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
14031	SPEN	rs772065708	SNP	missense variant	S/P	1687	431	0.43	1	benign	0	6001	likely benign	6
14032	SPEN	rs370600815	SNP	missense variant	S/F	1687	351	0.35	1	benign	0	9001	likely benign	9
14033	SPEN	rs527239966	SNP	missense variant	E/G	1688	11	0.01	37	benign	0.036	22001	likely benign	22
14034	SPEN	rs760509488	SNP	missense variant	E/D	1688	181	0.18	1	benign	0	2001	likely benign	2
14035	SPEN	rs1203124118	SNP	missense variant	P/L	1689	911	0.91	1	benign	0	1	likely benign	0
14036	SPEN	rs1394638881	SNP	missense variant	A/D	1690	201	0.2	207	benign	0.206	13001	likely benign	13
14037	SPEN	rs532673015	SNP	missense variant	P/S	1691	71	0.07	1	benign	0	9001	likely benign	9
14038	SPEN	rs1290156801	SNP	missense variant	P/S	1693	311	0.31	1	benign	0	6001	likely benign	6
14039	SPEN	rs149660885	SNP	missense variant	Q/L	1696	181	0.18	274	benign	0.273	17001	likely benign	17
14040	SPEN	rs1260835742	SNP	missense variant	Q/E	1699	441	0.44	24	benign	0.023	10001	likely benign	10

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