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
28881	ATR	rs1266555685	SNP	missense variant	L/Q	769	1	0	999	probably damaging	0.998	24001	likely benign	24
28882	ATR	rs1489808838	SNP	missense variant	L/I	769	21	0.02	992	probably damaging	0.991	22001	likely benign	22
28883	ATR	rs530165257	SNP	missense variant	L/I	767	81	0.08	193	benign	0.192	16001	likely benign	16
28884	ATR	rs1238634482	SNP	missense variant	P/T	765	21	0.02	844	possibly damaging	0.843	22001	likely benign	22
28885	ATR	rs77208665	SNP	missense variant	K/E	764	61	0.06	396	benign	0.395	20001	likely benign	20
28886	ATR	rs1036040776	SNP	missense variant	V/I	762	671	0.67	1	benign	0	1	likely benign	0
28887	ATR	rs777729532	SNP	missense variant	S/A	761	211	0.21	113	benign	0.112	17001	likely benign	17
28888	ATR	rs140901705	SNP	missense variant	A/V	760	121	0.12	662	possibly damaging	0.661	19001	likely benign	19
28889	ATR	rs1403551625	SNP	missense variant	Q/H	757	231	0.23	79	benign	0.078	16001	likely benign	16
28890	ATR	rs749078940	SNP	missense variant	S/L	754	201	0.2	1	benign	0	16001	likely benign	16

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