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
13711	SPEN	rs1299645944	SNP	missense variant	S/A	1152	231	0.23	1	benign	0	9001	likely benign	9
13712	SPEN	rs771410882	SNP	missense variant	E/K	1156	121	0.12	57	benign	0.056	22001	likely benign	22
13713	SPEN	rs78799629	SNP	missense variant	E/G	1157	1	0	716	possibly damaging	0.715	26001	likely benign	26
13714	SPEN	rs966208276	SNP	missense variant	I/V	1161	281	0.28	42	benign	0.041	19001	likely benign	19
13715	SPEN	rs1206861684	SNP	missense variant	H/Y	1165	261	0.26	16	benign	0.015	17001	likely benign	17
13716	SPEN	rs749550885	SNP	missense variant	T/M	1166	1	0	940	probably damaging	0.939	24001	likely benign	24
13717	SPEN	rs1309805749	SNP	missense variant	R/Q	1170	31	0.03	579	possibly damaging	0.578	25001	likely benign	25
13718	SPEN	rs1409348994	SNP	missense variant	R/C	1177	1	0	1000	probably damaging	0.999	26001	likely benign	26
13719	SPEN	rs761804754	SNP	missense variant	Q/R	1180	271	0.27	623	possibly damaging	0.622	23001	likely benign	23
13720	SPEN	rs1458311779	SNP	missense variant	Q/E	1181	1	0	139	benign	0.138	22001	likely benign	22

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