ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
MEL	MEL-JWCI-WGS-12	ACVR2B	SNP	Missense_Mutation	3	38519446	G	A	42	65
MEL	MEL-JWCI-WGS-12	ACVR2B	SNP	Missense_Mutation	3	38519758	C	T	22	98
MEL	MEL-Ma-Mel-105	ACVR2B	SNP	Missense_Mutation	3	38523951	A	C	11	92
MEL	MEL-Ma-Mel-37	ACVR2B	SNP	Missense_Mutation	3	38519878	C	T	30	68
MEL	MEL-UKRV-Mel-20	ACVR2B	SNP	Missense_Mutation	3	38523732	C	T	26	87
LUAD	TCGA-05-4382	ACVR2B	SNP	Missense_Mutation	3	38519453	G	T	42	63
LUAD	TCGA-05-4396	ACVR2B	SNP	Missense_Mutation	3	38519456	C	A	23	87
LUAD	TCGA-05-4396	ACVR2B	SNP	Missense_Mutation	3	38521287	G	T	42	84
OV	TCGA-09-2045	ACVR2B	SNP	Missense_Mutation	3	38518817	A	T	14	89
OV	TCGA-13-0900	ACVR2B	SNP	Missense	3	38520697	G	C	46	84
OV	TCGA-13-1407	ACVR2B	SNP	Missense	3	38520697	G	C	46	84
LUAD	TCGA-44-3398	ACVR2B	SNP	Missense_Mutation	3	38520636	G	C	33	69
LUAD	TCGA-44-3398	ACVR2B	SNP	Splice_Site	3	38524628	G	T	35	99
BRCA	TCGA-A2-A1FX	ACVR2B	SNP	Silent	3	38519699	C	T	31	45
UCEC	TCGA-A5-A0GP	ACVR2B	SNP	Silent	3	38518941	C	T	31	47
CRC	TCGA-AA-3516	ACVR2B	INS	Frame_Shift_Ins	3	38522929	-	A	41	50
CRC	TCGA-AA-3684	ACVR2B	SNP	Silent	3	38519664	C	T	24	71
CRC	TCGA-AA-3821	ACVR2B	SNP	Silent	3	38521171	C	A	28	54
CRC	TCGA-AA-3966	ACVR2B	SNP	Missense_Mutation	3	38518859	G	A	42	97
CRC	TCGA-AA-A00N	ACVR2B	SNP	Missense_Mutation	3	38519422	G	A	37	69
CRC	TCGA-AA-A010	ACVR2B	SNP	Missense_Mutation	3	38523772	G	T	48	86
AML	TCGA-AB-2973	ACVR2B	SNP	Missense_Mutation	3	38519671	C	T	19	64
CRC	TCGA-AG-A00Y	ACVR2B	INS	Frame_Shift_Ins	3	38518793	-	C	11	63
UCEC	TCGA-AP-A056	ACVR2B	SNP	Missense_Mutation	3	38519422	G	A	37	69
UCEC	TCGA-AX-A05Z	ACVR2B	SNP	Missense_Mutation	3	38519977	G	T	45	83
UCEC	TCGA-B5-A0JY	ACVR2B	SNP	Silent	3	38524664	C	T	28	86
UCEC	TCGA-B5-A11E	ACVR2B	SNP	Missense_Mutation	3	38524741	A	T	2	65
UCEC	TCGA-BS-A0UF	ACVR2B	SNP	Missense_Mutation	3	38518936	G	A	37	61
UCEC	TCGA-D1-A0ZO	ACVR2B	SNP	Missense_Mutation	3	38518825	G	A	38	97
UCEC	TCGA-D1-A103	ACVR2B	SNP	Missense_Mutation	3	38522888	G	A	40	67
BRCA	TCGA-D8-A1JE	ACVR2B	SNP	Nonsense_Mutation	3	38520670	A	T	9	69
KIRC	TCGA-EU-5905	ACVR2B	SNP	Missense_Mutation	3	38519652	A	G	10	70