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
12031	CBFB	rs547701828	SNP	missense variant	A/S	142	441	0.44	36	benign	0.035	22001	likely benign	22
12032	CBFB	rs774137566	SNP	missense variant	R/Q	147	371	0.37	449	possibly damaging	0.448	23001	likely benign	23
12033	CBFB	rs774137566	SNP	missense variant	R/P	147	121	0.12	665	possibly damaging	0.664	25001	likely benign	25
12034	CBFB	rs762321075	SNP	missense variant	R/S	148	151	0.15	988	probably damaging	0.987	25001	likely benign	25
12035	CBFB	rs1210173381	SNP	missense variant	R/G	149	1	0	988	probably damaging	0.987	31001	likely deleterious	31
12036	CBFB	rs547880442	SNP	missense variant	R/K	149	61	0.06	974	probably damaging	0.973	24001	likely benign	24
12037	CBFB	rs1277342356	SNP	missense variant	R/S	149	1	0	988	probably damaging	0.987	23001	likely benign	23
12038	CBFB	rs1467426352	SNP	missense variant	R/H	151	1	0	996	probably damaging	0.995	29001	likely benign	29
12039	CBFB	rs761036715	SNP	missense variant	E/K	152	71	0.07	151	benign	0.15	23001	likely benign	23
12040	CBFB	rs367668600	SNP	missense variant	R/I	156	31	0.03	997	probably damaging	0.996	28001	likely benign	28

Left 1203 1204 1205