DNM3

dynamin 3

Summary

This gene encodes a member of a family of guanosine triphosphate (GTP)-binding proteins that associate with microtubules and are involved in vesicular transport. The encoded protein functions in the development of megakaryocytes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]

Known Variants119 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs11583673	1:171,809,720	C/T	upstream gene variant	—
rs1313104093	1:171,810,819	A/G	—	uncertain significance
rs78415834	1:171,829,971	T/A	—	—
rs2421947	1:171,833,094	C/G	upstream gene variant	—
rs59396474	1:171,867,845	T/G	—	—
rs1291452147	1:171,890,895	C/T	—	uncertain significance
rs2529451951	1:171,890,943	C/T	—	uncertain significance
rs6681480	1:171,894,592	A/C	—	—
rs1998174	1:171,908,524	T/A	intron variant	—
rs183458045	1:171,912,053	G/A	intron variant	—
rs2038480	1:171,939,641	A/G	—	—
rs6662263	1:171,944,242	A/G	intron variant	—
rs6425522	1:171,946,082	T/C	intron variant	—
rs6684723	1:171,948,260	C/G	intron variant	—
rs10914144	1:171,949,750	T/A	—	—
rs12037133	1:171,949,999	G/A	—	—
rs1345200287	1:171,956,826	A/G	—	uncertain significance
rs371615077	1:171,958,120	A/T	—	uncertain significance
rs771642076	1:171,958,133	T/C	—	uncertain significance
rs915862931	1:171,958,138	G/T	—	uncertain significance
rs2530565507	1:171,958,169	G/T	—	uncertain significance
rs375401925	1:171,958,182	G/A	—	uncertain significance
rs534671967	1:171,979,848	G/T	—	—
rs1446545746	1:172,002,275	A/G	—	uncertain significance
rs759897946	1:172,002,316	G/T	—	uncertain significance
rs767005768	1:172,002,344	C/T	—	uncertain significance
rs749873284	1:172,002,345	G/A	—	likely benign
rs781193654	1:172,007,478	G/A	—	uncertain significance
rs757382462	1:172,007,546	G/A	—	uncertain significance
rs758244650	1:172,007,553	A/C	—	uncertain significance
rs552393073	1:172,007,565	C/A	—	likely benign
rs2531424872	1:172,011,165	G/T	—	uncertain significance
rs779122643	1:172,011,249	A/G	—	uncertain significance
rs367760498	1:172,013,588	A/G	—	uncertain significance
rs2531534037	1:172,017,816	A/G	—	uncertain significance
rs2531534141	1:172,017,822	C/G	—	uncertain significance
rs142151587	1:172,022,811	A/G	intron variant	—
rs9659615	1:172,025,643	G/A	intron variant	—
rs2531882863	1:172,037,977	C/G	—	uncertain significance
rs772354266	1:172,038,017	G/A	—	uncertain significance
rs760019506	1:172,038,053	G/T	—	likely benign
rs17346452	1:172,053,287	T/C	intron variant	—
rs61807763	1:172,088,225	C/T	intron variant	—
rs4604727	1:172,090,738	C/G	intron variant	—
rs569789251	1:172,100,308	T/C	—	likely benign
rs372889478	1:172,100,311	G/A	—	likely benign
rs373398423	1:172,100,349	T/C	—	uncertain significance
rs2421986	1:172,100,596	G/A	—	—
rs10489299	1:172,101,666	T/C	intron variant	—
rs16843915	1:172,118,702	G/C	regulatory region variant	—
rs61807786	1:172,124,828	C/T	intron variant	—
rs628479	1:172,134,090	T/A	intron variant	—
rs537444	1:172,134,469	C/G	intron variant	—
rs672740	1:172,137,119	T/G	regulatory region variant	—
rs17277127	1:172,137,134	A/T	regulatory region variant	—
rs11584955	1:172,138,105	C/A	intron variant	—
rs554019	1:172,140,548	C/T	intron variant	—
rs12125882	1:172,141,403	A/T	intron variant	—
rs590567	1:172,144,794	T/C	intron variant	—
rs61807788	1:172,147,974	T/C	intron variant	—
rs514864	1:172,162,621	A/T	—	—
rs112744418	1:172,163,708	G/A	intron variant	—
rs4394690	1:172,166,210	G/C	intron variant	—
rs2209098	1:172,167,226	T/C	intron variant	—
rs7535241	1:172,174,596	G/A	intron variant	—
rs55935473	1:172,175,590	T/G	intron variant	—
rs678962	1:172,189,889	T/G	intron variant	—
rs10797881	1:172,195,347	C/G	—	—
rs479336	1:172,199,573	T/A	—	—
rs609702	1:172,200,655	C/G	—	—
rs28600859	1:172,204,893	C/T	—	—
rs12075079	1:172,219,995	A/G	intron variant	—
rs2527155109	1:172,222,715	A/G	—	likely benign
rs2062275541	1:172,222,723	A/G	—	uncertain significance
rs12409899	1:172,227,011	C/A	—	—
rs12041600	1:172,230,229	G/A	intron variant	—
rs56682471	1:172,236,267	A/G	—	—
rs2421992	1:172,241,251	C/T	intron variant	—
rs2757495	1:172,268,191	T/G	—	—
rs9425568	1:172,316,593	G/A	upstream gene variant	—
rs10911624	1:172,316,842	G/A	upstream gene variant	—
rs17369011	1:172,321,641	A/T	regulatory region variant	—
rs9425573	1:172,330,437	G/T	regulatory region variant	—
rs4916251	1:172,346,396	T/A	intron variant	—
rs1011731	1:172,346,548	G/C	—	—
rs573884254	1:172,348,234	G/A	—	uncertain significance
rs374692919	1:172,348,254	A/G	—	uncertain significance
rs2068758544	1:172,348,260	A/C	—	uncertain significance
rs2526423097	1:172,348,320	A/C	—	uncertain significance
rs139523475	1:172,348,322	C/T	—	benign
rs768019	1:172,350,207	A/C	—	—
rs9425587	1:172,351,809	A/T	—	—
rs10797996	1:172,353,311	C/T	intron variant	—
rs4916252	1:172,354,017	T/A	—	—
rs10752943	1:172,354,992	C/T	intron variant	—
rs9425589	1:172,355,276	G/A	intron variant	—
rs768375311	1:172,356,341	G/A	—	uncertain significance
rs765996640	1:172,356,369	C/T	—	uncertain significance
rs2069235737	1:172,356,411	C/T	—	uncertain significance
rs1350184812	1:172,356,463	C/G	—	uncertain significance

Showing 100 of 119 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.