ASRGL1

asparaginase and isoaspartyl peptidase 1

Summary

Enables asparaginase activity and beta-aspartyl-peptidase activity. Involved in asparagine catabolic process via L-aspartate. Located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]

Known Variants227 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2463822	11:62,103,420	T/G	—	—
rs3741245	11:62,105,441	T/C	—	benign
rs2134555728	11:62,105,453	A/G	—	uncertain significance
rs1186341508	11:62,105,462	G/A	—	uncertain significance
rs183580478	11:62,105,465	G/A	—	uncertain significance
rs2495146250	11:62,105,470	C/T	—	likely benign
rs143657589	11:62,105,473	C/T	—	benign
rs2134555857	11:62,105,476	C/T	—	likely benign
rs1453590652	11:62,105,479	C/T	—	likely benign
rs766321690	11:62,105,480	G/A	—	uncertain significance
rs574757273	11:62,105,483	G/T	—	uncertain significance
rs746830715	11:62,105,486	G/A	—	uncertain significance
rs752659253	11:62,105,496	C/G	—	uncertain significance
rs543873786	11:62,105,499	A/G	—	uncertain significance
rs994536412	11:62,105,505	G/A	—	uncertain significance
rs2134556097	11:62,105,516	G/A	—	uncertain significance
rs1945768203	11:62,105,519	C/T	—	uncertain significance
rs751865225	11:62,105,525	G/T	—	uncertain significance
rs1945768578	11:62,105,527	C/T	—	likely benign
rs1180230618	11:62,105,531	G/A	—	uncertain significance
rs781496593	11:62,105,534	A/G	—	uncertain significance
rs148079160	11:62,105,545	C/T	—	likely benign
rs115409110	11:62,105,546	G/A	—	benign
rs771674934	11:62,105,548	G/C	—	likely benign
rs371350994	11:62,105,549	G/A	—	uncertain significance
rs1300898047	11:62,105,560	C/T	—	likely benign
rs533515407	11:62,105,564	C/T	—	uncertain significance
rs1344055752	11:62,105,565	G/A	—	uncertain significance
rs765198534	11:62,105,579	G/A	—	uncertain significance
rs775564099	11:62,105,586	A/G	—	uncertain significance
rs1393599376	11:62,105,590	C/G	—	likely benign
rs751622412	11:62,105,605	C/G	—	likely benign
rs142016448	11:62,105,611	C/T	—	benign
rs145018428	11:62,105,612	C/G	—	uncertain significance
rs373959296	11:62,105,619	A/G	—	uncertain significance
rs2495147815	11:62,105,625	C/T	—	uncertain significance
rs1333545878	11:62,105,638	A/G	—	uncertain significance
rs2134556791	11:62,105,651	T/C	—	likely benign
rs1285925310	11:62,105,654	C/T	—	likely benign
rs951677	11:62,107,249	G/T	—	—
rs141938564	11:62,112,519	A/G	intron variant	—
rs183005648	11:62,115,053	C/T	intron variant	—
rs191756451	11:62,116,432	G/T	intron variant	—
rs763962209	11:62,123,779	A/G	—	uncertain significance
rs1260441603	11:62,123,796	G/C	—	uncertain significance
rs150970142	11:62,123,797	G/A	—	uncertain significance
rs1183773629	11:62,123,798	T/C	—	likely benign
rs551053676	11:62,123,800	G/A	—	uncertain significance
rs1946294756	11:62,123,806	C/T	—	uncertain significance
rs2134605766	11:62,123,810	C/T	—	likely benign
rs754181082	11:62,123,811	T/C	—	likely benign
rs140751884	11:62,123,816	C/A	—	uncertain significance
rs2495207725	11:62,123,820	A/G	—	uncertain significance
rs769362763	11:62,123,843	T/C	—	likely benign
rs779850075	11:62,123,845	G/T	—	uncertain significance
rs150459367	11:62,123,853	G/A	—	uncertain significance
rs2495208021	11:62,123,855	T/C	—	likely benign
rs774341469	11:62,123,861	A/C	—	uncertain significance
rs754950129	11:62,123,864	C/T	—	likely benign
rs570756428	11:62,123,865	C/T	—	likely benign
rs1946297115	11:62,123,866	T/A	—	uncertain significance
rs1463386799	11:62,123,873	A/G	—	likely benign
rs201870863	11:62,123,886	G/T	—	uncertain significance
rs754170218	11:62,123,888	A/G	—	likely benign
rs567867048	11:62,123,896	G/T	—	uncertain significance
rs2495208397	11:62,123,898	A/G	—	uncertain significance
rs2495208421	11:62,123,899	T/A	—	uncertain significance
rs1946298288	11:62,123,901	G/A	—	uncertain significance
rs1374698423	11:62,123,902	C/A	—	uncertain significance
rs2134606226	11:62,123,906	T/C	—	likely benign
rs756806363	11:62,123,912	T/G	—	uncertain significance
rs2495208653	11:62,123,920	C/A	—	uncertain significance
rs780890144	11:62,123,923	G/A	—	uncertain significance
rs2495208775	11:62,123,931	A/G	—	uncertain significance
rs779576068	11:62,123,933	G/A	—	uncertain significance
rs1946299666	11:62,123,934	G/T	—	uncertain significance
rs982873806	11:62,123,939	G/T	—	uncertain significance
rs376734611	11:62,123,942	A/T	—	uncertain significance
rs536519740	11:62,123,944	A/G	—	uncertain significance
rs778797548	11:62,123,945	T/C	—	uncertain significance
rs1946300526	11:62,123,955	G/A	—	likely benign
rs753478917	11:62,124,439	C/A	—	likely benign
rs754768361	11:62,124,441	C/A	—	likely benign
rs1946313166	11:62,124,443	T/C	—	likely benign
rs1415268492	11:62,124,450	C/T	—	likely benign
rs758277116	11:62,124,488	C/T	—	likely benign
rs370679289	11:62,124,493	C/T	—	uncertain significance
rs770975541	11:62,124,494	G/A	—	likely benign
rs2134608186	11:62,124,496	A/C	—	uncertain significance
rs75102382	11:62,124,500	T/C	—	benign
rs770171289	11:62,124,503	A/T	—	likely benign
rs934405766	11:62,124,504	G/A	—	uncertain significance
rs763414105	11:62,124,510	A/G	—	likely benign
rs200094029	11:62,124,513	G/C	—	likely benign
rs765843116	11:62,124,524	G/A	—	likely benign
rs141452891	11:62,124,532	G/A	—	uncertain significance
rs754580834	11:62,124,536	A/G	—	likely benign
rs2134608467	11:62,124,545	G/C	—	likely benign
rs752425276	11:62,124,554	A/G	—	likely benign
rs1001341003	11:62,124,557	C/T	—	likely benign

Showing 100 of 227 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.