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
16841	ESR1	rs1436999383	SNP	missense variant	E/K	587	51	0.05	673	possibly damaging	0.672	24001	likely benign	24
16842	ESR1	rs749325025	SNP	missense variant	E/G	587	1	0	826	possibly damaging	0.825	26001	likely benign	26
16843	ESR1	rs769007417	SNP	missense variant	A/E	588	1001	1	4	benign	0.003	8001	likely benign	8
16844	ESR1	rs1218237385	SNP	missense variant	E/D	589	241	0.24	106	benign	0.105	13001	likely benign	13
16845	ESR1	rs372267992	SNP	missense variant	G/D	590	101	0.1	4	benign	0.003	4001	likely benign	4
16846	ESR1	rs1343738218	SNP	missense variant	F/L	591	591	0.59	6	benign	0.005	15001	likely benign	15
16847	ESR1	rs748564686	SNP	missense variant	F/S	591	1	0	404	benign	0.403	23001	likely benign	23
16848	ESR1	rs772367364	SNP	missense variant	P/H	592	11	0.01	910	probably damaging	0.909	23001	likely benign	23
16849	ESR1	rs772367364	SNP	missense variant	P/L	592	11	0.01	689	possibly damaging	0.688	23001	likely benign	23
16850	ESR1	rs1199517689	SNP	missense variant	T/A	594	141	0.14	27	benign	0.026	14001	likely benign	14

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