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
5801	CDH1	rs1567504603	SNP	missense variant	S/I	162	51	0.05	186	benign	0.185	15001	likely benign	15
5802	CDH1	rs748783182	SNP	missense variant	C/S	163	11	0.01	739	possibly damaging	0.738	24001	likely benign	24
5803	CDH1	rs1064794230	SNP	missense variant	C/W	163	1	0	998	probably damaging	0.997	24001	likely benign	24
5804	CDH1	rs1555515224	SNP	missense variant	N/K	166	1	0	1001	probably damaging	1	23001	likely benign	23
5805	CDH1	rs769076258	SNP	missense variant	E/K	167	401	0.4	707	possibly damaging	0.706	23001	likely benign	23
5806	CDH1	rs1483883033	SNP	missense variant	K/R	168	1001	1	121	benign	0.12	15001	likely benign	15
5807	CDH1	rs1284865285	SNP	missense variant	P/S	170	11	0.01	851	possibly damaging	0.85	23001	likely benign	23
5808	CDH1	rs762388314	SNP	missense variant	F/I	171	1	0	967	probably damaging	0.966	25001	likely benign	25
5809	CDH1	rs772622109	SNP	missense variant	F/C	171	1	0	997	probably damaging	0.996	27001	likely benign	27
5810	CDH1	rs571581856	SNP	missense variant	N/K	174	1001	1	15	benign	0.014	1	likely benign	0

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