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
15311	SPEN	rs183490080	SNP	missense variant	R/C	3403	1	0	928	probably damaging	0.927	28001	likely benign	28
15312	SPEN	rs549789481	SNP	missense variant	R/H	3403	761	0.76	23	benign	0.022	22001	likely benign	22
15313	SPEN	rs1312396255	SNP	missense variant	A/T	3406	791	0.79	1	benign	0	5001	likely benign	5
15314	SPEN	rs777908524	SNP	missense variant	P/S	3408	521	0.52	1	benign	0	10001	likely benign	10
15315	SPEN	rs1225784551	SNP	missense variant	P/L	3408	11	0.01	16	benign	0.015	22001	likely benign	22
15316	SPEN	rs1316512980	SNP	missense variant	N/I	3410	1	0	11	benign	0.01	10001	likely benign	10
15317	SPEN	rs368639527	SNP	missense variant	R/K	3411	141	0.14	225	benign	0.224	21001	likely benign	21
15318	SPEN	rs368639527	SNP	missense variant	R/M	3411	1	0	846	possibly damaging	0.845	25001	likely benign	25
15319	SPEN	rs1339546186	SNP	missense variant	P/A	3413	471	0.47	1	benign	0	5001	likely benign	5
15320	SPEN	rs971901910	SNP	missense variant	P/L	3415	51	0.05	220	benign	0.219	22001	likely benign	22

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