AGMAT
agmatinase (putative)
Summary
Enables arginase activity; guanidinobutyrase activity; and guanidinopropionase activity. Predicted to be involved in putrescine biosynthetic process from arginine, via agmatine. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6678650 | 1:15,900,152 | G/A | — | benign |
| rs202068651 | 1:15,900,201 | G/A | — | uncertain significance |
| rs2521754655 | 1:15,901,257 | A/G | — | likely benign |
| rs749080126 | 1:15,901,266 | G/T | — | uncertain significance |
| rs574567828 | 1:15,901,284 | A/G | — | uncertain significance |
| rs1248694641 | 1:15,901,293 | C/T | — | uncertain significance |
| rs1449683297 | 1:15,904,278 | C/G | — | uncertain significance |
| rs138227623 | 1:15,904,353 | G/A | — | uncertain significance |
| rs75133544 | 1:15,905,388 | G/A | — | benign |
| rs200508005 | 1:15,905,400 | C/T | — | uncertain significance |
| rs201546181 | 1:15,905,454 | C/T | — | uncertain significance |
| rs370906598 | 1:15,905,479 | G/T | — | uncertain significance |
| rs147805030 | 1:15,905,482 | T/G | — | uncertain significance |
| rs749470775 | 1:15,905,500 | C/T | — | uncertain significance |
| rs1639091509 | 1:15,906,632 | C/T | — | likely pathogenic |
| rs113177297 | 1:15,907,354 | C/T | downstream gene variant | — |
| rs140527149 | 1:15,908,132 | A/C | — | — |
| rs6664388 | 1:15,908,242 | C/T | downstream gene variant | — |
| rs6679837 | 1:15,908,534 | T/C | downstream gene variant | — |
| rs10803394 | 1:15,909,480 | G/A | — | — |
| rs750427999 | 1:15,909,757 | C/T | — | uncertain significance |
| rs772742125 | 1:15,909,822 | A/G | — | uncertain significance |
| rs148899500 | 1:15,909,873 | A/G | — | uncertain significance |
| rs549021034 | 1:15,909,879 | C/T | — | uncertain significance |
| rs2521792140 | 1:15,909,886 | C/T | — | uncertain significance |
| rs772410131 | 1:15,911,243 | C/A | — | uncertain significance |
| rs963058547 | 1:15,911,268 | C/A | — | uncertain significance |
| rs756967227 | 1:15,911,288 | T/C | — | uncertain significance |
| rs772601696 | 1:15,911,326 | C/T | — | uncertain significance |
| rs566899293 | 1:15,911,363 | G/A | — | uncertain significance |
| rs749883993 | 1:15,911,372 | G/A | — | uncertain significance |
| rs753214609 | 1:15,911,381 | G/C | — | uncertain significance |
| rs549635682 | 1:15,911,433 | G/A | — | likely benign |
| rs914510096 | 1:15,911,435 | C/A | — | uncertain significance |
| rs569552728 | 1:15,911,452 | A/C | — | uncertain significance |
| rs45619934 | 1:15,911,947 | G/C | — | — |
| rs57109480 | 1:15,912,476 | G/A | upstream gene variant | — |
| rs10159261 | 1:15,912,987 | G/T | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.