ASPG
asparaginase
Summary
Predicted to enable acyltransferase activity, transferring groups other than amino-acyl groups; asparaginase activity; and lysophospholipase activity. Predicted to be involved in asparagine metabolic process and phospholipid metabolic process. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1028966572 | 14:104,552,126 | C/T | — | likely benign |
| rs2511338924 | 14:104,559,021 | T/A | — | uncertain significance |
| rs767603910 | 14:104,559,031 | G/C | — | uncertain significance |
| rs201325717 | 14:104,559,048 | G/A | — | likely benign |
| rs988442636 | 14:104,559,050 | G/A | — | uncertain significance |
| rs776839328 | 14:104,559,880 | C/G | — | uncertain significance |
| rs748633326 | 14:104,561,877 | G/C | — | uncertain significance |
| rs759241387 | 14:104,561,887 | A/G | — | uncertain significance |
| rs200023747 | 14:104,561,935 | C/T | — | uncertain significance |
| rs968089615 | 14:104,563,912 | A/C | — | uncertain significance |
| rs765497573 | 14:104,563,922 | G/A | — | uncertain significance |
| rs371838478 | 14:104,565,206 | A/G | — | uncertain significance |
| rs373991126 | 14:104,565,250 | C/T | — | uncertain significance |
| rs2036748880 | 14:104,565,269 | G/C | — | uncertain significance |
| rs2511376710 | 14:104,565,290 | T/C | — | uncertain significance |
| rs759937851 | 14:104,569,917 | C/T | — | uncertain significance |
| rs111758905 | 14:104,569,928 | C/T | — | benign |
| rs776054502 | 14:104,570,644 | C/T | — | uncertain significance |
| rs771570066 | 14:104,570,738 | G/A | — | likely benign |
| rs762424237 | 14:104,570,749 | G/A | — | likely benign |
| rs763864204 | 14:104,570,771 | A/G | — | uncertain significance |
| rs2511402354 | 14:104,570,773 | T/C | — | uncertain significance |
| rs543090174 | 14:104,570,966 | C/G | — | uncertain significance |
| rs532395480 | 14:104,571,717 | G/T | — | uncertain significance |
| rs1230841371 | 14:104,571,728 | C/A | — | uncertain significance |
| rs2511409697 | 14:104,571,737 | A/C | — | uncertain significance |
| rs375752823 | 14:104,571,754 | G/A | — | likely benign |
| rs200194038 | 14:104,571,756 | T/C | — | uncertain significance |
| rs371179199 | 14:104,573,151 | C/T | — | uncertain significance |
| rs748461343 | 14:104,573,576 | C/T | — | uncertain significance |
| rs776166471 | 14:104,573,591 | G/C | — | uncertain significance |
| rs374170442 | 14:104,573,627 | G/A | — | uncertain significance |
| rs368121504 | 14:104,573,634 | C/T | — | uncertain significance |
| rs12587599 | 14:104,575,130 | C/T | intron variant | — |
| rs772634912 | 14:104,577,855 | G/A | — | uncertain significance |
| rs758204389 | 14:104,577,912 | T/C | — | uncertain significance |
| rs750221062 | 14:104,578,312 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.