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Variants search result for Homo sapiens
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12 records found for search term Rpp14
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15191814CV744081single nucleotide variantNM_007042.6(RPP14):c.163-8A>Gnot provided [RCV000910357]benign35831650758316507Humanname
407486323CV3476154single nucleotide variantNM_007042.6(RPP14):c.11C>T (p.Pro4Leu)not specified [RCV004665756]uncertain significance35831034058310340Humanname
156189581CV2328838single nucleotide variantNM_007042.6(RPP14):c.49T>G (p.Ser17Ala)not specified [RCV004178055]uncertain significance35831037858310378Humanname
405738510CV3320196single nucleotide variantNM_007042.6(RPP14):c.47C>T (p.Pro16Leu)not specified [RCV004452017]uncertain significance35831037658310376Humanname
598219939CV3902956single nucleotide variantNM_007042.6(RPP14):c.52G>A (p.Glu18Lys)not specified [RCV005272395]uncertain significance35831038158310381Humanname
155909358CV2359688single nucleotide variantNM_007042.6(RPP14):c.284A>G (p.Tyr95Cys)not specified [RCV004210513]uncertain significance35831695958316959Humanname
405738503CV3320195single nucleotide variantNM_007042.6(RPP14):c.175T>A (p.Leu59Ile)not specified [RCV004452016]uncertain significance35831652758316527Humanname
407486316CV3476153single nucleotide variantNM_007042.6(RPP14):c.146A>G (p.Lys49Arg)not specified [RCV004665755]uncertain significance35831057558310575Humanname
597709644CV3594271single nucleotide variantNM_007042.6(RPP14):c.255G>T (p.Leu85Phe)not specified [RCV004860863]uncertain significance35831693058316930Humanname
598219945CV3902957single nucleotide variantNM_007042.6(RPP14):c.289G>A (p.Gly97Ser)not specified [RCV005272396]uncertain significance35831696458316964Humanname
156072640CV2328837single nucleotide variantNM_007042.6(RPP14):c.352A>G (p.Ser118Gly)not specified [RCV004178054]uncertain significance35831747358317473Humanname
15137570CV709005single nucleotide variantNM_007042.6(RPP14):c.308G>A (p.Arg103Gln)not provided [RCV000965643]benign35831698358316983Humanname