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
21561	CCREBBP	rs944810089	SNP	missense variant	A/G	167	371	0.37	19	benign	0.018	20001	likely benign	20
21562	CCREBBP	rs1242423773	SNP	missense variant	A/S	167	251	0.25	361	benign	0.36	17001	likely benign	17
21563	CCREBBP	rs374119348	SNP	missense variant	P/H	166	31	0.03	152	benign	0.151	23001	likely benign	23
21564	CCREBBP	rs760912343	SNP	missense variant	P/A	166	451	0.45	67	benign	0.066	20001	likely benign	20
21565	CCREBBP	rs369771502	SNP	missense variant	S/R	165	281	0.28	711	possibly damaging	0.71	23001	likely benign	23
21566	CCREBBP	rs1487619883	SNP	missense variant	S/T	165	321	0.32	536	possibly damaging	0.535	22001	likely benign	22
21567	CCREBBP	rs757321118	SNP	missense variant	A/V	162	731	0.73	23	benign	0.022	16001	likely benign	16
21568	CCREBBP	rs765754292	SNP	missense variant	L/R	161	21	0.02	729	possibly damaging	0.728	25001	likely benign	25
21569	CCREBBP	rs1175854793	SNP	missense variant	V/L	159	231	0.23	433	benign	0.432	21001	likely benign	21
21570	CCREBBP	rs758936976	SNP	missense variant	Q/L	156	11	0.01	881	possibly damaging	0.88	26001	likely benign	26

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