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
11571	FBXW7	rs761747465	SNP	missense variant	K/T	371	61	0.06	46	benign	0.045	22001	likely benign	22
11572	FBXW7	rs745418631	SNP	missense variant	R/Q	367	191	0.19	7	benign	0.006	23001	likely benign	23
11573	FBXW7	rs775885576	SNP	missense variant	N/S	364	131	0.13	946	probably damaging	0.945	24001	likely benign	24
11574	FBXW7	rs1381320045	SNP	missense variant	T/S	363	361	0.36	4	benign	0.003	21001	likely benign	21
11575	FBXW7	rs1381320045	SNP	missense variant	T/N	363	251	0.25	4	benign	0.003	22001	likely benign	22
11576	FBXW7	rs1014611334	SNP	missense variant	H/R	359	31	0.03	11	benign	0.01	23001	likely benign	23
11577	FBXW7	rs1245385235	SNP	missense variant	I/N	356	121	0.12	650	possibly damaging	0.649	25001	likely benign	25
11578	FBXW7	rs762013076	SNP	missense variant	I/V	347	501	0.5	1	benign	0	21001	likely benign	21
11579	FBXW7	rs949285009	SNP	missense variant	P/R	344	71	0.07	8	benign	0.007	23001	likely benign	23
11580	FBXW7	rs765495879	SNP	missense variant	I/T	342	601	0.6	20	benign	0.019	21001	likely benign	21

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