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
24201	MLL2	rs538335897	SNP	missense variant	R/G	3087	1	0	42	benign	0.041	22001	likely benign	22
24202	MLL2	rs1467406954	SNP	missense variant	R/Q	3082	31	0.03	49	benign	0.048	23001	likely benign	23
24203	MLL2	rs988895659	SNP	missense variant	R/W	3082	1	0	929	probably damaging	0.928	27001	likely benign	27
24204	MLL2	rs767316622	SNP	missense variant	N/H	3077	1	0	895	possibly damaging	0.894	24001	likely benign	24
24205	MLL2	rs1174956128	SNP	missense variant	S/T	3075	71	0.07	629	possibly damaging	0.628	23001	likely benign	23
24206	MLL2	rs760565311	SNP	missense variant	L/M	3072	1	0	999	probably damaging	0.998	24001	likely benign	24
24207	MLL2	rs794727574	SNP	missense variant	R/K	3071	51	0.05	821	possibly damaging	0.82	22001	likely benign	22
24208	MLL2	rs765308296	SNP	missense variant	N/S	3067	141	0.14	160	benign	0.159	21001	likely benign	21
24209	MLL2	rs1381757467	SNP	missense variant	I/T	3065	11	0.01	445	benign	0.444	23001	likely benign	23
24210	MLL2	rs1474773103	SNP	missense variant	K/R	3063	1	0	995	probably damaging	0.994	26001	likely benign	26

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