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
9141	KM2TC-MLL3	rs776750473	SNP	missense variant	I/M	1303	121	0.12	216	benign	0.215	8001	likely benign	8
9142	KM2TC-MLL3	rs1230955155	SNP	missense variant	R/I	1300	161	0.16	992	probably damaging	0.991	24001	likely benign	24
9143	KM2TC-MLL3	rs1230955155	SNP	missense variant	R/T	1300	51	0.05	978	probably damaging	0.977	24001	likely benign	24
9144	KM2TC-MLL3	rs1261411890	SNP	missense variant	K/E	1299	1	0	981	probably damaging	0.98	26001	likely benign	26
9145	KM2TC-MLL3	rs1322825535	SNP	missense variant	K/E	1297	41	0.04	981	probably damaging	0.98	27001	likely benign	27
9146	KM2TC-MLL3	rs1268465923	SNP	missense variant	R/Q	1292	21	0.02	979	probably damaging	0.978	27001	likely benign	27
9147	KM2TC-MLL3	rs763465804	SNP	missense variant	S/N	1291	181	0.18	969	probably damaging	0.968	23001	likely benign	23
9148	KM2TC-MLL3	rs1174822708	SNP	missense variant	Q/R	1289	1	0	954	probably damaging	0.953	26001	likely benign	26
9149	KM2TC-MLL3	rs1345303559	SNP	missense variant	R/Q	1288	1	0	979	probably damaging	0.978	26001	likely benign	26
9150	KM2TC-MLL3	rs1301632462	SNP	missense variant	R/W	1288	1	0	994	probably damaging	0.993	28001	likely benign	28

Left 914 915 916