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
2781	GATA3	rs1164091515	SNP	missense variant	V/A	72	751	0.75	25	benign	0.024	22001	likely benign	22
2782	GATA3	rs755756354	SNP	missense variant	P/S	76	701	0.7	187	benign	0.186	22001	likely benign	22
2783	GATA3	rs1315804209	SNP	missense variant	P/L	76	31	0.03	503	possibly damaging	0.502	24001	likely benign	24
2784	GATA3	rs1325423656	SNP	missense variant	P/S	77	291	0.29	11	benign	0.01	22001	likely benign	22
2785	GATA3	rs1343882720	SNP	missense variant	P/L	77	21	0.02	16	benign	0.015	24001	likely benign	24
2786	GATA3	rs1004765920	SNP	missense variant	T/N	78	291	0.29	1	benign	0	22001	likely benign	22
2787	GATA3	rs1004765920	SNP	missense variant	T/I	78	181	0.18	10	benign	0.009	22001	likely benign	22
2788	GATA3	rs759839816	SNP	missense variant	G/R	81	11	0.01	178	benign	0.177	27001	likely benign	27
2789	GATA3	rs1460926411	SNP	missense variant	G/E	81	21	0.02	81	benign	0.08	15001	likely benign	15
2790	GATA3	rs764989707	SNP	missense variant	S/G	82	391	0.39	1	benign	0	22001	likely benign	22

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