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
13511	SPEN	rs775491800	SNP	missense variant	S/N	853	61	0.06	7	benign	0.006	16001	likely benign	16
13512	SPEN	rs1487428602	SNP	missense variant	C/F	854	151	0.15	1	benign	0	10001	likely benign	10
13513	SPEN	rs763596246	SNP	missense variant	N/H	855	61	0.06	460	possibly damaging	0.459	23001	likely benign	23
13514	SPEN	rs142778574	SNP	missense variant	N/K	855	221	0.22	55	benign	0.054	17001	likely benign	17
13515	SPEN	rs1211306704	SNP	missense variant	S/G	858	111	0.11	96	benign	0.095	21001	likely benign	21
13516	SPEN	rs932050686	SNP	missense variant	S/N	858	91	0.09	15	benign	0.014	19001	likely benign	19
13517	SPEN	rs767038690	SNP	missense variant	K/E	861	51	0.05	13	benign	0.012	23001	likely benign	23
13518	SPEN	rs754324744	SNP	missense variant	A/G	862	91	0.09	2	benign	0.001	19001	likely benign	19
13519	SPEN	rs1190587572	SNP	missense variant	K/R	864	51	0.05	979	probably damaging	0.978	23001	likely benign	23
13520	SPEN	rs1234686133	SNP	missense variant	G/V	866	1	0	938	probably damaging	0.937	25001	likely benign	25

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