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
11561	FBXW7	rs1560763656	SNP	missense variant	G/R	411	1	0	1001	probably damaging	1	27001	likely benign	27
11562	FBXW7	rs1560763689	SNP	missense variant	S/L	407	1	0	1000	probably damaging	0.999	32001	likely deleterious	32
11563	FBXW7	rs1390822119	SNP	missense variant	R/Q	393	21	0.02	130	benign	0.129	25001	likely benign	25
11564	FBXW7	rs1338105130	SNP	missense variant	L/V	387	1	0	978	probably damaging	0.977	23001	likely benign	23
11565	FBXW7	rs866269762	SNP	missense variant	T/K	385	1	0	1001	probably damaging	1	27001	likely benign	27
11566	FBXW7	rs1329859000	SNP	missense variant	G/A	378	261	0.26	1001	probably damaging	1	24001	likely benign	24
11567	FBXW7	rs1321798767	SNP	missense variant	V/A	375	101	0.1	383	benign	0.382	24001	likely benign	24
11568	FBXW7	rs937391131	SNP	missense variant	K/E	374	71	0.07	532	possibly damaging	0.531	27001	likely benign	27
11569	FBXW7	rs748952220	SNP	missense variant	P/R	373	151	0.15	896	possibly damaging	0.895	25001	likely benign	25
11570	FBXW7	rs761747465	SNP	missense variant	K/R	371	621	0.62	4	benign	0.003	19001	likely benign	19

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