Tmem129 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

58 records found for search term Tmem129

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156183413	CV2243267	single nucleotide variant	NM_001127266.2(TMEM129):c.31G>A (p.Ala11Thr)	not specified [RCV004110150]	uncertain significance	4	1720807	1720807	Human		name
156267918	CV2305707	single nucleotide variant	NM_001127266.2(TMEM129):c.67C>T (p.Pro23Ser)	not specified [RCV004167528]	uncertain significance	4	1720771	1720771	Human		name
405793503	CV3339508	single nucleotide variant	NM_001127266.2(TMEM129):c.64A>G (p.Thr22Ala)	not specified [RCV004474919]	uncertain significance	4	1720774	1720774	Human		name
598212263	CV3917238	single nucleotide variant	NM_001127266.2(TMEM129):c.75G>C (p.Glu25Asp)	not specified [RCV005292131]	uncertain significance	4	1720763	1720763	Human		name
156172573	CV2286933	single nucleotide variant	NM_001127266.2(TMEM129):c.221T>C (p.Met74Thr)	not specified [RCV004144539]	uncertain significance	4	1718611	1718611	Human		name
156390258	CV2373232	single nucleotide variant	NM_001127266.2(TMEM129):c.245G>A (p.Arg82Gln)	not specified [RCV004217902]	likely benign	4	1718587	1718587	Human		name
401752276	CV2682765	single nucleotide variant	NM_001127266.2(TMEM129):c.281G>A (p.Arg94Gln)	not specified [RCV004281739]	likely benign	4	1718551	1718551	Human		name
401725547	CV2721821	single nucleotide variant	NM_001127266.2(TMEM129):c.167C>A (p.Thr56Lys)	not specified [RCV004326337]	uncertain significance	4	1720671	1720671	Human		name
401880939	CV2763188	single nucleotide variant	NM_001127266.2(TMEM129):c.142T>A (p.Phe48Ile)	not specified [RCV004336227]	uncertain significance	4	1720696	1720696	Human		name
401876133	CV2789305	single nucleotide variant	NM_001127266.2(TMEM129):c.230C>T (p.Ala77Val)	not specified [RCV004365329]	uncertain significance	4	1718602	1718602	Human		name
405793478	CV3339500	single nucleotide variant	NM_001127266.2(TMEM129):c.176C>T (p.Thr59Met)	not specified [RCV004474911]	uncertain significance	4	1720662	1720662	Human		name
405793481	CV3339501	single nucleotide variant	NM_001127266.2(TMEM129):c.244C>T (p.Arg82Trp)	not specified [RCV004474912]	uncertain significance	4	1718588	1718588	Human		name
597785285	CV3616644	single nucleotide variant	NM_001127266.2(TMEM129):c.160C>G (p.Arg54Gly)	not specified [RCV004875042]	uncertain significance	4	1720678	1720678	Human		name
597785289	CV3616645	single nucleotide variant	NM_001127266.2(TMEM129):c.214G>A (p.Val72Met)	not specified [RCV004875043]	uncertain significance	4	1718618	1718618	Human		name
598212235	CV3917234	single nucleotide variant	NM_001127266.2(TMEM129):c.1050C>T (p.Arg350=)	not specified [RCV005292128]	likely benign	4	1717219	1717219	Human		name
598212245	CV3917235	single nucleotide variant	NM_001127266.2(TMEM129):c.125G>A (p.Gly42Asp)	not specified [RCV005292129]	uncertain significance	4	1720713	1720713	Human		name
598212255	CV3917237	single nucleotide variant	NM_001127266.2(TMEM129):c.250C>T (p.His84Tyr)	not specified [RCV005292130]	likely benign	4	1718582	1718582	Human		name
598212271	CV3917239	single nucleotide variant	NM_001127266.2(TMEM129):c.124G>A (p.Gly42Ser)	not specified [RCV005292132]	uncertain significance	4	1720714	1720714	Human		name
156112008	CV2217971	single nucleotide variant	NM_001127266.2(TMEM129):c.448C>T (p.Arg150Trp)	not specified [RCV004086421]	uncertain significance	4	1718384	1718384	Human		name
156203879	CV2234661	single nucleotide variant	NM_001127266.2(TMEM129):c.422T>C (p.Val141Ala)	not specified [RCV004102620]	uncertain significance	4	1718410	1718410	Human		name
156166954	CV2237198	single nucleotide variant	NM_001127266.2(TMEM129):c.815C>T (p.Pro272Leu)	not specified [RCV004114937]	uncertain significance	4	1717541	1717541	Human		name
155983919	CV2241057	single nucleotide variant	NM_001127266.2(TMEM129):c.851C>T (p.Ala284Val)	not specified [RCV004104103]	uncertain significance	4	1717418	1717418	Human		name
156248375	CV2263973	single nucleotide variant	NM_001127266.2(TMEM129):c.605A>T (p.Asp202Val)	not specified [RCV004138003]	uncertain significance	4	1718227	1718227	Human		name
155903353	CV2274861	single nucleotide variant	NM_001127266.2(TMEM129):c.661G>C (p.Val221Leu)	not specified [RCV004133054]	uncertain significance	4	1718171	1718171	Human		name
156003753	CV2290064	single nucleotide variant	NM_001127266.2(TMEM129):c.532C>G (p.Arg178Gly)	not specified [RCV004152747]	uncertain significance	4	1718300	1718300	Human		name
156012640	CV2358931	single nucleotide variant	NM_001127266.2(TMEM129):c.875G>A (p.Arg292His)	not specified [RCV004212266]	uncertain significance	4	1717394	1717394	Human		name
156015335	CV2360254	single nucleotide variant	NM_001127266.2(TMEM129):c.374C>T (p.Ala125Val)	not specified [RCV004208599]	uncertain significance	4	1718458	1718458	Human		name
156225583	CV2390629	single nucleotide variant	NM_001127266.2(TMEM129):c.529T>C (p.Tyr177His)	not specified [RCV004239152]	uncertain significance	4	1718303	1718303	Human		name
329400002	CV2444237	single nucleotide variant	NM_001127266.2(TMEM129):c.541G>A (p.Val181Met)	not specified [RCV004263008]	uncertain significance	4	1718291	1718291	Human		name
329368801	CV2450422	single nucleotide variant	NM_001127266.2(TMEM129):c.533G>A (p.Arg178Gln)	not specified [RCV004265350]	uncertain significance	4	1718299	1718299	Human		name
329398060	CV2466596	single nucleotide variant	NM_001127266.2(TMEM129):c.490G>A (p.Val164Met)	not specified [RCV004274124]	uncertain significance	4	1718342	1718342	Human		name
401718779	CV2679305	single nucleotide variant	NM_001127266.2(TMEM129):c.347G>A (p.Arg116His)	not specified [RCV004285847]	uncertain significance	4	1718485	1718485	Human		name
401740055	CV2684252	single nucleotide variant	NM_001127266.2(TMEM129):c.788C>T (p.Thr263Ile)	not specified [RCV004288912]	uncertain significance	4	1717568	1717568	Human		name
401735484	CV2687595	single nucleotide variant	NM_001127266.2(TMEM129):c.797C>T (p.Ser266Phe)	not specified [RCV004300817]	uncertain significance	4	1717559	1717559	Human		name
401719055	CV2704937	single nucleotide variant	NM_001127266.2(TMEM129):c.692C>G (p.Thr231Ser)	not specified [RCV004307506]	uncertain significance	4	1717664	1717664	Human		name
401750781	CV2715760	single nucleotide variant	NM_001127266.2(TMEM129):c.683T>G (p.Leu228Arg)	not specified [RCV004328899]	uncertain significance	4	1717673	1717673	Human		name
401763888	CV2725345	single nucleotide variant	NM_001127266.2(TMEM129):c.346C>T (p.Arg116Cys)	not specified [RCV004320000]	uncertain significance	4	1718486	1718486	Human		name
401879120	CV2778179	single nucleotide variant	NM_001127266.2(TMEM129):c.638G>A (p.Arg213His)	not specified [RCV004349903]	uncertain significance	4	1718194	1718194	Human		name
401867677	CV2780758	single nucleotide variant	NM_001127266.2(TMEM129):c.583C>T (p.Arg195Trp)	not specified [RCV004352085]	uncertain significance	4	1718249	1718249	Human		name
405793484	CV3339502	single nucleotide variant	NM_001127266.2(TMEM129):c.353G>A (p.Arg118Gln)	not specified [RCV004474913]	likely benign	4	1718479	1718479	Human		name
405793487	CV3339503	single nucleotide variant	NM_001127266.2(TMEM129):c.403C>G (p.Gln135Glu)	not specified [RCV004474914]	uncertain significance	4	1718429	1718429	Human		name
405793490	CV3339504	single nucleotide variant	NM_001127266.2(TMEM129):c.488G>A (p.Arg163His)	not specified [RCV004474915]	uncertain significance	4	1718344	1718344	Human		name
405793497	CV3339506	single nucleotide variant	NM_001127266.2(TMEM129):c.571G>A (p.Val191Met)	not specified [RCV004474917]	uncertain significance	4	1718261	1718261	Human		name
405793500	CV3339507	single nucleotide variant	NM_001127266.2(TMEM129):c.584G>A (p.Arg195Gln)	not specified [RCV004474918]	likely benign	4	1718248	1718248	Human		name
405793506	CV3339509	single nucleotide variant	NM_001127266.2(TMEM129):c.875G>C (p.Arg292Pro)	not specified [RCV004474920]	uncertain significance	4	1717394	1717394	Human		name
407458633	CV3486309	single nucleotide variant	NM_001127266.2(TMEM129):c.556G>T (p.Asp186Tyr)	not specified [RCV004686888]	uncertain significance	4	1718276	1718276	Human		name
597785282	CV3616643	single nucleotide variant	NM_001127266.2(TMEM129):c.376C>T (p.Arg126Cys)	not specified [RCV004875041]	uncertain significance	4	1718456	1718456	Human		name
597785296	CV3616647	single nucleotide variant	NM_001127266.2(TMEM129):c.608C>T (p.Ser203Leu)	not specified [RCV004875045]	uncertain significance	4	1718224	1718224	Human		name
598212214	CV3917230	single nucleotide variant	NM_001127266.2(TMEM129):c.457G>C (p.Asp153His)	not specified [RCV005292125]	uncertain significance	4	1718375	1718375	Human		name
598212223	CV3917231	single nucleotide variant	NM_001127266.2(TMEM129):c.637C>T (p.Arg213Cys)	not specified [RCV005292126]	uncertain significance	4	1718195	1718195	Human		name
598177954	CV3917236	single nucleotide variant	NM_001127266.2(TMEM129):c.431C>T (p.Ser144Phe)	not specified [RCV005285905]	uncertain significance	4	1718401	1718401	Human		name
156143239	CV2208618	single nucleotide variant	NM_001127266.2(TMEM129):c.1079C>T (p.Thr360Ile)	not specified [RCV004091137]	uncertain significance	4	1717190	1717190	Human		name
156108433	CV2254416	single nucleotide variant	NM_001127266.2(TMEM129):c.1051G>A (p.Ala351Thr)	not specified [RCV004123799]	uncertain significance	4	1717218	1717218	Human		name
401890204	CV2763697	single nucleotide variant	NM_001127266.2(TMEM129):c.1017G>T (p.Trp339Cys)	not specified [RCV004343196]	uncertain significance	4	1717252	1717252	Human		name
401881674	CV2784775	single nucleotide variant	NM_001127266.2(TMEM129):c.1015T>C (p.Trp339Arg)	not specified [RCV004352570]	uncertain significance	4	1717254	1717254	Human		name
401897290	CV2789988	single nucleotide variant	NM_001127266.2(TMEM129):c.1001T>C (p.Leu334Pro)	not specified [RCV004363950]	uncertain significance	4	1717268	1717268	Human		name
405793470	CV3339498	single nucleotide variant	NM_001127266.2(TMEM129):c.1027C>T (p.Arg343Cys)	not specified [RCV004474909]	uncertain significance	4	1717242	1717242	Human		name
597785292	CV3616646	single nucleotide variant	NM_001127266.2(TMEM129):c.1054C>T (p.Arg352Cys)	not specified [RCV004875044]	uncertain significance	4	1717215	1717215	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message