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
1721	ERBB2	rs1481595696	SNP	missense variant	D/H	382	271	0.27	4	benign	0.003	19001	likely benign	19
1722	ERBB2	rs751270411	SNP	missense variant	G/E	383	1	0	999	probably damaging	0.998	35001	likely deleterious	35
1723	ERBB2	rs753902259	SNP	missense variant	D/N	384	51	0.05	237	benign	0.236	23001	likely benign	23
1724	ERBB2	rs141116145	SNP	missense variant	A/D	386	141	0.14	2	benign	0.001	14001	likely benign	14
1725	ERBB2	rs141116145	SNP	missense variant	A/G	386	151	0.15	16	benign	0.015	14001	likely benign	14
1726	ERBB2	rs780881510	SNP	missense variant	N/H	388	91	0.09	54	benign	0.053	17001	likely benign	17
1727	ERBB2	rs750090147	SNP	missense variant	N/S	388	141	0.14	8	benign	0.007	4001	likely benign	4
1728	ERBB2	rs755701444	SNP	missense variant	A/T	390	101	0.1	84	benign	0.083	11001	likely benign	11
1729	ERBB2	rs587778264	SNP	missense variant	A/V	390	31	0.03	19	benign	0.018	11001	likely benign	11
1730	ERBB2	rs748700504	SNP	missense variant	P/L	391	11	0.01	732	possibly damaging	0.731	22001	likely benign	22

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