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
5871	CDH1	rs786203207	SNP	missense variant	I/T	225	151	0.15	919	probably damaging	0.918	22001	likely benign	22
5872	CDH1	rs1555515292	SNP	missense variant	A/V	226	121	0.12	40	benign	0.039	15001	likely benign	15
5873	CDH1	rs1064796018	SNP	missense variant	T/A	227	21	0.02	2	benign	0.001	17001	likely benign	17
5874	CDH1	rs1354439750	SNP	missense variant	T/I	229	481	0.48	8	benign	0.007	1	likely benign	0
5875	CDH1	rs1555515422	SNP	missense variant	S/C	232	21	0.02	987	probably damaging	0.986	26001	likely benign	26
5876	CDH1	rs1352098199	SNP	missense variant	H/Y	233	31	0.03	278	benign	0.277	23001	likely benign	23
5877	CDH1	rs115494727	SNP	missense variant	H/Q	233	21	0.02	676	possibly damaging	0.675	21001	likely benign	21
5878	CDH1	rs878854694	SNP	missense variant	A/T	234	11	0.01	1001	probably damaging	1	29001	likely benign	29
5879	CDH1	rs1377039383	SNP	missense variant	A/V	234	11	0.01	1001	probably damaging	1	27001	likely benign	27
5880	CDH1	rs730881664	SNP	missense variant	N/H	238	1	0	980	probably damaging	0.979	23001	likely benign	23

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