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
14111	SPEN	rs537211881	SNP	missense variant	E/K	1792	121	0.12	1	benign	0	20001	likely benign	20
14112	SPEN	rs75807604	SNP	missense variant	P/S	1795	471	0.47	4	benign	0.003	3001	likely benign	3
14113	SPEN	rs1463606926	SNP	missense variant	E/A	1796	21	0.02	886	possibly damaging	0.885	24001	likely benign	24
14114	SPEN	rs1331883564	SNP	missense variant	P/S	1799	161	0.16	40	benign	0.039	14001	likely benign	14
14115	SPEN	rs1172317666	SNP	missense variant	P/A	1800	261	0.26	25	benign	0.024	13001	likely benign	13
14116	SPEN	rs1381948969	SNP	missense variant	P/L	1800	381	0.38	37	benign	0.036	4001	likely benign	4
14117	SPEN	rs755913099	SNP	missense variant	A/V	1801	681	0.68	4	benign	0.003	14001	likely benign	14
14118	SPEN	rs748930885	SNP	missense variant	D/Y	1804	1	0	348	benign	0.347	23001	likely benign	23
14119	SPEN	rs768230840	SNP	missense variant	D/E	1804	221	0.22	37	benign	0.036	8001	likely benign	8
14120	SPEN	rs778550249	SNP	missense variant	E/K	1806	11	0.01	142	benign	0.141	23001	likely benign	23

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