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
14211	SPEN	rs201069603	SNP	missense variant	H/Y	1914	11	0.01	63	benign	0.062	19001	likely benign	19
14212	SPEN	rs1320111661	SNP	missense variant	H/Q	1914	161	0.16	1	benign	0	1	likely benign	0
14213	SPEN	rs980736587	SNP	missense variant	N/D	1916	741	0.74	7	benign	0.006	7001	likely benign	7
14214	SPEN	rs751269551	SNP	missense variant	N/S	1916	1001	1	1	benign	0	1	likely benign	0
14215	SPEN	rs756808528	SNP	missense variant	N/K	1916	231	0.23	11	benign	0.01	10001	likely benign	10
14216	SPEN	rs1298127512	SNP	missense variant	R/C	1917	21	0.02	4	benign	0.003	23001	likely benign	23
14217	SPEN	rs780910569	SNP	missense variant	R/H	1917	71	0.07	289	benign	0.288	20001	likely benign	20
14218	SPEN	rs1557760242	SNP	missense variant	S/P	1918	171	0.17	725	possibly damaging	0.724	22001	likely benign	22
14219	SPEN	rs1557760242	SNP	missense variant	S/A	1918	221	0.22	22	benign	0.021	16001	likely benign	16
14220	SPEN	rs375124168	SNP	missense variant	S/F	1918	1	0	855	possibly damaging	0.854	23001	likely benign	23

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