TRIM44

tripartite motif containing 44

Summary

This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, namely a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. [provided by RefSeq, Jul 2008]

Known Variants29 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1237661745	11:35,684,682	C/T	—	uncertain significance
rs1851291933	11:35,684,756	T/G	—	uncertain significance
rs946496646	11:35,684,783	C/T	—	uncertain significance
rs749414817	11:35,684,814	T/A	—	uncertain significance
rs34392570	11:35,684,833	C/T	—	benign
rs912518703	11:35,684,834	G/C	—	uncertain significance
rs2494690559	11:35,684,867	C/G	—	uncertain significance
rs766415812	11:35,684,868	C/T	—	uncertain significance
rs369326810	11:35,684,881	G/C	—	likely benign
rs1049198534	11:35,684,886	C/G	—	uncertain significance
rs1851295384	11:35,684,912	G/T	—	uncertain significance
rs992314092	11:35,684,919	A/G	—	uncertain significance
rs2494690845	11:35,684,948	G/A	—	uncertain significance
rs2494691336	11:35,685,077	G/A	—	uncertain significance
rs1851300008	11:35,685,092	A/G	—	uncertain significance
rs760616658	11:35,685,117	C/T	—	uncertain significance
rs886039241	11:35,685,122	G/A	missense variant	no classifications from unflagged records
rs2494691500	11:35,685,126	A/G	—	uncertain significance
rs756694211	11:35,685,196	T/C	—	likely benign
rs146343301	11:35,685,211	T/C	—	benign
rs139171417	11:35,685,238	T/C	—	benign
rs561637328	11:35,685,335	A/G	—	likely benign
rs7928794	11:35,701,236	A/C	intron variant	—
rs3740798	11:35,706,780	G/C	—	benign
rs77546297	11:35,746,616	A/G	—	—
rs962390951	11:35,747,523	C/G	—	uncertain significance
rs61758104	11:35,747,665	G/A	—	benign
rs138227319	11:35,756,978	A/T	—	uncertain significance
rs61881297	11:35,827,958	A/G	—	benign

Gene information from NCBI Gene. Variant classifications from ClinVar.