Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
Downloads

id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
20971	CCREBBP	rs375938207	SNP	missense variant	E/D	1012	361	0.36	1	benign	0	8001	likely benign	8
20972	CCREBBP	rs139896431	SNP	missense variant	P/L	1010	101	0.1	12	benign	0.011	22001	likely benign	22
20973	CCREBBP	rs139896431	SNP	missense variant	P/H	1010	51	0.05	238	benign	0.237	22001	likely benign	22
20974	CCREBBP	rs1283546321	SNP	missense variant	P/T	1010	431	0.43	1	benign	0	12001	likely benign	12
20975	CCREBBP	rs141734994	SNP	missense variant	D/Y	1009	1	0	1	benign	0	23001	likely benign	23
20976	CCREBBP	rs141734994	SNP	missense variant	D/N	1009	71	0.07	25	benign	0.024	22001	likely benign	22
20977	CCREBBP	rs774653315	SNP	missense variant	E/D	1007	261	0.26	226	benign	0.225	14001	likely benign	14
20978	CCREBBP	rs1317506171	SNP	missense variant	T/S	1006	541	0.54	1	benign	0	2001	likely benign	2
20979	CCREBBP	rs1317506171	SNP	missense variant	T/P	1006	171	0.17	1	benign	0	8001	likely benign	8
20980	CCREBBP	rs746265426	SNP	missense variant	E/D	1004	311	0.31	900	possibly damaging	0.899	17001	likely benign	17

Left 2097 2098 2099