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
11581	FBXW7	rs1247097813	SNP	missense variant	I/V	342	421	0.42	1	benign	0	19001	likely benign	19
11582	FBXW7	rs1485389861	SNP	missense variant	V/A	341	291	0.29	1	benign	0	22001	likely benign	22
11583	FBXW7	rs1184695126	SNP	missense variant	K/N	340	51	0.05	27	benign	0.026	23001	likely benign	23
11584	FBXW7	rs1185005670	SNP	missense variant	R/K	338	291	0.29	1	benign	0	22001	likely benign	22
11585	FBXW7	rs750480880	SNP	missense variant	K/Q	337	221	0.22	2	benign	0.001	22001	likely benign	22
11586	FBXW7	rs1046708929	SNP	missense variant	I/M	336	171	0.17	8	benign	0.007	19001	likely benign	19
11587	FBXW7	rs1207038641	SNP	missense variant	H/P	335	251	0.25	1	benign	0	22001	likely benign	22
11588	FBXW7	rs1183122092	SNP	missense variant	D/E	331	391	0.39	1	benign	0	18001	likely benign	18
11589	FBXW7	rs767438108	SNP	missense variant	I/F	330	141	0.14	69	benign	0.068	22001	likely benign	22
11590	FBXW7	rs767438108	SNP	missense variant	I/V	330	131	0.13	4	benign	0.003	22001	likely benign	22

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