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
13241	SPEN	rs1227508305	SNP	missense variant	M/V	404	71	0.07	39	benign	0.038	21001	likely benign	21
13242	SPEN	rs773963387	SNP	missense variant	Q/R	405	41	0.04	967	probably damaging	0.966	24001	likely benign	24
13243	SPEN	rs761057579	SNP	missense variant	E/K	407	31	0.03	967	probably damaging	0.966	29001	likely benign	29
13244	SPEN	rs1463367834	SNP	missense variant	E/D	407	231	0.23	280	benign	0.279	18001	likely benign	18
13245	SPEN	rs1399798498	SNP	missense variant	T/I	409	31	0.03	998	probably damaging	0.997	25001	likely benign	25
13246	SPEN	rs754406402	SNP	missense variant	I/V	412	541	0.54	1	benign	0	19001	likely benign	19
13247	SPEN	rs777234386	SNP	missense variant	R/H	423	11	0.01	999	probably damaging	0.998	29001	likely benign	29
13248	SPEN	rs938603695	SNP	missense variant	D/A	426	1	0	1000	probably damaging	0.999	28001	likely benign	28
13249	SPEN	rs760141792	SNP	missense variant	R/K	428	1	0	992	probably damaging	0.991	27001	likely benign	27
13250	SPEN	rs1262846873	SNP	missense variant	I/M	429	21	0.02	285	benign	0.284	22001	likely benign	22

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