AIMP2

aminoacyl tRNA synthetase complex interacting multifunctional protein 2

Summary

The protein encoded by this gene is part of the aminoacyl-tRNA synthetase complex, which contains nine different aminoacyl-tRNA synthetases and three non-enzymatic factors. The encoded protein is one of the non-enzymatic factors and is required for assembly and stability of the complex. [provided by RefSeq, May 2016]

Known Variants111 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs139842556	7:6,049,010	G/C	—	likely benign
rs1786347539	7:6,049,025	G/C	—	benign
rs145891242	7:6,049,037	C/G	—	uncertain significance
rs768787708	7:6,049,040	C/T	—	uncertain significance
rs774238548	7:6,049,044	G/A	—	uncertain significance
rs140169208	7:6,049,051	G/A	—	benign
rs766798963	7:6,049,055	C/T	—	uncertain significance
rs145382336	7:6,049,057	C/T	—	likely benign
rs201425558	7:6,049,063	C/T	—	likely benign
rs147658637	7:6,049,068	A/G	—	likely pathogenic
rs1786358808	7:6,049,069	C/A	—	pathogenic
rs756064767	7:6,049,075	C/T	—	likely benign
rs762176789	7:6,049,077	C/G	—	uncertain significance
rs780037791	7:6,049,081	C/G	—	uncertain significance
rs200865484	7:6,049,087	C/A	—	uncertain significance
rs200362634	7:6,049,088	G/T	—	likely benign
rs759928476	7:6,049,092	G/A	—	uncertain significance
rs373875101	7:6,049,095	G/A	—	uncertain significance
rs6977072	7:6,049,103	C/G	—	benign
rs753777297	7:6,049,108	G/T	—	likely benign
rs566052179	7:6,049,111	G/C	—	likely benign
rs747245459	7:6,049,113	G/C	—	uncertain significance
rs771332190	7:6,049,114	C/T	—	likely benign
rs1448273730	7:6,049,120	C/G	—	likely benign
rs746270222	7:6,049,121	C/T	—	uncertain significance
rs775895677	7:6,049,123	C/A	—	uncertain significance
rs2536738764	7:6,049,129	G/A	—	uncertain significance
rs750066868	7:6,049,140	G/T	—	likely benign
rs865834861	7:6,049,141	G/A	—	likely benign
rs766156266	7:6,049,142	G/C	—	likely benign
rs753828694	7:6,049,143	G/C	—	likely benign
rs376793759	7:6,054,767	G/C	—	benign
rs2128877989	7:6,054,777	G/A	—	uncertain significance
rs778920772	7:6,054,796	T/C	—	uncertain significance
rs1290887880	7:6,054,797	G/A	—	likely benign
rs577935179	7:6,054,813	C/T	—	uncertain significance
rs190724823	7:6,054,814	G/A	—	uncertain significance
rs140850823	7:6,054,834	C/T	—	conflicting classifications of pathogenicity
rs776388344	7:6,054,854	T/A	—	benign
rs765088234	7:6,054,867	C/T	—	uncertain significance
rs2536810020	7:6,054,897	G/A	—	uncertain significance
rs61751884	7:6,054,911	C/T	—	benign
rs775979886	7:6,054,912	A/G	—	uncertain significance
rs2536810189	7:6,054,918	A/T	—	uncertain significance
rs368845750	7:6,054,925	C/T	—	uncertain significance
rs1052534772	7:6,054,927	G/T	—	uncertain significance
rs764132138	7:6,054,953	T/C	—	likely benign
rs754061405	7:6,054,960	G/T	—	uncertain significance
rs6979676	7:6,054,987	G/A	—	benign
rs1787115101	7:6,057,453	G/A	—	likely benign
rs775788927	7:6,057,460	A/C	—	uncertain significance
rs764368950	7:6,057,467	T/C	—	uncertain significance
rs145256692	7:6,057,477	C/A	—	uncertain significance
rs747974072	7:6,057,485	C/T	—	uncertain significance
rs769933568	7:6,057,503	C/T	—	uncertain significance
rs137867185	7:6,057,504	C/T	—	likely benign
rs946176280	7:6,057,521	G/A	—	uncertain significance
rs774693908	7:6,057,522	G/A	—	likely benign
rs549852720	7:6,057,544	G/A	—	benign
rs2536824128	7:6,057,549	G/A	—	likely benign
rs534008494	7:6,057,555	G/A	—	likely benign
rs1787125039	7:6,057,561	C/T	—	likely benign
rs75895975	7:6,057,563	C/T	—	uncertain significance
rs61735883	7:6,057,564	G/T	—	likely benign
rs545201082	7:6,057,570	C/G	—	benign
rs1787127140	7:6,057,577	A/G	—	uncertain significance
rs931014900	7:6,057,579	G/C	—	uncertain significance
rs374110509	7:6,057,582	C/T	—	likely benign
rs34525431	7:6,057,598	C/A	—	benign
rs1787129648	7:6,057,603	G/A	—	likely benign
rs141537839	7:6,057,611	G/T	—	uncertain significance
rs542587504	7:6,057,625	A/C	—	uncertain significance
rs766723249	7:6,057,635	G/A	—	uncertain significance
rs929422782	7:6,057,681	G/A	—	uncertain significance
rs748822585	7:6,062,931	C/G	—	uncertain significance
rs869312968	7:6,062,932	A/G	—	pathogenic
rs776366708	7:6,062,937	C/T	—	uncertain significance
rs767064905	7:6,062,944	G/A	—	likely benign
rs11544566	7:6,062,981	G/A	—	uncertain significance
rs1787583537	7:6,062,983	A/G	—	likely benign
rs746283944	7:6,062,986	C/T	—	likely benign
rs749728733	7:6,062,997	T/C	—	uncertain significance
rs377482895	7:6,063,002	C/T	—	uncertain significance
rs150887968	7:6,063,003	G/A	—	uncertain significance
rs2536857516	7:6,063,013	C/G	—	uncertain significance
rs369386259	7:6,063,032	C/G	—	uncertain significance
rs139398981	7:6,063,036	A/G	—	uncertain significance
rs1310790068	7:6,063,039	C/T	—	uncertain significance
rs575274304	7:6,063,042	T/C	—	uncertain significance
rs764803060	7:6,063,046	C/T	—	likely benign
rs2536858033	7:6,063,050	A/G	—	uncertain significance
rs1787596232	7:6,063,056	A/G	—	uncertain significance
rs1787596576	7:6,063,057	T/C	—	uncertain significance
rs140208111	7:6,063,078	C/T	—	uncertain significance
rs1360732124	7:6,063,101	A/T	—	uncertain significance
rs767430426	7:6,063,119	G/A	—	uncertain significance
rs145632958	7:6,063,129	G/A	—	uncertain significance
rs1250422075	7:6,063,135	T/C	—	uncertain significance
rs997976538	7:6,063,162	G/A	—	uncertain significance
rs746501522	7:6,063,166	C/T	—	likely benign

Showing 100 of 111 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.