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Variants search result for Homo sapiens
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62 records found for search term Nln
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15164243CV777563deletionNM_020726.5(NLN):c.1527+15delnot provided [RCV000948292]benign56579266165792661Humanname
156267356CV2305023single nucleotide variantNM_020726.5(NLN):c.71T>C (p.Met24Thr)not specified [RCV004168912]uncertain significance56575859665758596Humanname
156194996CV2211007single nucleotide variantNM_020726.5(NLN):c.217G>A (p.Asp73Asn)not specified [RCV004088201]uncertain significance56575874265758742Humanname
156113822CV2224943single nucleotide variantNM_020726.5(NLN):c.124G>A (p.Val42Met)not specified [RCV004094793]uncertain significance56575864965758649Humanname
155994764CV2377634single nucleotide variantNM_020726.5(NLN):c.161C>T (p.Pro54Leu)not specified [RCV004227815]uncertain significance56575868665758686Humanname
329394702CV2461536single nucleotide variantNM_020726.5(NLN):c.233T>G (p.Leu78Arg)not specified [RCV004269454]uncertain significance56575875865758758Humanname
401757208CV2675166single nucleotide variantNM_020726.5(NLN):c.106G>A (p.Ala36Thr)not specified [RCV004289940]uncertain significance56575863165758631Humanname
156086818CV2258937single nucleotide variantNM_020726.5(NLN):c.776A>C (p.Glu259Ala)not specified [RCV004120217]uncertain significance56578137565781375Humanname
156173566CV2290114single nucleotide variantNM_020726.5(NLN):c.809C>T (p.Thr270Ile)not specified [RCV004152787]uncertain significance56578140865781408Humanname
156303506CV2308349single nucleotide variantNM_020726.5(NLN):c.302T>A (p.Val101Glu)not specified [RCV004164830]uncertain significance56576296065762960Humanname
156075435CV2350878single nucleotide variantNM_020726.5(NLN):c.940C>T (p.Arg314Cys)not specified [RCV004211715]uncertain significance56578589265785892Humanname
156157697CV2363735single nucleotide variantNM_020726.5(NLN):c.359C>A (p.Ala120Glu)not specified [RCV004218723]uncertain significance56576301765763017Humanname
329387983CV2440312single nucleotide variantNM_020726.5(NLN):c.460G>A (p.Asp154Asn)not specified [RCV004262792]uncertain significance56577743665777436Humanname
405707532CV3358828single nucleotide variantNM_020726.5(NLN):c.368C>G (p.Thr123Arg)not specified [RCV004493349]uncertain significance56576302665763026Humanname
405707539CV3358829single nucleotide variantNM_020726.5(NLN):c.785G>T (p.Arg262Ile)not specified [RCV004493350]uncertain significance56578138465781384Humanname
405707552CV3358831single nucleotide variantNM_020726.5(NLN):c.875A>G (p.Lys292Arg)not specified [RCV004493352]uncertain significance56578582765785827Humanname
405707559CV3358832single nucleotide variantNM_020726.5(NLN):c.892A>T (p.Thr298Ser)not specified [RCV004493353]uncertain significance56578584465785844Humanname
405707566CV3358833single nucleotide variantNM_020726.5(NLN):c.985T>G (p.Leu329Val)not specified [RCV004493354]uncertain significance56578814465788144Humanname
407508974CV3458692single nucleotide variantNM_020726.5(NLN):c.392G>A (p.Arg131His)not specified [RCV004647288]uncertain significance56576305065763050Humanname
407508977CV3458693single nucleotide variantNM_020726.5(NLN):c.391C>T (p.Arg131Cys)not specified [RCV004647289]uncertain significance56576304965763049Humanname
407508984CV3458695single nucleotide variantNM_020726.5(NLN):c.386T>C (p.Leu129Pro)not specified [RCV004647291]uncertain significance56576304465763044Humanname
407508987CV3458696single nucleotide variantNM_020726.5(NLN):c.830C>G (p.Thr277Ser)not specified [RCV004647292]uncertain significance56578578265785782Humanname
407508994CV3458701single nucleotide variantNM_020726.5(NLN):c.895C>T (p.His299Tyr)not specified [RCV004647294]uncertain significance56578584765785847Humanname
597651645CV3556428single nucleotide variantNM_020726.5(NLN):c.860G>A (p.Arg287Gln)not specified [RCV004826910]uncertain significance56578581265785812Humanname
597651669CV3556431single nucleotide variantNM_020726.5(NLN):c.379A>G (p.Lys127Glu)not specified [RCV004826913]uncertain significance56576303765763037Humanname
597651677CV3556432single nucleotide variantNM_020726.5(NLN):c.653C>T (p.Ala218Val)not specified [RCV004826914]uncertain significance56578027365780273Humanname
597651694CV3556434single nucleotide variantNM_020726.5(NLN):c.975G>T (p.Lys325Asn)not specified [RCV004826916]uncertain significance56578813465788134Humanname
598239312CV3994699single nucleotide variantNM_020726.5(NLN):c.862A>G (p.Thr288Ala)not specified [RCV005382901]likely benign56578581465785814Humanname
598193988CV3994700single nucleotide variantNM_020726.5(NLN):c.419G>T (p.Gly140Val)not specified [RCV005374652]uncertain significance56576307765763077Humanname
598193994CV3994701single nucleotide variantNM_020726.5(NLN):c.658C>T (p.Leu220Phe)not specified [RCV005374653]uncertain significance56578027865780278Humanname
156252808CV2192951single nucleotide variantNM_020726.5(NLN):c.1737T>G (p.Ile579Met)not specified [RCV004069509]uncertain significance56581005965810059Humanname
156050324CV2237759single nucleotide variantNM_020726.5(NLN):c.1394G>A (p.Arg465Gln)not specified [RCV004109012]uncertain significance56579252265792522Humanname
156026692CV2242380single nucleotide variantNM_020726.5(NLN):c.1558G>T (p.Val520Leu)not specified [RCV004111382]uncertain significance56580954565809545Humanname
156073818CV2263885single nucleotide variantNM_020726.5(NLN):c.1256C>A (p.Thr419Lys)not specified [RCV004137936]uncertain significance56578841565788415Humanname
156237356CV2265129single nucleotide variantNM_020726.5(NLN):c.1855C>T (p.Pro619Ser)not specified [RCV004126261]uncertain significance56581226665812266Humanname
155900957CV2298109single nucleotide variantNM_020726.5(NLN):c.2058G>C (p.Leu686Phe)not specified [RCV004159775]uncertain significance56582285865822858Humanname
156047699CV2315714single nucleotide variantNM_020726.5(NLN):c.1316T>A (p.Leu439His)not specified [RCV004169731]uncertain significance56578847565788475Humanname
156166734CV2345215single nucleotide variantNM_020726.5(NLN):c.1615G>A (p.Val539Ile)not specified [RCV004195954]likely benign56580960265809602Humanname
155993940CV2377346single nucleotide variantNM_020726.5(NLN):c.1468G>A (p.Asp490Asn)not specified [RCV004225527]uncertain significance56579259665792596Humanname
156263594CV2391722single nucleotide variantNM_020726.5(NLN):c.1549G>C (p.Gly517Arg)not specified [RCV004241875]uncertain significance56580953665809536Humanname
329360925CV2439892single nucleotide variantNM_020726.5(NLN):c.1172A>G (p.Glu391Gly)not specified [RCV004257929]uncertain significance56578833165788331Humanname
329361977CV2448176single nucleotide variantNM_020726.5(NLN):c.1509G>A (p.Met503Ile)not specified [RCV004263389]uncertain significance56579263765792637Humanname
329354511CV2448324single nucleotide variantNM_020726.5(NLN):c.1735A>G (p.Ile579Val)not specified [RCV004256612]uncertain significance56581005765810057Humanname
329401807CV2457442single nucleotide variantNM_020726.5(NLN):c.2095A>G (p.Arg699Gly)not specified [RCV004267265]uncertain significance56582289565822895Humanname
401748856CV2694520single nucleotide variantNM_020726.5(NLN):c.1628G>A (p.Arg543Gln)not specified [RCV004298653]uncertain significance56580961565809615Humanname
401876088CV2777653single nucleotide variantNM_020726.5(NLN):c.2063G>A (p.Arg688His)not specified [RCV004343492]uncertain significance56582286365822863Humanname
405707493CV3358822single nucleotide variantNM_020726.5(NLN):c.1417G>A (p.Val473Met)not specified [RCV004493343]uncertain significance56579254565792545Humanname
405707499CV3358823single nucleotide variantNM_020726.5(NLN):c.1450C>T (p.Pro484Ser)not specified [RCV004493344]uncertain significance56579257865792578Humanname
405707505CV3358824single nucleotide variantNM_020726.5(NLN):c.1504G>A (p.Val502Met)not specified [RCV004493345]uncertain significance56579263265792632Humanname
405707516CV3358826single nucleotide variantNM_020726.5(NLN):c.1673A>T (p.Asp558Val)not specified [RCV004493347]uncertain significance56580966065809660Humanname
405707524CV3358827single nucleotide variantNM_020726.5(NLN):c.1730G>C (p.Arg577Pro)not specified [RCV004493348]uncertain significance56581005265810052Humanname
407508980CV3458694single nucleotide variantNM_020726.5(NLN):c.1357G>C (p.Gly453Arg)not specified [RCV004647290]uncertain significance56579248565792485Humanname
407497590CV3458697single nucleotide variantNM_020726.5(NLN):c.1702C>A (p.Leu568Met)not specified [RCV004643787]uncertain significance56580968965809689Humanname
407497596CV3458698single nucleotide variantNM_020726.5(NLN):c.1510C>T (p.His504Tyr)not specified [RCV004643788]uncertain significance56579263865792638Humanname
597651638CV3556427single nucleotide variantNM_020726.5(NLN):c.1357G>A (p.Gly453Ser)not specified [RCV004826909]uncertain significance56579248565792485Humanname
597651654CV3556429single nucleotide variantNM_020726.5(NLN):c.1730G>A (p.Arg577His)not specified [RCV004826911]uncertain significance56581005265810052Humanname
597651660CV3556430single nucleotide variantNM_020726.5(NLN):c.1976C>T (p.Pro659Leu)not specified [RCV004826912]uncertain significance56581238765812387Humanname
597651686CV3556433single nucleotide variantNM_020726.5(NLN):c.1615G>C (p.Val539Leu)not specified [RCV004826915]uncertain significance56580960265809602Humanname
598239306CV3994698single nucleotide variantNM_020726.5(NLN):c.1932G>A (p.Met644Ile)not specified [RCV005382900]uncertain significance56581234365812343Humanname
598194000CV3994702single nucleotide variantNM_020726.5(NLN):c.1450C>G (p.Pro484Ala)not specified [RCV005374654]uncertain significance56579257865792578Humanname
598194007CV3994703single nucleotide variantNM_020726.5(NLN):c.1214T>A (p.Phe405Tyr)not specified [RCV005374655]uncertain significance56578837365788373Humanname
598194013CV3994704single nucleotide variantNM_020726.5(NLN):c.2089A>G (p.Met697Val)not specified [RCV005374656]uncertain significance56582288965822889Humanname