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Variants search result for Homo sapiens
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23 records found for search term Nrm
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405709225CV3359248single nucleotide variantNM_001384369.1(NRM):c.7C>T (p.Pro3Ser)not specified [RCV004493595]uncertain significance63069096830690968Humanname
156134983CV2213266single nucleotide variantNM_001384369.1(NRM):c.70G>C (p.Glu24Gln)not specified [RCV004085485]uncertain significance63069090530690905Humanname
156298650CV2329283single nucleotide variantNM_001384369.1(NRM):c.97C>T (p.Pro33Ser)not specified [RCV004174021]uncertain significance63069087830690878Humanname
329377669CV2462793single nucleotide variantNM_001384369.1(NRM):c.88T>A (p.Ser30Thr)not specified [RCV004278708]uncertain significance63069088730690887Humanname
405709219CV3359247single nucleotide variantNM_001384369.1(NRM):c.79C>T (p.Arg27Cys)not specified [RCV004493594]likely benign63069089630690896Humanname
401733040CV2685408single nucleotide variantNM_001384369.1(NRM):c.114C>G (p.Ile38Met)not specified [RCV004294442]likely benign63069086130690861Humanname
405709194CV3359244single nucleotide variantNM_001384369.1(NRM):c.106G>A (p.Gly36Arg)not specified [RCV004493591]uncertain significance63069086930690869Humanname
405709204CV3359245single nucleotide variantNM_001384369.1(NRM):c.221T>C (p.Val74Ala)not specified [RCV004493592]uncertain significance63069015630690156Humanname
597706720CV3576875single nucleotide variantNM_001384369.1(NRM):c.194G>T (p.Trp65Leu)not specified [RCV004840371]uncertain significance63069018330690183Humanname
597706730CV3576876single nucleotide variantNM_001384369.1(NRM):c.169C>T (p.Arg57Cys)not specified [RCV004840372]uncertain significance63069020830690208Humanname
597706742CV3576877single nucleotide variantNM_001384369.1(NRM):c.103C>T (p.Leu35Phe)not specified [RCV004840373]uncertain significance63069087230690872Humanname
155998330CV2260967single nucleotide variantNM_001384369.1(NRM):c.626T>G (p.Val209Gly)not specified [RCV004125847]uncertain significance63068882430688824Humanname
156066900CV2340931single nucleotide variantNM_001384369.1(NRM):c.727C>T (p.Arg243Trp)not specified [RCV004181425]uncertain significance63068872330688723Humanname
329377478CV2453356single nucleotide variantNM_001384369.1(NRM):c.422G>T (p.Cys141Phe)not specified [RCV004266979]uncertain significance63068936130689361Humanname
401770542CV2685761single nucleotide variantNM_001384369.1(NRM):c.667C>G (p.Leu223Val)not specified [RCV004294752]uncertain significance63068878330688783Humanname
401745106CV2693181single nucleotide variantNM_001384369.1(NRM):c.649C>T (p.Arg217Cys)not specified [RCV004293112]uncertain significance63068880130688801Humanname
401742811CV2697870single nucleotide variantNM_001384369.1(NRM):c.386G>A (p.Arg129Gln)not specified [RCV004300582]likely benign63068939730689397Humanname
401895754CV2771498single nucleotide variantNM_001384369.1(NRM):c.359C>T (p.Pro120Leu)not specified [RCV004348534]uncertain significance63068942430689424Humanname
405709211CV3359246single nucleotide variantNM_001384369.1(NRM):c.470T>C (p.Leu157Pro)not specified [RCV004493593]uncertain significance63068931330689313Humanname
407477241CV3465916single nucleotide variantNM_001384369.1(NRM):c.475T>C (p.Phe159Leu)not specified [RCV004638712]uncertain significance63068930830689308Humanname
407516937CV3465917single nucleotide variantNM_001384369.1(NRM):c.362A>G (p.Lys121Arg)not specified [RCV004650459]likely benign63068942130689421Humanname
597706751CV3576878single nucleotide variantNM_001384369.1(NRM):c.641G>T (p.Gly214Val)not specified [RCV004840374]uncertain significance63068880930688809Humanname
597706764CV3576879single nucleotide variantNM_001384369.1(NRM):c.299T>C (p.Leu100Pro)not specified [RCV004840375]uncertain significance63069007830690078Humanname