ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MED MD-054 SH2B2 SNP Missense_Mutation 7 101943890 C T 23 51 MEL ME009 SH2B2 SNP Silent 7 101950060 C T 21 59 MEL ME009 SH2B2 SNP Missense_Mutation 7 101957767 G A 35 96 MEL MEL-JWCI-WGS-11 SH2B2 SNP Missense_Mutation 7 101957815 C T 31 55 MEL MEL-Ma-Mel-114 SH2B2 SNP Silent 7 101957793 C T 31 50 MEL MEL-UKRV-Mel-20 SH2B2 SNP Missense_Mutation 7 101960936 C G 31 71 GBM TCGA-14-2554 SH2B2 SNP Missense_Mutation 7 101943880 G A 36 51 LUAD TCGA-38-4626 SH2B2 SNP Silent 7 101952177 C T 27 51 LUSC TCGA-60-2711 SH2B2 SNP Missense_Mutation 7 101960886 A T 6 73 LUAD TCGA-64-1676 SH2B2 SNP Silent 7 101944560 C T 21 55 UCEC TCGA-A5-A0GJ SH2B2 SNP Missense_Mutation 7 101960805 G C 38 93 BRCA TCGA-A8-A06Q SH2B2 SNP Missense_Mutation 7 101960937 G A 38 79 CRC TCGA-AA-3672 SH2B2 SNP Silent 7 101957772 G C 42 34 UCEC TCGA-B5-A11H SH2B2 SNP Missense_Mutation 7 101960877 G A 38 71 KIRC TCGA-CZ-5451 SH2B2 SNP Missense_Mutation 7 101952119 T G 50 85 HNSC TCGA-DQ-7595 SH2B2 SNP Missense_Mutation 7 101944494 G C 36 53 CARC Carc-DFCI-136 SH2B2 SNP Missense_Mutation 7 101952149 A G 6 85