ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-153 HSPB2 SNP Silent 11 111784208 C T 28 63 LUAD LUAD-CHTN-MAD06-00668 HSPB2 SNP Missense_Mutation 11 111784225 G T 39 88 MEL MEL-13567 HSPB2 SNP Missense_Mutation 11 111784566 C T 22 66 LUAD TCGA-05-4427 HSPB2 SNP Silent 11 111784229 C G 23 43 GBM TCGA-06-0185 HSPB2 SNP Silent 11 111784541 C T 29 59 OV TCGA-13-0885 HSPB2 SNP Silent 11 111784461 C A 27 54 LUAD TCGA-44-4112 HSPB2 SNP Missense_Mutation 11 111784250 C A 25 67 LUSC TCGA-66-2793 HSPB2 SNP Missense_Mutation 11 111784533 A G 6 62 CRC TCGA-AA-3833 HSPB2 SNP Missense_Mutation 11 111784519 G A 42 75 CRC TCGA-AG-A002 HSPB2 SNP Missense_Mutation 11 111784266 G A 37 73 UCEC TCGA-AP-A0LM HSPB2 SNP Missense_Mutation 11 111784387 G A 38 58 UCEC TCGA-B5-A0JY HSPB2 SNP Missense_Mutation 11 111784302 C A 32 88 UCEC TCGA-B5-A0JY HSPB2 SNP Missense_Mutation 11 111784329 G A 37 88 UCEC TCGA-B5-A11E HSPB2 SNP Missense_Mutation 11 111784206 G A 47 88 KIRC TCGA-BP-4775 HSPB2 SNP Missense_Mutation 11 111784450 T A 58 82 BLCA TCGA-BT-A20N HSPB2 SNP Missense_Mutation 11 111784284 G T 43 65 BLCA TCGA-DK-A3IQ HSPB2 SNP Missense_Mutation 11 111784264 C A 30 88