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
14411	SPEN	rs750396773	SNP	missense variant	S/C	2154	31	0.03	515	possibly damaging	0.514	21001	likely benign	21
14412	SPEN	rs750396773	SNP	missense variant	S/F	2154	11	0.01	441	benign	0.44	18001	likely benign	18
14413	SPEN	rs142682023	SNP	missense variant	S/C	2156	21	0.02	982	probably damaging	0.981	21001	likely benign	21
14414	SPEN	rs143503585	SNP	missense variant	G/E	2157	871	0.87	1	benign	0	1	likely benign	0
14415	SPEN	rs143503585	SNP	missense variant	G/V	2157	121	0.12	1	benign	0	1	likely benign	0
14416	SPEN	rs753484186	SNP	missense variant	P/A	2158	691	0.69	1	benign	0	1	likely benign	0
14417	SPEN	rs144493499	SNP	missense variant	P/L	2158	491	0.49	1	benign	0	1	likely benign	0
14418	SPEN	rs747561893	SNP	missense variant	P/A	2160	1	0	6	benign	0.005	10001	likely benign	10
14419	SPEN	rs757967848	SNP	missense variant	E/K	2161	51	0.05	506	possibly damaging	0.505	23001	likely benign	23
14420	SPEN	rs1405526402	SNP	missense variant	Q/E	2164	221	0.22	58	benign	0.057	14001	likely benign	14

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