Trim44 Variant Search Result - Rat Genome Database

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43 records found for search term Trim44

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
151663238	CV1333846	single nucleotide variant	NM_017583.6(TRIM44):c.*23A>G	Aniridia 3 [RCV001838947]\|not provided [RCV004718989]	benign	11	35806408	35806408	Human	1	name
405258346	CV3203683	single nucleotide variant	NM_017583.6(TRIM44):c.669+7A>G	TRIM44-related disorder [RCV003941876]	likely benign	11	35663787	35663787	Human		name , trait , alternate_id
151663237	CV1333845	single nucleotide variant	NM_017583.6(TRIM44):c.670-27G>C	Aniridia 3 [RCV001838946]\|not provided [RCV004718988]	benign	11	35685232	35685232	Human	1	name
156066503	CV2317851	single nucleotide variant	NM_017583.6(TRIM44):c.23C>T (p.Ala8Val)	not specified [RCV004175089]	uncertain significance	11	35663134	35663134	Human		name
405281724	CV3213530	single nucleotide variant	NM_017583.6(TRIM44):c.174C>T (p.Ala58=)	TRIM44-related disorder [RCV003907360]	benign	11	35663285	35663285	Human		name , trait , alternate_id
155913170	CV2245768	single nucleotide variant	NM_017583.6(TRIM44):c.97T>G (p.Cys33Gly)	not specified [RCV004111629]	uncertain significance	11	35663208	35663208	Human		name
597801871	CV3617788	single nucleotide variant	NM_017583.6(TRIM44):c.50C>T (p.Thr17Met)	not specified [RCV004880946]	uncertain significance	11	35663161	35663161	Human		name
598202742	CV3935470	single nucleotide variant	NM_017583.6(TRIM44):c.60G>C (p.Glu20Asp)	not specified [RCV005290425]	uncertain significance	11	35663171	35663171	Human		name
15156179	CV712809	single nucleotide variant	NM_017583.6(TRIM44):c.552T>C (p.Leu184=)	not provided [RCV000969064]	benign	11	35663663	35663663	Human		name
15156184	CV712810	single nucleotide variant	NM_017583.6(TRIM44):c.579T>C (p.Asp193=)	not provided [RCV000969065]	benign	11	35663690	35663690	Human		name
15104117	CV783986	single nucleotide variant	NM_017583.6(TRIM44):c.537T>C (p.Cys179=)	not provided [RCV000976155]	likely benign	11	35663648	35663648	Human		name
156038276	CV2214904	single nucleotide variant	NM_017583.6(TRIM44):c.209C>T (p.Pro70Leu)	not specified [RCV004084696]	uncertain significance	11	35663320	35663320	Human		name
155929460	CV2278131	single nucleotide variant	NM_017583.6(TRIM44):c.260A>G (p.Gln87Arg)	not specified [RCV004141341]	uncertain significance	11	35663371	35663371	Human		name
329386537	CV2456079	single nucleotide variant	NM_017583.6(TRIM44):c.222G>C (p.Glu74Asp)	not specified [RCV004272975]	likely benign	11	35663333	35663333	Human		name
401761316	CV2706300	single nucleotide variant	NM_017583.6(TRIM44):c.289G>A (p.Glu97Lys)	not specified [RCV004314961]	uncertain significance	11	35663400	35663400	Human		name
405790469	CV3337006	single nucleotide variant	NM_017583.6(TRIM44):c.124C>T (p.Arg42Cys)	not specified [RCV004473885]	uncertain significance	11	35663235	35663235	Human		name
405790473	CV3337007	single nucleotide variant	NM_017583.6(TRIM44):c.155T>A (p.Phe52Tyr)	not specified [RCV004473886]	uncertain significance	11	35663266	35663266	Human		name
405790475	CV3337008	single nucleotide variant	NM_017583.6(TRIM44):c.175G>C (p.Glu59Gln)	not specified [RCV004473887]	uncertain significance	11	35663286	35663286	Human		name
405790478	CV3337009	single nucleotide variant	NM_017583.6(TRIM44):c.208C>G (p.Pro70Ala)	not specified [RCV004473888]	uncertain significance	11	35663319	35663319	Human		name
405790481	CV3337010	single nucleotide variant	NM_017583.6(TRIM44):c.227C>G (p.Ala76Gly)	not specified [RCV004473889]	uncertain significance	11	35663338	35663338	Human		name
405790483	CV3337011	single nucleotide variant	NM_017583.6(TRIM44):c.253G>T (p.Val85Leu)	not specified [RCV004473890]	uncertain significance	11	35663364	35663364	Human		name
407453863	CV3490536	single nucleotide variant	NM_017583.6(TRIM44):c.294G>T (p.Glu98Asp)	not specified [RCV004684691]	uncertain significance	11	35663405	35663405	Human		name
597801863	CV3617784	single nucleotide variant	NM_017583.6(TRIM44):c.164A>G (p.His55Arg)	not specified [RCV004880942]	uncertain significance	11	35663275	35663275	Human		name
598202754	CV3935474	single nucleotide variant	NM_017583.6(TRIM44):c.206C>A (p.Pro69Gln)	not specified [RCV005290427]	uncertain significance	11	35663317	35663317	Human		name
156170182	CV2197875	single nucleotide variant	NM_017583.6(TRIM44):c.458C>T (p.Ala153Val)	not specified [RCV004077106]	uncertain significance	11	35663569	35663569	Human		name
156168550	CV2280043	single nucleotide variant	NM_017583.6(TRIM44):c.433A>G (p.Asn145Asp)	not specified [RCV004146401]	uncertain significance	11	35663544	35663544	Human		name
156051392	CV2386325	single nucleotide variant	NM_017583.6(TRIM44):c.992A>T (p.Asp331Val)	not specified [RCV004228667]	uncertain significance	11	35735430	35735430	Human		name
329376167	CV2465283	single nucleotide variant	NM_017583.6(TRIM44):c.467A>G (p.Glu156Gly)	not specified [RCV004281081]	uncertain significance	11	35663578	35663578	Human		name
11558025	CV259325	single nucleotide variant	NM_017583.6(TRIM44):c.463G>A (p.Gly155Arg)	Aniridia 3 [RCV000254593]	pathogenic\|no classifications from unflagged records	11	35663574	35663574	Human	1	name
405790487	CV3337012	single nucleotide variant	NM_017583.6(TRIM44):c.418G>A (p.Glu140Lys)	not specified [RCV004473891]	uncertain significance	11	35663529	35663529	Human		name
405790490	CV3337013	single nucleotide variant	NM_017583.6(TRIM44):c.799C>G (p.Gln267Glu)	not specified [RCV004473892]	uncertain significance	11	35725975	35725975	Human		name
407453866	CV3490537	single nucleotide variant	NM_017583.6(TRIM44):c.697G>A (p.Ala233Thr)	not specified [RCV004684692]	uncertain significance	11	35685286	35685286	Human		name
407453868	CV3490538	single nucleotide variant	NM_017583.6(TRIM44):c.604C>T (p.Pro202Ser)	not specified [RCV004684693]	uncertain significance	11	35663715	35663715	Human		name
597801861	CV3617782	single nucleotide variant	NM_017583.6(TRIM44):c.914G>A (p.Arg305Lys)	not specified [RCV004880941]	uncertain significance	11	35726090	35726090	Human		name
597801865	CV3617785	single nucleotide variant	NM_017583.6(TRIM44):c.322G>C (p.Glu108Gln)	not specified [RCV004880943]	uncertain significance	11	35663433	35663433	Human		name
597801869	CV3617787	single nucleotide variant	NM_017583.6(TRIM44):c.761A>G (p.Gln254Arg)	not specified [RCV004880945]	uncertain significance	11	35725937	35725937	Human		name
598202747	CV3935472	single nucleotide variant	NM_017583.6(TRIM44):c.616G>T (p.Ala206Ser)	not specified [RCV005290426]	uncertain significance	11	35663727	35663727	Human		name
598274176	CV3935473	single nucleotide variant	NM_017583.6(TRIM44):c.585G>C (p.Gln195His)	not specified [RCV005303796]	uncertain significance	11	35663696	35663696	Human		name
598274179	CV3935475	single nucleotide variant	NM_017583.6(TRIM44):c.947A>T (p.Gln316Leu)	not specified [RCV005303797]	uncertain significance	11	35726123	35726123	Human		name
15159783	CV724417	single nucleotide variant	NM_017583.6(TRIM44):c.941A>G (p.Lys314Arg)	not provided [RCV000881258]	benign	11	35726117	35726117	Human		name
8626979	CV82123	single nucleotide variant	NM_017583.5(TRIM44):c.755G>T (p.Arg252Leu)	Malignant melanoma [RCV000062202]	not provided	11	35725931	35725931	Human		name
597801867	CV3617786	single nucleotide variant	NM_017583.6(TRIM44):c.1012G>T (p.Ala338Ser)	not specified [RCV004880944]	uncertain significance	11	35806362	35806362	Human		name
598188554	CV4008597	duplication	NM_017583.6(TRIM44):c.319_336dup (p.Glu112_Thr113insSerGluGluGluSerGlu)	Aniridia 3 [RCV005396096]	uncertain significance	11	35663414	35663415	Human	1	name

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