MYO3B

myosin IIIB

Summary

This gene encodes one of the class III myosins. Myosins are ATPases, activated by actin, that move along actin filaments in the cell. This class of myosins are characterized by an amino-terminal kinase domain and shown to be present in photoreceptors. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]

Known Variants106 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2468043999	2:171,055,794	T/C	—	uncertain significance
rs200075965	2:171,056,676	T/C	—	uncertain significance
rs765463329	2:171,056,700	A/G	—	uncertain significance
rs200712982	2:171,056,754	C/T	—	uncertain significance
rs1374749310	2:171,056,756	G/C	—	uncertain significance
rs2092646176	2:171,056,758	T/A	—	uncertain significance
rs760455994	2:171,056,784	T/A	—	uncertain significance
rs61732478	2:171,070,907	G/T	—	uncertain significance
rs776450840	2:171,070,910	A/T	—	uncertain significance
rs199776057	2:171,070,946	C/T	—	uncertain significance
rs764517983	2:171,070,947	G/A	—	likely benign
rs754301736	2:171,070,961	A/G	—	likely benign
rs2468098682	2:171,071,250	T/A	—	uncertain significance
rs2468098701	2:171,071,251	T/A	—	uncertain significance
rs377640353	2:171,071,275	C/T	—	uncertain significance
rs78928255	2:171,073,826	T/C	—	benign
rs751804769	2:171,073,843	C/A	—	uncertain significance
rs55911154	2:171,073,856	G/A	—	likely benign
rs61744601	2:171,073,861	C/T	—	uncertain significance
rs2161916	2:171,073,887	G/A	—	benign
rs773287656	2:171,092,511	G/A	—	uncertain significance
rs757553236	2:171,092,552	G/A	—	uncertain significance
rs754007174	2:171,092,601	C/A	—	uncertain significance
rs573982927	2:171,183,777	C/T	—	—
rs10206079	2:171,188,108	T/A	—	—
rs144721721	2:171,191,900	C/T	—	uncertain significance
rs34509373	2:171,191,945	A/G	—	not provided
rs73016964	2:171,196,636	G/A	regulatory region variant	—
rs16858178	2:171,201,415	C/A	coding sequence variant	—
rs10209102	2:171,225,739	A/G	—	benign
rs367633802	2:171,225,758	G/A	—	uncertain significance
rs771014796	2:171,225,763	T/G	—	uncertain significance
rs757931168	2:171,225,793	A/G	—	uncertain significance
rs764731042	2:171,225,884	C/T	—	uncertain significance
rs773804372	2:171,238,527	C/T	—	uncertain significance
rs376329641	2:171,238,563	G/A	—	uncertain significance
rs569532415	2:171,238,581	T/A	—	uncertain significance
rs1000676831	2:171,239,682	A/T	—	uncertain significance
rs1260527308	2:171,240,232	T/C	—	uncertain significance
rs201471096	2:171,240,248	G/A	—	uncertain significance
rs2468649374	2:171,240,290	C/T	—	uncertain significance
rs2468670491	2:171,243,682	T/C	—	uncertain significance
rs201344786	2:171,243,796	T/C	—	uncertain significance
rs752494228	2:171,248,049	A/G	—	uncertain significance
rs374803318	2:171,248,059	A/G	—	uncertain significance
rs2094418285	2:171,248,913	A/G	—	uncertain significance
rs1558954885	2:171,248,940	G/C	—	uncertain significance
rs2094418604	2:171,248,959	T/G	—	uncertain significance
rs778612821	2:171,248,998	C/T	—	uncertain significance
rs373607305	2:171,249,001	A/T	—	uncertain significance
rs7561268	2:171,256,597	A/C	intron variant	—
rs749143819	2:171,256,748	C/G	—	uncertain significance
rs772115705	2:171,256,750	T/C	—	uncertain significance
rs148136770	2:171,256,771	C/T	—	uncertain significance
rs55911627	2:171,256,819	A/C	—	uncertain significance
rs1383880748	2:171,258,200	T/C	—	uncertain significance
rs767298458	2:171,259,417	A/G	—	uncertain significance
rs1300038166	2:171,259,428	T/C	—	uncertain significance
rs2094487448	2:171,259,455	A/T	—	uncertain significance
rs371410657	2:171,260,758	T/C	—	uncertain significance
rs771214819	2:171,260,793	G/C	—	uncertain significance
rs371579684	2:171,260,811	C/T	—	uncertain significance
rs368727850	2:171,260,838	A/G	—	uncertain significance
rs780808835	2:171,260,842	C/T	—	uncertain significance
rs2468774559	2:171,260,888	A/T	—	uncertain significance
rs372328011	2:171,262,078	T/C	—	uncertain significance
rs754572075	2:171,262,103	G/A	—	uncertain significance
rs2468783276	2:171,262,139	G/A	—	uncertain significance
rs2094520019	2:171,264,279	G/A	—	uncertain significance
rs1461185926	2:171,264,282	G/A	—	uncertain significance
rs969219284	2:171,264,285	G/A	—	uncertain significance
rs771656263	2:171,264,298	G/A	—	uncertain significance
rs2118674	2:171,318,894	A/T	intron variant	—
rs1248602218	2:171,319,896	A/G	—	uncertain significance
rs201168773	2:171,323,095	G/A	—	uncertain significance
rs1340797485	2:171,323,121	A/G	—	uncertain significance
rs1167426352	2:171,323,146	C/T	—	uncertain significance
rs368098559	2:171,323,172	C/T	—	uncertain significance
rs201311373	2:171,323,173	G/A	—	uncertain significance
rs374406879	2:171,323,193	C/T	—	uncertain significance
rs13035033	2:171,332,288	C/G	intron variant	—
rs12692954	2:171,349,315	G/A	intron variant	—
rs2083212	2:171,353,842	C/A	intron variant	—
rs376095782	2:171,355,124	G/A	—	uncertain significance
rs1385102716	2:171,356,189	A/C	—	uncertain significance
rs771135579	2:171,356,202	G/A	—	uncertain significance
rs1415415246	2:171,356,247	G/C	—	uncertain significance
rs10176755	2:171,365,889	A/C	—	—
rs935325928	2:171,371,445	C/A	—	uncertain significance
rs769944522	2:171,371,475	G/A	—	uncertain significance
rs756894438	2:171,371,503	A/G	—	uncertain significance
rs187423481	2:171,375,963	T/C	—	likely benign
rs184828372	2:171,376,004	C/A	—	uncertain significance
rs780588860	2:171,376,014	C/T	—	uncertain significance
rs148359602	2:171,399,430	A/G	—	benign
rs763022056	2:171,399,453	A/G	—	likely benign
rs199617422	2:171,400,394	T/C	—	benign
rs202081379	2:171,400,406	C/T	—	uncertain significance
rs748282949	2:171,400,407	G/A	—	likely benign
rs192058520	2:171,400,465	G/A	—	uncertain significance

Showing 100 of 106 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.