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
6881	KM2TC-MLL3	rs1388655093	SNP	missense variant	E/A	4376	1	0	412	benign	0.411	24001	likely benign	24
6882	KM2TC-MLL3	rs573014663	SNP	missense variant	P/S	4374	61	0.06	964	probably damaging	0.963	24001	likely benign	24
6883	KM2TC-MLL3	rs1057522023	SNP	missense variant	P/S	4373	321	0.32	943	probably damaging	0.942	23001	likely benign	23
6884	KM2TC-MLL3	rs1195009464	SNP	missense variant	K/E	4372	101	0.1	68	benign	0.067	17001	likely benign	17
6885	KM2TC-MLL3	rs750098046	SNP	missense variant	T/K	4370	31	0.03	59	benign	0.058	22001	likely benign	22
6886	KM2TC-MLL3	rs755732520	SNP	missense variant	G/R	4369	11	0.01	232	benign	0.231	23001	likely benign	23
6887	KM2TC-MLL3	rs1249814377	SNP	missense variant	I/N	4366	1	0	693	possibly damaging	0.692	25001	likely benign	25
6888	KM2TC-MLL3	rs767968866	SNP	missense variant	V/L	4365	11	0.01	704	possibly damaging	0.703	24001	likely benign	24
6889	KM2TC-MLL3	rs767968866	SNP	missense variant	V/I	4365	61	0.06	234	benign	0.233	20001	likely benign	20
6890	KM2TC-MLL3	rs373479151	SNP	missense variant	I/T	4364	1	0	992	probably damaging	0.991	26001	likely benign	26

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