ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
MEL	MEL-JWCI-WGS-1	TXNDC8	SNP	Silent	9	113096559	G	A	37	50
PRAD	PR-3035	TXNDC8	SNP	Missense_Mutation	9	113096558	C	T	27	64
CRC	TCGA-AA-3543	TXNDC8	SNP	Missense_Mutation	9	113096533	C	A	23	64
UCEC	TCGA-AP-A056	TXNDC8	SNP	Missense_Mutation	9	113091516	G	T	33	71
BRCA	TCGA-AR-A24H	TXNDC8	SNP	Missense_Mutation	9	113066787	C	A	32	72
UCEC	TCGA-AX-A05Z	TXNDC8	SNP	Missense_Mutation	9	113091516	G	T	33	71
UCEC	TCGA-AX-A0J1	TXNDC8	SNP	Splice_site	9	113091570	G	T	34	55
UCEC	TCGA-B5-A11E	TXNDC8	SNP	Missense_Mutation	9	113096539	G	A	37	75
UCEC	TCGA-BS-A0UF	TXNDC8	SNP	Splice_Site	9	113096601	C	A	32	75
HNSC	TCGA-CQ-6220	TXNDC8	SNP	Missense_Mutation	9	113096542	G	C	33	75
UCEC	TCGA-D1-A15X	TXNDC8	SNP	Missense_Mutation	9	113065829	A	G	5	71
UCEC	TCGA-D1-A17F	TXNDC8	SNP	Missense_Mutation	9	113096554	A	G	6	71
BRCA	TCGA-E2-A159	TXNDC8	SNP	Missense_Mutation	9	113065819	C	G	32	74