ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-1608 RSPH4A SNP Silent 6 116937807 G T 37 47 ESO ESO-539 RSPH4A SNP Missense_Mutation 6 116950858 A T 3 62 LUAD LUAD-RT-S01301 RSPH4A DNP Missense_Mutation 6 116949395 GA AC 41 95 MEL ME011 RSPH4A SNP Missense_Mutation 6 116949423 G A 44 62 MEL MEL-JWCI-27 RSPH4A SNP Missense_Mutation 6 116938229 A T 2 49 GBM TCGA-27-1835 RSPH4A SNP Nonsense_Mutation 6 116938051 G T 41 50 LUSC TCGA-37-5819 RSPH4A SNP Silent 6 116938131 T C 59 49 LUAD TCGA-44-2659 RSPH4A SNP Missense_Mutation 6 116938031 C A 24 52 LUAD TCGA-44-2659 RSPH4A SNP Missense_Mutation 6 116938033 G T 46 38 LUSC TCGA-46-3769 RSPH4A SNP Missense_Mutation 6 116948888 G A 46 96 LUAD TCGA-67-3771 RSPH4A SNP Silent 6 116949479 C T 32 63 BRCA TCGA-A2-A0EQ RSPH4A SNP Missense_Mutation 6 116949275 C G 30 75 CRC TCGA-AA-3710 RSPH4A SNP Nonsense_Mutation 6 116951637 C T 29 81 CRC TCGA-AA-3814 RSPH4A SNP Missense_Mutation 6 116948892 T A 54 88 CRC TCGA-AA-3949 RSPH4A SNP Silent 6 116949178 A G 2 67 CRC TCGA-AA-3977 RSPH4A SNP Silent 6 116953394 C A 28 49 CRC TCGA-AA-3984 RSPH4A SNP Missense_Mutation 6 116948877 G A 38 96 CRC TCGA-AA-3984 RSPH4A SNP Missense_Mutation 6 116951693 G A 34 81 CRC TCGA-AA-A00E RSPH4A SNP Missense_Mutation 6 116953382 T A 52 53 CRC TCGA-AA-A010 RSPH4A SNP Missense_Mutation 6 116949247 G T 33 55 CRC TCGA-AA-A01Q RSPH4A SNP Missense_Mutation 6 116937985 G A 34 54 CRC TCGA-AG-A002 RSPH4A SNP Missense_Mutation 6 116938122 G T 41 55 CRC TCGA-AG-A002 RSPH4A SNP Nonsense_Mutation 6 116949371 G T 35 95 UCEC TCGA-AP-A051 RSPH4A SNP Missense_Mutation 6 116938400 G A 34 54 UCEC TCGA-AP-A051 RSPH4A SNP Missense_Mutation 6 116950802 G A 37 93 UCEC TCGA-AP-A056 RSPH4A SNP Missense_Mutation 6 116938316 G T 33 52 UCEC TCGA-AX-A0J0 RSPH4A SNP Missense_Mutation 6 116938279 G A 41 54 UCEC TCGA-AX-A0J0 RSPH4A SNP Missense_Mutation 6 116938339 G T 33 59 UCEC TCGA-B5-A0JY RSPH4A SNP Nonsense_Mutation 6 116949323 C T 19 60 UCEC TCGA-B5-A0K9 RSPH4A SNP Missense_Mutation 6 116948817 T C 51 61 UCEC TCGA-B5-A11E RSPH4A SNP Missense_Mutation 6 116948838 A G 9 88 UCEC TCGA-B5-A11E RSPH4A SNP Missense_Mutation 6 116948931 G A 38 74 HNSC TCGA-BA-6868 RSPH4A SNP Missense_Mutation 6 116953560 G A 45 81 BRCA TCGA-BH-A18P RSPH4A SNP Nonsense_Mutation 6 116938343 C G 29 58 UCEC TCGA-BS-A0UF RSPH4A SNP Splice_Site 6 116943930 G T 33 85 HNSC TCGA-CN-4728 RSPH4A SNP Missense_Mutation 6 116949382 G C 36 57 HNSC TCGA-CN-6011 RSPH4A SNP Silent 6 116938128 G C 37 44 HNSC TCGA-CN-6013 RSPH4A SNP Missense_Mutation 6 116937941 G A 41 49 HNSC TCGA-CV-6961 RSPH4A SNP Missense_Mutation 6 116938309 G A 33 65 HNSC TCGA-CV-7252 RSPH4A SNP Missense_Mutation 6 116938138 C T 30 43 HNSC TCGA-CV-7422 RSPH4A SNP Silent 6 116938023 A G 8 52 HNSC TCGA-CV-7433 RSPH4A SNP Nonsense_Mutation 6 116938343 C G 29 58 UCEC TCGA-D1-A16Y RSPH4A SNP Silent 6 116938194 A G 4 60 UCEC TCGA-D1-A17U RSPH4A SNP Missense_Mutation 6 116938331 A G 7 52 BLCA TCGA-G2-A2EO RSPH4A SNP Missense_Mutation 6 116938321 G A 45 50 BLCA TCGA-G2-A3IE RSPH4A SNP Missense_Mutation 6 116949506 C T 29 95 HNSC TCGA-HD-7229 RSPH4A SNP Missense_Mutation 6 116949485 G C 33 80