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
31501	MLH1	rs1241839317	SNP	missense variant	P/H	310	31	0.03	8	benign	0.007	19001	likely benign	19
31502	MLH1	rs63751153	SNP	missense variant	Q/E	311	1001	1	1	benign	0	2001	likely benign	2
31503	MLH1	rs104895000	SNP	missense variant	Q/P	311	331	0.33	1	benign	0	12001	likely benign	12
31504	MLH1	rs104895000	SNP	missense variant	Q/R	311	471	0.47	1	benign	0	10001	likely benign	10
31505	MLH1	rs775776362	SNP	missense variant	Q/H	311	141	0.14	171	benign	0.17	16001	likely benign	16
31506	MLH1	rs761006237	SNP	missense variant	A/V	312	361	0.36	2	benign	0.001	7001	likely benign	7
31507	MLH1	rs535470039	SNP	missense variant	I/V	313	421	0.42	1	benign	0	1	likely benign	0
31508	MLH1	rs535470039	SNP	missense variant	I/F	313	61	0.06	4	benign	0.003	1	likely benign	0
31509	MLH1	rs786201951	SNP	missense variant	I/S	313	811	0.81	1	benign	0	1	likely benign	0
31510	MLH1	rs63750766	SNP	missense variant	T/I	315	181	0.18	52	benign	0.051	9001	likely benign	9

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