Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
Downloads

id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
27541	USP9X	rs1437371439	SNP	missense variant	M/I	2184	11	0.01	115	benign	0.114	24001	likely benign	24
27542	USP9X	rs1248098928	SNP	missense variant	N/S	2187	331	0.33	2	benign	0.001	21001	likely benign	21
27543	USP9X	rs1229265656	SNP	missense variant	G/V	2189	1	0	986	probably damaging	0.985		-
27544	USP9X	rs1265300035	SNP	missense variant	V/L	2190	881	0.88	1	benign	0	17001	likely benign	17
27545	USP9X	rs763663518	SNP	missense variant	A/S	2191	521	0.52	14	benign	0.013	20001	likely benign	20
27546	USP9X	rs943615606	SNP	missense variant	P/S	2202	41	0.04	294	benign	0.293	23001	likely benign	23
27547	USP9X	rs373269985	SNP	missense variant	A/T	2223	371	0.37	13	benign	0.012	22001	likely benign	22
27548	USP9X	rs1481990675	SNP	missense variant	A/V	2223	481	0.48	21	benign	0.02	22001	likely benign	22
27549	USP9X	rs760960427	SNP	missense variant	Y/C	2229	1	0	790	possibly damaging	0.789	27001	likely benign	27
27550	USP9X	rs777916760	SNP	missense variant	N/S	2240	41	0.04	1	benign	0	23001	likely benign	23

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