APOBEC3D
apolipoprotein B mRNA editing enzyme catalytic subunit 3D
Summary
This gene is a member of the cytidine deaminase gene family. It is one of a group of related genes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1 and inhibit retroviruses, such as HIV, by deaminating cytosine residues in nascent retroviral cDNA. [provided by RefSeq, Jul 2008]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs371353731 | 22:39,418,864 | G/A | — | uncertain significance |
| rs770105306 | 22:39,418,898 | G/A | — | uncertain significance |
| rs188724873 | 22:39,418,982 | C/T | — | uncertain significance |
| rs771281231 | 22:39,418,997 | G/T | — | likely benign |
| rs762513472 | 22:39,421,084 | C/T | — | uncertain significance |
| rs752483265 | 22:39,421,099 | G/C | — | uncertain significance |
| rs201748259 | 22:39,421,112 | T/G | — | uncertain significance |
| rs375631825 | 22:39,421,223 | T/C | — | uncertain significance |
| rs751837393 | 22:39,421,225 | G/T | — | uncertain significance |
| rs2518394014 | 22:39,421,229 | A/G | — | uncertain significance |
| rs778365707 | 22:39,421,238 | A/G | — | uncertain significance |
| rs553533578 | 22:39,421,295 | G/A | — | uncertain significance |
| rs1211503425 | 22:39,421,299 | G/T | — | uncertain significance |
| rs530222573 | 22:39,421,330 | C/T | — | uncertain significance |
| rs2518394981 | 22:39,421,580 | A/C | — | uncertain significance |
| rs776326105 | 22:39,421,658 | C/T | — | uncertain significance |
| rs762648654 | 22:39,425,436 | G/A | — | uncertain significance |
| rs367561607 | 22:39,425,439 | G/A | — | uncertain significance |
| rs770481293 | 22:39,425,495 | T/G | — | uncertain significance |
| rs368483208 | 22:39,425,499 | G/T | — | uncertain significance |
| rs200940247 | 22:39,425,510 | G/C | — | uncertain significance |
| rs779619670 | 22:39,427,720 | C/T | — | uncertain significance |
| rs1926232120 | 22:39,427,726 | G/A | — | uncertain significance |
| rs1249620028 | 22:39,427,730 | G/T | — | uncertain significance |
| rs2518405245 | 22:39,427,774 | A/G | — | uncertain significance |
| rs373001302 | 22:39,427,821 | G/C | — | uncertain significance |
| rs376105660 | 22:39,427,842 | G/C | — | uncertain significance |
| rs374093771 | 22:39,427,874 | C/T | — | uncertain significance |
| rs2518405716 | 22:39,427,921 | G/A | — | uncertain significance |
| rs1926256275 | 22:39,427,925 | G/A | — | uncertain significance |
| rs773716596 | 22:39,427,930 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.