DNAH10

dynein axonemal heavy chain 10

Summary

Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. The axonemal dyneins, found in cilia and flagella, are components of the outer and inner dynein arms attached to the peripheral microtubule doublets. DNAH10 is an inner arm dynein heavy chain (Maiti et al., 2000 [PubMed 11175280]).[supplied by OMIM, Mar 2008]

Known Variants468 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs766167753	12:124,252,159	T/C	—	uncertain significance
rs202082264	12:124,252,160	A/G	—	uncertain significance
rs1957096848	12:124,252,196	G/T	—	uncertain significance
rs190206140	12:124,252,221	G/A	—	uncertain significance
rs200881150	12:124,256,153	C/T	—	uncertain significance
rs775604149	12:124,256,154	G/A	—	likely benign
rs2541980340	12:124,256,245	A/C	—	uncertain significance
rs201210035	12:124,256,247	T/G	—	uncertain significance
rs201974470	12:124,257,388	C/T	—	likely benign
rs566985716	12:124,257,420	A/G	—	likely benign
rs1957306787	12:124,257,427	G/C	—	uncertain significance
rs147457213	12:124,257,461	C/T	—	benign
rs751553107	12:124,258,702	T/C	—	uncertain significance
rs374306028	12:124,258,772	C/T	—	likely benign
rs200209608	12:124,258,773	G/A	—	uncertain significance
rs202082455	12:124,258,820	G/A	—	likely benign
rs568067100	12:124,265,638	A/G	—	likely benign
rs766163811	12:124,265,664	C/T	—	uncertain significance
rs2542074609	12:124,265,671	A/C	—	likely benign
rs1565895023	12:124,265,672	A/G	—	uncertain significance
rs11057353	12:124,265,687	T/C	—	benign
rs201348789	12:124,265,707	C/G	—	benign
rs373979430	12:124,265,719	A/C	—	likely benign
rs1207962173	12:124,265,736	T/C	—	uncertain significance
rs765406956	12:124,265,762	A/G	—	uncertain significance
rs566020705	12:124,265,763	G/A	—	uncertain significance
rs11057354	12:124,267,638	A/G	—	benign
rs746639992	12:124,267,677	A/G	—	uncertain significance
rs11057355	12:124,267,703	T/C	—	benign
rs145614363	12:124,267,713	G/A	—	conflicting classifications of pathogenicity
rs369125793	12:124,267,780	C/T	—	uncertain significance
rs201619821	12:124,268,494	G/A	—	uncertain significance
rs377654704	12:124,268,620	A/G	—	uncertain significance
rs148358039	12:124,268,672	C/T	—	likely benign
rs141506707	12:124,268,693	G/A	—	uncertain significance
rs373894230	12:124,268,694	C/G	—	likely benign
rs147774367	12:124,270,348	T/C	—	uncertain significance
rs116082071	12:124,270,365	G/A	—	benign
rs116310078	12:124,270,467	C/T	—	benign
rs79726540	12:124,270,471	G/A	—	benign
rs765224002	12:124,272,359	G/C	—	uncertain significance
rs760229533	12:124,272,362	C/T	—	uncertain significance
rs139225647	12:124,272,382	C/T	—	benign
rs2542151858	12:124,272,411	G/C	—	uncertain significance
rs746846748	12:124,272,417	G/T	—	uncertain significance
rs144145237	12:124,272,420	C/T	—	likely benign
rs1452207029	12:124,272,422	A/G	—	uncertain significance
rs2542152209	12:124,272,430	A/T	—	uncertain significance
rs1247007253	12:124,272,431	C/T	—	uncertain significance
rs141195166	12:124,272,449	C/T	—	uncertain significance
rs1355478360	12:124,272,467	G/A	—	uncertain significance
rs567684796	12:124,272,481	C/T	—	uncertain significance
rs200152174	12:124,272,482	G/A	—	uncertain significance
rs976928734	12:124,272,495	C/G	—	uncertain significance
rs186760005	12:124,272,538	G/A	—	uncertain significance
rs1434715249	12:124,272,544	C/G	—	uncertain significance
rs10846559	12:124,274,474	G/A	—	benign
rs369738085	12:124,274,565	A/G	—	uncertain significance
rs751148187	12:124,274,566	C/T	—	likely benign
rs143737268	12:124,274,567	G/A	—	likely benign
rs75134035	12:124,274,625	A/C	—	benign
rs1114629	12:124,280,321	C/A	intron variant	—
rs76791219	12:124,281,322	T/C	—	benign
rs766899778	12:124,281,354	T/C	—	uncertain significance
rs118049936	12:124,283,801	A/G	—	benign
rs199570902	12:124,283,836	A/T	—	likely benign
rs2542243213	12:124,283,853	G/A	—	uncertain significance
rs773388313	12:124,284,775	A/G	—	likely benign
rs144164191	12:124,284,882	C/T	—	likely benign
rs376748704	12:124,284,899	C/T	—	uncertain significance
rs571838812	12:124,285,839	G/A	—	uncertain significance
rs138922654	12:124,285,870	G/T	—	benign
rs1958474673	12:124,285,875	T/C	—	uncertain significance
rs2542261277	12:124,285,887	A/G	—	uncertain significance
rs201207884	12:124,285,934	C/A	—	likely benign
rs750867553	12:124,285,947	C/T	—	uncertain significance
rs80041527	12:124,288,212	C/T	—	benign
rs77726895	12:124,288,213	G/A	—	benign
rs2542276939	12:124,288,259	C/T	—	uncertain significance
rs113378202	12:124,288,347	C/T	—	benign
rs143421929	12:124,289,410	G/A	—	uncertain significance
rs143052054	12:124,289,423	C/A	—	likely benign
rs764625697	12:124,289,442	C/T	—	uncertain significance
rs201914416	12:124,289,493	G/A	—	likely benign
rs745898168	12:124,289,509	G/A	—	uncertain significance
rs749051618	12:124,289,595	C/T	—	likely benign
rs374128515	12:124,293,486	G/A	—	uncertain significance
rs561113993	12:124,297,768	G/A	—	likely benign
rs146033482	12:124,297,780	G/C	—	uncertain significance
rs1959012114	12:124,297,800	T/G	—	uncertain significance
rs763093758	12:124,297,816	C/A	—	uncertain significance
rs757498037	12:124,297,837	G/C	—	uncertain significance
rs1959015064	12:124,297,853	A/T	—	uncertain significance
rs144699449	12:124,297,855	G/A	—	likely benign
rs148503528	12:124,297,874	A/G	—	benign
rs763183139	12:124,297,898	G/T	—	uncertain significance
rs118146260	12:124,297,903	C/T	—	conflicting classifications of pathogenicity
rs2542366605	12:124,297,961	A/G	—	uncertain significance
rs138151312	12:124,297,973	G/A	—	conflicting classifications of pathogenicity
rs150479083	12:124,298,011	A/G	—	uncertain significance

Showing 100 of 468 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.