ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-27 LAYN SNP Splice_Site 11 111420501 G A 44 85 MEL MEL-JWCI-WGS-34 LAYN SNP Missense_Mutation 11 111431007 G A 37 71 MEL MEL-Ma-Mel-102 LAYN SNP Missense_Mutation 11 111430885 G A 41 51 NB NB-0121 LAYN SNP Missense_Mutation 11 111425946 C A 28 51 LUAD TCGA-05-4398 LAYN DNP Missense_Mutation 11 111420459 GG AT 39 62 LUSC TCGA-34-5927 LAYN SNP Silent 11 111430955 G A 42 66 LUAD TCGA-67-6217 LAYN SNP Missense_Mutation 11 111425981 A C 3 51 KIRC TCGA-A3-3367 LAYN SNP Silent 11 111431066 G A 45 66 CRC TCGA-AA-3984 LAYN SNP Missense_Mutation 11 111431029 A C 10 85 CRC TCGA-AA-A00N LAYN SNP Silent 11 111414781 C T 31 44 CRC TCGA-AA-A010 LAYN SNP Silent 11 111420382 C A 32 64 CRC TCGA-AG-A02N LAYN SNP Missense_Mutation 11 111428283 G A 42 59 BRCA TCGA-AO-A0J4 LAYN SNP Missense_Mutation 11 111414758 G A 41 72 UCEC TCGA-AP-A051 LAYN SNP Missense_Mutation 11 111420416 G A 38 57 UCEC TCGA-AP-A0LM LAYN SNP Missense_Mutation 11 111414714 C A 32 59 UCEC TCGA-AX-A0J0 LAYN SNP Missense_Mutation 11 111431011 A G 10 53 UCEC TCGA-AX-A0J1 LAYN SNP Missense_Mutation 11 111414782 G A 37 70 BRCA TCGA-BH-A0AW LAYN SNP Silent 11 111414805 G C 45 54 UCEC TCGA-BK-A0C9 LAYN SNP Missense_Mutation 11 111425943 G A 33 60 UCEC TCGA-BS-A0U8 LAYN SNP Missense_Mutation 11 111414869 C T 27 51 BRCA TCGA-C8-A137 LAYN SNP Missense_Mutation 11 111414717 G A 37 61 HNSC TCGA-CR-5248 LAYN SNP Missense_Mutation 11 111428359 G A 48 47 UCEC TCGA-D1-A17Q LAYN SNP Missense_Mutation 11 111414717 G A 37 61 HNSC TCGA-DQ-7595 LAYN SNP Missense_Mutation 11 111428319 C T 24 68 BLCA TCGA-FD-A3B4 LAYN SNP Missense_Mutation 11 111414797 C A 17 93