FCRL5
Fc receptor like 5
Summary
This gene encodes a member of the immunoglobulin receptor superfamily and the Fc-receptor like family. This gene and several other Fc receptor-like gene members are clustered on the long arm of chromosome 1. The encoded protein is a single-pass type I membrane protein and contains 8 immunoglobulin-like C2-type domains. This gene is implicated in B cell development and lymphomagenesis. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Sep 2010]
Known Variants79 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs140510603 | 1:157,485,426 | G/C | — | uncertain significance |
| rs765035849 | 1:157,485,432 | A/G | — | likely benign |
| rs140845798 | 1:157,485,511 | G/A | — | uncertain significance |
| rs2873345 | 1:157,487,951 | T/C | intron variant | — |
| rs1571967 | 1:157,488,085 | C/A | intron variant | — |
| rs375192406 | 1:157,488,223 | A/T | — | uncertain significance |
| rs201504068 | 1:157,490,290 | C/T | — | uncertain significance |
| rs1051334871 | 1:157,490,296 | C/T | — | likely benign |
| rs771319382 | 1:157,490,309 | A/C | — | uncertain significance |
| rs771606459 | 1:157,490,329 | C/A | — | uncertain significance |
| rs200199101 | 1:157,490,335 | G/T | — | uncertain significance |
| rs1650160843 | 1:157,490,813 | T/C | — | uncertain significance |
| rs752961202 | 1:157,490,857 | T/C | — | uncertain significance |
| rs758054238 | 1:157,490,891 | C/A | — | uncertain significance |
| rs774152161 | 1:157,491,031 | G/A | — | likely benign |
| rs1650177955 | 1:157,491,055 | A/C | — | uncertain significance |
| rs74858059 | 1:157,491,066 | C/G | — | benign |
| rs113851024 | 1:157,491,767 | A/T | intron variant | — |
| rs557711548 | 1:157,492,543 | A/C | — | — |
| rs1217530344 | 1:157,494,093 | C/T | — | uncertain significance |
| rs750435883 | 1:157,494,114 | C/A | — | uncertain significance |
| rs185854028 | 1:157,494,131 | G/C | — | uncertain significance |
| rs746749785 | 1:157,494,171 | A/C | — | uncertain significance |
| rs76824212 | 1:157,494,217 | A/G | — | benign |
| rs113003110 | 1:157,494,243 | T/C | — | benign |
| rs199994796 | 1:157,494,301 | C/A | — | uncertain significance |
| rs141385857 | 1:157,494,800 | C/A | intron variant | — |
| rs181977070 | 1:157,497,058 | A/G | intron variant | — |
| rs11264750 | 1:157,497,160 | A/C | — | — |
| rs113288934 | 1:157,497,462 | C/T | — | likely benign |
| rs373506837 | 1:157,497,469 | G/A | — | uncertain significance |
| rs771555160 | 1:157,497,503 | G/A | — | uncertain significance |
| rs778591421 | 1:157,497,592 | C/A | — | uncertain significance |
| rs373102783 | 1:157,497,656 | T/C | — | uncertain significance |
| rs779447312 | 1:157,497,680 | C/T | — | uncertain significance |
| rs367673881 | 1:157,504,425 | C/T | — | uncertain significance |
| rs543656955 | 1:157,504,460 | G/A | — | uncertain significance |
| rs141517034 | 1:157,504,466 | T/C | — | likely benign |
| rs750361179 | 1:157,504,511 | A/G | — | likely benign |
| rs371783204 | 1:157,504,524 | A/T | — | uncertain significance |
| rs201978439 | 1:157,504,557 | C/T | — | uncertain significance |
| rs766185827 | 1:157,504,589 | C/T | — | uncertain significance |
| rs1650885205 | 1:157,504,591 | T/A | — | uncertain significance |
| rs139208993 | 1:157,504,647 | C/G | — | likely benign |
| rs1415904754 | 1:157,504,677 | C/G | — | uncertain significance |
| rs6427384 | 1:157,508,882 | C/T | missense variant | — |
| rs369083606 | 1:157,508,896 | G/A | — | uncertain significance |
| rs34868810 | 1:157,508,908 | T/C | — | benign |
| rs16838748 | 1:157,508,997 | G/T | missense variant | benign |
| rs377645767 | 1:157,509,010 | C/T | — | uncertain significance |
| rs149262706 | 1:157,509,011 | G/A | — | uncertain significance |
| rs371219221 | 1:157,509,026 | C/T | — | uncertain significance |
| rs2526216089 | 1:157,509,065 | T/C | — | uncertain significance |
| rs143613026 | 1:157,509,125 | T/G | — | uncertain significance |
| rs2526216673 | 1:157,509,139 | G/C | — | uncertain significance |
| rs945614254 | 1:157,509,149 | C/T | — | uncertain significance |
| rs139328860 | 1:157,512,768 | C/T | — | uncertain significance |
| rs565049633 | 1:157,512,825 | C/T | — | uncertain significance |
| rs12036228 | 1:157,514,091 | C/T | missense variant | — |
| rs750153521 | 1:157,514,146 | C/T | — | likely benign |
| rs142419505 | 1:157,514,216 | C/T | — | uncertain significance |
| rs149556320 | 1:157,514,233 | A/T | — | uncertain significance |
| rs2101642147 | 1:157,514,276 | A/C | — | uncertain significance |
| rs2526245725 | 1:157,514,321 | G/A | — | uncertain significance |
| rs140080936 | 1:157,514,324 | C/T | — | uncertain significance |
| rs778776602 | 1:157,514,638 | A/G | — | uncertain significance |
| rs11803066 | 1:157,514,685 | G/A | — | benign |
| rs1359772197 | 1:157,514,797 | T/C | — | uncertain significance |
| rs753400847 | 1:157,514,800 | G/A | — | uncertain significance |
| rs778238010 | 1:157,514,809 | C/T | — | likely benign |
| rs1651568234 | 1:157,516,775 | C/T | — | uncertain significance |
| rs747518639 | 1:157,516,784 | G/C | — | uncertain significance |
| rs149292734 | 1:157,516,823 | T/C | — | uncertain significance |
| rs112398428 | 1:157,516,828 | G/A | — | uncertain significance |
| rs377114139 | 1:157,516,836 | T/A | — | uncertain significance |
| rs376035021 | 1:157,516,891 | T/G | — | uncertain significance |
| rs964143961 | 1:157,516,960 | A/G | — | uncertain significance |
| rs184967438 | 1:157,521,982 | G/A | regulatory region variant | — |
| rs575866096 | 1:157,522,300 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.