ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62996 RELL2 SNP Synonymous 5 141019182 C A 23 55 LUAD LUAD-F00162 RELL2 SNP Missense_Mutation 5 141020004 G A 36 62 MEL MEL-Ma-Mel-114 RELL2 SNP Missense_Mutation 5 141019609 G A 41 59 MEL MEL-Ma-Mel-35 RELL2 SNP Silent 5 141019175 C T 26 52 LUSC TCGA-22-4604 RELL2 SNP Missense_Mutation 5 141019991 C A 17 62 LUAD TCGA-35-3621 RELL2 SNP Missense_Mutation 5 141018560 G A 45 85 LUSC TCGA-66-2768 RELL2 SNP Missense_Mutation 5 141019182 C T 23 55 LUSC TCGA-66-2783 RELL2 SNP Nonsense_Mutation 5 141019704 G T 35 51 LUAD TCGA-75-6205 RELL2 SNP Missense_Mutation 5 141018407 G C 38 57 BRCA TCGA-A2-A0T2 RELL2 SNP Missense_Mutation 5 141019995 G A 41 50 CRC TCGA-AA-3837 RELL2 SNP Missense_Mutation 5 141019845 G A 33 77 CRC TCGA-AG-A002 RELL2 SNP Missense_Mutation 5 141017850 C A 24 76 UCEC TCGA-AP-A051 RELL2 SNP Missense_Mutation 5 141018584 T A 58 66 UCEC TCGA-AX-A0J0 RELL2 SNP Silent 5 141019529 A G 2 51 UCEC TCGA-B5-A0JY RELL2 SNP Missense_Mutation 5 141019837 G T 34 52 UCEC TCGA-B5-A11Y RELL2 SNP Silent 5 141019613 G A 42 43 KIRC TCGA-BP-4999 RELL2 SNP Silent 5 141019628 G A 41 52 UCEC TCGA-BS-A0UF RELL2 SNP Missense_Mutation 5 141018406 C T 31 66 UCEC TCGA-BS-A0UV RELL2 SNP Silent 5 141018369 C T 19 43 HNSC TCGA-CN-4730 RELL2 SNP Silent 5 141019628 G C 41 52 HNSC TCGA-CR-7386 RELL2 SNP Silent 5 141019745 G A 41 52