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
15291	SPEN	rs375688033	SNP	missense variant	G/C	3378	1	0	467	possibly damaging	0.466	18001	likely benign	18
15292	SPEN	rs376476096	SNP	missense variant	S/N	3382	181	0.18	10	benign	0.009	16001	likely benign	16
15293	SPEN	rs1328669494	SNP	missense variant	K/T	3384	1	0	943	probably damaging	0.942	26001	likely benign	26
15294	SPEN	rs1228800333	SNP	missense variant	M/L	3385	411	0.41	1	benign	0	17001	likely benign	17
15295	SPEN	rs942125013	SNP	missense variant	M/I	3385	271	0.27	1	benign	0	17001	likely benign	17
15296	SPEN	rs1282973614	SNP	missense variant	P/L	3386	1	0	967	probably damaging	0.966	26001	likely benign	26
15297	SPEN	rs1205802663	SNP	missense variant	V/M	3388	101	0.1	929	probably damaging	0.928	24001	likely benign	24
15298	SPEN	rs528449671	SNP	missense variant	S/C	3389	1	0	974	probably damaging	0.973	25001	likely benign	25
15299	SPEN	rs1485569757	SNP	missense variant	A/S	3392	251	0.25	536	possibly damaging	0.535	23001	likely benign	23
15300	SPEN	rs1255647665	SNP	missense variant	A/V	3392	231	0.23	67	benign	0.066	23001	likely benign	23

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