MYH15
myosin heavy chain 15
Summary
Predicted to enable actin filament binding activity and microfilament motor activity. Predicted to be involved in extraocular skeletal muscle development. Located in cytosol and intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants173 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201226192 | 3:108,100,406 | C/A | — | benign |
| rs759844449 | 3:108,102,450 | C/G | — | uncertain significance |
| rs756722476 | 3:108,102,501 | C/G | — | uncertain significance |
| rs79837783 | 3:108,102,580 | T/A | — | likely benign |
| rs747814109 | 3:108,103,535 | G/A | — | likely benign |
| rs370570528 | 3:108,103,542 | C/T | — | uncertain significance |
| rs771645089 | 3:108,103,554 | T/G | — | uncertain significance |
| rs1169023362 | 3:108,103,561 | T/G | — | likely benign |
| rs973798055 | 3:108,103,599 | T/A | — | uncertain significance |
| rs576556260 | 3:108,107,842 | C/T | — | uncertain significance |
| rs61745216 | 3:108,107,849 | G/A | — | benign |
| rs1378191227 | 3:108,107,878 | C/G | — | uncertain significance |
| rs114502755 | 3:108,107,928 | C/A | — | benign |
| rs2472315967 | 3:108,110,625 | G/C | — | uncertain significance |
| rs1480479864 | 3:108,110,698 | T/C | — | uncertain significance |
| rs75064307 | 3:108,112,520 | C/T | intron variant | — |
| rs2290601 | 3:108,112,760 | C/T | intron variant | — |
| rs372356011 | 3:108,112,882 | A/G | — | likely benign |
| rs1444895313 | 3:108,112,910 | C/T | — | uncertain significance |
| rs759899590 | 3:108,112,931 | C/T | — | uncertain significance |
| rs748625019 | 3:108,112,940 | C/T | — | uncertain significance |
| rs56118396 | 3:108,112,954 | T/C | — | benign |
| rs763478257 | 3:108,112,958 | C/A | — | uncertain significance |
| rs199685285 | 3:108,112,964 | C/G | — | uncertain significance |
| rs372228730 | 3:108,117,545 | C/T | — | uncertain significance |
| rs2082481264 | 3:108,117,559 | C/G | — | uncertain significance |
| rs765108967 | 3:108,117,611 | C/T | — | likely benign |
| rs76478083 | 3:108,117,612 | G/A | — | likely benign |
| rs369120535 | 3:108,117,634 | C/A | — | uncertain significance |
| rs1442792908 | 3:108,117,657 | G/T | — | uncertain significance |
| rs187218353 | 3:108,117,950 | G/C | — | uncertain significance |
| rs763958814 | 3:108,117,969 | C/A | — | uncertain significance |
| rs761699091 | 3:108,117,975 | G/A | — | uncertain significance |
| rs1024468519 | 3:108,118,014 | C/T | — | uncertain significance |
| rs758857596 | 3:108,118,027 | C/A | — | uncertain significance |
| rs6786515 | 3:108,118,714 | C/T | intron variant | — |
| rs530022684 | 3:108,124,233 | T/C | — | uncertain significance |
| rs747904706 | 3:108,124,287 | C/T | — | uncertain significance |
| rs200741935 | 3:108,124,288 | G/A | — | uncertain significance |
| rs1381236156 | 3:108,127,144 | T/C | — | likely benign |
| rs1332521067 | 3:108,127,148 | C/G | — | uncertain significance |
| rs9878261 | 3:108,127,232 | T/C | — | benign |
| rs76765976 | 3:108,127,252 | C/A | — | benign |
| rs2472339934 | 3:108,129,451 | T/C | — | uncertain significance |
| rs1440550641 | 3:108,129,489 | G/A | — | uncertain significance |
| rs2472340119 | 3:108,129,514 | T/C | — | uncertain significance |
| rs370933466 | 3:108,129,568 | C/T | — | uncertain significance |
| rs1078456 | 3:108,129,586 | C/T | — | benign |
| rs368421301 | 3:108,129,652 | C/A | — | uncertain significance |
| rs769342956 | 3:108,129,670 | C/G | — | uncertain significance |
| rs368538771 | 3:108,129,673 | C/G | — | uncertain significance |
| rs200032613 | 3:108,129,724 | C/T | — | uncertain significance |
| rs2472340696 | 3:108,129,730 | C/T | — | uncertain significance |
| rs371195676 | 3:108,129,733 | C/T | — | uncertain significance |
| rs781352497 | 3:108,129,747 | G/A | — | uncertain significance |
| rs144890841 | 3:108,133,072 | T/C | — | benign |
| rs1252275172 | 3:108,133,153 | A/T | — | uncertain significance |
| rs1267055483 | 3:108,133,154 | T/C | — | uncertain significance |
| rs202066788 | 3:108,133,172 | C/T | — | uncertain significance |
| rs373059438 | 3:108,133,173 | G/A | — | uncertain significance |
| rs149020906 | 3:108,133,189 | G/A | — | benign |
| rs1456283634 | 3:108,133,217 | C/T | — | uncertain significance |
| rs768579358 | 3:108,133,235 | C/T | — | likely benign |
| rs1433192016 | 3:108,135,695 | A/C | — | uncertain significance |
| rs374236023 | 3:108,135,703 | G/A | — | likely benign |
| rs73207913 | 3:108,139,077 | C/T | intron variant | — |
| rs369737961 | 3:108,140,019 | G/A | — | uncertain significance |
| rs201690373 | 3:108,140,025 | G/A | — | uncertain significance |
| rs113330737 | 3:108,147,333 | A/G | — | benign |
| rs746369043 | 3:108,147,355 | T/C | — | uncertain significance |
| rs201473403 | 3:108,147,510 | A/G | — | likely benign |
| rs776507202 | 3:108,147,538 | C/T | — | likely benign |
| rs760486327 | 3:108,147,559 | G/A | — | uncertain significance |
| rs558561858 | 3:108,147,617 | G/T | — | uncertain significance |
| rs999832007 | 3:108,147,656 | C/T | — | uncertain significance |
| rs144965775 | 3:108,147,675 | G/A | — | benign |
| rs777324136 | 3:108,147,679 | C/T | — | uncertain significance |
| rs61744539 | 3:108,147,680 | A/G | — | likely benign |
| rs3900940 | 3:108,147,728 | T/A | missense variant | — |
| rs1531188 | 3:108,148,557 | C/T | intron variant | — |
| rs369281600 | 3:108,149,693 | C/A | — | uncertain significance |
| rs199968089 | 3:108,149,707 | T/C | — | uncertain significance |
| rs1227195542 | 3:108,149,710 | G/A | — | uncertain significance |
| rs2472365831 | 3:108,149,716 | A/C | — | uncertain significance |
| rs534599773 | 3:108,149,746 | A/G | — | uncertain significance |
| rs113689582 | 3:108,150,991 | C/T | intron variant | — |
| rs115721142 | 3:108,156,396 | C/A | — | benign |
| rs1209072266 | 3:108,156,449 | A/G | — | uncertain significance |
| rs201356810 | 3:108,156,459 | G/A | — | uncertain significance |
| rs371676709 | 3:108,156,493 | T/G | — | uncertain significance |
| rs2472377732 | 3:108,156,495 | C/G | — | uncertain significance |
| rs200949025 | 3:108,156,515 | G/A | — | uncertain significance |
| rs367902528 | 3:108,156,539 | C/G | — | uncertain significance |
| rs75221360 | 3:108,159,878 | G/A | — | uncertain significance |
| rs768199591 | 3:108,159,908 | A/G | — | uncertain significance |
| rs185257681 | 3:108,159,910 | T/G | — | likely benign |
| rs373858705 | 3:108,159,924 | C/T | — | uncertain significance |
| rs371327462 | 3:108,159,932 | T/G | — | uncertain significance |
| rs781725412 | 3:108,159,965 | C/T | — | uncertain significance |
| rs750956706 | 3:108,159,974 | G/A | — | uncertain significance |
Showing 100 of 173 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.