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
2971	GATA3	rs765797932	SNP	missense variant	T/A	315	11	0.01	979	probably damaging	0.978	27001	likely benign	27
2972	GATA3	rs759044265	SNP	missense variant	A/V	318	1	0	986	probably damaging	0.985	27001	likely benign	27
2973	GATA3	rs764474372	SNP	missense variant	N/K	319	1	0	1001	probably damaging	1	25001	likely benign	25
2974	GATA3	rs751874713	SNP	missense variant	C/S	320	11	0.01	1001	probably damaging	1	29001	likely benign	29
2975	GATA3	rs757598199	SNP	missense variant	T/A	324	31	0.03	580	possibly damaging	0.579	24001	likely benign	24
2976	GATA3	rs964378376	SNP	missense variant	T/A	326	21	0.02	994	probably damaging	0.993	27001	likely benign	27
2977	GATA3	rs1211413464	SNP	missense variant	A/D	332	11	0.01	927	probably damaging	0.926	25001	likely benign	25
2978	GATA3	rs1211413464	SNP	missense variant	A/G	332	91	0.09	91	benign	0.09	22001	likely benign	22
2979	GATA3	rs756230531	SNP	missense variant	N/S	333	141	0.14	843	possibly damaging	0.842	21001	likely benign	21
2980	GATA3	rs1238949082	SNP	missense variant	D/E	335	571	0.57	954	probably damaging	0.953	16001	likely benign	16

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