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
24971	MLL2	rs781460562	SNP	missense variant	A/T	2133	51	0.05	21	benign	0.02	18001	likely benign	18
24972	MLL2	rs770113503	SNP	missense variant	P/L	2132	21	0.02	374	benign	0.373	23001	likely benign	23
24973	MLL2	rs587778463	SNP	missense variant	T/I	2131	31	0.03	24	benign	0.023	23001	likely benign	23
24974	MLL2	rs587778463	SNP	missense variant	T/N	2131	71	0.07	126	benign	0.125	21001	likely benign	21
24975	MLL2	rs763310604	SNP	missense variant	T/A	2131	631	0.63	16	benign	0.015	6001	likely benign	6
24976	MLL2	rs763310604	SNP	missense variant	T/P	2131	341	0.34	1	benign	0	9001	likely benign	9
24977	MLL2	rs1218105017	SNP	missense variant	T/I	2130	131	0.13	32	benign	0.031	19001	likely benign	19
24978	MLL2	rs1232307242	SNP	missense variant	P/L	2129	1	0	36	benign	0.035	23001	likely benign	23
24979	MLL2	rs559685257	SNP	missense variant	P/S	2129	1	0	615	possibly damaging	0.614	25001	likely benign	25
24980	MLL2	rs1485524861	SNP	missense variant	S/N	2128	11	0.01	703	possibly damaging	0.702	24001	likely benign	24

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