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
7671	KM2TC-MLL3	rs372781879	SNP	missense variant	Q/E	3301	11	0.01	915	probably damaging	0.914	24001	likely benign	24
7672	KM2TC-MLL3	rs1306664007	SNP	missense variant	S/I	3300	21	0.02	277	benign	0.276	18001	likely benign	18
7673	KM2TC-MLL3	rs1289446225	SNP	missense variant	S/G	3300	351	0.35	1	benign	0	11001	likely benign	11
7674	KM2TC-MLL3	rs1469113009	SNP	missense variant	P/L	3297	61	0.06	2	benign	0.001	18001	likely benign	18
7675	KM2TC-MLL3	rs376425355	SNP	missense variant	P/R	3296	11	0.01	300	benign	0.299	22001	likely benign	22
7676	KM2TC-MLL3	rs755114138	SNP	missense variant	T/A	3295	941	0.94	1	benign	0	1	likely benign	0
7677	KM2TC-MLL3	rs1185981122	SNP	missense variant	G/D	3293	11	0.01	691	possibly damaging	0.69	23001	likely benign	23
7678	KM2TC-MLL3	rs965835568	SNP	missense variant	P/L	3292	11	0.01	998	probably damaging	0.997	25001	likely benign	25
7679	KM2TC-MLL3	rs144248018	SNP	missense variant	P/L	3289	81	0.08	402	benign	0.401	22001	likely benign	22
7680	KM2TC-MLL3	rs151063714	SNP	missense variant	P/A	3288	211	0.21	14	benign	0.013	14001	likely benign	14

Left 767 768 769