MYO18A
myosin XVIIIA
Summary
The protein encoded by this gene can bind GOLPH3, linking the Golgi to the cytoskeleton and influencing Golgi membrane trafficking. The encoded protein is also part of a complex that assembles lamellar actomyosin bundles and may be required for cell migration. [provided by RefSeq, Oct 2016]
Known Variants173 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1334867848 | 17:27,401,022 | A/C | — | uncertain significance |
| rs757416941 | 17:27,401,046 | C/T | — | likely benign |
| rs73986791 | 17:27,401,061 | C/T | — | benign |
| rs2545416684 | 17:27,401,076 | A/C | — | uncertain significance |
| rs76270749 | 17:27,401,080 | T/C | — | benign |
| rs78839711 | 17:27,401,105 | G/A | — | uncertain significance |
| rs750624381 | 17:27,401,117 | C/T | — | uncertain significance |
| rs1451396260 | 17:27,401,125 | A/T | — | uncertain significance |
| rs151013388 | 17:27,401,145 | G/A | — | likely benign |
| rs368933068 | 17:27,401,183 | G/A | — | uncertain significance |
| rs1185677962 | 17:27,401,211 | A/G | — | uncertain significance |
| rs200380774 | 17:27,401,852 | C/T | — | uncertain significance |
| rs773215389 | 17:27,401,855 | G/A | — | uncertain significance |
| rs200001601 | 17:27,401,872 | G/A | — | likely benign |
| rs372030853 | 17:27,401,880 | C/T | — | likely benign |
| rs752022497 | 17:27,401,890 | A/T | — | uncertain significance |
| rs757808931 | 17:27,401,898 | G/A | — | uncertain significance |
| rs1167874438 | 17:27,401,921 | T/A | — | uncertain significance |
| rs2545491048 | 17:27,409,425 | C/T | — | uncertain significance |
| rs375647301 | 17:27,413,506 | A/G | — | benign |
| rs201048224 | 17:27,413,528 | T/C | — | uncertain significance |
| rs185018719 | 17:27,413,554 | C/A | — | likely benign |
| rs139666837 | 17:27,413,960 | G/A | — | benign |
| rs144302282 | 17:27,413,975 | C/T | — | benign |
| rs35265675 | 17:27,413,981 | G/A | — | benign |
| rs370559537 | 17:27,413,991 | C/T | — | uncertain significance |
| rs1187911125 | 17:27,414,001 | C/T | — | uncertain significance |
| rs748567160 | 17:27,414,025 | G/A | — | uncertain significance |
| rs773518579 | 17:27,414,075 | G/A | — | uncertain significance |
| rs2544352802 | 17:27,414,076 | C/T | — | uncertain significance |
| rs374576391 | 17:27,414,096 | T/A | — | uncertain significance |
| rs752123909 | 17:27,417,032 | G/A | — | uncertain significance |
| rs913250612 | 17:27,417,065 | T/C | — | uncertain significance |
| rs1304367384 | 17:27,417,095 | C/A | — | uncertain significance |
| rs781091413 | 17:27,417,107 | G/C | — | uncertain significance |
| rs749532145 | 17:27,417,597 | C/T | — | uncertain significance |
| rs2544448503 | 17:27,417,608 | T/C | — | uncertain significance |
| rs2544448553 | 17:27,417,623 | T/C | — | uncertain significance |
| rs2066380607 | 17:27,417,848 | G/A | — | uncertain significance |
| rs565970571 | 17:27,417,851 | T/G | — | uncertain significance |
| rs767048813 | 17:27,417,892 | C/T | — | uncertain significance |
| rs533432831 | 17:27,417,907 | T/C | — | uncertain significance |
| rs199562933 | 17:27,417,916 | C/T | — | uncertain significance |
| rs115455253 | 17:27,417,925 | C/T | — | likely benign |
| rs751433687 | 17:27,419,441 | C/T | — | uncertain significance |
| rs377454229 | 17:27,419,449 | G/A | — | uncertain significance |
| rs745311924 | 17:27,419,898 | C/T | — | uncertain significance |
| rs368097941 | 17:27,419,904 | C/T | — | uncertain significance |
| rs758806767 | 17:27,419,983 | G/A | — | uncertain significance |
| rs749210452 | 17:27,420,003 | A/C | — | uncertain significance |
| rs752544509 | 17:27,420,366 | C/T | — | uncertain significance |
| rs1318578296 | 17:27,420,438 | T/G | — | uncertain significance |
| rs750280486 | 17:27,421,041 | C/T | — | not provided |
| rs751247065 | 17:27,422,022 | G/A | — | uncertain significance |
| rs375653114 | 17:27,422,036 | C/T | — | uncertain significance |
| rs2544547295 | 17:27,422,075 | A/C | — | uncertain significance |
| rs12938581 | 17:27,422,776 | T/C | upstream gene variant | — |
| rs2066528913 | 17:27,423,822 | C/T | — | uncertain significance |
| rs777594643 | 17:27,424,245 | C/T | — | uncertain significance |
| rs2544589947 | 17:27,424,319 | G/T | — | uncertain significance |
| rs201296071 | 17:27,424,356 | C/T | — | likely benign |
| rs1046179825 | 17:27,424,357 | G/A | — | uncertain significance |
| rs774237260 | 17:27,424,847 | C/T | — | uncertain significance |
| rs201591312 | 17:27,424,848 | G/A | — | uncertain significance |
| rs772944016 | 17:27,424,854 | G/A | — | uncertain significance |
| rs766466501 | 17:27,424,857 | G/A | — | uncertain significance |
| rs753243189 | 17:27,424,874 | A/G | — | uncertain significance |
| rs34191688 | 17:27,424,891 | C/T | — | benign |
| rs71369700 | 17:27,425,132 | C/T | — | benign |
| rs374966524 | 17:27,425,173 | C/T | — | uncertain significance |
| rs200040962 | 17:27,425,174 | G/A | — | likely benign |
| rs372665672 | 17:27,425,191 | C/T | — | uncertain significance |
| rs1329414528 | 17:27,425,209 | G/A | — | uncertain significance |
| rs1182327493 | 17:27,425,429 | T/G | — | uncertain significance |
| rs568992850 | 17:27,425,444 | C/T | — | uncertain significance |
| rs76590796 | 17:27,425,854 | C/T | — | likely benign |
| rs777985641 | 17:27,425,920 | G/A | — | uncertain significance |
| rs562045610 | 17:27,425,937 | T/A | — | uncertain significance |
| rs200673161 | 17:27,426,727 | T/G | — | uncertain significance |
| rs370961010 | 17:27,426,742 | C/A | — | uncertain significance |
| rs115267475 | 17:27,426,753 | G/A | — | benign |
| rs367942125 | 17:27,426,771 | G/A | — | uncertain significance |
| rs372597242 | 17:27,434,115 | C/A | — | uncertain significance |
| rs1032448858 | 17:27,434,139 | T/C | — | uncertain significance |
| rs762362806 | 17:27,434,196 | G/A | — | uncertain significance |
| rs149726067 | 17:27,436,868 | G/T | — | benign |
| rs763756760 | 17:27,436,882 | G/A | — | uncertain significance |
| rs749518766 | 17:27,436,915 | C/T | — | uncertain significance |
| rs377249402 | 17:27,436,941 | A/T | — | uncertain significance |
| rs763845502 | 17:27,436,942 | C/T | — | uncertain significance |
| rs758514569 | 17:27,436,984 | G/T | — | uncertain significance |
| rs372516386 | 17:27,437,013 | C/T | — | uncertain significance |
| rs375482122 | 17:27,437,016 | C/T | — | uncertain significance |
| rs977561607 | 17:27,437,017 | G/A | — | uncertain significance |
| rs768372239 | 17:27,437,026 | C/T | — | uncertain significance |
| rs200969774 | 17:27,437,032 | G/A | — | uncertain significance |
| rs1316653453 | 17:27,437,085 | A/G | — | uncertain significance |
| rs2544836183 | 17:27,437,515 | A/T | — | uncertain significance |
| rs377527263 | 17:27,437,537 | C/T | — | uncertain significance |
| rs763098744 | 17:27,437,539 | C/T | — | uncertain significance |
Showing 100 of 173 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.