EPS15L1
epidermal growth factor receptor pathway substrate 15 like 1
Summary
Enables cadherin binding activity. Predicted to be involved in endosomal transport and synaptic vesicle endocytosis. Located in membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs875622 | 19:16,467,759 | A/G | intron variant | — |
| rs144623166 | 19:16,472,595 | T/C | — | uncertain significance |
| rs370996327 | 19:16,472,694 | T/C | — | uncertain significance |
| rs776463184 | 19:16,472,731 | C/G | — | uncertain significance |
| rs144312610 | 19:16,472,751 | C/T | — | uncertain significance |
| rs10402422 | 19:16,475,388 | G/A | intron variant | — |
| rs146083535 | 19:16,487,943 | T/A | — | uncertain significance |
| rs780750731 | 19:16,487,960 | C/G | — | uncertain significance |
| rs1209088895 | 19:16,487,974 | G/C | — | uncertain significance |
| rs371897669 | 19:16,487,984 | G/C | — | uncertain significance |
| rs760069683 | 19:16,488,047 | A/G | — | uncertain significance |
| rs756964819 | 19:16,488,062 | G/A | — | uncertain significance |
| rs78663649 | 19:16,489,447 | C/A | — | — |
| rs7251806 | 19:16,499,569 | C/A | — | — |
| rs563892915 | 19:16,502,514 | G/A | — | — |
| rs2512769623 | 19:16,503,133 | G/C | — | uncertain significance |
| rs367867461 | 19:16,503,210 | G/A | — | uncertain significance |
| rs59326120 | 19:16,504,352 | T/G | — | — |
| rs371696682 | 19:16,504,806 | G/A | — | uncertain significance |
| rs2092512704 | 19:16,504,807 | G/A | — | uncertain significance |
| rs773806626 | 19:16,506,190 | T/C | — | uncertain significance |
| rs369675832 | 19:16,506,235 | G/A | — | uncertain significance |
| rs10404237 | 19:16,511,171 | A/C | — | — |
| rs544786872 | 19:16,513,262 | C/A | — | uncertain significance |
| rs202010883 | 19:16,513,263 | G/A | — | uncertain significance |
| rs757407541 | 19:16,513,265 | C/T | — | uncertain significance |
| rs149545861 | 19:16,514,569 | T/C | — | conflicting classifications of pathogenicity |
| rs1295704042 | 19:16,514,660 | C/T | — | uncertain significance |
| rs139234501 | 19:16,515,448 | C/T | — | conflicting classifications of pathogenicity |
| rs2512832258 | 19:16,515,455 | T/C | — | uncertain significance |
| rs1336398507 | 19:16,515,463 | T/G | — | uncertain significance |
| rs2512833023 | 19:16,515,519 | C/A | — | uncertain significance |
| rs1297220753 | 19:16,515,539 | G/A | — | uncertain significance |
| rs144869432 | 19:16,524,627 | C/T | — | uncertain significance |
| rs200246324 | 19:16,528,456 | T/C | — | likely benign |
| rs201102412 | 19:16,528,781 | G/C | — | uncertain significance |
| rs141848098 | 19:16,528,802 | G/A | — | uncertain significance |
| rs146251234 | 19:16,528,810 | T/G | — | uncertain significance |
| rs745463018 | 19:16,532,237 | C/G | — | uncertain significance |
| rs369307683 | 19:16,535,953 | C/T | — | uncertain significance |
| rs143789982 | 19:16,535,970 | G/A | — | uncertain significance |
| rs1234042385 | 19:16,535,976 | C/T | — | uncertain significance |
| rs377090366 | 19:16,536,034 | C/T | — | uncertain significance |
| rs2512946406 | 19:16,536,054 | G/T | — | uncertain significance |
| rs4808510 | 19:16,539,356 | C/G | — | — |
| rs2512963214 | 19:16,539,526 | T/G | — | uncertain significance |
| rs1304569912 | 19:16,545,211 | T/G | — | uncertain significance |
| rs2512988592 | 19:16,545,262 | G/A | — | uncertain significance |
| rs553724318 | 19:16,547,779 | G/A | — | uncertain significance |
| rs10411936 | 19:16,548,375 | A/C | — | — |
| rs747902043 | 19:16,548,591 | G/A | — | uncertain significance |
| rs57839742 | 19:16,559,368 | A/T | — | — |
| rs58166386 | 19:16,559,421 | A/G | intron variant | — |
| rs79788231 | 19:16,569,843 | G/A | intron variant | — |
| rs10408945 | 19:16,576,991 | G/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.