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_33300 | A variant on Chromosome 1 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCGTGGCGGCATGCGCCTGTAGTCCCAGCTGCTGGGGAGGCTGAAGCAGGAGAATGGCGTGAATCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGGACTCCAGCCTGGGTGACAGAGCAAGACTCCGTCTCAAAAAAAATAAAATAAAAATAAAAATAAAATAAAAACATAGTACACATTACGACTTAAGTAGTTGAAATTTGTGCCAAGTTTGAGCAACAAATGAGTT... | TCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCGTGGCGGCATGCGCCTGTAGTCCCAGCTGCTGGGGAGGCTGAAGCAGGAGAATGGCGTGAATCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGGACTCCAGCCTGGGTGACAGAGCAAGACTCCGTCTCAAAAAAAATAAAATAAAAATAAAAATAAAATAAAAACATAGTACACATTACGACTTAAGTAGTTGAAATTTGTGCCAAGTTTGAGCAACAAATGAGTT... |
Task1_train_33301 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GCGGCATGCGCCTGTAGTCCCAGCTGCTGGGGAGGCTGAAGCAGGAGAATGGCGTGAATCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGGACTCCAGCCTGGGTGACAGAGCAAGACTCCGTCTCAAAAAAAATAAAATAAAAATAAAAATAAAATAAAAACATAGTACACATTACGACTTAAGTAGTTGAAATTTGTGCCAAGTTTGAGCAACAAATGAGTTGCTCAAAAACATTTTAAGGTGATTACTTGGAAGAATAAACAAACACCTTCAAACTTTTCAGAATCGCTCATTGTAACTGGTATCCA... | GCGGCATGCGCCTGTAGTCCCAGCTGCTGGGGAGGCTGAAGCAGGAGAATGGCGTGAATCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGGACTCCAGCCTGGGTGACAGAGCAAGACTCCGTCTCAAAAAAAATAAAATAAAAATAAAAATAAAATAAAAACATAGTACACATTACGACTTAAGTAGTTGAAATTTGTGCCAAGTTTGAGCAACAAATGAGTTGCTCAAAAACATTTTAAGGTGATTACTTGGAAGAATAAACAAACACCTTCAAACTTTTCAGAATCGCTCATTGTAACTGGTATCCA... |
Task1_train_33302 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | TCCATAAATCTGCATAGATAGTACATACCATTTCTTTATGGTATGGTATGTGGTATATGATATGGACTGCCTGGATTTGTATCTCAGCCCAACTACTTTTAGATATATAATTTTGGAAAAATTACCAATTTTGGTTCCCCCCCCCCCTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCAGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCCTTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCACGCCTGGCTAATTTTTTATATAT... | TCCATAAATCTGCATAGATAGTACATACCATTTCTTTATGGTATGGTATGTGGTATATGATATGGACTGCCTGGATTTGTATCTCAGCCCAACTACTTTTAGATATATAATTTTGGAAAAATTACCAATTTTGGTTCCCCCCCCCCCTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCAGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCCTTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCACGCCTGGCTAATTTTTTATATAT... |
Task1_train_33303 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TCTAGTCTTTCTTCCTTCATTCTAATGACATGCTTTTCAACTTATTATTACCCTGGTTACCCCCCTTCAGATGACTTATTTTAACCCAATTGCAGAAGTTTACATTTATCCATATTAGTTTGGTTTACGATTGCAGCCTATAAAAATAAATTCATCTCATAATTTGGTCATTTGTTGGGTCAGCCATGCCTCCCAGCTTTCTGTCATCTGCAAGTTTGATAAGCATATCTTTGTGTCATCATCCTAAAATAATGGACAAGACCAAGGACAAAGCCTCATGTTCGTCTTCTCTTTCTTTCTTTTTTTTTTTTTTTTTCTGA... | TCTAGTCTTTCTTCCTTCATTCTAATGACATGCTTTTCAACTTATTATTACCCTGGTTACCCCCCTTCAGATGACTTATTTTAACCCAATTGCAGAAGTTTACATTTATCCATATTAGTTTGGTTTACGATTGCAGCCTATAAAAATAAATTCATCTCATAATTTGGTCATTTGTTGGGTCAGCCATGCCTCCCAGCTTTCTGTCATCTGCAAGTTTGATAAGCATATCTTTGTGTCATCATCCTAAAATAATGGACAAGACCAAGGACAAAGCCTCATGTTCGTCTTCTCTTTCTTTCTTTTTTTTTTTTTTTTTCTGA... |
Task1_train_33304 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | GATTTTGGCTATTCTAGGTTTTTTGCATTTCCGTGTAACTTTTAGAATCAGTTTGTTAGTTTCAACAACAACAACAACAAAAAGCCTGGTAGGATTTTCATTAGAATGGTATTGAATCTGTAGGTTAGTCAGTCTGGGGAGAATTCACATCTTAACAGTGTTGCCTTTTCTAATTCATGAACATGATATATTTTTCTATTTATTTAAATCTTTGAATATTTCTCTCATTAGTATTTCATTGTAGAGGTCTTATACATTTTAAAATTTATTCCCAAATGTTTTATGGTTTTTGATGCTAAAATTTTTTTTTTTCAGTTTCC... | GATTTTGGCTATTCTAGGTTTTTTGCATTTCCGTGTAACTTTTAGAATCAGTTTGTTAGTTTCAACAACAACAACAACAAAAAGCCTGGTAGGATTTTCATTAGAATGGTATTGAATCTGTAGGTTAGTCAGTCTGGGGAGAATTCACATCTTAACAGTGTTGCCTTTTCTAATTCATGAACATGATATATTTTTCTATTTATTTAAATCTTTGAATATTTCTCTCATTAGTATTTCATTGTAGAGGTCTTATACATTTTAAAATTTATTCCCAAATGTTTTATGGTTTTTGATGCTAAAATTTTTTTTTTTCAGTTTCC... |
Task1_train_33305 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AAAATATCAACTTTATTGATGTATAATTTATAAACAATAAAATGTACCTATTTTAAGTATGCAATTTGGTGAGTTTTCTCTCACACACACACACACACACACACACACACACACACATCTCCCTATAACCATCACCACAATCCAGAAATAGCATATTTCCTCATGTCTCTTTGCAACCAGTCCCTAATCTCAGTCCTGGGGAACCACTGATCTGCTTTGGGTGAAGATGTTTCATTTTTACCCAGAATGATATTAGTTACTGTCTTTTCTTCTATAACGTGGGTATAGCCCAAAGTAGTTTTATTGCTGTCTCTACATAG... | AAAATATCAACTTTATTGATGTATAATTTATAAACAATAAAATGTACCTATTTTAAGTATGCAATTTGGTGAGTTTTCTCTCACACACACACACACACACACACACACACACACACATCTCCCTATAACCATCACCACAATCCAGAAATAGCATATTTCCTCATGTCTCTTTGCAACCAGTCCCTAATCTCAGTCCTGGGGAACCACTGATCTGCTTTGGGTGAAGATGTTTCATTTTTACCCAGAATGATATTAGTTACTGTCTTTTCTTCTATAACGTGGGTATAGCCCAAAGTAGTTTTATTGCTGTCTCTACATAG... |
Task1_train_33306 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TAAGAAGGCCTCACAAGGCCGCTGTTGGTGCGCAGAGGCTCTCTTAAAAGTTTGTGTGCAGGTGCTCTCAGAGACATGGCCCTGCTGAGAGATTGTGTTTCCAAGTGTCAGTTGGGGTTGAATCCAACTCACAATGACTCCTTTGTCATCTTTCCCAATTTTCCATCCTCCAGAGGGCCTCCAGGGGACCCTGGATACAGCATAGTCTTTATGTGGTTTGGGGTTCCACAGCCAGACCCTGTCTCTCCAGAAAACACCCATGTCAGCCTGTGCCCTGGTCCTTGCTGCTTCTATTTCTCAATGACTGTGTTTCCATCTCC... | TAAGAAGGCCTCACAAGGCCGCTGTTGGTGCGCAGAGGCTCTCTTAAAAGTTTGTGTGCAGGTGCTCTCAGAGACATGGCCCTGCTGAGAGATTGTGTTTCCAAGTGTCAGTTGGGGTTGAATCCAACTCACAATGACTCCTTTGTCATCTTTCCCAATTTTCCATCCTCCAGAGGGCCTCCAGGGGACCCTGGATACAGCATAGTCTTTATGTGGTTTGGGGTTCCACAGCCAGACCCTGTCTCTCCAGAAAACACCCATGTCAGCCTGTGCCCTGGTCCTTGCTGCTTCTATTTCTCAATGACTGTGTTTCCATCTCC... |
Task1_train_33307 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGGTGTGTGGGCAGCACTGAAAGAAGGCTGCTGTGGCCGGAGGGAGGGAGGTGAGGCTGCAGAGACAGGCCGGGGGCGGAGGTGAGCGCTCATGGGCTCAGAGGCCTTGGCGAGGGCAGGGTTTGGAGGTTGGTGTTGGCATTTTGAGAAGCCACTGGAGAGGCTAACGGAAGTGACAGTTGGTTAACACTTTAGAAAGGTGGAGGATGGGCTACTGCAGGCAGGGGGAGGCAGGGCAGCTGAGGAGCAAGCTGCATGCTCGCCCAGCAGTGGTGGTTGGGCCTGGACTAGGGTTGTCAGTGTGCCCCTGGAGGAAGTGG... | TGGTGTGTGGGCAGCACTGAAAGAAGGCTGCTGTGGCCGGAGGGAGGGAGGTGAGGCTGCAGAGACAGGCCGGGGGCGGAGGTGAGCGCTCATGGGCTCAGAGGCCTTGGCGAGGGCAGGGTTTGGAGGTTGGTGTTGGCATTTTGAGAAGCCACTGGAGAGGCTAACGGAAGTGACAGTTGGTTAACACTTTAGAAAGGTGGAGGATGGGCTACTGCAGGCAGGGGGAGGCAGGGCAGCTGAGGAGCAAGCTGCATGCTCGCCCAGCAGTGGTGGTTGGGCCTGGACTAGGGTTGTCAGTGTGCCCCTGGAGGAAGTGG... |
Task1_train_33308 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TAGCCCCTCTCCCATCTTTGTCCCCTTTGCTGGGACACTGGCCTACTCCCATAGTCCCCTAGAGCCACCCCTTCCTCCAGTCCTGGTGGTGGGGAGGTCATGCTCCACAGGTTTTTTCCTGGGAAATCAGTACTGTGAGTGCATGTGAGATGGGGAACTGGCTTCACTTCCGAAATCCCTTTCCCCACCACTCACTTCATTCTGTCCCCTGCACACAAGCTTTGCAGCATGCACTATATTCAAATTCATGCATCAGCAAAATTGTAAATTACTGCATGTTATGAATCCTCAGGTTGTTTGCAAAGAATCATAACTGTTCT... | TAGCCCCTCTCCCATCTTTGTCCCCTTTGCTGGGACACTGGCCTACTCCCATAGTCCCCTAGAGCCACCCCTTCCTCCAGTCCTGGTGGTGGGGAGGTCATGCTCCACAGGTTTTTTCCTGGGAAATCAGTACTGTGAGTGCATGTGAGATGGGGAACTGGCTTCACTTCCGAAATCCCTTTCCCCACCACTCACTTCATTCTGTCCCCTGCACACAAGCTTTGCAGCATGCACTATATTCAAATTCATGCATCAGCAAAATTGTAAATTACTGCATGTTATGAATCCTCAGGTTGTTTGCAAAGAATCATAACTGTTCT... |
Task1_train_33309 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GACCTCAAGTGATCCACCCGCCTCAGCCTCCCAAAATGCTGGGATTACAGGTGTGAGCCACCGCTCCTGGTCAATAATGCCATTGTGTTAGGGACAGGATTATTGGGGGGAGTGTGTTTGAAAGCACTTGCAGTCCCGCCTGGCATAGAGCAGATGCCTAATCGGCGTTCCTGACTGGTCAAGGTCTCCCTTTGAGCTCAACCCCATGCTGTGGTCCTGTGGCTTGTGCATCAGGGGTCAGGGGTGAGGTTGGATGCAGCACCTTCTACTGGAGGTCAGATCCTGCTTGGTGTCTTCCTGATGTCTATCATCCTCATTGG... | GACCTCAAGTGATCCACCCGCCTCAGCCTCCCAAAATGCTGGGATTACAGGTGTGAGCCACCGCTCCTGGTCAATAATGCCATTGTGTTAGGGACAGGATTATTGGGGGGAGTGTGTTTGAAAGCACTTGCAGTCCCGCCTGGCATAGAGCAGATGCCTAATCGGCGTTCCTGACTGGTCAAGGTCTCCCTTTGAGCTCAACCCCATGCTGTGGTCCTGTGGCTTGTGCATCAGGGGTCAGGGGTGAGGTTGGATGCAGCACCTTCTACTGGAGGTCAGATCCTGCTTGGTGTCTTCCTGATGTCTATCATCCTCATTGG... |
Task1_train_33310 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ACCCACCAATTGCGGACACACCACCACCCATAATGCCACCTTGAAACCACTTTGTCTCCGTCAGGCCCTAAGCTTCTTGGACAAGCGGAGAGAAGTTCAATGTGGGAACAGCAGGGAGGGCCAAACAGTTTTGTTTCATTTTGGTTTACTTTTAACCCTTATTACAATCCTTATAACTAGTAAGTAGAAAAAGAATAAGAAAATGGTTAACAGCAGTGGTTTGACATAATAGGAAAAGCACTGTGCTTTAAAAAAAAAAAAAATTTCGGCCGGCCATGGTGGCTCACACCTGTAATCCCAGCAATTTGGGAGGCCGAGGT... | ACCCACCAATTGCGGACACACCACCACCCATAATGCCACCTTGAAACCACTTTGTCTCCGTCAGGCCCTAAGCTTCTTGGACAAGCGGAGAGAAGTTCAATGTGGGAACAGCAGGGAGGGCCAAACAGTTTTGTTTCATTTTGGTTTACTTTTAACCCTTATTACAATCCTTATAACTAGTAAGTAGAAAAAGAATAAGAAAATGGTTAACAGCAGTGGTTTGACATAATAGGAAAAGCACTGTGCTTTAAAAAAAAAAAAAATTTCGGCCGGCCATGGTGGCTCACACCTGTAATCCCAGCAATTTGGGAGGCCGAGGT... |
Task1_train_33311 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GAAAAAGAGAAGAGAAAAATTCTTGTGTCATTACTCAATATATGCTATTTGGTTTTGTAATTATTCGTGTCATTATTTTATATCTTCCTCTACGTGGGCTGAAAATTCCTAGAGGGGAGGAACTCTGGGTCTCAGAGCCTGCTGTCTCAGTTACCATCAGTTGTGGGCACAGGTAATGCTATTGAGCCATCACATCCTCTGGAGATTGTGAATTGGTCATGATCAAGCCCACTCTTCACTGGTATTTTTCCTAAATAAATTCATTGCTTGACCAACCCCGGGGCAGGATCAGGCCCAGGGTTCCACATGGACTCCAAGAA... | GAAAAAGAGAAGAGAAAAATTCTTGTGTCATTACTCAATATATGCTATTTGGTTTTGTAATTATTCGTGTCATTATTTTATATCTTCCTCTACGTGGGCTGAAAATTCCTAGAGGGGAGGAACTCTGGGTCTCAGAGCCTGCTGTCTCAGTTACCATCAGTTGTGGGCACAGGTAATGCTATTGAGCCATCACATCCTCTGGAGATTGTGAATTGGTCATGATCAAGCCCACTCTTCACTGGTATTTTTCCTAAATAAATTCATTGCTTGACCAACCCCGGGGCAGGATCAGGCCCAGGGTTCCACATGGACTCCAAGAA... |
Task1_train_33312 | A mutation is present on Chromosome 1. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CCTACGGAAAGATGGTGCTGCCTCTGACCATGGACCACTTCGTAGCCTTGACATCGTGCATGGCAGAGCACTTGCTCCGCTGCATGTTTTGTGAAGCTGGGTCAGGTTCTGCTATGGGAGTCATGAGCTGGGGAGCCACACCCAATGAATGTGCTATGCTAGCCCTAGAAATGACTCGGGGGAGGGGAAGAAAACTACTCAGCAACATCTACAGGATTTCCAAAATAGGAATCTGAAGGATGTGTAGGTGGAAGTTTGCGTGCCTGTGAGGCATGGTGTTTGAGCATCTGGAGCTGTGGATCATGTGAAATGGCATAACC... | CCTACGGAAAGATGGTGCTGCCTCTGACCATGGACCACTTCGTAGCCTTGACATCGTGCATGGCAGAGCACTTGCTCCGCTGCATGTTTTGTGAAGCTGGGTCAGGTTCTGCTATGGGAGTCATGAGCTGGGGAGCCACACCCAATGAATGTGCTATGCTAGCCCTAGAAATGACTCGGGGGAGGGGAAGAAAACTACTCAGCAACATCTACAGGATTTCCAAAATAGGAATCTGAAGGATGTGTAGGTGGAAGTTTGCGTGCCTGTGAGGCATGGTGTTTGAGCATCTGGAGCTGTGGATCATGTGAAATGGCATAACC... |
Task1_train_33313 | An alteration has been detected on Chromosome 1. Is it pathogenic, and if so, what disease is involved? | Benign | TTTACTTACAGTTCTGATAAGTGCTAGAAAGAGTTTACAGAGTGGTAGGGGAGTTGGAGAGAAGTGTTCTGCACTCTTAGAGTGGCCTCTACTAAAATCTCGAGGCAGAAACAAGCCTAGCCTATCCAATGAACTAAAAAAGGCCGCCATGTCTGGAGTTCAGGGAGCAAAGGGGAAAGTGGTACAAGAGGAGGCTAGTGACGTAGGGACCAGATCATGAGGGAGGCTGTGTTCAGAATTCTGGACTTTATGCCCCGGCTTGACAAGGTTTTCAAAGTAGGAGATCACTCTGGGTTCCAGTTATTTAACTCTGTGAGATT... | TTTACTTACAGTTCTGATAAGTGCTAGAAAGAGTTTACAGAGTGGTAGGGGAGTTGGAGAGAAGTGTTCTGCACTCTTAGAGTGGCCTCTACTAAAATCTCGAGGCAGAAACAAGCCTAGCCTATCCAATGAACTAAAAAAGGCCGCCATGTCTGGAGTTCAGGGAGCAAAGGGGAAAGTGGTACAAGAGGAGGCTAGTGACGTAGGGACCAGATCATGAGGGAGGCTGTGTTCAGAATTCTGGACTTTATGCCCCGGCTTGACAAGGTTTTCAAAGTAGGAGATCACTCTGGGTTCCAGTTATTTAACTCTGTGAGATT... |
Task1_train_33314 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTCTAGAATAACTGGAATATGACATAAACCACCTTCTCTAAGATAAAGCCCTTCTCCACTTCAAAGCCAAGACTCATAAAGATATATCCTAAGGGTAAAGCCATTTCTGCAGTCAAGTGAAATGATGGGATGTTGGACTGGGTTTGAGTTCCTCCAAAAACGGCGTTGCTTTGGGGGAGTTCATCATAGGGACCACTTCTGGGGATTCCTTTATTTATATAAAAACCAAAAAGCATCTTTCTCTAAAGAGGACCAGCCCCTCAGGCCTTCTTTTCAGTATTTGCATATGGCTTTGAGGGTAGGACAGGTTAGTCTTTTTC... | TTCTAGAATAACTGGAATATGACATAAACCACCTTCTCTAAGATAAAGCCCTTCTCCACTTCAAAGCCAAGACTCATAAAGATATATCCTAAGGGTAAAGCCATTTCTGCAGTCAAGTGAAATGATGGGATGTTGGACTGGGTTTGAGTTCCTCCAAAAACGGCGTTGCTTTGGGGGAGTTCATCATAGGGACCACTTCTGGGGATTCCTTTATTTATATAAAAACCAAAAAGCATCTTTCTCTAAAGAGGACCAGCCCCTCAGGCCTTCTTTTCAGTATTTGCATATGGCTTTGAGGGTAGGACAGGTTAGTCTTTTTC... |
Task1_train_33315 | Given this context: Chromosome 1 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTTATTTATATAAAAACCAAAAAGCATCTTTCTCTAAAGAGGACCAGCCCCTCAGGCCTTCTTTTCAGTATTTGCATATGGCTTTGAGGGTAGGACAGGTTAGTCTTTTTCCCCACCTTATCCCTGGAGCCCGGCCCAGTGCCCAGCATGTAATTCTAGAAGCAGTTTCTGATTGATTCAGGTTCCCCAACCCAAGGAACTCAACGTTTGATCAGCTCCCACTACTTTGTCTTTCCCTTTTCCAATTGCTTATGACCTCGGACACTCAGAACCACTGATGTGAAACCACCCACCTGGGTGCTCTCTCGGTGGTGACTTTC... | TTTATTTATATAAAAACCAAAAAGCATCTTTCTCTAAAGAGGACCAGCCCCTCAGGCCTTCTTTTCAGTATTTGCATATGGCTTTGAGGGTAGGACAGGTTAGTCTTTTTCCCCACCTTATCCCTGGAGCCCGGCCCAGTGCCCAGCATGTAATTCTAGAAGCAGTTTCTGATTGATTCAGGTTCCCCAACCCAAGGAACTCAACGTTTGATCAGCTCCCACTACTTTGTCTTTCCCTTTTCCAATTGCTTATGACCTCGGACACTCAGAACCACTGATGTGAAACCACCCACCTGGGTGCTCTCTCGGTGGTGACTTTC... |
Task1_train_33316 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCTATTCCTTCAGTGTAGCTGAGGTTAACACTAAACTATCCAAATACTAAACTATCAGAGGAAACAAATCAAAACCAATACACAAATTTACAAAACATAGAACTTCTTCCAATATAAGTAAAATCCAGCCACAGAACAGGCTTGGCTTCCACAGTTTGTTTTTCTCTTTGTCTTTCATCCTAGCTGTGGTCTTAACTCAAACCCACCGCCCCTCCCCACCAAAAGAAAACTCATTACACATTTAGATTTGAGGATGAAACAAGGTTACAATATATTTTTTTAGAAGGCTAGCAGTTTCCTACACAAAAGCTGATTCAAGC... | TCTATTCCTTCAGTGTAGCTGAGGTTAACACTAAACTATCCAAATACTAAACTATCAGAGGAAACAAATCAAAACCAATACACAAATTTACAAAACATAGAACTTCTTCCAATATAAGTAAAATCCAGCCACAGAACAGGCTTGGCTTCCACAGTTTGTTTTTCTCTTTGTCTTTCATCCTAGCTGTGGTCTTAACTCAAACCCACCGCCCCTCCCCACCAAAAGAAAACTCATTACACATTTAGATTTGAGGATGAAACAAGGTTACAATATATTTTTTTAGAAGGCTAGCAGTTTCCTACACAAAAGCTGATTCAAGC... |
Task1_train_33317 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | AGTCTCAGTTTTCTAGAGACTCCTTATAGAAACATTTGTGAGGATTAAAAACAATAACAGAGTCAACTTCAGAAACAAGTTACTGGATTTTATTATACCCCAAAACAAGGAAGAGAGTGGGTGCATTACTAAGGCAGTGACTCAGTGTTCAGGACTGTTGTTGTCACCCAGAGAGATTCACAAAACCTCCAACCTGTCCAGCAATACATTTAGAAGAAACAGGATTAGGGAAGACTCTGGAAGCAAAGAAGGCTTTATTAAACATAACCATGATCCATAGCTGGAGTATACATAGGAAATTTGGTAACTTGGATAAGGCA... | AGTCTCAGTTTTCTAGAGACTCCTTATAGAAACATTTGTGAGGATTAAAAACAATAACAGAGTCAACTTCAGAAACAAGTTACTGGATTTTATTATACCCCAAAACAAGGAAGAGAGTGGGTGCATTACTAAGGCAGTGACTCAGTGTTCAGGACTGTTGTTGTCACCCAGAGAGATTCACAAAACCTCCAACCTGTCCAGCAATACATTTAGAAGAAACAGGATTAGGGAAGACTCTGGAAGCAAAGAAGGCTTTATTAAACATAACCATGATCCATAGCTGGAGTATACATAGGAAATTTGGTAACTTGGATAAGGCA... |
Task1_train_33318 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | GACAGTGAGCAAGATGGGGAAAGCCTTGAACATTCTTTTTTTCCTGGTTAAAATAGAATGCCCTCCAATTGCCCATAGGAAATAAGGTAATGAACTGTGACGGTTAATATTGAGTGTCAACTTGATTGAGTTGAAGGATACAAAGTATTGTGACTGGGTGTGTCTGTGAGGGTGTTGCCGAAGGAGAGCAACATTTGAGTCAGTGGACTGGGAGAGGCAGACCCACATTCAGTCACGGTGGGCACCATCTAATCAGCTGCCAGCATGGCTAAAATAAAGCAGGCAGAAAATGAAAGAGCAGACAACTTGCTAAGACTTCT... | GACAGTGAGCAAGATGGGGAAAGCCTTGAACATTCTTTTTTTCCTGGTTAAAATAGAATGCCCTCCAATTGCCCATAGGAAATAAGGTAATGAACTGTGACGGTTAATATTGAGTGTCAACTTGATTGAGTTGAAGGATACAAAGTATTGTGACTGGGTGTGTCTGTGAGGGTGTTGCCGAAGGAGAGCAACATTTGAGTCAGTGGACTGGGAGAGGCAGACCCACATTCAGTCACGGTGGGCACCATCTAATCAGCTGCCAGCATGGCTAAAATAAAGCAGGCAGAAAATGAAAGAGCAGACAACTTGCTAAGACTTCT... |
Task1_train_33319 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGGTATGCAGGGACGTCAGGGCAGGAAATAAGACTGCGGGGCTCAGGAATTTACCCTTGCACGTCCTCTCACCTAAAATCAAAGAATCTGCTGTAAGAGGGGCCACCCTCTCTCATCTGACTGCACTACATTTCCTCTCAGACGGGTTTCCGCCAGCGGAACACCTCCCCACACACATCCCCCCAGCCCCACAAATGTCCACTTGTCCTTAGCAGGGGCGACAAACCAAGGATGGACAAGAACAAATTGTTGGTGGCTTCATGTTGTTGATTATTGGTTAGGAGTTCCTGATTCCCCAACCACTGGCCATCAAATATAAA... | TGGTATGCAGGGACGTCAGGGCAGGAAATAAGACTGCGGGGCTCAGGAATTTACCCTTGCACGTCCTCTCACCTAAAATCAAAGAATCTGCTGTAAGAGGGGCCACCCTCTCTCATCTGACTGCACTACATTTCCTCTCAGACGGGTTTCCGCCAGCGGAACACCTCCCCACACACATCCCCCCAGCCCCACAAATGTCCACTTGTCCTTAGCAGGGGCGACAAACCAAGGATGGACAAGAACAAATTGTTGGTGGCTTCATGTTGTTGATTATTGGTTAGGAGTTCCTGATTCCCCAACCACTGGCCATCAAATATAAA... |
Task1_train_33320 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCTGAACTCTATCGTTCCACTGGCCATGGGGGCCACTGTACCAACTGCCAGGATAACACAGATGGCGCCCACTGTGAGAGGTGCCGAGAGAACTTCTTCCGCCTTGGCAACAATGAAGCCTGCTCTTCATGCCACTGTAGTCCTGTGGGTAAGTGACAGGAAGATGGATTGAAAGACAAAATGATAGTTCCGTGGACCCCCGGAAAGGAAAGCTTTGTTTCCAAGGCATTTGGACAACTAAATGTGGAGATGTATACATTATTGTAACACAGAAATCAGTCAAGATCTGTCTCTACCCCATGCCTCCACCTTTTTTAACC... | CCTGAACTCTATCGTTCCACTGGCCATGGGGGCCACTGTACCAACTGCCAGGATAACACAGATGGCGCCCACTGTGAGAGGTGCCGAGAGAACTTCTTCCGCCTTGGCAACAATGAAGCCTGCTCTTCATGCCACTGTAGTCCTGTGGGTAAGTGACAGGAAGATGGATTGAAAGACAAAATGATAGTTCCGTGGACCCCCGGAAAGGAAAGCTTTGTTTCCAAGGCATTTGGACAACTAAATGTGGAGATGTATACATTATTGTAACACAGAAATCAGTCAAGATCTGTCTCTACCCCATGCCTCCACCTTTTTTAACC... |
Task1_train_33321 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TCAACATGAAAGCCAAAATGGTCCTTTCAAAATGTACCTCAGATTACACCACTTTTAAACCCTCCAATAGCTTCTTGATACACTAAAACCAAATCCTTTACTCTGACCTCCATGCTTCTACATGGGTTTGAACTGCTTCCATGGCTTATCTTGTTTTTCTGAAACTTTCTTCCCTTGGATATTATCCTGGCTGGTCTCTTCTCTGTCTTTCCATTGCTATCCCAATGTCTCCTTCTTACAGAGGCTTTCCCTACCCACCAATATAAAGTAGCCCTCACCTTCACCCCATCATGCTGCTCTATTTTGTTTAAATTTTTTAT... | TCAACATGAAAGCCAAAATGGTCCTTTCAAAATGTACCTCAGATTACACCACTTTTAAACCCTCCAATAGCTTCTTGATACACTAAAACCAAATCCTTTACTCTGACCTCCATGCTTCTACATGGGTTTGAACTGCTTCCATGGCTTATCTTGTTTTTCTGAAACTTTCTTCCCTTGGATATTATCCTGGCTGGTCTCTTCTCTGTCTTTCCATTGCTATCCCAATGTCTCCTTCTTACAGAGGCTTTCCCTACCCACCAATATAAAGTAGCCCTCACCTTCACCCCATCATGCTGCTCTATTTTGTTTAAATTTTTTAT... |
Task1_train_33322 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TACTTAAGATATAGGCTGGGTGCCCTGGGTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCTGGTGGATCATGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAATCCCGTCTCTACTAAAATACAAAAAATTAGCCAGGTGTGGTGGCACATGCCTGTAGTCCCAGCTACTCAGGAGACTGAGGTAGGGGAATCGCTTGAACCAGGGAGGCAGAGGTTGCAGTGAGCCAAAAAAAAAAAAAAAAAAAAAGATATACAGATCATGGCCAGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGG... | TACTTAAGATATAGGCTGGGTGCCCTGGGTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCTGGTGGATCATGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAATCCCGTCTCTACTAAAATACAAAAAATTAGCCAGGTGTGGTGGCACATGCCTGTAGTCCCAGCTACTCAGGAGACTGAGGTAGGGGAATCGCTTGAACCAGGGAGGCAGAGGTTGCAGTGAGCCAAAAAAAAAAAAAAAAAAAAAGATATACAGATCATGGCCAGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGG... |
Task1_train_33323 | This variant is located on Chromosome 1. Evaluate its biological effect and specify any disease association. | Benign | ACACCAGGCAAACCTGCCACATGATTCCTAAGACCTATCTGTATTAAGAAGGTGCATGGAGGTATAAAAGGATTCTCTGCTGTTGGAGGCTTGATCTCCTTCCTTGTATCTTTGCTCTACCTCCACTTTCTAGACTAGTTTGATGTGAATGCTCCATTTGTCTTTTGTCTCTAGCTTGCAACTGTAACCCCATGGGCTCAGAGCCTGTAGGATGTCGAAGTGATGGCACCTGTGTTTGCAAGCCAGGATTTGGTGGCCCCAACTGTGAGCATGGAGCATTCAGCTGTCCAGCTTGCTATAATCAAGTGAAGATTCAGGTA... | ACACCAGGCAAACCTGCCACATGATTCCTAAGACCTATCTGTATTAAGAAGGTGCATGGAGGTATAAAAGGATTCTCTGCTGTTGGAGGCTTGATCTCCTTCCTTGTATCTTTGCTCTACCTCCACTTTCTAGACTAGTTTGATGTGAATGCTCCATTTGTCTTTTGTCTCTAGCTTGCAACTGTAACCCCATGGGCTCAGAGCCTGTAGGATGTCGAAGTGATGGCACCTGTGTTTGCAAGCCAGGATTTGGTGGCCCCAACTGTGAGCATGGAGCATTCAGCTGTCCAGCTTGCTATAATCAAGTGAAGATTCAGGTA... |
Task1_train_33324 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | ACTTTTTGATCTAATGAGGTTTTAAATACTTTCTTAGGAGTAGGGTCTTCTTTCTAGCACATTTGAGTTTCAATTTATTATAGATAGTTTTGCTTCTATTGGTTACAGGTAAAATCCCAGACAGAACTAAGAAAGACTCCAGTGTCTGAAGCCAGAAAAACACCTGTAACTCAAACCCCAACTCAAGCAAGTAACTCCCAGTTCATCCCCATTCATCACCCTGGAGCCTTCCCTCCTCTTCCCAGCAGGCCAGGTAAATATGTTTTGTAATTTCTTCTACTTAATCTTTTCTGTGCAAGAATTTCTATTCAGTCACTGAG... | ACTTTTTGATCTAATGAGGTTTTAAATACTTTCTTAGGAGTAGGGTCTTCTTTCTAGCACATTTGAGTTTCAATTTATTATAGATAGTTTTGCTTCTATTGGTTACAGGTAAAATCCCAGACAGAACTAAGAAAGACTCCAGTGTCTGAAGCCAGAAAAACACCTGTAACTCAAACCCCAACTCAAGCAAGTAACTCCCAGTTCATCCCCATTCATCACCCTGGAGCCTTCCCTCCTCTTCCCAGCAGGCCAGGTAAATATGTTTTGTAATTTCTTCTACTTAATCTTTTCTGTGCAAGAATTTCTATTCAGTCACTGAG... |
Task1_train_33325 | Here is a variant on Chromosome 1. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GCCTTCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGATATTACAGGCACCCGCCACTGTGCCCGGCTAATTTTTGTATTTTCAGTAGAGACAGGTTTTCACCATGTTGGCCAGGCTGGTCTCAAACTTCTGACCTCAGGTGATCTACCCATCCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCACGCCCAGCCCAAATTAATCATTTTAAAGTGAATGATTCAGTGGCATTTATCACATTCACAATGCTGTGCAACTACTGCCTCTCTCTAATTCCAAAATATTTTCATCACCTCAGAAG... | GCCTTCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGATATTACAGGCACCCGCCACTGTGCCCGGCTAATTTTTGTATTTTCAGTAGAGACAGGTTTTCACCATGTTGGCCAGGCTGGTCTCAAACTTCTGACCTCAGGTGATCTACCCATCCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCACGCCCAGCCCAAATTAATCATTTTAAAGTGAATGATTCAGTGGCATTTATCACATTCACAATGCTGTGCAACTACTGCCTCTCTCTAATTCCAAAATATTTTCATCACCTCAGAAG... |
Task1_train_33326 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | TATGCCTTCTTATAGCAGACGGAGCTGAAAGGAACCTTAAAGATGAACTAGCCCACATTTCTTGTTTTACAGATGAGGAAACAGATTACTTGCCTTGGACAGTATATCTTTATGCTCTTCTAACAGTCTTTTGTCTAAGGTTGGCCTGGACTTACGACCTGTGAGTAATCTTCTTTGTAGCCCTAGTCTTATCGAACCAGTACAAAAGTTTAACTGCCAAAGGCACTTTCTTTCCTATAGTTCTGACAACTTCTCCTTTTGTTATATACCACTGATATCCAGGTTCAGTTCATCATCTATTTCAGACCATGTTTCTAATT... | TATGCCTTCTTATAGCAGACGGAGCTGAAAGGAACCTTAAAGATGAACTAGCCCACATTTCTTGTTTTACAGATGAGGAAACAGATTACTTGCCTTGGACAGTATATCTTTATGCTCTTCTAACAGTCTTTTGTCTAAGGTTGGCCTGGACTTACGACCTGTGAGTAATCTTCTTTGTAGCCCTAGTCTTATCGAACCAGTACAAAAGTTTAACTGCCAAAGGCACTTTCTTTCCTATAGTTCTGACAACTTCTCCTTTTGTTATATACCACTGATATCCAGGTTCAGTTCATCATCTATTTCAGACCATGTTTCTAATT... |
Task1_train_33327 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ATGAACTAGCCCACATTTCTTGTTTTACAGATGAGGAAACAGATTACTTGCCTTGGACAGTATATCTTTATGCTCTTCTAACAGTCTTTTGTCTAAGGTTGGCCTGGACTTACGACCTGTGAGTAATCTTCTTTGTAGCCCTAGTCTTATCGAACCAGTACAAAAGTTTAACTGCCAAAGGCACTTTCTTTCCTATAGTTCTGACAACTTCTCCTTTTGTTATATACCACTGATATCCAGGTTCAGTTCATCATCTATTTCAGACCATGTTTCTAATTGGATTCTCTGTAGCCTGGTTCATGTTGTAGTCTGCCATTTTC... | ATGAACTAGCCCACATTTCTTGTTTTACAGATGAGGAAACAGATTACTTGCCTTGGACAGTATATCTTTATGCTCTTCTAACAGTCTTTTGTCTAAGGTTGGCCTGGACTTACGACCTGTGAGTAATCTTCTTTGTAGCCCTAGTCTTATCGAACCAGTACAAAAGTTTAACTGCCAAAGGCACTTTCTTTCCTATAGTTCTGACAACTTCTCCTTTTGTTATATACCACTGATATCCAGGTTCAGTTCATCATCTATTTCAGACCATGTTTCTAATTGGATTCTCTGTAGCCTGGTTCATGTTGTAGTCTGCCATTTTC... |
Task1_train_33328 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TAACTGCCAAAGGCACTTTCTTTCCTATAGTTCTGACAACTTCTCCTTTTGTTATATACCACTGATATCCAGGTTCAGTTCATCATCTATTTCAGACCATGTTTCTAATTGGATTCTCTGTAGCCTGGTTCATGTTGTAGTCTGCCATTTTCTGGCAACAAATTGGATCTATTTTAATAATGATCAGAGATGCTGGATTTGTCATGTTGGGATCTTTTTAACTCAGTATCCCAAATTGTGGACATAGGATTTCATGAAATAAAAATAAACCTCAACAGTACTTCTTTAAATAATACTCACTATATACCCAGAATAAAACT... | TAACTGCCAAAGGCACTTTCTTTCCTATAGTTCTGACAACTTCTCCTTTTGTTATATACCACTGATATCCAGGTTCAGTTCATCATCTATTTCAGACCATGTTTCTAATTGGATTCTCTGTAGCCTGGTTCATGTTGTAGTCTGCCATTTTCTGGCAACAAATTGGATCTATTTTAATAATGATCAGAGATGCTGGATTTGTCATGTTGGGATCTTTTTAACTCAGTATCCCAAATTGTGGACATAGGATTTCATGAAATAAAAATAAACCTCAACAGTACTTCTTTAAATAATACTCACTATATACCCAGAATAAAACT... |
Task1_train_33329 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGCACTTTCTTTCCTATAGTTCTGACAACTTCTCCTTTTGTTATATACCACTGATATCCAGGTTCAGTTCATCATCTATTTCAGACCATGTTTCTAATTGGATTCTCTGTAGCCTGGTTCATGTTGTAGTCTGCCATTTTCTGGCAACAAATTGGATCTATTTTAATAATGATCAGAGATGCTGGATTTGTCATGTTGGGATCTTTTTAACTCAGTATCCCAAATTGTGGACATAGGATTTCATGAAATAAAAATAAACCTCAACAGTACTTCTTTAAATAATACTCACTATATACCCAGAATAAAACTATATTCCAGTA... | GGCACTTTCTTTCCTATAGTTCTGACAACTTCTCCTTTTGTTATATACCACTGATATCCAGGTTCAGTTCATCATCTATTTCAGACCATGTTTCTAATTGGATTCTCTGTAGCCTGGTTCATGTTGTAGTCTGCCATTTTCTGGCAACAAATTGGATCTATTTTAATAATGATCAGAGATGCTGGATTTGTCATGTTGGGATCTTTTTAACTCAGTATCCCAAATTGTGGACATAGGATTTCATGAAATAAAAATAAACCTCAACAGTACTTCTTTAAATAATACTCACTATATACCCAGAATAAAACTATATTCCAGTA... |
Task1_train_33330 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AAGTGGCAGCAAATGTGAAATAAGCATAAGCAAAGTGCTTTCATTTAAGTGCTTAGAGGATTAATCAAGGAGCACTTCCTAGAAGTGTGTTTTGAAGATTTTAAGAGAAGGTACAAATATTCACTGGTGACGAGGATGGAGTCAGAAAGAGGGAAGTAAAACACACATTATGCATTGGGAGCTGCATTAGAAAGGGGAATGGATGCTAACAAAAAGAAAAAACATCTCTTGCAGGATGGTGAAGCAGGCTTTCAGCTGGGATGGAGAAGGGATGCTGAGTTACAATCATTGGTGAAGTTATTGAGATGTCATTTCAGCCT... | AAGTGGCAGCAAATGTGAAATAAGCATAAGCAAAGTGCTTTCATTTAAGTGCTTAGAGGATTAATCAAGGAGCACTTCCTAGAAGTGTGTTTTGAAGATTTTAAGAGAAGGTACAAATATTCACTGGTGACGAGGATGGAGTCAGAAAGAGGGAAGTAAAACACACATTATGCATTGGGAGCTGCATTAGAAAGGGGAATGGATGCTAACAAAAAGAAAAAACATCTCTTGCAGGATGGTGAAGCAGGCTTTCAGCTGGGATGGAGAAGGGATGCTGAGTTACAATCATTGGTGAAGTTATTGAGATGTCATTTCAGCCT... |
Task1_train_33331 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TTTTAGTTGCTATGTATTTAGCATTTTGTACTAGTAAATGTGTTTTTCATCAAATTTGGGGAAATTCTGGCCACCACTCTTTCTTCAAAAATTTTTTCTGTCCCTTTTTTTTTCTACTTCTGTTGTTTACATGCATGTTGGATTGTCTGACATGTAGCAAATCTCTGTTGGTCTACTCACTTTTTAAAGATAATTTTTCTCTTTGTTGTTTACTTTTAATAATTTCTATTGCTCTATCTTCAAGTTCCCTACTTTTTCTTTTGTAATTTTTTTTGGCTGTTAAATTCACCCAGTGAATTTTTTATTTCTAAAATTATAAT... | TTTTAGTTGCTATGTATTTAGCATTTTGTACTAGTAAATGTGTTTTTCATCAAATTTGGGGAAATTCTGGCCACCACTCTTTCTTCAAAAATTTTTTCTGTCCCTTTTTTTTTCTACTTCTGTTGTTTACATGCATGTTGGATTGTCTGACATGTAGCAAATCTCTGTTGGTCTACTCACTTTTTAAAGATAATTTTTCTCTTTGTTGTTTACTTTTAATAATTTCTATTGCTCTATCTTCAAGTTCCCTACTTTTTCTTTTGTAATTTTTTTTGGCTGTTAAATTCACCCAGTGAATTTTTTATTTCTAAAATTATAAT... |
Task1_train_33332 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TTTTTCCCCTCCCCAAAGTGAATTCTCCATCAGATTTACTACTCCCTGACTCAATTATATTTACCTGGAATATCTGAATGCAGGTATTTATCCTCTCAGAAAAGAATATGTTTACCTGGGATCTAAACATACTGTACACGAATATACATAACTGCAATACAGCACTGCTGTTTTTAACAGCTCCACTTACACCTCATCAGTACCTCACAACCGTGTTTTAGGAAAAAGTTTTGTGTAATGTTATGGTAAAGAGAAGAAAATTATGTCTCTTAAATATTCCTTTAGAACAAATTCAGGCAAGTTTAAAAAATAAATAAAAT... | TTTTTCCCCTCCCCAAAGTGAATTCTCCATCAGATTTACTACTCCCTGACTCAATTATATTTACCTGGAATATCTGAATGCAGGTATTTATCCTCTCAGAAAAGAATATGTTTACCTGGGATCTAAACATACTGTACACGAATATACATAACTGCAATACAGCACTGCTGTTTTTAACAGCTCCACTTACACCTCATCAGTACCTCACAACCGTGTTTTAGGAAAAAGTTTTGTGTAATGTTATGGTAAAGAGAAGAAAATTATGTCTCTTAAATATTCCTTTAGAACAAATTCAGGCAAGTTTAAAAAATAAATAAAAT... |
Task1_train_33333 | Consider a variant on Chromosome 1. Determine its clinical classification and disease relevance. | Benign | GTATTTTTCTGAAGGAGAAAAGAACAACTCCTTTTAATCTTTTGGAAGCAAGTCTCTTCCATTTTCAACATTAATGGTTATAGGTCACCATCCGTTAAGAAGATGTGTTTTGTCTATTTCCATTAAAATGTAAGTTCTAGGAGGAAGGAACAAAGTTGTTTTTCGCCATGGTATCCCCAGTGCTTGGTATATAACAGAGACTCAATTAGCTTGCTGAATGACCAAACAAATGATTTCAGCTTTTGATAACATCTTTGGAACTTGAGAGCATACACCTTGGCTTTTGTCTTTATTCATTTATTTATTTATTCATTCATTTT... | GTATTTTTCTGAAGGAGAAAAGAACAACTCCTTTTAATCTTTTGGAAGCAAGTCTCTTCCATTTTCAACATTAATGGTTATAGGTCACCATCCGTTAAGAAGATGTGTTTTGTCTATTTCCATTAAAATGTAAGTTCTAGGAGGAAGGAACAAAGTTGTTTTTCGCCATGGTATCCCCAGTGCTTGGTATATAACAGAGACTCAATTAGCTTGCTGAATGACCAAACAAATGATTTCAGCTTTTGATAACATCTTTGGAACTTGAGAGCATACACCTTGGCTTTTGTCTTTATTCATTTATTTATTTATTCATTCATTTT... |
Task1_train_33334 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ACATCTTTGGAACTTGAGAGCATACACCTTGGCTTTTGTCTTTATTCATTTATTTATTTATTCATTCATTTTGTGCCCTTCTGGGAATGAACCAGGACTATTTGAATGGAAAGAGAAAAAAAAAAGCTGTCATAGTTTAAAAATTGGCATATGTTCTCTTCCAGATTAAATTCCCTTGGACCTTTTAATTTATGCTAGAACAAGCACTTATCTTTTCTTTTTTTTATTACTAAGCCCAACACAGTGCGTGGCATGCAGTAACTGTTCAAATAATGTTTGTTTAATTGACGGGTTTTAAGCTCGATAACTTAGCTAAGCCC... | ACATCTTTGGAACTTGAGAGCATACACCTTGGCTTTTGTCTTTATTCATTTATTTATTTATTCATTCATTTTGTGCCCTTCTGGGAATGAACCAGGACTATTTGAATGGAAAGAGAAAAAAAAAAGCTGTCATAGTTTAAAAATTGGCATATGTTCTCTTCCAGATTAAATTCCCTTGGACCTTTTAATTTATGCTAGAACAAGCACTTATCTTTTCTTTTTTTTATTACTAAGCCCAACACAGTGCGTGGCATGCAGTAACTGTTCAAATAATGTTTGTTTAATTGACGGGTTTTAAGCTCGATAACTTAGCTAAGCCC... |
Task1_train_33335 | An alteration has been detected on Chromosome 1. Is it pathogenic, and if so, what disease is involved? | Benign | CATGTGTGATTTTCTTCACCTTGGTATGGTTTCTAAAATGAGAATTTCAGATGTAAAAAAATGACCATTTTTAGAGTTTTTAATTTATATTCACATTTCTTTGTGGGACTGTTATGTTGTTTTACATTTCTACCAGCAACATGTGAGAGTGTCCATTTTACAACCCCTTGCGAGTATTTGATGTTATTGTAAAATCTTTGCTAATTTGATAGAAGAAAATGGTATGGGCCAGCTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCAGATCACGAGGTCAAATCGAGACCATCCTGGCCAACA... | CATGTGTGATTTTCTTCACCTTGGTATGGTTTCTAAAATGAGAATTTCAGATGTAAAAAAATGACCATTTTTAGAGTTTTTAATTTATATTCACATTTCTTTGTGGGACTGTTATGTTGTTTTACATTTCTACCAGCAACATGTGAGAGTGTCCATTTTACAACCCCTTGCGAGTATTTGATGTTATTGTAAAATCTTTGCTAATTTGATAGAAGAAAATGGTATGGGCCAGCTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCAGATCACGAGGTCAAATCGAGACCATCCTGGCCAACA... |
Task1_train_33336 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CCTGTTGGGAGGTGTCTCTTAGTTAGGGGGCACGAGGTTCAAGGACCCACTTGAGGAGGCAGTCTGTCTCTTAGCAGAGCTCGAGCGCTGTGCTGGGAGATCCACTGCTCTCTTCAGAGCCGGCAGGCAGGAACGTTTAAGTCTGCTGAAACTGTGCCCACAGCCGCAGCTTCCCCCAGGTGCTCTGTCCCAGGGAGATAGGAGTTTTATCTACAAGCTCCTGAGTGGGGCTGCTACCTTTCTTTCAGAGGTGCCCTGCCCAGAGAGGAGGAATCTAGAGAGGTAATTTGGCTACAGTGGCTTTGGGGCGCTGCGGTGGG... | CCTGTTGGGAGGTGTCTCTTAGTTAGGGGGCACGAGGTTCAAGGACCCACTTGAGGAGGCAGTCTGTCTCTTAGCAGAGCTCGAGCGCTGTGCTGGGAGATCCACTGCTCTCTTCAGAGCCGGCAGGCAGGAACGTTTAAGTCTGCTGAAACTGTGCCCACAGCCGCAGCTTCCCCCAGGTGCTCTGTCCCAGGGAGATAGGAGTTTTATCTACAAGCTCCTGAGTGGGGCTGCTACCTTTCTTTCAGAGGTGCCCTGCCCAGAGAGGAGGAATCTAGAGAGGTAATTTGGCTACAGTGGCTTTGGGGCGCTGCGGTGGG... |
Task1_train_33337 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TTATCCAAGCAAATTATGTATGGGTCCTTCTCCATATGTAGTATTCCTCAGGGCTTTTTTGGAGGGTTAAGAGGTTTTTGTTTTTTTTTTTTTTTGTATTTTAAAATTACTTGTTGGGAGAAAAACTTTTTCTATGAAATAGTATTCTTATGGAGGTTGTTATATATTCTTAAAGATGTTCTGTATGTGTGCCCCCTCCAAGGGACCTTTAAAAATTTGACTATGTCCCGAAAAACTATTTATGAAAGCTCTCCCGCAAGTGTAATAAAGGCCAAATAGTCTAAGGATGTAATTAAGATTATTGAGAACAGTTAATTATC... | TTATCCAAGCAAATTATGTATGGGTCCTTCTCCATATGTAGTATTCCTCAGGGCTTTTTTGGAGGGTTAAGAGGTTTTTGTTTTTTTTTTTTTTTGTATTTTAAAATTACTTGTTGGGAGAAAAACTTTTTCTATGAAATAGTATTCTTATGGAGGTTGTTATATATTCTTAAAGATGTTCTGTATGTGTGCCCCCTCCAAGGGACCTTTAAAAATTTGACTATGTCCCGAAAAACTATTTATGAAAGCTCTCCCGCAAGTGTAATAAAGGCCAAATAGTCTAAGGATGTAATTAAGATTATTGAGAACAGTTAATTATC... |
Task1_train_33338 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TCTAGTTATATTTCCTGAAGAGCAGAGTGTGAAGTTCACCTGCAAGTTATCCCTAGTCTTGAGCAGGAGGCTCAGGAGTGGGGCATGGAAAGAAGATAAGTTAATAAAGGATTTCCTATGTGGCTGGACAGATGTGCTAGGAACCCTCCAAGAAACCATATAGATGCACCTCAGAAGGCTCCCTCGGAGGGACAGGAAGTTGGGTATTTATACATGACATATTTCCTCCACTCCCCAGAGAAGCTTACACTGCTGCACTTGCTGGCTGTGGCCTTCTGGGGCTTTGGATAAAGCCCTGGTCCAAAAAAAAAAAAACAAAA... | TCTAGTTATATTTCCTGAAGAGCAGAGTGTGAAGTTCACCTGCAAGTTATCCCTAGTCTTGAGCAGGAGGCTCAGGAGTGGGGCATGGAAAGAAGATAAGTTAATAAAGGATTTCCTATGTGGCTGGACAGATGTGCTAGGAACCCTCCAAGAAACCATATAGATGCACCTCAGAAGGCTCCCTCGGAGGGACAGGAAGTTGGGTATTTATACATGACATATTTCCTCCACTCCCCAGAGAAGCTTACACTGCTGCACTTGCTGGCTGTGGCCTTCTGGGGCTTTGGATAAAGCCCTGGTCCAAAAAAAAAAAAACAAAA... |
Task1_train_33339 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | ATAGCTCTATGGCTGGCCTGCAAGGCCAGCTCTCTCTTGCAGTGTTAGCAGCTTAACTCTTTCTCTCTGGGGACGAGCTGGTTCCTGCCTGCCTTAAAGGAGCCTGGCTCTCCCTTACAGTGGTCAGTAGTATTACTCTCTCTCTCTGGGCACACGCAAGCCATGTCAAGCCATGCTATGCCATGCCAAACTGAGCCCCGTGCACAGTGTCGCAGAGCAGTTATACCTTCTACAGACAATAGTGGCTCAGAGCCAAGTATGAACTTACACAAACAGGTTATATAACAAGTAGAGTTGTGTGCCTGCGCATCAATCCCACT... | ATAGCTCTATGGCTGGCCTGCAAGGCCAGCTCTCTCTTGCAGTGTTAGCAGCTTAACTCTTTCTCTCTGGGGACGAGCTGGTTCCTGCCTGCCTTAAAGGAGCCTGGCTCTCCCTTACAGTGGTCAGTAGTATTACTCTCTCTCTCTGGGCACACGCAAGCCATGTCAAGCCATGCTATGCCATGCCAAACTGAGCCCCGTGCACAGTGTCGCAGAGCAGTTATACCTTCTACAGACAATAGTGGCTCAGAGCCAAGTATGAACTTACACAAACAGGTTATATAACAAGTAGAGTTGTGTGCCTGCGCATCAATCCCACT... |
Task1_train_33340 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CATGAAGAGTTGATTCTGGAAATTTCATGAGTCTTTAAGGTGGCTTTACTCCCCTCTTTACTAAATTATTTTTCCAAATAGGTCAAAGATCACAAAGAAATTATCAGCACTTACTTTTACTTTGTACCTGTCTTATGTTGTTTTCCAGAACCTCCAGTCTTCAAAGGTGATTATCCTTCTAACTGGATTGAACCACTTGGTGGGAATGCAATCCTGAATTGTGAGGTGAAAGGAGACCCCACCCCAACCATCCAGTGGAACAGAAAGGGAGTGGATATTGAAATTAGCCACAGAATCCGGCAACTGGGCAATGGCTCCCT... | CATGAAGAGTTGATTCTGGAAATTTCATGAGTCTTTAAGGTGGCTTTACTCCCCTCTTTACTAAATTATTTTTCCAAATAGGTCAAAGATCACAAAGAAATTATCAGCACTTACTTTTACTTTGTACCTGTCTTATGTTGTTTTCCAGAACCTCCAGTCTTCAAAGGTGATTATCCTTCTAACTGGATTGAACCACTTGGTGGGAATGCAATCCTGAATTGTGAGGTGAAAGGAGACCCCACCCCAACCATCCAGTGGAACAGAAAGGGAGTGGATATTGAAATTAGCCACAGAATCCGGCAACTGGGCAATGGCTCCCT... |
Task1_train_33341 | Here is a variant on Chromosome 1. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GTAGTTGTGTTTTTAGTTCTTGTTTTTTTGCATCATCTAGATAGCATGATGTTTTATGCCAACTCCAGTTTATATTATCATTCTCCCTTTTTTCTTGCTATCATTCCATTCTTATAAAAGAAACACTTGAACTCTACAACATTTTGTATCTTGAAGTCCAATTCTAGTTAGGATTTTCCATATTGATTAAAAAATAAAAATAAAAAAGTCTTTAGCTGAAAACCTGTATTTATATGTAGTAGAAATGACACAGAAATGAATAAATGTTACCCAATTGTTAACCCTCCAATTAAAAATGCATCTATATTAAATGGCATTAT... | GTAGTTGTGTTTTTAGTTCTTGTTTTTTTGCATCATCTAGATAGCATGATGTTTTATGCCAACTCCAGTTTATATTATCATTCTCCCTTTTTTCTTGCTATCATTCCATTCTTATAAAAGAAACACTTGAACTCTACAACATTTTGTATCTTGAAGTCCAATTCTAGTTAGGATTTTCCATATTGATTAAAAAATAAAAATAAAAAAGTCTTTAGCTGAAAACCTGTATTTATATGTAGTAGAAATGACACAGAAATGAATAAATGTTACCCAATTGTTAACCCTCCAATTAAAAATGCATCTATATTAAATGGCATTAT... |
Task1_train_33342 | An alteration has been detected on Chromosome 1. Is it pathogenic, and if so, what disease is involved? | Benign | CCAGCTTCCAGGCTGCTTTGTTTACCTAAGCAAGCCTGGGAAATGGCGGGCGCCCCTCCCCCAGCCTCACTGCTGCCTTGCAGTTTGATCTCAGACTGCTGTGCTAGCAATCAGCCAGACTCCATGGGCATAGGACCCTCTGAGCCAGGTGCAGGATATAATCTCCTGGTGCGCCATTTTTTAAGCCTGTCAGAAAAGCACAGTATTCGGGTGGGAGTGACCCGATTTTCCAGGTGCCATCAGTTACCCCTTTGTTTGACTAGGAACGGGAACTCCCTGACCTCTTGCACTTCCCGAGTGAGGCAATGCCTCACCCTGCT... | CCAGCTTCCAGGCTGCTTTGTTTACCTAAGCAAGCCTGGGAAATGGCGGGCGCCCCTCCCCCAGCCTCACTGCTGCCTTGCAGTTTGATCTCAGACTGCTGTGCTAGCAATCAGCCAGACTCCATGGGCATAGGACCCTCTGAGCCAGGTGCAGGATATAATCTCCTGGTGCGCCATTTTTTAAGCCTGTCAGAAAAGCACAGTATTCGGGTGGGAGTGACCCGATTTTCCAGGTGCCATCAGTTACCCCTTTGTTTGACTAGGAACGGGAACTCCCTGACCTCTTGCACTTCCCGAGTGAGGCAATGCCTCACCCTGCT... |
Task1_train_33343 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GGATGTCTAGGGAGTGAAGATGGTTAGAAAGTGATGAGACATTGAGAGAACATTTTGATAAAGATAATACTTTATGTTATGAAATATTTGGTCAGATTACCTAAAGTTTAGGTAGAACTCTGAAAAAAAAATGATGAAGGCGATGCTGGCCAACTTTCTTTACAGAATTCATAAGACAGTCAGCGTCCCAACTTAAAATAATAAAACCACTCAGAACCTCAATACTTCATTTTTTAAGTGTAATAACCAAACTATCTTGAGATTCACTACTTAGTTGTTTCAGTATAGATACTACTTACAGGTGTCTATATATCTAAAAA... | GGATGTCTAGGGAGTGAAGATGGTTAGAAAGTGATGAGACATTGAGAGAACATTTTGATAAAGATAATACTTTATGTTATGAAATATTTGGTCAGATTACCTAAAGTTTAGGTAGAACTCTGAAAAAAAAATGATGAAGGCGATGCTGGCCAACTTTCTTTACAGAATTCATAAGACAGTCAGCGTCCCAACTTAAAATAATAAAACCACTCAGAACCTCAATACTTCATTTTTTAAGTGTAATAACCAAACTATCTTGAGATTCACTACTTAGTTGTTTCAGTATAGATACTACTTACAGGTGTCTATATATCTAAAAA... |
Task1_train_33344 | An alteration has been detected on Chromosome 1. Is it pathogenic, and if so, what disease is involved? | Benign | AATTTTTGCAAATGAGAGCCAAGTACAAATTTTAGTCTCCTAGTCCTGTTTTTATTTTCCCATTGTCAAGATTGCTTTGTTAATGAATATTGCCCTATGTATTTATTTTTAGCCTTCCATCTATACTTTTCAATTTGTCTTGTCTAAGTTCCACAAAAGTGGAAATTATCTTGAATTTTTGTAAGGTCCACCAGTTCTTATAATGCATAAATATACTTCAAGAATCATTCTCTAGGATCGAAGCTCATTTCTCAATAATTGGCTATACTTACTTGTTCCTGACAGTCACGTCTGGCTTGCTGCTCATTACTTAAAGCTGT... | AATTTTTGCAAATGAGAGCCAAGTACAAATTTTAGTCTCCTAGTCCTGTTTTTATTTTCCCATTGTCAAGATTGCTTTGTTAATGAATATTGCCCTATGTATTTATTTTTAGCCTTCCATCTATACTTTTCAATTTGTCTTGTCTAAGTTCCACAAAAGTGGAAATTATCTTGAATTTTTGTAAGGTCCACCAGTTCTTATAATGCATAAATATACTTCAAGAATCATTCTCTAGGATCGAAGCTCATTTCTCAATAATTGGCTATACTTACTTGTTCCTGACAGTCACGTCTGGCTTGCTGCTCATTACTTAAAGCTGT... |
Task1_train_33345 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCTTAGAAAAACAACCTCATTAAAAAGTAGGCAGAGGATATGAACAGACACTTTTCAAAAGAAGACATACATGCAGCCAAGAATCGTATGAAAAAAAACTCAGCATTACTATCGGTAGAGAAACACAAATGAAAACCACAATGAGATACCATCTCACACCAGTCAGAATCGCTGTTATTAAAAAGTCAAAAAATAACAGATGCTGGCAAGGCTGCAGAGAAAAAGGAATGCTTATAAACCGTTGGTGGGAGTATAAATAAGTTCAACCATTGTGGAAGGCAGTGTGTTGATTCCTCAAAGACCTAAAAACAGAGATACCA... | TCTTAGAAAAACAACCTCATTAAAAAGTAGGCAGAGGATATGAACAGACACTTTTCAAAAGAAGACATACATGCAGCCAAGAATCGTATGAAAAAAAACTCAGCATTACTATCGGTAGAGAAACACAAATGAAAACCACAATGAGATACCATCTCACACCAGTCAGAATCGCTGTTATTAAAAAGTCAAAAAATAACAGATGCTGGCAAGGCTGCAGAGAAAAAGGAATGCTTATAAACCGTTGGTGGGAGTATAAATAAGTTCAACCATTGTGGAAGGCAGTGTGTTGATTCCTCAAAGACCTAAAAACAGAGATACCA... |
Task1_train_33346 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | ATTAATTGTTGATTCAATTTCTTTAATAGATATGCACCTATTTAGATTGTCTATTTCTTCTTATGTAAATTTTGGTAGATTCTATCTTTTAAGAAATCGATCCATTTCATCTAGGTTATCAAATTCGTGAGCATAGAGTTGTTTGTAGTATTTCTTCTGTTATCCTTTCAATGTCCACGCGATCTGTAATAATGTCCCTTATCATTTCTGATATTAGTAGTTTTGTTCTCTCTCTCTCATCCTTTTTTTTTTTTTTCTTAGCATGGCTAATGGCTCATTGATCTTATTGATTTTTTCAAAGAACCAAAGTTTGGTTGCAT... | ATTAATTGTTGATTCAATTTCTTTAATAGATATGCACCTATTTAGATTGTCTATTTCTTCTTATGTAAATTTTGGTAGATTCTATCTTTTAAGAAATCGATCCATTTCATCTAGGTTATCAAATTCGTGAGCATAGAGTTGTTTGTAGTATTTCTTCTGTTATCCTTTCAATGTCCACGCGATCTGTAATAATGTCCCTTATCATTTCTGATATTAGTAGTTTTGTTCTCTCTCTCTCATCCTTTTTTTTTTTTTTCTTAGCATGGCTAATGGCTCATTGATCTTATTGATTTTTTCAAAGAACCAAAGTTTGGTTGCAT... |
Task1_train_33347 | A mutation is present on Chromosome 1. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TCCCGGCAGGATTCATTACCTGCTGACTAAACAGCACTTGAGCACTAAAGAACCAGCAGCAATACCATAAATAGCATGTCGTGGGCCTGGGGAGAGATTCTGGGATGTGCTGGCTTCAGGTGAGACCTAGCACATTCTGAGGTATGGTAGCTACTATGAGAGATTCCTTCTACTTGAGAAAAGCAGAGGGAAAATTTAAAGAGGCTTGGTCTTTCACCTTAGTTACCATCTCAGCCACAGTGAGGTAGAGCACCATGCAGGCTCTTAGGGTTCCTGATTCCAGGACTTGGCCCTTGGATGGCATTTCTGGACTTGCCCTG... | TCCCGGCAGGATTCATTACCTGCTGACTAAACAGCACTTGAGCACTAAAGAACCAGCAGCAATACCATAAATAGCATGTCGTGGGCCTGGGGAGAGATTCTGGGATGTGCTGGCTTCAGGTGAGACCTAGCACATTCTGAGGTATGGTAGCTACTATGAGAGATTCCTTCTACTTGAGAAAAGCAGAGGGAAAATTTAAAGAGGCTTGGTCTTTCACCTTAGTTACCATCTCAGCCACAGTGAGGTAGAGCACCATGCAGGCTCTTAGGGTTCCTGATTCCAGGACTTGGCCCTTGGATGGCATTTCTGGACTTGCCCTG... |
Task1_train_33348 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TTCTTTTATTATTGTTGTTAATCTCTTACTCTGCCTAATTTATAAATTAAACTTTATCATAGGCAAGTATGTATAGGAAAATAGCATGTATAGGGTTCAGTACTATCCGAGGTTTTAGGCATCCACCGAGGGTCTTGGAACGTGTCCACCACGGATAAGGGGGAACGATTATGATATCAGCTCACCTAGAGTGAGGAAGCTACAGCAAACATCAGTTTGTTCAGTTATAACAAAGAAGAGTAAGAGACAGGAATTAAACATTATAACATTATAACCTACCCAATGTTTACAATCTATTATTCCTTGCTTCCTAATAGTAT... | TTCTTTTATTATTGTTGTTAATCTCTTACTCTGCCTAATTTATAAATTAAACTTTATCATAGGCAAGTATGTATAGGAAAATAGCATGTATAGGGTTCAGTACTATCCGAGGTTTTAGGCATCCACCGAGGGTCTTGGAACGTGTCCACCACGGATAAGGGGGAACGATTATGATATCAGCTCACCTAGAGTGAGGAAGCTACAGCAAACATCAGTTTGTTCAGTTATAACAAAGAAGAGTAAGAGACAGGAATTAAACATTATAACATTATAACCTACCCAATGTTTACAATCTATTATTCCTTGCTTCCTAATAGTAT... |
Task1_train_33349 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | TAAGTTTGTATTGTGCTGTGTCCATTTGATTCTTAAAACCATCTGACAAGTTGTTATTTCTGATTTTTGATCCAATTTTAAGATAGCACATGATTTATGAGTCAATTTTATTTTGAATATCTTTTTTAAATTTTCATTTCTATATTTTCTATAGTTCCTTTAATGTTCCTAAAATAGCTGTTATAAAGACCTAACACTAATTCTAACATCTGAATCTGAGTGTCTAGTTCTACTGAATATTTATTTTCTCTTTTTGTTCACAGTTGTTTTTGCTTTTTTGTGTATCTTTTAATTTTTATTCAAAATCGTATTTTTAAACA... | TAAGTTTGTATTGTGCTGTGTCCATTTGATTCTTAAAACCATCTGACAAGTTGTTATTTCTGATTTTTGATCCAATTTTAAGATAGCACATGATTTATGAGTCAATTTTATTTTGAATATCTTTTTTAAATTTTCATTTCTATATTTTCTATAGTTCCTTTAATGTTCCTAAAATAGCTGTTATAAAGACCTAACACTAATTCTAACATCTGAATCTGAGTGTCTAGTTCTACTGAATATTTATTTTCTCTTTTTGTTCACAGTTGTTTTTGCTTTTTTGTGTATCTTTTAATTTTTATTCAAAATCGTATTTTTAAACA... |
Task1_train_33350 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AAGAATATTTATATGTGTGTGTGTGTATGTGTGTATTGAAATTCTTTTTAACCTATTGCATAAGGTTTATTGAAATAGAAACATATTTCATGGAAAACATTAATACCATTTTGTTATTGAAAGTACTAGATAATCTACAAATAATCCCATGAAAAGAGCAAATTTTCTGAAAAATATATAAACCTGTTAATATAATAAACAAGATAGCACTCAAATGTATTTGTCAAAATTAATATATAATAACTCAGTAAAATGTAATTATATTGTACCTTACTTAAATATATTTTATGACATCAAAATTATTTTTCTCTCCAATTAAA... | AAGAATATTTATATGTGTGTGTGTGTATGTGTGTATTGAAATTCTTTTTAACCTATTGCATAAGGTTTATTGAAATAGAAACATATTTCATGGAAAACATTAATACCATTTTGTTATTGAAAGTACTAGATAATCTACAAATAATCCCATGAAAAGAGCAAATTTTCTGAAAAATATATAAACCTGTTAATATAATAAACAAGATAGCACTCAAATGTATTTGTCAAAATTAATATATAATAACTCAGTAAAATGTAATTATATTGTACCTTACTTAAATATATTTTATGACATCAAAATTATTTTTCTCTCCAATTAAA... |
Task1_train_33351 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | CAGCAAATACTTTAAATTAAATAATAATGATTGTGGTACACATTAAAATCAATGGGATACAGCTGAAACAGAGATGTATTTAGCATTATAACATGCATCAGAAAAAACAAATAAAAAAATAAAAGCAACAGGTACTACAATCTAGAAGGTAGACAGGAATGTACACCCAACAAAAATAGAAGGAAAGAATCATTCAAGCATAAATAGTTGACCATTAATCTTAAGAAAAATAAATTGATGAGAATGTTAAAAACATGTCAAAATATTGAAAAACAGAAATAAGCAAAATACTTTTGATAAATATGAAATACTTTATCATA... | CAGCAAATACTTTAAATTAAATAATAATGATTGTGGTACACATTAAAATCAATGGGATACAGCTGAAACAGAGATGTATTTAGCATTATAACATGCATCAGAAAAAACAAATAAAAAAATAAAAGCAACAGGTACTACAATCTAGAAGGTAGACAGGAATGTACACCCAACAAAAATAGAAGGAAAGAATCATTCAAGCATAAATAGTTGACCATTAATCTTAAGAAAAATAAATTGATGAGAATGTTAAAAACATGTCAAAATATTGAAAAACAGAAATAAGCAAAATACTTTTGATAAATATGAAATACTTTATCATA... |
Task1_train_33352 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | TTGACTCCATGTCTCACATTCAGGTCATGCTGATGCAAGAGATGGGCTCCCACAGCCTTGTGCAGATGTGGCTTTGTCCCCCTCCTGGTTGCTTTCATGGGCTGGCATTGAGTGTCTGTGGCTTTTCCAGGAACATAGTGCAAGCTATTGATGGATCTACCATTCTGGGGCTTCAATGATTGTGGTCCTGTTCTCACAGCTCCACAAGGCAGTGCCTCAGTGGGGACTCTATGTGAGGGCTCTGACCCCACATTTCCTTTCCTCAATGGCCTAGCAGAGGTTCTCCATGTGGGCTCCCCCCTGCAGCAAACTTCTGCCTG... | TTGACTCCATGTCTCACATTCAGGTCATGCTGATGCAAGAGATGGGCTCCCACAGCCTTGTGCAGATGTGGCTTTGTCCCCCTCCTGGTTGCTTTCATGGGCTGGCATTGAGTGTCTGTGGCTTTTCCAGGAACATAGTGCAAGCTATTGATGGATCTACCATTCTGGGGCTTCAATGATTGTGGTCCTGTTCTCACAGCTCCACAAGGCAGTGCCTCAGTGGGGACTCTATGTGAGGGCTCTGACCCCACATTTCCTTTCCTCAATGGCCTAGCAGAGGTTCTCCATGTGGGCTCCCCCCTGCAGCAAACTTCTGCCTG... |
Task1_train_33353 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGGAAAGAGGTGTAATTGACTCACAATTCCACATGGCTGGGAGGCCTCAGGAAACTTACAACCCTGGTGGAAGGGTAAGCAAACATGTCCTTCTTCACATGATGACAGGAAGGAGAAGTGCAAAGCAAAGACAGAAAAGCTCCTTATAAAACCATCAGATCTCAGGAGAACTCACGCAGTATCATGAGAACAGCAGCAGAGGAAAAATCGCCCTCATGATTCAATTTTCTCCCACCAGGTCCCATCCACAACACGTGAGGATTATGGCAATTGCAATTCACGATGAGATTTGGGTGGGGACACAGCTAAACCTGTTCTGC... | AGGAAAGAGGTGTAATTGACTCACAATTCCACATGGCTGGGAGGCCTCAGGAAACTTACAACCCTGGTGGAAGGGTAAGCAAACATGTCCTTCTTCACATGATGACAGGAAGGAGAAGTGCAAAGCAAAGACAGAAAAGCTCCTTATAAAACCATCAGATCTCAGGAGAACTCACGCAGTATCATGAGAACAGCAGCAGAGGAAAAATCGCCCTCATGATTCAATTTTCTCCCACCAGGTCCCATCCACAACACGTGAGGATTATGGCAATTGCAATTCACGATGAGATTTGGGTGGGGACACAGCTAAACCTGTTCTGC... |
Task1_train_33354 | This variant is located on Chromosome 1. Evaluate its biological effect and specify any disease association. | Benign | ACTTTTCTTCGATAATAAATTAACCTTAGTTTATGTTGACCTTTTTACTTCATCAACTTTAATTTTTATGTCTTTCGAGATAATATTTAGCTTAAAAAACATTGTAGAGATGTACAAAAGATTTTTTCTTTCTGTTCTTGTGCTATAAGCTTTTATCTTTTAAATATTTTACTTATTTATTTACTTTTTAAACCTTTTTGTTAAAAACAGACACAAACACACATATTAACCTCAGCCTACAAAGGGTTAGGATCATCAGTATCACTGTCTTCTTCCTCCGCTCTTGTCCCACTAGAAGATCTTCAGGGCAGTAACAGGCA... | ACTTTTCTTCGATAATAAATTAACCTTAGTTTATGTTGACCTTTTTACTTCATCAACTTTAATTTTTATGTCTTTCGAGATAATATTTAGCTTAAAAAACATTGTAGAGATGTACAAAAGATTTTTTCTTTCTGTTCTTGTGCTATAAGCTTTTATCTTTTAAATATTTTACTTATTTATTTACTTTTTAAACCTTTTTGTTAAAAACAGACACAAACACACATATTAACCTCAGCCTACAAAGGGTTAGGATCATCAGTATCACTGTCTTCTTCCTCCGCTCTTGTCCCACTAGAAGATCTTCAGGGCAGTAACAGGCA... |
Task1_train_33355 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCCTGCTTAAACTCCTCTAGAATTTGTTTTGTCTGGAGCATAAAGACTAAATTTTTTCTGTCTTAAAAATCTATCCACAATCTTACTCCCTCTATTGCCAACCTGGTCCCATATCACTTTTTATTGTTTCTAGTTTTTTGATTTTTCCACGTTATCTCTTGCAATTGGAATATTCTTCTATACCTTTTACTGGGCTATTTCTAATTCATACTTCAGTGTAACATTTCAACTTAAATGTTACTCACTCTGGGAAGTCTCTGACCATGGAGACTAGCTTGATTTCCCATTCTGTGTTTCCTGAAACATACACTTCTCATGTT... | TCCTGCTTAAACTCCTCTAGAATTTGTTTTGTCTGGAGCATAAAGACTAAATTTTTTCTGTCTTAAAAATCTATCCACAATCTTACTCCCTCTATTGCCAACCTGGTCCCATATCACTTTTTATTGTTTCTAGTTTTTTGATTTTTCCACGTTATCTCTTGCAATTGGAATATTCTTCTATACCTTTTACTGGGCTATTTCTAATTCATACTTCAGTGTAACATTTCAACTTAAATGTTACTCACTCTGGGAAGTCTCTGACCATGGAGACTAGCTTGATTTCCCATTCTGTGTTTCCTGAAACATACACTTCTCATGTT... |
Task1_train_33356 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | CTCTGACCATGGAGACTAGCTTGATTTCCCATTCTGTGTTTCCTGAAACATACACTTCTCATGTTGTATTATAATTATACTTCCTTGTTCAATTAAGTTCCTTGAGGACAGCAACTAAGTATATCTTACTCATTGTCTATTTATAACACCCACTACAGCATTTGGCACATTTCTAGCACTTGACATTTCTTGAATTAAAACATTATTTCTAAATTTAACAGTAATCCAGTAAGATATGAACATATCACATCTGGGTTAAAGCCTGGGTTATTGCAGGTAAAAAGAAATAGCTGAAGTACTTAGATTCAGTTCCTGGATCT... | CTCTGACCATGGAGACTAGCTTGATTTCCCATTCTGTGTTTCCTGAAACATACACTTCTCATGTTGTATTATAATTATACTTCCTTGTTCAATTAAGTTCCTTGAGGACAGCAACTAAGTATATCTTACTCATTGTCTATTTATAACACCCACTACAGCATTTGGCACATTTCTAGCACTTGACATTTCTTGAATTAAAACATTATTTCTAAATTTAACAGTAATCCAGTAAGATATGAACATATCACATCTGGGTTAAAGCCTGGGTTATTGCAGGTAAAAAGAAATAGCTGAAGTACTTAGATTCAGTTCCTGGATCT... |
Task1_train_33357 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | TTCAGAAAGGTCAGTCAGAAATAAACCTACAATGTGACCTACTGATTCCCACAATTATCTGGGCTGAACTTGGAAAAAAAGGAAGGGGAAGGGGACAGGAGGGAGAGAGGGAGGGAAGGAGGGAGGGAGGGAGGGAGCGAGGGAGGGAGGAAGGAAGGAAGGAAGGAGCAAAATGTCCTCCTCTTAGTAAATCAGCACCTCAATCTTGAGCAGTATTTTCCCAAATTGTGCAGAAAACTCTAGTTTCCTAGGATGCTCAAAGAAGTACCTCCAAAGTATCTTGCGGTAAAATGATTTAAGGAAATACTGGGTTAAGCAAA... | TTCAGAAAGGTCAGTCAGAAATAAACCTACAATGTGACCTACTGATTCCCACAATTATCTGGGCTGAACTTGGAAAAAAAGGAAGGGGAAGGGGACAGGAGGGAGAGAGGGAGGGAAGGAGGGAGGGAGGGAGGGAGCGAGGGAGGGAGGAAGGAAGGAAGGAAGGAGCAAAATGTCCTCCTCTTAGTAAATCAGCACCTCAATCTTGAGCAGTATTTTCCCAAATTGTGCAGAAAACTCTAGTTTCCTAGGATGCTCAAAGAAGTACCTCCAAAGTATCTTGCGGTAAAATGATTTAAGGAAATACTGGGTTAAGCAAA... |
Task1_train_33358 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GTGTATATTTTTATACTTTTTGGAAAACATGGCTATAGTGCTTTATATAAGCAAATTAAATATTTCCATTAAGAGAGCTTTTTAATCTTGAAAAGATGAATTTTGACCTTGATTTGATGAATAGAAAAAGGCATTATTGCTCTGCAGAACACTAATAACTTATCCTTCAAACTTTATACATACTTTCATACATTATTTAAGTATGCTTAAAAAACAGCTTTAAGATTAAGGCAATTAGTGGGTTAACAGTTTCATCAGCTTCAGGCTAGTTTTGATAAGTTTTGATATCTTGATCAGTTCATGCTCAACCAGATTAGTAT... | GTGTATATTTTTATACTTTTTGGAAAACATGGCTATAGTGCTTTATATAAGCAAATTAAATATTTCCATTAAGAGAGCTTTTTAATCTTGAAAAGATGAATTTTGACCTTGATTTGATGAATAGAAAAAGGCATTATTGCTCTGCAGAACACTAATAACTTATCCTTCAAACTTTATACATACTTTCATACATTATTTAAGTATGCTTAAAAAACAGCTTTAAGATTAAGGCAATTAGTGGGTTAACAGTTTCATCAGCTTCAGGCTAGTTTTGATAAGTTTTGATATCTTGATCAGTTCATGCTCAACCAGATTAGTAT... |
Task1_train_33359 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GGCCCGATAAAAAAGTTGGTTGACCACAACATGAATAAATAAATAACCATAAGCTTGGAAATGCTACCTGTAGTATTTCAGAGTGTCGATCACATTTGTAGTCATCACTTAAAGAATTAATGTCTGCCAATGTTATCATCTAAAATGTATTTACAGAGGTCAGAAGAGCTATGTCTGTCCTCCTCTATGCAAAGAGGTGATGACATCAAGGGGTATGTCACAAGCCAAAGTTTAGTTAGCCTAAGTTAGTTAGCTGGTTTGCAGTTTTTATCCACTAAGTCTGATCTTCTGACCCCTCAGTTTTACAACTTTCCACTCTC... | GGCCCGATAAAAAAGTTGGTTGACCACAACATGAATAAATAAATAACCATAAGCTTGGAAATGCTACCTGTAGTATTTCAGAGTGTCGATCACATTTGTAGTCATCACTTAAAGAATTAATGTCTGCCAATGTTATCATCTAAAATGTATTTACAGAGGTCAGAAGAGCTATGTCTGTCCTCCTCTATGCAAAGAGGTGATGACATCAAGGGGTATGTCACAAGCCAAAGTTTAGTTAGCCTAAGTTAGTTAGCTGGTTTGCAGTTTTTATCCACTAAGTCTGATCTTCTGACCCCTCAGTTTTACAACTTTCCACTCTC... |
Task1_train_33360 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CCACAACATGAATAAATAAATAACCATAAGCTTGGAAATGCTACCTGTAGTATTTCAGAGTGTCGATCACATTTGTAGTCATCACTTAAAGAATTAATGTCTGCCAATGTTATCATCTAAAATGTATTTACAGAGGTCAGAAGAGCTATGTCTGTCCTCCTCTATGCAAAGAGGTGATGACATCAAGGGGTATGTCACAAGCCAAAGTTTAGTTAGCCTAAGTTAGTTAGCTGGTTTGCAGTTTTTATCCACTAAGTCTGATCTTCTGACCCCTCAGTTTTACAACTTTCCACTCTCTGTGCTGCATAGCACCTCTCCAC... | CCACAACATGAATAAATAAATAACCATAAGCTTGGAAATGCTACCTGTAGTATTTCAGAGTGTCGATCACATTTGTAGTCATCACTTAAAGAATTAATGTCTGCCAATGTTATCATCTAAAATGTATTTACAGAGGTCAGAAGAGCTATGTCTGTCCTCCTCTATGCAAAGAGGTGATGACATCAAGGGGTATGTCACAAGCCAAAGTTTAGTTAGCCTAAGTTAGTTAGCTGGTTTGCAGTTTTTATCCACTAAGTCTGATCTTCTGACCCCTCAGTTTTACAACTTTCCACTCTCTGTGCTGCATAGCACCTCTCCAC... |
Task1_train_33361 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | ACTTGATTTGCAACACTAGCCTAGCTATTATCAAGGCAGAGCTATTCTGAATGAAGAGTAAAATAAACAAAGAAAATCAGTAAAATAAAAAAGCATAGACCACGAAGCAATTCTAATGCTGAAAAGATTTATTAAAGGCATTCTCTTTATAACATTTCTTGTCAGTGCACATAATTCCAATAGCAAATATTTTTTCACCATTCATTCAAATACAGTATCACAATGTGTTTAGTATAAATATGTATACAAAATTTTATAAAGACACTAAAAAGTTTCTGACCAATTAAGTCATGAGTTTACAAAGCACAAACTGAAGATTA... | ACTTGATTTGCAACACTAGCCTAGCTATTATCAAGGCAGAGCTATTCTGAATGAAGAGTAAAATAAACAAAGAAAATCAGTAAAATAAAAAAGCATAGACCACGAAGCAATTCTAATGCTGAAAAGATTTATTAAAGGCATTCTCTTTATAACATTTCTTGTCAGTGCACATAATTCCAATAGCAAATATTTTTTCACCATTCATTCAAATACAGTATCACAATGTGTTTAGTATAAATATGTATACAAAATTTTATAAAGACACTAAAAAGTTTCTGACCAATTAAGTCATGAGTTTACAAAGCACAAACTGAAGATTA... |
Task1_train_33362 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | ACCCTGTAATCTACAGTCATCCTCCCCTGAAGAGAGAACCCAATAGTCACCATGCAGATCTGGTCAAAGCTGGCATGCTACCCTTGGTCTTTCCCTCTTAGCTCTCTTGTGGATTCACTTCTTTCTTTGTCCATATAACTTACATATATACCCATATCCTATTTCGGGCTTTATGGCTCTATTTTGGTCTTCCAGCATGCGTGACCTATATTTTAAACAATCTAGCACTTTTTTTTTCTCACACTATCTTCTACTACTCTTTAGTTTTCCAATTTTTTCTCCTTTATCTTTCCTCTCTTTGCCCACTTTTTTTTTTTTGA... | ACCCTGTAATCTACAGTCATCCTCCCCTGAAGAGAGAACCCAATAGTCACCATGCAGATCTGGTCAAAGCTGGCATGCTACCCTTGGTCTTTCCCTCTTAGCTCTCTTGTGGATTCACTTCTTTCTTTGTCCATATAACTTACATATATACCCATATCCTATTTCGGGCTTTATGGCTCTATTTTGGTCTTCCAGCATGCGTGACCTATATTTTAAACAATCTAGCACTTTTTTTTTCTCACACTATCTTCTACTACTCTTTAGTTTTCCAATTTTTTCTCCTTTATCTTTCCTCTCTTTGCCCACTTTTTTTTTTTTGA... |
Task1_train_33363 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGGTCACTGACAATAGGCAACTCACTTTTTCAATTGATGCACAGTTGATTCTCATTATCTGTGGTAGTTATGTTCTATAAAGTAAAATTGACGCAAATCCTGAATTAGCAAATACTGAACCCTTGCCCCTGGGGAAATATAGGGTTAGGTTCCCGTGAGCCTTTGGTCACGACATTTTGCATCAACTGATTAATATATAACCTTATGTTATGTGAGTTTCTGCTTAAGGACACCTTACTTAATATGGGTTGTTGATTCATTAACTCATGGCCAACAGCACTGTAACTCATACCCAGATGAAGCTTACCTAGCACACATAT... | TGGTCACTGACAATAGGCAACTCACTTTTTCAATTGATGCACAGTTGATTCTCATTATCTGTGGTAGTTATGTTCTATAAAGTAAAATTGACGCAAATCCTGAATTAGCAAATACTGAACCCTTGCCCCTGGGGAAATATAGGGTTAGGTTCCCGTGAGCCTTTGGTCACGACATTTTGCATCAACTGATTAATATATAACCTTATGTTATGTGAGTTTCTGCTTAAGGACACCTTACTTAATATGGGTTGTTGATTCATTAACTCATGGCCAACAGCACTGTAACTCATACCCAGATGAAGCTTACCTAGCACACATAT... |
Task1_train_33364 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | ATGGTGCCCTGCTTCCCCCCTGGACAAGTAGCTGGTCCTGATGGTTTTCCCATTCCAGGGCCCAGATGACTGCCATTGTAACAGGCTCCCAAGCCAGCCCTCCCAGCCAAGTTCCCAGACTCTAAGAAAAGAGTGGGGCTTCCCGGACTCCTCTGGGAGAAGACTCAAGCTTCTTAGATGCACAGAAGGGACTGACCCAGGACCCTGCAGGGTTGGCCAAGGGCTCGTCCTCTGGTAGCAGGCGTCTCTGTCTCTTCTGGGAACTCCCTTTCATAGTGGACACTGAAATGGAAGCAAGGCTGGGTGAACCAGAGAAGGCT... | ATGGTGCCCTGCTTCCCCCCTGGACAAGTAGCTGGTCCTGATGGTTTTCCCATTCCAGGGCCCAGATGACTGCCATTGTAACAGGCTCCCAAGCCAGCCCTCCCAGCCAAGTTCCCAGACTCTAAGAAAAGAGTGGGGCTTCCCGGACTCCTCTGGGAGAAGACTCAAGCTTCTTAGATGCACAGAAGGGACTGACCCAGGACCCTGCAGGGTTGGCCAAGGGCTCGTCCTCTGGTAGCAGGCGTCTCTGTCTCTTCTGGGAACTCCCTTTCATAGTGGACACTGAAATGGAAGCAAGGCTGGGTGAACCAGAGAAGGCT... |
Task1_train_33365 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | TAATATCACCAGTAATGGGACAAGTCAAGACTGGTGTCACCTAATAGCTTGTAATGAGAACACAGAATCATTTCTGTGGCATTCTTATCCAAGATGCATATCCTAGTAATCAGACAAACCCCAACTGAGGGACATACTGACCTGCAGTCTTCAAGTGTCAAGATCGTGTCAAGGAAAGACTGATGAACTCTTCCAGATGGAAGAGATGAAAGAGATAAGGCAACTCAATGCACTGTCTGATTCTGGATTGGATCCTTTTGCTATAAAGGACATTTACTGGGACAGCAAATGAAATTTGAATGGGGTCTGAGGATTAGAAT... | TAATATCACCAGTAATGGGACAAGTCAAGACTGGTGTCACCTAATAGCTTGTAATGAGAACACAGAATCATTTCTGTGGCATTCTTATCCAAGATGCATATCCTAGTAATCAGACAAACCCCAACTGAGGGACATACTGACCTGCAGTCTTCAAGTGTCAAGATCGTGTCAAGGAAAGACTGATGAACTCTTCCAGATGGAAGAGATGAAAGAGATAAGGCAACTCAATGCACTGTCTGATTCTGGATTGGATCCTTTTGCTATAAAGGACATTTACTGGGACAGCAAATGAAATTTGAATGGGGTCTGAGGATTAGAAT... |
Task1_train_33366 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ATGACAGTGCCAGTTCCCACCTCATGCAGGTCCAGGGCCCTGTCTCCAGCCCTGCACAGGCCTTAGGAACCCAGCTGCTACCCATTAGGGTTTAGGCCTAGGCCTAAAATGTCCTTGGAAGTCAGTTCACAAGCTCGCTGCTCTGGCTTTGGGTCACTTCTTTGTTTCTGCCACTAAAAGACTTCCTTTTCATTCCAGGAAACATCATTCTTATGCCTTATGCAGCAGTGTTACTTGTTTGTAGTGGGGAGGGCACTGAGTTTGTCCACCGTGTTGTTGGAACTGGTCAGTCTTTTCTCGTATCCTACTCGTCTCACGGT... | ATGACAGTGCCAGTTCCCACCTCATGCAGGTCCAGGGCCCTGTCTCCAGCCCTGCACAGGCCTTAGGAACCCAGCTGCTACCCATTAGGGTTTAGGCCTAGGCCTAAAATGTCCTTGGAAGTCAGTTCACAAGCTCGCTGCTCTGGCTTTGGGTCACTTCTTTGTTTCTGCCACTAAAAGACTTCCTTTTCATTCCAGGAAACATCATTCTTATGCCTTATGCAGCAGTGTTACTTGTTTGTAGTGGGGAGGGCACTGAGTTTGTCCACCGTGTTGTTGGAACTGGTCAGTCTTTTCTCGTATCCTACTCGTCTCACGGT... |
Task1_train_33367 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | ATGGAAGGTTTCAAGCCTGGGGCAACAGAGGTCAGGAATAGGTAGCCTTGGATATGGAACCTCAAACTGCAGAGTGGCCCCCTCATGCCAAAATTAGGCTTACCCCTCCTCAGCCCCATGACATTGTCTGGAGAAGGCACTGGGCAGCCTAAGTCAGGACAGCTCCACAGCAGCCCCTACCCATCTCAGTATCTGCACCATCAGCCAAAACTCCCCAAGCATACCCTCAACCCACCCCCACAAGCAATCCCATGTCAGAGAAACAGTAAACCCCTCTCCAGTGGGCTAGAAGGCTCCCAGAACAACCCTGAGTGTGCACA... | ATGGAAGGTTTCAAGCCTGGGGCAACAGAGGTCAGGAATAGGTAGCCTTGGATATGGAACCTCAAACTGCAGAGTGGCCCCCTCATGCCAAAATTAGGCTTACCCCTCCTCAGCCCCATGACATTGTCTGGAGAAGGCACTGGGCAGCCTAAGTCAGGACAGCTCCACAGCAGCCCCTACCCATCTCAGTATCTGCACCATCAGCCAAAACTCCCCAAGCATACCCTCAACCCACCCCCACAAGCAATCCCATGTCAGAGAAACAGTAAACCCCTCTCCAGTGGGCTAGAAGGCTCCCAGAACAACCCTGAGTGTGCACA... |
Task1_train_33368 | This alteration occurs on Chromosome 1. Is it associated with a disease or is it a benign variant? | Benign | AGTGGCGCAATCTCTGATCACTACAACATCTGCCTCTGGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACATGCCACCAAGCCTGGCTACTTTTTGTATTTTTAATAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGATCTCAGGTGATACGACTGCCTTGGCCTCCCAAAGTGCTGGGATTACATGCGTGAGCCCCTGCGCCTGCCCGGAACTCACAAAATCTCATTCCCTTCCTAGTCTTGGCAGAGCCTTCAGACTCCTTGCTCACCCACTCTCAAAGAA... | AGTGGCGCAATCTCTGATCACTACAACATCTGCCTCTGGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACATGCCACCAAGCCTGGCTACTTTTTGTATTTTTAATAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGATCTCAGGTGATACGACTGCCTTGGCCTCCCAAAGTGCTGGGATTACATGCGTGAGCCCCTGCGCCTGCCCGGAACTCACAAAATCTCATTCCCTTCCTAGTCTTGGCAGAGCCTTCAGACTCCTTGCTCACCCACTCTCAAAGAA... |
Task1_train_33369 | A variant on Chromosome 1 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GCCAAATTTTGATGCTTTCTGTTTTCCAAAGCCTTGGTGCGAGTTATCTCTCCTGGTGCTGAGCTGGGTTCTACTGAATTACTGTCACAGACATAGAACATATGTGTCATGCCTCTGCTTAGACCTTCTCTAGCCATCAATTATTTTCAGATCAGATCCAGACTAATTGCACAGCCTCTAGAACTCCTTTCTGTTGCATGTCCTCATCTCCCACAACACCCTAGCAAGAATCTCTGGGTTAGGCATCCTCACGCTCCATACAGACCTTTCCTTTTCTGCTTCCTGTATTCCTTCCCCATCTAGGAACTGACACTCCTCCT... | GCCAAATTTTGATGCTTTCTGTTTTCCAAAGCCTTGGTGCGAGTTATCTCTCCTGGTGCTGAGCTGGGTTCTACTGAATTACTGTCACAGACATAGAACATATGTGTCATGCCTCTGCTTAGACCTTCTCTAGCCATCAATTATTTTCAGATCAGATCCAGACTAATTGCACAGCCTCTAGAACTCCTTTCTGTTGCATGTCCTCATCTCCCACAACACCCTAGCAAGAATCTCTGGGTTAGGCATCCTCACGCTCCATACAGACCTTTCCTTTTCTGCTTCCTGTATTCCTTCCCCATCTAGGAACTGACACTCCTCCT... |
Task1_train_33370 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | TGGGTTTGGAAGTATAGAATCCCAGAGCTGAAAATAAGCCTCATTGCTCATAACTGTAGCCCCTCATTTTACTTGGGGGGAATTGACACCTGAGGTCCAGAGGTGACCTGTCCAAGGTAACATGGGGAGTTTGTGGCTGAGCTGGTCTAAGCCAGGATTTCTGAATGGCCAGCCTTGCTGCCTTAGGTCACACTGTGTCATACCATCAAGCTGATATCCCCATTCCTATTTCCCCGGCAGCCATCCCCCCAAGAGTGGTGGTCCCACTGGCGGAGACCCACTGTGAGGAGCAGGGTGACGCAGTCTTTGAATGTACCCTC... | TGGGTTTGGAAGTATAGAATCCCAGAGCTGAAAATAAGCCTCATTGCTCATAACTGTAGCCCCTCATTTTACTTGGGGGGAATTGACACCTGAGGTCCAGAGGTGACCTGTCCAAGGTAACATGGGGAGTTTGTGGCTGAGCTGGTCTAAGCCAGGATTTCTGAATGGCCAGCCTTGCTGCCTTAGGTCACACTGTGTCATACCATCAAGCTGATATCCCCATTCCTATTTCCCCGGCAGCCATCCCCCCAAGAGTGGTGGTCCCACTGGCGGAGACCCACTGTGAGGAGCAGGGTGACGCAGTCTTTGAATGTACCCTC... |
Task1_train_33371 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGAGGTCCAGAGGTGACCTGTCCAAGGTAACATGGGGAGTTTGTGGCTGAGCTGGTCTAAGCCAGGATTTCTGAATGGCCAGCCTTGCTGCCTTAGGTCACACTGTGTCATACCATCAAGCTGATATCCCCATTCCTATTTCCCCGGCAGCCATCCCCCCAAGAGTGGTGGTCCCACTGGCGGAGACCCACTGTGAGGAGCAGGGTGACGCAGTCTTTGAATGTACCCTCTCCAGCCCCTGCCCTAGTGCAGCCTGGCATTTCCGGCACCGGCTACTCCACCCCAGTGACAAATATGAAGTGTATGTGTCCCCTGACGGG... | TGAGGTCCAGAGGTGACCTGTCCAAGGTAACATGGGGAGTTTGTGGCTGAGCTGGTCTAAGCCAGGATTTCTGAATGGCCAGCCTTGCTGCCTTAGGTCACACTGTGTCATACCATCAAGCTGATATCCCCATTCCTATTTCCCCGGCAGCCATCCCCCCAAGAGTGGTGGTCCCACTGGCGGAGACCCACTGTGAGGAGCAGGGTGACGCAGTCTTTGAATGTACCCTCTCCAGCCCCTGCCCTAGTGCAGCCTGGCATTTCCGGCACCGGCTACTCCACCCCAGTGACAAATATGAAGTGTATGTGTCCCCTGACGGG... |
Task1_train_33372 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GATTATTCTCCACCCACTGCAGTGCAGACCTTCATGGCCAACCCAACCCTTCTCAGCTGTGCCTGCTCTACTGGGTCTCTTGGAATTACTTTGGGGCACAGATGGCTCTAGGGTCCTAGGCAGCCTTGGGACAGTGGCCCAGGTTCAGTCTGGATGAGAAGCCCCTGCACCAGACCAGAGAGCACTCTCAAACTTCCCTGGGGATAGAAATTTGCGTTCCAGATGTTCCCAGGAAAGTGTAAATTGGACATAAGTAAGGCAGGTGGTTGAGCAAGTCGATATTTTAAAAACCATGCACCTGCTGCGGCAGTTTGATAAAC... | GATTATTCTCCACCCACTGCAGTGCAGACCTTCATGGCCAACCCAACCCTTCTCAGCTGTGCCTGCTCTACTGGGTCTCTTGGAATTACTTTGGGGCACAGATGGCTCTAGGGTCCTAGGCAGCCTTGGGACAGTGGCCCAGGTTCAGTCTGGATGAGAAGCCCCTGCACCAGACCAGAGAGCACTCTCAAACTTCCCTGGGGATAGAAATTTGCGTTCCAGATGTTCCCAGGAAAGTGTAAATTGGACATAAGTAAGGCAGGTGGTTGAGCAAGTCGATATTTTAAAAACCATGCACCTGCTGCGGCAGTTTGATAAAC... |
Task1_train_33373 | Given this context: Chromosome 1 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GCCTGCTCTACTGGGTCTCTTGGAATTACTTTGGGGCACAGATGGCTCTAGGGTCCTAGGCAGCCTTGGGACAGTGGCCCAGGTTCAGTCTGGATGAGAAGCCCCTGCACCAGACCAGAGAGCACTCTCAAACTTCCCTGGGGATAGAAATTTGCGTTCCAGATGTTCCCAGGAAAGTGTAAATTGGACATAAGTAAGGCAGGTGGTTGAGCAAGTCGATATTTTAAAAACCATGCACCTGCTGCGGCAGTTTGATAAACAAATGACTTTTGGCTTATGCGTTTTCTCCAAAACCCTCATGAAGCCTATAGCAGGGTGGC... | GCCTGCTCTACTGGGTCTCTTGGAATTACTTTGGGGCACAGATGGCTCTAGGGTCCTAGGCAGCCTTGGGACAGTGGCCCAGGTTCAGTCTGGATGAGAAGCCCCTGCACCAGACCAGAGAGCACTCTCAAACTTCCCTGGGGATAGAAATTTGCGTTCCAGATGTTCCCAGGAAAGTGTAAATTGGACATAAGTAAGGCAGGTGGTTGAGCAAGTCGATATTTTAAAAACCATGCACCTGCTGCGGCAGTTTGATAAACAAATGACTTTTGGCTTATGCGTTTTCTCCAAAACCCTCATGAAGCCTATAGCAGGGTGGC... |
Task1_train_33374 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AACAAATGACTTTTGGCTTATGCGTTTTCTCCAAAACCCTCATGAAGCCTATAGCAGGGTGGCCTGCGGGTATAGGACTAGGGAGGTGGTGATGGGATTCACCCATCCATCCCTGGAACACCCTGGCTTCCTTCCCAGGTGGTCACCTTGCTTCTCTCCTGGGGAAGTCCAGGTCAGGCAAGCAGCTGGGCTCAGGCAGGTGCTTTGGCCGGATTTAACAGGAGTTTTGGTATTTTCTCTTGTCTCTCCATGTGGGCACTGACCTTCCATATGAATAACCCCTCACTGAAGCTGGGAAGGATAAAGACCTTCAGTCCACA... | AACAAATGACTTTTGGCTTATGCGTTTTCTCCAAAACCCTCATGAAGCCTATAGCAGGGTGGCCTGCGGGTATAGGACTAGGGAGGTGGTGATGGGATTCACCCATCCATCCCTGGAACACCCTGGCTTCCTTCCCAGGTGGTCACCTTGCTTCTCTCCTGGGGAAGTCCAGGTCAGGCAAGCAGCTGGGCTCAGGCAGGTGCTTTGGCCGGATTTAACAGGAGTTTTGGTATTTTCTCTTGTCTCTCCATGTGGGCACTGACCTTCCATATGAATAACCCCTCACTGAAGCTGGGAAGGATAAAGACCTTCAGTCCACA... |
Task1_train_33375 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGGGCTTTCCAGTAGCAGAGGGAAGCAGAGCCACTCTTCCCAGGGAAAATCAATCCCACAGAGAGGGAGGCTGGGCCAGAAGCCTTGCAGAGAGGCCCCATCTACAGGGAGAGAGCTCAGAATCAGGGTTGGGCCTCCCAGAAAAACAACAGCAAGATCGTGGCAGAGACAGCAACAGTGATGAATGCTGGAGGAAAGCAGGAGGCTGGGAGGCTGGGTCCAGTCGGCTTCAGGCTGGAGGACTGGGGAGCAGCAGGGAAGGAAAGGAGCACAGAGGGGACAGTGGAAGACAACTGGACAGGCATGCCCCAGAGCAACTG... | AGGGCTTTCCAGTAGCAGAGGGAAGCAGAGCCACTCTTCCCAGGGAAAATCAATCCCACAGAGAGGGAGGCTGGGCCAGAAGCCTTGCAGAGAGGCCCCATCTACAGGGAGAGAGCTCAGAATCAGGGTTGGGCCTCCCAGAAAAACAACAGCAAGATCGTGGCAGAGACAGCAACAGTGATGAATGCTGGAGGAAAGCAGGAGGCTGGGAGGCTGGGTCCAGTCGGCTTCAGGCTGGAGGACTGGGGAGCAGCAGGGAAGGAAAGGAGCACAGAGGGGACAGTGGAAGACAACTGGACAGGCATGCCCCAGAGCAACTG... |
Task1_train_33376 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GGAGATGGGGTCACTGGATGAGTCAGGTCATAGGAATGGGATTGGAGGTTATGGGGAAATGGGGTCAGGTTATAGGGAGGATTTGGGGGCTCCTGAGGGAATGGGCACAGGGAGCAAGGCAGGTTATAGGGATGGCTTAAGGGGTTCTGGAGAAATGAGGTCAATGGATGAGGCAGGTTATAGGAAAAATTTGGGAGCTCCTGAGAGAATGGATTCAGGGAGCAAGGCAGGTTACAGGGGTGGTTTAAGGGGTTCTGGGGAAATGGGGTTAATTGAGGCAGGCTATAGGAAAGATTTGGGGGTTTCTGAGGGAGGGGGTT... | GGAGATGGGGTCACTGGATGAGTCAGGTCATAGGAATGGGATTGGAGGTTATGGGGAAATGGGGTCAGGTTATAGGGAGGATTTGGGGGCTCCTGAGGGAATGGGCACAGGGAGCAAGGCAGGTTATAGGGATGGCTTAAGGGGTTCTGGAGAAATGAGGTCAATGGATGAGGCAGGTTATAGGAAAAATTTGGGAGCTCCTGAGAGAATGGATTCAGGGAGCAAGGCAGGTTACAGGGGTGGTTTAAGGGGTTCTGGGGAAATGGGGTTAATTGAGGCAGGCTATAGGAAAGATTTGGGGGTTTCTGAGGGAGGGGGTT... |
Task1_train_33377 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TCCTGAGGGAATGGGTTCAGGGAGTAAGGCAGGTTTCAGGGATGGTTTAGGGGGTTCTGGAGAAATGGGGTCAGTGAATGAAGCAGGTTATAGGAAGGATTTGGGTGCTCCTAAGGGAATAGGTTCAGGGAGCAAGGCAGATTTTAGGGATGCTTTAGGGAGTTCTGGGGAAATGGGGTCAATGGATGAGGCAGGTTATAGGAAGGATTTGTGGGCTCCTGAGGGAATAGGTTCAGGAAGTAAGGCAGGTTTTAGGGATGGTTTAGGGAGTTCTGTAGAAATGGGGTCAGTGAATGAGGCAGGTTATAGGAAGGATTTGG... | TCCTGAGGGAATGGGTTCAGGGAGTAAGGCAGGTTTCAGGGATGGTTTAGGGGGTTCTGGAGAAATGGGGTCAGTGAATGAAGCAGGTTATAGGAAGGATTTGGGTGCTCCTAAGGGAATAGGTTCAGGGAGCAAGGCAGATTTTAGGGATGCTTTAGGGAGTTCTGGGGAAATGGGGTCAATGGATGAGGCAGGTTATAGGAAGGATTTGTGGGCTCCTGAGGGAATAGGTTCAGGAAGTAAGGCAGGTTTTAGGGATGGTTTAGGGAGTTCTGTAGAAATGGGGTCAGTGAATGAGGCAGGTTATAGGAAGGATTTGG... |
Task1_train_33378 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GAGTAAGGAAGGTTTCAGGGATGGTTTAGGGGGTTCTGAGGAAATGGGGTCAATGGATGAGGCAGGTTATAGGAAGGATTTGGGGGCTCCTGAGGGAATAGGTTCAGGGAGTAAGGCAGGTTTCAGGGATGGTTTAGGGGGTTCTGAAGAAATGCGGTCAATGGATGAGGCAGGTTATAGGAAGGATTTGGGGGCTCCTGAGAGAATAGGTTCAGGAAGTAAGGCAGGTTTTAGGGATGGTTTAGGGAGTTCTGTAGAAATGGGGTCAGTGAATGAGGCAGGTTATAGGAAGGATTTAGGGGCTCCTAAGGGAATGGGTT... | GAGTAAGGAAGGTTTCAGGGATGGTTTAGGGGGTTCTGAGGAAATGGGGTCAATGGATGAGGCAGGTTATAGGAAGGATTTGGGGGCTCCTGAGGGAATAGGTTCAGGGAGTAAGGCAGGTTTCAGGGATGGTTTAGGGGGTTCTGAAGAAATGCGGTCAATGGATGAGGCAGGTTATAGGAAGGATTTGGGGGCTCCTGAGAGAATAGGTTCAGGAAGTAAGGCAGGTTTTAGGGATGGTTTAGGGAGTTCTGTAGAAATGGGGTCAGTGAATGAGGCAGGTTATAGGAAGGATTTAGGGGCTCCTAAGGGAATGGGTT... |
Task1_train_33379 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | GAAAATTATGCCTGCCTGAGTGCACAGCTGGGCGTGTGGGTGAAGGGGATGAGCAGGCTATTGCCAAGGTTAACAGTCTGTGGCTTCTGAGTTTTGGATGCAACTTCTGACTGGTGGTTTGACACCCAGTCTTTCTGGGAGCTCAAACCATGGGAGTTTCCTGCTGTCTGTGACTCCCTGCAGAGATGAAAAAGGACCAAGTCGAGTGCCAGCCCCTCCCCAGCTTGTGTGGCTAGATCTGGTGCAGAAGGGAATTACCCAGTTGCCTAACGACCTCCCCTACACACACATACTCTCTCTCTCTCAGGGAGGGGCAGGGG... | GAAAATTATGCCTGCCTGAGTGCACAGCTGGGCGTGTGGGTGAAGGGGATGAGCAGGCTATTGCCAAGGTTAACAGTCTGTGGCTTCTGAGTTTTGGATGCAACTTCTGACTGGTGGTTTGACACCCAGTCTTTCTGGGAGCTCAAACCATGGGAGTTTCCTGCTGTCTGTGACTCCCTGCAGAGATGAAAAAGGACCAAGTCGAGTGCCAGCCCCTCCCCAGCTTGTGTGGCTAGATCTGGTGCAGAAGGGAATTACCCAGTTGCCTAACGACCTCCCCTACACACACATACTCTCTCTCTCTCAGGGAGGGGCAGGGG... |
Task1_train_33380 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GGTAGGACAACACGGCCACCGAGAGCCAGCCTGAGGGCTGTGCAAGGCCACTGGCTATGGCCCCAGGCTGGGGTGCAAGCCTGTCTCTCCAGGCTGGGCCAAGACACAGCTGTGCAGATTTGGCCCAGGGCTAATATCCTGAGAGTTTAGTGACACTGGCCTTGGCCCAATTAGGGGTGTCCAGAGGGTGACCTTGGGTGGTGTGCACACACAAGGGGTCACCATCTTTTTGAGGTTAAAGAGCAAAAGGAGGAAGGCTGATGTCCAGGCAAGATCCATATTCCACAAGCCCTGGGATTCCCAGGTGATGGAAAGAGAGT... | GGTAGGACAACACGGCCACCGAGAGCCAGCCTGAGGGCTGTGCAAGGCCACTGGCTATGGCCCCAGGCTGGGGTGCAAGCCTGTCTCTCCAGGCTGGGCCAAGACACAGCTGTGCAGATTTGGCCCAGGGCTAATATCCTGAGAGTTTAGTGACACTGGCCTTGGCCCAATTAGGGGTGTCCAGAGGGTGACCTTGGGTGGTGTGCACACACAAGGGGTCACCATCTTTTTGAGGTTAAAGAGCAAAAGGAGGAAGGCTGATGTCCAGGCAAGATCCATATTCCACAAGCCCTGGGATTCCCAGGTGATGGAAAGAGAGT... |
Task1_train_33381 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | GAGCTGCAGGGGAAGCAGGACGCAGTGACATGGAGACACAGGCAGGGTAGTAGGTCACCATGCGGCTGGGGTAGGACTGGGGTGCCAAAGGGGAGAGGAGCAGGCTGGAGCTGCCTCCAGGGGCAGAATAGGACAGCAGCCTGAGGCTGGAGGGAAGCTTCTCCGCCCCACATTTCACCCCCACCAGCAAGCAGAGGCCACAGGGAGAGAAGCACGAGGCCCCGGAGGAGCCAGAGAAGGAAACCTGTGGGCTGAAGCAGAGGAGGAAGGGCTGGGAGCCTGGGGCCCTCCAAGGAGGAATGGGATAGCTGGAAGGTAGG... | GAGCTGCAGGGGAAGCAGGACGCAGTGACATGGAGACACAGGCAGGGTAGTAGGTCACCATGCGGCTGGGGTAGGACTGGGGTGCCAAAGGGGAGAGGAGCAGGCTGGAGCTGCCTCCAGGGGCAGAATAGGACAGCAGCCTGAGGCTGGAGGGAAGCTTCTCCGCCCCACATTTCACCCCCACCAGCAAGCAGAGGCCACAGGGAGAGAAGCACGAGGCCCCGGAGGAGCCAGAGAAGGAAACCTGTGGGCTGAAGCAGAGGAGGAAGGGCTGGGAGCCTGGGGCCCTCCAAGGAGGAATGGGATAGCTGGAAGGTAGG... |
Task1_train_33382 | This alteration occurs on Chromosome 1. Is it associated with a disease or is it a benign variant? | Benign | TCATGGCATGAACATATGAAAGTTCTCTGAGGTCATCTGCTTGAAGTTCAGAGAAGGAAAATGGCTCAGGGTCACACCTGAGGTCTGGGCAGAGCCAGAGCTGTTTAGATGTCCCGAGGCTTAGGCAGGACTCAATCCGTTCCTCGGCCCTGCCCCAGCCTTGTCCTCCAACTCTCGGCTATGAAGTTGGAACACTCACAAAGCCCCAGCACTAGCAGTGGGTGGGAGGTGCTCGGGGCAGGGACCCCAGGTCCCGATATCCCTCACTCAGGCACAGGAGACTCACTGACCAGAGGTGGGTCAGCCTGGGGCACTGGGAC... | TCATGGCATGAACATATGAAAGTTCTCTGAGGTCATCTGCTTGAAGTTCAGAGAAGGAAAATGGCTCAGGGTCACACCTGAGGTCTGGGCAGAGCCAGAGCTGTTTAGATGTCCCGAGGCTTAGGCAGGACTCAATCCGTTCCTCGGCCCTGCCCCAGCCTTGTCCTCCAACTCTCGGCTATGAAGTTGGAACACTCACAAAGCCCCAGCACTAGCAGTGGGTGGGAGGTGCTCGGGGCAGGGACCCCAGGTCCCGATATCCCTCACTCAGGCACAGGAGACTCACTGACCAGAGGTGGGTCAGCCTGGGGCACTGGGAC... |
Task1_train_33383 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | TCAAAGCATAGTCCTCAGGCTTCTTGCATCAACACCAGCGAGCCCAGGAATCCTTGTTAAACCTGCAGACCCACAGCCCCCCAACCAGGCCTGCTGGAGCAGGGGCTTCCCCTCCCTTACACTGTTCGTGGTCTCCCTCCCAGAAAGCCCCCTTTCCCTGTCCTAACCTCAAGGCTAAACCCTCATCCCCCTTTGGGGCCCCACCCAAGCCCTGCCTCCTCTGAGCAGCTCTCCCTGATCCTTCCCCATCCTTGTTCCATCTTATCCCGCCTGAGTTCATCCTGTTAATCCCATCCCCCTGCCAGATCTGGAGCCCTGGG... | TCAAAGCATAGTCCTCAGGCTTCTTGCATCAACACCAGCGAGCCCAGGAATCCTTGTTAAACCTGCAGACCCACAGCCCCCCAACCAGGCCTGCTGGAGCAGGGGCTTCCCCTCCCTTACACTGTTCGTGGTCTCCCTCCCAGAAAGCCCCCTTTCCCTGTCCTAACCTCAAGGCTAAACCCTCATCCCCCTTTGGGGCCCCACCCAAGCCCTGCCTCCTCTGAGCAGCTCTCCCTGATCCTTCCCCATCCTTGTTCCATCTTATCCCGCCTGAGTTCATCCTGTTAATCCCATCCCCCTGCCAGATCTGGAGCCCTGGG... |
Task1_train_33384 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CCCCCTTTCCCTGTCCTAACCTCAAGGCTAAACCCTCATCCCCCTTTGGGGCCCCACCCAAGCCCTGCCTCCTCTGAGCAGCTCTCCCTGATCCTTCCCCATCCTTGTTCCATCTTATCCCGCCTGAGTTCATCCTGTTAATCCCATCCCCCTGCCAGATCTGGAGCCCTGGGCAAGGACTGCACCTTCCCCTCATGTGCCCTACCGCACAGCCTGGCACAAGGAGGGCGGGTGCAGGTACTCAGAAAATAGCCTGAACATGGCCAAATAGAAAGAACCAGAGCCTCCAGGCCCCCCACCTGCGAGTTAGGGTTGTTTCC... | CCCCCTTTCCCTGTCCTAACCTCAAGGCTAAACCCTCATCCCCCTTTGGGGCCCCACCCAAGCCCTGCCTCCTCTGAGCAGCTCTCCCTGATCCTTCCCCATCCTTGTTCCATCTTATCCCGCCTGAGTTCATCCTGTTAATCCCATCCCCCTGCCAGATCTGGAGCCCTGGGCAAGGACTGCACCTTCCCCTCATGTGCCCTACCGCACAGCCTGGCACAAGGAGGGCGGGTGCAGGTACTCAGAAAATAGCCTGAACATGGCCAAATAGAAAGAACCAGAGCCTCCAGGCCCCCCACCTGCGAGTTAGGGTTGTTTCC... |
Task1_train_33385 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CCTTCCCCATCCTTGTTCCATCTTATCCCGCCTGAGTTCATCCTGTTAATCCCATCCCCCTGCCAGATCTGGAGCCCTGGGCAAGGACTGCACCTTCCCCTCATGTGCCCTACCGCACAGCCTGGCACAAGGAGGGCGGGTGCAGGTACTCAGAAAATAGCCTGAACATGGCCAAATAGAAAGAACCAGAGCCTCCAGGCCCCCCACCTGCGAGTTAGGGTTGTTTCCGAGTTTTCTTTCTTGGGTTTCATCTGAAATGAGAAGGAAAGGCATTGTTGTGTGGGAGTCCCCGGGAAATCGGTGGCCCCCTCGAGTGAGGA... | CCTTCCCCATCCTTGTTCCATCTTATCCCGCCTGAGTTCATCCTGTTAATCCCATCCCCCTGCCAGATCTGGAGCCCTGGGCAAGGACTGCACCTTCCCCTCATGTGCCCTACCGCACAGCCTGGCACAAGGAGGGCGGGTGCAGGTACTCAGAAAATAGCCTGAACATGGCCAAATAGAAAGAACCAGAGCCTCCAGGCCCCCCACCTGCGAGTTAGGGTTGTTTCCGAGTTTTCTTTCTTGGGTTTCATCTGAAATGAGAAGGAAAGGCATTGTTGTGTGGGAGTCCCCGGGAAATCGGTGGCCCCCTCGAGTGAGGA... |
Task1_train_33386 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | GAGGCTGGGGGCAGTGGCTTGGGCACCTCTGCTTCTTCCACGCTCGGTAGTCTGAATCAGAAGATGGGAGACAGAATCAGAGGATAGAGGTGGAAGATACCCTAAGTATACCTAACCCAATGGAGATGCTGCCAGGGCCACCAAGGAGGAGGTGAGGATGTCAGGCCCTGGCCTCCCCGGCTCACCACCACCTTTATCCACTCGATATATTGCACTTCCAAGGTATCATCTGAGCAAAGCACACTATGCTTTTTAAAAAGCTTATAAATTCCTATGAAGTCCAACGACTCCATGTTCAGACGTAGTCAACAGACTCTGAA... | GAGGCTGGGGGCAGTGGCTTGGGCACCTCTGCTTCTTCCACGCTCGGTAGTCTGAATCAGAAGATGGGAGACAGAATCAGAGGATAGAGGTGGAAGATACCCTAAGTATACCTAACCCAATGGAGATGCTGCCAGGGCCACCAAGGAGGAGGTGAGGATGTCAGGCCCTGGCCTCCCCGGCTCACCACCACCTTTATCCACTCGATATATTGCACTTCCAAGGTATCATCTGAGCAAAGCACACTATGCTTTTTAAAAAGCTTATAAATTCCTATGAAGTCCAACGACTCCATGTTCAGACGTAGTCAACAGACTCTGAA... |
Task1_train_33387 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AGTCTGAGGCAACCAGTCCATCCCCATCCATCAGGATAGAAACCTGAGCACCTACCTCTCAGAAGCAGAGGCCTGCCGGTCTCCATTCTGGCTGAGCCTGGGAGCCTCATCGTCCGTGGTGGAGCTCAGGTTGCGGTGCCGCCGCCTGCGCTCGCGCTCCTGTTCCTCCTCATCCTCCAGAGTCCTCTGCCGGGCAAGGCTGGGGGAGGGGAGGAGAGGGTCAGCACAGCTGGGGAAACCCAGGACCCTCCCGAGGCAGGCTCCTCTAGGGCTGGGAGAAGAGACCAAATGCCCTCTAGGCCTGCACTGGCTACTAGCAG... | AGTCTGAGGCAACCAGTCCATCCCCATCCATCAGGATAGAAACCTGAGCACCTACCTCTCAGAAGCAGAGGCCTGCCGGTCTCCATTCTGGCTGAGCCTGGGAGCCTCATCGTCCGTGGTGGAGCTCAGGTTGCGGTGCCGCCGCCTGCGCTCGCGCTCCTGTTCCTCCTCATCCTCCAGAGTCCTCTGCCGGGCAAGGCTGGGGGAGGGGAGGAGAGGGTCAGCACAGCTGGGGAAACCCAGGACCCTCCCGAGGCAGGCTCCTCTAGGGCTGGGAGAAGAGACCAAATGCCCTCTAGGCCTGCACTGGCTACTAGCAG... |
Task1_train_33388 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TCGCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCACCACCATGTCCAACTAATTTTTGTATTTTTAGTAGAGACGCGGTTTCACCATCTCGGCCAGGCTAGTCTCAAACTCCTGACCTCAGCTGATTCGCCCACCTCCGCCTCCAAAAGTGCAGGAATTACAGGCATGAGCCACTGCGCCCAGCCTAAGTACTGCATTTTCTACATCTGCACAGAAAAAGTTGTGAGATATCCCCCAGCAAATAATCTTGTTTCATTTTGCTTAATCCATTGTTCCCTAAACTCATTTAACCAT... | TCGCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCACCACCATGTCCAACTAATTTTTGTATTTTTAGTAGAGACGCGGTTTCACCATCTCGGCCAGGCTAGTCTCAAACTCCTGACCTCAGCTGATTCGCCCACCTCCGCCTCCAAAAGTGCAGGAATTACAGGCATGAGCCACTGCGCCCAGCCTAAGTACTGCATTTTCTACATCTGCACAGAAAAAGTTGTGAGATATCCCCCAGCAAATAATCTTGTTTCATTTTGCTTAATCCATTGTTCCCTAAACTCATTTAACCAT... |
Task1_train_33389 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCTCACTCTTGCCACCCAGGCTGGAGGGCAGTGGCGTGATCACAGCTCACTGCAGCCTTGAACTCTTGGGCTTAAGTAATTCTCCTGTCGCAGCCTCCTGAGTAGCTGGGATTACAAGCATGTGCCACCATGCATGGCTTCTCACAGGATATTAAACCGTCCAGGCACTGGGATCCTGGGGACCTTTGAGGCTTTATGGAGAAATGCTACCTAGGAAAAGCATATGCTCTGCACTTTCTCCATCTATTTCTGTTTCCTCTGATAGACATTCTTTGTTGTGGCTTTTACACCTGTGTTTGTATATTTTCTTCTTCTTCTGC... | TCTCACTCTTGCCACCCAGGCTGGAGGGCAGTGGCGTGATCACAGCTCACTGCAGCCTTGAACTCTTGGGCTTAAGTAATTCTCCTGTCGCAGCCTCCTGAGTAGCTGGGATTACAAGCATGTGCCACCATGCATGGCTTCTCACAGGATATTAAACCGTCCAGGCACTGGGATCCTGGGGACCTTTGAGGCTTTATGGAGAAATGCTACCTAGGAAAAGCATATGCTCTGCACTTTCTCCATCTATTTCTGTTTCCTCTGATAGACATTCTTTGTTGTGGCTTTTACACCTGTGTTTGTATATTTTCTTCTTCTTCTGC... |
Task1_train_33390 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GCCGGCGAGGACTGCCTGTGGTACCTGGACCGGAATGGCTCCTGGCATCCGGGGTTTAACTGCGAGTTCTTCACCTTCTGCTGCGGGACCTGCTACCATCGGTACTGCTGCAGGGACCTGACCTTGCTTATCACCGAGAGGCAGCAGAAGCACTGCCTGGCCTTCAGGTGGGTTCCTGCCTCCTCACCCTCACCACCTCCTCTATCCTTTTCTCCAGAGGCCTCCTCTTCCTCCCTCCCGGACTCCTGCCTCCTCCGTTGTCGACCTCCACATTCTTAGCTGAATAGAGTCACCAGGACTCAAGCCTGGCGGCAGAGCTA... | GCCGGCGAGGACTGCCTGTGGTACCTGGACCGGAATGGCTCCTGGCATCCGGGGTTTAACTGCGAGTTCTTCACCTTCTGCTGCGGGACCTGCTACCATCGGTACTGCTGCAGGGACCTGACCTTGCTTATCACCGAGAGGCAGCAGAAGCACTGCCTGGCCTTCAGGTGGGTTCCTGCCTCCTCACCCTCACCACCTCCTCTATCCTTTTCTCCAGAGGCCTCCTCTTCCTCCCTCCCGGACTCCTGCCTCCTCCGTTGTCGACCTCCACATTCTTAGCTGAATAGAGTCACCAGGACTCAAGCCTGGCGGCAGAGCTA... |
Task1_train_33391 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GCCCTGGACAGTGCCATCTTCTCAGTGATGTGCTAAAAGGACTCTTCTTGTCCAGAAACCTGAGCTCCATGTACTAAAGCAAAATTTGGAGAGCCTCAGAGACAAGAAAAGGAAAGTGAGAAGAGATAAGGCATCCTTCCTTGAGCGTGACCCAGGCCTGGACTCTCCCATGGCAGAATAGGGACATCCACAGCAGGTCAGCCAGGGATGGGGTGGGCAGGGTCTGTGTAGCCCTGGGAGGTGAGGCCTGAGCAGTCATGGCATTGGCAGATGGTGCCTGGCAGCCTGGTCCTACTGAAGCAGTTTGGGCACTTCCACCT... | GCCCTGGACAGTGCCATCTTCTCAGTGATGTGCTAAAAGGACTCTTCTTGTCCAGAAACCTGAGCTCCATGTACTAAAGCAAAATTTGGAGAGCCTCAGAGACAAGAAAAGGAAAGTGAGAAGAGATAAGGCATCCTTCCTTGAGCGTGACCCAGGCCTGGACTCTCCCATGGCAGAATAGGGACATCCACAGCAGGTCAGCCAGGGATGGGGTGGGCAGGGTCTGTGTAGCCCTGGGAGGTGAGGCCTGAGCAGTCATGGCATTGGCAGATGGTGCCTGGCAGCCTGGTCCTACTGAAGCAGTTTGGGCACTTCCACCT... |
Task1_train_33392 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | GTTGCTAATTTTCCAGCTGATATAATACAATCCAGCTTTATTCGAAAGATAAGTATTCTAACTCTTGTTCGGTGTTTATTCAAACTTGTGTTTGCATGTATTTGTTTGGACTATAAATTTTGAGACTATAGTGAGTATGTTTTTGACTATAATATTTTAAATGGAAGATGAAATTTAAATTAGTATTTGCTTGTTTCTTTTTACAATAAAATAGGTAGCTTTGCAGTTTGGGGAGGGCTGTTTTCCATGATTGACTGTAGTATGGTTCAAGTCAGAGGAAAGGAAGATCCCTGGAACTCCATCACAAGTGGTGCCTTAAC... | GTTGCTAATTTTCCAGCTGATATAATACAATCCAGCTTTATTCGAAAGATAAGTATTCTAACTCTTGTTCGGTGTTTATTCAAACTTGTGTTTGCATGTATTTGTTTGGACTATAAATTTTGAGACTATAGTGAGTATGTTTTTGACTATAATATTTTAAATGGAAGATGAAATTTAAATTAGTATTTGCTTGTTTCTTTTTACAATAAAATAGGTAGCTTTGCAGTTTGGGGAGGGCTGTTTTCCATGATTGACTGTAGTATGGTTCAAGTCAGAGGAAAGGAAGATCCCTGGAACTCCATCACAAGTGGTGCCTTAAC... |
Task1_train_33393 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | AGTGTCGTGACCTGTTTTCTTGTGCGTCTGCTAAAATGTGAGTTAGGCTATGAACACCATAGGAAGAGGAATTGTGCCGGACTTATTCAAACTGTACCCCAGGCACTTAGCTTAACAACTGGTGTCTAGCAGATACTCAGCAAAAGTGCATTGCATCGAAGACTGAATAATTTCAAGATAGGAGTATTCAACGTCTAATATGTACCAAGCGCTGTTCTCAATGCTACAGAAAAGCAGGTTTCTAAGGTTTCTGGAGTTAAACAAAAAACCCTGACATTGAACTTACATGGAATATTAAAGTCATTATCTACCATAAGCAT... | AGTGTCGTGACCTGTTTTCTTGTGCGTCTGCTAAAATGTGAGTTAGGCTATGAACACCATAGGAAGAGGAATTGTGCCGGACTTATTCAAACTGTACCCCAGGCACTTAGCTTAACAACTGGTGTCTAGCAGATACTCAGCAAAAGTGCATTGCATCGAAGACTGAATAATTTCAAGATAGGAGTATTCAACGTCTAATATGTACCAAGCGCTGTTCTCAATGCTACAGAAAAGCAGGTTTCTAAGGTTTCTGGAGTTAAACAAAAAACCCTGACATTGAACTTACATGGAATATTAAAGTCATTATCTACCATAAGCAT... |
Task1_train_33394 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | TGACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCGCTGTGCCCAGCCGCCAGTTTCTGCCTGGGAGGTACCACTTCCAAAGAAAAAACGAAAAATGTCCTGTCATGGAAGACACAATCCATTAGACATACCCCCACTTCTTGCTGTGACCTGAACCTTGAGTCACTCTATTGTTGGTTTGATGAAGTCCGCGTCCTCTGACAGTAGGATTGGTCAGGACTTTAGCAGCACCTACTGTTCGGTTGGAGGCTTGCATTTTAATGCGGGGACTCCGGAGCTAATGGTAGTTAATAAT... | TGACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCGCTGTGCCCAGCCGCCAGTTTCTGCCTGGGAGGTACCACTTCCAAAGAAAAAACGAAAAATGTCCTGTCATGGAAGACACAATCCATTAGACATACCCCCACTTCTTGCTGTGACCTGAACCTTGAGTCACTCTATTGTTGGTTTGATGAAGTCCGCGTCCTCTGACAGTAGGATTGGTCAGGACTTTAGCAGCACCTACTGTTCGGTTGGAGGCTTGCATTTTAATGCGGGGACTCCGGAGCTAATGGTAGTTAATAAT... |
Task1_train_33395 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | AGAGCCGGGTAGGGGAGCGCAGCGGCCAGATACCTCAGCGCTACCTGGCGGAACTGGATTTCTCTCCCGCCTGCCGGCCTGCCTGCCACAGCCGGACTCCGCCACTCCGGTAGGATTCCCCGCCTGTCATTCCCTAGCCCAGCTCTTGGGAAACTGCAGAGGGGTCCAGAGGATTTGCAGTTCTGAACCTGCACACTCCAGTCTAGGATCTCCGAGCAAGAGCGTAGGTGTCCTGAGGGTCAAAGAACAGAGAGAGATTGTCTCTGGGAAGGCAGAATGGCCATGACGCCGCTAGTCTGGCTCCAGGGCCCCAGAGATCT... | AGAGCCGGGTAGGGGAGCGCAGCGGCCAGATACCTCAGCGCTACCTGGCGGAACTGGATTTCTCTCCCGCCTGCCGGCCTGCCTGCCACAGCCGGACTCCGCCACTCCGGTAGGATTCCCCGCCTGTCATTCCCTAGCCCAGCTCTTGGGAAACTGCAGAGGGGTCCAGAGGATTTGCAGTTCTGAACCTGCACACTCCAGTCTAGGATCTCCGAGCAAGAGCGTAGGTGTCCTGAGGGTCAAAGAACAGAGAGAGATTGTCTCTGGGAAGGCAGAATGGCCATGACGCCGCTAGTCTGGCTCCAGGGCCCCAGAGATCT... |
Task1_train_33396 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | GGTTTCAATGACAGCAGCATAATGCCGTGGGAGTTGGGAGGAGGGAATGATCTGACTCACTCTGGGGCAGGTCTTCGAGTTAATTCTCCAGTGGATTCTCCTAGGCATCGTGTGGTCCGTCCTCAGAACTGTGCCTCCCTAATGTGGCTGAGTGGATTCACTACCCACCCCATGCTTGGGCTCTGCCTCGACCTCTCCCTCCCATGCACAGCCAAAGCCGCTCAAAGCTGCTGGTTTTCCTTGACTCTGGGCTTCTCTCCATCACCCACTGCCTCCCAACAGAACCCCCGGTCTCTGCATCCTCCTGTTCCAGATTGCTA... | GGTTTCAATGACAGCAGCATAATGCCGTGGGAGTTGGGAGGAGGGAATGATCTGACTCACTCTGGGGCAGGTCTTCGAGTTAATTCTCCAGTGGATTCTCCTAGGCATCGTGTGGTCCGTCCTCAGAACTGTGCCTCCCTAATGTGGCTGAGTGGATTCACTACCCACCCCATGCTTGGGCTCTGCCTCGACCTCTCCCTCCCATGCACAGCCAAAGCCGCTCAAAGCTGCTGGTTTTCCTTGACTCTGGGCTTCTCTCCATCACCCACTGCCTCCCAACAGAACCCCCGGTCTCTGCATCCTCCTGTTCCAGATTGCTA... |
Task1_train_33397 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | GGGAGTTGGGAGGAGGGAATGATCTGACTCACTCTGGGGCAGGTCTTCGAGTTAATTCTCCAGTGGATTCTCCTAGGCATCGTGTGGTCCGTCCTCAGAACTGTGCCTCCCTAATGTGGCTGAGTGGATTCACTACCCACCCCATGCTTGGGCTCTGCCTCGACCTCTCCCTCCCATGCACAGCCAAAGCCGCTCAAAGCTGCTGGTTTTCCTTGACTCTGGGCTTCTCTCCATCACCCACTGCCTCCCAACAGAACCCCCGGTCTCTGCATCCTCCTGTTCCAGATTGCTAGGACCCCAGCTGCCCATCAGGGACCCCT... | GGGAGTTGGGAGGAGGGAATGATCTGACTCACTCTGGGGCAGGTCTTCGAGTTAATTCTCCAGTGGATTCTCCTAGGCATCGTGTGGTCCGTCCTCAGAACTGTGCCTCCCTAATGTGGCTGAGTGGATTCACTACCCACCCCATGCTTGGGCTCTGCCTCGACCTCTCCCTCCCATGCACAGCCAAAGCCGCTCAAAGCTGCTGGTTTTCCTTGACTCTGGGCTTCTCTCCATCACCCACTGCCTCCCAACAGAACCCCCGGTCTCTGCATCCTCCTGTTCCAGATTGCTAGGACCCCAGCTGCCCATCAGGGACCCCT... |
Task1_train_33398 | This variant is located on Chromosome 1. Evaluate its biological effect and specify any disease association. | Benign | AGCCACTGTGCCTGACCATATTTGCTTTTCTTACAAGTATTACTGTTATAAGGCACCTCTGAGGGGGCCGCTCTTTATCTTTCCTTTAACCTGGTAGCCCAGTAAATTTAGGGTTTGGGCCCCTGCTGTGTGCCCTCTTTTTTTTTTTTTTTTTGAGAGAGAGGAGGTCTCACTATATTGCCTAGGCCGGTCTCTAATTCCTGGACTCAGGAGATCCTCTCACCTCAGCCTCCCAAAGTGCTGGGATTTTGGGCATGAGCTACCATGCCTGGCTCAGCCCTCTCCCTTTGTCAGCCAGAACAGGGCAGCCTTGAACTCAA... | AGCCACTGTGCCTGACCATATTTGCTTTTCTTACAAGTATTACTGTTATAAGGCACCTCTGAGGGGGCCGCTCTTTATCTTTCCTTTAACCTGGTAGCCCAGTAAATTTAGGGTTTGGGCCCCTGCTGTGTGCCCTCTTTTTTTTTTTTTTTTTGAGAGAGAGGAGGTCTCACTATATTGCCTAGGCCGGTCTCTAATTCCTGGACTCAGGAGATCCTCTCACCTCAGCCTCCCAAAGTGCTGGGATTTTGGGCATGAGCTACCATGCCTGGCTCAGCCCTCTCCCTTTGTCAGCCAGAACAGGGCAGCCTTGAACTCAA... |
Task1_train_33399 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | GCTCTTTATCTTTCCTTTAACCTGGTAGCCCAGTAAATTTAGGGTTTGGGCCCCTGCTGTGTGCCCTCTTTTTTTTTTTTTTTTTGAGAGAGAGGAGGTCTCACTATATTGCCTAGGCCGGTCTCTAATTCCTGGACTCAGGAGATCCTCTCACCTCAGCCTCCCAAAGTGCTGGGATTTTGGGCATGAGCTACCATGCCTGGCTCAGCCCTCTCCCTTTGTCAGCCAGAACAGGGCAGCCTTGAACTCAACTGCTCCTTCCAGCTGCCTGCCTCTTCCCACTCCCAGCCAGGCCCTGTGGCTCCGACATGCATCCAGCA... | GCTCTTTATCTTTCCTTTAACCTGGTAGCCCAGTAAATTTAGGGTTTGGGCCCCTGCTGTGTGCCCTCTTTTTTTTTTTTTTTTTGAGAGAGAGGAGGTCTCACTATATTGCCTAGGCCGGTCTCTAATTCCTGGACTCAGGAGATCCTCTCACCTCAGCCTCCCAAAGTGCTGGGATTTTGGGCATGAGCTACCATGCCTGGCTCAGCCCTCTCCCTTTGTCAGCCAGAACAGGGCAGCCTTGAACTCAACTGCTCCTTCCAGCTGCCTGCCTCTTCCCACTCCCAGCCAGGCCCTGTGGCTCCGACATGCATCCAGCA... |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.