FCAMR
Fc alpha and mu receptor
Summary
Predicted to enable IgA binding activity; IgM binding activity; and transmembrane signaling receptor activity. Predicted to be involved in signal transduction. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2526335217 | 1:207,131,868 | C/T | — | uncertain significance |
| rs749562507 | 1:207,131,904 | G/A | — | uncertain significance |
| rs555854947 | 1:207,131,911 | G/A | — | uncertain significance |
| rs757911937 | 1:207,131,977 | G/C | — | uncertain significance |
| rs41275382 | 1:207,133,059 | A/G | — | uncertain significance |
| rs1680424598 | 1:207,133,120 | T/C | — | uncertain significance |
| rs372937296 | 1:207,133,126 | C/T | — | likely benign |
| rs1425270586 | 1:207,133,797 | C/G | — | uncertain significance |
| rs140563378 | 1:207,133,830 | G/A | — | uncertain significance |
| rs371658246 | 1:207,134,010 | C/A | — | uncertain significance |
| rs1680476192 | 1:207,134,077 | C/A | — | uncertain significance |
| rs1007881396 | 1:207,134,289 | C/G | — | uncertain significance |
| rs745380215 | 1:207,134,308 | G/A | — | uncertain significance |
| rs548403472 | 1:207,134,376 | C/T | — | likely benign |
| rs940097389 | 1:207,134,397 | G/A | — | uncertain significance |
| rs2526356163 | 1:207,134,409 | G/A | — | uncertain significance |
| rs1453504402 | 1:207,134,439 | G/A | — | uncertain significance |
| rs1376085905 | 1:207,134,443 | T/C | — | uncertain significance |
| rs1319143764 | 1:207,134,500 | C/T | — | uncertain significance |
| rs769273194 | 1:207,135,581 | C/T | — | uncertain significance |
| rs2526363569 | 1:207,135,605 | C/G | — | uncertain significance |
| rs972627590 | 1:207,135,649 | T/G | — | uncertain significance |
| rs200786919 | 1:207,135,705 | G/A | — | uncertain significance |
| rs759028700 | 1:207,135,713 | T/C | — | uncertain significance |
| rs561968221 | 1:207,135,716 | C/T | — | uncertain significance |
| rs188207561 | 1:207,135,723 | G/A | missense variant | — |
| rs377470491 | 1:207,135,765 | T/C | — | uncertain significance |
| rs368893206 | 1:207,135,773 | C/T | — | uncertain significance |
| rs374305028 | 1:207,135,779 | C/T | — | uncertain significance |
| rs147389157 | 1:207,135,828 | G/A | missense variant | — |
| rs1428362770 | 1:207,135,830 | C/T | — | uncertain significance |
| rs778235453 | 1:207,135,846 | C/T | — | uncertain significance |
| rs764296824 | 1:207,139,138 | A/G | — | uncertain significance |
| rs2526397776 | 1:207,140,995 | T/C | — | uncertain significance |
| rs1856746 | 1:207,143,422 | A/G | intron variant | — |
| rs2526410603 | 1:207,143,452 | C/A | — | likely benign |
| rs748430335 | 1:207,143,460 | T/A | — | uncertain significance |
| rs12066378 | 1:207,144,619 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.