ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-137 KLHL35 SNP Missense_Mutation 11 75133690 C G 28 57 MEL ME017 KLHL35 SNP Missense_Mutation 11 75134848 G A 34 95 LUSC TCGA-60-2698 KLHL35 SNP Missense_Mutation 11 75139655 C T 29 96 LUAD TCGA-64-5779 KLHL35 SNP Missense_Mutation 11 75136592 C T 27 95 UCEC TCGA-B5-A11N KLHL35 DEL In_Frame_Del 11 75139545 GGGCAGGCT - 39 28 HNSC TCGA-BB-7862 KLHL35 SNP Silent 11 75139659 T G 53 45 BRCA TCGA-BH-A18H KLHL35 SNP Missense_Mutation 11 75133746 C T 32 97 BRCA TCGA-E9-A1NA KLHL35 SNP Missense_Mutation 11 75136581 C T 19 81