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
28081	ATR	rs2229032	SNP	missense variant	R/Q	2425	231	0.23	1	benign	0	1	likely benign	0
28082	ATR	rs909033162	SNP	missense variant	K/R	2422	331	0.33	12	benign	0.011	21001	likely benign	21
28083	ATR	rs1211640581	SNP	missense variant	L/F	2421	71	0.07	994	probably damaging	0.993	23001	likely benign	23
28084	ATR	rs753611213	SNP	missense variant	K/N	2420	1	0	941	probably damaging	0.94	24001	likely benign	24
28085	ATR	rs756990664	SNP	missense variant	S/C	2418	21	0.02	410	benign	0.409	24001	likely benign	24
28086	ATR	rs1345846388	SNP	missense variant	P/Q	2412	11	0.01	835	possibly damaging	0.834	27001	likely benign	27
28087	ATR	rs1233586936	SNP	missense variant	M/I	2410	851	0.85	6	benign	0.005	17001	likely benign	17
28088	ATR	rs778835776	SNP	missense variant	R/H	2407	1	0	891	possibly damaging	0.89	27001	likely benign	27
28089	ATR	rs746049210	SNP	missense variant	R/C	2407	1	0	944	probably damaging	0.943	32001	likely deleterious	32
28090	ATR	rs758671096	SNP	missense variant	Y/C	2400	21	0.02	936	probably damaging	0.935	29001	likely benign	29

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