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
24881	MLL2	rs587783724	SNP	missense variant	A/S	2214	201	0.2	46	benign	0.045	1	likely benign	0
24882	MLL2	rs587783724	SNP	missense variant	A/P	2214	331	0.33	244	benign	0.243	1	likely benign	0
24883	MLL2	rs587783724	SNP	missense variant	A/T	2214	521	0.52	1	benign	0	1	likely benign	0
24884	MLL2	rs368767696	SNP	missense variant	G/V	2213	31	0.03	187	benign	0.186	17001	likely benign	17
24885	MLL2	rs368767696	SNP	missense variant	G/D	2213	11	0.01	187	benign	0.186	17001	likely benign	17
24886	MLL2	rs750666025	SNP	missense variant	L/V	2212	211	0.21	8	benign	0.007	9001	likely benign	9
24887	MLL2	rs201190869	SNP	missense variant	P/L	2210	51	0.05	1	benign	0	14001	likely benign	14
24888	MLL2	rs201190869	SNP	missense variant	P/Q	2210	111	0.11	113	benign	0.112	13001	likely benign	13
24889	MLL2	rs1324674144	SNP	missense variant	P/S	2210	101	0.1	1	benign	0	8001	likely benign	8
24890	MLL2	rs747613578	SNP	missense variant	A/V	2207	321	0.32	1	benign	0	1	likely benign	0

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