FCGRT
Fc gamma receptor and transporter
Summary
This gene encodes a receptor that binds the Fc region of monomeric immunoglobulin G. The encoded protein transfers immunoglobulin G antibodies from mother to fetus across the placenta. This protein also binds immunoglobulin G to protect the antibody from degradation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs187804944 | 19:50,016,300 | T/A | regulatory region variant | — |
| rs2079985451 | 19:50,016,674 | C/G | — | uncertain significance |
| rs748687030 | 19:50,016,709 | C/T | — | uncertain significance |
| rs1337482068 | 19:50,017,190 | C/T | — | uncertain significance |
| rs11551281 | 19:50,017,191 | G/T | — | benign |
| rs2079990336 | 19:50,017,216 | G/A | — | uncertain significance |
| rs375492056 | 19:50,017,258 | C/G | — | uncertain significance |
| rs201043787 | 19:50,017,381 | G/C | — | uncertain significance |
| rs201701956 | 19:50,017,450 | T/C | intron variant | — |
| rs544444357 | 19:50,017,474 | A/G | — | uncertain significance |
| rs150420714 | 19:50,017,538 | G/C | — | benign |
| rs777412760 | 19:50,017,658 | C/A | — | uncertain significance |
| rs554770888 | 19:50,017,690 | C/G | — | uncertain significance |
| rs766823478 | 19:50,017,719 | G/T | — | uncertain significance |
| rs2514078647 | 19:50,017,731 | C/A | — | uncertain significance |
| rs117080418 | 19:50,025,208 | T/A | intron variant | — |
| rs780596384 | 19:50,027,770 | C/A | — | uncertain significance |
| rs1031342092 | 19:50,027,773 | C/G | — | uncertain significance |
| rs147601685 | 19:50,027,872 | G/A | missense variant | — |
| rs374238496 | 19:50,027,895 | G/A | — | uncertain significance |
| rs1168003686 | 19:50,027,910 | G/A | — | uncertain significance |
| rs748983920 | 19:50,027,972 | G/C | — | uncertain significance |
| rs3810194 | 19:50,028,040 | T/G | — | — |
| rs770697747 | 19:50,028,723 | C/G | — | uncertain significance |
| rs144900355 | 19:50,028,758 | G/A | — | uncertain significance |
| rs199588435 | 19:50,028,762 | T/C | — | uncertain significance |
| rs142797093 | 19:50,028,828 | C/G | — | uncertain significance |
| rs756324491 | 19:50,029,285 | G/A | — | uncertain significance |
| rs1393639273 | 19:50,029,294 | A/C | — | uncertain significance |
| rs34072018 | 19:50,029,298 | C/T | — | benign |
| rs535861974 | 19:50,029,324 | A/G | — | uncertain significance |
| rs2514099574 | 19:50,029,326 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.