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
26991	USP9X	rs1304318647	SNP	missense variant	D/G	37	161	0.16	25	benign	0.024	22001	likely benign	22
26992	USP9X	rs755870817	SNP	missense variant	S/F	43	91	0.09	16	benign	0.015	22001	likely benign	22
26993	USP9X	rs149866601	SNP	missense variant	P/R	44	121	0.12	132	benign	0.131	22001	likely benign	22
26994	USP9X	rs149866601	SNP	missense variant	P/L	44	151	0.15	11	benign	0.01	22001	likely benign	22
26995	USP9X	rs760972686	SNP	missense variant	P/L	48	21	0.02	1	benign	0	23001	likely benign	23
26996	USP9X	rs866511878	SNP	missense variant	A/G	56	271	0.27	1	benign	0	19001	likely benign	19
26997	USP9X	rs866511878	SNP	missense variant	A/V	56	221	0.22	1	benign	0	19001	likely benign	19
26998	USP9X	rs1384577833	SNP	missense variant	P/A	58	261	0.26	1	benign	0	16001	likely benign	16
26999	USP9X	rs1569160145	SNP	missense variant	D/E	62	541	0.54	1	benign	0	13001	likely benign	13
27000	USP9X	rs1263301936	SNP	missense variant	P/T	65	201	0.2	551	possibly damaging	0.55	22001	likely benign	22

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