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
28011	ATR	rs758432141	SNP	missense variant	D/N	2629	431	0.43	996	probably damaging	0.995	23001	likely benign	23
28012	ATR	rs1279843589	SNP	missense variant	A/V	2627	1	0	998	probably damaging	0.997	29001	likely benign	29
28013	ATR	rs112027460	SNP	missense variant	A/S	2627	61	0.06	964	probably damaging	0.963	23001	likely benign	23
28014	ATR	rs374127772	SNP	missense variant	Y/H	2622	361	0.36	16	benign	0.015	22001	likely benign	22
28015	ATR	rs781420658	SNP	missense variant	V/M	2620	1	0	1001	probably damaging	1	26001	likely benign	26
28016	ATR	rs1034620994	SNP	missense variant	P/L	2613	11	0.01	991	probably damaging	0.99	29001	likely benign	29
28017	ATR	rs1349108610	SNP	missense variant	R/K	2608	1001	1	6	benign	0.005	18001	likely benign	18
28018	ATR	rs1315255360	SNP	missense variant	N/K	2607	11	0.01	915	probably damaging	0.914	23001	likely benign	23
28019	ATR	rs199948706	SNP	missense variant	R/Q	2606	21	0.02	73	benign	0.072	23001	likely benign	23
28020	ATR	rs771519566	SNP	missense variant	K/R	2604	121	0.12	294	benign	0.293	23001	likely benign	23

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