Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
Downloads

id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
4071	MAP3K1	rs762482085	SNP	missense variant	K/R	554	241	0.24	7	benign	0.006	19001	likely benign	19
4072	MAP3K1	rs763710987	SNP	missense variant	L/V	556	121	0.12	71	benign	0.07	13001	likely benign	13
4073	MAP3K1	rs1416272340	SNP	missense variant	A/T	557	31	0.03	990	probably damaging	0.989	27001	likely benign	27
4074	MAP3K1	rs899646671	SNP	missense variant	E/K	558	51	0.05	981	probably damaging	0.98	29001	likely benign	29
4075	MAP3K1	rs750985690	SNP	missense variant	P/A	559	11	0.01	995	probably damaging	0.994	24001	likely benign	24
4076	MAP3K1	rs1163509195	SNP	missense variant	I/F	561	1	0	732	possibly damaging	0.731	25001	likely benign	25
4077	MAP3K1	rs757294454	SNP	missense variant	Q/R	562	51	0.05	26	benign	0.025	25001	likely benign	25
4078	MAP3K1	rs1291113510	SNP	missense variant	M/V	566	251	0.25	36	benign	0.035	21001	likely benign	21
4079	MAP3K1	rs1453683035	SNP	missense variant	M/I	566	171	0.17	58	benign	0.057	23001	likely benign	23
4080	MAP3K1	rs779917428	SNP	missense variant	L/F	568	1	0	995	probably damaging	0.994	26001	likely benign	26

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