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
1	id	Variant ID	Class	Conseq. Type	AA	AA coord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
2	TP53	rs1567535890	SNP	missense variant	H/Y	342			292	benign	0.291	2001	likely benign	2
3	TP53	rs764432741	SNP	missense variant	S/P	341			251	benign	0.25	1	likely benign	0
4	TP53	rs1378564917	SNP	missense variant	G/E	340			970	probably damaging	0.969	2001	likely benign	2
5	TP53	rs753947213	SNP	missense variant	G/R	340			980	probably damaging	0.979	4001	likely benign	4
6	TP53	rs554512119	SNP	missense variant	G/R	339			1	benign	0	1	likely benign	0
7	TP53	rs554512119	SNP	missense variant	G/S	339			1	benign	0	1	likely benign	0
8	TP53	rs144366923	SNP	missense variant	R/T	337	1	0	96	benign	0.095	1001	likely benign	1
9	TP53	rs1483708811	SNP	missense variant	P/L	335	131	0.13	1	benign	0	5001	likely benign	5
10	TP53	rs1486846348	SNP	missense variant	T/I	333	71	0.07	106	benign	0.105	2001	likely benign	2

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