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
7921	KM2TC-MLL3	rs772095859	SNP	missense variant	T/A	2898	461	0.46	7	benign	0.006	1	likely benign	0
7922	KM2TC-MLL3	rs199939847	SNP	missense variant	S/F	2897	1	0	276	benign	0.275	20001	likely benign	20
7923	KM2TC-MLL3	rs758355940	SNP	missense variant	A/T	2896	81	0.08	1	benign	0	13001	likely benign	13
7924	KM2TC-MLL3	rs1484349722	SNP	missense variant	Q/R	2895	241	0.24	1	benign	0	2001	likely benign	2
7925	KM2TC-MLL3	rs1180489534	SNP	missense variant	V/I	2893	221	0.22	1	benign	0	3001	likely benign	3
7926	KM2TC-MLL3	rs1207158010	SNP	missense variant	N/I	2892	81	0.08	22	benign	0.021	7001	likely benign	7
7927	KM2TC-MLL3	rs1242846407	SNP	missense variant	N/D	2892	701	0.7	11	benign	0.01	1	likely benign	0
7928	KM2TC-MLL3	rs144267618	SNP	missense variant	S/T	2890	61	0.06	1	benign	0	1	likely benign	0
7929	KM2TC-MLL3	rs763198348	SNP	missense variant	S/R	2890	31	0.03	25	benign	0.024	4001	likely benign	4
7930	KM2TC-MLL3	rs368995188	SNP	missense variant	P/A	2889	421	0.42	1	benign	0	1	likely benign	0

Left 792 793 794