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
3811	MAP3K1	rs1433829054	SNP	missense variant	S/L	127	551	0.55	1	benign	0	14001	likely benign	14
3812	MAP3K1	rs1252128480	SNP	missense variant	V/M	128	141	0.14	86	benign	0.085	15001	likely benign	15
3813	MAP3K1	rs1431311260	SNP	missense variant	A/V	129	351	0.35	132	benign	0.131	16001	likely benign	16
3814	MAP3K1	rs557606535	SNP	missense variant	D/N	132	81	0.08	957	probably damaging	0.956	23001	likely benign	23
3815	MAP3K1	rs557606535	SNP	missense variant	D/H	132	21	0.02	991	probably damaging	0.99	25001	likely benign	25
3816	MAP3K1	rs1441612510	SNP	missense variant	S/G	133	91	0.09	8	benign	0.007	22001	likely benign	22
3817	MAP3K1	rs945114075	SNP	missense variant	S/R	133	61	0.06	1	benign	0	22001	likely benign	22
3818	MAP3K1	rs773710793	SNP	missense variant	A/T	141	31	0.03	957	probably damaging	0.956	25001	likely benign	25
3819	MAP3K1	rs1324275241	SNP	missense variant	E/D	142	511	0.51	1	benign	0	18001	likely benign	18
3820	MAP3K1	rs1051553256	SNP	missense variant	G/R	144	271	0.27	1	benign	0	20001	likely benign	20

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