SERINC5
serine incorporator 5
Summary
Enables phospholipid scramblase activity. Involved in antiviral innate immune response and plasma membrane phospholipid scrambling. Located in several cellular components, including centrosome; cytosol; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs536295821 | 5:79,409,430 | C/T | — | likely benign |
| rs1275313774 | 5:79,439,491 | C/T | — | uncertain significance |
| rs1327320126 | 5:79,439,493 | G/C | — | uncertain significance |
| rs552728668 | 5:79,439,507 | G/A | — | likely benign |
| rs537411704 | 5:79,439,524 | C/T | — | uncertain significance |
| rs756068379 | 5:79,441,929 | C/T | — | uncertain significance |
| rs116691179 | 5:79,441,930 | G/A | — | benign |
| rs368333548 | 5:79,441,966 | G/T | — | uncertain significance |
| rs1174209289 | 5:79,443,106 | A/G | — | uncertain significance |
| rs769873829 | 5:79,446,740 | C/T | — | uncertain significance |
| rs768554900 | 5:79,446,751 | G/A | — | uncertain significance |
| rs73772260 | 5:79,446,904 | G/A | intron variant | — |
| rs372110753 | 5:79,454,723 | T/G | — | likely benign |
| rs1252650207 | 5:79,454,762 | C/G | — | uncertain significance |
| rs150438751 | 5:79,454,763 | A/G | — | benign |
| rs1373117689 | 5:79,462,289 | G/A | — | uncertain significance |
| rs144763991 | 5:79,465,166 | A/G | — | uncertain significance |
| rs1273070025 | 5:79,465,197 | G/C | — | uncertain significance |
| rs115205303 | 5:79,465,284 | A/G | — | benign |
| rs759732415 | 5:79,465,311 | T/C | — | uncertain significance |
| rs1373349611 | 5:79,465,320 | C/A | — | uncertain significance |
| rs1747517504 | 5:79,465,367 | G/A | — | uncertain significance |
| rs558072691 | 5:79,469,905 | G/A | — | — |
| rs905335326 | 5:79,473,161 | G/A | — | uncertain significance |
| rs199907400 | 5:79,473,173 | C/T | — | uncertain significance |
| rs763674377 | 5:79,473,185 | T/C | — | uncertain significance |
| rs1016883055 | 5:79,473,729 | C/T | — | uncertain significance |
| rs556072650 | 5:79,498,759 | G/A | — | likely benign |
| rs1164431400 | 5:79,498,815 | T/A | — | uncertain significance |
| rs4704640 | 5:79,520,202 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.