACACTTTGTTTATCCAATCTAC... | CTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCTTGTTGACCAGGCTGGTCTTGAACTCCTGACTTCAGGTGACCCGCCTATCTTGGCCTCCCAAAGTGCGGGGATTACAGGCATTAGCCACCGAGCCCAGCCTCAGCTCCCACTTACAAGTGAGAACATGCAGTATTTGGTTTTCTGTCCTGCACTAATTTACTTAGGATAATGGCCTCCAGTTCCATCCATGTTGCTGCAAAGGACACGATTTCATTCTTTTTTATGGCTGTGCAGTAGTCCATGATGTATATGTACCACACTTTGTTTATCCAATCTAC... |
Task1_train_34660 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GAAATAGTACAGAGTGTGCCTATAATACTCTCTCACACAATTTCTCTATTATTAACATTAATGTGATATATTTGTTATAAGTAATGAACTGATATTAGTACAGTCCATGGTTTATTCAGACTTCTTAGTTTCTACTTAAACTAAGTTTTCTTAAACTAAGATTTCCTTAGTTTTACTACTTTTTCTGTTTCAGAATCACATCCAGGATACCACATTACATTAACTTGTAATGTCTCTTTAGGTCCCTCTTGGCTGTGACAGTTTAATCTTTTTTTTTTTTTTTTTAAACAGGTCTAGATGTGATGATACTTATCTCTTTG... | GAAATAGTACAGAGTGTGCCTATAATACTCTCTCACACAATTTCTCTATTATTAACATTAATGTGATATATTTGTTATAAGTAATGAACTGATATTAGTACAGTCCATGGTTTATTCAGACTTCTTAGTTTCTACTTAAACTAAGTTTTCTTAAACTAAGATTTCCTTAGTTTTACTACTTTTTCTGTTTCAGAATCACATCCAGGATACCACATTACATTAACTTGTAATGTCTCTTTAGGTCCCTCTTGGCTGTGACAGTTTAATCTTTTTTTTTTTTTTTTTAAACAGGTCTAGATGTGATGATACTTATCTCTTTG... |
Task1_train_34661 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | ATTAATTCTGAATTAGCCTTCCAAAAGCAAACCAGCAAAAACTAGGAATATAACAAAGTTATTCAAATATTCTAATATTAAAAATCTTCTTTGTCTTTCTGATGGTTTCATTTGTAGAAATAACTCTAAACATCTGGATGGGTCACCAAAAGGTGTTGTGGCCTCTTAGTTCTACTTTGAAATTAAAGGCCCTTTTTAGAGGAAAAAAATATCTGAAGTCCAACCCTCACCCCTCCTCCTGCCTTGTCTAGGATCTTCAGCATTAGAAAGATTGCTGGCCGGTTACCATAACACCCAGGGCCCTTGGTGGCTGCTCTGTG... | ATTAATTCTGAATTAGCCTTCCAAAAGCAAACCAGCAAAAACTAGGAATATAACAAAGTTATTCAAATATTCTAATATTAAAAATCTTCTTTGTCTTTCTGATGGTTTCATTTGTAGAAATAACTCTAAACATCTGGATGGGTCACCAAAAGGTGTTGTGGCCTCTTAGTTCTACTTTGAAATTAAAGGCCCTTTTTAGAGGAAAAAAATATCTGAAGTCCAACCCTCACCCCTCCTCCTGCCTTGTCTAGGATCTTCAGCATTAGAAAGATTGCTGGCCGGTTACCATAACACCCAGGGCCCTTGGTGGCTGCTCTGTG... |
Task1_train_34662 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | TCCAGAACCAAGAGAAAAGTGACAGAAAGTTCCTAAGTCATTACAGTCCAGAATATCTAGCATGGGGATTTTGTAGGAGCTGGAAGAATGGAGACATCCTTCAAAACAAGGGTAAGGGTACAACAGGACAACAGCACCCACACGCAAGACAATCCAGAGCCTGTTTAATCCTTTTGCAGAACTTCTTGCTTGGTTACATCAATTTACATCATTTTAACATTTAAAAAACATCTTTAAGGAGGTTAAATTCCCTTGCCTAGTAAGAATAAAAACCAAATCAAATGTACACATTCTTAAACCACAGGAAATGATGGAAATAA... | TCCAGAACCAAGAGAAAAGTGACAGAAAGTTCCTAAGTCATTACAGTCCAGAATATCTAGCATGGGGATTTTGTAGGAGCTGGAAGAATGGAGACATCCTTCAAAACAAGGGTAAGGGTACAACAGGACAACAGCACCCACACGCAAGACAATCCAGAGCCTGTTTAATCCTTTTGCAGAACTTCTTGCTTGGTTACATCAATTTACATCATTTTAACATTTAAAAAACATCTTTAAGGAGGTTAAATTCCCTTGCCTAGTAAGAATAAAAACCAAATCAAATGTACACATTCTTAAACCACAGGAAATGATGGAAATAA... |
Task1_train_34663 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GGCGGCAAGCAAAGAGAGAGGTTGTGCAGGCAAACTCCCATTTTTAAAGCCATCAGATCTTGTGAGACTTGTTCACTATTGTGAGAACAGCATGGAAAAGACCCACCCCCATGTTTCAGTTATCTCCCACTGGGTCCCTCCCACAACACGTGGGAATTATGGGAGCTACAAGATGAAATTTGGGTAGGGACAGAAAGCCAAACCACATCACCCTGAAAAATACTTTTGAAGTGGCATCGTAATTATTTCTAAATAAATAGCAAACACTTAACACTTTCCTCCCAGTGTAATTCCATATATTAGTTTGGGACAAATGTGTG... | GGCGGCAAGCAAAGAGAGAGGTTGTGCAGGCAAACTCCCATTTTTAAAGCCATCAGATCTTGTGAGACTTGTTCACTATTGTGAGAACAGCATGGAAAAGACCCACCCCCATGTTTCAGTTATCTCCCACTGGGTCCCTCCCACAACACGTGGGAATTATGGGAGCTACAAGATGAAATTTGGGTAGGGACAGAAAGCCAAACCACATCACCCTGAAAAATACTTTTGAAGTGGCATCGTAATTATTTCTAAATAAATAGCAAACACTTAACACTTTCCTCCCAGTGTAATTCCATATATTAGTTTGGGACAAATGTGTG... |
Task1_train_34664 | This genomic variant is located on Chromosome 2. Can you determine its pathogenicity and name any linked disease? | Benign | GGGAGGGGCACAAATCTAGGAGGCTGAGGTTGCAGTGAGCTGTAACCGCACCACTGCACTTCAGCCTGGGCAACAGAGCAGACCTTGTCTTAAAAAAAAAAAGTGGGACGCTGGGATCCAGGAGAGTAAGCAACCAAGGCTGGGTCCCTGGGGAATGTGGGAAGTGGGGAGGGTTTGACAAGAATAGTATTGCAAGGAAATTTGATCCTCTATTACCCAGTTCCACTTGTAGAATAAGAAAATACTAGTTAATGTTTTGTCTACCACCTACCATTTAGGAACTCAAGACTCTGTGGCTTTTCAAAGGTGGTTTGAGGAAT... | GGGAGGGGCACAAATCTAGGAGGCTGAGGTTGCAGTGAGCTGTAACCGCACCACTGCACTTCAGCCTGGGCAACAGAGCAGACCTTGTCTTAAAAAAAAAAAGTGGGACGCTGGGATCCAGGAGAGTAAGCAACCAAGGCTGGGTCCCTGGGGAATGTGGGAAGTGGGGAGGGTTTGACAAGAATAGTATTGCAAGGAAATTTGATCCTCTATTACCCAGTTCCACTTGTAGAATAAGAAAATACTAGTTAATGTTTTGTCTACCACCTACCATTTAGGAACTCAAGACTCTGTGGCTTTTCAAAGGTGGTTTGAGGAAT... |
Task1_train_34665 | This variant is present on Chromosome 2. Is the change likely to result in a pathogenic outcome? | Benign | TGCTTTCAGGATACAGTTCAAACACCTTTGCTTGACCTACATGAAATGCAAGGACCTGGCTCCTGCTCCTGTTGTAGCCCCAGGTCCTGTCACGCCCCACATATCCAGATCTTCTGTTAGGCCAGGAAGCTTCCTGCCTCTCTGCTTTTATTTGGAATAGCCTCCTCAGCTCACACCTTCACAACTCAGCTCCTGTAATACCTTCCCCAGCCAGTTCCTTGTGTCCACCTCTCCCTCATCCCCCAAACCCAGATTAGGAGTCTACGCTCCCAGAGGCCTGTGCAGGTCTCCTTCATCGCGTTAATCACACCGTATCAAAA... | TGCTTTCAGGATACAGTTCAAACACCTTTGCTTGACCTACATGAAATGCAAGGACCTGGCTCCTGCTCCTGTTGTAGCCCCAGGTCCTGTCACGCCCCACATATCCAGATCTTCTGTTAGGCCAGGAAGCTTCCTGCCTCTCTGCTTTTATTTGGAATAGCCTCCTCAGCTCACACCTTCACAACTCAGCTCCTGTAATACCTTCCCCAGCCAGTTCCTTGTGTCCACCTCTCCCTCATCCCCCAAACCCAGATTAGGAGTCTACGCTCCCAGAGGCCTGTGCAGGTCTCCTTCATCGCGTTAATCACACCGTATCAAAA... |
Task1_train_34666 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | GGGCTCCTACAACCTTGGACATTCTGTCCCTGTGCCTTTGCAAGGTATAGCCCCACTCCTGGCTGCTTTCATAGGCTGGCATTGAGTGTCTGCAGTTCTTCCAGGTGCACAGTGCAAGCTGTCAGTGGATCTACCATTCTGGGGTCTGGAGAATGGTGACCCTCTTCTCACAGCTCTACTAGGCAGTGCCCCAGTGGGGACTCTAAGTGGAGTTCCAACCCCACATTTCCTTTCTGAACTGCCTTAGCAGTTCTTCATGAAGTTCTTCATGAGGGCTCTGCCCTTGCGGCACACTTCTGCCTGGACACCCAGACATTTAC... | GGGCTCCTACAACCTTGGACATTCTGTCCCTGTGCCTTTGCAAGGTATAGCCCCACTCCTGGCTGCTTTCATAGGCTGGCATTGAGTGTCTGCAGTTCTTCCAGGTGCACAGTGCAAGCTGTCAGTGGATCTACCATTCTGGGGTCTGGAGAATGGTGACCCTCTTCTCACAGCTCTACTAGGCAGTGCCCCAGTGGGGACTCTAAGTGGAGTTCCAACCCCACATTTCCTTTCTGAACTGCCTTAGCAGTTCTTCATGAAGTTCTTCATGAGGGCTCTGCCCTTGCGGCACACTTCTGCCTGGACACCCAGACATTTAC... |
Task1_train_34667 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GACTGTTCCAAGCATGGGAGTGTTAACAGCCTCTTCTCCACCAAAGAGAATCCACAATTAGCAGTTAATTCCCACCCACCTACCGCTCTGAAAGAGGGGAATCTTCCTTAGAGTGAGGCTGCACTCATGTACAAGAATAGCAAATGGGGAGAAGGAAAGAAGATTGGGCTGGCAGGGAGTCAGGGAGTCTCTGAGGGGAAGGGGAATTTGTGTAATTGAATCCATTTGAAATTTCAAGAATTTTGAGTGGAGATTGGGATTCATTTTAAAGACCTATGATTCTTGAATATTACCTCTTGTGCACTTCACCGCTCTAAGTG... | GACTGTTCCAAGCATGGGAGTGTTAACAGCCTCTTCTCCACCAAAGAGAATCCACAATTAGCAGTTAATTCCCACCCACCTACCGCTCTGAAAGAGGGGAATCTTCCTTAGAGTGAGGCTGCACTCATGTACAAGAATAGCAAATGGGGAGAAGGAAAGAAGATTGGGCTGGCAGGGAGTCAGGGAGTCTCTGAGGGGAAGGGGAATTTGTGTAATTGAATCCATTTGAAATTTCAAGAATTTTGAGTGGAGATTGGGATTCATTTTAAAGACCTATGATTCTTGAATATTACCTCTTGTGCACTTCACCGCTCTAAGTG... |
Task1_train_34668 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GTCCGGGAGGGAGGCGGGGGGGGGGGGGGGGGTCGGCCAGCCGCCCGGTCCGGGAGGGAGGTGGGGGGGGTCAGCCCCCCTTCCGGCCGGCCGCCCCGTCCGGGAGGTGAGGGGCGCCTCTGCCCGGCCGCCCCTACTGGGAAGTGAGGACCCCTCTGCCCGGCCAGCCGCCCCGTCCGGGAGGGAGGTGGGGGGGACAGCCCCCCGCCCAGCCAGCCGCCCTATCCAGGAGGTGAGGGGCGCGTCTGCCCGGCCGTCCCTACTGGGAAGTGAGGAGCCCCTCTGCCTGGCCAGCCGCCCCGTCCGGGAGGGTGGTGGGG... | GTCCGGGAGGGAGGCGGGGGGGGGGGGGGGGGTCGGCCAGCCGCCCGGTCCGGGAGGGAGGTGGGGGGGGTCAGCCCCCCTTCCGGCCGGCCGCCCCGTCCGGGAGGTGAGGGGCGCCTCTGCCCGGCCGCCCCTACTGGGAAGTGAGGACCCCTCTGCCCGGCCAGCCGCCCCGTCCGGGAGGGAGGTGGGGGGGACAGCCCCCCGCCCAGCCAGCCGCCCTATCCAGGAGGTGAGGGGCGCGTCTGCCCGGCCGTCCCTACTGGGAAGTGAGGAGCCCCTCTGCCTGGCCAGCCGCCCCGTCCGGGAGGGTGGTGGGG... |
Task1_train_34669 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGCTAATTTTTGTAGTTTTTTTGGTAGAGATGGGGTTTTGCCATGTTGGCCAAGCTGGTCTTGAACTCCTGAGCTCCTGCGTCAGCTTCCCAAAGTGCTAGGATTATAGGCGTGAGCTATCACACCCAGCCTGGAAAGCTTAACTTTTTACTGTGTCACAGCACTTTTATGCTTGAAGTTTACACAACTATTCTGCAAGAACTGACATGAACAATTTCTATGATTTTGTTTAAGGGAATGCCCAGTTCCTAAACCAAACTCAGGTCAGCAAAGCCACAACTTCACCCATAGGGAAAAAGCAACACATTGCCCAAGGGTCT... | AGCTAATTTTTGTAGTTTTTTTGGTAGAGATGGGGTTTTGCCATGTTGGCCAAGCTGGTCTTGAACTCCTGAGCTCCTGCGTCAGCTTCCCAAAGTGCTAGGATTATAGGCGTGAGCTATCACACCCAGCCTGGAAAGCTTAACTTTTTACTGTGTCACAGCACTTTTATGCTTGAAGTTTACACAACTATTCTGCAAGAACTGACATGAACAATTTCTATGATTTTGTTTAAGGGAATGCCCAGTTCCTAAACCAAACTCAGGTCAGCAAAGCCACAACTTCACCCATAGGGAAAAAGCAACACATTGCCCAAGGGTCT... |
Task1_train_34670 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TTATGTCTTCTAGGAAAATAGTGTAAAATTCAGCACGTTAAGAAGCTTTTGGTTTTCTGAATTATGTTTGACATGTTATTGTTGACAAACAGAGGACTCTGATTAATAGCTCCAGGAAGCCATCACTATTGTTGCGAGTTTAAAGGTTAAAGACCCAAGATTTAGGAAGAGTTAACACTAAATAATCCTAGATTCTGACTGTTTTTCAGGAAATAAATCTTTATATGTATTTGTGTTCTCTATATATACACACATACAGTAGGCTAATATACATATACATACAGTAGGCTAAACTTAGGCTACACATTTTTTTAAAATGC... | TTATGTCTTCTAGGAAAATAGTGTAAAATTCAGCACGTTAAGAAGCTTTTGGTTTTCTGAATTATGTTTGACATGTTATTGTTGACAAACAGAGGACTCTGATTAATAGCTCCAGGAAGCCATCACTATTGTTGCGAGTTTAAAGGTTAAAGACCCAAGATTTAGGAAGAGTTAACACTAAATAATCCTAGATTCTGACTGTTTTTCAGGAAATAAATCTTTATATGTATTTGTGTTCTCTATATATACACACATACAGTAGGCTAATATACATATACATACAGTAGGCTAAACTTAGGCTACACATTTTTTTAAAATGC... |
Task1_train_34671 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CGTGGGTTCTTTGTATATTATTCTTGCAAATTTTCTCTAAGTTTGAAATTATTTTTACATTAAAAAGTTATACTTCTCTTAACCAATCCTACCCAAAGCAAATCAGTTTTTGGCCTTTTAGCAGTTATGTATTATGCTTGTAGGATATTATTTTGAATTTCTGATGTATTGCTTTGGATTTAAATTTAAATTGTCCTCTCTCTATGTCTCATTTCCTTTCATGATAGCATGAATTTCTCATGAGTGGTGATGAAGAGAGCGATTATATTATTGCTTGCCACTGTCCTGACACTTTTTTTTTTTGAGACGGTGTCTCACTC... | CGTGGGTTCTTTGTATATTATTCTTGCAAATTTTCTCTAAGTTTGAAATTATTTTTACATTAAAAAGTTATACTTCTCTTAACCAATCCTACCCAAAGCAAATCAGTTTTTGGCCTTTTAGCAGTTATGTATTATGCTTGTAGGATATTATTTTGAATTTCTGATGTATTGCTTTGGATTTAAATTTAAATTGTCCTCTCTCTATGTCTCATTTCCTTTCATGATAGCATGAATTTCTCATGAGTGGTGATGAAGAGAGCGATTATATTATTGCTTGCCACTGTCCTGACACTTTTTTTTTTTGAGACGGTGTCTCACTC... |
Task1_train_34672 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTATATTCTACCAGAACAGCAGCTGGCAGAGGGACATGAGTAGGTCCTGCTGCCCAATAAATGAGCTTTGCAGGCACCAAAGCTTGGTTATGACATGATCAAGCTCCTCACTTTATCCCTCCTTGCCTGAGTGCCCTGGTTTTTTACATTTTCACCAAAGGACAAGGAGGGCAGGGAAAGGGAGTGATTTTCAGATCAGGTAGGCTTTAAAACTTCAAGGAGTGACACTGGAGCCAGGAGTGTCAATCCACTAATTTACTTCCCATGTGGTCTTGAGTAAATCATTTCTCTAGTCTGAGCTTAATTTCCTTAGCTGTCAG... | TTATATTCTACCAGAACAGCAGCTGGCAGAGGGACATGAGTAGGTCCTGCTGCCCAATAAATGAGCTTTGCAGGCACCAAAGCTTGGTTATGACATGATCAAGCTCCTCACTTTATCCCTCCTTGCCTGAGTGCCCTGGTTTTTTACATTTTCACCAAAGGACAAGGAGGGCAGGGAAAGGGAGTGATTTTCAGATCAGGTAGGCTTTAAAACTTCAAGGAGTGACACTGGAGCCAGGAGTGTCAATCCACTAATTTACTTCCCATGTGGTCTTGAGTAAATCATTTCTCTAGTCTGAGCTTAATTTCCTTAGCTGTCAG... |
Task1_train_34673 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | TTCTCCACATCCTCTCCAGCACATGTTGTTTCCTGACTTTTTAATGATTGCCATTCTATCTGGTGTGAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCTGATGGCCAGTGATGATGAGCATTTTTTCATGTGTCTGTTGGGTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATGTGCTTCGCCCACTTTTTGATGGGGTTGTTTGTTTTTTTCTTGTAAATTTGTTTGAGTTTTTTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGATTGCAAAAATTTTCTCCCATTCTGTAGGTTGCCTGT... | TTCTCCACATCCTCTCCAGCACATGTTGTTTCCTGACTTTTTAATGATTGCCATTCTATCTGGTGTGAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCTGATGGCCAGTGATGATGAGCATTTTTTCATGTGTCTGTTGGGTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATGTGCTTCGCCCACTTTTTGATGGGGTTGTTTGTTTTTTTCTTGTAAATTTGTTTGAGTTTTTTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGATTGCAAAAATTTTCTCCCATTCTGTAGGTTGCCTGT... |
Task1_train_34674 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TCCTCTCCAGCACATGTTGTTTCCTGACTTTTTAATGATTGCCATTCTATCTGGTGTGAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCTGATGGCCAGTGATGATGAGCATTTTTTCATGTGTCTGTTGGGTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATGTGCTTCGCCCACTTTTTGATGGGGTTGTTTGTTTTTTTCTTGTAAATTTGTTTGAGTTTTTTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGATTGCAAAAATTTTCTCCCATTCTGTAGGTTGCCTGTTCACTCTGA... | TCCTCTCCAGCACATGTTGTTTCCTGACTTTTTAATGATTGCCATTCTATCTGGTGTGAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCTGATGGCCAGTGATGATGAGCATTTTTTCATGTGTCTGTTGGGTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATGTGCTTCGCCCACTTTTTGATGGGGTTGTTTGTTTTTTTCTTGTAAATTTGTTTGAGTTTTTTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGATTGCAAAAATTTTCTCCCATTCTGTAGGTTGCCTGTTCACTCTGA... |
Task1_train_34675 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GTGATGATGAGCATTTTTTCATGTGTCTGTTGGGTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATGTGCTTCGCCCACTTTTTGATGGGGTTGTTTGTTTTTTTCTTGTAAATTTGTTTGAGTTTTTTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGATTGCAAAAATTTTCTCCCATTCTGTAGGTTGCCTGTTCACTCTGATGATATTTTAATATGTCCAGATACTGCATTTTACCAGGTGTAATATTTCTGATTTATCTTACTTAGGAAAGGGAATTCTTGAAGAATTATGTCCAGCGAATAGT... | GTGATGATGAGCATTTTTTCATGTGTCTGTTGGGTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATGTGCTTCGCCCACTTTTTGATGGGGTTGTTTGTTTTTTTCTTGTAAATTTGTTTGAGTTTTTTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGATTGCAAAAATTTTCTCCCATTCTGTAGGTTGCCTGTTCACTCTGATGATATTTTAATATGTCCAGATACTGCATTTTACCAGGTGTAATATTTCTGATTTATCTTACTTAGGAAAGGGAATTCTTGAAGAATTATGTCCAGCGAATAGT... |
Task1_train_34676 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | TTTAAAAAAATCACAGCTTTTAAATTTATATGCACGTATGGTAGGTATACAAGAATCTTTTTTTCTTTGCTGTTCTATTTGTATTGAAAGTGGGACAGAAGATATGGCACCTATTTCATTAAGATTCAGAATTTCAGACTGGAACTGGAAGAAAGTATAATTGATTATGTAATACTTATTGGTGTCTACAAGACCAAAAGTGAAATGGACATTAGTTAATCACTAGGTATTTGTTGATCCTTCATTTTTGTTGGAGAATTGCTCAAGCAGAAGACGTTCTCTCCCTTGAAAAGTTTACCCTGTGCAGAACAGGGGCCAAT... | TTTAAAAAAATCACAGCTTTTAAATTTATATGCACGTATGGTAGGTATACAAGAATCTTTTTTTCTTTGCTGTTCTATTTGTATTGAAAGTGGGACAGAAGATATGGCACCTATTTCATTAAGATTCAGAATTTCAGACTGGAACTGGAAGAAAGTATAATTGATTATGTAATACTTATTGGTGTCTACAAGACCAAAAGTGAAATGGACATTAGTTAATCACTAGGTATTTGTTGATCCTTCATTTTTGTTGGAGAATTGCTCAAGCAGAAGACGTTCTCTCCCTTGAAAAGTTTACCCTGTGCAGAACAGGGGCCAAT... |
Task1_train_34677 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | GCAGCCAGCCCTTCTGATCATCCCCATATCTCTTGAGTTTTCATTCATCTAACCTTTATTAGAAGTTCATCAAGTATTTTTTTTTCTATTGTTACAACAGGACACATAAGTATATAAGGTAATGATGATCCATACACTTGCTCTTTTAGAGATGATTGAATTTTATTATTTTTCCCCAAATCTTTTCCAGATAACTACATTTAGCTCTAATGACCACAGTGAACTACTTTGACCTTAAAACACAAGTGGGACAATAAAGCCTTTTGGATTGTTGAATAAATAAAAGTAAAAATGTGTTATCTAATTTCTGTGAAGCACCT... | GCAGCCAGCCCTTCTGATCATCCCCATATCTCTTGAGTTTTCATTCATCTAACCTTTATTAGAAGTTCATCAAGTATTTTTTTTTCTATTGTTACAACAGGACACATAAGTATATAAGGTAATGATGATCCATACACTTGCTCTTTTAGAGATGATTGAATTTTATTATTTTTCCCCAAATCTTTTCCAGATAACTACATTTAGCTCTAATGACCACAGTGAACTACTTTGACCTTAAAACACAAGTGGGACAATAAAGCCTTTTGGATTGTTGAATAAATAAAAGTAAAAATGTGTTATCTAATTTCTGTGAAGCACCT... |
Task1_train_34678 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | AATATGCATTTTTTCTCCAATGATGTCACTTTCTACTTGAAGATCACGATTCTGAATTTCAGTATAAAAAAGCAATTTTTTAGGGTTCTGACTTTTCAGAAATAAATTGAAGATAAAAGTGAAAACCTAAGAGGGCAGACTAACAAAGTATATGCTATCATATAGGAAACATTAGAAAATTATATAGAGATTATTATTCCTGAAGTGTATGTATTAGTATTATATATAATGTTTGTATACATAAACATGCAGTGCTTGAGAAAAATTCTTTTCTGATAATATCACAATTCTATCATTAAAATTCATGATAGAGATTTTAT... | AATATGCATTTTTTCTCCAATGATGTCACTTTCTACTTGAAGATCACGATTCTGAATTTCAGTATAAAAAAGCAATTTTTTAGGGTTCTGACTTTTCAGAAATAAATTGAAGATAAAAGTGAAAACCTAAGAGGGCAGACTAACAAAGTATATGCTATCATATAGGAAACATTAGAAAATTATATAGAGATTATTATTCCTGAAGTGTATGTATTAGTATTATATATAATGTTTGTATACATAAACATGCAGTGCTTGAGAAAAATTCTTTTCTGATAATATCACAATTCTATCATTAAAATTCATGATAGAGATTTTAT... |
Task1_train_34679 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GTAACACTTAAGTAGTGCTTACTTCTAAATTAGTTTATTGAACACTCATACTAATGTAAGAACTGTTACTATTCCTGTTCAACAGATGAGGAAACTGCATCTTAGAGTTGTTAAGTAAGATATTCAAGGTAACACAGTTTAATAAGGTGTGGAGCCTCAAAAAAAAAAGTTGAAATACTACTATTGTCATCACTGTTTTTGAGTGAAGAAATGAAGGCAAAGACATTAACTTTTTGAAGCTCATACCACTAGTGAATGGTGAAAGCCAGGATTTGAAATGCAGCTAACTGACTTTAGAGCTCATTCTTTAGCTACAACTT... | GTAACACTTAAGTAGTGCTTACTTCTAAATTAGTTTATTGAACACTCATACTAATGTAAGAACTGTTACTATTCCTGTTCAACAGATGAGGAAACTGCATCTTAGAGTTGTTAAGTAAGATATTCAAGGTAACACAGTTTAATAAGGTGTGGAGCCTCAAAAAAAAAAGTTGAAATACTACTATTGTCATCACTGTTTTTGAGTGAAGAAATGAAGGCAAAGACATTAACTTTTTGAAGCTCATACCACTAGTGAATGGTGAAAGCCAGGATTTGAAATGCAGCTAACTGACTTTAGAGCTCATTCTTTAGCTACAACTT... |
Task1_train_34680 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TGGTAAACAATGCCAGAGACATTTTATAATCAGCAGCAAAATGAAAACTAGGCTAATCTTATCTTTGATTTTCATAACCATTACCATGCATTAAAGTGTTTAATTCACACATTTTAAACTTGGCATAACCGAGTCAGTGTAATCGAAAAAAATGTAAACCTAACAATAATAACAACAACAACAACAAGCATTGCTGGTGTGTGCTGTGATTTAACATAAAATATTGTCTTGAAGTTTTCATATGTAATTAGAGTAACTTATAGTTTTTGAAAGTCTTAAAGCAGTTCTCTTAGAATTATTTTATGTTAGAATCATTTCCA... | TGGTAAACAATGCCAGAGACATTTTATAATCAGCAGCAAAATGAAAACTAGGCTAATCTTATCTTTGATTTTCATAACCATTACCATGCATTAAAGTGTTTAATTCACACATTTTAAACTTGGCATAACCGAGTCAGTGTAATCGAAAAAAATGTAAACCTAACAATAATAACAACAACAACAACAAGCATTGCTGGTGTGTGCTGTGATTTAACATAAAATATTGTCTTGAAGTTTTCATATGTAATTAGAGTAACTTATAGTTTTTGAAAGTCTTAAAGCAGTTCTCTTAGAATTATTTTATGTTAGAATCATTTCCA... |
Task1_train_34681 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | AATATAGTATCAAGATTAGGATGTTGACATTGATATAATCAAGGTATGGAATAGTTCTGCCTGCCAGAGGATCCCTGGTGTTGCCCTTTTATAGCCACACTGATTTCCCTTTAGCTCTGTCCATGCCTAACCCCAGGAAACCACTAATCTTTTCTTCATTTCTGTAATTTTTTTAATTTTAAGATTGTTATTTAAATGGAATTATATAATATTTAACTTTTGGGGGTTGACTGTTACACTTGGCATAATTCCACTGAGTCATCCAAGATGTTGTGTGGATCAGTAGCTGATCATGTTATTAAATTGCTGAGTAGTTGTTG... | AATATAGTATCAAGATTAGGATGTTGACATTGATATAATCAAGGTATGGAATAGTTCTGCCTGCCAGAGGATCCCTGGTGTTGCCCTTTTATAGCCACACTGATTTCCCTTTAGCTCTGTCCATGCCTAACCCCAGGAAACCACTAATCTTTTCTTCATTTCTGTAATTTTTTTAATTTTAAGATTGTTATTTAAATGGAATTATATAATATTTAACTTTTGGGGGTTGACTGTTACACTTGGCATAATTCCACTGAGTCATCCAAGATGTTGTGTGGATCAGTAGCTGATCATGTTATTAAATTGCTGAGTAGTTGTTG... |
Task1_train_34682 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | GTATATATATACAGATATATCTATCTATATATATATATACACACATATGTGTGTGTACATGTATGTATCTATGCCAGTGTTAGAAAAGGAATATATGGACAAATCAGAGTGTGATTAGGAGGATCAGTTCATGTGGAATAGGAGTCCAAGTTGTTTAAGGTGTCACAGAGGAGGCCACATAGTGGAGGGGATGAGAAGAGTCAGAAAAAAGTACTTCCAAATCTGATTAGCTATCAGTGGGTTTGTATTTATATTTTTGCCTTAACTTCTACAAATAATTCCTCTCACAAAAGTCATTTTGGAAACTTATCTTTCAAAGT... | GTATATATATACAGATATATCTATCTATATATATATATACACACATATGTGTGTGTACATGTATGTATCTATGCCAGTGTTAGAAAAGGAATATATGGACAAATCAGAGTGTGATTAGGAGGATCAGTTCATGTGGAATAGGAGTCCAAGTTGTTTAAGGTGTCACAGAGGAGGCCACATAGTGGAGGGGATGAGAAGAGTCAGAAAAAAGTACTTCCAAATCTGATTAGCTATCAGTGGGTTTGTATTTATATTTTTGCCTTAACTTCTACAAATAATTCCTCTCACAAAAGTCATTTTGGAAACTTATCTTTCAAAGT... |
Task1_train_34683 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AAACATATGTGCAAACCAACTATTGTGGCAAAAACAGTTTTTGTTGGTGAAGGGACTAGCTGCCATTTGGTGATTTTTCAGATAGTCAAATTTGAAAAATCAATTGGATCTTCTCTTCTCTTCTCTTTTCTCTTTTTGAGATGGAGTCGCAGTCCCCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCTGCCTTCCGGGTTCAAGTGATTTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACACGCCACCATGCCTGGCTAATTTTTTTTTTTTTTGTATTTTTAGTAGAGACGGGGTTTC... | AAACATATGTGCAAACCAACTATTGTGGCAAAAACAGTTTTTGTTGGTGAAGGGACTAGCTGCCATTTGGTGATTTTTCAGATAGTCAAATTTGAAAAATCAATTGGATCTTCTCTTCTCTTCTCTTTTCTCTTTTTGAGATGGAGTCGCAGTCCCCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCTGCCTTCCGGGTTCAAGTGATTTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACACGCCACCATGCCTGGCTAATTTTTTTTTTTTTTGTATTTTTAGTAGAGACGGGGTTTC... |
Task1_train_34684 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CTATATTATTGTGTAAATAGCTCCCATCTGAGCTAGGTGTCTTGCTAACTCAGATCAATTAGTACTTGTAATTGAAGCTCAATAATAATTACTGCTACATCTAGTGAGCATTTAATTCCTGTGTGCCAGGCATAGCTATAGATACAGTTTAAGCTGCTCAAGTTTAACACAGTAAAAATGATAAGAGCATAGGTGCTTATAAAGAATTACTATTACAAGGAAACTGGGTATGAATACAGTTTTTAAGGGTATAATTTTGGGCCAGGCTTGGTGGCTCACGCCACACTCCCAACACTTTGAGAGGCCTAGTCGGGTGGATC... | CTATATTATTGTGTAAATAGCTCCCATCTGAGCTAGGTGTCTTGCTAACTCAGATCAATTAGTACTTGTAATTGAAGCTCAATAATAATTACTGCTACATCTAGTGAGCATTTAATTCCTGTGTGCCAGGCATAGCTATAGATACAGTTTAAGCTGCTCAAGTTTAACACAGTAAAAATGATAAGAGCATAGGTGCTTATAAAGAATTACTATTACAAGGAAACTGGGTATGAATACAGTTTTTAAGGGTATAATTTTGGGCCAGGCTTGGTGGCTCACGCCACACTCCCAACACTTTGAGAGGCCTAGTCGGGTGGATC... |
Task1_train_34685 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | CTTTTGCACTAAGAAGGCAGAGCTGAACCGCTATGATAGAGATTTCATGGCCTGCAAAGCTGAAAACATTTACTCTAACTGCACCTTTAAGAAAGAACTTACAAAACTCTGGCCTAGACCCTAGGGATCCTCATTAATAAAGATAAATTATTCTTATGGTTAGAAGAAAAAGTCGCCACCAATATAAGTAAATGCTTGCCTGATAGTCCAAAAATTTCCCAGAAAGCAAAATATATAAATTACTATGTATTAGCCAGCAAAATGAACAAAAATAATCATTACACTAGCTACTTATGTCTATAACTTTGTTTACAATAGCT... | CTTTTGCACTAAGAAGGCAGAGCTGAACCGCTATGATAGAGATTTCATGGCCTGCAAAGCTGAAAACATTTACTCTAACTGCACCTTTAAGAAAGAACTTACAAAACTCTGGCCTAGACCCTAGGGATCCTCATTAATAAAGATAAATTATTCTTATGGTTAGAAGAAAAAGTCGCCACCAATATAAGTAAATGCTTGCCTGATAGTCCAAAAATTTCCCAGAAAGCAAAATATATAAATTACTATGTATTAGCCAGCAAAATGAACAAAAATAATCATTACACTAGCTACTTATGTCTATAACTTTGTTTACAATAGCT... |
Task1_train_34686 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TGTAGCAAGCAAACACCACATTCTTTTAGATTAAGACACACATTATTTATCATTTATTCTATCACAACCACCAAACTCAATACTTTACATACATGTAAAATTTCATTTTGTTTCTTCCATAAAAGCTCCCTAAGAGATGGAATTTATTGTCTGCTTTGTTCACTAACAAATCCCCAATACCCAGAATAGGGTCTGGCACTTTATGGGTGCTCAATAAATTTATGATTATTAATGAATCCTCACAAGAAAATAAGCTAATCATTAGTATTACTCATATCCGGAAAATGAGAGATGAATAACTTGGCCTACTCAATAGTGTC... | TGTAGCAAGCAAACACCACATTCTTTTAGATTAAGACACACATTATTTATCATTTATTCTATCACAACCACCAAACTCAATACTTTACATACATGTAAAATTTCATTTTGTTTCTTCCATAAAAGCTCCCTAAGAGATGGAATTTATTGTCTGCTTTGTTCACTAACAAATCCCCAATACCCAGAATAGGGTCTGGCACTTTATGGGTGCTCAATAAATTTATGATTATTAATGAATCCTCACAAGAAAATAAGCTAATCATTAGTATTACTCATATCCGGAAAATGAGAGATGAATAACTTGGCCTACTCAATAGTGTC... |
Task1_train_34687 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | TGCCAGCATAATATTAATGAGACTTATTTACCTTGTATGACTCAATAATCTGCTTATTTTTATTGTTGTGTTGTATTTTAATATATGAATAAACCACAATTTGTTTTGCCATTTTTTTATAGAGATTTGATTACCTGGCTCCACTTTTAGCTATTATCAAGAAATAAACATCAGCATACAAGTCTTCATATAGGTGTATATTTTCATTTTCTTGGATAAATACCCAAGAGTAGAATGCAGCCTCATACGGATCTACTGTTTTACTTCATTAGAAGCTGTCACACTATTTTCCAAATGACTGTGTTGTTTCCCATGCTAAC... | TGCCAGCATAATATTAATGAGACTTATTTACCTTGTATGACTCAATAATCTGCTTATTTTTATTGTTGTGTTGTATTTTAATATATGAATAAACCACAATTTGTTTTGCCATTTTTTTATAGAGATTTGATTACCTGGCTCCACTTTTAGCTATTATCAAGAAATAAACATCAGCATACAAGTCTTCATATAGGTGTATATTTTCATTTTCTTGGATAAATACCCAAGAGTAGAATGCAGCCTCATACGGATCTACTGTTTTACTTCATTAGAAGCTGTCACACTATTTTCCAAATGACTGTGTTGTTTCCCATGCTAAC... |
Task1_train_34688 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GTTTGATTAAAGACTTAAATGTAAAACCCCAAATTATAAAAACCCTGGAAGACAGCCTAGGCAACACAATTCTAGACACAGGAAATGGTAAATATTTTATGACAAAGATGCCAAAAGCAATCAAAATAAAAGCAAAAGTTGACAAATGGGATCTAATTAAACTTAACAGCTTCTGCACAGCAAAGAAACCATCAACAGAATAAACAGACAACCTACAGAATGGGAGAACATTTTTGCAAACTATGCATCTGAAAAAGGTCTAATATCCAACATCTATAAGGAAGTTCAACAAATTTACAAGAAAAAAAAAAAACTCCACT... | GTTTGATTAAAGACTTAAATGTAAAACCCCAAATTATAAAAACCCTGGAAGACAGCCTAGGCAACACAATTCTAGACACAGGAAATGGTAAATATTTTATGACAAAGATGCCAAAAGCAATCAAAATAAAAGCAAAAGTTGACAAATGGGATCTAATTAAACTTAACAGCTTCTGCACAGCAAAGAAACCATCAACAGAATAAACAGACAACCTACAGAATGGGAGAACATTTTTGCAAACTATGCATCTGAAAAAGGTCTAATATCCAACATCTATAAGGAAGTTCAACAAATTTACAAGAAAAAAAAAAAACTCCACT... |
Task1_train_34689 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTTCGTTTTTTTTATTCAAGATGACTTTGACTCTTCAGAGTCCCTTGCATTTCCACATGATTTTTAGAATCAGCTTGTCCATTTCTGCAAAACAACGCAGTTGGAATTTTCATAGGTATTGTGTTGAATCTGTAGATCAATTTGGGAAATGTTACCATCCTAAGAATATTAAATCTTCCAGTCTGTGAACATGGGGTGTCTTTAATTTCTTTAACATTGTCTTGTGAAGTAGAATTGTTTTCTTAATTTTTTTCTCATTCACTGCTAATGTATATTTTAATACAATTGATTTTTATATATTGATCATATATCCTGCGGCT... | CTTCGTTTTTTTTATTCAAGATGACTTTGACTCTTCAGAGTCCCTTGCATTTCCACATGATTTTTAGAATCAGCTTGTCCATTTCTGCAAAACAACGCAGTTGGAATTTTCATAGGTATTGTGTTGAATCTGTAGATCAATTTGGGAAATGTTACCATCCTAAGAATATTAAATCTTCCAGTCTGTGAACATGGGGTGTCTTTAATTTCTTTAACATTGTCTTGTGAAGTAGAATTGTTTTCTTAATTTTTTTCTCATTCACTGCTAATGTATATTTTAATACAATTGATTTTTATATATTGATCATATATCCTGCGGCT... |
Task1_train_34690 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | TATGAACTACTAATTTTTTACTAATAATTATTTCCATTTCCACTATTTACTATTCTGAATGTCACATTTATTTATTTATGTTTTTTGGGATGGAGTCTTGCTCTGTCCCCCATGCTGGAGTTCAATGGCACAATCTCAGCTCACTGCAACCTCCGCCTTCTGGGTTCAAGCCATTCTCCTACCTCAGCCTTCTGAGTAGCCGGGACCAAAGACGCCCACTGCCATGCCTGGTAACATTTGTATTTTTAATAGAGACAAGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCTGCCTCA... | TATGAACTACTAATTTTTTACTAATAATTATTTCCATTTCCACTATTTACTATTCTGAATGTCACATTTATTTATTTATGTTTTTTGGGATGGAGTCTTGCTCTGTCCCCCATGCTGGAGTTCAATGGCACAATCTCAGCTCACTGCAACCTCCGCCTTCTGGGTTCAAGCCATTCTCCTACCTCAGCCTTCTGAGTAGCCGGGACCAAAGACGCCCACTGCCATGCCTGGTAACATTTGTATTTTTAATAGAGACAAGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCTGCCTCA... |
Task1_train_34691 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AGGCCATATAAAGTACTAACTTATGACAGAGCTAGATTTGTGAAGGGTTTCACATTCCAATCTCTGACTCAGAAAGTCAAAGCAAGGTTCACATAAAAAGCAAACGATTGGCCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACCTGAGGTCAGGAATTCGAGACCACCCTGACCAATACGGTGAAACCCCGTCTCTACTAAAAATATGAAAATTAGCTGGGTGTGGTGGCATGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCTGGA... | AGGCCATATAAAGTACTAACTTATGACAGAGCTAGATTTGTGAAGGGTTTCACATTCCAATCTCTGACTCAGAAAGTCAAAGCAAGGTTCACATAAAAAGCAAACGATTGGCCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACCTGAGGTCAGGAATTCGAGACCACCCTGACCAATACGGTGAAACCCCGTCTCTACTAAAAATATGAAAATTAGCTGGGTGTGGTGGCATGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCTGGA... |
Task1_train_34692 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGTTCCTCTTCCTTCATCTCTTCCTTTGCAGTCCTTTCCTAAGTCTCTGTCTTAGGTCTTTTTCTCACCTCTATCTCCCTAGATAATTTCCCCTAATGCCTCAATTTCTCTTGTCATTACTTCTCTCTAGTGACTCCTAAGTCTCTTACTTTAGTCGTCACCTCAAGCCTTGGCTCCAGGTCTCAGTTTCCACCTTTCTGCTGGATGTGTCCAAGTGGACGGGCTGCTGACATGTGGATGAGCCCAATCAGACTCCATCATCCTAAGTCACCCTTCCACCTTATGTTCCCAACTTTGTCAACTGCTGCTCACTCCCTTAA... | GGTTCCTCTTCCTTCATCTCTTCCTTTGCAGTCCTTTCCTAAGTCTCTGTCTTAGGTCTTTTTCTCACCTCTATCTCCCTAGATAATTTCCCCTAATGCCTCAATTTCTCTTGTCATTACTTCTCTCTAGTGACTCCTAAGTCTCTTACTTTAGTCGTCACCTCAAGCCTTGGCTCCAGGTCTCAGTTTCCACCTTTCTGCTGGATGTGTCCAAGTGGACGGGCTGCTGACATGTGGATGAGCCCAATCAGACTCCATCATCCTAAGTCACCCTTCCACCTTATGTTCCCAACTTTGTCAACTGCTGCTCACTCCCTTAA... |
Task1_train_34693 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TATAGATAATGACCAGCTGTCCAGTGATAGTCTAAGAAGAAGCTCTAATAAGCAGTTGTACCTAAGTTTAGTGCTACATAGGCAGGTTCTGTCCCTTAAGCAGAAATAACTGGCAACGCTATGGAGATTTAAGGAGTCGATGGCAGTCATTAACACAGGTCATGTGAAAGCAAGCCCTGCCTTTTCCATCTTCTCCACCAACCTGTATTAGGGCCACTTTTCCCTCTAACATGGTTTGTAATTCTCAGTTGTTATGATATTATCAGTTCCAGAAGGCCACTGTTAAAGGGCTATCTGGGAGGAAAATGAAGCTTTCTGAT... | TATAGATAATGACCAGCTGTCCAGTGATAGTCTAAGAAGAAGCTCTAATAAGCAGTTGTACCTAAGTTTAGTGCTACATAGGCAGGTTCTGTCCCTTAAGCAGAAATAACTGGCAACGCTATGGAGATTTAAGGAGTCGATGGCAGTCATTAACACAGGTCATGTGAAAGCAAGCCCTGCCTTTTCCATCTTCTCCACCAACCTGTATTAGGGCCACTTTTCCCTCTAACATGGTTTGTAATTCTCAGTTGTTATGATATTATCAGTTCCAGAAGGCCACTGTTAAAGGGCTATCTGGGAGGAAAATGAAGCTTTCTGAT... |
Task1_train_34694 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CGATTCTTAAGAGAACAAAAGCAAGAAGTATCTGAAACACTTCTTTTCCATGTTAAAGACAAGCTGTGTTTTTTTTCTAGCCAACCGAATATCAGAAAAGCCAGTGATTTCATTTCAAAAATGTATTTTAAGAAAAGAAACTCTCATTACTTCTTACATATGCATGAAAGAGGACACATTTCACTCATAAAGGAACTACAACTTTTCTAAAGGGCAGTTTGGCAATATCTCTTAAAATTACAAAGGCATTTGGCTTTGGACTTAGCAATTATACCTCTTGCAATTTAGGCTACACACTATCTGATGTACAGAAAATGTTA... | CGATTCTTAAGAGAACAAAAGCAAGAAGTATCTGAAACACTTCTTTTCCATGTTAAAGACAAGCTGTGTTTTTTTTCTAGCCAACCGAATATCAGAAAAGCCAGTGATTTCATTTCAAAAATGTATTTTAAGAAAAGAAACTCTCATTACTTCTTACATATGCATGAAAGAGGACACATTTCACTCATAAAGGAACTACAACTTTTCTAAAGGGCAGTTTGGCAATATCTCTTAAAATTACAAAGGCATTTGGCTTTGGACTTAGCAATTATACCTCTTGCAATTTAGGCTACACACTATCTGATGTACAGAAAATGTTA... |
Task1_train_34695 | This variant is present on Chromosome 2. Is the change likely to result in a pathogenic outcome? | Benign | GCTTCACTCGGAAGCTGAGTGACCTTGGCACAAAGGTTTTTGCTGCTCTTTCCCTACCCCCAGCCCTGGTTTCTAAATGTGCCCCGTGCTTCCCTCACTGTGAAGTACAAAGGCCAGCCTGCTGGGCAGGGGTAAGAAGTCACACTTACTTAGCAGGGGCACCACCCTCTGTTTTCATCCACCTGTGGAGAGAAAGTGGGCTCAGGGTAAATCATCGTACTTTCTCCCTAGAGCCCAGCCCCACCCATGCCCAGACCCTCTGCAGGAAGGTCTGGGGAGAGGAGCTGCCCCCCATTCCCCCCTCATTCCCCCATTCCCCC... | GCTTCACTCGGAAGCTGAGTGACCTTGGCACAAAGGTTTTTGCTGCTCTTTCCCTACCCCCAGCCCTGGTTTCTAAATGTGCCCCGTGCTTCCCTCACTGTGAAGTACAAAGGCCAGCCTGCTGGGCAGGGGTAAGAAGTCACACTTACTTAGCAGGGGCACCACCCTCTGTTTTCATCCACCTGTGGAGAGAAAGTGGGCTCAGGGTAAATCATCGTACTTTCTCCCTAGAGCCCAGCCCCACCCATGCCCAGACCCTCTGCAGGAAGGTCTGGGGAGAGGAGCTGCCCCCCATTCCCCCCTCATTCCCCCATTCCCCC... |
Task1_train_34696 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ATCAGGAGACACAAGTTGTGTCTCCAGTGCTTAGTCAATTTCAACCTATGATTTACACTCCCTTATGCTTCTGGGATCTGTCTCCGGGCGAGTGTGAGGGGAGAGGTCAGCTCCCTTTCCTGGCAGCCGTGTGCTAAGGAAGGTCTCTGGGTTAGGCAGCTGGGCCATGCAACTGCTGCAGGCTGCCTTTCTCTGTCTGAAGCCCCAGGCCCCACTGCTGCCGTGGCCTGTTTAACGAGCTGTCAGAGGCGGCTGCAGTCCCACGTGCCTTCCTGTGTTGACTCCAAAGGCTATTTTAAGCAGGGAAGATGGTGGGAAAC... | ATCAGGAGACACAAGTTGTGTCTCCAGTGCTTAGTCAATTTCAACCTATGATTTACACTCCCTTATGCTTCTGGGATCTGTCTCCGGGCGAGTGTGAGGGGAGAGGTCAGCTCCCTTTCCTGGCAGCCGTGTGCTAAGGAAGGTCTCTGGGTTAGGCAGCTGGGCCATGCAACTGCTGCAGGCTGCCTTTCTCTGTCTGAAGCCCCAGGCCCCACTGCTGCCGTGGCCTGTTTAACGAGCTGTCAGAGGCGGCTGCAGTCCCACGTGCCTTCCTGTGTTGACTCCAAAGGCTATTTTAAGCAGGGAAGATGGTGGGAAAC... |
Task1_train_34697 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | TTGTGTCTCCAGTGCTTAGTCAATTTCAACCTATGATTTACACTCCCTTATGCTTCTGGGATCTGTCTCCGGGCGAGTGTGAGGGGAGAGGTCAGCTCCCTTTCCTGGCAGCCGTGTGCTAAGGAAGGTCTCTGGGTTAGGCAGCTGGGCCATGCAACTGCTGCAGGCTGCCTTTCTCTGTCTGAAGCCCCAGGCCCCACTGCTGCCGTGGCCTGTTTAACGAGCTGTCAGAGGCGGCTGCAGTCCCACGTGCCTTCCTGTGTTGACTCCAAAGGCTATTTTAAGCAGGGAAGATGGTGGGAAACAGGAAGTGTCCCAGC... | TTGTGTCTCCAGTGCTTAGTCAATTTCAACCTATGATTTACACTCCCTTATGCTTCTGGGATCTGTCTCCGGGCGAGTGTGAGGGGAGAGGTCAGCTCCCTTTCCTGGCAGCCGTGTGCTAAGGAAGGTCTCTGGGTTAGGCAGCTGGGCCATGCAACTGCTGCAGGCTGCCTTTCTCTGTCTGAAGCCCCAGGCCCCACTGCTGCCGTGGCCTGTTTAACGAGCTGTCAGAGGCGGCTGCAGTCCCACGTGCCTTCCTGTGTTGACTCCAAAGGCTATTTTAAGCAGGGAAGATGGTGGGAAACAGGAAGTGTCCCAGC... |
Task1_train_34698 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCAGTCTGGCCCCAACCTGCCCTTACCCACTGCACATACAACCCTCTGCAAGTCGGGAAGCCAATAGTTTCAGTGAGTGTCTTTAGTCTTGGGCAACTGGTAACCCAACTTGGGAGAAGAGAACATCAGAGGGAGTCTCACCCACAGCCATGCAAATGACACCCAAGATCAGAGTCCACTCTCCCCTCCCGTCTCTTGCCACCCTAGGTCACTCTCTGAAAACTCTTCCCAGACCCTTCCAGGCACTCATCATGGCTACACCCAGGTCCCCACGGCTCTCGGCACCACCTCTCTCCCAGCCAGGGAGAGAAAGCCACTCT... | GCAGTCTGGCCCCAACCTGCCCTTACCCACTGCACATACAACCCTCTGCAAGTCGGGAAGCCAATAGTTTCAGTGAGTGTCTTTAGTCTTGGGCAACTGGTAACCCAACTTGGGAGAAGAGAACATCAGAGGGAGTCTCACCCACAGCCATGCAAATGACACCCAAGATCAGAGTCCACTCTCCCCTCCCGTCTCTTGCCACCCTAGGTCACTCTCTGAAAACTCTTCCCAGACCCTTCCAGGCACTCATCATGGCTACACCCAGGTCCCCACGGCTCTCGGCACCACCTCTCTCCCAGCCAGGGAGAGAAAGCCACTCT... |
Task1_train_34699 | Located on Chromosome 2, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GATCCTTACCCTCCAGCCCCATCCAGAGACACATAGTAAGACCTCAGAGGCACACATCCATTTTTCTCATTCCCTGAAGTTCAAGTTGAAACCTATGTGAATGACACTGTGAAGGTGTGTGCTCTTCCCCAATTCACTGACGTCGCTCCTGATCTACTCTCTACCCTGATCTGCATCCCTGAAGGCAGACTTTTATTTACTATGTCATCCAGACCCCCTTAGTCTCTGGCTCAGGATAGCTTTGGCCTTTGGCTAGTAAGGAGGGACTGGCAGGGTATGAGAGGGAGGGAGAGAGAAGGGCAAGGTGCCAGTGGCTACAT... | GATCCTTACCCTCCAGCCCCATCCAGAGACACATAGTAAGACCTCAGAGGCACACATCCATTTTTCTCATTCCCTGAAGTTCAAGTTGAAACCTATGTGAATGACACTGTGAAGGTGTGTGCTCTTCCCCAATTCACTGACGTCGCTCCTGATCTACTCTCTACCCTGATCTGCATCCCTGAAGGCAGACTTTTATTTACTATGTCATCCAGACCCCCTTAGTCTCTGGCTCAGGATAGCTTTGGCCTTTGGCTAGTAAGGAGGGACTGGCAGGGTATGAGAGGGAGGGAGAGAGAAGGGCAAGGTGCCAGTGGCTACAT... |
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