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Variants search result for Homo sapiens
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71 records found for search term Opn4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401907553CV2809438single nucleotide variantNM_033282.4(OPN4):c.291-825T>Gnot provided [RCV003422699]likely benign108665720786657207Humanname
15143385CV744458single nucleotide variantNM_033282.4(OPN4):c.1074-10G>Anot provided [RCV000899828]likely benign108666224286662242Humanname
407505579CV3469826single nucleotide variantNM_033282.4(OPN4):c.16G>T (p.Gly6Trp)not specified [RCV004646164]uncertain significance108665479986654799Humanname
598255489CV3998559single nucleotide variantNM_033282.4(OPN4):c.56G>T (p.Cys19Phe)not specified [RCV005385671]uncertain significance108665483986654839Humanname
15100068CV752310single nucleotide variantNM_033282.4(OPN4):c.999G>T (p.Ser333=)not provided [RCV000914551]likely benign108666131486661314Humanname
155925433CV2348386single nucleotide variantNM_033282.4(OPN4):c.224C>A (p.Thr75Lys)not specified [RCV004193581]uncertain significance108665623486656234Humanname
155957565CV2387516single nucleotide variantNM_033282.4(OPN4):c.122G>A (p.Arg41Gln)not specified [RCV004240369]likely benign108665490586654905Humanname
329385804CV2462352single nucleotide variantNM_033282.4(OPN4):c.293G>A (p.Ser98Asn)not specified [RCV004266335]uncertain significance108665803486658034Humanname
401723553CV2674994single nucleotide variantNM_033282.4(OPN4):c.226G>A (p.Val76Met)not specified [RCV004296300]uncertain significance108665623686656236Humanname
407527419CV3469827single nucleotide variantNM_033282.4(OPN4):c.201C>G (p.Asp67Glu)not specified [RCV004655206]uncertain significance108665621186656211Humanname
598255517CV3998565single nucleotide variantNM_033282.4(OPN4):c.106A>C (p.Ile36Leu)not specified [RCV005385676]uncertain significance108665488986654889Humanname
15105413CV712493single nucleotide variantNM_033282.4(OPN4):c.1320C>G (p.Leu440=)not provided [RCV000959880]benign108666372486663724Humanname
156061607CV2263147single nucleotide variantNM_033282.4(OPN4):c.662G>A (p.Cys221Tyr)not specified [RCV004131384]uncertain significance108665933086659330Humanname
156294541CV2293205single nucleotide variantNM_033282.4(OPN4):c.956C>G (p.Ala319Gly)not specified [RCV004150714]uncertain significance108666005086660050Humanname
155910328CV2303570single nucleotide variantNM_033282.4(OPN4):c.907C>T (p.Leu303Phe)not specified [RCV004161660]uncertain significance108666000186660001Humanname
156289586CV2324819single nucleotide variantNM_033282.4(OPN4):c.580G>C (p.Val194Leu)not specified [RCV004173049]uncertain significance108665863986658639Humanname
155968725CV2339342single nucleotide variantNM_033282.4(OPN4):c.545C>T (p.Ala182Val)not specified [RCV004191572]likely benign108665860486658604Humanname
156143874CV2358616single nucleotide variantNM_033282.4(OPN4):c.376G>C (p.Val126Leu)not specified [RCV004207492]uncertain significance108665811786658117Humanname
155997377CV2393302single nucleotide variantNM_033282.4(OPN4):c.970G>A (p.Ala324Thr)not provided [RCV003491310]|not specified [RCV004228812]uncertain significance108666128586661285Humanname
156058181CV2396437single nucleotide variantNM_033282.4(OPN4):c.854G>A (p.Arg285Gln)not specified [RCV004242150]uncertain significance108665994886659948Humanname
156045508CV2397251single nucleotide variantNM_033282.4(OPN4):c.817G>A (p.Gly273Arg)not specified [RCV004238785]uncertain significance108665991186659911Humanname
329369348CV2450613single nucleotide variantNM_033282.4(OPN4):c.859C>T (p.Arg287Trp)not provided [RCV004696385]|not specified [RCV004265506]uncertain significance108665995386659953Humanname
401751638CV2672524single nucleotide variantNM_033282.4(OPN4):c.560C>T (p.Ala187Val)not specified [RCV004287563]uncertain significance108665861986658619Humanname
401731119CV2674267single nucleotide variantNM_033282.4(OPN4):c.694G>A (p.Val232Met)not specified [RCV004289151]uncertain significance108665936286659362Humanname
401867043CV2759079single nucleotide variantNM_033282.4(OPN4):c.320T>G (p.Met107Arg)not specified [RCV004342382]uncertain significance108665806186658061Humanname
401892004CV2775876single nucleotide variantNM_033282.4(OPN4):c.539G>A (p.Gly180Asp)not specified [RCV004344908]uncertain significance108665859886658598Humanname
401896684CV2791921single nucleotide variantNM_033282.4(OPN4):c.397T>C (p.Tyr133His)not specified [RCV004359352]uncertain significance108665813886658138Humanname
405752108CV3356194single nucleotide variantNM_033282.4(OPN4):c.985C>A (p.Pro329Thr)not specified [RCV004499291]uncertain significance108666130086661300Humanname
405752114CV3356195single nucleotide variantNM_033282.4(OPN4):c.988T>C (p.Tyr330His)not specified [RCV004499292]uncertain significance108666130386661303Humanname
405752148CV3356200single nucleotide variantNM_033282.4(OPN4):c.521G>A (p.Arg174His)not specified [RCV004499297]uncertain significance108665858086658580Humanname
405752163CV3356202single nucleotide variantNM_033282.4(OPN4):c.554G>A (p.Arg185Lys)not specified [RCV004499299]uncertain significance108665861386658613Humanname
405752170CV3356203single nucleotide variantNM_033282.4(OPN4):c.580G>A (p.Val194Ile)not specified [RCV004499300]uncertain significance108665863986658639Humanname
405752178CV3356204single nucleotide variantNM_033282.4(OPN4):c.709A>G (p.Met237Val)not specified [RCV004499301]uncertain significance108665937786659377Humanname
405752186CV3356205single nucleotide variantNM_033282.4(OPN4):c.916G>A (p.Val306Met)not specified [RCV004499302]uncertain significance108666001086660010Humanname
405752192CV3356206single nucleotide variantNM_033282.4(OPN4):c.947C>T (p.Ala316Val)not specified [RCV004499303]uncertain significance108666004186660041Humanname
407527410CV3469823single nucleotide variantNM_033282.4(OPN4):c.860G>A (p.Arg287Gln)not specified [RCV004655203]uncertain significance108665995486659954Humanname
407527416CV3469825single nucleotide variantNM_033282.4(OPN4):c.940G>A (p.Ala314Thr)not specified [RCV004655205]likely benign108666003486660034Humanname
597687460CV3573947single nucleotide variantNM_033282.4(OPN4):c.953T>C (p.Val318Ala)not specified [RCV004838318]uncertain significance108666004786660047Humanname
597687468CV3573948single nucleotide variantNM_033282.4(OPN4):c.889A>G (p.Ile297Val)not specified [RCV004838319]uncertain significance108665998386659983Humanname
597687477CV3573950single nucleotide variantNM_033282.4(OPN4):c.832A>C (p.Asn278His)not specified [RCV004838320]uncertain significance108665992686659926Humanname
597687495CV3573953single nucleotide variantNM_033282.4(OPN4):c.393C>G (p.Ser131Arg)not specified [RCV004838322]uncertain significance108665813486658134Humanname
597687504CV3573954single nucleotide variantNM_033282.4(OPN4):c.871G>A (p.Glu291Lys)not specified [RCV004838323]uncertain significance108665996586659965Humanname
597687514CV3573955single nucleotide variantNM_033282.4(OPN4):c.787C>T (p.Arg263Trp)not specified [RCV004838324]uncertain significance108665945586659455Humanname
598255500CV3998562single nucleotide variantNM_033282.4(OPN4):c.520C>T (p.Arg174Cys)not specified [RCV005385673]uncertain significance108665857986658579Humanname
598255506CV3998563single nucleotide variantNM_033282.4(OPN4):c.631G>C (p.Ala211Pro)not specified [RCV005385674]uncertain significance108665929986659299Humanname
598255512CV3998564single nucleotide variantNM_033282.4(OPN4):c.676A>C (p.Met226Leu)not specified [RCV005385675]uncertain significance108665934486659344Humanname
598255522CV3998566single nucleotide variantNM_033282.4(OPN4):c.736C>G (p.Leu246Val)not specified [RCV005385677]uncertain significance108665940486659404Humanname
598255529CV3998567single nucleotide variantNM_033282.4(OPN4):c.304C>T (p.Arg102Trp)not specified [RCV005385678]uncertain significance108665804586658045Humanname
598255535CV3998568single nucleotide variantNM_033282.4(OPN4):c.352C>T (p.Leu118Phe)not specified [RCV005385679]uncertain significance108665809386658093Humanname
15193646CV752311duplicationNM_033282.4(OPN4):c.1412dup (p.Ser473fs)not provided [RCV000910900]benign108666572586665726Humanname
8633749CV88965single nucleotide variantNM_001030015.2(OPN4):c.186G>A (p.Thr62=)Malignant melanoma [RCV000069062]not provided108665619686656196Humanname
156229575CV2199498single nucleotide variantNM_033282.4(OPN4):c.1220G>C (p.Arg407Thr)not specified [RCV004071050]uncertain significance108666239886662398Humanname
156238610CV2217062single nucleotide variantNM_033282.4(OPN4):c.1223G>A (p.Arg408His)not specified [RCV004085744]uncertain significance108666240186662401Humanname
156333174CV2335941single nucleotide variantNM_033282.4(OPN4):c.1378G>A (p.Glu460Lys)not specified [RCV004189551]uncertain significance108666378286663782Humanname
156088297CV2337149single nucleotide variantNM_033282.4(OPN4):c.1206G>C (p.Trp402Cys)not specified [RCV004192908]uncertain significance108666238486662384Humanname
155925611CV2348439single nucleotide variantNM_033282.4(OPN4):c.1070A>G (p.Tyr357Cys)not specified [RCV004193629]uncertain significance108666138586661385Humanname
156383969CV2361767single nucleotide variantNM_033282.4(OPN4):c.1015G>A (p.Ala339Thr)not specified [RCV004223241]uncertain significance108666133086661330Humanname
155954832CV2389828single nucleotide variantNM_033282.4(OPN4):c.1313G>A (p.Arg438Gln)not specified [RCV004236051]uncertain significance108666371786663717Humanname
401727927CV2675866single nucleotide variantNM_033282.4(OPN4):c.1130G>A (p.Arg377Gln)not specified [RCV004281870]likely benign108666230886662308Humanname
405752127CV3356197single nucleotide variantNM_033282.4(OPN4):c.1282G>T (p.Val428Leu)not specified [RCV004499294]uncertain significance108666368686663686Humanname
405752134CV3356198single nucleotide variantNM_033282.4(OPN4):c.1324G>A (p.Gly442Ser)not specified [RCV004499295]likely benign108666372886663728Humanname
405752141CV3356199single nucleotide variantNM_033282.4(OPN4):c.1402A>G (p.Lys468Glu)not specified [RCV004499296]uncertain significance108666571686665716Humanname
407527413CV3469824single nucleotide variantNM_033282.4(OPN4):c.1384G>A (p.Glu462Lys)not specified [RCV004655204]uncertain significance108666378886663788Humanname
597660776CV3573949single nucleotide variantNM_033282.4(OPN4):c.1169G>A (p.Arg390His)not specified [RCV004834972]uncertain significance108666234786662347Humanname
597687485CV3573952single nucleotide variantNM_033282.4(OPN4):c.1214T>A (p.Ile405Lys)not specified [RCV004838321]uncertain significance108666239286662392Humanname
597687522CV3573956single nucleotide variantNM_033282.4(OPN4):c.1136G>A (p.Ser379Asn)not specified [RCV004838325]uncertain significance108666231486662314Humanname
598255484CV3998558single nucleotide variantNM_033282.4(OPN4):c.1102C>G (p.Leu368Val)not specified [RCV005385670]uncertain significance108666228086662280Humanname
598182332CV3998560single nucleotide variantNM_033282.4(OPN4):c.1168C>T (p.Arg390Cys)not specified [RCV005395121]uncertain significance108666234686662346Humanname
598255494CV3998561single nucleotide variantNM_033282.4(OPN4):c.1037A>T (p.Asn346Ile)not specified [RCV005385672]uncertain significance108666135286661352Humanname
15127587CV712494single nucleotide variantNM_033282.4(OPN4):c.1331G>A (p.Gly444Asp)not provided [RCV000963931]benign108666373586663735Humanname
8633750CV88966single nucleotide variantNM_001030015.2(OPN4):c.1086C>T (p.Ala362=)Malignant melanoma [RCV000069063]not provided108666136886661368Humanname