NPFFR2
neuropeptide FF receptor 2
Summary
This gene encodes a member of a subfamily of G-protein-coupled neuropeptide receptors. This protein is activated by the neuropeptides A-18-amide (NPAF) and F-8-amide (NPFF) and may function in pain modulation and regulation of the opioid system. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs568137320 | 4:72,897,638 | C/T | — | likely benign |
| rs115834666 | 4:72,897,723 | C/G | — | benign |
| rs750299127 | 4:72,897,815 | A/C | — | uncertain significance |
| rs139488490 | 4:72,897,848 | A/T | — | uncertain significance |
| rs528947248 | 4:72,916,263 | C/T | — | — |
| rs143106299 | 4:72,920,085 | A/T | intron variant | — |
| rs183365738 | 4:72,954,415 | G/A | intron variant | — |
| rs111817580 | 4:72,955,605 | C/A | intron variant | — |
| rs4129733 | 4:72,963,020 | T/G | intron variant | — |
| rs189643183 | 4:72,971,639 | G/C | intron variant | — |
| rs758998304 | 4:72,994,321 | T/C | — | uncertain significance |
| rs376287922 | 4:72,994,452 | C/G | — | uncertain significance |
| rs143711179 | 4:72,994,486 | A/G | — | uncertain significance |
| rs1468143710 | 4:72,994,492 | G/A | — | uncertain significance |
| rs77812923 | 4:72,994,525 | A/G | — | benign |
| rs1722154079 | 4:72,994,633 | G/A | — | uncertain significance |
| rs11940196 | 4:73,003,569 | A/T | — | — |
| rs765897220 | 4:73,003,780 | T/C | — | uncertain significance |
| rs77060411 | 4:73,003,816 | G/A | — | conflicting classifications of pathogenicity |
| rs181995385 | 4:73,006,445 | T/G | intron variant | — |
| rs61733659 | 4:73,012,709 | T/C | — | benign |
| rs377571805 | 4:73,012,711 | T/C | — | uncertain significance |
| rs201155248 | 4:73,012,745 | C/G | — | uncertain significance |
| rs149509872 | 4:73,012,817 | T/G | — | uncertain significance |
| rs747727510 | 4:73,012,979 | T/C | — | uncertain significance |
| rs2475737575 | 4:73,013,072 | A/G | — | uncertain significance |
| rs371971346 | 4:73,013,179 | A/G | — | uncertain significance |
| rs1393782380 | 4:73,013,194 | A/T | — | uncertain significance |
| rs148058374 | 4:73,013,366 | C/T | — | uncertain significance |
| rs141753805 | 4:73,013,458 | A/C | — | uncertain significance |
| rs1182382513 | 4:73,013,504 | A/C | — | uncertain significance |
| rs2475738623 | 4:73,013,517 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.