ABLIM1
actin binding LIM protein 1
Summary
This gene encodes a LIM zinc-binding domain-containing protein that binds to actin filaments and mediates interactions between actin and cytoplasmic targets. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2017]
Known Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs530174120 | 10:116,196,105 | C/T | — | uncertain significance |
| rs200083344 | 10:116,196,107 | C/A | — | uncertain significance |
| rs1260510217 | 10:116,197,629 | T/C | — | uncertain significance |
| rs2059652561 | 10:116,197,656 | T/C | — | uncertain significance |
| rs139367133 | 10:116,198,996 | C/A | — | uncertain significance |
| rs941853 | 10:116,199,175 | G/A | intron variant | — |
| rs935379889 | 10:116,200,802 | T/C | — | uncertain significance |
| rs201140669 | 10:116,200,811 | T/C | — | uncertain significance |
| rs753542135 | 10:116,201,482 | C/T | — | uncertain significance |
| rs780911994 | 10:116,203,827 | A/G | — | uncertain significance |
| rs143955890 | 10:116,203,838 | C/T | — | uncertain significance |
| rs1473633676 | 10:116,203,839 | G/A | — | uncertain significance |
| rs727532 | 10:116,204,776 | A/G | intron variant | — |
| rs768395853 | 10:116,205,156 | T/C | — | uncertain significance |
| rs780288120 | 10:116,207,684 | T/A | — | uncertain significance |
| rs2505264023 | 10:116,207,693 | T/A | — | uncertain significance |
| rs200090370 | 10:116,207,753 | A/C | — | uncertain significance |
| rs777212178 | 10:116,213,168 | C/T | — | uncertain significance |
| rs778437966 | 10:116,213,213 | G/T | — | uncertain significance |
| rs143815431 | 10:116,213,225 | C/T | — | uncertain significance |
| rs141945341 | 10:116,225,483 | C/T | — | uncertain significance |
| rs1373772536 | 10:116,225,489 | G/A | — | uncertain significance |
| rs868447773 | 10:116,225,511 | G/A | — | uncertain significance |
| rs760395146 | 10:116,225,517 | A/C | — | uncertain significance |
| rs1661779234 | 10:116,225,555 | T/A | — | uncertain significance |
| rs375611769 | 10:116,225,564 | C/T | — | uncertain significance |
| rs745604571 | 10:116,227,966 | T/A | — | uncertain significance |
| rs2506699403 | 10:116,227,968 | C/T | — | uncertain significance |
| rs2066893774 | 10:116,232,795 | A/G | — | uncertain significance |
| rs531917073 | 10:116,232,958 | G/A | — | — |
| rs2507322474 | 10:116,233,657 | G/A | — | uncertain significance |
| rs772641158 | 10:116,233,675 | C/G | — | uncertain significance |
| rs372492992 | 10:116,233,678 | G/C | — | uncertain significance |
| rs11196758 | 10:116,237,760 | C/G | — | — |
| rs200728197 | 10:116,247,767 | C/T | — | uncertain significance |
| rs766636587 | 10:116,251,584 | C/G | — | uncertain significance |
| rs2508965827 | 10:116,251,616 | G/A | — | uncertain significance |
| rs758650622 | 10:116,251,631 | C/T | — | uncertain significance |
| rs1366832886 | 10:116,304,846 | G/A | — | uncertain significance |
| rs1303154038 | 10:116,307,514 | T/C | — | uncertain significance |
| rs2483547 | 10:116,318,672 | C/T | — | — |
| rs10885582 | 10:116,327,550 | T/C | intron variant | — |
| rs1488751953 | 10:116,331,058 | C/T | — | uncertain significance |
| rs200432876 | 10:116,331,163 | C/T | — | uncertain significance |
| rs931524045 | 10:116,335,249 | C/G | — | uncertain significance |
| rs144719371 | 10:116,335,260 | C/T | — | uncertain significance |
| rs769390756 | 10:116,335,275 | C/T | — | uncertain significance |
| rs2511441710 | 10:116,335,281 | T/C | — | uncertain significance |
| rs776165405 | 10:116,335,283 | C/T | — | uncertain significance |
| rs367711981 | 10:116,335,329 | A/G | — | uncertain significance |
| rs141394205 | 10:116,336,469 | C/T | intron variant | — |
| rs1441751878 | 10:116,361,712 | G/C | — | uncertain significance |
| rs10885588 | 10:116,390,793 | G/A | intron variant | — |
| rs201341957 | 10:116,417,737 | A/G | — | uncertain significance |
| rs753417432 | 10:116,417,743 | G/A | — | uncertain significance |
| rs2513379271 | 10:116,417,784 | T/C | — | uncertain significance |
| rs200655611 | 10:116,417,796 | G/C | — | uncertain significance |
| rs747877624 | 10:116,417,865 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.