ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0015 NCK2 SNP Missense_Mutation 2 106509536 C G 30 56 LUAD LUAD-B00416 NCK2 SNP Missense_Mutation 2 106498476 G C 37 97 LUAD LUAD-CHTN-MAD06-00668 NCK2 SNP Silent 2 106498364 A T 13 59 LUAD LUAD-CHTN-MAD06-00668 NCK2 SNP Missense_Mutation 2 106498366 G T 34 97 LUAD LUAD-RT-S01699 NCK2 SNP Missense_Mutation 2 106498374 G T 39 75 LUAD LUAD-RT-S01777 NCK2 SNP Missense_Mutation 2 106471635 G T 47 100 LUAD LUAD-RT-S01777 NCK2 SNP Missense_Mutation 2 106471637 C G 27 68 LUAD LUAD-VUMN6 NCK2 SNP Missense_Mutation 2 106498290 G T 43 98 MEL MEL-JWCI-27 NCK2 SNP Missense_Mutation 2 106471716 C T 30 99 MEL MEL-JWCI-WGS-1 NCK2 SNP Missense_Mutation 2 106498039 C T 22 97 MEL MEL-JWCI-WGS-12 NCK2 SNP Silent 2 106497908 C T 31 42 MEL MEL-Ma-Mel-35 NCK2 SNP Silent 2 106509536 C T 30 56 LUAD TCGA-05-4396 NCK2 SNP Missense_Mutation 2 106498006 G T 39 97 OV TCGA-13-0714 NCK2 SNP Missense_Mutation 2 106471535 A T 16 79 LUSC TCGA-21-1071 NCK2 SNP Missense_Mutation 2 106498233 G C 45 98 LUSC TCGA-43-2578 NCK2 SNP Missense_Mutation 2 106498213 G T 43 97 LUAD TCGA-64-5781 NCK2 SNP Nonsense_Mutation 2 106498470 G T 41 84 LUAD TCGA-67-3771 NCK2 SNP Missense_Mutation 2 106498084 C G 30 83 CRC TCGA-A6-2672 NCK2 SNP Silent 2 106471730 C T 24 67 BRCA TCGA-A8-A07E NCK2 SNP Missense_Mutation 2 106471553 G T 41 100 BRCA TCGA-A8-A09G NCK2 SNP Silent 2 106509512 C T 32 57 CRC TCGA-AA-A00N NCK2 SNP Silent 2 106497917 C T 31 52 UCEC TCGA-AP-A051 NCK2 SNP Silent 2 106471675 G A 40 47 UCEC TCGA-AP-A0LE NCK2 SNP Missense_Mutation 2 106509519 A G 8 88 UCEC TCGA-AP-A0LM NCK2 SNP Silent 2 106498475 C T 27 47 UCEC TCGA-AP-A0LM NCK2 SNP Missense_Mutation 2 106509466 C T 27 96 UCEC TCGA-AP-A0LT NCK2 SNP Missense_Mutation 2 106471637 C T 27 68 UCEC TCGA-B5-A0JY NCK2 SNP Missense_Mutation 2 106471619 G A 37 100 UCEC TCGA-BG-A0M4 NCK2 SNP Silent 2 106509618 A C 7 52 UCEC TCGA-BS-A0UJ NCK2 SNP Missense_Mutation 2 106498188 G A 37 97 UCEC TCGA-BS-A0UV NCK2 SNP Missense_Mutation 2 106471537 T G 63 58 HNSC TCGA-CN-4729 NCK2 SNP Missense_Mutation 2 106497993 G A 37 97 HNSC TCGA-CN-4730 NCK2 SNP Missense_Mutation 2 106498068 G A 37 97 HNSC TCGA-CN-6011 NCK2 SNP Silent 2 106498397 C T 31 54 HNSC TCGA-CN-6024 NCK2 SNP Silent 2 106497977 C T 29 60 HNSC TCGA-CR-6480 NCK2 SNP Silent 2 106498358 A G 6 44 HNSC TCGA-CR-7397 NCK2 SNP Missense_Mutation 2 106497876 G A 37 98 HNSC TCGA-CV-5444 NCK2 SNP Silent 2 106498121 G A 45 55 UCEC TCGA-D1-A103 NCK2 SNP Missense_Mutation 2 106497898 T A 50 77 UCEC TCGA-D1-A177 NCK2 SNP Missense_Mutation 2 106498393 G A 38 67