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
22311	DNMT3A	rs751918466	SNP	missense variant	A/T	149	641	0.64	2	benign	0.001	18001	likely benign	18
22312	DNMT3A	rs1210750462	SNP	missense variant	A/E	147	461	0.46	4	benign	0.003	15001	likely benign	15
22313	DNMT3A	rs759826795	SNP	missense variant	A/T	145	571	0.57	1	benign	0	17001	likely benign	17
22314	DNMT3A	rs745432645	SNP	missense variant	R/Q	143	351	0.35	1	benign	0	21001	likely benign	21
22315	DNMT3A	rs1449714685	SNP	missense variant	G/D	142	531	0.53	31	benign	0.03	19001	likely benign	19
22316	DNMT3A	rs1310435543	SNP	missense variant	E/Q	141	191	0.19	7	benign	0.006	21001	likely benign	21
22317	DNMT3A	rs1310158529	SNP	missense variant	T/I	138	81	0.08	2	benign	0.001	18001	likely benign	18
22318	DNMT3A	rs1310158529	SNP	missense variant	T/N	138	21	0.02	1	benign	0	20001	likely benign	20
22319	DNMT3A	rs1423789971	SNP	missense variant	C/S	137	171	0.17	588	possibly damaging	0.587	23001	likely benign	23
22320	DNMT3A	rs1322950644	SNP	missense variant	G/S	135	141	0.14	935	probably damaging	0.934	23001	likely benign	23

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