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
16511	ESR1	rs1201514802	SNP	missense variant	G/D	57	561	0.56	662	possibly damaging	0.661	23001	likely benign	23
16512	ESR1	rs1199270277	SNP	missense variant	A/T	58	821	0.82	27	benign	0.026	21001	likely benign	21
16513	ESR1	rs1199270277	SNP	missense variant	A/S	58	1001	1	45	benign	0.044	19001	likely benign	19
16514	ESR1	rs1243016506	SNP	missense variant	A/G	58	241	0.24	2	benign	0.001	22001	likely benign	22
16515	ESR1	rs1180943277	SNP	missense variant	Y/H	60	151	0.15	978	probably damaging	0.977	27001	likely benign	27
16516	ESR1	rs1236724118	SNP	missense variant	Y/C	60	1	0	984	probably damaging	0.983	32001	likely deleterious	32
16517	ESR1	rs756751297	SNP	missense variant	N/D	63	831	0.83	187	benign	0.186	21001	likely benign	21
16518	ESR1	rs780595074	SNP	missense variant	N/S	63	1001	1	8	benign	0.007	17001	likely benign	17
16519	ESR1	rs1172047540	SNP	missense variant	A/T	65	111	0.11	994	probably damaging	0.993	25001	likely benign	25
16520	ESR1	rs1172047540	SNP	missense variant	A/P	65	1001	1	999	probably damaging	0.998	23001	likely benign	23

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