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
4391	MAP3K1	rs939394998	SNP	missense variant	L/F	978	171	0.17	1	benign	0	4001	likely benign	4
4392	MAP3K1	rs746481448	SNP	missense variant	M/T	979	201	0.2	1	benign	0	2001	likely benign	2
4393	MAP3K1	rs1421356880	SNP	missense variant	M/I	979	101	0.1	1	benign	0	13001	likely benign	13
4394	MAP3K1	rs1421356880	SNP	missense variant	M/I	979	101	0.1	1	benign	0	13001	likely benign	13
4395	MAP3K1	rs565036596	SNP	missense variant	F/L	980	241	0.24	4	benign	0.003	8001	likely benign	8
4396	MAP3K1	rs770325439	SNP	missense variant	A/G	982	91	0.09	1	benign	0	12001	likely benign	12
4397	MAP3K1	rs1163745945	SNP	missense variant	S/L	984	291	0.29	108	benign	0.107	17001	likely benign	17
4398	MAP3K1	rs776591269	SNP	missense variant	P/S	986	101	0.1	2	benign	0.001	11001	likely benign	11
4399	MAP3K1	rs745800039	SNP	missense variant	S/T	988	251	0.25	1	benign	0	6001	likely benign	6
4400	MAP3K1	rs1326307145	SNP	missense variant	S/F	988	1	0	47	benign	0.046	18001	likely benign	18

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