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
28171	ATR	rs1337844230	SNP	missense variant	K/R	2166	71	0.07	77	benign	0.076	23001	likely benign	23
28172	ATR	rs1288613889	SNP	missense variant	A/T	2165	11	0.01	449	possibly damaging	0.448	25001	likely benign	25
28173	ATR	rs1164077204	SNP	missense variant	I/V	2163	41	0.04	453	possibly damaging	0.452	24001	likely benign	24
28174	ATR	rs1281243044	SNP	missense variant	E/D	2162	521	0.52	13	benign	0.012	18001	likely benign	18
28175	ATR	rs538022321	SNP	missense variant	M/V	2161	261	0.26	32	benign	0.031	20001	likely benign	20
28176	ATR	rs765977826	SNP	missense variant	V/F	2158	111	0.11	102	benign	0.101	19001	likely benign	19
28177	ATR	rs202193482	SNP	missense variant	D/N	2154	371	0.37	8	benign	0.007	21001	likely benign	21
28178	ATR	rs747991579	SNP	missense variant	H/Y	2153	91	0.09	2	benign	0.001	18001	likely benign	18
28179	ATR	rs1170670205	SNP	missense variant	H/P	2151	1	0	946	probably damaging	0.945	27001	likely benign	27
28180	ATR	rs1470834016	SNP	missense variant	R/Q	2148	1	0	920	probably damaging	0.919	27001	likely benign	27

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