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
21131	CCREBBP	rs187842756	SNP	missense variant	L/V	843	211	0.21	316	benign	0.315	20001	likely benign	20
21132	CCREBBP	rs970929591	SNP	missense variant	Q/P	842	181	0.18	67	benign	0.066	22001	likely benign	22
21133	CCREBBP	rs1335692925	SNP	missense variant	L/P	836	311	0.31	485	possibly damaging	0.484	23001	likely benign	23
21134	CCREBBP	rs759041100	SNP	missense variant	M/I	835	301	0.3	29	benign	0.028	17001	likely benign	17
21135	CCREBBP	rs767051018	SNP	missense variant	M/V	835	341	0.34	48	benign	0.047	19001	likely benign	19
21136	CCREBBP	rs1205756499	SNP	missense variant	N/S	834	461	0.46	295	benign	0.294	17001	likely benign	17
21137	CCREBBP	rs200474872	SNP	missense variant	L/F	833	71	0.07	107	benign	0.106	16001	likely benign	16
21138	CCREBBP	rs755952440	SNP	missense variant	P/H	832	1	0	242	benign	0.241	24001	likely benign	24
21139	CCREBBP	rs376047316	SNP	missense variant	P/S	832	571	0.57	1	benign	0	16001	likely benign	16
21140	CCREBBP	rs1400600409	SNP	missense variant	P/R	830	11	0.01	974	probably damaging	0.973	25001	likely benign	25

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