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
16531	ESR1	rs775435150	SNP	missense variant	G/S	74	1001	1	24	benign	0.023	14001	likely benign	14
16532	ESR1	rs775435150	SNP	missense variant	G/R	74	21	0.02	874	possibly damaging	0.873	23001	likely benign	23
16533	ESR1	rs775435150	SNP	missense variant	G/C	74	21	0.02	947	probably damaging	0.946	24001	likely benign	24
16534	ESR1	rs905397493	SNP	missense variant	Q/E	75	411	0.41	115	benign	0.114	19001	likely benign	19
16535	ESR1	rs746640340	SNP	missense variant	T/N	76	91	0.09	7	benign	0.006	15001	likely benign	15
16536	ESR1	rs746640340	SNP	missense variant	T/S	76	1001	1	4	benign	0.003	9001	likely benign	9
16537	ESR1	rs9340773	SNP	missense variant	G/S	77	1001	1	8	benign	0.007	16001	likely benign	16
16538	ESR1	rs9340773	SNP	missense variant	G/R	77	161	0.16	579	possibly damaging	0.578	23001	likely benign	23
16539	ESR1	rs767847192	SNP	missense variant	L/F	78	131	0.13	877	possibly damaging	0.876	22001	likely benign	22
16540	ESR1	rs1172645166	SNP	missense variant	P/A	79	601	0.6	1	benign	0	2001	likely benign	2

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