RNPEP
arginyl aminopeptidase
Summary
Predicted to enable metalloaminopeptidase activity. Predicted to be involved in proteolysis. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs747061104 | 1:201,951,799 | C/T | — | uncertain significance |
| rs770984111 | 1:201,951,835 | G/A | — | uncertain significance |
| rs2526992140 | 1:201,951,865 | A/T | — | uncertain significance |
| rs1682981215 | 1:201,951,897 | G/A | — | uncertain significance |
| rs1325609679 | 1:201,951,939 | C/T | — | uncertain significance |
| rs564306427 | 1:201,951,946 | G/A | — | uncertain significance |
| rs922112100 | 1:201,951,975 | G/T | — | uncertain significance |
| rs911914805 | 1:201,951,981 | G/A | — | uncertain significance |
| rs2526992938 | 1:201,952,072 | T/C | — | uncertain significance |
| rs549263851 | 1:201,952,084 | G/T | — | uncertain significance |
| rs201819747 | 1:201,952,168 | C/T | — | uncertain significance |
| rs1281876553 | 1:201,952,191 | G/T | — | uncertain significance |
| rs1376183425 | 1:201,952,228 | G/A | — | uncertain significance |
| rs4950806 | 1:201,952,574 | T/C | regulatory region variant | — |
| rs12059693 | 1:201,953,994 | A/G | intron variant | — |
| rs770570576 | 1:201,958,050 | G/A | — | uncertain significance |
| rs762297316 | 1:201,958,110 | C/T | — | uncertain significance |
| rs79043888 | 1:201,958,136 | G/A | — | benign |
| rs777775930 | 1:201,958,143 | G/A | — | uncertain significance |
| rs1010317728 | 1:201,958,168 | T/C | — | uncertain significance |
| rs147777734 | 1:201,958,634 | C/T | synonymous variant | — |
| rs6691690 | 1:201,960,453 | G/C | — | — |
| rs1191114043 | 1:201,965,310 | C/T | — | uncertain significance |
| rs1683542851 | 1:201,965,330 | G/A | — | uncertain significance |
| rs201672156 | 1:201,965,336 | A/G | — | uncertain significance |
| rs2527030304 | 1:201,965,366 | C/T | — | uncertain significance |
| rs148809029 | 1:201,965,367 | T/C | — | uncertain significance |
| rs59698324 | 1:201,965,855 | C/T | downstream gene variant | — |
| rs2527033437 | 1:201,966,488 | G/A | — | uncertain significance |
| rs140055683 | 1:201,966,514 | G/A | — | uncertain significance |
| rs1348330939 | 1:201,966,521 | C/T | — | uncertain significance |
| rs79980228 | 1:201,966,541 | C/T | — | benign |
| rs374485540 | 1:201,966,544 | T/A | — | uncertain significance |
| rs1227783070 | 1:201,966,566 | A/G | — | uncertain significance |
| rs777820375 | 1:201,966,607 | G/A | — | uncertain significance |
| rs747119651 | 1:201,966,611 | A/G | — | uncertain significance |
| rs2527034204 | 1:201,966,621 | A/C | — | uncertain significance |
| rs114130028 | 1:201,966,632 | A/G | — | uncertain significance |
| rs200764787 | 1:201,966,652 | G/A | — | uncertain significance |
| rs765846112 | 1:201,969,032 | G/A | — | uncertain significance |
| rs750504839 | 1:201,969,041 | A/T | — | uncertain significance |
| rs140175504 | 1:201,969,060 | C/T | — | uncertain significance |
| rs770743142 | 1:201,969,066 | G/A | — | uncertain significance |
| rs202127308 | 1:201,969,078 | G/A | — | uncertain significance |
| rs1571642336 | 1:201,969,086 | A/G | — | uncertain significance |
| rs140770038 | 1:201,969,125 | C/G | — | uncertain significance |
| rs2527046062 | 1:201,970,504 | G/A | — | uncertain significance |
| rs368925698 | 1:201,970,506 | G/A | — | uncertain significance |
| rs774786362 | 1:201,970,560 | G/A | — | uncertain significance |
| rs1683803675 | 1:201,970,567 | A/T | — | uncertain significance |
| rs772103009 | 1:201,970,596 | C/G | — | uncertain significance |
| rs2527047445 | 1:201,970,827 | A/C | — | uncertain significance |
| rs146663755 | 1:201,972,448 | C/G | — | uncertain significance |
| rs758550677 | 1:201,972,479 | C/T | — | uncertain significance |
| rs2527053312 | 1:201,972,495 | G/A | — | uncertain significance |
| rs749095534 | 1:201,972,503 | T/C | — | uncertain significance |
| rs1034480331 | 1:201,973,503 | A/G | — | uncertain significance |
| rs770961749 | 1:201,973,545 | G/A | — | uncertain significance |
| rs190562495 | 1:201,974,732 | G/T | — | uncertain significance |
| rs139066886 | 1:201,974,735 | G/A | — | uncertain significance |
| rs758735913 | 1:201,974,824 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.