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
4441	MAP3K1	rs1408304086	SNP	missense variant	N/I	1036	51	0.05	1	benign	0	22001	likely benign	22
4442	MAP3K1	rs377648645	SNP	missense variant	D/H	1038	1	0	621	possibly damaging	0.62	26001	likely benign	26
4443	MAP3K1	rs148803468	SNP	missense variant	S/P	1039	551	0.55	1	benign	0	19001	likely benign	19
4444	MAP3K1	rs1444422239	SNP	missense variant	S/L	1039	421	0.42	1	benign	0	20001	likely benign	20
4445	MAP3K1	rs761299133	SNP	missense variant	K/I	1041	1	0	500	possibly damaging	0.499	25001	likely benign	25
4446	MAP3K1	rs1345704990	SNP	missense variant	S/P	1043	1	0	987	probably damaging	0.986	27001	likely benign	27
4447	MAP3K1	rs766945040	SNP	missense variant	S/Y	1043	21	0.02	992	probably damaging	0.991	25001	likely benign	25
4448	MAP3K1	rs755413206	SNP	missense variant	T/I	1047	1	0	992	probably damaging	0.991	25001	likely benign	25
4449	MAP3K1	rs1561200313	SNP	missense variant	R/G	1050	1	0	978	probably damaging	0.977	25001	likely benign	25
4450	MAP3K1	rs1273847896	SNP	missense variant	R/T	1050	1	0	978	probably damaging	0.977	26001	likely benign	26

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