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
3841	MAP3K1	rs748846611	SNP	missense variant	K/R	167	31	0.03	58	benign	0.057	24001	likely benign	24
3842	MAP3K1	rs1284046424	SNP	missense variant	L/V	170	1	0	273	benign	0.272	22001	likely benign	22
3843	MAP3K1	rs368874835	SNP	missense variant	G/E	172	1	0	974	probably damaging	0.973	26001	likely benign	26
3844	MAP3K1	rs368874835	SNP	missense variant	G/A	172	31	0.03	294	benign	0.293	23001	likely benign	23
3845	MAP3K1	rs1418554317	SNP	missense variant	M/V	176	1	0	825	possibly damaging	0.824	25001	likely benign	25
3846	MAP3K1	rs761784150	SNP	missense variant	M/T	176	61	0.06	886	possibly damaging	0.885	24001	likely benign	24
3847	MAP3K1	rs767390050	SNP	missense variant	R/G	179	1	0	988	probably damaging	0.987	27001	likely benign	27
3848	MAP3K1	rs767390050	SNP	missense variant	R/C	179	1	0	994	probably damaging	0.993	30001	likely deleterious	30
3849	MAP3K1	rs1446304905	SNP	missense variant	R/H	179	1	0	992	probably damaging	0.991	29001	likely benign	29
3850	MAP3K1	rs1380166875	SNP	missense variant	P/L	180	51	0.05	998	probably damaging	0.997	24001	likely benign	24

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