Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
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id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
13681	SPEN	rs780888765	SNP	missense variant	S/T	1095	81	0.08	79	benign	0.078	10001	likely benign	10
13682	SPEN	rs1165595104	SNP	missense variant	Q/R	1099	101	0.1	375	benign	0.374	20001	likely benign	20
13683	SPEN	rs1427820860	SNP	missense variant	V/D	1101	151	0.15	22	benign	0.021	8001	likely benign	8
13684	SPEN	rs755778364	SNP	missense variant	Q/L	1102	381	0.38	1	benign	0	12001	likely benign	12
13685	SPEN	rs907075014	SNP	missense variant	S/A	1103	161	0.16	50	benign	0.049	7001	likely benign	7
13686	SPEN	rs998597411	SNP	missense variant	K/N	1105	11	0.01	544	possibly damaging	0.543	15001	likely benign	15
13687	SPEN	rs1250141856	SNP	missense variant	I/V	1107	571	0.57	1	benign	0	2001	likely benign	2
13688	SPEN	rs779704335	SNP	missense variant	P/A	1108	891	0.89	1	benign	0	1	likely benign	0
13689	SPEN	rs779704335	SNP	missense variant	P/S	1108	731	0.73	1	benign	0	1	likely benign	0
13690	SPEN	rs1300674129	SNP	missense variant	P/L	1108	231	0.23	1	benign	0	15001	likely benign	15

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