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
1511	ERBB2	rs1187611727	SNP	missense variant	L/F	49	51	0.05	852	possibly damaging	0.851	23001	likely benign	23
1512	ERBB2	rs1390107974	SNP	missense variant	Q/R	51	231	0.23	1	benign	0	20001	likely benign	20
1513	ERBB2	rs1220384939	SNP	missense variant	Q/H	51	41	0.04	1	benign	0	21001	likely benign	21
1514	ERBB2	rs140441229	SNP	missense variant	Q/R	57	21	0.02	856	possibly damaging	0.855	26001	likely benign	26
1515	ERBB2	rs1298421770	SNP	missense variant	G/E	58	291	0.29	913	probably damaging	0.912	24001	likely benign	24
1516	ERBB2	rs1332501526	SNP	missense variant	L/V	60	1	0	1001	probably damaging	1	23001	likely benign	23
1517	ERBB2	rs766186178	SNP	missense variant	E/Q	61	1	0	1001	probably damaging	1	27001	likely benign	27
1518	ERBB2	rs1013215187	SNP	missense variant	L/V	62	101	0.1	49	benign	0.048	21001	likely benign	21
1519	ERBB2	rs753655456	SNP	missense variant	T/I	63	1	0	1001	probably damaging	1	25001	likely benign	25
1520	ERBB2	rs1364385133	SNP	missense variant	P/L	66	281	0.28	38	benign	0.037	19001	likely benign	19

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