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
17001	FOXA1	rs1401881303	SNP	missense variant	S/L	307	51	0.05	59	benign	0.058	22001	likely benign	22
17002	FOXA1	rs764636331	SNP	missense variant	S/R	304	71	0.07	114	benign	0.113	15001	likely benign	15
17003	FOXA1	rs1183289159	SNP	missense variant	S/G	304	321	0.32	1	benign	0	13001	likely benign	13
17004	FOXA1	rs997215836	SNP	missense variant	P/L	303	21	0.02	1	benign	0	21001	likely benign	21
17005	FOXA1	rs997215836	SNP	missense variant	P/H	303	41	0.04	95	benign	0.094	21001	likely benign	21
17006	FOXA1	rs753453381	SNP	missense variant	S/T	301	261	0.26	4	benign	0.003	5001	likely benign	5
17007	FOXA1	rs1293965921	SNP	missense variant	A/T	300	391	0.39	1	benign	0	3001	likely benign	3
17008	FOXA1	rs577631417	SNP	missense variant	P/L	297	171	0.17	6	benign	0.005	22001	likely benign	22
17009	FOXA1	rs577631417	SNP	missense variant	P/H	297	101	0.1	636	possibly damaging	0.635	23001	likely benign	23
17010	FOXA1	rs1231726284	SNP	missense variant	P/S	297	531	0.53	87	benign	0.086	21001	likely benign	21

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