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Variants search result for Homo sapiens
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38 records found for search term Lpcat2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
14399433CV614157single nucleotide variantNM_017839.5(LPCAT2):c.172-6188G>AMulticentric osteolysis nodulosis arthropathy spectrum [RCV000767860]pathogenic165551932055519320Human1name
401764190CV2700536single nucleotide variantNM_017839.5(LPCAT2):c.52G>C (p.Gly18Arg)not specified [RCV004312951]uncertain significance165550923355509233Humanname
597796240CV3702067single nucleotide variantNM_017839.5(LPCAT2):c.65T>C (p.Val22Ala)not specified [RCV004935094]likely benign165550924655509246Humanname
598238922CV3991906single nucleotide variantNM_017839.5(LPCAT2):c.91C>T (p.Arg31Cys)not specified [RCV005364337]uncertain significance165550927255509272Humanname
401903224CV2807951single nucleotide variantNM_017839.5(LPCAT2):c.1173T>C (p.Pro391=)not provided [RCV003419332]likely benign165555106055551060Humanname
15161612CV703738single nucleotide variantNM_017839.5(LPCAT2):c.265G>A (p.Val89Ile)not provided [RCV000947703]benign165552560155525601Humanname
155925912CV2208066single nucleotide variantNM_017839.5(LPCAT2):c.347G>A (p.Arg116His)not specified [RCV004086757]likely benign165552841255528412Humanname
156248889CV2222046single nucleotide variantNM_017839.5(LPCAT2):c.863T>C (p.Val288Ala)not specified [RCV004103030]uncertain significance165554574555545745Humanname
156189870CV2356675single nucleotide variantNM_017839.5(LPCAT2):c.601G>A (p.Glu201Lys)not specified [RCV004202034]uncertain significance165552990655529906Humanname
156336407CV2360731single nucleotide variantNM_017839.5(LPCAT2):c.920G>A (p.Arg307Gln)not specified [RCV004213517]uncertain significance165554580255545802Humanname
155905347CV2385767single nucleotide variantNM_017839.5(LPCAT2):c.846A>C (p.Glu282Asp)not specified [RCV004226517]uncertain significance165553762655537626Humanname
329400982CV2445986single nucleotide variantNM_017839.5(LPCAT2):c.553G>C (p.Val185Leu)not specified [RCV004270573]uncertain significance165552985855529858Humanname
329396230CV2462446single nucleotide variantNM_017839.5(LPCAT2):c.925T>G (p.Leu309Val)not specified [RCV004276637]likely benign165554580755545807Humanname
401742775CV2697861single nucleotide variantNM_017839.5(LPCAT2):c.811A>G (p.Met271Val)not specified [RCV004300573]likely benign165553759155537591Humanname
401760819CV2706106single nucleotide variantNM_017839.5(LPCAT2):c.380C>T (p.Ala127Val)not specified [RCV004314796]uncertain significance165552844555528445Humanname
401757526CV2707831single nucleotide variantNM_017839.5(LPCAT2):c.500A>G (p.Asn167Ser)not specified [RCV004309114]uncertain significance165552856555528565Humanname
405815550CV3284162single nucleotide variantNM_017839.5(LPCAT2):c.391A>C (p.Lys131Gln)not specified [RCV004410559]uncertain significance165552845655528456Humanname
407471475CV3445950single nucleotide variantNM_017839.5(LPCAT2):c.707C>G (p.Ala236Gly)not specified [RCV004637409]uncertain significance165553282755532827Humanname
407471479CV3445951single nucleotide variantNM_017839.5(LPCAT2):c.876T>G (p.Asn292Lys)not specified [RCV004637410]uncertain significance165554575855545758Humanname
407461269CV3445952single nucleotide variantNM_017839.5(LPCAT2):c.455G>T (p.Gly152Val)not specified [RCV004634084]uncertain significance165552852055528520Humanname
597623472CV3702064single nucleotide variantNM_017839.5(LPCAT2):c.887A>G (p.Lys296Arg)not specified [RCV004936496]uncertain significance165554576955545769Humanname
597623473CV3702065single nucleotide variantNM_017839.5(LPCAT2):c.504G>C (p.Glu168Asp)not specified [RCV004936497]uncertain significance165552856955528569Humanname
598230920CV3991904single nucleotide variantNM_017839.5(LPCAT2):c.799A>G (p.Ile267Val)not specified [RCV005362784]uncertain significance165553757955537579Humanname
598238915CV3991905single nucleotide variantNM_017839.5(LPCAT2):c.880G>A (p.Glu294Lys)not specified [RCV005364336]uncertain significance165554576255545762Humanname
15186690CV703739single nucleotide variantNM_017839.5(LPCAT2):c.382G>A (p.Val128Ile)not provided [RCV000953360]benign165552844755528447Humanname
156147946CV2196995single nucleotide variantNM_017839.5(LPCAT2):c.1573G>A (p.Ala525Thr)not specified [RCV004071450]uncertain significance165558303655583036Humanname
156079741CV2258076single nucleotide variantNM_017839.5(LPCAT2):c.1241G>A (p.Arg414Gln)not specified [RCV004121475]uncertain significance165557465655574656Humanname
405815548CV3284160single nucleotide variantNM_017839.5(LPCAT2):c.1108A>G (p.Ile370Val)not specified [RCV004410557]uncertain significance165555099555550995Humanname
405815549CV3284161single nucleotide variantNM_017839.5(LPCAT2):c.1261G>A (p.Ala421Thr)not specified [RCV004410558]uncertain significance165557467655574676Humanname
407471471CV3445949single nucleotide variantNM_017839.5(LPCAT2):c.1324G>A (p.Val442Ile)not specified [RCV004637408]uncertain significance165557911855579118Humanname
597623471CV3702063single nucleotide variantNM_017839.5(LPCAT2):c.1624A>G (p.Lys542Glu)not specified [RCV004936495]uncertain significance165558308755583087Humanname
597796073CV3702066single nucleotide variantNM_017839.5(LPCAT2):c.1111G>A (p.Ala371Thr)not specified [RCV004935093]uncertain significance165555099855550998Humanname
598238886CV3991899single nucleotide variantNM_017839.5(LPCAT2):c.1015A>G (p.Met339Val)not specified [RCV005364331]uncertain significance165554935655549356Humanname
598238899CV3991901single nucleotide variantNM_017839.5(LPCAT2):c.1102G>A (p.Ala368Thr)not specified [RCV005364333]uncertain significance165555098955550989Humanname
598238904CV3991902single nucleotide variantNM_017839.5(LPCAT2):c.1493A>T (p.Lys498Met)not specified [RCV005364334]uncertain significance165558295655582956Humanname
598238909CV3991903single nucleotide variantNM_017839.5(LPCAT2):c.1241G>C (p.Arg414Pro)not specified [RCV005364335]uncertain significance165557465655574656Humanname
15186694CV703740single nucleotide variantNM_017839.5(LPCAT2):c.1346C>T (p.Thr449Met)not provided [RCV000953361]benign165557914055579140Human1name
15186694CV703740single nucleotide variantNM_017839.5(LPCAT2):c.1346C>T (p.Thr449Met)not provided [RCV000953361]benign165557914055579141Human1name