ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW163 FADS2 SNP Silent 11 61608179 C T 31 51 ESO ESO-0013 FADS2 SNP Nonsense_Mutation 11 61584116 C A 31 56 ESO ESO-117 FADS2 SNP Missense_Mutation 11 61607911 G A 38 62 HNSC HN_62505 FADS2 SNP Synonymous 11 61608179 C T 31 51 LUAD LUAD-NYU315 FADS2 SNP Splice_Site 11 61632623 G T 34 89 MEL MEL-JWCI-WGS-1 FADS2 SNP Silent 11 61605270 C T 18 53 MEL MEL-JWCI-WGS-1 FADS2 SNP Silent 11 61630757 C T 30 57 MEL MEL-Ma-Mel-85 FADS2 SNP Silent 11 61607982 C T 24 52 MM MM-0525 FADS2 SNP Missense_Mutation 11 61583785 G C 48 60 OV TCGA-09-2056 FADS2 SNP Missense_Mutation 11 61605272 C G 24 51 LUAD TCGA-17-Z032 FADS2 SNP Missense_Mutation 11 61608169 T C 58 63 LUSC TCGA-66-2795 FADS2 SNP Missense_Mutation 11 61624947 C G 22 76 GBM TCGA-81-5911 FADS2 SNP Silent 11 61615699 G A 35 61 CRC TCGA-AA-3870 FADS2 SNP Missense_Mutation 11 61607903 A T 6 84 CRC TCGA-AA-A00O FADS2 SNP Missense_Mutation 11 61615706 G A 37 93 CRC TCGA-AA-A022 FADS2 SNP Missense_Mutation 11 61632644 G A 39 89 CRC TCGA-AG-3898 FADS2 SNP Missense_Mutation 11 61607828 G A 39 63 BRCA TCGA-AN-A0AT FADS2 SNP Silent 11 61608167 T A 63 25 UCEC TCGA-AP-A059 FADS2 SNP Missense_Mutation 11 61631197 G A 40 61 UCEC TCGA-AP-A0LM FADS2 SNP Missense_Mutation 11 61615676 G A 38 80 UCEC TCGA-B5-A0JY FADS2 SNP Silent 11 61624518 T C 50 53 BRCA TCGA-B6-A0I5 FADS2 SNP Missense_Mutation 11 61607902 C T 21 91 BRCA TCGA-B6-A0IJ FADS2 SNP Silent 11 61615738 C G 27 45 BRCA TCGA-BH-A0DZ FADS2 SNP Missense_Mutation 11 61583860 C T 29 55 BRCA TCGA-BH-A18T FADS2 SNP Missense_Mutation 11 61631214 C G 29 80 KIRC TCGA-BP-5004 FADS2 SNP Missense_Mutation 11 61608124 A C 16 57 UCEC TCGA-BS-A0UV FADS2 SNP Silent 11 61630802 C T 31 50 HNSC TCGA-CV-7252 FADS2 SNP Missense_Mutation 11 61632693 G T 34 60 KIRC TCGA-CW-5585 FADS2 SNP Missense_Mutation 11 61624985 G A 40 50 UCEC TCGA-D1-A17Q FADS2 SNP Silent 11 61631196 C T 19 48 HNSC TCGA-D6-6516 FADS2 SNP Splice_Site 11 61583899 G T 44 53 BRCA TCGA-D8-A1Y1 FADS2 SNP Silent 11 61607877 C T 19 49 BRCA TCGA-E2-A14W FADS2 SNP Missense_Mutation 11 61624993 G C 33 48