SYNPO
synaptopodin
Summary
Synaptopodin is an actin-associated protein that may play a role in actin-based cell shape and motility. The name synaptopodin derives from the protein's associations with postsynaptic densities and dendritic spines and with renal podocytes (Mundel et al., 1997 [PubMed 9314539]).[supplied by OMIM, Mar 2008]
Known Variants181 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11740208 | 5:149,976,487 | G/A | — | — |
| rs76537501 | 5:149,997,474 | G/A | — | benign |
| rs58237678 | 5:149,997,536 | T/C | — | benign |
| rs59962087 | 5:149,997,659 | C/A | — | benign |
| rs6579796 | 5:149,997,911 | G/A | — | benign |
| rs371137506 | 5:149,998,046 | G/T | — | uncertain significance |
| rs6579797 | 5:149,998,128 | G/C | missense variant | benign |
| rs369739500 | 5:149,998,318 | C/T | — | likely benign |
| rs2480369868 | 5:150,027,554 | A/C | — | uncertain significance |
| rs1310889102 | 5:150,027,581 | A/G | — | uncertain significance |
| rs1233176451 | 5:150,027,587 | C/T | — | uncertain significance |
| rs751195238 | 5:150,027,605 | A/G | — | uncertain significance |
| rs1175307647 | 5:150,027,611 | G/A | — | uncertain significance |
| rs757549506 | 5:150,027,710 | G/C | — | uncertain significance |
| rs187039904 | 5:150,027,767 | C/T | — | uncertain significance |
| rs770697443 | 5:150,027,849 | C/T | — | likely benign |
| rs373884404 | 5:150,027,852 | A/G | — | likely benign |
| rs759517134 | 5:150,027,980 | G/A | — | uncertain significance |
| rs2480375137 | 5:150,028,000 | C/T | — | uncertain significance |
| rs142079099 | 5:150,028,009 | C/T | — | uncertain significance |
| rs370579156 | 5:150,028,056 | T/A | — | likely benign |
| rs200631093 | 5:150,028,061 | C/T | — | uncertain significance |
| rs555455244 | 5:150,028,074 | G/A | — | likely benign |
| rs201288895 | 5:150,028,109 | C/T | — | conflicting classifications of pathogenicity |
| rs2480376279 | 5:150,028,121 | A/T | — | uncertain significance |
| rs145720408 | 5:150,028,134 | C/T | — | likely benign |
| rs369769452 | 5:150,028,139 | C/T | — | uncertain significance |
| rs373212175 | 5:150,028,160 | G/A | — | uncertain significance |
| rs151142897 | 5:150,028,170 | T/C | — | likely benign |
| rs2480377443 | 5:150,028,196 | A/C | — | uncertain significance |
| rs1561654787 | 5:150,028,198 | G/A | — | uncertain significance |
| rs533483214 | 5:150,028,218 | C/T | — | likely benign |
| rs761117289 | 5:150,028,256 | A/T | — | uncertain significance |
| rs184098652 | 5:150,028,274 | C/T | — | likely benign |
| rs750474276 | 5:150,028,307 | T/C | — | uncertain significance |
| rs2480378793 | 5:150,028,327 | G/A | — | uncertain significance |
| rs777440231 | 5:150,028,361 | C/T | — | uncertain significance |
| rs745358433 | 5:150,028,380 | G/A | — | benign |
| rs893008241 | 5:150,028,393 | G/C | — | uncertain significance |
| rs2480380039 | 5:150,028,403 | C/G | — | uncertain significance |
| rs769889153 | 5:150,028,406 | G/A | — | uncertain significance |
| rs201230432 | 5:150,028,408 | T/A | — | likely benign |
| rs201930365 | 5:150,028,488 | G/A | — | likely benign |
| rs1275338233 | 5:150,028,537 | T/C | — | uncertain significance |
| rs41336050 | 5:150,028,577 | C/T | — | uncertain significance |
| rs150372498 | 5:150,028,578 | G/A | — | likely benign |
| rs149502965 | 5:150,028,613 | T/C | — | uncertain significance |
| rs144793851 | 5:150,028,620 | G/C | — | uncertain significance |
| rs41520647 | 5:150,028,639 | A/G | — | uncertain significance |
| rs142043265 | 5:150,028,646 | C/T | — | uncertain significance |
| rs371488666 | 5:150,028,647 | G/A | — | likely benign |
| rs2480383419 | 5:150,028,648 | G/A | — | uncertain significance |
| rs146345840 | 5:150,028,651 | C/T | — | likely benign |
| rs374045522 | 5:150,028,661 | C/G | — | uncertain significance |
| rs148505175 | 5:150,028,663 | A/G | — | likely benign |
| rs756648276 | 5:150,028,684 | C/T | — | uncertain significance |
| rs141856687 | 5:150,028,685 | G/A | — | uncertain significance |
| rs375811693 | 5:150,028,709 | G/A | — | uncertain significance |
| rs367675794 | 5:150,028,718 | T/C | — | uncertain significance |
| rs2480384322 | 5:150,028,722 | G/A | — | likely benign |
| rs762832656 | 5:150,028,752 | G/A | — | likely benign |
| rs150686584 | 5:150,028,761 | G/A | — | likely benign |
| rs1320261343 | 5:150,028,774 | G/A | — | uncertain significance |
| rs34850457 | 5:150,028,796 | C/A | — | benign |
| rs779357633 | 5:150,028,807 | A/T | — | uncertain significance |
| rs749255472 | 5:150,028,829 | C/T | — | uncertain significance |
| rs759292082 | 5:150,028,856 | A/G | — | uncertain significance |
| rs928489254 | 5:150,028,910 | C/T | — | uncertain significance |
| rs1343433161 | 5:150,028,928 | C/T | — | uncertain significance |
| rs771829726 | 5:150,028,946 | C/T | — | uncertain significance |
| rs745691549 | 5:150,028,967 | G/A | — | uncertain significance |
| rs1259489802 | 5:150,029,056 | C/T | — | uncertain significance |
| rs199673919 | 5:150,029,071 | G/C | — | uncertain significance |
| rs200584473 | 5:150,029,083 | G/A | — | uncertain significance |
| rs34838671 | 5:150,029,146 | C/T | — | uncertain significance |
| rs771544767 | 5:150,029,163 | C/T | — | likely benign |
| rs775723716 | 5:150,029,169 | G/A | — | likely benign |
| rs143457316 | 5:150,029,171 | C/T | — | conflicting classifications of pathogenicity |
| rs200798227 | 5:150,029,229 | G/A | — | likely benign |
| rs144726615 | 5:150,029,232 | G/A | — | benign |
| rs775685409 | 5:150,029,253 | C/A | — | uncertain significance |
| rs2480391895 | 5:150,029,295 | C/T | — | likely benign |
| rs202036742 | 5:150,029,325 | C/T | — | benign |
| rs755997156 | 5:150,029,342 | C/T | — | uncertain significance |
| rs1345645545 | 5:150,029,390 | C/T | — | uncertain significance |
| rs2480392814 | 5:150,029,392 | T/A | — | uncertain significance |
| rs374090784 | 5:150,029,410 | G/A | — | uncertain significance |
| rs3733931 | 5:150,029,415 | C/T | — | benign |
| rs969736241 | 5:150,029,416 | G/A | — | uncertain significance |
| rs2480393699 | 5:150,029,441 | G/A | — | uncertain significance |
| rs368637681 | 5:150,029,450 | G/A | — | uncertain significance |
| rs202224903 | 5:150,029,501 | T/C | — | likely benign |
| rs149554571 | 5:150,029,503 | C/T | — | uncertain significance |
| rs767231888 | 5:150,029,524 | C/T | — | uncertain significance |
| rs1264912311 | 5:150,029,540 | G/A | — | uncertain significance |
| rs375476992 | 5:150,029,575 | C/T | — | uncertain significance |
| rs144240217 | 5:150,029,579 | C/T | — | likely benign |
| rs1327534417 | 5:150,029,600 | C/A | — | uncertain significance |
| rs368497168 | 5:150,029,603 | C/T | — | uncertain significance |
| rs1429864228 | 5:150,029,638 | A/C | — | uncertain significance |
Showing 100 of 181 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.