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
28211	ATR	rs574382204	SNP	missense variant	T/A	2092	31	0.03	14	benign	0.013	22001	likely benign	22
28212	ATR	rs1270466103	SNP	missense variant	M/T	2090	1	0	597	possibly damaging	0.596	25001	likely benign	25
28213	ATR	rs1032148842	SNP	missense variant	R/Q	2089	1	0	963	probably damaging	0.962	31001	likely deleterious	31
28214	ATR	rs1480463477	SNP	missense variant	M/I	2087	11	0.01	693	possibly damaging	0.692	25001	likely benign	25
28215	ATR	rs757353909	SNP	missense variant	M/V	2087	1	0	598	possibly damaging	0.597	25001	likely benign	25
28216	ATR	rs1423459834	SNP	missense variant	I/V	2083	11	0.01	259	benign	0.258	23001	likely benign	23
28217	ATR	rs1183951151	SNP	missense variant	Y/H	2078	1	0	520	possibly damaging	0.519	27001	likely benign	27
28218	ATR	rs372864251	SNP	missense variant	L/V	2076	1	0	833	possibly damaging	0.832	24001	likely benign	24
28219	ATR	rs1282142308	SNP	missense variant	G/V	2073	1	0	977	probably damaging	0.976	26001	likely benign	26
28220	ATR	rs1330121617	SNP	missense variant	G/S	2073	61	0.06	916	probably damaging	0.915	24001	likely benign	24

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