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
15271	SPEN	rs1333065783	SNP	missense variant	L/V	3351	241	0.24	433	benign	0.432	9001	likely benign	9
15272	SPEN	rs764860707	SNP	missense variant	P/S	3354	811	0.81	4	benign	0.003	1	likely benign	0
15273	SPEN	rs752417115	SNP	missense variant	Q/H	3355	11	0.01	846	possibly damaging	0.845	14001	likely benign	14
15274	SPEN	rs1162919224	SNP	missense variant	V/L	3357	261	0.26	1	benign	0	1001	likely benign	1
15275	SPEN	rs377740771	SNP	missense variant	S/T	3359	91	0.09	10	benign	0.009	1	likely benign	0
15276	SPEN	rs756610754	SNP	missense variant	A/T	3363	181	0.18	1	benign	0	8001	likely benign	8
15277	SPEN	rs756610754	SNP	missense variant	A/P	3363	51	0.05	2	benign	0.001	9001	likely benign	9
15278	SPEN	rs780471620	SNP	missense variant	A/V	3363	161	0.16	1	benign	0	5001	likely benign	5
15279	SPEN	rs998961195	SNP	missense variant	Q/H	3364	61	0.06	361	benign	0.36	1	likely benign	0
15280	SPEN	rs749647806	SNP	missense variant	P/S	3367	141	0.14	1	benign	0	10001	likely benign	10

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