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
14891	SPEN	rs779271032	SNP	missense variant	P/L	2797	1	0	37	benign	0.036	20001	likely benign	20
14892	SPEN	rs772466830	SNP	missense variant	A/V	2798	501	0.5	60	benign	0.059	13001	likely benign	13
14893	SPEN	rs140025266	SNP	missense variant	A/T	2800	1001	1	1	benign	0	1	likely benign	0
14894	SPEN	rs367966477	SNP	missense variant	A/V	2800	21	0.02	24	benign	0.023	19001	likely benign	19
14895	SPEN	rs777036247	SNP	missense variant	G/D	2801	51	0.05	944	probably damaging	0.943	23001	likely benign	23
14896	SPEN	rs1275384688	SNP	missense variant	S/L	2802	1	0	119	benign	0.118	22001	likely benign	22
14897	SPEN	rs769982439	SNP	missense variant	A/V	2804	1	0	108	benign	0.107	21001	likely benign	21
14898	SPEN	rs762890376	SNP	missense variant	G/R	2805	1	0	946	probably damaging	0.945	25001	likely benign	25
14899	SPEN	rs1335827333	SNP	missense variant	G/E	2805	1	0	884	possibly damaging	0.883	25001	likely benign	25
14900	SPEN	rs764040616	SNP	missense variant	R/C	2807	1	0	998	probably damaging	0.997	26001	likely benign	26

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