EVL
Enah/Vasp-like
Summary
Predicted to enable SH3 domain binding activity and profilin binding activity. Involved in negative regulation of epithelial cell migration; negative regulation of ruffle assembly; and positive regulation of stress fiber assembly. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1190983 | 14:100,497,986 | T/C | regulatory region variant | — |
| rs747052307 | 14:100,551,100 | C/T | — | uncertain significance |
| rs760877640 | 14:100,551,128 | A/G | — | uncertain significance |
| rs143412382 | 14:100,551,130 | A/G | — | uncertain significance |
| rs1010337733 | 14:100,563,822 | T/C | — | uncertain significance |
| rs2549041191 | 14:100,563,834 | C/T | — | uncertain significance |
| rs1450563732 | 14:100,563,867 | C/T | — | uncertain significance |
| rs35006525 | 14:100,563,868 | G/A | — | benign |
| rs1169191067 | 14:100,563,956 | A/G | — | uncertain significance |
| rs768934626 | 14:100,563,988 | A/C | — | uncertain significance |
| rs11160570 | 14:100,581,636 | T/A | — | — |
| rs3783332 | 14:100,586,757 | A/G | intron variant | — |
| rs141817237 | 14:100,589,878 | C/A | — | uncertain significance |
| rs2549070596 | 14:100,589,884 | A/G | — | uncertain significance |
| rs1887837386 | 14:100,589,930 | T/A | — | uncertain significance |
| rs370658826 | 14:100,594,876 | C/T | — | uncertain significance |
| rs780082762 | 14:100,594,940 | C/T | — | uncertain significance |
| rs780661759 | 14:100,594,996 | G/A | — | uncertain significance |
| rs201550659 | 14:100,595,047 | G/A | — | uncertain significance |
| rs368376778 | 14:100,595,909 | G/A | — | uncertain significance |
| rs140562245 | 14:100,595,924 | A/G | — | uncertain significance |
| rs1188324139 | 14:100,596,006 | A/G | — | uncertain significance |
| rs34073270 | 14:100,602,266 | C/G | — | benign |
| rs750723779 | 14:100,603,959 | C/T | — | uncertain significance |
| rs1252884127 | 14:100,607,525 | C/T | — | uncertain significance |
| rs201712062 | 14:100,607,527 | G/A | — | uncertain significance |
| rs2549098009 | 14:100,608,115 | G/A | — | uncertain significance |
| rs549778510 | 14:100,610,049 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.