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
12831	SF3B1	rs535085463	SNP	missense variant	E/D	490	351	0.35	44	benign	0.043	19001	likely benign	19
12832	SF3B1	rs771481374	SNP	missense variant	P/T	489	551	0.55	7	benign	0.006	21001	likely benign	21
12833	SF3B1	rs1488105943	SNP	missense variant	T/A	486	681	0.68	1	benign	0	22001	likely benign	22
12834	SF3B1	rs1032673609	SNP	missense variant	D/N	483	171	0.17	34	benign	0.033	23001	likely benign	23
12835	SF3B1	rs888908728	SNP	missense variant	I/V	472	541	0.54	1	benign	0	19001	likely benign	19
12836	SF3B1	rs866844931	SNP	missense variant	P/L	465	31	0.03	443	benign	0.442	24001	likely benign	24
12837	SF3B1	rs758559038	SNP	missense variant	V/F	456	51	0.05	95	benign	0.094	22001	likely benign	22
12838	SF3B1	rs758559038	SNP	missense variant	V/I	456	421	0.42	4	benign	0.003	19001	likely benign	19
12839	SF3B1	rs777705664	SNP	missense variant	R/Q	451	351	0.35	29	benign	0.028	23001	likely benign	23
12840	SF3B1	rs369794291	SNP	missense variant	R/G	451	271	0.27	16	benign	0.015	20001	likely benign	20

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