ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62421 EFEMP2 SNP Splice_Site_SNP 11 65638130 C G 32 96 LUAD LUAD_E00565 EFEMP2 SNP Silent 11 65638689 G T 39 39 MEL MEL-Ma-Mel-53 EFEMP2 SNP Missense_Mutation 11 65638693 G A 35 70 LUAD TCGA-05-4396 EFEMP2 SNP Missense_Mutation 11 65637348 C A 23 64 LUAD TCGA-05-4396 EFEMP2 SNP Missense_Mutation 11 65638705 G T 39 71 LUAD TCGA-05-5428 EFEMP2 SNP Missense_Mutation 11 65635480 G A 45 57 LUAD TCGA-05-5428 EFEMP2 SNP Missense_Mutation 11 65635499 G C 33 66 LUAD TCGA-17-Z031 EFEMP2 SNP Missense_Mutation 11 65638652 G C 42 71 LUSC TCGA-21-1076 EFEMP2 SNP Silent 11 65638668 G A 42 77 LUSC TCGA-34-5231 EFEMP2 SNP Missense_Mutation 11 65635425 G T 40 56 LUSC TCGA-34-5231 EFEMP2 SNP Missense_Mutation 11 65635437 G C 38 55 LUSC TCGA-39-5030 EFEMP2 SNP Missense_Mutation 11 65635415 T C 50 88 LUSC TCGA-39-5037 EFEMP2 SNP Silent 11 65634506 C T 29 66 LUAD TCGA-44-6777 EFEMP2 SNP Missense_Mutation 11 65637376 G A 37 97 LUAD TCGA-50-5941 EFEMP2 SNP Silent 11 65635362 A T 7 1 OV TCGA-61-2102 EFEMP2 SNP Silent 11 65635353 C T 27 46 CRC TCGA-AA-A00E EFEMP2 SNP Silent 11 65638689 G A 39 39 CRC TCGA-AA-A01R EFEMP2 SNP Missense_Mutation 11 65638763 A G 15 86 UCEC TCGA-AP-A059 EFEMP2 SNP Missense_Mutation 11 65635525 C T 27 96 UCEC TCGA-AP-A0LD EFEMP2 SNP Missense_Mutation 11 65637375 C A 27 83 UCEC TCGA-AP-A0LM EFEMP2 SNP Missense_Mutation 11 65635408 G A 38 96 UCEC TCGA-AP-A0LM EFEMP2 SNP Silent 11 65638023 G A 37 35 UCEC TCGA-AP-A0LM EFEMP2 SNP Silent 11 65639778 C T 27 65 BRCA TCGA-AR-A256 EFEMP2 SNP Missense_Mutation 11 65638053 C G 20 62 UCEC TCGA-B5-A0JY EFEMP2 SNP Missense_Mutation 11 65637603 C T 27 74 HNSC TCGA-BA-5152 EFEMP2 SNP Silent 11 65635368 G T 41 68 HNSC TCGA-BA-5559 EFEMP2 SNP Missense_Mutation 11 65638052 A T 6 88 HNSC TCGA-BB-4223 EFEMP2 SNP Nonsense_Mutation 11 65638808 C A 29 94 KIRC TCGA-BP-4961 EFEMP2 SNP Missense_Mutation 11 65637667 C T 19 96 HNSC TCGA-CR-7398 EFEMP2 SNP Missense_Mutation 11 65637634 C T 31 74 HNSC TCGA-CV-5441 EFEMP2 SNP Missense_Mutation 11 65638688 C T 27 80 HNSC TCGA-CV-7248 EFEMP2 SNP Silent 11 65634509 C A 23 26 HNSC TCGA-CV-7429 EFEMP2 SNP Missense_Mutation 11 65635459 A T 8 88 KIRC TCGA-CZ-5465 EFEMP2 SNP Missense_Mutation 11 65635794 C T 19 55