ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
LUAD	LUAD-B01246	CCND1	SNP	Silent	11	69465912	G	A	33	86
LUAD	LUAD-RT-S01810	CCND1	SNP	Silent	11	69462802	G	T	39	25
LUAD	LUAD_E00565	CCND1	SNP	Missense_Mutation	11	69457826	G	A	41	95
MEL	ME024	CCND1	SNP	Missense_Mutation	11	69466022	C	T	22	87
MEL	ME049	CCND1	SNP	Missense_Mutation	11	69465970	G	A	42	60
MM	MM-0322	CCND1	SNP	Missense_Mutation	11	69456092	A	G	7	73
MM	MM-0335	CCND1	SNP	Missense	11	69456219	A	T	4	59
MM	MM-0427	CCND1	SNP	Missense_Mutation	11	69456241	C	G	26	92
MM	MM-0429	CCND1	SNP	Missense_Mutation	11	69456104	G	A	46	92
MM	MM-0429	CCND1	SNP	Silent	11	69456210	C	G	24	55
MM	MM-0451	CCND1	SNP	Missense_Mutation	11	69458005	G	C	35	34
MM	MM-0635	CCND1	SNP	Missense_Mutation	11	69462891	G	C	33	68
MM	MM-442	CCND1	SNP	Silent	11	69456108	A	G	3	56
MM	MM-442	CCND1	SNP	Missense_Mutation	11	69456133	C	T	22	78
MM	MM-442	CCND1	SNP	Silent	11	69456201	C	T	24	61
LUAD	TCGA-05-4426	CCND1	SNP	Silent	11	69462817	C	A	23	47
LUSC	TCGA-34-2608	CCND1	SNP	Missense_Mutation	11	69458669	G	A	45	73
GBM	TCGA-41-4097	CCND1	SNP	Missense_Mutation	11	69457803	G	T	46	95
LUAD	TCGA-49-6742	CCND1	DNP	Missense_Mutation	11	69458698	GG	TA	39	32
LUAD	TCGA-67-3771	CCND1	SNP	Missense_Mutation	11	69456155	A	C	10	73
UCEC	TCGA-AP-A054	CCND1	SNP	Missense_Mutation	11	69465889	T	C	55	91
UCEC	TCGA-AP-A0LM	CCND1	SNP	Missense_Mutation	11	69458005	G	T	35	34
UCEC	TCGA-AX-A05Z	CCND1	SNP	Missense_Mutation	11	69462881	T	C	56	74
UCEC	TCGA-AX-A062	CCND1	SNP	Nonsense_Mutation	11	69465985	G	T	41	64
UCEC	TCGA-AX-A063	CCND1	SNP	Missense_Mutation	11	69462905	G	A	45	94
UCEC	TCGA-AX-A0J0	CCND1	SNP	Missense_Mutation	11	69458697	C	T	27	54
UCEC	TCGA-B5-A0JV	CCND1	SNP	Missense_Mutation	11	69466019	C	T	17	100
HNSC	TCGA-BA-4075	CCND1	SNP	Silent	11	69462871	C	T	26	94
UCEC	TCGA-BG-A0M7	CCND1	SNP	Missense_Mutation	11	69466019	C	T	17	100
UCEC	TCGA-BG-A0MQ	CCND1	SNP	Missense_Mutation	11	69465892	C	A	24	62
UCEC	TCGA-BG-A0VW	CCND1	SNP	Silent	11	69457918	C	T	25	68
BRCA	TCGA-BH-A0BP	CCND1	SNP	Missense_Mutation	11	69465940	C	T	27	68
UCEC	TCGA-BS-A0TJ	CCND1	INS	In_Frame_Ins	11	69466031	-	GCG	59	92
UCEC	TCGA-BS-A0U5	CCND1	SNP	Missense_Mutation	11	69466040	T	G	59	79
BLCA	TCGA-BT-A20J	CCND1	SNP	Missense_Mutation	11	69456203	C	T	31	92
HNSC	TCGA-CN-4728	CCND1	SNP	Silent	11	69457891	C	T	26	68
HNSC	TCGA-CV-6441	CCND1	SNP	Missense_Mutation	11	69466006	G	C	41	86
HNSC	TCGA-CV-6441	CCND1	DEL	In_Frame_Del	11	69466013	CTTGCACAC	-	28	87
UCEC	TCGA-D1-A0ZO	CCND1	SNP	Missense_Mutation	11	69466019	C	T	17	100
UCEC	TCGA-D1-A0ZU	CCND1	SNP	Missense_Mutation	11	69466021	C	T	18	100
UCEC	TCGA-D1-A163	CCND1	SNP	Missense_Mutation	11	69466019	C	T	17	100
UCEC	TCGA-D1-A16D	CCND1	DEL	In_Frame_Del	11	69466027	GACGTGCGG	-	37	100
UCEC	TCGA-D1-A174	CCND1	SNP	Missense_Mutation	11	69466022	C	A	22	87
UCEC	TCGA-D1-A17D	CCND1	SNP	Missense_Mutation	11	69466021	C	T	18	100
BLCA	TCGA-DK-A1AC	CCND1	SNP	Silent	11	69458749	C	T	32	49