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
961	MYC	rs775427980	SNP	missense variant	S/T	229	651	0.65	1	benign	0	5001	likely benign	5
962	MYC	rs1476455361	SNP	missense variant	A/T	230	231	0.23	1	benign	0	13001	likely benign	13
963	MYC	rs544792311	SNP	missense variant	A/V	230	201	0.2	1	benign	0	16001	likely benign	16
964	MYC	rs1020933770	SNP	missense variant	S/P	232	221	0.22	14	benign	0.013	24001	likely benign	24
965	MYC	rs147506213	SNP	missense variant	P/T	233	211	0.21	2	benign	0.001	1	likely benign	0
966	MYC	rs147506213	SNP	missense variant	P/A	233	271	0.27	1	benign	0	1	likely benign	0
967	MYC	rs147506213	SNP	missense variant	P/S	233	321	0.32	1	benign	0	1	likely benign	0
968	MYC	rs1221550924	SNP	missense variant	P/Q	233	181	0.18	105	benign	0.104	19001	likely benign	19
969	MYC	rs1221550924	SNP	missense variant	P/L	233	111	0.11	1	benign	0	20001	likely benign	20
970	MYC	rs765003654	SNP	missense variant	L/V	239	541	0.54	377	benign	0.376	23001	likely benign	23

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