MOV10L1

Mov10 like RNA helicase 1

Summary

This gene is similar to a mouse gene that encodes a putative RNA helicase and shows testis-specific expression. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]

Known Variants97 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1451840900	22:50,528,536	A/G	—	uncertain significance
rs1237156816	22:50,528,602	G/C	—	uncertain significance
rs777895411	22:50,530,450	G/C	—	uncertain significance
rs368506169	22:50,530,502	T/C	—	uncertain significance
rs544105826	22:50,530,555	C/A	—	uncertain significance
rs778083042	22:50,530,556	A/G	—	uncertain significance
rs1166720923	22:50,530,565	T/C	—	uncertain significance
rs746064791	22:50,530,571	T/C	—	uncertain significance
rs738490	22:50,530,651	G/T	—	—
rs150821412	22:50,537,888	A/G	—	uncertain significance
rs762299641	22:50,537,902	G/A	—	uncertain significance
rs140532446	22:50,537,980	G/A	—	benign
rs781497595	22:50,538,011	C/G	—	uncertain significance
rs146380250	22:50,538,028	G/A	—	uncertain significance
rs915047666	22:50,546,565	G/C	—	uncertain significance
rs1036345284	22:50,546,609	A/T	—	uncertain significance
rs56022779	22:50,546,612	C/T	—	uncertain significance
rs774769069	22:50,546,632	C/G	—	uncertain significance
rs147590689	22:50,546,633	G/A	—	uncertain significance
rs3810971	22:50,546,666	C/T	—	benign
rs200767181	22:50,547,183	G/A	—	uncertain significance
rs367878826	22:50,547,278	G/A	—	pathogenic
rs369127945	22:50,552,112	A/G	—	likely benign
rs1271026193	22:50,552,163	C/T	—	uncertain significance
rs746813089	22:50,552,187	G/A	—	uncertain significance
rs2518581607	22:50,552,898	A/G	—	uncertain significance
rs148394255	22:50,552,916	G/A	—	uncertain significance
rs2518582275	22:50,552,953	C/T	—	uncertain significance
rs1246569472	22:50,553,019	G/A	—	likely benign
rs200879347	22:50,553,033	A/G	—	uncertain significance
rs199722978	22:50,553,645	A/G	—	uncertain significance
rs766951729	22:50,553,648	C/A	—	uncertain significance
rs188656814	22:50,554,895	T/C	intron variant	—
rs138222	22:50,555,619	C/T	—	benign
rs882753	22:50,555,635	C/T	—	benign
rs760749	22:50,555,686	A/C	—	benign
rs756762868	22:50,555,735	C/T	—	uncertain significance
rs778485550	22:50,555,736	G/A	—	likely benign
rs138229	22:50,557,407	A/G	regulatory region variant	—
rs763942893	22:50,558,975	T/G	—	uncertain significance
rs775542421	22:50,563,855	C/T	—	uncertain significance
rs375117683	22:50,563,912	T/C	—	uncertain significance
rs371629719	22:50,563,924	T/C	—	likely benign
rs186275301	22:50,563,972	C/T	—	uncertain significance
rs143354163	22:50,563,989	C/G	—	uncertain significance
rs774122746	22:50,563,995	G/A	—	likely benign
rs2518663247	22:50,564,636	A/C	—	uncertain significance
rs1260289962	22:50,564,664	A/G	—	uncertain significance
rs750220679	22:50,566,860	G/A	—	uncertain significance
rs2518677908	22:50,566,861	T/C	—	uncertain significance
rs746576478	22:50,566,911	A/G	—	uncertain significance
rs2062752780	22:50,572,476	A/T	—	uncertain significance
rs2062768230	22:50,573,000	A/G	—	uncertain significance
rs779257855	22:50,580,538	A/T	—	uncertain significance
rs989644791	22:50,580,579	C/T	—	uncertain significance
rs769563161	22:50,580,591	C/A	—	uncertain significance
rs2063008265	22:50,580,621	A/G	—	likely pathogenic
rs2518774246	22:50,581,550	T/C	—	uncertain significance
rs778510267	22:50,581,589	A/G	—	uncertain significance
rs779178382	22:50,582,551	G/A	—	uncertain significance
rs1479684172	22:50,582,614	G/T	—	likely pathogenic
rs774313159	22:50,582,644	G/A	—	uncertain significance
rs761285275	22:50,582,667	G/A	—	uncertain significance
rs138263	22:50,583,245	C/T	intron variant	—
rs139935120	22:50,584,133	G/A	—	likely benign
rs2518796971	22:50,584,150	A/C	—	uncertain significance
rs1278182234	22:50,584,154	G/A	—	uncertain significance
rs776426358	22:50,584,178	C/T	—	uncertain significance
rs146761404	22:50,584,179	G/A	—	uncertain significance
rs769328111	22:50,584,184	C/T	—	uncertain significance
rs763186580	22:50,588,082	G/A	—	uncertain significance
rs760908056	22:50,589,167	G/A	—	uncertain significance
rs766119000	22:50,589,186	T/C	—	uncertain significance
rs201713542	22:50,589,218	G/T	—	uncertain significance
rs780483629	22:50,589,228	A/G	—	uncertain significance
rs199998051	22:50,589,260	A/G	—	uncertain significance
rs767062478	22:50,589,267	G/A	—	uncertain significance
rs758849727	22:50,589,289	A/C	—	uncertain significance
rs1602347225	22:50,589,321	C/T	—	uncertain significance
rs56173861	22:50,591,470	G/T	splice region variant	—
rs745731029	22:50,591,511	C/T	—	uncertain significance
rs373995577	22:50,591,571	C/G	—	uncertain significance
rs982658399	22:50,591,577	T/C	—	uncertain significance
rs781058862	22:50,591,646	G/A	—	uncertain significance
rs143387727	22:50,596,534	G/A	—	uncertain significance
rs185921944	22:50,597,274	T/C	intron variant	—
rs73187226	22:50,597,466	C/T	intron variant	—
rs139398528	22:50,598,132	G/A	—	uncertain significance
rs1356453369	22:50,598,158	G/T	—	uncertain significance
rs369728929	22:50,599,120	C/T	—	uncertain significance
rs755129454	22:50,599,190	A/C	—	uncertain significance
rs149143559	22:50,599,253	G/A	—	uncertain significance
rs2063546617	22:50,599,430	C/G	—	uncertain significance
rs759812049	22:50,599,453	G/A	—	likely benign
rs147087173	22:50,599,472	A/G	—	uncertain significance
rs2518896913	22:50,599,474	T/C	—	uncertain significance
rs2518896963	22:50,599,478	T/G	—	uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.