MYO1B
myosin IB
Summary
Enables ATP binding activity; actin filament binding activity; and microfilament motor activity. Involved in actin filament organization and post-Golgi vesicle-mediated transport. Located in several cellular components, including actin filament; endosome; and trans-Golgi network membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs13019004 | 2:192,110,219 | C/G | — | — |
| rs13030978 | 2:192,117,238 | C/T | intron variant | — |
| rs1823913 | 2:192,118,047 | T/G | — | — |
| rs10931491 | 2:192,120,813 | G/C | — | — |
| rs1688970086 | 2:192,160,871 | C/T | — | uncertain significance |
| rs16833579 | 2:192,160,939 | C/T | — | benign |
| rs1456538068 | 2:192,194,665 | G/T | — | uncertain significance |
| rs1436274669 | 2:192,206,222 | G/A | — | uncertain significance |
| rs571631275 | 2:192,206,271 | A/G | — | uncertain significance |
| rs1433259503 | 2:192,206,280 | C/T | — | uncertain significance |
| rs142741123 | 2:192,207,115 | T/C | intron variant | — |
| rs772294497 | 2:192,214,910 | T/G | — | uncertain significance |
| rs372393246 | 2:192,227,012 | G/C | — | uncertain significance |
| rs981011943 | 2:192,228,458 | C/T | — | uncertain significance |
| rs139492822 | 2:192,228,907 | A/G | — | uncertain significance |
| rs764901908 | 2:192,228,982 | A/G | — | uncertain significance |
| rs780531601 | 2:192,234,335 | G/A | — | uncertain significance |
| rs2469557214 | 2:192,246,277 | G/C | — | uncertain significance |
| rs2469593569 | 2:192,250,668 | C/T | — | uncertain significance |
| rs751800512 | 2:192,250,712 | C/T | — | uncertain significance |
| rs751651155 | 2:192,251,974 | G/A | — | uncertain significance |
| rs756300060 | 2:192,252,035 | A/G | — | uncertain significance |
| rs73984118 | 2:192,255,030 | G/A | — | benign |
| rs746831096 | 2:192,255,148 | T/G | — | uncertain significance |
| rs775824635 | 2:192,255,170 | A/G | — | uncertain significance |
| rs754453637 | 2:192,255,205 | A/C | — | uncertain significance |
| rs746728776 | 2:192,256,887 | C/T | — | uncertain significance |
| rs148260477 | 2:192,256,898 | T/A | — | uncertain significance |
| rs201068066 | 2:192,256,914 | G/A | — | uncertain significance |
| rs149384034 | 2:192,257,809 | T/C | — | uncertain significance |
| rs746233050 | 2:192,257,899 | T/C | — | uncertain significance |
| rs2469652238 | 2:192,257,925 | G/A | — | uncertain significance |
| rs766138754 | 2:192,257,932 | G/C | — | uncertain significance |
| rs1480988061 | 2:192,257,937 | A/G | — | uncertain significance |
| rs114890021 | 2:192,261,160 | A/G | — | benign |
| rs1696077711 | 2:192,261,165 | G/A | — | uncertain significance |
| rs750662699 | 2:192,261,179 | A/C | — | uncertain significance |
| rs200675888 | 2:192,265,123 | C/T | — | uncertain significance |
| rs1173087972 | 2:192,265,190 | C/T | — | uncertain significance |
| rs185761535 | 2:192,267,362 | G/A | — | benign |
| rs138223215 | 2:192,267,400 | A/G | — | uncertain significance |
| rs750974260 | 2:192,267,404 | A/T | — | uncertain significance |
| rs2469742681 | 2:192,267,442 | A/C | — | uncertain significance |
| rs762439233 | 2:192,272,875 | A/G | — | uncertain significance |
| rs570289277 | 2:192,273,803 | A/T | — | uncertain significance |
| rs2469787167 | 2:192,273,840 | C/T | — | uncertain significance |
| rs770628445 | 2:192,275,832 | T/G | — | uncertain significance |
| rs2126176875 | 2:192,278,779 | G/A | — | uncertain significance |
| rs1140895 | 2:192,278,782 | A/T | — | uncertain significance |
| rs2469827597 | 2:192,279,309 | A/G | — | uncertain significance |
| rs149460981 | 2:192,279,339 | A/G | — | uncertain significance |
| rs763461462 | 2:192,279,381 | G/A | — | likely benign |
| rs2469895280 | 2:192,288,608 | T/G | — | uncertain significance |
| rs1265082528 | 2:192,288,627 | G/A | — | uncertain significance |
| rs2469895614 | 2:192,288,658 | A/G | — | uncertain significance |
| rs148878483 | 2:192,288,678 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.