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Variants search result for Homo sapiens
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27 records found for search term Ubtd1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401875645CV2766946single nucleotide variantNM_024954.5(UBTD1):c.4G>T (p.Gly2Cys)not specified [RCV004343332]uncertain significance109749920797499207Humanname
155963920CV2194193single nucleotide variantNM_024954.5(UBTD1):c.73C>T (p.Arg25Cys)not specified [RCV004077274]uncertain significance109756791697567916Humanname
156286407CV2334930single nucleotide variantNM_024954.5(UBTD1):c.74G>A (p.Arg25His)not specified [RCV004182033]uncertain significance109756791797567917Humanname
156006595CV2394195single nucleotide variantNM_024954.5(UBTD1):c.54C>A (p.His18Gln)not specified [RCV004236388]uncertain significance109749925797499257Humanname
407523093CV3491203single nucleotide variantNM_024954.5(UBTD1):c.47C>G (p.Pro16Arg)not specified [RCV004677925]uncertain significance109749925097499250Humanname
155944707CV2237843single nucleotide variantNM_024954.5(UBTD1):c.133G>C (p.Gly45Arg)not specified [RCV004109080]uncertain significance109756797697567976Humanname
329365210CV2440142single nucleotide variantNM_024954.5(UBTD1):c.250G>A (p.Glu84Lys)not provided [RCV004696364]|not specified [RCV004260604]uncertain significance109756809397568093Humanname
329394775CV2461481single nucleotide variantNM_024954.5(UBTD1):c.151C>G (p.Arg51Gly)not specified [RCV004269412]uncertain significance109756799497567994Humanname
405800325CV3337823single nucleotide variantNM_024954.5(UBTD1):c.223G>A (p.Ala75Thr)not specified [RCV004477210]uncertain significance109756806697568066Humanname
597684672CV3622718single nucleotide variantNM_024954.5(UBTD1):c.170C>T (p.Thr57Ile)not specified [RCV004883968]uncertain significance109756801397568013Humanname
156265650CV2312249single nucleotide variantNM_024954.5(UBTD1):c.433G>A (p.Val145Met)not specified [RCV004165136]uncertain significance109757027297570272Humanname
156188998CV2342332single nucleotide variantNM_024954.5(UBTD1):c.553G>A (p.Glu185Lys)not specified [RCV004191898]uncertain significance109757039297570392Humanname
156387523CV2372773single nucleotide variantNM_024954.5(UBTD1):c.440G>A (p.Arg147His)not specified [RCV004221960]uncertain significance109757027997570279Humanname
156047160CV2382414single nucleotide variantNM_024954.5(UBTD1):c.392C>T (p.Thr131Met)not specified [RCV004230753]uncertain significance109757023197570231Humanname
156221243CV2392421single nucleotide variantNM_024954.5(UBTD1):c.550A>C (p.Ile184Leu)not specified [RCV004244002]uncertain significance109757038997570389Humanname
401896056CV2777352single nucleotide variantNM_024954.5(UBTD1):c.460C>T (p.Arg154Cys)not specified [RCV004354363]uncertain significance109757029997570299Humanname
405800327CV3337824single nucleotide variantNM_024954.5(UBTD1):c.304C>T (p.Leu102Phe)not specified [RCV004477211]uncertain significance109757014397570143Humanname
405800329CV3337825single nucleotide variantNM_024954.5(UBTD1):c.332A>G (p.Asn111Ser)not specified [RCV004477212]uncertain significance109757017197570171Humanname
405800331CV3337826single nucleotide variantNM_024954.5(UBTD1):c.601C>T (p.Arg201Cys)not specified [RCV004477213]uncertain significance109757044097570440Humanname
407523090CV3491202single nucleotide variantNM_024954.5(UBTD1):c.583G>A (p.Gly195Arg)not specified [RCV004677924]uncertain significance109757042297570422Humanname
597684625CV3622713single nucleotide variantNM_024954.5(UBTD1):c.449C>T (p.Pro150Leu)not specified [RCV004883963]uncertain significance109757028897570288Humanname
597684634CV3622714single nucleotide variantNM_024954.5(UBTD1):c.385G>C (p.Glu129Gln)not specified [RCV004883964]uncertain significance109757022497570224Humanname
597684654CV3622716single nucleotide variantNM_024954.5(UBTD1):c.439C>T (p.Arg147Cys)not specified [RCV004883966]uncertain significance109757027897570278Humanname
597684662CV3622717single nucleotide variantNM_024954.5(UBTD1):c.652A>G (p.Ile218Val)not specified [RCV004883967]uncertain significance109757049197570491Humanname
597684682CV3622719single nucleotide variantNM_024954.5(UBTD1):c.335G>A (p.Arg112His)not specified [RCV004883969]uncertain significance109757017497570174Humanname
597684692CV3622720single nucleotide variantNM_024954.5(UBTD1):c.359T>G (p.Leu120Arg)not specified [RCV004883970]uncertain significance109757019897570198Humanname
598265696CV3929079single nucleotide variantNM_024954.5(UBTD1):c.334C>T (p.Arg112Cys)not specified [RCV005301782]uncertain significance109757017397570173Humanname