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
13551	SPEN	rs1325016087	SNP	missense variant	T/A	907	351	0.35	1	benign	0	1	likely benign	0
13552	SPEN	rs1404197854	SNP	missense variant	T/I	907	21	0.02	48	benign	0.047	14001	likely benign	14
13553	SPEN	rs200414729	SNP	missense variant	K/T	909	91	0.09	995	probably damaging	0.994	22001	likely benign	22
13554	SPEN	rs200414729	SNP	missense variant	K/I	909	11	0.01	998	probably damaging	0.997	23001	likely benign	23
13555	SPEN	rs1296493092	SNP	missense variant	Q/R	915	1	0	680	possibly damaging	0.679	23001	likely benign	23
13556	SPEN	rs1437811812	SNP	missense variant	L/I	917	421	0.42	24	benign	0.023	10001	likely benign	10
13557	SPEN	rs527854339	SNP	missense variant	Q/E	918	351	0.35	51	benign	0.05	14001	likely benign	14
13558	SPEN	rs757565246	SNP	missense variant	V/A	919	561	0.56	1	benign	0	6001	likely benign	6
13559	SPEN	rs781407526	SNP	missense variant	S/A	920	511	0.51	2	benign	0.001	14001	likely benign	14
13560	SPEN	rs1229346868	SNP	missense variant	Q/H	921	201	0.2	7	benign	0.006	7001	likely benign	7

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