ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62415 GGTLC2 SNP Synonymous 22 22989556 C T 21 44 MEL ME016 GGTLC2 SNP Splice_site 22 22989453 G A 43 76 MEL ME018 GGTLC2 SNP Silent 22 22989341 C T 29 63 MEL MEL-Ma-Mel-67 GGTLC2 SNP Silent 22 22989484 G A 37 48 GBM TCGA-19-1790 GGTLC2 SNP Missense_Mutation 22 22989259 T A 50 71 OV TCGA-24-2290 GGTLC2 SNP Silent 22 22989329 A T 6 54 LUSC TCGA-63-5128 GGTLC2 SNP Nonsense_Mutation 22 22989255 G T 37 76 BRCA TCGA-A2-A0CX GGTLC2 SNP Silent 22 22989670 C T 31 51 UCEC TCGA-A5-A0G5 GGTLC2 SNP Missense_Mutation 22 22989735 C T 19 64 CRC TCGA-AG-4008 GGTLC2 SNP Silent 22 22989502 C T 19 51 UCEC TCGA-AP-A059 GGTLC2 SNP Silent 22 22988905 C T 17 50 KIRC TCGA-B0-4707 GGTLC2 SNP Silent 22 22989281 T C 51 55 UCEC TCGA-B5-A0JY GGTLC2 SNP Missense_Mutation 22 22990110 G A 38 48 UCEC TCGA-B5-A11E GGTLC2 SNP Silent 22 22988953 C T 19 52 BLCA TCGA-BT-A2LB GGTLC2 SNP Missense_Mutation 22 22989480 C T 23 76 HNSC TCGA-CV-5432 GGTLC2 SNP Silent 22 22989484 G C 37 48 HNSC TCGA-CV-7407 GGTLC2 SNP Silent 22 22988944 C G 31 44 HNSC TCGA-CV-7432 GGTLC2 SNP Missense_Mutation 22 22988902 C G 32 56