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_43300 | This alteration occurs on Chromosome 14. Is it associated with a disease or is it a benign variant? | Benign | CTGCCTCAGCCTCCCAAGTAGCTGGAATTACAGGCACGTGCCACTACGCCTGGCTAATTTTTGGATTTTCAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTTCAAGCTCCTGACCTCAAGTGATGTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTGAGTCACTACAGGTGTGAGCCAGCACACTTGGCCACTTTTTTTTTTTTAATCACTGTTCTTGAAGTGGTTGCAGAAGAGAAATAAGACCAATGCCACTGGAGCACAGTAGGGGAGGGGAGGTCATAGGAATGATGTCACAGAAACAGGCCTGCCTGG... | CTGCCTCAGCCTCCCAAGTAGCTGGAATTACAGGCACGTGCCACTACGCCTGGCTAATTTTTGGATTTTCAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTTCAAGCTCCTGACCTCAAGTGATGTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTGAGTCACTACAGGTGTGAGCCAGCACACTTGGCCACTTTTTTTTTTTTAATCACTGTTCTTGAAGTGGTTGCAGAAGAGAAATAAGACCAATGCCACTGGAGCACAGTAGGGGAGGGGAGGTCATAGGAATGATGTCACAGAAACAGGCCTGCCTGG... |
Task1_train_43301 | A variant on Chromosome 14 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | ACTGGTCTGTAATTCCCTTTCCCTCATGGTCCACCAGGAAAATTCTTATTCTTTGCCTTGTACATTTGGTCAAAGATCACCCCTTCTGTGAAGCTATTTTTGACTTATTAAGTAGACTTAGGTACTTCTCTCTGTGAATATTTCCACCGTATCTTGCACACCTGTCTGGCTCCACTATACCATGGGCTCCACAAGACATGGGCAGGATCTTGTTCAATATTTTATGCAATAATGTAGGAATACAGTGGGCAATCGACAAAGATTTATCAAATGAATGAATTTCTTTGTAATTGACTGTTTGTACCCCCTCAATACTTGTT... | ACTGGTCTGTAATTCCCTTTCCCTCATGGTCCACCAGGAAAATTCTTATTCTTTGCCTTGTACATTTGGTCAAAGATCACCCCTTCTGTGAAGCTATTTTTGACTTATTAAGTAGACTTAGGTACTTCTCTCTGTGAATATTTCCACCGTATCTTGCACACCTGTCTGGCTCCACTATACCATGGGCTCCACAAGACATGGGCAGGATCTTGTTCAATATTTTATGCAATAATGTAGGAATACAGTGGGCAATCGACAAAGATTTATCAAATGAATGAATTTCTTTGTAATTGACTGTTTGTACCCCCTCAATACTTGTT... |
Task1_train_43302 | Consider a variant on Chromosome 14. Determine its clinical classification and disease relevance. | Benign | GACCCTGGATGTGACTGCATGACTCTCTAGATACGTCACATCACCTTCCCGACCTTAATTTTCTCATCTATAAATAACTTGACTAAGTTATTCAAGGTCCCTTCCAGCTTGAAAATCCGGTAATTCCATGGTTGTCTCTTTCCAAGGGCTTCCGTGTCAAAGGAGAGTTCAGGGTTTTCTCTCTTCCTCTGTCAATTCAGAGGGGCCCCGTGGATAAGGTAGAAGTTACAGTGCTACCACCAGCAGAAGACAGTGCTGATTTCAGGGGAAATGAATAAGCAGGCACAGAGAGGAACACTTGGTTTTAAAAATTCTGTCAG... | GACCCTGGATGTGACTGCATGACTCTCTAGATACGTCACATCACCTTCCCGACCTTAATTTTCTCATCTATAAATAACTTGACTAAGTTATTCAAGGTCCCTTCCAGCTTGAAAATCCGGTAATTCCATGGTTGTCTCTTTCCAAGGGCTTCCGTGTCAAAGGAGAGTTCAGGGTTTTCTCTCTTCCTCTGTCAATTCAGAGGGGCCCCGTGGATAAGGTAGAAGTTACAGTGCTACCACCAGCAGAAGACAGTGCTGATTTCAGGGGAAATGAATAAGCAGGCACAGAGAGGAACACTTGGTTTTAAAAATTCTGTCAG... |
Task1_train_43303 | This alteration on Chromosome 14 may affect genome function. Does it lead to a disease or is it benign? | Benign | ATCTTCAGTCTGATTGAAGGCCACTTTTCTTTCCCATCCCCCAGTCCCAGAGCCAAAGTCTGAATGTGAGATATTATGACTAACAGACCCTGCACAGGGTAGCTGGAGTCGTAAAATTAACCTCTCAGTGTATTGTCCATGATTGGCCATAAACTGGCCCTTTTACCTACATCGAGGGCAGTGTGAGAAAGATGTCTCTTCAGAAGCCATCTAGAAATGAATCACTTCCAGCACCACAGCTAATACGTTAATGAGTCCCCAAAGAATATAAATTCAGAAGCTGCCCTGAAAAGCTGCTTAGCAGCTCAGCTGAGAAGAAT... | ATCTTCAGTCTGATTGAAGGCCACTTTTCTTTCCCATCCCCCAGTCCCAGAGCCAAAGTCTGAATGTGAGATATTATGACTAACAGACCCTGCACAGGGTAGCTGGAGTCGTAAAATTAACCTCTCAGTGTATTGTCCATGATTGGCCATAAACTGGCCCTTTTACCTACATCGAGGGCAGTGTGAGAAAGATGTCTCTTCAGAAGCCATCTAGAAATGAATCACTTCCAGCACCACAGCTAATACGTTAATGAGTCCCCAAAGAATATAAATTCAGAAGCTGCCCTGAAAAGCTGCTTAGCAGCTCAGCTGAGAAGAAT... |
Task1_train_43304 | A variant on Chromosome 14 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GTAATAGCATGATGTCCTTTTGAAGATACTATATTAATTATTTCTTGAATACCTTTTCAAGTAAGTTACTGTTATTTGAAATTCCACTTAATGCCAGCCCTGGCCCCTCAACATTTCATCCCAATCTCGTTGTTTTTGAAAGGCTCAGAGTCATATTGGGCACTTCTTTCATTACTGCCTTTAACTGACCATTTCCTCTTTTCTTTCCTGCAACAGATTGCAGATTGAGCTTAACCAAGAAGTTCGTAGGCTAATCAAGGCTGGCTTGACCTACAAAAGAAGAAGAGAGTTCTGCCTGCCCACTTGGGCTTGTGTTGACA... | GTAATAGCATGATGTCCTTTTGAAGATACTATATTAATTATTTCTTGAATACCTTTTCAAGTAAGTTACTGTTATTTGAAATTCCACTTAATGCCAGCCCTGGCCCCTCAACATTTCATCCCAATCTCGTTGTTTTTGAAAGGCTCAGAGTCATATTGGGCACTTCTTTCATTACTGCCTTTAACTGACCATTTCCTCTTTTCTTTCCTGCAACAGATTGCAGATTGAGCTTAACCAAGAAGTTCGTAGGCTAATCAAGGCTGGCTTGACCTACAAAAGAAGAAGAGAGTTCTGCCTGCCCACTTGGGCTTGTGTTGACA... |
Task1_train_43305 | This sequence change occurs on Chromosome 14. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ATTTCTAAAAATTATGCTTATAATTGAAAACCAAATTATTCTTAACCATCAAAAATAAATGCATATGGCTTTGCTTACATCTATAAGCTCCATGTACAGTCTTGGTTCAAGCAAACTTGAAAAAAATAGTTCAATTATTGACTCTATCAATTATGCCTCAGTTTAAAAAACAAAATAAAATTTTTTAAAAAAATAGTGACCTGATAAAGTCAACTGCTGATGGTTCTCACATAGGTTACCCTCACACATGTAACTATCCTAGGGATGAGTGGCTTCCCGGCACCAAGGCAGATTCTTTGTCTCTCTTCATTATATGTCAC... | ATTTCTAAAAATTATGCTTATAATTGAAAACCAAATTATTCTTAACCATCAAAAATAAATGCATATGGCTTTGCTTACATCTATAAGCTCCATGTACAGTCTTGGTTCAAGCAAACTTGAAAAAAATAGTTCAATTATTGACTCTATCAATTATGCCTCAGTTTAAAAAACAAAATAAAATTTTTTAAAAAAATAGTGACCTGATAAAGTCAACTGCTGATGGTTCTCACATAGGTTACCCTCACACATGTAACTATCCTAGGGATGAGTGGCTTCCCGGCACCAAGGCAGATTCTTTGTCTCTCTTCATTATATGTCAC... |
Task1_train_43306 | A variant was discovered on Chromosome 14. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CATGGACAGTAAGAACTGTTAGGGAGGATGTGGAGAATTGTAAGTTTCATAAAACTGCTGGTGGCAATGTAAAATGGTGCAGTAACTTTGGAAAACAATTTGGTAGTTCCTCAAAATCCTAAAGACAGAGTTACCATGTGACCCAGCAATTCCACTCCTACATACATACCCAAGAGAACTGAAAACACGTTCACAGAAAAACTTGTACACATATGCTAATCCACACCATTAGTCATAACAGCCATGATGGGGTTCAAGACACACTCCCCGCAAATATTTTAAAGTGAAATAATTTGAGAAAAATGTAGAAGCAGGAAGTT... | CATGGACAGTAAGAACTGTTAGGGAGGATGTGGAGAATTGTAAGTTTCATAAAACTGCTGGTGGCAATGTAAAATGGTGCAGTAACTTTGGAAAACAATTTGGTAGTTCCTCAAAATCCTAAAGACAGAGTTACCATGTGACCCAGCAATTCCACTCCTACATACATACCCAAGAGAACTGAAAACACGTTCACAGAAAAACTTGTACACATATGCTAATCCACACCATTAGTCATAACAGCCATGATGGGGTTCAAGACACACTCCCCGCAAATATTTTAAAGTGAAATAATTTGAGAAAAATGTAGAAGCAGGAAGTT... |
Task1_train_43307 | A genomic change on Chromosome 14 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ACTCAGGCCAAGAAGCTTTAAACGAGACAAAGAATGGCATTTTCTAATGATAAGAAATAAATCATAATGAAGATAAAACATTCATCAGTATTTACATACCAAATAACAAAGCAGAAGCTTCCAGTATTTACGTACCAAATAACAAAGCAGAAGCTTCCACACAGCAAAAACTGCCTAAGATTGAAAGGAGAAATAGACCCCACTAACATAAGGAAACAAACACACCTGGGTAGCCCTGAACAGTTCAAGTGGACAAAATCGTTAAGATACAAAATACCTGAACAATATAACCAAAAGGTTATATATAAACTCAATTCTGT... | ACTCAGGCCAAGAAGCTTTAAACGAGACAAAGAATGGCATTTTCTAATGATAAGAAATAAATCATAATGAAGATAAAACATTCATCAGTATTTACATACCAAATAACAAAGCAGAAGCTTCCAGTATTTACGTACCAAATAACAAAGCAGAAGCTTCCACACAGCAAAAACTGCCTAAGATTGAAAGGAGAAATAGACCCCACTAACATAAGGAAACAAACACACCTGGGTAGCCCTGAACAGTTCAAGTGGACAAAATCGTTAAGATACAAAATACCTGAACAATATAACCAAAAGGTTATATATAAACTCAATTCTGT... |
Task1_train_43308 | A variant found on Chromosome 14 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AAAGAAAGTGAGGCAGAGAGGAGTTATAATAGATAACCCACCAAGGCCACACAGTGAAGTGGCAGAACCCAGAAGACACTCTTGGCAATCTTCTCTTTAGTCTACATTCTTTTTGTTTTGTTTCGCTTTGGTTTGGTTTTTGGGTTTTTTTGTTTGTTTGTGTTTTGAACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTGTGATCCCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCGTGCTACCAAGACTGGCTAATTTTTT... | AAAGAAAGTGAGGCAGAGAGGAGTTATAATAGATAACCCACCAAGGCCACACAGTGAAGTGGCAGAACCCAGAAGACACTCTTGGCAATCTTCTCTTTAGTCTACATTCTTTTTGTTTTGTTTCGCTTTGGTTTGGTTTTTGGGTTTTTTTGTTTGTTTGTGTTTTGAACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTGTGATCCCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCGTGCTACCAAGACTGGCTAATTTTTT... |
Task1_train_43309 | A genomic change on Chromosome 14 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GATTCATCAACAGTTGGGAGGGAGTGATTCTGGTGCCCTGAATAGTGTTTCTAGAAAGCTTTCTGTGAAGGTATTCACCATGTAAATGATCTCAGCCACCAGTAGGCCTCAGCAGCAAAGGGATATAGACAAAGTATTTCTCTACTCCAGTATGGAGAGAAGGATGGAACCTTTACTCTTATGTGAATCTATGACATCATAGCTTTAAAAAGACACTAACCTCTTAAACCATCAGATATAAAGGTGGAAATTAATGATTCCAAGATTTTACCCAGAATAAGAACATTCTGTCCTCTCATTTATAAAAGTATAAGAAAAAT... | GATTCATCAACAGTTGGGAGGGAGTGATTCTGGTGCCCTGAATAGTGTTTCTAGAAAGCTTTCTGTGAAGGTATTCACCATGTAAATGATCTCAGCCACCAGTAGGCCTCAGCAGCAAAGGGATATAGACAAAGTATTTCTCTACTCCAGTATGGAGAGAAGGATGGAACCTTTACTCTTATGTGAATCTATGACATCATAGCTTTAAAAAGACACTAACCTCTTAAACCATCAGATATAAAGGTGGAAATTAATGATTCCAAGATTTTACCCAGAATAAGAACATTCTGTCCTCTCATTTATAAAAGTATAAGAAAAAT... |
Task1_train_43310 | A change on Chromosome 14 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CCAAGTGACTATTTATTACTGAGTCGACACAGGATGTCACCAGTGAGCCTCATCTCCAGTCCAATGGAGGAGTTGACTTAGACCTTCCTTGGACAGGAAGGGTCTCATAAGCAATGCCAGAACTTCAACAGAGCCTAAAGGTCTGGGGACAGGGAGATGGGACTTCATGTGCTCCAGGCAGGGAAGAGCTGTGCATTTTTGAGAAATGGGCAGGGACAGGTCTTCCATGGTACCAGTGGTTGAGGATGTCGTGGGTACAACTTTCCCTGGAGGTCAGAAAGCATGAGACAGTTTCTGGAAGTCTCCGCTAGTGCTGTGAT... | CCAAGTGACTATTTATTACTGAGTCGACACAGGATGTCACCAGTGAGCCTCATCTCCAGTCCAATGGAGGAGTTGACTTAGACCTTCCTTGGACAGGAAGGGTCTCATAAGCAATGCCAGAACTTCAACAGAGCCTAAAGGTCTGGGGACAGGGAGATGGGACTTCATGTGCTCCAGGCAGGGAAGAGCTGTGCATTTTTGAGAAATGGGCAGGGACAGGTCTTCCATGGTACCAGTGGTTGAGGATGTCGTGGGTACAACTTTCCCTGGAGGTCAGAAAGCATGAGACAGTTTCTGGAAGTCTCCGCTAGTGCTGTGAT... |
Task1_train_43311 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | AAGATAAAAGATTGTGGAGACCAAGTTTATTGTGCAGAGGAAGCTCTCAGTATAGCAGACCTCAGAGAGAGAGCAGATTGTAAAATTTGTCTTGTCGGACCTAAAAGGGTGCCTGGCTCTTAGTTGGTTATCTCCTGGATTTGGAAAGGAAAGAAGGAAAACAAAGGGGAAAAGAGATTCTCTATAGAATGTGGTTTTTTCCCACAAGAGATTTTGCAGGGCAATTTCAAGATATGGCAAGGAAATATATCTTGGGGTTAAATATTTTGATTTTTTTTTCCTTGTCTCATAATATTATGCCAGAATCAGATTGGAAAGTA... | AAGATAAAAGATTGTGGAGACCAAGTTTATTGTGCAGAGGAAGCTCTCAGTATAGCAGACCTCAGAGAGAGAGCAGATTGTAAAATTTGTCTTGTCGGACCTAAAAGGGTGCCTGGCTCTTAGTTGGTTATCTCCTGGATTTGGAAAGGAAAGAAGGAAAACAAAGGGGAAAAGAGATTCTCTATAGAATGTGGTTTTTTCCCACAAGAGATTTTGCAGGGCAATTTCAAGATATGGCAAGGAAATATATCTTGGGGTTAAATATTTTGATTTTTTTTTCCTTGTCTCATAATATTATGCCAGAATCAGATTGGAAAGTA... |
Task1_train_43312 | Mutation context: Chromosome 14. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCTTTTACATATTGTCTGTGGCAGCTTTTACACTAAAAAGCAGAGTTGACCAGTTGTAACAGACTGTATCACCCTGCAAATCCTGAAGCATTTGCTACCTGGCCCTTTGTAGAAAAAATTTGCCAACCCTTGATATAGAAAAAGTCCATTACCTCAAAGAGTTCCCCCTAGTCCTTTGCCGTCAGTCCCCTCCTGACAAATCCCTGGCAACCACTGATCTGCTCTTTCGCCTATAGTTTTACCTTTTCTATAAGTTCATAGAAATGGAATCATGTATCGTTTTGGGTCTGGCTTTTTTCAGTTATCTTAATGATCTTGAG... | TCTTTTACATATTGTCTGTGGCAGCTTTTACACTAAAAAGCAGAGTTGACCAGTTGTAACAGACTGTATCACCCTGCAAATCCTGAAGCATTTGCTACCTGGCCCTTTGTAGAAAAAATTTGCCAACCCTTGATATAGAAAAAGTCCATTACCTCAAAGAGTTCCCCCTAGTCCTTTGCCGTCAGTCCCCTCCTGACAAATCCCTGGCAACCACTGATCTGCTCTTTCGCCTATAGTTTTACCTTTTCTATAAGTTCATAGAAATGGAATCATGTATCGTTTTGGGTCTGGCTTTTTTCAGTTATCTTAATGATCTTGAG... |
Task1_train_43313 | Given this context: Chromosome 14 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GTACTGTGAATATACATAATATCTATGCAACCTGTTTAACCTTGCTGAATGTCAGTTCTCATTTATACAATAAAGATACTGCCTACCGTCATAGGGTCATTGTGAGGACTGAGTCAGTATCTATGGTACCTGGCACATAACTCAATAAGTAGCTGTTATTGCAGACATGGTGCCTCTTCTTTAAAAAAAACCTTCCTACTTAAGATAGTCTCACCTCTGAACTTCTGAGTCAAGGTCACTCTCCACAATAATATTAAGTTTCCACTTCAGATTTAACTTCCTTGAGAGCAGTCTAATACAACAGTAATTACTAGATTTGT... | GTACTGTGAATATACATAATATCTATGCAACCTGTTTAACCTTGCTGAATGTCAGTTCTCATTTATACAATAAAGATACTGCCTACCGTCATAGGGTCATTGTGAGGACTGAGTCAGTATCTATGGTACCTGGCACATAACTCAATAAGTAGCTGTTATTGCAGACATGGTGCCTCTTCTTTAAAAAAAACCTTCCTACTTAAGATAGTCTCACCTCTGAACTTCTGAGTCAAGGTCACTCTCCACAATAATATTAAGTTTCCACTTCAGATTTAACTTCCTTGAGAGCAGTCTAATACAACAGTAATTACTAGATTTGT... |
Task1_train_43314 | Here is a genetic alteration on Chromosome 14. Based on the data, is it a benign variant or a cause of disease? | Benign | AAAAAGTGCTTAATTCATATTTATTTATTAGGCTGAATATTAAAGAACTGCATCTTCTACCGGGGACTTTCCTTAGATTCTCAGCTGAATTCATCTTTCTTTTAAATTTAAGAAACCTGGACGTCTCAGGATTTGCCTTAACAAAGTGCCACCTTCCCAACTCCAGAATCACTCTGGAGAATCACGGCCAAGATATGTAAGCTGTATCCACACACACTCCAACCTGGAGAATTATATTAGGATTGGGTACACTTTCCTGGATGCTTTTTTCAGATATCTCTTGAGCAAACTAAACAAATGCACCCCTGGGGTGCCACATC... | AAAAAGTGCTTAATTCATATTTATTTATTAGGCTGAATATTAAAGAACTGCATCTTCTACCGGGGACTTTCCTTAGATTCTCAGCTGAATTCATCTTTCTTTTAAATTTAAGAAACCTGGACGTCTCAGGATTTGCCTTAACAAAGTGCCACCTTCCCAACTCCAGAATCACTCTGGAGAATCACGGCCAAGATATGTAAGCTGTATCCACACACACTCCAACCTGGAGAATTATATTAGGATTGGGTACACTTTCCTGGATGCTTTTTTCAGATATCTCTTGAGCAAACTAAACAAATGCACCCCTGGGGTGCCACATC... |
Task1_train_43315 | An alteration has been detected on Chromosome 14. Is it pathogenic, and if so, what disease is involved? | Benign | TTCTCCTTTGAGCTAAACTAAATAAATTCTGCCAGGAGATCCCTCTTGTAATCTATTTCAACTGACAGCGACTACTTTTGTCTGATTTATTACAGCTGTAAGCCCTTCCTTCTGGAAGGGGGAGGGGCTGCGATCTCTTTTAAAGCTAGACCAATTTTACACTGGCAGGGGCCGTGTGTGCGGCTCTACATTACAGCGCCCTACAGGATGCATCTAAACTAGTTTGGTCAGCTTATCCATTCCCTGAAAGCAAGGAAGCCGCCACATCAGTAACTCCGTTGCTAAGGCAACTGCTTACTTTCCATATCAACTGCAAACTC... | TTCTCCTTTGAGCTAAACTAAATAAATTCTGCCAGGAGATCCCTCTTGTAATCTATTTCAACTGACAGCGACTACTTTTGTCTGATTTATTACAGCTGTAAGCCCTTCCTTCTGGAAGGGGGAGGGGCTGCGATCTCTTTTAAAGCTAGACCAATTTTACACTGGCAGGGGCCGTGTGTGCGGCTCTACATTACAGCGCCCTACAGGATGCATCTAAACTAGTTTGGTCAGCTTATCCATTCCCTGAAAGCAAGGAAGCCGCCACATCAGTAACTCCGTTGCTAAGGCAACTGCTTACTTTCCATATCAACTGCAAACTC... |
Task1_train_43316 | A mutation is present on Chromosome 14. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AACATAGTTTAAAGGTAGCAGTGTGTGATTTAACCCTTGCTTGGCATGGCCTTAGGTCTTGTTTATGATTTAGTGTCATATTGTCACAGAATCTATTCTGCCAGTCTTACGATCTCTGGTCAGTTGTGTTTAAACCGCAGAAGGGAGGGGATATAACAGGCATGTCTGAGCTCCCATCTCATCATGGCCCGGAACTCAGTTTTTAAGGTTTCTCTGGGGTCCCCTTAGCCAAGATTTTTATTTTTAGTTCTCATCTAGAGACATATGCATATGTATTGATTTGCAAATCTTTTGATGTAGAATAATGTTGAATTCTCTTT... | AACATAGTTTAAAGGTAGCAGTGTGTGATTTAACCCTTGCTTGGCATGGCCTTAGGTCTTGTTTATGATTTAGTGTCATATTGTCACAGAATCTATTCTGCCAGTCTTACGATCTCTGGTCAGTTGTGTTTAAACCGCAGAAGGGAGGGGATATAACAGGCATGTCTGAGCTCCCATCTCATCATGGCCCGGAACTCAGTTTTTAAGGTTTCTCTGGGGTCCCCTTAGCCAAGATTTTTATTTTTAGTTCTCATCTAGAGACATATGCATATGTATTGATTTGCAAATCTTTTGATGTAGAATAATGTTGAATTCTCTTT... |
Task1_train_43317 | Assess the clinical impact of this variant found on Chromosome 14. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACAAGACCCTCATCTCTACAAAAATTTGAAAATTAGCCAGGCATAGTGTGCACAGCTGCAGTCCCAGCTACTTGGAAGGCTGAGGCAGGAGGATCACCTGAACCTGGTAGTTTTAGGCTGCAGTGAGGTGTGATTGCACCACAGTACTCCAGCCTGTGGGACAGAGAGCAAGATCCCATCTCTTTAAAAAAAAAAAAAAAGAGAGAGGTTTGATGGTTTGATTTTAATAAGAAACTGACTCAGGGAGGCATGCTCAGTATTCTTTTTATTTTTTAATGGTGTTTGTAGTCAGAGTGACTCTGATGCCAACCCCTCCACCC... | ACAAGACCCTCATCTCTACAAAAATTTGAAAATTAGCCAGGCATAGTGTGCACAGCTGCAGTCCCAGCTACTTGGAAGGCTGAGGCAGGAGGATCACCTGAACCTGGTAGTTTTAGGCTGCAGTGAGGTGTGATTGCACCACAGTACTCCAGCCTGTGGGACAGAGAGCAAGATCCCATCTCTTTAAAAAAAAAAAAAAAGAGAGAGGTTTGATGGTTTGATTTTAATAAGAAACTGACTCAGGGAGGCATGCTCAGTATTCTTTTTATTTTTTAATGGTGTTTGTAGTCAGAGTGACTCTGATGCCAACCCCTCCACCC... |
Task1_train_43318 | A variant has been detected on Chromosome 14. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTTCCTCAAGTTGAGGGTTGTTTCTGTGAAAAGGCATCAAGGGGAGCAGCTGACGACCTGTCTGTCGCTAAGGAACACCCGGTGGGCTTCTGCCTACAGCCACCTGTAGCTCAGGGACTGGGGACGAGCAGGAGAGGGCAGTAGTGGGGCTGGGCTGGCCAGTTTCCCACCGTGCCCTGGGAGGTGCTCTCGTGCGCTGCCCTGCCTGCTGCTGCCCGCTGCGTCCGTCAGTTGCCAGCCAAAATTATACACTGGCTTTTCTAAATGTGCTGAGGAGATACAAGTATACAGCAATTCTAAAGAGAGGAAAACAAAACAAA... | CTTCCTCAAGTTGAGGGTTGTTTCTGTGAAAAGGCATCAAGGGGAGCAGCTGACGACCTGTCTGTCGCTAAGGAACACCCGGTGGGCTTCTGCCTACAGCCACCTGTAGCTCAGGGACTGGGGACGAGCAGGAGAGGGCAGTAGTGGGGCTGGGCTGGCCAGTTTCCCACCGTGCCCTGGGAGGTGCTCTCGTGCGCTGCCCTGCCTGCTGCTGCCCGCTGCGTCCGTCAGTTGCCAGCCAAAATTATACACTGGCTTTTCTAAATGTGCTGAGGAGATACAAGTATACAGCAATTCTAAAGAGAGGAAAACAAAACAAA... |
Task1_train_43319 | This mutation on Chromosome 14 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CACACCCGCAATGGGACCCCCATCTGTGCTGTGACGACCCTGAGATCCCAGAGGAGGCAGGTGGAGCTGGCCGTTCATGGCTTCGAACCGCCCCCTTTGTAGACCCTTGGGCCCTTCTCACGGCCTCAGGAGCCCAGTCTCCTCCTGTGGCCCCCGCCGCCCCAGACCCTCCTGCCCAGCAAGGCTACCTCCTGAATTTTCCTTTTTCTCTTCTTCTTCCTCAAAACCCCTGTTCCTCAGGTTCCATGGGCAACTGCCATGTCATGGGCATAGTGCTCAATTGAGAATCAAGTCACCTGGGTTTAAGTCTCCACCTTCCA... | CACACCCGCAATGGGACCCCCATCTGTGCTGTGACGACCCTGAGATCCCAGAGGAGGCAGGTGGAGCTGGCCGTTCATGGCTTCGAACCGCCCCCTTTGTAGACCCTTGGGCCCTTCTCACGGCCTCAGGAGCCCAGTCTCCTCCTGTGGCCCCCGCCGCCCCAGACCCTCCTGCCCAGCAAGGCTACCTCCTGAATTTTCCTTTTTCTCTTCTTCTTCCTCAAAACCCCTGTTCCTCAGGTTCCATGGGCAACTGCCATGTCATGGGCATAGTGCTCAATTGAGAATCAAGTCACCTGGGTTTAAGTCTCCACCTTCCA... |
Task1_train_43320 | Here is a genetic alteration on Chromosome 14. Based on the data, is it a benign variant or a cause of disease? | Benign | AGCCCATTGCATGCCCCCTGTGGTGGTGGTGACCCATTAGAAAAACAAATAAAATAGGATTCAATTGATGCCAACTTAAACACACCTGAGGAGGGGTGGAAAGCTGTCACCGTACAGGAAATCTTTGTCCTTCACATCTGTCTCTGGTTGCACGTGTAACAGCTTCCCCCACCTAGTGGCAAGGAAAGTGGTGGATTCCAACTGTGGAGGAAGGGTCGCCGGCATGCAGAGGGAGGGGTGCAGGGGGAGGGGTGCAGAGGGAGGGGCACAGAGGGAGGGGTGGAGGGGCGCAGAGGGAGGGGCGCAGAGGGAGGGGTGGA... | AGCCCATTGCATGCCCCCTGTGGTGGTGGTGACCCATTAGAAAAACAAATAAAATAGGATTCAATTGATGCCAACTTAAACACACCTGAGGAGGGGTGGAAAGCTGTCACCGTACAGGAAATCTTTGTCCTTCACATCTGTCTCTGGTTGCACGTGTAACAGCTTCCCCCACCTAGTGGCAAGGAAAGTGGTGGATTCCAACTGTGGAGGAAGGGTCGCCGGCATGCAGAGGGAGGGGTGCAGGGGGAGGGGTGCAGAGGGAGGGGCACAGAGGGAGGGGTGGAGGGGCGCAGAGGGAGGGGCGCAGAGGGAGGGGTGGA... |
Task1_train_43321 | The following genetic variant occurs on Chromosome 14. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GCACAAGAATCACTTGAACCTGGGAGGTGGAGCTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCCATCTCAAAACAAACAAACAAAAACTGCAATAAATAATTTATTTCCCCACAGTCTATAGGCGATAAATGAAAACAAGCATCTGAAGTGGCACACAACCTAGTTCTGCTTGATGCTCTCAACAGTCTGGGAGCCACTTAATATCCTACACTTCCCTCTTAGAGATTAAAAATTCACATTAGCTTAAAAAGAAAGAGTTCTGCCAGGTTCTACAGTAAAGAAACCTGGTTAA... | GCACAAGAATCACTTGAACCTGGGAGGTGGAGCTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCCATCTCAAAACAAACAAACAAAAACTGCAATAAATAATTTATTTCCCCACAGTCTATAGGCGATAAATGAAAACAAGCATCTGAAGTGGCACACAACCTAGTTCTGCTTGATGCTCTCAACAGTCTGGGAGCCACTTAATATCCTACACTTCCCTCTTAGAGATTAAAAATTCACATTAGCTTAAAAAGAAAGAGTTCTGCCAGGTTCTACAGTAAAGAAACCTGGTTAA... |
Task1_train_43322 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TTTCTAAAACTTTCAAGGAGGAAGGCAGAGAGGAATGACATCAACTGAGCACCCATCATGTGTGAGGCACTCTTCTAACCATGTTTATGTACATCTGCTTATTTAATCCTCATAAAATGGCCAGGCACCATGGCTCACAACTGTAATCCCAGCATTTGGGAGGCCGAGGTGGGCGGATCACTTGAGGCCAGGAGTTGGAGACCAGCCTGGCTGATATGGTGAAACCCCATCTCTACTAAAACTAGAAAAATTAGCAGGGCATGTTGGCAGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCACAAGAATTGCTTGA... | TTTCTAAAACTTTCAAGGAGGAAGGCAGAGAGGAATGACATCAACTGAGCACCCATCATGTGTGAGGCACTCTTCTAACCATGTTTATGTACATCTGCTTATTTAATCCTCATAAAATGGCCAGGCACCATGGCTCACAACTGTAATCCCAGCATTTGGGAGGCCGAGGTGGGCGGATCACTTGAGGCCAGGAGTTGGAGACCAGCCTGGCTGATATGGTGAAACCCCATCTCTACTAAAACTAGAAAAATTAGCAGGGCATGTTGGCAGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCACAAGAATTGCTTGA... |
Task1_train_43323 | A variant was discovered on Chromosome 14. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TGTGTGAGGCACTCTTCTAACCATGTTTATGTACATCTGCTTATTTAATCCTCATAAAATGGCCAGGCACCATGGCTCACAACTGTAATCCCAGCATTTGGGAGGCCGAGGTGGGCGGATCACTTGAGGCCAGGAGTTGGAGACCAGCCTGGCTGATATGGTGAAACCCCATCTCTACTAAAACTAGAAAAATTAGCAGGGCATGTTGGCAGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCACAAGAATTGCTTGAACCTGGGGGGCAGAGGTTGCAGTGAATAGAGATCGCACCACTATACTCCACCCTGGAC... | TGTGTGAGGCACTCTTCTAACCATGTTTATGTACATCTGCTTATTTAATCCTCATAAAATGGCCAGGCACCATGGCTCACAACTGTAATCCCAGCATTTGGGAGGCCGAGGTGGGCGGATCACTTGAGGCCAGGAGTTGGAGACCAGCCTGGCTGATATGGTGAAACCCCATCTCTACTAAAACTAGAAAAATTAGCAGGGCATGTTGGCAGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCACAAGAATTGCTTGAACCTGGGGGGCAGAGGTTGCAGTGAATAGAGATCGCACCACTATACTCCACCCTGGAC... |
Task1_train_43324 | A sequence alteration has been identified on Chromosome 14. Is it disease-inducing or harmless? | Benign | CGTACAAGCAAGCATATATATGTGCACATGTACAGCAACTGGTATGGCAACTAGAAAAGGTACATTGAAGGTCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCAAGGCAGGAGGATCACCTGCGGTCTCAGGAGTTCGAGATCAGCCTGGCCAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCACACGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCGAAGGTTGCAGCGAGCCGAGATCGCGCCACTGCAT... | CGTACAAGCAAGCATATATATGTGCACATGTACAGCAACTGGTATGGCAACTAGAAAAGGTACATTGAAGGTCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCAAGGCAGGAGGATCACCTGCGGTCTCAGGAGTTCGAGATCAGCCTGGCCAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCACACGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCGAAGGTTGCAGCGAGCCGAGATCGCGCCACTGCAT... |
Task1_train_43325 | Given this variant on Chromosome 14, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TCTTGTCCTAATTTCATTTTTCTTTTAATAAATGAAATTTTATAAGGTTTCCTTCACTCAGTTTAAAAAATTTATCCAGTATTGGGGCAAGGTTTTTTTGTTTCATGTTATTTGCCGTAAATTTTTATTTTTATTTATATATATATACATATATTTTTGGAGACGGAGTCTCACTCTGTCACCCAGTCTGGAGGGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCACGTCCCGGGTTCAAGCAATTCTCCTGGCTCAGCCTCCCAAGCAGCTGGGACTACAGGCGCACGCTTCCATGCCCAGCTGATTCTTTTGTATT... | TCTTGTCCTAATTTCATTTTTCTTTTAATAAATGAAATTTTATAAGGTTTCCTTCACTCAGTTTAAAAAATTTATCCAGTATTGGGGCAAGGTTTTTTTGTTTCATGTTATTTGCCGTAAATTTTTATTTTTATTTATATATATATACATATATTTTTGGAGACGGAGTCTCACTCTGTCACCCAGTCTGGAGGGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCACGTCCCGGGTTCAAGCAATTCTCCTGGCTCAGCCTCCCAAGCAGCTGGGACTACAGGCGCACGCTTCCATGCCCAGCTGATTCTTTTGTATT... |
Task1_train_43326 | A mutation is present on Chromosome 14. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GGGCGTGGTGGCTCACACATGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAAAAGGGCAAAACCCTATCTCTACTAAAAGTACAAAAAATTAGCTGGGCGTGGTGGTAGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTCGGAGGCAGGGGTTGCAGTGAGCCAAGATCACTGCACTCCAGGCTGGGCGACAGTGAGACTCTGACTCAAAAAAAAAAAAAAAAAAAAAGAAAGAAAAAAAAAAAAGAAAGAAATC... | GGGCGTGGTGGCTCACACATGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAAAAGGGCAAAACCCTATCTCTACTAAAAGTACAAAAAATTAGCTGGGCGTGGTGGTAGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTCGGAGGCAGGGGTTGCAGTGAGCCAAGATCACTGCACTCCAGGCTGGGCGACAGTGAGACTCTGACTCAAAAAAAAAAAAAAAAAAAAAGAAAGAAAAAAAAAAAAGAAAGAAATC... |
Task1_train_43327 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | AAACGGGGTGCCGTAAACAACGGAAGTGTATTGTCTTGTGGTTCCGGAGGCCAGAAGCCTGAAGGAGAGTCTGTCCCAGGCCCCTCTTGCCTCTCTGCCCTTGGCTGTCTTCATCTTTGCCCAGGTTCTCCCTGCATGTCCAGTTTTCTCCTTTTTATAAGGATTCTTGTGTCCTGAAAGAACCTCCTTAAAAACAACTAAAACCAAGAACTTCTGGGGCTGTTCACACATTGTTCGAGTCACCCCAAGATCGTTCTGGCATGCTGAGCTGAACACCACCATCTTTGTTCATTCTCTCTCTAATGGGCAAAGCAGGATCA... | AAACGGGGTGCCGTAAACAACGGAAGTGTATTGTCTTGTGGTTCCGGAGGCCAGAAGCCTGAAGGAGAGTCTGTCCCAGGCCCCTCTTGCCTCTCTGCCCTTGGCTGTCTTCATCTTTGCCCAGGTTCTCCCTGCATGTCCAGTTTTCTCCTTTTTATAAGGATTCTTGTGTCCTGAAAGAACCTCCTTAAAAACAACTAAAACCAAGAACTTCTGGGGCTGTTCACACATTGTTCGAGTCACCCCAAGATCGTTCTGGCATGCTGAGCTGAACACCACCATCTTTGTTCATTCTCTCTCTAATGGGCAAAGCAGGATCA... |
Task1_train_43328 | This genomic variant is located on Chromosome 14. Can you determine its pathogenicity and name any linked disease? | Benign | GTAAACAACGGAAGTGTATTGTCTTGTGGTTCCGGAGGCCAGAAGCCTGAAGGAGAGTCTGTCCCAGGCCCCTCTTGCCTCTCTGCCCTTGGCTGTCTTCATCTTTGCCCAGGTTCTCCCTGCATGTCCAGTTTTCTCCTTTTTATAAGGATTCTTGTGTCCTGAAAGAACCTCCTTAAAAACAACTAAAACCAAGAACTTCTGGGGCTGTTCACACATTGTTCGAGTCACCCCAAGATCGTTCTGGCATGCTGAGCTGAACACCACCATCTTTGTTCATTCTCTCTCTAATGGGCAAAGCAGGATCATCGAGTTGAAAA... | GTAAACAACGGAAGTGTATTGTCTTGTGGTTCCGGAGGCCAGAAGCCTGAAGGAGAGTCTGTCCCAGGCCCCTCTTGCCTCTCTGCCCTTGGCTGTCTTCATCTTTGCCCAGGTTCTCCCTGCATGTCCAGTTTTCTCCTTTTTATAAGGATTCTTGTGTCCTGAAAGAACCTCCTTAAAAACAACTAAAACCAAGAACTTCTGGGGCTGTTCACACATTGTTCGAGTCACCCCAAGATCGTTCTGGCATGCTGAGCTGAACACCACCATCTTTGTTCATTCTCTCTCTAATGGGCAAAGCAGGATCATCGAGTTGAAAA... |
Task1_train_43329 | A variant on Chromosome 14 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GCTTGATGGACGAGCAGTCCGCCTTGTTGAGGAGTGAGCTCCTTGTCACGGGAAGCATCCAAGAGGAGGCGGCGTGCACATCTGTCAGGAATGTGGAGGAGGCGCCCTGGCTCTGGTCTGAGGTTGCCCTTGAACGATTTCGAGGCTCCCTCGGGCAAGGCTGTGGCTCCGAGTGGGACGAACTCCCCGCCAGCTCTGGGCCTCCCCACCTGCCGGCCCGCGGTCGGCGCCGGCACAGGCGGAGGGCGTCTTCCTTCCCCTGCGGCCCCAAGCCAAGTGGAAGACTTTTCTCTAAGTTTCCCTCTCCGAAGCCCCGCGGG... | GCTTGATGGACGAGCAGTCCGCCTTGTTGAGGAGTGAGCTCCTTGTCACGGGAAGCATCCAAGAGGAGGCGGCGTGCACATCTGTCAGGAATGTGGAGGAGGCGCCCTGGCTCTGGTCTGAGGTTGCCCTTGAACGATTTCGAGGCTCCCTCGGGCAAGGCTGTGGCTCCGAGTGGGACGAACTCCCCGCCAGCTCTGGGCCTCCCCACCTGCCGGCCCGCGGTCGGCGCCGGCACAGGCGGAGGGCGTCTTCCTTCCCCTGCGGCCCCAAGCCAAGTGGAAGACTTTTCTCTAAGTTTCCCTCTCCGAAGCCCCGCGGG... |
Task1_train_43330 | Here is a mutation located on Chromosome 14. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TCCCAGCGTCTCACTCCCCAATCCGGTGACACAGGGCGAGTGCTTTCATGTTTCTGAGCCTCTTACCCTCATCTGTGAACTGGGGGCAAGGCCTATGATCAGGGGTCGGCAAGATAACCCAGGTAAAGCAAGGAGCCCGTGGGCTCACGCGCAGCAAGAACGCCATGGATGTTTGCTCCTCTGATTATCCTTGATGTTATTTTCCATAGTTTTCTTAAGGGTGAATTCCTCCCAGGAGTGAAGAGCCCTGGGTGAAAGGCTGGCTGCACCAATTCACAAGGAACTCTGCATCTGCCTGGGTCATCCTCTGTCCAGCTCCA... | TCCCAGCGTCTCACTCCCCAATCCGGTGACACAGGGCGAGTGCTTTCATGTTTCTGAGCCTCTTACCCTCATCTGTGAACTGGGGGCAAGGCCTATGATCAGGGGTCGGCAAGATAACCCAGGTAAAGCAAGGAGCCCGTGGGCTCACGCGCAGCAAGAACGCCATGGATGTTTGCTCCTCTGATTATCCTTGATGTTATTTTCCATAGTTTTCTTAAGGGTGAATTCCTCCCAGGAGTGAAGAGCCCTGGGTGAAAGGCTGGCTGCACCAATTCACAAGGAACTCTGCATCTGCCTGGGTCATCCTCTGTCCAGCTCCA... |
Task1_train_43331 | Assess the clinical impact of this variant found on Chromosome 14. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAGATCACCTGAGGTCAGGAGTTAAGACCAGCCTGGCCAACATGGTGAAACCCGGCCTCTGCTAAAAATACAAAAATTAGCTGGACCTGTAATATCAGCTACTCGGGAGGCTGAGGCAGGAGAATAGCTTGAACTTGGGAGGTGGAAGCTGCAGTGAGCCGAGATCGCGCCACTGCACTCTAGCCTGGGACACAGAGCAAGACTCTGTCTCAACCAAAAAAAAAAAAAAAAGAAGTTATTAAAATTAATTTCACCTTCTAAATGTGGCTACTAGAACATTTACCATGG... | GTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAGATCACCTGAGGTCAGGAGTTAAGACCAGCCTGGCCAACATGGTGAAACCCGGCCTCTGCTAAAAATACAAAAATTAGCTGGACCTGTAATATCAGCTACTCGGGAGGCTGAGGCAGGAGAATAGCTTGAACTTGGGAGGTGGAAGCTGCAGTGAGCCGAGATCGCGCCACTGCACTCTAGCCTGGGACACAGAGCAAGACTCTGTCTCAACCAAAAAAAAAAAAAAAAGAAGTTATTAAAATTAATTTCACCTTCTAAATGTGGCTACTAGAACATTTACCATGG... |
Task1_train_43332 | Given a variant located on Chromosome 14, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GCATCAGTCATATAAAAATTCCACTCAGCAGTATTTGTGAGTGCCTACTGTGTGCTAGACTCTGGGAATTCATTGGTGAGCAAAACAGACATAATCTTTATCCAGCCACTGCCCCACTTTCCCCAAGAACAAGAAGCATGTTAAAAAAATACGTAATTATAAAACATGAAGGACTGTGAAGCAAAAGAATAGGGTATGTACAGATAATGATTGACCTAACTTAGCTGGAAAGGAGAACTCTGAAGCAAATGACATTTGAGTGAAGACCAAGAACAAGAAAGTTAACCATGAAAGAGTTCTTGGCAAAAGGAACAACGTGC... | GCATCAGTCATATAAAAATTCCACTCAGCAGTATTTGTGAGTGCCTACTGTGTGCTAGACTCTGGGAATTCATTGGTGAGCAAAACAGACATAATCTTTATCCAGCCACTGCCCCACTTTCCCCAAGAACAAGAAGCATGTTAAAAAAATACGTAATTATAAAACATGAAGGACTGTGAAGCAAAAGAATAGGGTATGTACAGATAATGATTGACCTAACTTAGCTGGAAAGGAGAACTCTGAAGCAAATGACATTTGAGTGAAGACCAAGAACAAGAAAGTTAACCATGAAAGAGTTCTTGGCAAAAGGAACAACGTGC... |
Task1_train_43333 | A mutation on Chromosome 14 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AAATGGAGGTCTTCACTCTTATAGACAAATATGCCACAGCTGCACCCAATGGGACTTTTCCCTCCTTTTCTCATACCAGGCGCCAAGGAGAGGGCACATCAGCAGAAGAAACACAGCGGTTTTGAAGATGAACTCTCAGAGGTTCTTGAGAACCAGAGCAGCCAGGCCGAGCTGAAAGGTCTGTCCCAGCCGGTCTGGCCGGAGGTGGGGAAGGGAGGGTGGCAGTGGGAACAGTGGCTATGATGGACCCAGGGTTCCAGTGAGTCGGGAGCCCCACCCATAATCCCTTATTTCCCTCTCTCTACAAATGGGGAAACTGC... | AAATGGAGGTCTTCACTCTTATAGACAAATATGCCACAGCTGCACCCAATGGGACTTTTCCCTCCTTTTCTCATACCAGGCGCCAAGGAGAGGGCACATCAGCAGAAGAAACACAGCGGTTTTGAAGATGAACTCTCAGAGGTTCTTGAGAACCAGAGCAGCCAGGCCGAGCTGAAAGGTCTGTCCCAGCCGGTCTGGCCGGAGGTGGGGAAGGGAGGGTGGCAGTGGGAACAGTGGCTATGATGGACCCAGGGTTCCAGTGAGTCGGGAGCCCCACCCATAATCCCTTATTTCCCTCTCTCTACAAATGGGGAAACTGC... |
Task1_train_43334 | A mutation is present on Chromosome 14. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TGTACTTGGGAGCACTTTGTTCAGTGGTTATCATTCTAATGACGGGAGGAATTTTCACTTGTTCAAAGGCTGTCTTTAAGGCAGCCACAATAAAATACCTTTTAATGAAACCCTAAAATATTGCAGAATTGAGCCCTTTCACAGGATGCTGAAGACAGAGAAGCCCCACATGGAGGGGAGAATGAAGTTGCAGTCATGGTGCCTCTTACACAGAGAGGTTAAGCAACTTGCCCAAGATCACACAGCTGACATTAATTTTCAGTTCAGGCTTTATCTCCTGGATTAATCTTAAGGTCTGGTTTTTTGTTTTTGTTCTTTGA... | TGTACTTGGGAGCACTTTGTTCAGTGGTTATCATTCTAATGACGGGAGGAATTTTCACTTGTTCAAAGGCTGTCTTTAAGGCAGCCACAATAAAATACCTTTTAATGAAACCCTAAAATATTGCAGAATTGAGCCCTTTCACAGGATGCTGAAGACAGAGAAGCCCCACATGGAGGGGAGAATGAAGTTGCAGTCATGGTGCCTCTTACACAGAGAGGTTAAGCAACTTGCCCAAGATCACACAGCTGACATTAATTTTCAGTTCAGGCTTTATCTCCTGGATTAATCTTAAGGTCTGGTTTTTTGTTTTTGTTCTTTGA... |
Task1_train_43335 | Chromosome 14 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | ATCAAGATGTATTTCCCAAGATGGAAGGAAAGTACAGTTTAAGCTCTTCTTACATAATTGTAAATCCTGACTCTAATATCTAGTTCTTGGGTTTTTCAGCTCAGGACGGTTAAAATGTACCTGCCTGGCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCTGAGGCGGGTGGATCACGAGGTCAGGAGTTCGGGACCAGCCTGGCCAACACAGTGAAACCCTGTCTCTACTAAAAATACAAAATTAGCTGGGAGTGGGGGCGGGTGCCTGTAATCCCAGTTACTCCGGAGGCTGAGACAGGAGAATC... | ATCAAGATGTATTTCCCAAGATGGAAGGAAAGTACAGTTTAAGCTCTTCTTACATAATTGTAAATCCTGACTCTAATATCTAGTTCTTGGGTTTTTCAGCTCAGGACGGTTAAAATGTACCTGCCTGGCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCTGAGGCGGGTGGATCACGAGGTCAGGAGTTCGGGACCAGCCTGGCCAACACAGTGAAACCCTGTCTCTACTAAAAATACAAAATTAGCTGGGAGTGGGGGCGGGTGCCTGTAATCCCAGTTACTCCGGAGGCTGAGACAGGAGAATC... |
Task1_train_43336 | This sequence variant lies on Chromosome 14. Is it clinically significant, and what condition might it cause if any? | Benign | CCACAGGGTAAAGGAGGAAAAGACCGTAAGAGAAACTATAGTTTTGGGAGAAATCAGCGTTGTTGACACCCAATAGAAAACCTATTTACTTCAAAGTGCATGTAATTCATTTACCCGGTAGCTCATAAACGCTCCCTAGCCCTGCATAGTTTTCGAGTGAGTGTGAGTGATTCATAGTTTTTTATATATATACATACATAGAAAAGAGGATCCCAAATATCCTGCAGAGGAAGGAATGCTTAGAAAGCCTCTTTTCTTCTAAGTGCTACGGCTGTGTGTTTATGTGTTTGTAAAAATACAAAGTAAATGCTCAAATAATG... | CCACAGGGTAAAGGAGGAAAAGACCGTAAGAGAAACTATAGTTTTGGGAGAAATCAGCGTTGTTGACACCCAATAGAAAACCTATTTACTTCAAAGTGCATGTAATTCATTTACCCGGTAGCTCATAAACGCTCCCTAGCCCTGCATAGTTTTCGAGTGAGTGTGAGTGATTCATAGTTTTTTATATATATACATACATAGAAAAGAGGATCCCAAATATCCTGCAGAGGAAGGAATGCTTAGAAAGCCTCTTTTCTTCTAAGTGCTACGGCTGTGTGTTTATGTGTTTGTAAAAATACAAAGTAAATGCTCAAATAATG... |
Task1_train_43337 | Chromosome 14 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GTAAACTTTATGGGTTGCAACATATGAACTCTTTCCTCATTAACATATTTTGGGGTTTATCTTGGATTTAAAAATGGCCACATGGGTGTAGAAGGGAGGACGTAGAAACAAGTTCAACAGGCACTCAAAGTGACCGGTTTGTTTATGTAGGATTAGGGATCATAAGTGTCAAAGATTCTTTCTGGGATTCATGAGATCCGTAATAGTTACACGTGGTAAGCGCCTCAGAGAAGAGTCTTACTTTAATAGGAGGAAATGTTATTTTCTGTTTTCTTTTTCCTTTGTTTACTCTTTCAGTCCATAATCATTCGTGGAGCTTT... | GTAAACTTTATGGGTTGCAACATATGAACTCTTTCCTCATTAACATATTTTGGGGTTTATCTTGGATTTAAAAATGGCCACATGGGTGTAGAAGGGAGGACGTAGAAACAAGTTCAACAGGCACTCAAAGTGACCGGTTTGTTTATGTAGGATTAGGGATCATAAGTGTCAAAGATTCTTTCTGGGATTCATGAGATCCGTAATAGTTACACGTGGTAAGCGCCTCAGAGAAGAGTCTTACTTTAATAGGAGGAAATGTTATTTTCTGTTTTCTTTTTCCTTTGTTTACTCTTTCAGTCCATAATCATTCGTGGAGCTTT... |
Task1_train_43338 | A genomic change on Chromosome 14 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGCGCCTCAGAGAAGAGTCTTACTTTAATAGGAGGAAATGTTATTTTCTGTTTTCTTTTTCCTTTGTTTACTCTTTCAGTCCATAATCATTCGTGGAGCTTTTGAGATGACAAGTGGCTTTTCTAAGCTTTTTCTGTGTGTTGCGTGTCTCATTATCAAATGTAGAGTACAGTATTTTGCATTCACACCGTATAAGGTGCATGTACTGTTAGGCTGTGTCTATGCCAGTTACCAAATCCCATAAAGGCAGATTTTTTTTTCTTTTTTGGAAAGCCCAAGATCCACTCATTTTGTTTAATTTCCTTTCGCCAAATCAGCCT... | AGCGCCTCAGAGAAGAGTCTTACTTTAATAGGAGGAAATGTTATTTTCTGTTTTCTTTTTCCTTTGTTTACTCTTTCAGTCCATAATCATTCGTGGAGCTTTTGAGATGACAAGTGGCTTTTCTAAGCTTTTTCTGTGTGTTGCGTGTCTCATTATCAAATGTAGAGTACAGTATTTTGCATTCACACCGTATAAGGTGCATGTACTGTTAGGCTGTGTCTATGCCAGTTACCAAATCCCATAAAGGCAGATTTTTTTTTCTTTTTTGGAAAGCCCAAGATCCACTCATTTTGTTTAATTTCCTTTCGCCAAATCAGCCT... |
Task1_train_43339 | Here is a variant on Chromosome 14. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTGCTTCAAAGCAATTTGAAAACCCACTGCCCCAGATGAGCTCCTTGGGTCCCTAAGGCTTGGCCTGTGCATGCCCTGCCAGATGCCTCTTCTCACTTGCAGCTCCAGTCTACACATGTGCTGGCTGAATCCTATAAGTAGATGGTGTCTGTTGACATCCAGAGGTTCTGGAGGGGTGGCTCCCAGGAGACTGCTAGGTAGTTGTTCTGCTTCACTGATGAGTGGGCAGGAGACAAACGTTTACTTATCAAGATAAAGCAGGGAATGCCACCTCCACACCCTCTGGTCCCTGCACACAGTAGGTGTTGAATGGAGTTGAT... | CTGCTTCAAAGCAATTTGAAAACCCACTGCCCCAGATGAGCTCCTTGGGTCCCTAAGGCTTGGCCTGTGCATGCCCTGCCAGATGCCTCTTCTCACTTGCAGCTCCAGTCTACACATGTGCTGGCTGAATCCTATAAGTAGATGGTGTCTGTTGACATCCAGAGGTTCTGGAGGGGTGGCTCCCAGGAGACTGCTAGGTAGTTGTTCTGCTTCACTGATGAGTGGGCAGGAGACAAACGTTTACTTATCAAGATAAAGCAGGGAATGCCACCTCCACACCCTCTGGTCCCTGCACACAGTAGGTGTTGAATGGAGTTGAT... |
Task1_train_43340 | This is a variant located on Chromosome 14. Is this mutation a likely cause of disease or not? | Benign | TGGGGGACTCCCCCACCCCTCCTTGAACTGGGCTGACTCCTTCTCTGGGCAACCCCAGCCCCTGAGCTCCTCTCCCTCTGCATCCACGTCCCCCACACCTGCATCCACCTCCCTCCTGAGTCTGAACCCAAGGCCAGAGCAAGGACCCTTCACCTTCATTCTCAGTCGGTGCTCAGCACATAAGCGAGGGGCTCTAGGACCATGGAGAGGCAGCCCTGGGCACCTGTCAGGGACTCCTGGGCTGGCTGGGGCTGATCTCACTGCCTGCTGGTAAGGGGTTGTGAGGGGGATGAGTCCAAACCCCTGCCCCTGCCCCTGAG... | TGGGGGACTCCCCCACCCCTCCTTGAACTGGGCTGACTCCTTCTCTGGGCAACCCCAGCCCCTGAGCTCCTCTCCCTCTGCATCCACGTCCCCCACACCTGCATCCACCTCCCTCCTGAGTCTGAACCCAAGGCCAGAGCAAGGACCCTTCACCTTCATTCTCAGTCGGTGCTCAGCACATAAGCGAGGGGCTCTAGGACCATGGAGAGGCAGCCCTGGGCACCTGTCAGGGACTCCTGGGCTGGCTGGGGCTGATCTCACTGCCTGCTGGTAAGGGGTTGTGAGGGGGATGAGTCCAAACCCCTGCCCCTGCCCCTGAG... |
Task1_train_43341 | This sequence variant lies on Chromosome 14. Is it clinically significant, and what condition might it cause if any? | Benign | ATGCACTGGGCTGGTTCAGCAGCTGACCAATGAGGGTCATGCTTGCATACTGGCCTTGGGTGAGTGGCTCAGGAACAGTTTGCAAGACCGTGTTGAAGCTACTTGTAACTAGACCATTTTCCCAGCTTGACCATGAGCTTCTTCAAGGCATCTCTTCTCAGTCTCCACTGTAGCTCTGTAAGACCTGTATGAGCTCAGAGCATGTAATGTTGGTTAAGTGAATAAATGCATGGATGGGGGGTGGGTGGGCAGAGATGATGATGAAGCTGCCTCCTCCTTAAGCAGGCTGTTTTCTGAACCAACTCTGGCTCTGACCCTAT... | ATGCACTGGGCTGGTTCAGCAGCTGACCAATGAGGGTCATGCTTGCATACTGGCCTTGGGTGAGTGGCTCAGGAACAGTTTGCAAGACCGTGTTGAAGCTACTTGTAACTAGACCATTTTCCCAGCTTGACCATGAGCTTCTTCAAGGCATCTCTTCTCAGTCTCCACTGTAGCTCTGTAAGACCTGTATGAGCTCAGAGCATGTAATGTTGGTTAAGTGAATAAATGCATGGATGGGGGGTGGGTGGGCAGAGATGATGATGAAGCTGCCTCCTCCTTAAGCAGGCTGTTTTCTGAACCAACTCTGGCTCTGACCCTAT... |
Task1_train_43342 | A mutation on Chromosome 14 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGGCTGCGGGGCTCCTGACTGCCCCAGGCAAGACTCCAACTTGAGCTAGTCCTGCTCCTTAGCCCAGGCTGCATTTGTGTTTAGCCCCCCATCAGCTCTTCTTTCCATAGCTACATTGGTGCCTGGTGCAGTAAGGTCCTAAGGTCTCTATTAGTCTACAAACTTGAGCACCCACTAGGTGAAGGGTCAGTGTAGAAGGTGCATAGAGGAACTTCCCACCTGGTCTTCATATGTAGCTCCACACTGACACATCACACACAGGCACACGCACACACACAGTACACACCCATCAACATCCATGTGTGCTTTCTGCACACCCA... | TGGCTGCGGGGCTCCTGACTGCCCCAGGCAAGACTCCAACTTGAGCTAGTCCTGCTCCTTAGCCCAGGCTGCATTTGTGTTTAGCCCCCCATCAGCTCTTCTTTCCATAGCTACATTGGTGCCTGGTGCAGTAAGGTCCTAAGGTCTCTATTAGTCTACAAACTTGAGCACCCACTAGGTGAAGGGTCAGTGTAGAAGGTGCATAGAGGAACTTCCCACCTGGTCTTCATATGTAGCTCCACACTGACACATCACACACAGGCACACGCACACACACAGTACACACCCATCAACATCCATGTGTGCTTTCTGCACACCCA... |
Task1_train_43343 | With a mutation on Chromosome 14, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ATTGCCAAGTATCCTGTATTTACTGGGAATGGACATCACAGTAGCATGCCTTCCTAGCCACATCTATGAGGTTTTGTTCATTTTCATTCTGCTTTTTGTTTGAGCTAAACCTGCCTTGGGAGGCAGAAAAGAAAAGATAACATCTGATTCCCCCGATCAACCAACCAATCAACTAGGTCAGGGCCACGTAAATTCATTCAGGACAAGCACTGAGGTCAAACTCCCCAGTGATCCTCACCCTCCTCCAGAATTTCCACTTCCCGAAATGAAGCAAAGAGCGGTAGACAGGAGTCATCCCTTCTTGTGGCTCCCAACCTGGG... | ATTGCCAAGTATCCTGTATTTACTGGGAATGGACATCACAGTAGCATGCCTTCCTAGCCACATCTATGAGGTTTTGTTCATTTTCATTCTGCTTTTTGTTTGAGCTAAACCTGCCTTGGGAGGCAGAAAAGAAAAGATAACATCTGATTCCCCCGATCAACCAACCAATCAACTAGGTCAGGGCCACGTAAATTCATTCAGGACAAGCACTGAGGTCAAACTCCCCAGTGATCCTCACCCTCCTCCAGAATTTCCACTTCCCGAAATGAAGCAAAGAGCGGTAGACAGGAGTCATCCCTTCTTGTGGCTCCCAACCTGGG... |
Task1_train_43344 | Here is a genetic alteration on Chromosome 14. Based on the data, is it a benign variant or a cause of disease? | Benign | CAGAACGTAAAATACTGATGGACTCAATGAATGAATCAGCCAGGCACCCTGTGACAGATGCTGGGGATAGAGTGGAAAAAAAGACAAATGCTGCCCTGCCTTCAGGAAACTTATAGCTCACTGGAGGAGACATTAAATCACGGTGCATTCAATGAAATTGTGCTGAGCGTTTGCCAGTACAGAAAGGTAGAGTTTGTATAGGGTGTGGGCAAGAGTTGTACCTGGTTTTCATGTTTCTGAGCCATGTCTCCACCAAGTCTGTGGTCAGGTAGTCTTCAAGGGCGAGGTGGTCACCCATTTTCTCCATGAGGACCACCAGC... | CAGAACGTAAAATACTGATGGACTCAATGAATGAATCAGCCAGGCACCCTGTGACAGATGCTGGGGATAGAGTGGAAAAAAAGACAAATGCTGCCCTGCCTTCAGGAAACTTATAGCTCACTGGAGGAGACATTAAATCACGGTGCATTCAATGAAATTGTGCTGAGCGTTTGCCAGTACAGAAAGGTAGAGTTTGTATAGGGTGTGGGCAAGAGTTGTACCTGGTTTTCATGTTTCTGAGCCATGTCTCCACCAAGTCTGTGGTCAGGTAGTCTTCAAGGGCGAGGTGGTCACCCATTTTCTCCATGAGGACCACCAGC... |
Task1_train_43345 | This alteration occurs on Chromosome 14. Is it associated with a disease or is it a benign variant? | Benign | AGTTTGAGGACATGACAACGAAAATTCTTGTCAAAGGTGGAGGCAAACTTGCCTGCACCGTACATCATGGGCACCTTAATGGTCTTGTACTTGTCCAGGTGGAAAGTGTCGACTTCGGTGAAGACAGGGTCAAATGGGGTCAACCATTTCCCTGAACAAGTAAGAGAAGAACTCATTGCAGAAATTCCCTCTTTGAAAAGCATTGTTCTTGCTCAAATAATAGAGAGGGAGCCTTCTATCTCACTTCTCTCACTTCTCGTCTTCTCGTTCCAACTAGGAAAGGCGTTCCCTAATTGGGTTGGCTTTTCCACAGCTCAGGC... | AGTTTGAGGACATGACAACGAAAATTCTTGTCAAAGGTGGAGGCAAACTTGCCTGCACCGTACATCATGGGCACCTTAATGGTCTTGTACTTGTCCAGGTGGAAAGTGTCGACTTCGGTGAAGACAGGGTCAAATGGGGTCAACCATTTCCCTGAACAAGTAAGAGAAGAACTCATTGCAGAAATTCCCTCTTTGAAAAGCATTGTTCTTGCTCAAATAATAGAGAGGGAGCCTTCTATCTCACTTCTCTCACTTCTCGTCTTCTCGTTCCAACTAGGAAAGGCGTTCCCTAATTGGGTTGGCTTTTCCACAGCTCAGGC... |
Task1_train_43346 | This is a variant located on Chromosome 14. Is this mutation a likely cause of disease or not? | Benign | TTGTTCATTGGTCGCCTTTAGTTTTCCAAAATAAGTGTCATCTTTAGCTGAAATCATTCATTAATTCAGACACCAAATCTCACAGATCGAAGGAGTCAGAAATTCCTTTGAAACAACTTAGCCCAAACCTTTCTGTGTCAGTATGGATAAATCAAGGCCCAATGTCTAGAAGGTCTTGGGCAAAGTTGAAATTCAGGGTCAGTGACACAACCTCAAGGGAGGCCCCGAAAGTGCCAGCTGCACAGCAGTCCCCTGCCTGGCTTTGCTGTTTGACCACGTCCCGTGTCAGTGAATCACGGGCATCTTCAGGAGCTCAGCCT... | TTGTTCATTGGTCGCCTTTAGTTTTCCAAAATAAGTGTCATCTTTAGCTGAAATCATTCATTAATTCAGACACCAAATCTCACAGATCGAAGGAGTCAGAAATTCCTTTGAAACAACTTAGCCCAAACCTTTCTGTGTCAGTATGGATAAATCAAGGCCCAATGTCTAGAAGGTCTTGGGCAAAGTTGAAATTCAGGGTCAGTGACACAACCTCAAGGGAGGCCCCGAAAGTGCCAGCTGCACAGCAGTCCCCTGCCTGGCTTTGCTGTTTGACCACGTCCCGTGTCAGTGAATCACGGGCATCTTCAGGAGCTCAGCCT... |
Task1_train_43347 | Given this variant on Chromosome 14, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AACATGGCTAAGAGGTGTGGGCAGCTTCTTGGTCACCCTCAGGTTGGGGAATCACCTTCTGTCTTCATTTTCCAGGAACTTGGTGATGATATCGTGGGTGAGTTCATTTTCCAGGTGCTGTAGTTTCCCCTCATCAGGCAGGAAGAAGATGGCGGTGGCATTGCCCAGGTATTTCATCAGCAGCACCCAGCTGGACAGCTTCTTACAGTGCTGGATGTTAAACATGCCTAAACGCTTCATCATAGGCACCTTCACGGTGGTCACCTGGTCCACGTGGAAGTCCTCTTCCTCGGTGTCCTTGACTTCAAAGGGTCTCTCCC... | AACATGGCTAAGAGGTGTGGGCAGCTTCTTGGTCACCCTCAGGTTGGGGAATCACCTTCTGTCTTCATTTTCCAGGAACTTGGTGATGATATCGTGGGTGAGTTCATTTTCCAGGTGCTGTAGTTTCCCCTCATCAGGCAGGAAGAAGATGGCGGTGGCATTGCCCAGGTATTTCATCAGCAGCACCCAGCTGGACAGCTTCTTACAGTGCTGGATGTTAAACATGCCTAAACGCTTCATCATAGGCACCTTCACGGTGGTCACCTGGTCCACGTGGAAGTCCTCTTCCTCGGTGTCCTTGACTTCAAAGGGTCTCTCCC... |
Task1_train_43348 | Given this variant on Chromosome 14, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AGAGTCTATGGCACTCCCTTCTGTGATGGGGGCAAGGAGAAGACTCACCCCAAAGGAGCCAGGGACTATGGGGCTGAAATTAGCAACTGACTAGAGCCGTGGAGCTTCATGGACAACAGGAATAATCTCTTAAATCCTGGCCTCTCCCCTTGGCCCGTGCCTCTTATTTGGTGTTTTAATCTCTGCCCAAACACAAAATGCCTTCTCTATCCCTGGTACCTCAGTGTGAATGGGGTGCTGAGAGAAGTCACTTTTGGATATGTGGGGTGGCTAGTGCCTCCCAGGTTGTGGTGGATTCAAGATGACCGTCAAAAGGTGGC... | AGAGTCTATGGCACTCCCTTCTGTGATGGGGGCAAGGAGAAGACTCACCCCAAAGGAGCCAGGGACTATGGGGCTGAAATTAGCAACTGACTAGAGCCGTGGAGCTTCATGGACAACAGGAATAATCTCTTAAATCCTGGCCTCTCCCCTTGGCCCGTGCCTCTTATTTGGTGTTTTAATCTCTGCCCAAACACAAAATGCCTTCTCTATCCCTGGTACCTCAGTGTGAATGGGGTGCTGAGAGAAGTCACTTTTGGATATGTGGGGTGGCTAGTGCCTCCCAGGTTGTGGTGGATTCAAGATGACCGTCAAAAGGTGGC... |
Task1_train_43349 | A sequence alteration has been identified on Chromosome 14. Is it disease-inducing or harmless? | Benign | GTTGACAGATGAATTCATATTTTAGTTTTATTGAATGTGTTATTGTAATTCTGCAATAGAGGTGCCTAACCTGGGTTGGCGTATTTCCATTCCTGGGAGCCCCAAGGAATGGAAATATGGTAACCCAGCAACATCCCATGAAGCTAGTTACCTGGGAGAATTTGTGGAAAAGGGCACTGACTGGGGTTAATGGGTGTTGGCTTGTGACTGGGGTCCCTGTTGATGGTTTGGTGATTGAGCCTTGGAAGTGGCATCCCTGCCAGCGAATCCAGCTCCACTGGGGTCAAATGCACCCTCAGAACAGAAAGAGGGATGTGGTT... | GTTGACAGATGAATTCATATTTTAGTTTTATTGAATGTGTTATTGTAATTCTGCAATAGAGGTGCCTAACCTGGGTTGGCGTATTTCCATTCCTGGGAGCCCCAAGGAATGGAAATATGGTAACCCAGCAACATCCCATGAAGCTAGTTACCTGGGAGAATTTGTGGAAAAGGGCACTGACTGGGGTTAATGGGTGTTGGCTTGTGACTGGGGTCCCTGTTGATGGTTTGGTGATTGAGCCTTGGAAGTGGCATCCCTGCCAGCGAATCCAGCTCCACTGGGGTCAAATGCACCCTCAGAACAGAAAGAGGGATGTGGTT... |
Task1_train_43350 | A mutation on Chromosome 14 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GTGCAGAGGTGAAAAAGCAGTCAGCAAGGGAGTCTATGGCAGAAACCAACAGGAGACGTCCAGTAGCAATGGAAGCTCATCAACCACCCACTCACTGTCCGGAATACCTCCTCAGCAGCACTTCCTGATGCAAGCCCTGCTAATAATGCCCTAGAGCAGCAAAGTCCAGCAGAACTTCCTGTGATGCTGGGAAGATCCTAGACCTGCACTCTCCAGTACGGTAGCCATTAGCCATGTGTGGCTACTGAGCAACTTAAACAGTGGCTTGTGCAAATGAGAAACTAAAATGTTAATTTTACTACATTTCAGTTAACTTAAGT... | GTGCAGAGGTGAAAAAGCAGTCAGCAAGGGAGTCTATGGCAGAAACCAACAGGAGACGTCCAGTAGCAATGGAAGCTCATCAACCACCCACTCACTGTCCGGAATACCTCCTCAGCAGCACTTCCTGATGCAAGCCCTGCTAATAATGCCCTAGAGCAGCAAAGTCCAGCAGAACTTCCTGTGATGCTGGGAAGATCCTAGACCTGCACTCTCCAGTACGGTAGCCATTAGCCATGTGTGGCTACTGAGCAACTTAAACAGTGGCTTGTGCAAATGAGAAACTAAAATGTTAATTTTACTACATTTCAGTTAACTTAAGT... |
Task1_train_43351 | A mutation on Chromosome 14 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGCAGAACTTCCTGTGATGCTGGGAAGATCCTAGACCTGCACTCTCCAGTACGGTAGCCATTAGCCATGTGTGGCTACTGAGCAACTTAAACAGTGGCTTGTGCAAATGAGAAACTAAAATGTTAATTTTACTACATTTCAGTTAACTTAAGTGTAAATTACTGCAGGTGGCTTAGCGGCTACTATATTGAACAGCACCACCTGATAATTTAGCACAATATTTTTTTTCCTCTGCAATGGTTTCCCTGAACCAAGAGTAAACAGCCCACATGTGTTGAACTTCTTTTTTTTAAGATGGAGTCTCACTCTGTCGCTCAGGC... | AGCAGAACTTCCTGTGATGCTGGGAAGATCCTAGACCTGCACTCTCCAGTACGGTAGCCATTAGCCATGTGTGGCTACTGAGCAACTTAAACAGTGGCTTGTGCAAATGAGAAACTAAAATGTTAATTTTACTACATTTCAGTTAACTTAAGTGTAAATTACTGCAGGTGGCTTAGCGGCTACTATATTGAACAGCACCACCTGATAATTTAGCACAATATTTTTTTTCCTCTGCAATGGTTTCCCTGAACCAAGAGTAAACAGCCCACATGTGTTGAACTTCTTTTTTTTAAGATGGAGTCTCACTCTGTCGCTCAGGC... |
Task1_train_43352 | A mutation on Chromosome 14 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGCCATTAGCCATGTGTGGCTACTGAGCAACTTAAACAGTGGCTTGTGCAAATGAGAAACTAAAATGTTAATTTTACTACATTTCAGTTAACTTAAGTGTAAATTACTGCAGGTGGCTTAGCGGCTACTATATTGAACAGCACCACCTGATAATTTAGCACAATATTTTTTTTCCTCTGCAATGGTTTCCCTGAACCAAGAGTAAACAGCCCACATGTGTTGAACTTCTTTTTTTTAAGATGGAGTCTCACTCTGTCGCTCAGGCTGGAGTGCAATGGCACAGTCTCTGCTCACTGCAACCTCCACCCCGTGGGTTCAAG... | AGCCATTAGCCATGTGTGGCTACTGAGCAACTTAAACAGTGGCTTGTGCAAATGAGAAACTAAAATGTTAATTTTACTACATTTCAGTTAACTTAAGTGTAAATTACTGCAGGTGGCTTAGCGGCTACTATATTGAACAGCACCACCTGATAATTTAGCACAATATTTTTTTTCCTCTGCAATGGTTTCCCTGAACCAAGAGTAAACAGCCCACATGTGTTGAACTTCTTTTTTTTAAGATGGAGTCTCACTCTGTCGCTCAGGCTGGAGTGCAATGGCACAGTCTCTGCTCACTGCAACCTCCACCCCGTGGGTTCAAG... |
Task1_train_43353 | This alteration on Chromosome 14 may affect genome function. Does it lead to a disease or is it benign? | Benign | AATTAAAAATAGAATTAGTTAAATAGAACAACATAAACTGAAGGTAACTTAGTAAGGGCTCAAACCATACCAGTTTTCTTTCCTTCTCTTTCCTCTTTGCAGGATGGATGGATAAATGGGTGGATAGCCTGGCAGATGGAGGGTGGATGGATAGATGAATAGCTAATGGATAAATGGTTGGCTGGCTGGGTGGATAGATGGATTAATGGATGAATGGATGGATGGATGAACCGATAGAGGGATAGATAGATGAATAGATTAGTGGATAGGTGGTTGGCTAGCTAGATGGCTAGCTAGGTGGATGAATGGATGCATGGATG... | AATTAAAAATAGAATTAGTTAAATAGAACAACATAAACTGAAGGTAACTTAGTAAGGGCTCAAACCATACCAGTTTTCTTTCCTTCTCTTTCCTCTTTGCAGGATGGATGGATAAATGGGTGGATAGCCTGGCAGATGGAGGGTGGATGGATAGATGAATAGCTAATGGATAAATGGTTGGCTGGCTGGGTGGATAGATGGATTAATGGATGAATGGATGGATGGATGAACCGATAGAGGGATAGATAGATGAATAGATTAGTGGATAGGTGGTTGGCTAGCTAGATGGCTAGCTAGGTGGATGAATGGATGCATGGATG... |
Task1_train_43354 | A sequence alteration has been identified on Chromosome 14. Is it disease-inducing or harmless? | Benign | GATAGCCTGGCAGATGGAGGGTGGATGGATAGATGAATAGCTAATGGATAAATGGTTGGCTGGCTGGGTGGATAGATGGATTAATGGATGAATGGATGGATGGATGAACCGATAGAGGGATAGATAGATGAATAGATTAGTGGATAGGTGGTTGGCTAGCTAGATGGCTAGCTAGGTGGATGAATGGATGCATGGATGGATGGATGGATGGATGGATGGATGGATAGATGGATGAACTGATGGATGGATAAATGGGTGGATAGTTTGCTGGATGGGTAGATGAAGGGTGGAGGGATGAACAGGTTAATGGATAAATGGTT... | GATAGCCTGGCAGATGGAGGGTGGATGGATAGATGAATAGCTAATGGATAAATGGTTGGCTGGCTGGGTGGATAGATGGATTAATGGATGAATGGATGGATGGATGAACCGATAGAGGGATAGATAGATGAATAGATTAGTGGATAGGTGGTTGGCTAGCTAGATGGCTAGCTAGGTGGATGAATGGATGCATGGATGGATGGATGGATGGATGGATGGATGGATAGATGGATGAACTGATGGATGGATAAATGGGTGGATAGTTTGCTGGATGGGTAGATGAAGGGTGGAGGGATGAACAGGTTAATGGATAAATGGTT... |
Task1_train_43355 | This alteration occurs on Chromosome 14. Is it associated with a disease or is it a benign variant? | Benign | AGCCTGGCAGATGGAGGGTGGATGGATAGATGAATAGCTAATGGATAAATGGTTGGCTGGCTGGGTGGATAGATGGATTAATGGATGAATGGATGGATGGATGAACCGATAGAGGGATAGATAGATGAATAGATTAGTGGATAGGTGGTTGGCTAGCTAGATGGCTAGCTAGGTGGATGAATGGATGCATGGATGGATGGATGGATGGATGGATGGATGGATAGATGGATGAACTGATGGATGGATAAATGGGTGGATAGTTTGCTGGATGGGTAGATGAAGGGTGGAGGGATGAACAGGTTAATGGATAAATGGTTGGC... | AGCCTGGCAGATGGAGGGTGGATGGATAGATGAATAGCTAATGGATAAATGGTTGGCTGGCTGGGTGGATAGATGGATTAATGGATGAATGGATGGATGGATGAACCGATAGAGGGATAGATAGATGAATAGATTAGTGGATAGGTGGTTGGCTAGCTAGATGGCTAGCTAGGTGGATGAATGGATGCATGGATGGATGGATGGATGGATGGATGGATGGATAGATGGATGAACTGATGGATGGATAAATGGGTGGATAGTTTGCTGGATGGGTAGATGAAGGGTGGAGGGATGAACAGGTTAATGGATAAATGGTTGGC... |
Task1_train_43356 | A variant on Chromosome 14 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AGACCATTCTCTCTCCACTGCTGAGCCCCACGGCCACTCTGCAAGGGATTTCCCACCCACCTGTTTGGGGCCCTTTGGAGTTTGGTTTTAATTGGGTCACGGGATGCTGTGACAGGCTGCCCCTGCCTGGTGGGGATCTGGGGTCACTGATGACATTGTGCCCATGGAGAGAGCCCAGCAGAAAGGGATTCCCTCCAAGGCGACACACAGGGCAAAGCTCACATCAGAAGCCAGGCAGGCCCTCTGCACCTGGTAATTAGCCAGCCTGGGTGCTGTCAGGCTCACACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG... | AGACCATTCTCTCTCCACTGCTGAGCCCCACGGCCACTCTGCAAGGGATTTCCCACCCACCTGTTTGGGGCCCTTTGGAGTTTGGTTTTAATTGGGTCACGGGATGCTGTGACAGGCTGCCCCTGCCTGGTGGGGATCTGGGGTCACTGATGACATTGTGCCCATGGAGAGAGCCCAGCAGAAAGGGATTCCCTCCAAGGCGACACACAGGGCAAAGCTCACATCAGAAGCCAGGCAGGCCCTCTGCACCTGGTAATTAGCCAGCCTGGGTGCTGTCAGGCTCACACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG... |
Task1_train_43357 | Assess the clinical impact of this variant found on Chromosome 14. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CCACGGCCACTCTGCAAGGGATTTCCCACCCACCTGTTTGGGGCCCTTTGGAGTTTGGTTTTAATTGGGTCACGGGATGCTGTGACAGGCTGCCCCTGCCTGGTGGGGATCTGGGGTCACTGATGACATTGTGCCCATGGAGAGAGCCCAGCAGAAAGGGATTCCCTCCAAGGCGACACACAGGGCAAAGCTCACATCAGAAGCCAGGCAGGCCCTCTGCACCTGGTAATTAGCCAGCCTGGGTGCTGTCAGGCTCACACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAAGCATGTACCCTATGGTA... | CCACGGCCACTCTGCAAGGGATTTCCCACCCACCTGTTTGGGGCCCTTTGGAGTTTGGTTTTAATTGGGTCACGGGATGCTGTGACAGGCTGCCCCTGCCTGGTGGGGATCTGGGGTCACTGATGACATTGTGCCCATGGAGAGAGCCCAGCAGAAAGGGATTCCCTCCAAGGCGACACACAGGGCAAAGCTCACATCAGAAGCCAGGCAGGCCCTCTGCACCTGGTAATTAGCCAGCCTGGGTGCTGTCAGGCTCACACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAAGCATGTACCCTATGGTA... |
Task1_train_43358 | Given this context: Chromosome 14 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | ATGACATTGTGCCCATGGAGAGAGCCCAGCAGAAAGGGATTCCCTCCAAGGCGACACACAGGGCAAAGCTCACATCAGAAGCCAGGCAGGCCCTCTGCACCTGGTAATTAGCCAGCCTGGGTGCTGTCAGGCTCACACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAAGCATGTACCCTATGGTACAGTTGAGAATATGGAGGCCTCAGATGGGGCTTTTGCCAGAAACTGCCATGCCTACTGCTCACACTTCCATAGCACGTGCCCCCAAGCACCCCATGGTGTAGGTGCTGTTATTATCACTATC... | ATGACATTGTGCCCATGGAGAGAGCCCAGCAGAAAGGGATTCCCTCCAAGGCGACACACAGGGCAAAGCTCACATCAGAAGCCAGGCAGGCCCTCTGCACCTGGTAATTAGCCAGCCTGGGTGCTGTCAGGCTCACACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAAGCATGTACCCTATGGTACAGTTGAGAATATGGAGGCCTCAGATGGGGCTTTTGCCAGAAACTGCCATGCCTACTGCTCACACTTCCATAGCACGTGCCCCCAAGCACCCCATGGTGTAGGTGCTGTTATTATCACTATC... |
Task1_train_43359 | Given a variant located on Chromosome 14, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCACCAGCTACATCCAGCTCCCTGAGGCAGGTAATCCATGATGTTTTACATCCTGGGAGCGGAGGAATCTGTTTTTCCAGGAGAGTTTTAGGCAGCAGCCTGGAGTGTGTGGAGTGTGAGGGGTAAGCAGAGGCCAGGAGGAGGTGTACTCAGGTGTTAGGGGCCAGGGGTCTGTTCTTGGCTGCCACTGATTCCCTGTGCCTTTTTTAGAGGCATCCTCTGTGTCTGGGTTTTCACACCTGCAAAGGGTGGAGGTGCCCTGGGGCCTCTATGGTCATTTCTGCCTTGATACTTACAGATTCGGATTTGAGTCAGCTGTG... | CCACCAGCTACATCCAGCTCCCTGAGGCAGGTAATCCATGATGTTTTACATCCTGGGAGCGGAGGAATCTGTTTTTCCAGGAGAGTTTTAGGCAGCAGCCTGGAGTGTGTGGAGTGTGAGGGGTAAGCAGAGGCCAGGAGGAGGTGTACTCAGGTGTTAGGGGCCAGGGGTCTGTTCTTGGCTGCCACTGATTCCCTGTGCCTTTTTTAGAGGCATCCTCTGTGTCTGGGTTTTCACACCTGCAAAGGGTGGAGGTGCCCTGGGGCCTCTATGGTCATTTCTGCCTTGATACTTACAGATTCGGATTTGAGTCAGCTGTG... |
Task1_train_43360 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AAGAAAAAAGCATGCTCAGGTTGTCCAGAAAAAAAAGGAAACCTGAAAAAAAAAAAAAAACCACAATAGCGAGAAAGGGGGTCTAAGTTTCCTCGGAGGTCCTCAACTGTCTGTAGAAGTGCCCCACCCAGAACCCAAAATAAAATGAAGTAACCCCGCCCCTGGTCAGGGTCCTGTCTTTTTTATTATCCAGACACACGTATCAGAGCCTGCTAACATCCAGTTGTGGGAAGAGCAGCAAGCAGTACACCAGGAGCCACAGGAAGAGAATAAAATACATCATATCCGGCTGCTGGACAAGCTGTGTCAGGGAGTCACTC... | AAGAAAAAAGCATGCTCAGGTTGTCCAGAAAAAAAAGGAAACCTGAAAAAAAAAAAAAAACCACAATAGCGAGAAAGGGGGTCTAAGTTTCCTCGGAGGTCCTCAACTGTCTGTAGAAGTGCCCCACCCAGAACCCAAAATAAAATGAAGTAACCCCGCCCCTGGTCAGGGTCCTGTCTTTTTTATTATCCAGACACACGTATCAGAGCCTGCTAACATCCAGTTGTGGGAAGAGCAGCAAGCAGTACACCAGGAGCCACAGGAAGAGAATAAAATACATCATATCCGGCTGCTGGACAAGCTGTGTCAGGGAGTCACTC... |
Task1_train_43361 | Assess the clinical impact of this variant found on Chromosome 14. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TGAGCCGAGATCGCACCACTGCACTCCAGCCTGGGCAAAAAGAGCGAAACTCCATCTCAAAATAATTATAATAACAATAATAATAATAACTCAGAGCCAGGCTTGTGGATGGAAATATAGTGCCCAAGTCACATTCTGCTTAAAGTTGTAACAAATACAGACGAGTTAAAAGAAAAAAAAAAGTACGCTTTCTGAGTCAGCCCCAAGGGCTCTCCTTGGCAGCACGGGTTTCCTGCCGGTGAAATGTCCTAGTTGCCTAGGACCCGGGTCCCCAAGGGCAGAGCTCACAGTGAAAGGCAAAGGGTCAGTGTGTGTGAGAC... | TGAGCCGAGATCGCACCACTGCACTCCAGCCTGGGCAAAAAGAGCGAAACTCCATCTCAAAATAATTATAATAACAATAATAATAATAACTCAGAGCCAGGCTTGTGGATGGAAATATAGTGCCCAAGTCACATTCTGCTTAAAGTTGTAACAAATACAGACGAGTTAAAAGAAAAAAAAAAGTACGCTTTCTGAGTCAGCCCCAAGGGCTCTCCTTGGCAGCACGGGTTTCCTGCCGGTGAAATGTCCTAGTTGCCTAGGACCCGGGTCCCCAAGGGCAGAGCTCACAGTGAAAGGCAAAGGGTCAGTGTGTGTGAGAC... |
Task1_train_43362 | Assess the clinical impact of this variant found on Chromosome 14. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GTGGCTCACAGAGGTGAGTATCTCCCGGGCCCAGCAGCATGGGCCTATCCCGAGAGCTTGTTAGAAATGCAGAATCGAATTGTGGGCCCTAGCCAGATCTACTAACTCAGAGTCTGCATTTTATCTTATTTCATTATTTTTTGTTGATTGATTGATTGATTGAAATGGGGTCTTGCTTTGTCACCAGGCTGGAGTGCAGTGGCACAATCACAGCTCCCTGCAGCCTCAAACTCCTGGGCTCAAGTGATCCTCCCACCTCAGGCCCCTGAGTAGCTGGAACTACAGGAGCACACCACCATGTCCAGTTAATTTTTAAATAT... | GTGGCTCACAGAGGTGAGTATCTCCCGGGCCCAGCAGCATGGGCCTATCCCGAGAGCTTGTTAGAAATGCAGAATCGAATTGTGGGCCCTAGCCAGATCTACTAACTCAGAGTCTGCATTTTATCTTATTTCATTATTTTTTGTTGATTGATTGATTGATTGAAATGGGGTCTTGCTTTGTCACCAGGCTGGAGTGCAGTGGCACAATCACAGCTCCCTGCAGCCTCAAACTCCTGGGCTCAAGTGATCCTCCCACCTCAGGCCCCTGAGTAGCTGGAACTACAGGAGCACACCACCATGTCCAGTTAATTTTTAAATAT... |
Task1_train_43363 | Here is a genetic alteration on Chromosome 14. Based on the data, is it a benign variant or a cause of disease? | Benign | AATTTATGTATGAGCTGTGCTTGGGTTTTAAAGAGAGAACTATTGTATCACGCGCATTTTAAAAAACCATCAAGTTCCTTATCCAGCCAACAATGATCAACGGTCAGCCTACTTACAGTCCACGTTTCAGAACATTTATTCTTAATCCCAAAGTTGGTTTAACTGAACACCTCTGGACTCATTAAGAATACTTAGCAAAGCAATTCTAAAAACAAATACCAATGTTAGACTTTGGAACTGAGGAGTAAACAGAAAGACAGTTTGTCATTTTGCTGAGCTCAAGACTCAGTTGTTTGAGGTCAGGAACCATCAGATAAATA... | AATTTATGTATGAGCTGTGCTTGGGTTTTAAAGAGAGAACTATTGTATCACGCGCATTTTAAAAAACCATCAAGTTCCTTATCCAGCCAACAATGATCAACGGTCAGCCTACTTACAGTCCACGTTTCAGAACATTTATTCTTAATCCCAAAGTTGGTTTAACTGAACACCTCTGGACTCATTAAGAATACTTAGCAAAGCAATTCTAAAAACAAATACCAATGTTAGACTTTGGAACTGAGGAGTAAACAGAAAGACAGTTTGTCATTTTGCTGAGCTCAAGACTCAGTTGTTTGAGGTCAGGAACCATCAGATAAATA... |
Task1_train_43364 | A mutation on Chromosome 14 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTAGATGCGTGTAAACTGACTTTGTAAGATAGCCTCCTAACTCCCAGTTCCTAGTGTTACTCTGCCATATAACTTTGCAGTCAGCATTTTCTGCCCCAGATGGAATCACCACCGTCTATCACATATGAAATAATGATTATCATTAAAATTCATTCTTGGATGTGATTTTCTAATTTTCAGGAGTAGCTCTCTGATTCTGAGTTAATTTCAAGTGATATTTGTAAGAACTACCACTGCATATTGCAGTTTTTGAAAACTAAAGTGTGAGAGAGATTAACCATGTGTAAACAGTTACTTGTGGATCCGCAGGATTCATTTTA... | TTAGATGCGTGTAAACTGACTTTGTAAGATAGCCTCCTAACTCCCAGTTCCTAGTGTTACTCTGCCATATAACTTTGCAGTCAGCATTTTCTGCCCCAGATGGAATCACCACCGTCTATCACATATGAAATAATGATTATCATTAAAATTCATTCTTGGATGTGATTTTCTAATTTTCAGGAGTAGCTCTCTGATTCTGAGTTAATTTCAAGTGATATTTGTAAGAACTACCACTGCATATTGCAGTTTTTGAAAACTAAAGTGTGAGAGAGATTAACCATGTGTAAACAGTTACTTGTGGATCCGCAGGATTCATTTTA... |
Task1_train_43365 | This variant is found on Chromosome 14. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ATATTTCTTAATTCTCGCACCCAGCTCTCAGTCATCATAAAGGTAAAAGTTTTGTAATCGGCATCATTGTAAAAAGTGAGTTTTGATAGACTTTGTATTTGAGGACAGAGTTTGAAGAAAGTAAAAAAACACACAAATTATGCTAGTTGTTTTTGTTGATGGAGCATCAAACATCACCATGATGAACAACTTGAATTCATCAGGGTATTCTACTATGTCTAGATATTTGGCATTATAAAGACATTTTGATGATTAATGGAATTTACCCTTTATTGGCAGCTGCCAAAGAGCTAGCTGTTGTTTCTTTACTAGCACCCAGA... | ATATTTCTTAATTCTCGCACCCAGCTCTCAGTCATCATAAAGGTAAAAGTTTTGTAATCGGCATCATTGTAAAAAGTGAGTTTTGATAGACTTTGTATTTGAGGACAGAGTTTGAAGAAAGTAAAAAAACACACAAATTATGCTAGTTGTTTTTGTTGATGGAGCATCAAACATCACCATGATGAACAACTTGAATTCATCAGGGTATTCTACTATGTCTAGATATTTGGCATTATAAAGACATTTTGATGATTAATGGAATTTACCCTTTATTGGCAGCTGCCAAAGAGCTAGCTGTTGTTTCTTTACTAGCACCCAGA... |
Task1_train_43366 | A mutation on Chromosome 14 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GTATGAGGTACTCAGAGTGGTCTCATTCATAAAGTGGAATGGTAGCTGCCAGGGGCTGGAGGGAGTCGAGGATGGGAAGTTAATGTTAGTAACAGGTACGGAGTCTCAGTTTGGGAAGATAAAAAGTTCTGGAGGTGGATAGTGCCGACGGTTCCACATGTCAATGCACTTAATGCCACCAAACTGTACTCTTAAAAACAGTTGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGGGGCCGAGGCGGGCGGATCACAAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTAC... | GTATGAGGTACTCAGAGTGGTCTCATTCATAAAGTGGAATGGTAGCTGCCAGGGGCTGGAGGGAGTCGAGGATGGGAAGTTAATGTTAGTAACAGGTACGGAGTCTCAGTTTGGGAAGATAAAAAGTTCTGGAGGTGGATAGTGCCGACGGTTCCACATGTCAATGCACTTAATGCCACCAAACTGTACTCTTAAAAACAGTTGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGGGGCCGAGGCGGGCGGATCACAAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTAC... |
Task1_train_43367 | A mutation on Chromosome 14 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGATCCTTCCTGGATATGTGCCCTAAGATAGCATTCGAATGAGAGAAACAGAACTGGTAAGATATATATAGGTGTATATAAAGAGATTTATTATACAGAGTTGACTCGTGATTTTGGAGACCAGCAAGTCCTGAGATCCGCAGGATGAGTCAGCAAGCGGGAGACCCAGGATGGCCAGTGGTGTGGTTCCATCTGAAGCCCTGCAGGCTCAAGGCCCAGGAAGAGCTACCTGAAAATCAACAGTTCGAGTCCAAAGGCAGGAAAAAGCCATTGTCCCAGCTTGAAGGCAGGCAGGCAGGAGGAATTTGGGGGAATGTCAG... | TGATCCTTCCTGGATATGTGCCCTAAGATAGCATTCGAATGAGAGAAACAGAACTGGTAAGATATATATAGGTGTATATAAAGAGATTTATTATACAGAGTTGACTCGTGATTTTGGAGACCAGCAAGTCCTGAGATCCGCAGGATGAGTCAGCAAGCGGGAGACCCAGGATGGCCAGTGGTGTGGTTCCATCTGAAGCCCTGCAGGCTCAAGGCCCAGGAAGAGCTACCTGAAAATCAACAGTTCGAGTCCAAAGGCAGGAAAAAGCCATTGTCCCAGCTTGAAGGCAGGCAGGCAGGAGGAATTTGGGGGAATGTCAG... |
Task1_train_43368 | This sequence variant lies on Chromosome 14. Is it clinically significant, and what condition might it cause if any? | Benign | GCACTTTGGGAGGCCGAGGCGGGTGGATTGTTTGAGGTCAGGAGTTCGAGACCAACCTGGCCAACATGGCAAAACCTCATCTCTACCAAAAATACAAAAATTAGCCAGGCATGGTGGCAGGCACCTGTGATCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAAGATTACGCCATTGTACTCCAGCCTGGGTGACAGAGAGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAATTACGCTTCAAACACATGATCTCTCACCACTGTTGAATTTTCTT... | GCACTTTGGGAGGCCGAGGCGGGTGGATTGTTTGAGGTCAGGAGTTCGAGACCAACCTGGCCAACATGGCAAAACCTCATCTCTACCAAAAATACAAAAATTAGCCAGGCATGGTGGCAGGCACCTGTGATCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAAGATTACGCCATTGTACTCCAGCCTGGGTGACAGAGAGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAATTACGCTTCAAACACATGATCTCTCACCACTGTTGAATTTTCTT... |
Task1_train_43369 | This sequence variant lies on Chromosome 14. Is it clinically significant, and what condition might it cause if any? | Benign | TACTAAAGTCTAATAAAATTATCCCAATCCTTTCCAAACAGTAGAGGATATACCACAGTTGAAGTATTTTCTTACATCATTTATCAATCAGTCTAAGTACTGGCACCAGTTTTGTGCCCATTTGTTTTACTAGGCTACAAGCTACCAGAAAACATAAGCACTGTCTTCTACTCACTCTGCATTCCCGACACCAGCCTGGCCAGAGTTACCTATTTACTAGACACTGAGTAGACACAAGCTGAATGATTAACAGATATCCATAAAAACTCATATGCGTCTTTAATAAGTGACTTATTAAATTTACGAGAACACAAATAAAG... | TACTAAAGTCTAATAAAATTATCCCAATCCTTTCCAAACAGTAGAGGATATACCACAGTTGAAGTATTTTCTTACATCATTTATCAATCAGTCTAAGTACTGGCACCAGTTTTGTGCCCATTTGTTTTACTAGGCTACAAGCTACCAGAAAACATAAGCACTGTCTTCTACTCACTCTGCATTCCCGACACCAGCCTGGCCAGAGTTACCTATTTACTAGACACTGAGTAGACACAAGCTGAATGATTAACAGATATCCATAAAAACTCATATGCGTCTTTAATAAGTGACTTATTAAATTTACGAGAACACAAATAAAG... |
Task1_train_43370 | A sequence alteration has been identified on Chromosome 14. Is it disease-inducing or harmless? | Benign | ATATTTACTCATTGATTATGAACACCATAGGGCTTCTTTAGCATTCAATCAAGTTTATCAGCAGGAGAAATGGTGTTTTTTTTTTTAATGAGTATGTTTTTAAAAATTAGAATAACTTTTTTAAAAATTGAGACAGGGTGTTGCTCTGTTGCCCAGGTTGGAGTGCAGTGGTAGGACCACGACTCACTGCAGCCTAGACCCTCCTGGGCTTAAGCACTCCTCCTGCCTCAGCCTGGGCCACCAAGTAGCTGGGACCACAGGCACATGTGACTATGCCCAGCCAATATTTAAAAAAAATTTTTTTTTTTTTTTGTAGAGAC... | ATATTTACTCATTGATTATGAACACCATAGGGCTTCTTTAGCATTCAATCAAGTTTATCAGCAGGAGAAATGGTGTTTTTTTTTTTAATGAGTATGTTTTTAAAAATTAGAATAACTTTTTTAAAAATTGAGACAGGGTGTTGCTCTGTTGCCCAGGTTGGAGTGCAGTGGTAGGACCACGACTCACTGCAGCCTAGACCCTCCTGGGCTTAAGCACTCCTCCTGCCTCAGCCTGGGCCACCAAGTAGCTGGGACCACAGGCACATGTGACTATGCCCAGCCAATATTTAAAAAAAATTTTTTTTTTTTTTTGTAGAGAC... |
Task1_train_43371 | Chromosome 14 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGGCAGGCTTGGGACCCACTGCTGCCGAGAGCCAAGGGCCCCTCCCTCACCCCGTCTCTCTGTCTCTCTCTCTCCTGCATGGCTCAGAACAGCAGTGCCTTCCTCCATGGCCAGCAGGAACCCCACCCATGATCCCAGCTCCTCTGGTTCTTCTTCTTCTTCTTCTTTTTTTTTTTTTTTTTGAGGTGGAGTCTCACTCTGTTTCCCGGGTTGGAGTGCAGTGGGGCAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTTGAGCAATTCTCCTACCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACGTGCCACCC... | AGGCAGGCTTGGGACCCACTGCTGCCGAGAGCCAAGGGCCCCTCCCTCACCCCGTCTCTCTGTCTCTCTCTCTCCTGCATGGCTCAGAACAGCAGTGCCTTCCTCCATGGCCAGCAGGAACCCCACCCATGATCCCAGCTCCTCTGGTTCTTCTTCTTCTTCTTCTTTTTTTTTTTTTTTTTGAGGTGGAGTCTCACTCTGTTTCCCGGGTTGGAGTGCAGTGGGGCAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTTGAGCAATTCTCCTACCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACGTGCCACCC... |
Task1_train_43372 | Consider a variant on Chromosome 14. Determine its clinical classification and disease relevance. | Benign | GTTTGTGTGTGTGAGTGTACACCTCTCCACGCCCATACAGCCCATCCTATATCCCCCATCAGAGTGTGTGTGTGTGTACACATCTCCACACCCATACAGCCCGTCCTGTATCCCCCATCAGTGTGTGTGTGTGTGTGTGTGTGTGTACACATCTCCACACCCATACAGCCCGTCCTGTATCCCCCATCAGTGTGTGTGTGTGTGTGTGTACATATCTCTACACCCATACAGCCCATCCTGTATCCCCCATCGGTGTGTTTGTGTGTGTGTGTGAGTGTACACCTCTCCACGCCCATACAGCCCATCCTATATCCCCCATC... | GTTTGTGTGTGTGAGTGTACACCTCTCCACGCCCATACAGCCCATCCTATATCCCCCATCAGAGTGTGTGTGTGTGTACACATCTCCACACCCATACAGCCCGTCCTGTATCCCCCATCAGTGTGTGTGTGTGTGTGTGTGTGTGTACACATCTCCACACCCATACAGCCCGTCCTGTATCCCCCATCAGTGTGTGTGTGTGTGTGTGTACATATCTCTACACCCATACAGCCCATCCTGTATCCCCCATCGGTGTGTTTGTGTGTGTGTGTGAGTGTACACCTCTCCACGCCCATACAGCCCATCCTATATCCCCCATC... |
Task1_train_43373 | Mutation context: Chromosome 14. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TTTACTCATTCAGCAGTTTCTGGCACTTTTGTTAGTTACTGGCTCCATGCTGGATGCCAGAGCCACAGTGAGAAGTCAGACTAGGCCCTGTTCTGGCTGGGACGGACAGAGATGTCATTTACTGTCCAAGGCCTTGTGATCGAAGTGTGTGCCAGGTACCGTGAGGACCCACCCAGAACAGTGGAGACTGGGGTTGGGGGTAGGGGTTCCTGGAGTCTGAAAAGAAGAGGAAGGGTGCACCAATAGGGGGTTGCACTGAGGGGGGTGGCAGCTAGGGGGATGGCACTGAGTGGGTATGGCACTGAGGGGGGTACACCTGG... | TTTACTCATTCAGCAGTTTCTGGCACTTTTGTTAGTTACTGGCTCCATGCTGGATGCCAGAGCCACAGTGAGAAGTCAGACTAGGCCCTGTTCTGGCTGGGACGGACAGAGATGTCATTTACTGTCCAAGGCCTTGTGATCGAAGTGTGTGCCAGGTACCGTGAGGACCCACCCAGAACAGTGGAGACTGGGGTTGGGGGTAGGGGTTCCTGGAGTCTGAAAAGAAGAGGAAGGGTGCACCAATAGGGGGTTGCACTGAGGGGGGTGGCAGCTAGGGGGATGGCACTGAGTGGGTATGGCACTGAGGGGGGTACACCTGG... |
Task1_train_43374 | Chromosome 14 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GCTGGGAGTGGTGGTACACACCCGCGGTCCCAGCTACATGGGAGGCTGGGGTAGGAGGATTGCTTGAGCCTGGGAGGTCAAGGGTGCAGAGAGCAATGATTGCACCACTGCACTGTGACCTGGATGACAGAGCAAAACCCTGTCTCCAGAAAAAGAAAGAAAGAAAGAAAGCAGGTCTCAAAAGCAATGGATGAGTATTCTTTAACTACAATGTAGCAGACTCTTTATTAAAAATGAAATTTGATGTTTATTTTTAATCATGTTCAACCCACTTTATTCTCAGATATAGTCTTCCTGTGAATAACTTTCTTTTCAGAATG... | GCTGGGAGTGGTGGTACACACCCGCGGTCCCAGCTACATGGGAGGCTGGGGTAGGAGGATTGCTTGAGCCTGGGAGGTCAAGGGTGCAGAGAGCAATGATTGCACCACTGCACTGTGACCTGGATGACAGAGCAAAACCCTGTCTCCAGAAAAAGAAAGAAAGAAAGAAAGCAGGTCTCAAAAGCAATGGATGAGTATTCTTTAACTACAATGTAGCAGACTCTTTATTAAAAATGAAATTTGATGTTTATTTTTAATCATGTTCAACCCACTTTATTCTCAGATATAGTCTTCCTGTGAATAACTTTCTTTTCAGAATG... |
Task1_train_43375 | Assess the clinical impact of this variant found on Chromosome 14. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GAGAGCAACATGGCACCACCCTCTGGCAGTGTGAAAATTTGGTTCTGTTGATTATTTCCCTTAATAAAGGAAGATCTTCATCTGAGCTTTGGAAATCACTTCCCCTTGCCTGGAGATTCTGTTGTGAGAACATTTTTAATAATAAGATTTGACCAGCATTTGGTTGAACATATTGTGAATTGCTAGAGTCATAGACATGCCCAAGTCATATTATAACTGTAAAGAAAGCTCCAAAGCCCCATCTAATTTCATAAAAGCTATTCACTGTTTGTTAGTATCTGATTCTTCCTCATTAGCATGGGTCATCATCAACTTGACTC... | GAGAGCAACATGGCACCACCCTCTGGCAGTGTGAAAATTTGGTTCTGTTGATTATTTCCCTTAATAAAGGAAGATCTTCATCTGAGCTTTGGAAATCACTTCCCCTTGCCTGGAGATTCTGTTGTGAGAACATTTTTAATAATAAGATTTGACCAGCATTTGGTTGAACATATTGTGAATTGCTAGAGTCATAGACATGCCCAAGTCATATTATAACTGTAAAGAAAGCTCCAAAGCCCCATCTAATTTCATAAAAGCTATTCACTGTTTGTTAGTATCTGATTCTTCCTCATTAGCATGGGTCATCATCAACTTGACTC... |
Task1_train_43376 | Consider a variant on Chromosome 14. Determine its clinical classification and disease relevance. | Benign | CTCCTGTAGCTGAAGGAGAAGAAGGGATGGGAGCTGGCCTCACAGAGGGCTTTGTAGAGCCACGGGGCCCCAGGGTCAGACCTTGTGCCGGTCATGCCAACATCCAGGGCCACCTCCTTGCTGCTCCATCTACTGCCTCCTGTTGGGCAGCTGCAGCCAGTGCCCTTGGCCCTGCATGTTTACTCAATCATGCTACTTAGCATGTTTTATTCAGGACACCTCTTTGGTACCAGCATCCCTACTAGCACGCTAGTCCTGTTGGGAGCAGGACCTGTGTTGTCTCAGTCATCCCTGCCTCTCTAGAACAAGTACAGAGGCGA... | CTCCTGTAGCTGAAGGAGAAGAAGGGATGGGAGCTGGCCTCACAGAGGGCTTTGTAGAGCCACGGGGCCCCAGGGTCAGACCTTGTGCCGGTCATGCCAACATCCAGGGCCACCTCCTTGCTGCTCCATCTACTGCCTCCTGTTGGGCAGCTGCAGCCAGTGCCCTTGGCCCTGCATGTTTACTCAATCATGCTACTTAGCATGTTTTATTCAGGACACCTCTTTGGTACCAGCATCCCTACTAGCACGCTAGTCCTGTTGGGAGCAGGACCTGTGTTGTCTCAGTCATCCCTGCCTCTCTAGAACAAGTACAGAGGCGA... |
Task1_train_43377 | This mutation on Chromosome 14 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GCAACTGCGCCACCACCACGCCGCCCCACTGCTCAACGGCATGCAGCCTTGGCCCAGCTCCCATCACAGGGATGCCCTCCCTGCCCCCCCCCCCCAGGATGCCTTTCCTGCCCCCTCTTTGCCCTGTCACCTCCTAAGGATGCTCTCAGGACGCAGGGAGCCTGGCCGCAAAACCAGGACAGCGGGGCCAGCACCAGGCACCCAGAGCCTCTCACTTTGCTCAGGAAAGGTAAAGGCTCATGGCTCACGGCAGGCACTCTTGCCAACTTGCTCTGCCATCTCCTGAGGCGGGCACCTCTCCCCTCCGCCCCGTCACCTCC... | GCAACTGCGCCACCACCACGCCGCCCCACTGCTCAACGGCATGCAGCCTTGGCCCAGCTCCCATCACAGGGATGCCCTCCCTGCCCCCCCCCCCCAGGATGCCTTTCCTGCCCCCTCTTTGCCCTGTCACCTCCTAAGGATGCTCTCAGGACGCAGGGAGCCTGGCCGCAAAACCAGGACAGCGGGGCCAGCACCAGGCACCCAGAGCCTCTCACTTTGCTCAGGAAAGGTAAAGGCTCATGGCTCACGGCAGGCACTCTTGCCAACTTGCTCTGCCATCTCCTGAGGCGGGCACCTCTCCCCTCCGCCCCGTCACCTCC... |
Task1_train_43378 | A genomic change on Chromosome 14 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGGTCAGATGACCCCCAAGGTTCCTCCCAGCCCTCCCCAGGAGTTCCACAGCATACGGGAGGCAGCTACCACTGCTGGGACCAGACGATGCTGGGCTGCAGCTCACCTCCCAGGAGAAACCACAGCAGTCACAAACCCACATAGAGGCTTCCAGCTCCTGAGGCCCCAGTTACCCCGGGATGCAGTCACAGGCTAGCCACCCAATGTATCTTGGGTTTCAAACATTTAAAAGTCATGGTATCTCAGTATGCTGCCATGGGATTAAAAAAAGAGGAAGAAAGAAAAAGTTGGCTGGGCGCAGTGGCTCACACCTGTAATCC... | GGGTCAGATGACCCCCAAGGTTCCTCCCAGCCCTCCCCAGGAGTTCCACAGCATACGGGAGGCAGCTACCACTGCTGGGACCAGACGATGCTGGGCTGCAGCTCACCTCCCAGGAGAAACCACAGCAGTCACAAACCCACATAGAGGCTTCCAGCTCCTGAGGCCCCAGTTACCCCGGGATGCAGTCACAGGCTAGCCACCCAATGTATCTTGGGTTTCAAACATTTAAAAGTCATGGTATCTCAGTATGCTGCCATGGGATTAAAAAAAGAGGAAGAAAGAAAAAGTTGGCTGGGCGCAGTGGCTCACACCTGTAATCC... |
Task1_train_43379 | Chromosome 14 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TGCTGAATGGCCAGGCTGCACCAGCGTGTTCACGCCCTTCATTAGCTTGCCTTGCAGATGAGAAAACAGGCTCTCAGATGTATCCGCAACTGCCCAGGTCACATGGCCAAGGCTGCTGTCAGGGTCCAAGGGCACACGCACCCCTGAGCTGGCCCCTTCGACTCCAGGGCAAGGGTGCTGAATGAAGCCCTTTCCTCCACCATATGCAAAGGCAGCCTCGCCACTTAAAAAACAAAGAACACTTTATTCCCTTGACAGTTTCTGTACAGCGACACCAGGCTGTGCAAAGCCCAGTGTCGTCTTCACTGAGCACATTCCCC... | TGCTGAATGGCCAGGCTGCACCAGCGTGTTCACGCCCTTCATTAGCTTGCCTTGCAGATGAGAAAACAGGCTCTCAGATGTATCCGCAACTGCCCAGGTCACATGGCCAAGGCTGCTGTCAGGGTCCAAGGGCACACGCACCCCTGAGCTGGCCCCTTCGACTCCAGGGCAAGGGTGCTGAATGAAGCCCTTTCCTCCACCATATGCAAAGGCAGCCTCGCCACTTAAAAAACAAAGAACACTTTATTCCCTTGACAGTTTCTGTACAGCGACACCAGGCTGTGCAAAGCCCAGTGTCGTCTTCACTGAGCACATTCCCC... |
Task1_train_43380 | A change on Chromosome 14 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CCAAAGGCATTTTTAAAGTCCTGTCTCTTTCTCTGTAGGCATTGTCTCTTCAGGTCTTCTTTTTTTTTCTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCACTCAGGCTAGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTTCTGTCTCAGCCTCTCAAGTAGCTGGGACTACAGGCGCCTGCCACCATGTCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGCTTTGCCATATTGGTCAGACTAGTCTTGAACTCCTGACCTCAGGTGATCCACCAACCTTGG... | CCAAAGGCATTTTTAAAGTCCTGTCTCTTTCTCTGTAGGCATTGTCTCTTCAGGTCTTCTTTTTTTTTCTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCACTCAGGCTAGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTTCTGTCTCAGCCTCTCAAGTAGCTGGGACTACAGGCGCCTGCCACCATGTCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGCTTTGCCATATTGGTCAGACTAGTCTTGAACTCCTGACCTCAGGTGATCCACCAACCTTGG... |
Task1_train_43381 | Chromosome 14 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GTAATTTTCTAAAGGCAACGTAGTAAAAGATTGGAGCTCCGCGGGGCTGAGGCTGTTTGTGAAACCCACTTGCTGTATCTCAGGGGGTGGTTTTGGGGAACTGGTGGGCTCTGCAATTGGATTTTCTGGGATGTCTGTGGAGGGAGTTGCCAGGCTGAGAGGTGAAGAGATTGGGCTTCTGCCAGCACGAGAGGAGGTGGGCCAGCTGTCGGCTATCCTCAGTGGGGAAGGGGGCTTTGGGACTCCTGGGCAGCGGACATAACAGACAGAGTGGCCACTGTCTTCACTTGGACCTCCCTGAACAATGCTTCCCAGCAGCT... | GTAATTTTCTAAAGGCAACGTAGTAAAAGATTGGAGCTCCGCGGGGCTGAGGCTGTTTGTGAAACCCACTTGCTGTATCTCAGGGGGTGGTTTTGGGGAACTGGTGGGCTCTGCAATTGGATTTTCTGGGATGTCTGTGGAGGGAGTTGCCAGGCTGAGAGGTGAAGAGATTGGGCTTCTGCCAGCACGAGAGGAGGTGGGCCAGCTGTCGGCTATCCTCAGTGGGGAAGGGGGCTTTGGGACTCCTGGGCAGCGGACATAACAGACAGAGTGGCCACTGTCTTCACTTGGACCTCCCTGAACAATGCTTCCCAGCAGCT... |
Task1_train_43382 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GGTTGGGGGATGGGGGTTGGGGGGCGGGGGCGGGAGCTCAGGGGAGCAGGAGCACCGGCAGTGGAGGTAGAAGAAGTCAGTGGAGCACCCGAGGTCAGTGTCCCAGGGTGGCCATCACCAGGCCGGGTGGGGGGCCCCGTCACCTGCTTGCTTGGCTGCGCCTGCTGTGCCTGCTTCTTCATCTGGCCACGCGTCATGGGGTCACTTCCTGCTCACCACTGCTTTCTCCCTCATGGATGTCACTCCCGGGCATGGGCTTGGGACCTGGAGAACGGAGAACTCGTAGCCCAGGGCTGGCGCTGGGTCTCTGAGGACTGGGT... | GGTTGGGGGATGGGGGTTGGGGGGCGGGGGCGGGAGCTCAGGGGAGCAGGAGCACCGGCAGTGGAGGTAGAAGAAGTCAGTGGAGCACCCGAGGTCAGTGTCCCAGGGTGGCCATCACCAGGCCGGGTGGGGGGCCCCGTCACCTGCTTGCTTGGCTGCGCCTGCTGTGCCTGCTTCTTCATCTGGCCACGCGTCATGGGGTCACTTCCTGCTCACCACTGCTTTCTCCCTCATGGATGTCACTCCCGGGCATGGGCTTGGGACCTGGAGAACGGAGAACTCGTAGCCCAGGGCTGGCGCTGGGTCTCTGAGGACTGGGT... |
Task1_train_43383 | Chromosome 14 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CATCAGGACCACATTACCTTTGCCATGCTGCTGGCAAGAATCAAACTGAAGGGCACCGTGGGGTAAGAGCACTCACGCCCACAGGAGGATGCCATATTGCTGGTGGCCCCCAAGGGTTTCATGATCAGATACATGCTTTTATTATTTCTTTTATTTTCTCTTTTATTTTCTTTATTTTATTTTTTGAGACGGAGTCTCCCTTTGTTGCCTAGGCTGGAGTGCCGTGGTGTAATCTCACCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTCCTGCTTCAGTCTCCGAAGTAGCTAGGACTATAGGCGCAGGCCA... | CATCAGGACCACATTACCTTTGCCATGCTGCTGGCAAGAATCAAACTGAAGGGCACCGTGGGGTAAGAGCACTCACGCCCACAGGAGGATGCCATATTGCTGGTGGCCCCCAAGGGTTTCATGATCAGATACATGCTTTTATTATTTCTTTTATTTTCTCTTTTATTTTCTTTATTTTATTTTTTGAGACGGAGTCTCCCTTTGTTGCCTAGGCTGGAGTGCCGTGGTGTAATCTCACCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTCCTGCTTCAGTCTCCGAAGTAGCTAGGACTATAGGCGCAGGCCA... |
Task1_train_43384 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | CCTCGTGATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCGGCCTTACCTGAGATTTTTCTTACTTGGTTGAAACCAGCTCGTGAGCATCTGAGTTTAGGGCATCCCACACCTGCTCAGCGAGTTACTGGAATCCCAACAGAATGTGCAGCTACCAAGCAGAAGAATGTTTATTTATTTTTTTAAAAAATCATATACAACTGGATCCTTCGAAAGCTTTATTTTGTGAGACTTTAAACCATGAAGTGTCTGAAACCTATTTCTCTAATTCATCACATTAAATTGGGGGCATGTCTT... | CCTCGTGATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCGGCCTTACCTGAGATTTTTCTTACTTGGTTGAAACCAGCTCGTGAGCATCTGAGTTTAGGGCATCCCACACCTGCTCAGCGAGTTACTGGAATCCCAACAGAATGTGCAGCTACCAAGCAGAAGAATGTTTATTTATTTTTTTAAAAAATCATATACAACTGGATCCTTCGAAAGCTTTATTTTGTGAGACTTTAAACCATGAAGTGTCTGAAACCTATTTCTCTAATTCATCACATTAAATTGGGGGCATGTCTT... |
Task1_train_43385 | This variant is present on Chromosome 14. Is the change likely to result in a pathogenic outcome? | Benign | CTCTCTTGTGACCTGCGCGCCGCCCCCCCTACAGCCATCTCCCCAGCCTTCTGTCCCCCAGCCCTCCCTGCTGCTGGGCTCTGCCCACGGCCTTGACGTCCGACTCCCCTGGGACTCCCAGGCCCTCTGTAGAGGCAGAACGGCACCACCCCCCTGCTCAGACACCTCCCCTACAGCAAGGGCAGCCCTCAAGGCTGCACCAGGGTCTCAAATGGGTTTAAAAGGAGCCCGGGGAAAGGCCTGCACTGCACCCTGCTCTGGAACATTATGGCAAGCCTCCCTTCCGGTCTGAAAATTACGGCAAGCCTCACTTCCGGTCT... | CTCTCTTGTGACCTGCGCGCCGCCCCCCCTACAGCCATCTCCCCAGCCTTCTGTCCCCCAGCCCTCCCTGCTGCTGGGCTCTGCCCACGGCCTTGACGTCCGACTCCCCTGGGACTCCCAGGCCCTCTGTAGAGGCAGAACGGCACCACCCCCCTGCTCAGACACCTCCCCTACAGCAAGGGCAGCCCTCAAGGCTGCACCAGGGTCTCAAATGGGTTTAAAAGGAGCCCGGGGAAAGGCCTGCACTGCACCCTGCTCTGGAACATTATGGCAAGCCTCCCTTCCGGTCTGAAAATTACGGCAAGCCTCACTTCCGGTCT... |
Task1_train_43386 | A genomic change on Chromosome 14 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GAACTGAACTATATATTTTTAGAAATATCTGCATATGCCACATAAATTTTTAAAATCATAAGAATGCTAAACAGCACATTCAGGACAGGGTGAAGAAACAGGCATGCAGGTTGTGCAGTAGGAAGCTGGGTAACATTGTTCCTTATGGCTTTGTTGTCGCTTCCAGAATTTCATTAAAAACTTTTTAAAAAACATGGGCCCACATTATGAATTACGTCTGCTTTTAGAGTACTAAAAACTCCAAGCAAAAACACATGGGTAACGCCGGGCACGGTGGTTCATGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGCGGACA... | GAACTGAACTATATATTTTTAGAAATATCTGCATATGCCACATAAATTTTTAAAATCATAAGAATGCTAAACAGCACATTCAGGACAGGGTGAAGAAACAGGCATGCAGGTTGTGCAGTAGGAAGCTGGGTAACATTGTTCCTTATGGCTTTGTTGTCGCTTCCAGAATTTCATTAAAAACTTTTTAAAAAACATGGGCCCACATTATGAATTACGTCTGCTTTTAGAGTACTAAAAACTCCAAGCAAAAACACATGGGTAACGCCGGGCACGGTGGTTCATGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGCGGACA... |
Task1_train_43387 | Given this context: Chromosome 14 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CAAAAACACATGGGTAACGCCGGGCACGGTGGTTCATGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGCGGACAGATCATGAGGTCAGGAGTTTGAGACCACCCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCAAGCGCCTGTAATCAGGGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGAGAGGCAGAGGTTGCACTGAGCTGAGATAGCGCCACTGCATTCCAGCCTGGACCACAGAGCGAGACTTCATCTTAAAAAAAAATTAGCTGGTCATGG... | CAAAAACACATGGGTAACGCCGGGCACGGTGGTTCATGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGCGGACAGATCATGAGGTCAGGAGTTTGAGACCACCCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCAAGCGCCTGTAATCAGGGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGAGAGGCAGAGGTTGCACTGAGCTGAGATAGCGCCACTGCATTCCAGCCTGGACCACAGAGCGAGACTTCATCTTAAAAAAAAATTAGCTGGTCATGG... |
Task1_train_43388 | A variant was discovered on Chromosome 14. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CCAAGCCCAGCTTATATCACTGTGGTCTCTGGTCAGAAAGGTCTGGAAAATACCACCTTAGTACAAACACATTACATCAACTTTTATATGTAAGATGTAATTTAGAAAAAATGTCAATAATGGTTTTATGACGAGACTGAAATTGCAGACATGTTCATAAGCACAATGCTTCTTTTCTCTTTCTTGTCTTTCTGTACGTAAGCAACTAGAAGCCATTTGTGTCAAGGTAACGTCTGGAGAAACAAAAGGTCAGGAAAGGCCAATGCTCCTACCGACCACAATCCAGCCCCAAACTGCAAGAAAGAGCCAGCTGCCCCGGG... | CCAAGCCCAGCTTATATCACTGTGGTCTCTGGTCAGAAAGGTCTGGAAAATACCACCTTAGTACAAACACATTACATCAACTTTTATATGTAAGATGTAATTTAGAAAAAATGTCAATAATGGTTTTATGACGAGACTGAAATTGCAGACATGTTCATAAGCACAATGCTTCTTTTCTCTTTCTTGTCTTTCTGTACGTAAGCAACTAGAAGCCATTTGTGTCAAGGTAACGTCTGGAGAAACAAAAGGTCAGGAAAGGCCAATGCTCCTACCGACCACAATCCAGCCCCAAACTGCAAGAAAGAGCCAGCTGCCCCGGG... |
Task1_train_43389 | Here is a variant on Chromosome 14. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CCACTGCACCTTGCCTCATTTATTAATTCTAATATTTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTAATCTTTAGGCATTTCTACATATAAGATCATATCTGCAAATAGAGATAACCTTTTTTTTTTTTTTTTTTTTTTGAGACGAAGTTTTGCTCTGTCACCCAGGCTGGAGTGTAATGGCGTAATATCAGCTCACTGCAACCTCCATCTCCTGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCGAGTAGGTGGGATTACAGGTGCCCACCATCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTT... | CCACTGCACCTTGCCTCATTTATTAATTCTAATATTTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTAATCTTTAGGCATTTCTACATATAAGATCATATCTGCAAATAGAGATAACCTTTTTTTTTTTTTTTTTTTTTTGAGACGAAGTTTTGCTCTGTCACCCAGGCTGGAGTGTAATGGCGTAATATCAGCTCACTGCAACCTCCATCTCCTGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCGAGTAGGTGGGATTACAGGTGCCCACCATCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTT... |
Task1_train_43390 | A genetic alteration is present on Chromosome 14. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ATTTAACATTTGAAAACAAGACAGGTCCTGGCTTTTATTCTGGCTCTAGCCAGAACCTATCAACTAGGCACTTAAAAAATTATATATATAAATTTTTTTTTTGAGACGGGAGTCGCACTTTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTACTGACTCAGCCTCCCCAGTAGCTGGGATTACAGGCACCCGCCATCATGCCCGGCTAATTTTTTTTTGTATTTTTGTAGAGATGGGGTTTTACCATTTTGGTCAGGCTGGTCTGAAACTCCTGACT... | ATTTAACATTTGAAAACAAGACAGGTCCTGGCTTTTATTCTGGCTCTAGCCAGAACCTATCAACTAGGCACTTAAAAAATTATATATATAAATTTTTTTTTTGAGACGGGAGTCGCACTTTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTACTGACTCAGCCTCCCCAGTAGCTGGGATTACAGGCACCCGCCATCATGCCCGGCTAATTTTTTTTTGTATTTTTGTAGAGATGGGGTTTTACCATTTTGGTCAGGCTGGTCTGAAACTCCTGACT... |
Task1_train_43391 | With a mutation on Chromosome 14, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AACTTAGATAAATAGTATTTATAGTTAAATACTAAAATGACACAATTAAAAACTATACTTGGCCAGGTGCAGTGGCTCGCACCTATAATCCCAGCACTTTGGGAAGCCGAGGCAGGAGGATCACTTGAGGCCAGGAGTTCAAGGCAAGCCAGGGCAACATAGTAAGACCCCCATCTCTAAAAAGTAAAAATAAAAAAATTAGCCGGACGTGGTTATGCACACCTACAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGGATCACCTGAGCACAGGAGTTTGAGGTTGAGATTACAGTGAGCTACAATCATGCCACTGCAT... | AACTTAGATAAATAGTATTTATAGTTAAATACTAAAATGACACAATTAAAAACTATACTTGGCCAGGTGCAGTGGCTCGCACCTATAATCCCAGCACTTTGGGAAGCCGAGGCAGGAGGATCACTTGAGGCCAGGAGTTCAAGGCAAGCCAGGGCAACATAGTAAGACCCCCATCTCTAAAAAGTAAAAATAAAAAAATTAGCCGGACGTGGTTATGCACACCTACAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGGATCACCTGAGCACAGGAGTTTGAGGTTGAGATTACAGTGAGCTACAATCATGCCACTGCAT... |
Task1_train_43392 | This alteration occurs on Chromosome 14. Is it associated with a disease or is it a benign variant? | Benign | CAACATGGTGAAACCCCGTCTCTACTAAAAACACATAAATTAGCTGGGCTTGGTGGCATGTGCCTGTAATCTCAGTCACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGATGCAGTGAGCCGAGGTCACGCCACTGCACTCCAGCCTCGCAACAGAGCAAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAGTGTTGGTTTATCCATGTATACCATTGATTAAATCAGAGATTCTGTGAGCCTGGGTGGAAAGTTGTGGAAACCAGAAGATCTATGCTGGTAAATACTTGGGACATTTTATGTTT... | CAACATGGTGAAACCCCGTCTCTACTAAAAACACATAAATTAGCTGGGCTTGGTGGCATGTGCCTGTAATCTCAGTCACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGATGCAGTGAGCCGAGGTCACGCCACTGCACTCCAGCCTCGCAACAGAGCAAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAGTGTTGGTTTATCCATGTATACCATTGATTAAATCAGAGATTCTGTGAGCCTGGGTGGAAAGTTGTGGAAACCAGAAGATCTATGCTGGTAAATACTTGGGACATTTTATGTTT... |
Task1_train_43393 | Given a variant located on Chromosome 14, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CTGGTCTTCATCTGTAAACAGAGACATTTTGAGTAAATAGTCTCAGATCCTTTCCATTCCAAAGTTCTGTTGACTTTAGTATCTCAAGTCATGACCTTCTTTTTTTTTTAGTCATGTTTATGAAAGATAAGCTTTGGCTCCAAATTAGTTTATTTTTAACTCTTAACAGCTGTTGATTTTATTTCTCTCAGCAGTCCAAAAAGGCACATTAAGCTCCTGTTATTCCACTTTCATAGAGCAACAGGCAGGAGTTTCTTAGAAATAACCTTTGGACTAAGATGTTGTAGATCGTGTTGTTAGAAAGAGTGAGAGGGAGCTGG... | CTGGTCTTCATCTGTAAACAGAGACATTTTGAGTAAATAGTCTCAGATCCTTTCCATTCCAAAGTTCTGTTGACTTTAGTATCTCAAGTCATGACCTTCTTTTTTTTTTAGTCATGTTTATGAAAGATAAGCTTTGGCTCCAAATTAGTTTATTTTTAACTCTTAACAGCTGTTGATTTTATTTCTCTCAGCAGTCCAAAAAGGCACATTAAGCTCCTGTTATTCCACTTTCATAGAGCAACAGGCAGGAGTTTCTTAGAAATAACCTTTGGACTAAGATGTTGTAGATCGTGTTGTTAGAAAGAGTGAGAGGGAGCTGG... |
Task1_train_43394 | This sequence change occurs on Chromosome 14. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ACCATCCACCATCCATCCATCCACCCATCTATATGTCCATTCACCCATTCGCCATCCACTCATCCACCACCCACCATTCATCTATCATCCCTCATCCACTGTCTACCATCCACCATTCATCCATCCACCCATTCACCCATCCACCATCCATCCATCCACCATCCACTTATCCACAATCTGCCATCCACCATTCGCCATTCATCCATCCATTCATCCACCACCCATCACCATTCACATCCACCATCGGCCATTCACCATCCACCATCCACCATCCACCTATTCACCATCCACCATTCACTCATTCACCACCCATCCTTCCA... | ACCATCCACCATCCATCCATCCACCCATCTATATGTCCATTCACCCATTCGCCATCCACTCATCCACCACCCACCATTCATCTATCATCCCTCATCCACTGTCTACCATCCACCATTCATCCATCCACCCATTCACCCATCCACCATCCATCCATCCACCATCCACTTATCCACAATCTGCCATCCACCATTCGCCATTCATCCATCCATTCATCCACCACCCATCACCATTCACATCCACCATCGGCCATTCACCATCCACCATCCACCATCCACCTATTCACCATCCACCATTCACTCATTCACCACCCATCCTTCCA... |
Task1_train_43395 | Here is a mutation located on Chromosome 14. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GGCTCAGTCTCAAGTGGCCAGGGGCAGGCCCTGGGGGAGGGGTCGGCTCAAGGGAAGATGAGGCCGGGCCCTTGCTGGGGGCTGGAGCTGGGAGGGCGCGGGCGCTGAGGACCGGCGGCCAGCCCCGCGGTGGGCGTGAGTGCGAGGGAGGCCGGGAGAGCGCGTGTGGGCGGGGAGCGCGAGAAGGAGAGCGAGCCGGGAGAGCGCGGAGCCAGCGGAGCGCGGAGGCCCCAGCGCCAGCACCCGCGCGGGCGGTGAGCGTGAGTGTGGCGCAGGGTCGCCCCTCCCCAGCCTGGCCCCGGCAGTGCGGGCCCCGGGAG... | GGCTCAGTCTCAAGTGGCCAGGGGCAGGCCCTGGGGGAGGGGTCGGCTCAAGGGAAGATGAGGCCGGGCCCTTGCTGGGGGCTGGAGCTGGGAGGGCGCGGGCGCTGAGGACCGGCGGCCAGCCCCGCGGTGGGCGTGAGTGCGAGGGAGGCCGGGAGAGCGCGTGTGGGCGGGGAGCGCGAGAAGGAGAGCGAGCCGGGAGAGCGCGGAGCCAGCGGAGCGCGGAGGCCCCAGCGCCAGCACCCGCGCGGGCGGTGAGCGTGAGTGTGGCGCAGGGTCGCCCCTCCCCAGCCTGGCCCCGGCAGTGCGGGCCCCGGGAG... |
Task1_train_43396 | Consider this mutation on Chromosome 14. Is this a benign change or a disease-causing variant? | Benign | GCGCGGCCAGGGGCAGACTCTGTCCCTCTGTGAGCCTCAGGTTCCTCATCTGTGAAATGGGCAAATGACAACCCCTAACTTTGATGTCACAGTAGCTGATCTGTGTCAGGCATCGAGCTGGGCACACAGTAGGTGCTTACTAAGTGTGAGTTCTCCCAAACAAGAAGGCGGGGCCTGGCTTGTCCTTCCCCACATCCCCGCCTCCGTCCTCTTGACAGCGGTGGATGCAGCATGTGCTGAACCGTTCTCTTCACAACACCCCTGCCCTGCTGGGCGCCGGCCCCCATGCCAAGCATGAAGGGGCACCGGGGAGAGAGAAG... | GCGCGGCCAGGGGCAGACTCTGTCCCTCTGTGAGCCTCAGGTTCCTCATCTGTGAAATGGGCAAATGACAACCCCTAACTTTGATGTCACAGTAGCTGATCTGTGTCAGGCATCGAGCTGGGCACACAGTAGGTGCTTACTAAGTGTGAGTTCTCCCAAACAAGAAGGCGGGGCCTGGCTTGTCCTTCCCCACATCCCCGCCTCCGTCCTCTTGACAGCGGTGGATGCAGCATGTGCTGAACCGTTCTCTTCACAACACCCCTGCCCTGCTGGGCGCCGGCCCCCATGCCAAGCATGAAGGGGCACCGGGGAGAGAGAAG... |
Task1_train_43397 | Chromosome 14 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CCACAGACAGACACTCCTGGGCCGGAGCTGCAGAGTCCCAAGGAGGCTGAGGAGCCACAGACTCCAGCTCAGGGCTCCCGGCGAACAAGCAGCAGGAAAGAGCCCAATGCCCACCGCAAGGATGGCACAAGGCTGGGCCTGGGCTCCCTGAGGCAGGCCTTCTCCCGGGCCAGCCAGCGGGCTTTGACCCAGGTCTCCAAGGAAGATACGGGCCTGTTCCGGCGAAGCTCCTGCTCCCTGTTCCGGTCCTTCCGGCAAGCCCTGAATGACGGCCCAGCTACCGGCCATTCCCAGGCCACTCCTGAGGTGCCCTCGGGGGT... | CCACAGACAGACACTCCTGGGCCGGAGCTGCAGAGTCCCAAGGAGGCTGAGGAGCCACAGACTCCAGCTCAGGGCTCCCGGCGAACAAGCAGCAGGAAAGAGCCCAATGCCCACCGCAAGGATGGCACAAGGCTGGGCCTGGGCTCCCTGAGGCAGGCCTTCTCCCGGGCCAGCCAGCGGGCTTTGACCCAGGTCTCCAAGGAAGATACGGGCCTGTTCCGGCGAAGCTCCTGCTCCCTGTTCCGGTCCTTCCGGCAAGCCCTGAATGACGGCCCAGCTACCGGCCATTCCCAGGCCACTCCTGAGGTGCCCTCGGGGGT... |
Task1_train_43398 | A mutation located on Chromosome 14 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TCGCAGGGTTCCGAGGCCACATGGTTGGACCAAGCCATCCAGTGCGTGGCTGAGATCCTGGGCGAGACCTACAAAGATGACATCCAGCGGCACCTGGAGACTCTTATCCGGAGCTACCCCGACATCAGGTGTGTACCCCACCTGCTTCCACTAGCTTCCTACCAGAGCTTCAGGGCCAAGGGGGCTGGTATTGGAGCAACCCCAGCCCAGACCTGACTGCCCAGGGGCCTGAAGACCAGAGGCAGGAGGTAGGCCTTGGACCCTCAGACCCTCAAGGCTGGAGGGGGAATGGAGAGAGCCCCTTCTCCTAATCTGCTCTT... | TCGCAGGGTTCCGAGGCCACATGGTTGGACCAAGCCATCCAGTGCGTGGCTGAGATCCTGGGCGAGACCTACAAAGATGACATCCAGCGGCACCTGGAGACTCTTATCCGGAGCTACCCCGACATCAGGTGTGTACCCCACCTGCTTCCACTAGCTTCCTACCAGAGCTTCAGGGCCAAGGGGGCTGGTATTGGAGCAACCCCAGCCCAGACCTGACTGCCCAGGGGCCTGAAGACCAGAGGCAGGAGGTAGGCCTTGGACCCTCAGACCCTCAAGGCTGGAGGGGGAATGGAGAGAGCCCCTTCTCCTAATCTGCTCTT... |
Task1_train_43399 | A variant was discovered on Chromosome 14. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GCCTGGCCTCTTGGGAACTGCTTTCTGCATCTGCGAGAAGAGGGTAAGGACTGCTCCTGCCCTATGGGCCCCATTGGCTGTCATCCCTTGGGCCTCCATGCTGCCCCATTTTCAGAAGACTTTCCTTGTCTTGAGGACTTCACGTATGTTACCATTGACCCTCATGCCTGAGCTTAGAGAGGGGAAGTGACTGGTGCAGACACAAGTCCAAGGCAGCAGCCTCGTTTCCCAATCCCCAGCCGGTGCTCTGGGCGGGCCACTGCCGTCAGTGGGGGACAAGGGTGGCAGCCCCGCCTCAGCCCTGCAAAGCCCGTGGAGAC... | GCCTGGCCTCTTGGGAACTGCTTTCTGCATCTGCGAGAAGAGGGTAAGGACTGCTCCTGCCCTATGGGCCCCATTGGCTGTCATCCCTTGGGCCTCCATGCTGCCCCATTTTCAGAAGACTTTCCTTGTCTTGAGGACTTCACGTATGTTACCATTGACCCTCATGCCTGAGCTTAGAGAGGGGAAGTGACTGGTGCAGACACAAGTCCAAGGCAGCAGCCTCGTTTCCCAATCCCCAGCCGGTGCTCTGGGCGGGCCACTGCCGTCAGTGGGGGACAAGGGTGGCAGCCCCGCCTCAGCCCTGCAAAGCCCGTGGAGAC... |
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