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
12011	CBFB	rs1280921900	SNP	missense variant	P/A	100	331	0.33	952	probably damaging	0.951	23001	likely benign	23
12012	CBFB	rs201816595	SNP	missense variant	I/T	109	551	0.55	319	benign	0.318	22001	likely benign	22
12013	CBFB	rs536650594	SNP	missense variant	I/M	109	241	0.24	15	benign	0.014	15001	likely benign	15
12014	CBFB	rs767709685	SNP	missense variant	W/C	113	21	0.02	997	probably damaging	0.996	32001	likely deleterious	32
12015	CBFB	rs1397697429	SNP	missense variant	L/F	116	11	0.01	988	probably damaging	0.987	25001	likely benign	25
12016	CBFB	rs1334666202	SNP	missense variant	L/P	116	1	0	997	probably damaging	0.996	29001	likely benign	29
12017	CBFB	rs1361619079	SNP	missense variant	Q/H	117	131	0.13	2	benign	0.001	18001	likely benign	18
12018	CBFB	rs141277554	SNP	missense variant	M/T	122	351	0.35	890	possibly damaging	0.889	23001	likely benign	23
12019	CBFB	rs1434504398	SNP	missense variant	C/Y	124	111	0.11	20	benign	0.019	23001	likely benign	23
12020	CBFB	rs1434504398	SNP	missense variant	C/S	124	111	0.11	335	benign	0.334	23001	likely benign	23

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