AFAP1L1
actin filament associated protein 1 like 1
Summary
Predicted to be located in several cellular components, including actin cytoskeleton; anchoring junction; and cell projection. Predicted to be active in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs62378114 | 5:148,651,395 | A/T | regulatory region variant | — |
| rs771932913 | 5:148,679,123 | A/G | — | uncertain significance |
| rs768682537 | 5:148,679,141 | C/T | — | uncertain significance |
| rs372800883 | 5:148,679,159 | T/C | — | uncertain significance |
| rs1475004663 | 5:148,680,714 | T/A | — | uncertain significance |
| rs1323240480 | 5:148,680,752 | G/A | — | uncertain significance |
| rs199689420 | 5:148,680,783 | G/T | — | uncertain significance |
| rs369530534 | 5:148,682,000 | C/T | — | uncertain significance |
| rs571245239 | 5:148,682,059 | G/A | — | uncertain significance |
| rs2481091034 | 5:148,682,071 | G/A | — | uncertain significance |
| rs373024375 | 5:148,682,077 | A/G | — | uncertain significance |
| rs200939762 | 5:148,685,890 | C/T | — | uncertain significance |
| rs550069903 | 5:148,685,952 | G/A | — | uncertain significance |
| rs759695857 | 5:148,687,049 | A/C | — | uncertain significance |
| rs370079883 | 5:148,687,124 | G/A | — | uncertain significance |
| rs2481111320 | 5:148,687,175 | T/C | — | uncertain significance |
| rs567317757 | 5:148,689,684 | G/A | — | uncertain significance |
| rs544299473 | 5:148,691,682 | G/A | — | uncertain significance |
| rs775982070 | 5:148,691,736 | C/T | — | uncertain significance |
| rs757240110 | 5:148,691,741 | C/T | — | uncertain significance |
| rs374903729 | 5:148,695,459 | C/T | — | uncertain significance |
| rs369601847 | 5:148,695,786 | G/A | — | uncertain significance |
| rs746515510 | 5:148,695,800 | T/C | — | uncertain significance |
| rs141357304 | 5:148,697,448 | G/A | — | uncertain significance |
| rs777886501 | 5:148,699,215 | C/T | — | uncertain significance |
| rs370935371 | 5:148,699,230 | A/G | — | uncertain significance |
| rs1348259951 | 5:148,700,003 | G/A | — | uncertain significance |
| rs200188866 | 5:148,702,193 | G/A | — | uncertain significance |
| rs969182346 | 5:148,702,208 | C/T | — | uncertain significance |
| rs745394391 | 5:148,702,214 | G/A | — | uncertain significance |
| rs114805975 | 5:148,702,241 | C/T | — | uncertain significance |
| rs774281613 | 5:148,702,251 | C/T | — | uncertain significance |
| rs140123570 | 5:148,702,255 | G/C | — | uncertain significance |
| rs10044242 | 5:148,706,299 | C/G | regulatory region variant | — |
| rs201232986 | 5:148,709,259 | G/A | — | uncertain significance |
| rs199896142 | 5:148,709,292 | A/G | — | uncertain significance |
| rs755708543 | 5:148,709,322 | C/T | — | uncertain significance |
| rs1220707446 | 5:148,709,327 | C/T | — | uncertain significance |
| rs2481210293 | 5:148,712,283 | A/C | — | uncertain significance |
| rs143616929 | 5:148,712,303 | C/T | — | uncertain significance |
| rs148055999 | 5:148,712,330 | G/A | — | uncertain significance |
| rs1463628851 | 5:148,712,359 | G/A | — | uncertain significance |
| rs760627807 | 5:148,712,405 | G/A | — | uncertain significance |
| rs1231506226 | 5:148,712,426 | C/T | — | uncertain significance |
| rs150030700 | 5:148,715,247 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.