MYO1F

myosin IF

Summary

Myosins are molecular motors that use the energy from ATP hydrolysis to generate force on actin filaments. The protein encoded by this gene is an unconventional myosin that may be involved in the intracellular movement of membrane-enclosed compartments. There is evidence to suggest that mutations in this gene can result in hearing loss. [provided by RefSeq, Jan 2017]

Known Variants242 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs13346588	19:8,586,226	C/G	—	benign
rs141749665	19:8,586,373	T/C	—	likely benign
rs190908621	19:8,586,378	G/A	—	likely benign
rs756797956	19:8,586,417	T/G	—	uncertain significance
rs547516698	19:8,586,427	G/A	—	likely benign
rs775985136	19:8,586,481	C/T	—	likely benign
rs184207950	19:8,586,510	G/A	—	likely benign
rs144467959	19:8,587,052	G/A	—	benign
rs139911601	19:8,587,195	C/T	—	benign
rs145346891	19:8,587,201	C/T	—	benign
rs182853755	19:8,587,205	C/T	—	likely benign
rs376380813	19:8,587,291	C/T	—	uncertain significance
rs199953551	19:8,587,293	T/G	—	conflicting classifications of pathogenicity
rs748515052	19:8,587,306	C/T	—	uncertain significance
rs191981941	19:8,587,341	C/T	—	uncertain significance
rs145269171	19:8,587,349	G/T	—	benign
rs1209334245	19:8,587,353	C/G	—	uncertain significance
rs199886043	19:8,587,372	G/A	—	uncertain significance
rs200864651	19:8,587,401	C/T	—	likely benign
rs201982814	19:8,587,411	C/T	—	likely benign
rs898006078	19:8,587,412	G/T	—	uncertain significance
rs765257989	19:8,587,416	C/T	—	conflicting classifications of pathogenicity
rs201578688	19:8,587,483	C/G	—	likely benign
rs201056652	19:8,587,513	C/T	—	likely benign
rs73922133	19:8,587,553	T/C	—	benign
rs199971487	19:8,587,575	C/T	—	uncertain significance
rs773074453	19:8,587,576	G/A	—	uncertain significance
rs775501333	19:8,587,582	G/C	—	uncertain significance
rs1400726405	19:8,587,584	G/A	—	uncertain significance
rs1470651579	19:8,587,592	G/C	—	uncertain significance
rs570160376	19:8,587,614	G/A	—	uncertain significance
rs780576676	19:8,587,623	C/T	—	likely benign
rs754535521	19:8,587,624	G/C	—	uncertain significance
rs201832487	19:8,587,708	C/A	—	likely benign
rs10408143	19:8,587,782	T/C	—	benign
rs73002701	19:8,587,900	A/T	—	benign
rs10402716	19:8,590,170	T/G	—	benign
rs201618281	19:8,590,368	G/C	—	uncertain significance
rs753576044	19:8,590,408	T/G	—	likely benign
rs201645601	19:8,590,419	C/T	—	uncertain significance
rs1972231594	19:8,590,446	T/C	—	uncertain significance
rs57842422	19:8,591,021	G/A	—	benign
rs1005137511	19:8,591,358	C/A	—	uncertain significance
rs757976654	19:8,591,362	C/T	—	likely benign
rs1972271714	19:8,591,364	C/A	—	uncertain significance
rs371111771	19:8,591,366	C/T	—	uncertain significance
rs376154461	19:8,591,389	A/G	—	likely benign
rs1271488358	19:8,591,421	G/A	—	uncertain significance
rs367667498	19:8,591,435	C/G	—	uncertain significance
rs2512333694	19:8,591,478	A/T	—	uncertain significance
rs368127869	19:8,591,489	T/C	—	likely benign
rs2303687	19:8,591,572	C/G	—	benign
rs2512335148	19:8,591,736	C/T	—	uncertain significance
rs114946243	19:8,591,778	G/T	—	likely benign
rs115485773	19:8,591,779	C/T	—	likely benign
rs182601554	19:8,591,786	C/G	—	conflicting classifications of pathogenicity
rs2340539	19:8,592,043	G/C	—	benign
rs111542097	19:8,592,149	C/T	—	likely benign
rs2967774	19:8,592,207	A/G	—	benign
rs200225777	19:8,592,235	C/T	—	likely benign
rs771666143	19:8,592,237	C/T	—	uncertain significance
rs1394251312	19:8,592,303	T/C	—	uncertain significance
rs201723456	19:8,592,315	C/T	—	uncertain significance
rs375036959	19:8,592,322	T/C	—	uncertain significance
rs779362654	19:8,592,357	C/T	—	uncertain significance
rs201198914	19:8,592,358	G/C	—	uncertain significance
rs3815907	19:8,594,893	C/T	—	benign
rs1156708600	19:8,595,091	G/A	—	uncertain significance
rs374767520	19:8,595,095	G/A	—	likely benign
rs780966187	19:8,595,108	G/C	—	uncertain significance
rs775707003	19:8,595,124	C/T	—	uncertain significance
rs766761177	19:8,595,150	C/T	—	uncertain significance
rs377604689	19:8,595,151	G/A	—	uncertain significance
rs996910823	19:8,595,157	C/T	—	uncertain significance
rs755770493	19:8,595,158	G/A	—	likely benign
rs769899272	19:8,595,213	C/T	—	uncertain significance
rs3213834	19:8,595,254	G/A	—	benign
rs1406211383	19:8,595,361	C/T	—	uncertain significance
rs201305709	19:8,595,369	C/T	—	uncertain significance
rs200375822	19:8,595,378	A/T	—	uncertain significance
rs749484151	19:8,595,379	C/T	—	uncertain significance
rs1177544539	19:8,595,411	G/A	—	uncertain significance
rs375465378	19:8,595,439	C/T	—	likely benign
rs143347435	19:8,595,468	G/A	—	likely benign
rs114211438	19:8,595,495	T/G	—	likely benign
rs78936828	19:8,600,969	G/A	—	benign
rs758642752	19:8,601,165	T/C	—	uncertain significance
rs200911217	19:8,601,206	C/T	—	uncertain significance
rs201646155	19:8,601,234	C/T	—	conflicting classifications of pathogenicity
rs573248456	19:8,601,242	C/T	—	uncertain significance
rs781374288	19:8,601,248	C/T	—	uncertain significance
rs200744759	19:8,601,250	C/T	—	benign
rs770548153	19:8,601,251	G/A	—	uncertain significance
rs75948259	19:8,601,351	G/T	—	benign
rs115875216	19:8,601,357	G/A	—	benign
rs1248587093	19:8,601,423	C/T	—	uncertain significance
rs199981303	19:8,601,430	G/A	—	likely benign
rs149369796	19:8,601,534	G/A	—	likely benign
rs75679944	19:8,601,770	C/G	—	benign
rs148281976	19:8,601,851	C/T	—	uncertain significance

Showing 100 of 242 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.