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
1701	ERBB2	rs1263270004	SNP	missense variant	E/G	348	1001	1	1	benign	0	23001	likely benign	23
1702	ERBB2	rs559242250	SNP	missense variant	L/F	350	191	0.19	405	benign	0.404	17001	likely benign	17
1703	ERBB2	rs775972596	SNP	missense variant	R/Q	351	651	0.65	6	benign	0.005	22001	likely benign	22
1704	ERBB2	rs763367024	SNP	missense variant	E/G	352	971	0.97	1	benign	0	21001	likely benign	21
1705	ERBB2	rs769082334	SNP	missense variant	V/M	353	81	0.08	351	benign	0.35	19001	likely benign	19
1706	ERBB2	rs769082334	SNP	missense variant	V/L	353	121	0.12	10	benign	0.009	17001	likely benign	17
1707	ERBB2	rs1197249604	SNP	missense variant	V/A	353	861	0.86	4	benign	0.003	1001	likely benign	1
1708	ERBB2	rs918747921	SNP	missense variant	R/W	354	21	0.02	644	possibly damaging	0.643	25001	likely benign	25
1709	ERBB2	rs1385831939	SNP	missense variant	T/A	357	1	0	51	benign	0.05	23001	likely benign	23
1710	ERBB2	rs373474372	SNP	missense variant	N/I	360	21	0.02	897	possibly damaging	0.896	27001	likely benign	27

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