TBC1D22A
TBC1 domain family member 22A
Summary
Enables 14-3-3 protein binding activity and protein homodimerization activity. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2084457782 | 22:47,188,422 | A/G | — | uncertain significance |
| rs188509845 | 22:47,189,435 | G/A | — | uncertain significance |
| rs141580250 | 22:47,189,568 | C/T | — | uncertain significance |
| rs373618433 | 22:47,189,601 | G/A | — | uncertain significance |
| rs146025212 | 22:47,189,616 | T/C | — | benign |
| rs112995262 | 22:47,189,678 | C/A | — | uncertain significance |
| rs201151937 | 22:47,189,679 | C/G | — | uncertain significance |
| rs749281882 | 22:47,189,681 | A/G | — | uncertain significance |
| rs563554988 | 22:47,189,706 | C/T | — | uncertain significance |
| rs141713070 | 22:47,189,747 | G/C | — | benign |
| rs762974977 | 22:47,193,344 | G/T | — | uncertain significance |
| rs1267287718 | 22:47,193,352 | G/A | — | uncertain significance |
| rs759900287 | 22:47,193,358 | G/A | — | uncertain significance |
| rs187687977 | 22:47,193,392 | C/T | — | uncertain significance |
| rs141698918 | 22:47,193,404 | C/T | — | benign |
| rs146205023 | 22:47,193,415 | A/G | — | uncertain significance |
| rs761726540 | 22:47,193,446 | C/T | — | uncertain significance |
| rs569400492 | 22:47,193,485 | A/G | — | uncertain significance |
| rs710119 | 22:47,199,148 | A/T | — | — |
| rs4823878 | 22:47,200,354 | T/C | intron variant | — |
| rs801652 | 22:47,202,691 | C/T | intron variant | — |
| rs764993895 | 22:47,287,213 | C/G | — | uncertain significance |
| rs775351336 | 22:47,290,684 | A/G | — | uncertain significance |
| rs139839482 | 22:47,290,705 | G/A | — | uncertain significance |
| rs758517657 | 22:47,290,719 | A/G | — | uncertain significance |
| rs988342620 | 22:47,308,003 | C/T | — | uncertain significance |
| rs199657694 | 22:47,370,218 | G/A | — | uncertain significance |
| rs138491114 | 22:47,432,980 | G/A | synonymous variant | — |
| rs1438074649 | 22:47,433,023 | C/T | — | uncertain significance |
| rs753037531 | 22:47,433,075 | G/A | — | uncertain significance |
| rs768020083 | 22:47,507,411 | C/T | — | uncertain significance |
| rs367838104 | 22:47,507,440 | G/A | — | uncertain significance |
| rs1198950585 | 22:47,507,468 | G/A | — | uncertain significance |
| rs5766691 | 22:47,532,396 | A/T | — | — |
| rs373398596 | 22:47,569,177 | C/A | — | uncertain significance |
| rs746462660 | 22:47,569,213 | G/A | — | uncertain significance |
| rs1569483166 | 22:47,569,246 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.