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
8561	KM2TC-MLL3	rs769437118	SNP	missense variant	P/T	2097	41	0.04	173	benign	0.172	20001	likely benign	20
8562	KM2TC-MLL3	rs1262981837	SNP	missense variant	Q/H	2096	181	0.18	13	benign	0.012	14001	likely benign	14
8563	KM2TC-MLL3	rs1191511092	SNP	missense variant	Y/C	2094	1	0	817	possibly damaging	0.816	25001	likely benign	25
8564	KM2TC-MLL3	rs558139040	SNP	missense variant	P/L	2093	1	0	27	benign	0.026	23001	likely benign	23
8565	KM2TC-MLL3	rs558139040	SNP	missense variant	P/Q	2093	21	0.02	124	benign	0.123	22001	likely benign	22
8566	KM2TC-MLL3	rs140719911	SNP	missense variant	D/V	2092	1	0	193	benign	0.192	23001	likely benign	23
8567	KM2TC-MLL3	rs140719911	SNP	missense variant	D/G	2092	11	0.01	19	benign	0.018	23001	likely benign	23
8568	KM2TC-MLL3	rs773701046	SNP	missense variant	N/S	2088	591	0.59	2	benign	0.001	1	likely benign	0
8569	KM2TC-MLL3	rs574167397	SNP	missense variant	N/H	2088	1	0	260	benign	0.259	15001	likely benign	15
8570	KM2TC-MLL3	rs1259700034	SNP	missense variant	H/R	2087	11	0.01	556	possibly damaging	0.555	23001	likely benign	23

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