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
2131	ERBB2	rs748800582	SNP	missense variant	S/F	1078	21	0.02	178	benign	0.177	22001	likely benign	22
2132	ERBB2	rs1038581447	SNP	missense variant	E/K	1079	911	0.91	179	benign	0.178	19001	likely benign	19
2133	ERBB2	rs772604432	SNP	missense variant	A/T	1081	221	0.22	2	benign	0.001	16001	likely benign	16
2134	ERBB2	rs772604432	SNP	missense variant	A/P	1081	151	0.15	2	benign	0.001	16001	likely benign	16
2135	ERBB2	rs1449896791	SNP	missense variant	S/A	1083	331	0.33	16	benign	0.015	21001	likely benign	21
2136	ERBB2	rs200796676	SNP	missense variant	D/N	1084	651	0.65	181	benign	0.18	22001	likely benign	22
2137	ERBB2	rs200796676	SNP	missense variant	D/Y	1084	11	0.01	644	possibly damaging	0.643	26001	likely benign	26
2138	ERBB2	rs779955263	SNP	missense variant	D/E	1084	781	0.78	66	benign	0.065	17001	likely benign	17
2139	ERBB2	rs1208224755	SNP	missense variant	V/I	1085	531	0.53	68	benign	0.067	19001	likely benign	19
2140	ERBB2	rs1193632490	SNP	missense variant	G/S	1088	491	0.49	4	benign	0.003	21001	likely benign	21

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