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Variants search result for Homo sapiens
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25 records found for search term Cenph
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156152315CV2369256single nucleotide variantNM_022909.4(CENPH):c.20T>G (p.Met7Arg)not specified [RCV004208171]uncertain significance56918965469189654Humanname
598208046CV3951437single nucleotide variantNM_022909.4(CENPH):c.14C>T (p.Pro5Leu)not specified [RCV005315392]uncertain significance56918964869189648Humanname
598208039CV3951436single nucleotide variantNM_022909.4(CENPH):c.61C>T (p.Arg21Trp)not specified [RCV005315391]uncertain significance56918969569189695Humanname
155979024CV2215130single nucleotide variantNM_022909.4(CENPH):c.142G>A (p.Ala48Thr)not specified [RCV004086851]uncertain significance56919180269191802Humanname
155999233CV2378566single nucleotide variantNM_022909.4(CENPH):c.245T>G (p.Ile82Ser)not specified [RCV004229002]uncertain significance56919572269195722Humanname
405761709CV3300242single nucleotide variantNM_022909.4(CENPH):c.140G>C (p.Arg47Thr)not specified [RCV004433759]uncertain significance56919180069191800Humanname
405761715CV3300243single nucleotide variantNM_022909.4(CENPH):c.205C>T (p.Pro69Ser)not specified [RCV004433760]uncertain significance56919466169194661Humanname
405761722CV3300244single nucleotide variantNM_022909.4(CENPH):c.233T>A (p.Ile78Asn)not specified [RCV004433761]uncertain significance56919468969194689Humanname
407461758CV3418991single nucleotide variantNM_022909.4(CENPH):c.114C>G (p.Asp38Glu)not specified [RCV004612692]uncertain significance56918974869189748Humanname
597779465CV3645488single nucleotide variantNM_022909.4(CENPH):c.242A>T (p.Lys81Ile)not specified [RCV004899274]uncertain significance56919571969195719Humanname
597779477CV3645492single nucleotide variantNM_022909.4(CENPH):c.131T>C (p.Leu44Pro)not specified [RCV004899277]uncertain significance56918976569189765Humanname
598208053CV3951438single nucleotide variantNM_022909.4(CENPH):c.180G>T (p.Met60Ile)not specified [RCV005315393]uncertain significance56919184069191840Humanname
156134377CV2235528single nucleotide variantNM_022909.4(CENPH):c.591C>G (p.Ile197Met)not specified [RCV004109562]uncertain significance56920829969208299Humanname
156061871CV2240026single nucleotide variantNM_022909.4(CENPH):c.422T>C (p.Met141Thr)not specified [RCV004110808]uncertain significance56920255669202556Humanname
156142721CV2257398single nucleotide variantNM_022909.4(CENPH):c.515T>C (p.Leu172Pro)not specified [RCV004125485]uncertain significance56920822369208223Humanname
156057574CV2383221single nucleotide variantNM_022909.4(CENPH):c.383A>G (p.Asp128Gly)not specified [RCV004220230]uncertain significance56920251769202517Humanname
329390417CV2450293single nucleotide variantNM_022909.4(CENPH):c.596G>A (p.Arg199Gln)not specified [RCV004271387]likely benign56920830469208304Humanname
405761733CV3300246single nucleotide variantNM_022909.4(CENPH):c.486G>T (p.Leu162Phe)not specified [RCV004433763]uncertain significance56920296969202969Humanname
405761739CV3300247single nucleotide variantNM_022909.4(CENPH):c.552T>G (p.Ile184Met)not specified [RCV004433764]uncertain significance56920826069208260Humanname
407461753CV3418989single nucleotide variantNM_022909.4(CENPH):c.706A>G (p.Ile236Val)not specified [RCV004612690]uncertain significance56920976169209761Humanname
407461756CV3418990single nucleotide variantNM_022909.4(CENPH):c.476A>G (p.Lys159Arg)not specified [RCV004612691]uncertain significance56920295969202959Humanname
597779469CV3645490single nucleotide variantNM_022909.4(CENPH):c.617T>C (p.Ile206Thr)not specified [RCV004899275]uncertain significance56920832569208325Humanname
597779473CV3645491single nucleotide variantNM_022909.4(CENPH):c.418A>G (p.Ile140Val)not specified [RCV004899276]uncertain significance56920255269202552Humanname
597779481CV3645493single nucleotide variantNM_022909.4(CENPH):c.535A>G (p.Lys179Glu)not specified [RCV004899278]uncertain significance56920824369208243Humanname
38460602CV800941single nucleotide variantNM_022909.4(CENPH):c.635T>C (p.Ile212Thr)Recurrent spontaneous abortion [RCV001250899]uncertain significance56920834369208343Human2name