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
26061	MLL2	rs368472158	SNP	missense variant	R/L	688	11	0.01	13	benign	0.012	21001	likely benign	21
26062	MLL2	rs368472158	SNP	missense variant	R/H	688	91	0.09	1	benign	0	17001	likely benign	17
26063	MLL2	rs371076182	SNP	missense variant	R/C	688	91	0.09	166	benign	0.165	20001	likely benign	20
26064	MLL2	rs745659904	SNP	missense variant	A/T	686	121	0.12	1	benign	0	19001	likely benign	19
26065	MLL2	rs1484438278	SNP	missense variant	S/Y	681	11	0.01	426	benign	0.425	23001	likely benign	23
26066	MLL2	rs202185563	SNP	missense variant	T/M	680	261	0.26	2	benign	0.001	4001	likely benign	4
26067	MLL2	rs1488924024	SNP	missense variant	T/P	680	31	0.03	1	benign	0	14001	likely benign	14
26068	MLL2	rs773307440	SNP	missense variant	P/S	679	31	0.03	2	benign	0.001	21001	likely benign	21
26069	MLL2	rs1184175230	SNP	missense variant	S/P	678	201	0.2	1	benign	0	13001	likely benign	13
26070	MLL2	rs759891414	SNP	missense variant	P/L	674	131	0.13	1	benign	0	21001	likely benign	21

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