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Variants search result for Homo sapiens
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23 records found for search term Ubl7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156136328CV2284805single nucleotide variantNM_032907.5(UBL7):c.10T>C (p.Ser4Pro)not specified [RCV004142982]uncertain significance157445885874458858Humanname
598189299CV3928907single nucleotide variantNM_032907.5(UBL7):c.26C>A (p.Ala9Glu)not specified [RCV005288054]uncertain significance157445884274458842Humanname
155943832CV2294878single nucleotide variantNM_032907.5(UBL7):c.64A>G (p.Ile22Val)not specified [RCV004156034]uncertain significance157445880474458804Humanname
405799924CV3341446single nucleotide variantNM_032907.5(UBL7):c.71G>C (p.Arg24Pro)not specified [RCV004476999]uncertain significance157445879774458797Humanname
15173739CV726245single nucleotide variantNM_032907.5(UBL7):c.609T>C (p.Pro203=)not provided [RCV000884059]benign157444999174449991Humanname
15156605CV726246single nucleotide variantNM_032907.5(UBL7):c.70C>G (p.Arg24Gly)not provided [RCV000880663]benign157445879874458798Humanname
156153935CV2303866single nucleotide variantNM_032907.5(UBL7):c.231C>G (p.Asp77Glu)not specified [RCV004168154]uncertain significance157445662574456625Humanname
329359046CV2450814single nucleotide variantNM_032907.5(UBL7):c.229G>C (p.Asp77His)not specified [RCV004267731]uncertain significance157445662774456627Humanname
401739008CV2708280single nucleotide variantNM_032907.5(UBL7):c.248C>T (p.Pro83Leu)not specified [RCV004311621]uncertain significance157445660874456608Humanname
597682488CV3625955single nucleotide variantNM_032907.5(UBL7):c.260T>C (p.Val87Ala)not specified [RCV004883767]uncertain significance157445659674456596Humanname
156297340CV2240846single nucleotide variantNM_032907.5(UBL7):c.731C>T (p.Pro244Leu)not specified [RCV004102135]uncertain significance157444933774449337Humanname
156000691CV2296337single nucleotide variantNM_032907.5(UBL7):c.866C>T (p.Pro289Leu)not specified [RCV004148095]uncertain significance157444920274449202Humanname
156352954CV2324075single nucleotide variantNM_032907.5(UBL7):c.580C>T (p.His194Tyr)not specified [RCV004178370]uncertain significance157445002074450020Humanname
155968511CV2339321single nucleotide variantNM_032907.5(UBL7):c.598G>A (p.Ala200Thr)not specified [RCV004191553]likely benign157445000274450002Humanname
329363740CV2465099single nucleotide variantNM_032907.5(UBL7):c.355G>A (p.Ala119Thr)not specified [RCV004286823]uncertain significance157445232874452328Humanname
405799920CV3341444single nucleotide variantNM_032907.5(UBL7):c.463A>G (p.Ile155Val)not specified [RCV004476997]uncertain significance157445144574451445Humanname
405799922CV3341445single nucleotide variantNM_032907.5(UBL7):c.652C>T (p.Arg218Trp)not specified [RCV004476998]uncertain significance157444994874449948Humanname
597682499CV3625956single nucleotide variantNM_032907.5(UBL7):c.628C>T (p.Arg210Trp)not specified [RCV004883768]uncertain significance157444997274449972Humanname
597682512CV3625957single nucleotide variantNM_032907.5(UBL7):c.341G>C (p.Arg114Pro)not specified [RCV004883769]uncertain significance157445234274452342Humanname
597682529CV3625959single nucleotide variantNM_032907.5(UBL7):c.871C>G (p.Pro291Ala)not specified [RCV004883771]uncertain significance157444919774449197Humanname
598189316CV3928909single nucleotide variantNM_032907.5(UBL7):c.653G>A (p.Arg218Gln)not specified [RCV005288056]uncertain significance157444994774449947Humanname
156004244CV2295894single nucleotide variantNM_032907.5(UBL7):c.1132G>A (p.Gly378Arg)not specified [RCV004151801]uncertain significance157444610174446101Humanname
598189307CV3928908single nucleotide variantNM_032907.5(UBL7):c.1029G>C (p.Gln343His)not specified [RCV005288055]uncertain significance157444620474446204Humanname