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73 records found for search term Trim41
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405790416CV3336987single nucleotide variantNM_033549.5(TRIM41):c.22C>T (p.Pro8Ser)not specified [RCV004473866]uncertain significance5181224021181224021Humanname
15184368CV709858single nucleotide variantNM_033549.5(TRIM41):c.516C>T (p.Pro172=)not provided [RCV000975096]benign5181224515181224515Humanname
156239973CV2350308single nucleotide variantNM_033549.5(TRIM41):c.163G>A (p.Asp55Asn)not specified [RCV004202259]uncertain significance5181224162181224162Humanname
401918206CV2825654single nucleotide variantNM_033549.5(TRIM41):c.1653C>T (p.Cys551=)not provided [RCV003430060]likely benign5181234535181234535Humanname
597801807CV3617753single nucleotide variantNM_033549.5(TRIM41):c.203G>C (p.Gly68Ala)not specified [RCV004880914]uncertain significance5181224202181224202Humanname
597801821CV3617761single nucleotide variantNM_033549.5(TRIM41):c.199G>A (p.Asp67Asn)not specified [RCV004880921]uncertain significance5181224198181224198Humanname
15157571CV699049single nucleotide variantNM_033549.5(TRIM41):c.185A>G (p.Glu62Gly)not provided [RCV000946908]benign5181224184181224184Humanname
156275239CV2202723single nucleotide variantNM_033549.5(TRIM41):c.440G>A (p.Gly147Glu)not specified [RCV004082967]uncertain significance5181224439181224439Humanname
156086801CV2241273single nucleotide variantNM_033549.5(TRIM41):c.997C>T (p.Arg333Trp)not specified [RCV004102425]uncertain significance5181232746181232746Humanname
156161012CV2319425single nucleotide variantNM_033549.5(TRIM41):c.874A>G (p.Lys292Glu)not specified [RCV004185012]uncertain significance5181230804181230804Humanname
155976013CV2342729single nucleotide variantNM_033549.5(TRIM41):c.998G>A (p.Arg333Gln)not specified [RCV004196801]uncertain significance5181232747181232747Humanname
329361918CV2468442single nucleotide variantNM_033549.5(TRIM41):c.799G>A (p.Val267Met)not specified [RCV004277748]uncertain significance5181224798181224798Humanname
401721409CV2709949single nucleotide variantNM_033549.5(TRIM41):c.331G>A (p.Gly111Ser)not specified [RCV004315020]uncertain significance5181224330181224330Humanname
401760443CV2718842single nucleotide variantNM_033549.5(TRIM41):c.918G>C (p.Met306Ile)not specified [RCV004328584]uncertain significance5181232667181232667Humanname
401773990CV2727697single nucleotide variantNM_033549.5(TRIM41):c.637C>T (p.Pro213Ser)not specified [RCV004329866]uncertain significance5181224636181224636Humanname
401869304CV2772347single nucleotide variantNM_033549.5(TRIM41):c.473A>G (p.Glu158Gly)not specified [RCV004353359]uncertain significance5181224472181224472Humanname
401871599CV2783551single nucleotide variantNM_033549.5(TRIM41):c.595C>G (p.Leu199Val)not specified [RCV004365880]uncertain significance5181224594181224594Humanname
405790419CV3336988single nucleotide variantNM_033549.5(TRIM41):c.465A>C (p.Glu155Asp)not specified [RCV004473867]uncertain significance5181224464181224464Humanname
405790421CV3336989single nucleotide variantNM_033549.5(TRIM41):c.511C>A (p.Leu171Met)not specified [RCV004473868]uncertain significance5181224510181224510Humanname
405790424CV3336990single nucleotide variantNM_033549.5(TRIM41):c.674G>T (p.Gly225Val)not specified [RCV004473869]uncertain significance5181224673181224673Humanname
407453810CV3490516single nucleotide variantNM_033549.5(TRIM41):c.348C>G (p.Ser116Arg)not specified [RCV004684673]uncertain significance5181224347181224347Humanname
407453816CV3490518single nucleotide variantNM_033549.5(TRIM41):c.998G>C (p.Arg333Pro)not specified [RCV004684675]uncertain significance5181232747181232747Humanname
597801813CV3617757single nucleotide variantNM_033549.5(TRIM41):c.634C>T (p.His212Tyr)not specified [RCV004880917]uncertain significance5181224633181224633Humanname
597801825CV3617763single nucleotide variantNM_033549.5(TRIM41):c.965G>A (p.Arg322Gln)not specified [RCV004880923]uncertain significance5181232714181232714Humanname
598274159CV3935459single nucleotide variantNM_033549.5(TRIM41):c.311A>T (p.Glu104Val)not specified [RCV005303788]uncertain significance5181224310181224310Humanname
598274161CV3935460single nucleotide variantNM_033549.5(TRIM41):c.767A>G (p.Lys256Arg)not specified [RCV005303789]uncertain significance5181224766181224766Humanname
598202719CV3935461single nucleotide variantNM_033549.5(TRIM41):c.382G>A (p.Asp128Asn)not specified [RCV005290421]uncertain significance5181224381181224381Humanname
8631591CV86795single nucleotide variantNM_033549.4(TRIM41):c.518C>T (p.Pro173Leu)Malignant melanoma [RCV000066886]not provided5181224517181224517Humanname
156221926CV2232613single nucleotide variantNM_033549.5(TRIM41):c.1046C>A (p.Ala349Glu)not specified [RCV004101288]uncertain significance5181232795181232795Humanname
155914158CV2242625single nucleotide variantNM_033549.5(TRIM41):c.1571A>T (p.Asp524Val)not specified [RCV004113684]uncertain significance5181234453181234453Humanname
156184534CV2255466single nucleotide variantNM_033549.5(TRIM41):c.1604G>A (p.Arg535His)not specified [RCV004117817]uncertain significance5181234486181234486Humanname
156187444CV2292464single nucleotide variantNM_033549.5(TRIM41):c.1765C>T (p.Arg589Cys)not specified [RCV004150253]uncertain significance5181234647181234647Humanname
156079581CV2300934single nucleotide variantNM_033549.5(TRIM41):c.1718G>A (p.Ser573Asn)not specified [RCV004158120]uncertain significance5181234600181234600Humanname
156020535CV2309564single nucleotide variantNM_033549.5(TRIM41):c.1867G>A (p.Gly623Ser)not specified [RCV004158945]uncertain significance5181234749181234749Humanname
156046430CV2315602single nucleotide variantNM_033549.5(TRIM41):c.1543C>T (p.Pro515Ser)not specified [RCV004169639]likely benign5181234425181234425Humanname
156089552CV2344447single nucleotide variantNM_033549.5(TRIM41):c.1267C>T (p.Arg423Trp)not specified [RCV004195192]uncertain significance5181233739181233739Humanname
156159877CV2361670single nucleotide variantNM_033549.5(TRIM41):c.1351C>T (p.Arg451Trp)not specified [RCV004223158]uncertain significance5181234233181234233Humanname
156252960CV2366086single nucleotide variantNM_033549.5(TRIM41):c.1583C>T (p.Ser528Leu)not specified [RCV004210123]uncertain significance5181234465181234465Humanname
156156404CV2368021single nucleotide variantNM_033549.5(TRIM41):c.1558G>A (p.Val520Met)not specified [RCV004223106]uncertain significance5181234440181234440Humanname
156304541CV2369120single nucleotide variantNM_033549.5(TRIM41):c.1375C>T (p.Arg459Trp)not specified [RCV004208046]uncertain significance5181234257181234257Humanname
156209073CV2370065single nucleotide variantNM_033549.5(TRIM41):c.1703C>T (p.Thr568Met)not specified [RCV004210960]uncertain significance5181234585181234585Humanname
156258572CV2395395single nucleotide variantNM_033549.5(TRIM41):c.1085G>A (p.Arg362His)not specified [RCV004241273]uncertain significance5181232834181232834Humanname
155997393CV2398710single nucleotide variantNM_033549.5(TRIM41):c.1402C>T (p.Arg468Cys)not specified [RCV004240054]uncertain significance5181234284181234284Humanname
329369533CV2424850single nucleotide variantNM_033549.5(TRIM41):c.1372C>T (p.Arg458Trp)not specified [RCV004248735]uncertain significance5181234254181234254Humanname
329372594CV2443181single nucleotide variantNM_033549.5(TRIM41):c.1732C>T (p.Arg578Cys)not specified [RCV004255374]uncertain significance5181234614181234614Humanname
329381753CV2471238single nucleotide variantNM_033549.5(TRIM41):c.1541G>A (p.Gly514Asp)not specified [RCV004278477]uncertain significance5181234423181234423Humanname
401736191CV2672846single nucleotide variantNM_033549.5(TRIM41):c.1046C>T (p.Ala349Val)not specified [RCV004281621]uncertain significance5181232795181232795Humanname
405790387CV3336977single nucleotide variantNM_033549.5(TRIM41):c.1051A>G (p.Ser351Gly)not specified [RCV004473856]uncertain significance5181232800181232800Humanname
405790390CV3336978single nucleotide variantNM_033549.5(TRIM41):c.1072G>A (p.Ala358Thr)not specified [RCV004473857]uncertain significance5181232821181232821Humanname
405790393CV3336979single nucleotide variantNM_033549.5(TRIM41):c.1119G>T (p.Gln373His)not specified [RCV004473858]uncertain significance5181232868181232868Humanname
405790396CV3336980single nucleotide variantNM_033549.5(TRIM41):c.1222C>G (p.His408Asp)not specified [RCV004473859]uncertain significance5181233694181233694Humanname
405790402CV3336982single nucleotide variantNM_033549.5(TRIM41):c.1301C>T (p.Thr434Met)not specified [RCV004473861]uncertain significance5181234183181234183Humanname
405790405CV3336983single nucleotide variantNM_033549.5(TRIM41):c.1321C>T (p.His441Tyr)not specified [RCV004473862]uncertain significance5181234203181234203Humanname
405790407CV3336984single nucleotide variantNM_033549.5(TRIM41):c.1400A>G (p.Lys467Arg)not specified [RCV004473863]uncertain significance5181234282181234282Humanname
405790410CV3336985single nucleotide variantNM_033549.5(TRIM41):c.1525C>T (p.His509Tyr)not specified [RCV004473864]uncertain significance5181234407181234407Humanname
405790413CV3336986single nucleotide variantNM_033549.5(TRIM41):c.1874G>A (p.Arg625His)not specified [RCV004473865]uncertain significance5181234756181234756Humanname
407453812CV3490517single nucleotide variantNM_033549.5(TRIM41):c.1373G>A (p.Arg458Gln)not specified [RCV004684674]uncertain significance5181234255181234255Humanname
407453818CV3490519single nucleotide variantNM_033549.5(TRIM41):c.1835G>A (p.Arg612His)not specified [RCV004684676]uncertain significance5181234717181234717Humanname
407453822CV3490520single nucleotide variantNM_033549.5(TRIM41):c.1108C>T (p.Arg370Trp)not specified [RCV004684677]uncertain significance5181232857181232857Humanname
407453826CV3490521single nucleotide variantNM_033549.5(TRIM41):c.1865A>G (p.Lys622Arg)not specified [RCV004684678]uncertain significance5181234747181234747Humanname
407453828CV3490522single nucleotide variantNM_033549.5(TRIM41):c.1343C>T (p.Pro448Leu)not specified [RCV004684679]uncertain significance5181234225181234225Humanname
597801803CV3617751single nucleotide variantNM_033549.5(TRIM41):c.1263G>C (p.Met421Ile)not specified [RCV004880912]uncertain significance5181233735181233735Humanname
597801805CV3617752single nucleotide variantNM_033549.5(TRIM41):c.1585C>T (p.Arg529Cys)not specified [RCV004880913]uncertain significance5181234467181234467Humanname
597801809CV3617754single nucleotide variantNM_033549.5(TRIM41):c.1567G>A (p.Gly523Arg)not specified [RCV004880915]uncertain significance5181234449181234449Humanname
597801811CV3617756single nucleotide variantNM_033549.5(TRIM41):c.1606C>T (p.Arg536Trp)not specified [RCV004880916]uncertain significance5181234488181234488Humanname
597801815CV3617758single nucleotide variantNM_033549.5(TRIM41):c.1550G>A (p.Gly517Asp)not specified [RCV004880918]uncertain significance5181234432181234432Humanname
597801817CV3617759single nucleotide variantNM_033549.5(TRIM41):c.1103A>G (p.Gln368Arg)not specified [RCV004880919]uncertain significance5181232852181232852Humanname
597801819CV3617760single nucleotide variantNM_033549.5(TRIM41):c.1594C>T (p.His532Tyr)not specified [RCV004880920]uncertain significance5181234476181234476Humanname
597801823CV3617762single nucleotide variantNM_033549.5(TRIM41):c.1346A>G (p.Asp449Gly)not specified [RCV004880922]uncertain significance5181234228181234228Humanname
597801827CV3617764single nucleotide variantNM_033549.5(TRIM41):c.1846T>C (p.Phe616Leu)not specified [RCV004880924]uncertain significance5181234728181234728Humanname
598202698CV3935456single nucleotide variantNM_033549.5(TRIM41):c.1444C>T (p.Arg482Cys)not specified [RCV005290418]uncertain significance5181234326181234326Humanname
598202704CV3935457single nucleotide variantNM_033549.5(TRIM41):c.1279C>G (p.Gln427Glu)not specified [RCV005290419]uncertain significance5181233751181233751Humanname
598202711CV3935458single nucleotide variantNM_033549.5(TRIM41):c.1033C>A (p.Arg345Ser)not specified [RCV005290420]uncertain significance5181232782181232782Humanname