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
5131	ZNF217	rs746990012	SNP	missense variant	T/M	668	111	0.11	1	benign	0	1	likely benign	0
5132	ZNF217	rs546115875	SNP	missense variant	E/G	665	211	0.21	166	benign	0.165	13001	likely benign	13
5133	ZNF217	rs1393197465	SNP	missense variant	K/R	664	751	0.75	1	benign	0	1	likely benign	0
5134	ZNF217	rs370634538	SNP	missense variant	P/S	663	891	0.89	11	benign	0.01	5001	likely benign	5
5135	ZNF217	rs768555897	SNP	missense variant	S/R	662	361	0.36	26	benign	0.025	1	likely benign	0
5136	ZNF217	rs1204964480	SNP	missense variant	V/I	661	461	0.46	4	benign	0.003	3001	likely benign	3
5137	ZNF217	rs1488894032	SNP	missense variant	N/I	658	471	0.47	1	benign	0	1	likely benign	0
5138	ZNF217	rs1305256233	SNP	missense variant	N/D	658	501	0.5	8	benign	0.007	1	likely benign	0
5139	ZNF217	rs747768875	SNP	missense variant	S/R	654	531	0.53	2	benign	0.001	2001	likely benign	2
5140	ZNF217	rs769344360	SNP	missense variant	S/I	654	191	0.19	1	benign	0	6001	likely benign	6

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