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Variants search result for Homo sapiens
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42 records found for search term Ubqln4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156267872CV2275579single nucleotide variantNM_020131.5(UBQLN4):c.68A>G (p.Lys23Arg)not specified [RCV004137216]uncertain significance1156053634156053634Humanname
401933067CV2806054single nucleotide variantNM_020131.5(UBQLN4):c.522C>T (p.Gly174=)not provided [RCV003409140]likely benign1156050510156050510Humanname
598189542CV3928963single nucleotide variantNM_020131.5(UBQLN4):c.83T>C (p.Ile28Thr)not specified [RCV005288086]uncertain significance1156053619156053619Humanname
401764394CV2725611single nucleotide variantNM_020131.5(UBQLN4):c.100G>A (p.Val34Ile)not specified [RCV004321994]uncertain significance1156053602156053602Humanname
401933066CV2806053single nucleotide variantNM_020131.5(UBQLN4):c.1542C>T (p.Pro514=)not provided [RCV003409139]likely benign1156041596156041596Humanname
597683383CV3626022single nucleotide variantNM_020131.5(UBQLN4):c.207G>C (p.Gln69His)not specified [RCV004883834]uncertain significance1156051759156051759Humanname
597684552CV3626026single nucleotide variantNM_020131.5(UBQLN4):c.128G>A (p.Arg43Gln)not specified [RCV004883838]uncertain significance1156051838156051838Humanname
15121104CV706729single nucleotide variantNM_020131.5(UBQLN4):c.1593C>T (p.Ser531=)not provided [RCV000962831]benign1156041545156041545Humanname
15166944CV718274single nucleotide variantNM_020131.5(UBQLN4):c.1251C>T (p.Pro417=)not provided [RCV000882746]likely benign1156042789156042789Humanname
150547479CV1292041single nucleotide variantNM_020131.5(UBQLN4):c.931G>A (p.Gly311Arg)not specified [RCV001733707]uncertain significance1156044193156044193Humanname
329387437CV2470699single nucleotide variantNM_020131.5(UBQLN4):c.434C>T (p.Pro145Leu)not specified [RCV004275947]uncertain significance1156051154156051154Humanname
401740937CV2680511single nucleotide variantNM_020131.5(UBQLN4):c.407G>A (p.Arg136Gln)not specified [RCV004291151]uncertain significance1156051181156051181Humanname
401884544CV2761829single nucleotide variantNM_020131.5(UBQLN4):c.647G>A (p.Arg216His)not specified [RCV004339473]uncertain significance1156050385156050385Humanname
405800272CV3337673single nucleotide variantNM_020131.5(UBQLN4):c.346G>A (p.Ala116Thr)not specified [RCV004477060]uncertain significance1156051242156051242Humanname
405800270CV3337674single nucleotide variantNM_020131.5(UBQLN4):c.953C>T (p.Ser318Phe)not specified [RCV004477061]uncertain significance1156044171156044171Humanname
407522935CV3491138single nucleotide variantNM_020131.5(UBQLN4):c.378T>G (p.Ser126Arg)not specified [RCV004677870]uncertain significance1156051210156051210Humanname
407522938CV3491139single nucleotide variantNM_020131.5(UBQLN4):c.449G>A (p.Gly150Glu)not specified [RCV004677871]uncertain significance1156051139156051139Humanname
597683405CV3626024single nucleotide variantNM_020131.5(UBQLN4):c.494T>C (p.Ile165Thr)not specified [RCV004883836]uncertain significance1156050538156050538Humanname
597684545CV3626027single nucleotide variantNM_020131.5(UBQLN4):c.686T>C (p.Met229Thr)not specified [RCV004883839]uncertain significance1156050346156050346Humanname
598265403CV3928960single nucleotide variantNM_020131.5(UBQLN4):c.691C>T (p.Arg231Trp)not specified [RCV005301721]uncertain significance1156050341156050341Humanname
598265411CV3928962single nucleotide variantNM_020131.5(UBQLN4):c.800G>A (p.Arg267Gln)not specified [RCV005301723]uncertain significance1156048601156048601Humanname
15161881CV706730single nucleotide variantNM_020131.5(UBQLN4):c.893G>A (p.Arg298Gln)not provided [RCV000970168]benign1156048508156048508Humanname
155911768CV2313384single nucleotide variantNM_020131.5(UBQLN4):c.1004C>T (p.Pro335Leu)not specified [RCV004163709]uncertain significance1156044120156044120Humanname
156068264CV2345945single nucleotide variantNM_020131.5(UBQLN4):c.1030G>C (p.Gly344Arg)not specified [RCV004198981]uncertain significance1156044094156044094Humanname
329372009CV2454940single nucleotide variantNM_020131.5(UBQLN4):c.1382C>T (p.Thr461Ile)not specified [RCV004270429]uncertain significance1156041956156041956Humanname
401752115CV2682706single nucleotide variantNM_020131.5(UBQLN4):c.1661C>T (p.Thr554Met)not specified [RCV004281686]uncertain significance1156037123156037123Humanname
401749266CV2694603single nucleotide variantNM_020131.5(UBQLN4):c.1131G>T (p.Met377Ile)not specified [RCV004298721]uncertain significance1156042909156042909Humanname
401890471CV2768266single nucleotide variantNM_020131.5(UBQLN4):c.1220G>A (p.Arg407His)not specified [RCV004350256]uncertain significance1156042820156042820Humanname
405800032CV3337668single nucleotide variantNM_020131.5(UBQLN4):c.1291G>A (p.Ala431Thr)not specified [RCV004477055]uncertain significance1156042212156042212Humanname
405800033CV3337669single nucleotide variantNM_020131.5(UBQLN4):c.1360C>T (p.Pro454Ser)not specified [RCV004477056]uncertain significance1156041978156041978Humanname
405800035CV3337670single nucleotide variantNM_020131.5(UBQLN4):c.1490G>A (p.Arg497Gln)not specified [RCV004477057]uncertain significance1156041648156041648Humanname
405800275CV3337671single nucleotide variantNM_020131.5(UBQLN4):c.1559C>T (p.Thr520Met)not specified [RCV004477058]uncertain significance1156041579156041579Humanname
405800274CV3337672single nucleotide variantNM_020131.5(UBQLN4):c.1579A>G (p.Thr527Ala)not specified [RCV004477059]likely benign1156041559156041559Humanname
407522932CV3491137single nucleotide variantNM_020131.5(UBQLN4):c.1013C>T (p.Pro338Leu)not specified [RCV004677869]uncertain significance1156044111156044111Humanname
597683373CV3626021single nucleotide variantNM_020131.5(UBQLN4):c.1058C>T (p.Ser353Leu)not specified [RCV004883833]uncertain significance1156044066156044066Humanname
597683394CV3626023single nucleotide variantNM_020131.5(UBQLN4):c.1556C>T (p.Ala519Val)not specified [RCV004883835]uncertain significance1156041582156041582Humanname
597683415CV3626025single nucleotide variantNM_020131.5(UBQLN4):c.1489C>T (p.Arg497Trp)not specified [RCV004883837]uncertain significance1156041649156041649Humanname
598189535CV3928958single nucleotide variantNM_020131.5(UBQLN4):c.1007C>T (p.Ser336Leu)not specified [RCV005288085]uncertain significance1156044117156044117Humanname
598265398CV3928959single nucleotide variantNM_020131.5(UBQLN4):c.1513A>G (p.Ser505Gly)not specified [RCV005301720]uncertain significance1156041625156041625Humanname
14725865CV655043single nucleotide variantNM_020131.5(UBQLN4):c.1485A>G (p.Ile495Met)not provided [RCV000833624]benign1156041653156041653Human3name
14725865CV655043single nucleotide variantNM_020131.5(UBQLN4):c.1485A>G (p.Ile495Met)not provided [RCV000833624]benign1156041653156041654Human3name
8624729CV79843single nucleotide variantNM_020131.4(UBQLN4):c.1642G>T (p.Gly548Ter)Malignant melanoma [RCV000059919]not provided1156041496156041496Humanname