ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62506 KLRC3 SNP Splice_site 12 10572963 C A 24 49 MEL ME018 KLRC3 SNP Splice_Site 12 10569367 C T 32 67 MEL MEL-13575 KLRC3 SNP Missense_Mutation 12 10570954 C T 29 64 MEL MEL-JWCI-WGS-22 KLRC3 SNP Missense_Mutation 12 10568386 C T 32 55 MEL MEL-JWCI-WGS-7 KLRC3 SNP Missense_Mutation 12 10569321 G A 37 53 MM MM-0191 KLRC3 SNP Synonymous 12 10587978 G A 39 49 MM MM-0191 KLRC3 SNP Missense 12 10588531 G A 38 38 LUAD TCGA-05-4403 KLRC3 SNP Nonsense_Mutation 12 10573032 G A 47 50 LUAD TCGA-05-4403 KLRC3 SNP Silent 12 10573045 T C 60 41 GBM TCGA-06-0124 KLRC3 SNP Missense_Mutation 12 10573119 C A 20 46 GBM TCGA-06-0124 KLRC3 SNP Missense_Mutation 12 10588555 C A 20 48 GBM TCGA-06-0141 KLRC3 SNP Missense_Mutation 12 10573038 T C 52 62 OV TCGA-13-0804 KLRC3 SNP Missense_Mutation 12 10572978 T C 52 47 OV TCGA-13-1488 KLRC3 SNP Silent 12 10570982 G A 36 50 LUSC TCGA-22-5477 KLRC3 SNP Silent 12 10569292 T A 63 45 LUSC TCGA-39-5035 KLRC3 SNP Missense_Mutation 12 10588420 C G 29 52 LUAD TCGA-44-6145 KLRC3 SNP Missense_Mutation 12 10568380 C A 32 44 LUSC TCGA-70-6722 KLRC3 SNP Missense_Mutation 12 10568344 G T 40 0 UCEC TCGA-A5-A0GP KLRC3 SNP Missense_Mutation 12 10568248 A C 4 52 CRC TCGA-AA-3845 KLRC3 SNP Missense_Mutation 12 10568344 G A 40 0 CRC TCGA-AG-A002 KLRC3 SNP Missense_Mutation 12 10570992 G A 34 51 KIRC TCGA-B0-5092 KLRC3 SNP Missense_Mutation 12 10588502 T A 64 48 UCEC TCGA-B5-A0JY KLRC3 SNP Missense_Mutation 12 10588453 G T 33 51 UCEC TCGA-B5-A11E KLRC3 SNP Missense_Mutation 12 10588443 G T 35 50 BRCA TCGA-BH-A0AW KLRC3 SNP Missense_Mutation 12 10570980 G C 33 54 HNSC TCGA-CN-6988 KLRC3 SNP Missense_Mutation 12 10569330 C A 21 52 HNSC TCGA-CV-5441 KLRC3 SNP Nonsense_Mutation 12 10569334 C T 30 66 HNSC TCGA-CV-6961 KLRC3 SNP Missense_Mutation 12 10570960 C G 32 64 BLCA TCGA-DK-A1A6 KLRC3 SNP Missense_Mutation 12 10572972 C G 29 43