MYO5B

myosin VB

Summary

The protein encoded by this gene, together with other proteins, may be involved in plasma membrane recycling. Mutations in this gene are associated with microvillous inclusion disease. [provided by RefSeq, Sep 2009]

Known Variants1,392 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1331960796	18:47,349,201	T/C	—	uncertain significance
rs1276336111	18:47,349,297	G/A	—	uncertain significance
rs1190572023	18:47,349,413	A/G	—	uncertain significance
rs879173424	18:47,349,418	C/A	—	uncertain significance
rs373429782	18:47,349,450	T/C	—	uncertain significance
rs377694296	18:47,349,460	C/G	—	uncertain significance
rs371267343	18:47,349,462	T/G	—	uncertain significance
rs9947614	18:47,349,473	C/G	—	benign
rs375545150	18:47,349,476	A/G	—	uncertain significance
rs777915881	18:47,349,477	T/C	—	uncertain significance
rs1201555709	18:47,349,484	C/T	—	uncertain significance
rs369420591	18:47,349,490	T/G	—	uncertain significance
rs1342001906	18:47,349,499	G/C	—	uncertain significance
rs371306335	18:47,349,500	A/G	—	uncertain significance
rs886053853	18:47,349,524	G/A	—	uncertain significance
rs558262946	18:47,349,526	A/G	—	uncertain significance
rs367570644	18:47,349,541	T/C	—	uncertain significance
rs368155236	18:47,349,549	A/G	—	uncertain significance
rs371042751	18:47,349,559	C/T	—	uncertain significance
rs9947739	18:47,349,568	C/G	—	uncertain significance
rs1598810725	18:47,349,602	T/C	—	uncertain significance
rs200885001	18:47,349,621	G/A	—	uncertain significance
rs201748833	18:47,349,628	T/C	—	uncertain significance
rs368561623	18:47,349,633	A/G	—	uncertain significance
rs75335611	18:47,349,653	C/T	—	uncertain significance
rs886053854	18:47,349,680	T/G	—	uncertain significance
rs372278198	18:47,349,683	C/T	—	uncertain significance
rs375530149	18:47,349,684	C/G	—	uncertain significance
rs544138887	18:47,349,688	A/G	—	uncertain significance
rs368309880	18:47,349,692	T/G	—	uncertain significance
rs183415958	18:47,349,715	T/G	—	uncertain significance
rs188815832	18:47,349,717	C/T	—	uncertain significance
rs113215300	18:47,349,739	G/T	—	uncertain significance
rs73959716	18:47,349,768	A/C	—	uncertain significance
rs78201339	18:47,349,776	A/G	—	uncertain significance
rs1366788070	18:47,349,792	C/T	—	uncertain significance
rs112057683	18:47,349,841	G/A	—	uncertain significance
rs115831173	18:47,349,867	T/C	—	uncertain significance
rs76811062	18:47,349,881	A/G	—	uncertain significance
rs1167522718	18:47,349,885	C/T	—	uncertain significance
rs144518115	18:47,349,918	T/C	—	uncertain significance
rs148796775	18:47,349,919	G/A	—	uncertain significance
rs115116077	18:47,349,922	G/A	—	uncertain significance
rs147973380	18:47,349,925	T/G	—	uncertain significance
rs886053855	18:47,349,929	A/G	—	uncertain significance
rs116888891	18:47,349,931	C/A	—	uncertain significance
rs117972198	18:47,349,933	G/A	—	uncertain significance
rs372605995	18:47,349,945	T/A	—	uncertain significance
rs77754378	18:47,349,970	C/G	—	uncertain significance
rs72925912	18:47,349,981	A/G	—	uncertain significance
rs72925913	18:47,350,003	G/T	—	uncertain significance
rs375226833	18:47,350,013	C/A	—	uncertain significance
rs369480218	18:47,350,014	T/C	—	uncertain significance
rs373003146	18:47,350,016	A/T	—	uncertain significance
rs11876859	18:47,350,094	T/G	—	benign
rs369797807	18:47,350,111	G/T	—	uncertain significance
rs369742971	18:47,350,146	T/C	—	uncertain significance
rs373513902	18:47,350,148	A/G	—	uncertain significance
rs375423515	18:47,350,169	G/A	—	uncertain significance
rs373899751	18:47,350,175	T/G	—	uncertain significance
rs796115232	18:47,350,195	C/T	—	uncertain significance
rs140855200	18:47,350,196	A/C	—	benign
rs114480066	18:47,350,201	C/T	—	uncertain significance
rs190516330	18:47,350,270	T/C	—	likely benign
rs113741260	18:47,350,291	C/A	—	uncertain significance
rs183150275	18:47,350,303	C/T	—	likely benign
rs113647716	18:47,350,304	C/T	—	uncertain significance
rs111868213	18:47,350,307	G/A	—	uncertain significance
rs796631271	18:47,350,330	C/A	—	uncertain significance
rs140222157	18:47,350,376	C/T	—	uncertain significance
rs141004090	18:47,350,444	A/G	—	uncertain significance
rs374402517	18:47,350,494	A/G	—	uncertain significance
rs377539134	18:47,350,502	A/G	—	uncertain significance
rs74812451	18:47,350,525	T/A	—	uncertain significance
rs57818618	18:47,350,548	A/C	—	benign
rs77330305	18:47,350,552	G/T	—	uncertain significance
rs59318525	18:47,350,558	A/G	—	benign
rs886053857	18:47,350,582	C/T	—	uncertain significance
rs78050801	18:47,350,585	G/A	—	uncertain significance
rs114048807	18:47,350,593	G/A	—	uncertain significance
rs607552	18:47,350,601	T/C	—	uncertain significance
rs72925916	18:47,350,622	C/G	—	uncertain significance
rs886053858	18:47,350,626	A/G	—	uncertain significance
rs72925917	18:47,350,630	A/G	—	uncertain significance
rs1045170751	18:47,350,637	A/G	—	uncertain significance
rs375542187	18:47,350,654	G/A	—	uncertain significance
rs774764763	18:47,350,658	G/A	—	uncertain significance
rs886053859	18:47,350,670	A/G	—	uncertain significance
rs74651470	18:47,350,683	C/T	—	uncertain significance
rs73959721	18:47,350,712	T/C	—	uncertain significance
rs1040969957	18:47,350,727	G/A	—	uncertain significance
rs1297286387	18:47,350,743	A/G	—	uncertain significance
rs75318758	18:47,350,753	T/C	—	uncertain significance
rs79509391	18:47,350,832	A/T	—	uncertain significance
rs75305404	18:47,350,848	G/C	—	uncertain significance
rs75032645	18:47,350,866	A/G	—	uncertain significance
rs192996713	18:47,350,874	G/A	—	uncertain significance
rs78555149	18:47,350,876	G/A	—	uncertain significance
rs111319402	18:47,350,920	C/G	—	benign
rs79745077	18:47,350,945	G/T	—	uncertain significance

Showing 100 of 1,392 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.