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
23321	MLL2	rs1441362256	SNP	missense variant	P/L	4287	361	0.36	58	benign	0.057	18001	likely benign	18
23322	MLL2	rs750203743	SNP	missense variant	P/S	4287	251	0.25	6	benign	0.005	17001	likely benign	17
23323	MLL2	rs750203743	SNP	missense variant	P/T	4287	91	0.09	58	benign	0.057	17001	likely benign	17
23324	MLL2	rs1365424828	SNP	missense variant	P/L	4286	291	0.29	1	benign	0	20001	likely benign	20
23325	MLL2	rs893293173	SNP	missense variant	G/V	4285	1	0	671	possibly damaging	0.67	24001	likely benign	24
23326	MLL2	rs749164970	SNP	missense variant	Q/R	4284	1	0	22	benign	0.021	23001	likely benign	23
23327	MLL2	rs768584961	SNP	missense variant	P/L	4283	21	0.02	12	benign	0.011	23001	likely benign	23
23328	MLL2	rs768584961	SNP	missense variant	P/R	4283	11	0.01	18	benign	0.017	23001	likely benign	23
23329	MLL2	rs1020472849	SNP	missense variant	R/L	4282	11	0.01	7	benign	0.006	22001	likely benign	22
23330	MLL2	rs1020472849	SNP	missense variant	R/Q	4282	201	0.2	441	benign	0.44	20001	likely benign	20

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