ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-E00918 DGAT2 SNP Missense_Mutation 11 75509364 A T 3 68 MEL ME029 DGAT2 SNP Nonsense_Mutation 11 75501756 C T 31 64 MEL ME030 DGAT2 SNP Missense_Mutation 11 75495752 A T 8 73 MEL MEL-Ma-Mel-48 DGAT2 SNP Silent 11 75511547 G A 45 60 MEL MEL-Ma-Mel-86 DGAT2 SNP Silent 11 75509389 C T 31 31 PRAD P05-2212 DGAT2 SNP Silent 11 75511517 C T 31 43 LUSC TCGA-18-3409 DGAT2 SNP Missense_Mutation 11 75501768 C T 30 94 LUSC TCGA-43-2578 DGAT2 SNP Missense_Mutation 11 75508290 C T 27 97 LUSC TCGA-56-1622 DGAT2 SNP Missense_Mutation 11 75509352 G T 37 74 CRC TCGA-AA-3525 DGAT2 SNP Missense_Mutation 11 75507491 A C 3 88 CRC TCGA-AA-3555 DGAT2 SNP Missense_Mutation 11 75511497 G A 37 73 CRC TCGA-AA-3977 DGAT2 SNP Missense_Mutation 11 75507381 G T 33 64 CRC TCGA-AA-3984 DGAT2 SNP Silent 11 75511496 C T 31 49 CRC TCGA-AG-A002 DGAT2 SNP Missense_Mutation 11 75511508 G T 33 66 UCEC TCGA-AP-A059 DGAT2 SNP Missense_Mutation 11 75508212 C A 24 96 UCEC TCGA-AP-A0LM DGAT2 SNP Missense_Mutation 11 75507431 A G 8 88 UCEC TCGA-AX-A05Z DGAT2 SNP Missense_Mutation 11 75507472 G A 33 96 UCEC TCGA-B5-A0JY DGAT2 SNP Missense_Mutation 11 75508249 G T 33 58 UCEC TCGA-B5-A11H DGAT2 SNP Silent 11 75509344 C A 24 58 UCEC TCGA-B5-A11N DGAT2 SNP Missense_Mutation 11 75495695 G A 41 79 BRCA TCGA-B6-A0IK DGAT2 SNP Missense_Mutation 11 75509333 G A 37 68 UCEC TCGA-BG-A18B DGAT2 SNP Missense_Mutation 11 75509447 C T 26 82 HNSC TCGA-CQ-5327 DGAT2 SNP Missense_Mutation 11 75508295 G C 45 97 BRCA TCGA-E2-A1LK DGAT2 SNP Missense_Mutation 11 75501262 A G 8 85