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
14611	SPEN	rs770443691	SNP	missense variant	S/G	2416	131	0.13	7	benign	0.006	1001	likely benign	1
14612	SPEN	rs780855299	SNP	missense variant	V/F	2417	51	0.05	35	benign	0.034	5001	likely benign	5
14613	SPEN	rs1392141313	SNP	missense variant	E/K	2419	131	0.13	932	probably damaging	0.931	23001	likely benign	23
14614	SPEN	rs1333768300	SNP	missense variant	T/I	2421	21	0.02	980	probably damaging	0.979	22001	likely benign	22
14615	SPEN	rs745353021	SNP	missense variant	T/A	2423	431	0.43	1	benign	0	3001	likely benign	3
14616	SPEN	rs769345412	SNP	missense variant	K/R	2424	161	0.16	2	benign	0.001	7001	likely benign	7
14617	SPEN	rs1045264	SNP	missense variant	A/S	2425	171	0.17	16	benign	0.015	1001	likely benign	1
14618	SPEN	rs148508636	SNP	missense variant	S/F	2426	1	0	134	benign	0.133	16001	likely benign	16
14619	SPEN	rs370674242	SNP	missense variant	P/S	2428	501	0.5	95	benign	0.094	8001	likely benign	8
14620	SPEN	rs773388165	SNP	missense variant	P/S	2429	181	0.18	980	probably damaging	0.979	16001	likely benign	16

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