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
5401	ZNF217	rs760608608	SNP	missense variant	C/G	286	41	0.04	15	benign	0.014	22001	likely benign	22
5402	ZNF217	rs763868677	SNP	missense variant	R/T	285	121	0.12	1	benign	0	1	likely benign	0
5403	ZNF217	rs1427352375	SNP	missense variant	V/A	284	1001	1	1	benign	0	3001	likely benign	3
5404	ZNF217	rs1014353902	SNP	missense variant	V/I	284	51	0.05	4	benign	0.003	3001	likely benign	3
5405	ZNF217	rs776464913	SNP	missense variant	P/L	283	71	0.07	4	benign	0.003	10001	likely benign	10
5406	ZNF217	rs761427801	SNP	missense variant	P/T	283	11	0.01	15	benign	0.014	13001	likely benign	13
5407	ZNF217	rs897677828	SNP	missense variant	K/N	282	11	0.01	388	benign	0.387	20001	likely benign	20
5408	ZNF217	rs764907375	SNP	missense variant	K/R	281	261	0.26	4	benign	0.003	1001	likely benign	1
5409	ZNF217	rs750067497	SNP	missense variant	K/E	281	171	0.17	6	benign	0.005	7001	likely benign	7
5410	ZNF217	rs765812399	SNP	missense variant	G/V	280	341	0.34	1	benign	0	1	likely benign	0

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