Tmem129 Variant Search Result - Rat Genome Database

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58 records found for search term Tmem129

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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

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