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
27571	USP9X	rs1230275240	SNP	missense variant	C/S	2307	721	0.72	2	benign	0.001	21001	likely benign	21
27572	USP9X	rs778609510	SNP	missense variant	F/L	2313	61	0.06	16	benign	0.015	17001	likely benign	17
27573	USP9X	rs771978688	SNP	missense variant	L/H	2321	1	0	907	possibly damaging	0.906	27001	likely benign	27
27574	USP9X	rs768106392	SNP	missense variant	Y/F	2327	371	0.37	4	benign	0.003	21001	likely benign	21
27575	USP9X	rs756203778	SNP	missense variant	R/W	2334	1	0	86	benign	0.085	24001	likely benign	24
27576	USP9X	rs1182060907	SNP	missense variant	Y/C	2336	1	0	115	benign	0.114	24001	likely benign	24
27577	USP9X	rs1313600621	SNP	missense variant	L/F	2344	1	0	60	benign	0.059	21001	likely benign	21
27578	USP9X	rs978873138	SNP	missense variant	L/V	2345	51	0.05	14	benign	0.013	22001	likely benign	22
27579	USP9X	rs1569203086	SNP	missense variant	H/P	2353	81	0.08	643	possibly damaging	0.642	24001	likely benign	24
27580	USP9X	rs969515565	SNP	missense variant	I/V	2355	61	0.06	66	benign	0.065	21001	likely benign	21

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