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
20471	CCREBBP	rs868301787	SNP	missense variant	E/K	1965	761	0.76	84	benign	0.083	17001	likely benign	17
20472	CCREBBP	rs867327595	SNP	missense variant	R/P	1964	101	0.1	113	benign	0.112	20001	likely benign	20
20473	CCREBBP	rs867327595	SNP	missense variant	R/H	1964	31	0.03	154	benign	0.153	22001	likely benign	22
20474	CCREBBP	rs1278592398	SNP	missense variant	R/C	1964	11	0.01	271	benign	0.27	23001	likely benign	23
20475	CCREBBP	rs1052651750	SNP	missense variant	E/K	1963	1	0	139	benign	0.138	22001	likely benign	22
20476	CCREBBP	rs759839179	SNP	missense variant	R/P	1960	61	0.06	325	benign	0.324	20001	likely benign	20
20477	CCREBBP	rs759839179	SNP	missense variant	R/Q	1960	231	0.23	82	benign	0.081	18001	likely benign	18
20478	CCREBBP	rs772270271	SNP	missense variant	R/W	1960	11	0.01	452	possibly damaging	0.451	22001	likely benign	22
20479	CCREBBP	rs986406817	SNP	missense variant	A/V	1958	651	0.65	6	benign	0.005	16001	likely benign	16
20480	CCREBBP	rs1170288988	SNP	missense variant	A/S	1954	31	0.03	143	benign	0.142	22001	likely benign	22

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