MYOM3
myomesin 3
Summary
Predicted to enable protein homodimerization activity. Predicted to be involved in sarcomere organization. Predicted to be located in cytoplasm. Predicted to be active in M band. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants131 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs767491269 | 1:24,383,861 | C/T | — | uncertain significance |
| rs201761830 | 1:24,383,918 | G/A | — | uncertain significance |
| rs200459313 | 1:24,383,958 | G/A | — | uncertain significance |
| rs377022872 | 1:24,384,024 | G/A | — | uncertain significance |
| rs1339263607 | 1:24,384,034 | A/G | — | likely benign |
| rs545471092 | 1:24,384,045 | C/T | — | uncertain significance |
| rs768039253 | 1:24,384,096 | C/T | — | likely benign |
| rs201441408 | 1:24,384,114 | G/T | — | uncertain significance |
| rs540279109 | 1:24,384,413 | C/T | — | — |
| rs753915841 | 1:24,385,433 | G/C | — | uncertain significance |
| rs961510485 | 1:24,385,442 | G/A | — | uncertain significance |
| rs754458069 | 1:24,388,450 | T/G | — | uncertain significance |
| rs762828925 | 1:24,388,524 | G/T | — | uncertain significance |
| rs755699689 | 1:24,388,567 | C/T | — | uncertain significance |
| rs371553713 | 1:24,388,573 | C/T | — | uncertain significance |
| rs748384660 | 1:24,389,641 | A/G | — | uncertain significance |
| rs140762098 | 1:24,389,690 | G/A | — | likely benign |
| rs766889836 | 1:24,389,706 | A/G | — | uncertain significance |
| rs2522788453 | 1:24,390,577 | C/A | — | uncertain significance |
| rs142799431 | 1:24,390,604 | C/A | — | uncertain significance |
| rs1187253364 | 1:24,390,638 | C/A | — | uncertain significance |
| rs139328461 | 1:24,392,325 | T/C | — | likely benign |
| rs926555960 | 1:24,392,392 | A/C | — | uncertain significance |
| rs765255132 | 1:24,392,402 | C/T | — | likely benign |
| rs371522272 | 1:24,392,413 | C/T | — | uncertain significance |
| rs779589433 | 1:24,393,516 | A/G | — | uncertain significance |
| rs372855664 | 1:24,393,536 | T/C | — | uncertain significance |
| rs200672813 | 1:24,394,714 | G/A | — | likely benign |
| rs376479533 | 1:24,394,755 | C/T | — | uncertain significance |
| rs201010210 | 1:24,394,770 | C/T | — | uncertain significance |
| rs1408015765 | 1:24,394,773 | T/C | — | uncertain significance |
| rs2522807013 | 1:24,394,788 | C/A | — | uncertain significance |
| rs145156576 | 1:24,394,835 | C/G | — | uncertain significance |
| rs374495623 | 1:24,394,836 | G/C | — | uncertain significance |
| rs190172239 | 1:24,395,465 | C/T | intron variant | — |
| rs371240271 | 1:24,397,608 | G/A | — | uncertain significance |
| rs1045216533 | 1:24,397,617 | A/G | — | uncertain significance |
| rs780458567 | 1:24,397,649 | C/G | — | uncertain significance |
| rs374619324 | 1:24,397,675 | C/T | — | uncertain significance |
| rs952599438 | 1:24,398,464 | T/C | — | uncertain significance |
| rs373813223 | 1:24,400,658 | G/A | — | uncertain significance |
| rs376787618 | 1:24,400,659 | T/A | — | uncertain significance |
| rs200099929 | 1:24,400,719 | C/G | — | uncertain significance |
| rs190544582 | 1:24,401,933 | C/T | — | uncertain significance |
| rs550247481 | 1:24,401,958 | A/C | — | uncertain significance |
| rs143415979 | 1:24,402,670 | C/T | — | uncertain significance |
| rs1027026608 | 1:24,402,681 | G/A | — | uncertain significance |
| rs767537845 | 1:24,402,685 | T/C | — | uncertain significance |
| rs1643646877 | 1:24,406,505 | C/T | — | uncertain significance |
| rs375791231 | 1:24,406,528 | G/A | — | uncertain significance |
| rs1194628210 | 1:24,406,540 | A/T | — | uncertain significance |
| rs1340725587 | 1:24,406,598 | G/A | — | uncertain significance |
| rs374933004 | 1:24,406,607 | C/T | — | uncertain significance |
| rs779858144 | 1:24,406,610 | T/C | — | uncertain significance |
| rs200017159 | 1:24,406,651 | C/T | — | uncertain significance |
| rs199679581 | 1:24,406,652 | G/A | — | uncertain significance |
| rs765920079 | 1:24,406,655 | C/T | — | uncertain significance |
| rs201302124 | 1:24,407,913 | A/G | — | uncertain significance |
| rs527935454 | 1:24,407,928 | C/T | — | uncertain significance |
| rs367603089 | 1:24,408,501 | C/G | — | uncertain significance |
| rs2522854250 | 1:24,408,517 | G/C | — | uncertain significance |
| rs369571711 | 1:24,408,595 | G/T | — | uncertain significance |
| rs2522854673 | 1:24,408,621 | A/T | — | uncertain significance |
| rs760274173 | 1:24,409,098 | C/A | — | uncertain significance |
| rs148441250 | 1:24,409,181 | G/C | — | uncertain significance |
| rs1336729033 | 1:24,410,962 | T/G | — | uncertain significance |
| rs2522864522 | 1:24,411,022 | A/G | — | uncertain significance |
| rs373823143 | 1:24,413,146 | G/A | — | uncertain significance |
| rs367585562 | 1:24,413,152 | C/T | — | uncertain significance |
| rs776323581 | 1:24,413,172 | G/A | — | uncertain significance |
| rs953479746 | 1:24,413,197 | T/A | — | uncertain significance |
| rs200272032 | 1:24,413,222 | C/T | — | likely benign |
| rs183173497 | 1:24,413,248 | C/T | — | uncertain significance |
| rs1458750184 | 1:24,413,281 | A/G | — | uncertain significance |
| rs114127073 | 1:24,413,883 | C/A | downstream gene variant | — |
| rs1240977992 | 1:24,416,074 | T/G | — | uncertain significance |
| rs535235744 | 1:24,416,111 | C/T | — | uncertain significance |
| rs201031583 | 1:24,416,117 | C/T | — | uncertain significance |
| rs200021174 | 1:24,416,143 | A/T | — | uncertain significance |
| rs752583370 | 1:24,416,602 | G/A | — | uncertain significance |
| rs2522886514 | 1:24,417,289 | G/A | — | uncertain significance |
| rs2522886778 | 1:24,417,338 | C/T | — | uncertain significance |
| rs140717407 | 1:24,417,350 | C/T | — | uncertain significance |
| rs201540067 | 1:24,417,373 | G/T | — | uncertain significance |
| rs777864474 | 1:24,417,376 | C/G | — | uncertain significance |
| rs201416125 | 1:24,417,383 | G/A | — | uncertain significance |
| rs368225792 | 1:24,417,389 | G/A | — | uncertain significance |
| rs184649466 | 1:24,417,428 | G/A | — | uncertain significance |
| rs746117980 | 1:24,417,430 | C/T | — | uncertain significance |
| rs527719064 | 1:24,417,470 | C/T | — | uncertain significance |
| rs201180005 | 1:24,418,697 | C/T | — | uncertain significance |
| rs1448807976 | 1:24,418,746 | C/T | — | uncertain significance |
| rs778312960 | 1:24,418,767 | G/T | — | uncertain significance |
| rs199675940 | 1:24,418,800 | C/T | — | uncertain significance |
| rs780664587 | 1:24,419,481 | G/A | — | uncertain significance |
| rs367570862 | 1:24,419,491 | G/A | — | uncertain significance |
| rs764993464 | 1:24,419,538 | A/T | — | uncertain significance |
| rs200618328 | 1:24,419,556 | G/A | — | uncertain significance |
| rs374208248 | 1:24,419,571 | C/T | — | uncertain significance |
| rs778378166 | 1:24,419,580 | G/A | — | uncertain significance |
Showing 100 of 131 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.