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
12051	CBFB	rs1163696533	SNP	missense variant	T/S	175	591	0.59	6	benign	0.005	29001	likely benign	29
12052	CBFB	rs1179158329	SNP	missense variant	K/R	177	581	0.58	894	possibly damaging	0.893	29001	likely benign	29
12053	CBFB	rs547825285	SNP	missense variant	T/K	179	51	0.05	776	possibly damaging	0.775	21001	likely benign	21
12054	CBFB	rs763106753	SNP	missense variant	T/A	180	671	0.67	1	benign	0	7001	likely benign	7
12055	CBFB	rs1238322571	SNP	missense variant	T/R	180	31	0.03	52	benign	0.051	21001	likely benign	21
12056	CBFB	rs147332258	SNP	missense variant	P/T	182	1	0	902	possibly damaging	0.901	23001	likely benign	23
12057	MDM2	rs781195441	SNP	missense variant	S/F	3	1	0	992	probably damaging	0.991	28001	likely benign	28
12058	MDM2	rs577736495	SNP	missense variant	P/S	5	881	0.88	1	benign	0	13001	likely benign	13
12059	MDM2	rs201821879	SNP	missense variant	P/L	5	341	0.34	1	benign	0	22001	likely benign	22
12060	MDM2	rs1450828029	SNP	missense variant	T/A	6	201	0.2	982	probably damaging	0.981	23001	likely benign	23

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