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
25161	MLL2	rs759354387	SNP	missense variant	L/I	1875	1	0	968	probably damaging	0.967	24001	likely benign	24
25162	MLL2	rs1296651659	SNP	missense variant	S/C	1873	31	0.03	892	possibly damaging	0.891	25001	likely benign	25
25163	MLL2	rs1369797487	SNP	missense variant	S/A	1873	131	0.13	179	benign	0.178	21001	likely benign	21
25164	MLL2	rs1369797487	SNP	missense variant	S/P	1873	701	0.7	6	benign	0.005	20001	likely benign	20
25165	MLL2	rs752658829	SNP	missense variant	S/N	1872	1	0	589	possibly damaging	0.588	24001	likely benign	24
25166	MLL2	rs762856028	SNP	missense variant	S/G	1872	31	0.03	485	possibly damaging	0.484	24001	likely benign	24
25167	MLL2	rs767630148	SNP	missense variant	L/F	1871	1	0	992	probably damaging	0.991	26001	likely benign	26
25168	MLL2	rs886049481	SNP	missense variant	T/I	1865	11	0.01	289	benign	0.288	23001	likely benign	23
25169	MLL2	rs750400711	SNP	missense variant	P/S	1863	81	0.08	995	probably damaging	0.994	24001	likely benign	24
25170	MLL2	rs1213998643	SNP	missense variant	K/N	1862	141	0.14	615	possibly damaging	0.614	22001	likely benign	22

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