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
20481	CCREBBP	rs1303431695	SNP	missense variant	P/R	1952	1	0	232	benign	0.231	23001	likely benign	23
20482	CCREBBP	rs1176184150	SNP	missense variant	Q/P	1950	341	0.34	463	possibly damaging	0.462	23001	likely benign	23
20483	CCREBBP	rs1380660032	SNP	missense variant	A/T	1949	651	0.65	8	benign	0.007	18001	likely benign	18
20484	CCREBBP	rs557611780	SNP	missense variant	P/L	1948	511	0.51	29	benign	0.028	22001	likely benign	22
20485	CCREBBP	rs1231016252	SNP	missense variant	P/S	1948	431	0.43	4	benign	0.003	19001	likely benign	19
20486	CCREBBP	rs577591403	SNP	missense variant	P/S	1947	111	0.11	7	benign	0.006	21001	likely benign	21
20487	CCREBBP	rs765600316	SNP	missense variant	P/L	1946	501	0.5	1	benign	0	21001	likely benign	21
20488	CCREBBP	rs765600316	SNP	missense variant	P/R	1946	251	0.25	11	benign	0.01	21001	likely benign	21
20489	CCREBBP	rs765600316	SNP	missense variant	P/Q	1946	621	0.62	1	benign	0	19001	likely benign	19
20490	CCREBBP	rs1321085895	SNP	missense variant	P/A	1946	421	0.42	1	benign	0	15001	likely benign	15

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