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
12481	CDNK2B	rs1475218156	SNP	missense variant	G/A	103	1	0	719	possibly damaging	0.718	25001	likely benign	25
12482	CDNK2B	rs1475218156	SNP	missense variant	G/E	103	21	0.02	433	benign	0.432	24001	likely benign	24
12483	CDNK2B	rs1425823622	SNP	missense variant	R/Q	101	441	0.44	97	benign	0.096	16001	likely benign	16
12484	CDNK2B	rs967713185	SNP	missense variant	R/W	101	1	0	880	possibly damaging	0.879	24001	likely benign	24
12485	CDNK2B	rs979009141	SNP	missense variant	H/L	100	711	0.71	4	benign	0.003	20001	likely benign	20
12486	CDNK2B	rs779087967	SNP	missense variant	V/M	98	21	0.02	23	benign	0.022	18001	likely benign	18
12487	CDNK2B	rs748001006	SNP	missense variant	T/M	95	11	0.01	996	probably damaging	0.995	29001	likely benign	29
12488	CDNK2B	rs1357609907	SNP	missense variant	T/S	95	1	0	926	probably damaging	0.925	28001	likely benign	28
12489	CDNK2B	rs758215089	SNP	missense variant	D/E	94	91	0.09	850	possibly damaging	0.849	23001	likely benign	23
12490	CDNK2B	rs917099997	SNP	missense variant	D/H	94	1	0	993	probably damaging	0.992	32001	likely deleterious	32

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