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
15041	SPEN	rs747592629	SNP	missense variant	P/L	3033	11	0.01	832	possibly damaging	0.831	22001	likely benign	22
15042	SPEN	rs771632933	SNP	missense variant	S/L	3035	31	0.03	1	benign	0	17001	likely benign	17
15043	SPEN	rs1310807352	SNP	missense variant	F/L	3036	1	0	959	probably damaging	0.958	22001	likely benign	22
15044	SPEN	rs777119046	SNP	missense variant	P/Q	3037	11	0.01	573	possibly damaging	0.572	23001	likely benign	23
15045	SPEN	rs376872398	SNP	missense variant	R/G	3038	1	0	916	probably damaging	0.915	23001	likely benign	23
15046	SPEN	rs1482118387	SNP	missense variant	S/N	3040	1	0	87	benign	0.086	22001	likely benign	22
15047	SPEN	rs549639590	SNP	missense variant	A/S	3046	1001	1	2	benign	0.001	1	likely benign	0
15048	SPEN	rs1252524754	SNP	missense variant	S/C	3047	11	0.01	982	probably damaging	0.981	23001	likely benign	23
15049	SPEN	rs763414538	SNP	missense variant	T/M	3048	1	0	347	benign	0.346	21001	likely benign	21
15050	SPEN	rs774692728	SNP	missense variant	A/V	3049	181	0.18	4	benign	0.003	15001	likely benign	15

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