NXPE1
neurexophilin and PC-esterase domain family member 1
Summary
Predicted to be located in extracellular region and membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9326244 | 11:114,390,106 | C/T | downstream gene variant | — |
| rs11215031 | 11:114,390,447 | T/G | downstream gene variant | — |
| rs560863314 | 11:114,392,724 | T/C | — | uncertain significance |
| rs141275411 | 11:114,392,755 | T/C | — | uncertain significance |
| rs150910581 | 11:114,392,805 | T/C | — | uncertain significance |
| rs562986823 | 11:114,392,890 | C/G | — | uncertain significance |
| rs1214444884 | 11:114,393,012 | T/C | — | uncertain significance |
| rs116712555 | 11:114,393,032 | G/C | — | uncertain significance |
| rs199812582 | 11:114,393,037 | C/T | — | uncertain significance |
| rs566770021 | 11:114,393,073 | G/A | — | uncertain significance |
| rs77697681 | 11:114,393,119 | G/A | — | benign |
| rs781055560 | 11:114,393,123 | G/A | — | uncertain significance |
| rs746197216 | 11:114,393,153 | G/A | — | likely benign |
| rs2496760180 | 11:114,393,182 | T/A | — | uncertain significance |
| rs369017531 | 11:114,393,645 | G/A | — | uncertain significance |
| rs755390673 | 11:114,393,661 | A/G | — | uncertain significance |
| rs115978809 | 11:114,393,689 | T/C | — | uncertain significance |
| rs79538449 | 11:114,393,757 | C/T | — | benign |
| rs377195015 | 11:114,393,810 | C/T | — | uncertain significance |
| rs1318849 | 11:114,397,748 | C/G | — | — |
| rs143110380 | 11:114,398,591 | C/T | — | uncertain significance |
| rs754269717 | 11:114,398,592 | G/A | — | uncertain significance |
| rs1380179859 | 11:114,398,613 | C/G | — | uncertain significance |
| rs141451498 | 11:114,400,928 | G/C | — | uncertain significance |
| rs2496826920 | 11:114,400,954 | G/T | — | uncertain significance |
| rs45609739 | 11:114,400,991 | G/C | missense variant | — |
| rs188537245 | 11:114,401,000 | A/G | — | uncertain significance |
| rs1332358992 | 11:114,401,054 | A/G | — | uncertain significance |
| rs2496828928 | 11:114,401,063 | T/A | — | uncertain significance |
| rs1206772474 | 11:114,401,086 | T/C | — | uncertain significance |
| rs142774949 | 11:114,401,160 | C/T | — | benign |
| rs1282386428 | 11:114,401,165 | C/A | — | uncertain significance |
| rs1369909638 | 11:114,401,198 | G/T | — | uncertain significance |
| rs1458793297 | 11:114,401,209 | C/A | — | uncertain significance |
| rs1329307339 | 11:114,401,276 | C/T | — | uncertain significance |
| rs9667301 | 11:114,408,846 | A/G | — | — |
| rs6589441 | 11:114,424,863 | G/A | — | — |
| rs11215054 | 11:114,425,969 | G/A | intron variant | — |
| rs678170 | 11:114,431,956 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.