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
6081	CDH1	rs773441320	SNP	missense variant	N/S	417	861	0.86	16	benign	0.015	14001	likely benign	14
6082	CDH1	rs1555515902	SNP	missense variant	N/K	417	291	0.29	59	benign	0.058	4001	likely benign	4
6083	CDH1	rs1379626654	SNP	missense variant	D/A	418	11	0.01	855	possibly damaging	0.854	24001	likely benign	24
6084	CDH1	rs1057520936	SNP	missense variant	D/E	418	31	0.03	379	benign	0.378	16001	likely benign	16
6085	CDH1	rs878854677	SNP	missense variant	G/D	420	371	0.37	6	benign	0.005	8001	likely benign	8
6086	CDH1	rs747256664	SNP	missense variant	G/R	421	1	0	776	possibly damaging	0.775	17001	likely benign	17
6087	CDH1	rs786202027	SNP	missense variant	F/L	423	1	0	1001	probably damaging	1	18001	likely benign	18
6088	CDH1	rs1555515904	SNP	missense variant	V/A	424	411	0.41	6	benign	0.005	1	likely benign	0
6089	CDH1	rs570930882	SNP	missense variant	V/I	425	1001	1	28	benign	0.027	8001	likely benign	8
6090	CDH1	rs570930882	SNP	missense variant	V/L	425	31	0.03	454	possibly damaging	0.453	22001	likely benign	22

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