ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-041 SCRN1 SNP Silent 7 29976189 T C 62 63 LUAD LUAD-5V8LT SCRN1 SNP Missense_Mutation 7 29966154 C G 30 65 LUAD LUAD-F00257 SCRN1 SNP Missense_Mutation 7 29980462 G A 37 95 MEL ME001 SCRN1 SNP Missense_Mutation 7 29963586 T C 56 85 MEL MEL-JWCI-WGS-1 SCRN1 SNP Silent 7 29983621 C T 30 51 MEL MEL-Ma-Mel-86 SCRN1 SNP Silent 7 30008609 C T 30 57 PRAD PR-04-3113 SCRN1 SNP Splice_site 7 29980490 C T 22 92 OV TCGA-04-1367 SCRN1 SNP Missense_Mutation 7 29980316 T A 55 86 LUAD TCGA-05-4396 SCRN1 SNP Silent 7 29963594 C A 23 45 LUAD TCGA-05-4396 SCRN1 SNP Missense_Mutation 7 29976211 G T 39 85 LUAD TCGA-05-4396 SCRN1 SNP Missense_Mutation 7 29976301 C A 23 98 OV TCGA-23-1120 SCRN1 SNP Missense_Mutation 7 29983757 A G 13 91 LUSC TCGA-33-4533 SCRN1 SNP Missense_Mutation 7 29980442 C A 25 66 LUAD TCGA-44-2656 SCRN1 SNP Missense_Mutation 7 29966088 C T 25 57 LUAD TCGA-44-2656 SCRN1 SNP Missense_Mutation 7 29980415 C G 27 95 LUAD TCGA-44-3918 SCRN1 SNP Missense_Mutation 7 29980336 T A 58 52 LUSC TCGA-56-1622 SCRN1 SNP Missense_Mutation 7 29966073 C A 29 65 LUAD TCGA-64-1680 SCRN1 SNP Missense_Mutation 7 30008662 A G 13 72 UCEC TCGA-A5-A0VP SCRN1 SNP Silent 7 29966080 G A 37 51 UCEC TCGA-A5-A0VP SCRN1 SNP Missense_Mutation 7 29983652 C T 19 86 BRCA TCGA-A8-A06Q SCRN1 SNP Silent 7 29963714 C T 29 54 BRCA TCGA-A8-A09A SCRN1 SNP Silent 7 29994932 T G 61 47 CRC TCGA-AA-3979 SCRN1 SNP Silent 7 30008594 C A 26 49 BRCA TCGA-AN-A0AR SCRN1 SNP Missense_Mutation 7 30008626 C T 21 70 UCEC TCGA-AP-A0LD SCRN1 SNP Silent 7 29966215 G A 40 50 UCEC TCGA-AX-A06H SCRN1 SNP Missense_Mutation 7 30008541 G A 39 66 KIRC TCGA-B0-4833 SCRN1 SNP Missense_Mutation 7 29994903 C A 30 99 UCEC TCGA-B5-A0JY SCRN1 SNP Nonsense_Mutation 7 29980430 C A 30 95 UCEC TCGA-B5-A11E SCRN1 SNP Silent 7 29983741 G T 35 52 UCEC TCGA-BG-A18B SCRN1 SNP Missense_Mutation 7 29983772 G A 48 84 UCEC TCGA-BS-A0UF SCRN1 SNP Missense_Mutation 7 29966137 C A 32 75 KIRC TCGA-CJ-4638 SCRN1 SNP Missense_Mutation 7 29963599 C A 29 93 HNSC TCGA-CN-6010 SCRN1 SNP Missense_Mutation 7 29983623 C G 24 99 HNSC TCGA-CR-7388 SCRN1 SNP Missense_Mutation 7 29980412 G C 45 61 KIRC TCGA-CZ-5465 SCRN1 INS Frame_Shift_Ins 7 29980329 - C 6 62 UCEC TCGA-D1-A17Q SCRN1 SNP Missense_Mutation 7 29976225 C A 32 71 UCEC TCGA-D1-A17Q SCRN1 SNP Silent 7 30029821 C T 31 48