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
7321	KM2TC-MLL3	rs537682415	SNP	missense variant	E/G	3726	51	0.05	38	benign	0.037	18001	likely benign	18
7322	KM2TC-MLL3	rs779566409	SNP	missense variant	E/Q	3726	421	0.42	2	benign	0.001	6001	likely benign	6
7323	KM2TC-MLL3	rs143269206	SNP	missense variant	T/P	3725	471	0.47	1	benign	0	6001	likely benign	6
7324	KM2TC-MLL3	rs1054637537	SNP	missense variant	E/D	3724	221	0.22	12	benign	0.011	6001	likely benign	6
7325	KM2TC-MLL3	rs115580901	SNP	missense variant	A/P	3723	151	0.15	4	benign	0.003	1	likely benign	0
7326	KM2TC-MLL3	rs115580901	SNP	missense variant	A/T	3723	491	0.49	4	benign	0.003	1	likely benign	0
7327	KM2TC-MLL3	rs748055632	SNP	missense variant	L/M	3720	41	0.04	389	benign	0.388	14001	likely benign	14
7328	KM2TC-MLL3	rs372143700	SNP	missense variant	K/I	3719	1	0	641	possibly damaging	0.64	23001	likely benign	23
7329	KM2TC-MLL3	rs777577307	SNP	missense variant	K/E	3719	11	0.01	412	benign	0.411	22001	likely benign	22
7330	KM2TC-MLL3	rs746124863	SNP	missense variant	I/R	3718	41	0.04	4	benign	0.003	15001	likely benign	15

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