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
14351	SPEN	rs546998631	SNP	missense variant	P/L	2067	101	0.1	1	benign	0	7001	likely benign	7
14352	SPEN	rs1221512785	SNP	missense variant	A/V	2068	521	0.52	25	benign	0.024	8001	likely benign	8
14353	SPEN	rs1344997486	SNP	missense variant	P/A	2069	161	0.16	367	benign	0.366	15001	likely benign	15
14354	SPEN	rs1375827370	SNP	missense variant	P/L	2069	311	0.31	23	benign	0.022	17001	likely benign	17
14355	SPEN	rs1281222537	SNP	missense variant	E/D	2070	121	0.12	629	possibly damaging	0.628	17001	likely benign	17
14356	SPEN	rs754077907	SNP	missense variant	S/P	2073	121	0.12	2	benign	0.001	16001	likely benign	16
14357	SPEN	rs1553179827	SNP	missense variant	S/F	2073	91	0.09	50	benign	0.049	15001	likely benign	15
14358	SPEN	rs577325205	SNP	missense variant	K/T	2074	1	0	916	probably damaging	0.915	24001	likely benign	24
14359	SPEN	rs577325205	SNP	missense variant	K/R	2074	111	0.11	101	benign	0.1	21001	likely benign	21
14360	SPEN	rs752765121	SNP	missense variant	S/L	2075	221	0.22	4	benign	0.003	20001	likely benign	20

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