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
1711	ERBB2	rs1324411001	SNP	missense variant	A/S	365	661	0.66	6	benign	0.005	13001	likely benign	13
1712	ERBB2	rs767588058	SNP	missense variant	G/R	366	11	0.01	888	possibly damaging	0.887	28001	likely benign	28
1713	ERBB2	rs1435728387	SNP	missense variant	G/A	366	11	0.01	563	possibly damaging	0.562	25001	likely benign	25
1714	ERBB2	rs1275492389	SNP	missense variant	I/M	370	1	0	1000	probably damaging	0.999	24001	likely benign	24
1715	ERBB2	rs1243660575	SNP	missense variant	F/C	371	171	0.17	989	probably damaging	0.988	25001	likely benign	25
1716	ERBB2	rs149567593	SNP	missense variant	F/L	371	601	0.6	565	possibly damaging	0.564	20001	likely benign	20
1717	ERBB2	rs752664566	SNP	missense variant	A/T	375	381	0.38	555	possibly damaging	0.554	24001	likely benign	24
1718	ERBB2	rs752664566	SNP	missense variant	A/S	375	521	0.52	407	benign	0.406	22001	likely benign	22
1719	ERBB2	rs758210687	SNP	missense variant	P/L	378	171	0.17	841	possibly damaging	0.84	22001	likely benign	22
1720	ERBB2	rs148068883	SNP	missense variant	S/G	380	501	0.5	822	possibly damaging	0.821	24001	likely benign	24

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