MYO5C
myosin VC
Summary
Predicted to enable actin filament binding activity and microfilament motor activity. Predicted to be involved in actin filament organization. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants104 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2543094188 | 15:52,486,140 | T/C | — | uncertain significance |
| rs2543094288 | 15:52,486,167 | A/G | — | uncertain significance |
| rs374653735 | 15:52,486,235 | C/T | — | uncertain significance |
| rs774601490 | 15:52,487,582 | T/G | — | uncertain significance |
| rs2543100812 | 15:52,488,543 | T/C | — | uncertain significance |
| rs752080146 | 15:52,497,132 | C/G | — | uncertain significance |
| rs200915830 | 15:52,497,163 | C/A | — | uncertain significance |
| rs970778597 | 15:52,497,196 | C/G | — | uncertain significance |
| rs199835263 | 15:52,497,249 | C/T | — | uncertain significance |
| rs1260741198 | 15:52,497,329 | T/G | — | uncertain significance |
| rs977286918 | 15:52,497,341 | G/A | — | uncertain significance |
| rs1328438643 | 15:52,498,097 | A/G | — | uncertain significance |
| rs2543125161 | 15:52,498,109 | C/G | — | uncertain significance |
| rs755213572 | 15:52,500,759 | C/T | — | uncertain significance |
| rs771161538 | 15:52,500,773 | A/G | — | uncertain significance |
| rs200009646 | 15:52,500,824 | A/G | — | uncertain significance |
| rs764025562 | 15:52,503,950 | T/C | — | uncertain significance |
| rs1186888446 | 15:52,503,963 | C/G | — | uncertain significance |
| rs754670620 | 15:52,504,004 | C/T | — | uncertain significance |
| rs570238090 | 15:52,504,010 | G/A | — | uncertain significance |
| rs552636024 | 15:52,504,069 | C/T | — | uncertain significance |
| rs758993594 | 15:52,504,070 | G/T | — | uncertain significance |
| rs112120821 | 15:52,505,468 | G/A | — | likely benign |
| rs201122601 | 15:52,506,853 | A/G | — | uncertain significance |
| rs770508177 | 15:52,510,735 | C/T | — | uncertain significance |
| rs201307143 | 15:52,510,748 | G/T | — | likely benign |
| rs2543153466 | 15:52,510,877 | C/T | — | uncertain significance |
| rs73404874 | 15:52,510,884 | C/G | — | benign |
| rs141240489 | 15:52,510,885 | C/T | — | uncertain significance |
| rs1211888232 | 15:52,511,986 | C/T | — | likely benign |
| rs1205380035 | 15:52,513,449 | T/A | — | uncertain significance |
| rs376832628 | 15:52,515,791 | T/C | — | uncertain significance |
| rs1221655572 | 15:52,515,842 | G/C | — | uncertain significance |
| rs2543167221 | 15:52,515,843 | A/C | — | uncertain significance |
| rs749738365 | 15:52,515,865 | G/A | — | uncertain significance |
| rs201708880 | 15:52,517,099 | G/A | — | uncertain significance |
| rs199650912 | 15:52,517,178 | C/G | — | uncertain significance |
| rs777538927 | 15:52,517,653 | T/C | — | uncertain significance |
| rs1182095059 | 15:52,517,705 | T/C | — | uncertain significance |
| rs772122535 | 15:52,521,401 | G/C | — | uncertain significance |
| rs374398546 | 15:52,524,828 | C/T | — | likely benign |
| rs763437157 | 15:52,524,829 | G/A | — | uncertain significance |
| rs778862426 | 15:52,527,881 | G/A | — | uncertain significance |
| rs199903966 | 15:52,529,717 | C/T | — | conflicting classifications of pathogenicity |
| rs143555762 | 15:52,531,980 | T/C | — | uncertain significance |
| rs267604253 | 15:52,531,989 | C/T | — | uncertain significance |
| rs766392804 | 15:52,532,034 | G/A | — | uncertain significance |
| rs779928665 | 15:52,534,249 | C/T | — | uncertain significance |
| rs772298768 | 15:52,534,269 | G/T | — | uncertain significance |
| rs1349755844 | 15:52,534,337 | G/C | — | uncertain significance |
| rs755980618 | 15:52,534,345 | C/T | — | uncertain significance |
| rs746099723 | 15:52,534,365 | T/C | — | uncertain significance |
| rs769021351 | 15:52,534,391 | C/T | — | uncertain significance |
| rs781503261 | 15:52,536,550 | T/C | — | uncertain significance |
| rs906563408 | 15:52,537,630 | C/G | — | uncertain significance |
| rs753890613 | 15:52,537,655 | A/G | — | uncertain significance |
| rs765244762 | 15:52,538,169 | G/T | — | uncertain significance |
| rs539335624 | 15:52,538,216 | T/C | — | uncertain significance |
| rs372776812 | 15:52,539,168 | G/A | — | uncertain significance |
| rs781590712 | 15:52,539,755 | G/C | — | uncertain significance |
| rs76586635 | 15:52,540,805 | T/G | — | — |
| rs917252559 | 15:52,540,924 | C/T | — | uncertain significance |
| rs2543236149 | 15:52,540,934 | A/T | — | uncertain significance |
| rs773799844 | 15:52,545,611 | A/G | — | uncertain significance |
| rs766863204 | 15:52,545,632 | T/A | — | uncertain significance |
| rs2543252980 | 15:52,548,915 | A/G | — | uncertain significance |
| rs375051159 | 15:52,553,138 | A/G | — | uncertain significance |
| rs201603903 | 15:52,553,141 | C/T | — | uncertain significance |
| rs779133127 | 15:52,553,153 | C/T | — | uncertain significance |
| rs200250841 | 15:52,553,156 | A/G | — | uncertain significance |
| rs949593584 | 15:52,553,223 | C/G | — | uncertain significance |
| rs200784696 | 15:52,553,259 | C/G | — | uncertain significance |
| rs1010156958 | 15:52,553,303 | C/A | — | uncertain significance |
| rs2543269379 | 15:52,556,394 | G/A | — | uncertain significance |
| rs200785449 | 15:52,556,403 | T/C | — | likely benign |
| rs189317194 | 15:52,556,415 | G/A | — | uncertain significance |
| rs180901348 | 15:52,556,426 | C/T | — | likely benign |
| rs778653472 | 15:52,556,467 | C/T | — | likely benign |
| rs754545758 | 15:52,562,049 | C/T | — | uncertain significance |
| rs752692442 | 15:52,562,054 | C/T | — | uncertain significance |
| rs749596996 | 15:52,564,025 | T/G | — | uncertain significance |
| rs943150513 | 15:52,564,028 | C/T | — | uncertain significance |
| rs888364551 | 15:52,564,832 | A/G | — | uncertain significance |
| rs749415370 | 15:52,564,871 | C/G | — | uncertain significance |
| rs1017902309 | 15:52,564,878 | G/A | — | uncertain significance |
| rs201635310 | 15:52,564,893 | T/C | — | uncertain significance |
| rs374820157 | 15:52,564,896 | G/A | — | uncertain significance |
| rs945382386 | 15:52,567,760 | T/G | — | uncertain significance |
| rs759423675 | 15:52,567,785 | C/T | — | uncertain significance |
| rs576864172 | 15:52,567,803 | C/T | — | likely benign |
| rs747741199 | 15:52,567,824 | C/T | — | uncertain significance |
| rs200743352 | 15:52,571,110 | T/C | — | likely benign |
| rs767371909 | 15:52,571,113 | G/T | — | uncertain significance |
| rs756100925 | 15:52,571,125 | C/T | — | uncertain significance |
| rs770573242 | 15:52,571,163 | T/C | — | uncertain significance |
| rs1204838499 | 15:52,571,164 | C/T | — | uncertain significance |
| rs2543307736 | 15:52,571,178 | A/C | — | uncertain significance |
| rs775863790 | 15:52,571,828 | C/T | — | uncertain significance |
| rs77023030 | 15:52,573,016 | A/T | regulatory region variant | — |
| rs754976668 | 15:52,575,022 | C/T | — | uncertain significance |
Showing 100 of 104 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.