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
25921	MLL2	rs748254982	SNP	missense variant	Q/H	827	111	0.11	1	benign	0	1	likely benign	0
25922	MLL2	rs1325574684	SNP	missense variant	Q/R	827	661	0.66	1	benign	0	1	likely benign	0
25923	MLL2	rs542972001	SNP	missense variant	P/R	826	1	0	249	benign	0.248	14001	likely benign	14
25924	MLL2	rs542972001	SNP	missense variant	P/H	826	1	0	398	benign	0.397	14001	likely benign	14
25925	MLL2	rs766963404	SNP	missense variant	P/S	826	91	0.09	89	benign	0.088	6001	likely benign	6
25926	MLL2	rs766963404	SNP	missense variant	P/A	826	31	0.03	24	benign	0.023	8001	likely benign	8
25927	MLL2	rs1202698255	SNP	missense variant	S/F	825	1	0	284	benign	0.283	17001	likely benign	17
25928	MLL2	rs200528183	SNP	missense variant	L/F	824	1	0	329	benign	0.328	1001	likely benign	1
25929	MLL2	rs1188737662	SNP	missense variant	P/S	822	21	0.02	1	benign	0	9001	likely benign	9
25930	MLL2	rs1263065363	SNP	missense variant	E/K	820	81	0.08	1	benign	0	15001	likely benign	15

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