RAI14
retinoic acid induced 14
Summary
Predicted to enable actin binding activity. Predicted to be involved in cell differentiation and spermatogenesis. Located in cytosol; fibrillar center; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs455213 | 5:34,660,235 | T/C | regulatory region variant | — |
| rs6880536 | 5:34,726,063 | T/G | intron variant | — |
| rs142482062 | 5:34,728,419 | G/C | intron variant | — |
| rs114642247 | 5:34,757,629 | T/G | — | benign |
| rs2478997997 | 5:34,757,689 | T/G | — | uncertain significance |
| rs559732278 | 5:34,758,231 | G/A | — | — |
| rs369411268 | 5:34,796,115 | C/G | — | uncertain significance |
| rs369052260 | 5:34,803,825 | G/A | — | uncertain significance |
| rs200207291 | 5:34,808,695 | A/T | — | uncertain significance |
| rs1341637602 | 5:34,808,704 | T/C | — | uncertain significance |
| rs201315302 | 5:34,808,727 | G/A | — | uncertain significance |
| rs1025530803 | 5:34,811,181 | T/A | — | uncertain significance |
| rs755062513 | 5:34,812,006 | C/A | — | uncertain significance |
| rs755186988 | 5:34,812,299 | A/G | — | uncertain significance |
| rs771350937 | 5:34,813,709 | A/G | — | uncertain significance |
| rs761936931 | 5:34,814,717 | A/G | — | uncertain significance |
| rs199515102 | 5:34,814,746 | C/T | — | uncertain significance |
| rs1756531180 | 5:34,818,903 | C/G | — | uncertain significance |
| rs747432780 | 5:34,818,921 | G/A | — | uncertain significance |
| rs776926297 | 5:34,818,947 | A/G | — | uncertain significance |
| rs371610339 | 5:34,818,948 | G/C | — | uncertain significance |
| rs761402081 | 5:34,821,954 | A/C | — | uncertain significance |
| rs746815082 | 5:34,823,076 | G/A | — | uncertain significance |
| rs377452240 | 5:34,823,090 | C/A | — | uncertain significance |
| rs779981720 | 5:34,823,134 | C/T | — | uncertain significance |
| rs139982390 | 5:34,823,176 | A/G | — | uncertain significance |
| rs2479746139 | 5:34,823,200 | A/T | — | uncertain significance |
| rs540309181 | 5:34,823,414 | G/C | — | uncertain significance |
| rs549636576 | 5:34,823,492 | C/A | — | uncertain significance |
| rs1223304448 | 5:34,823,493 | A/G | — | likely benign |
| rs2479752519 | 5:34,823,524 | G/A | — | uncertain significance |
| rs2479753883 | 5:34,823,584 | G/C | — | uncertain significance |
| rs748653495 | 5:34,823,643 | G/A | — | uncertain significance |
| rs2479755101 | 5:34,823,649 | G/C | — | uncertain significance |
| rs186771212 | 5:34,823,665 | T/A | — | uncertain significance |
| rs565597265 | 5:34,823,676 | G/A | — | uncertain significance |
| rs138949061 | 5:34,824,081 | G/A | — | uncertain significance |
| rs767058997 | 5:34,824,091 | A/C | — | uncertain significance |
| rs370210803 | 5:34,824,168 | C/T | — | uncertain significance |
| rs1757193130 | 5:34,824,190 | A/T | — | uncertain significance |
| rs752004465 | 5:34,824,271 | A/T | — | uncertain significance |
| rs774301029 | 5:34,824,303 | C/T | — | uncertain significance |
| rs139761677 | 5:34,824,416 | G/T | — | uncertain significance |
| rs771898528 | 5:34,824,492 | G/A | — | uncertain significance |
| rs776281580 | 5:34,824,501 | C/T | — | uncertain significance |
| rs2479771775 | 5:34,824,589 | A/T | — | uncertain significance |
| rs2479793995 | 5:34,826,447 | T/C | — | uncertain significance |
| rs762044517 | 5:34,826,549 | C/G | — | uncertain significance |
| rs187066273 | 5:34,828,207 | T/C | intron variant | — |
| rs112077697 | 5:34,829,851 | A/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.