ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-12 SPRY1 SNP Missense_Mutation 4 124323531 C T 26 67 LUAD TCGA-05-4398 SPRY1 SNP Missense_Mutation 4 124322828 G A 33 72 LUAD TCGA-05-4427 SPRY1 SNP Silent 4 124323229 G T 45 64 OV TCGA-10-0935 SPRY1 SNP Missense_Mutation 4 124323351 T C 63 65 CRC TCGA-AA-A00D SPRY1 SNP Missense_Mutation 4 124323423 A G 3 87 CRC TCGA-AA-A01Q SPRY1 SNP Missense_Mutation 4 124323323 A G 6 75 CRC TCGA-AG-A002 SPRY1 SNP Missense_Mutation 4 124322919 C T 31 94 CRC TCGA-AG-A002 SPRY1 SNP Silent 4 124323508 C T 28 60 BRCA TCGA-AN-A0FD SPRY1 SNP Silent 4 124323154 A G 15 49 UCEC TCGA-AP-A059 SPRY1 SNP Splice_Site 4 124322691 G A 35 94 HNSC TCGA-CN-4734 SPRY1 SNP Missense_Mutation 4 124323279 A G 3 54 UCEC TCGA-D1-A16Y SPRY1 SNP Missense_Mutation 4 124323012 A G 14 56 UCEC TCGA-D1-A17Q SPRY1 SNP Missense_Mutation 4 124322781 C T 31 80 BRCA TCGA-D8-A1XJ SPRY1 SNP Missense_Mutation 4 124323620 C T 31 65 BLCA TCGA-FD-A3B8 SPRY1 SNP Missense_Mutation 4 124322883 C A 26 81