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
5701	CDH1	rs1064793867	SNP	missense variant	V/M	82	151	0.15	258	benign	0.257	14001	likely benign	14
5702	CDH1	rs1064793867	SNP	missense variant	V/L	82	141	0.14	171	benign	0.17	12001	likely benign	12
5703	CDH1	rs942284129	SNP	missense variant	V/G	82	11	0.01	346	benign	0.345	16001	likely benign	16
5704	CDH1	rs754388534	SNP	missense variant	T/I	84	381	0.38	78	benign	0.077	5001	likely benign	5
5705	CDH1	rs1555514427	SNP	missense variant	V/I	85	61	0.06	106	benign	0.105	17001	likely benign	17
5706	CDH1	rs878854688	SNP	missense variant	V/A	85	511	0.51	269	benign	0.268	18001	likely benign	18
5707	CDH1	rs1160169015	SNP	missense variant	K/R	86	181	0.18	32	benign	0.031	6001	likely benign	6
5708	CDH1	rs878854689	SNP	missense variant	R/S	87	11	0.01	77	benign	0.076	14001	likely benign	14
5709	CDH1	rs779313390	SNP	missense variant	P/T	88	131	0.13	689	possibly damaging	0.688	16001	likely benign	16
5710	CDH1	rs779313390	SNP	missense variant	P/S	88	491	0.49	310	benign	0.309	11001	likely benign	11

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