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
18631	KDM6A	rs1163288010	SNP	missense variant	C/G	293	1	0	963	probably damaging	0.962	31001	likely deleterious	31
18632	KDM6A	rs755266795	SNP	missense variant	S/A	295	401	0.4	872	possibly damaging	0.871	23001	likely benign	23
18633	KDM6A	rs777683511	SNP	missense variant	I/V	311	211	0.21	744	possibly damaging	0.743	23001	likely benign	23
18634	KDM6A	rs749434836	SNP	missense variant	A/T	316	1	0	988	probably damaging	0.987	27001	likely benign	27
18635	KDM6A	rs771046931	SNP	missense variant	T/I	320	21	0.02	992	probably damaging	0.991	25001	likely benign	25
18636	KDM6A	rs1397939870	SNP	missense variant	D/V	348	1	0	997	probably damaging	0.996	26001	likely benign	26
18637	KDM6A	rs1313792775	SNP	missense variant	H/L	349	11	0.01	949	probably damaging	0.948	25001	likely benign	25
18638	KDM6A	rs756591426	SNP	missense variant	A/T	352	81	0.08	200	benign	0.199	23001	likely benign	23
18639	KDM6A	rs1281139041	SNP	missense variant	T/I	360	541	0.54	995	probably damaging	0.994	22001	likely benign	22
18640	KDM6A	rs778404068	SNP	missense variant	S/F	364	1	0	993	probably damaging	0.992	25001	likely benign	25

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