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Variants search result for Homo sapiens
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34 records found for search term Ptger2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156086971CV2258947single nucleotide variantNM_000956.4(PTGER2):c.5G>A (p.Gly2Asp)not specified [RCV004120227]uncertain significance145231455352314553Humanname
156268696CV2326323single nucleotide variantNM_000956.4(PTGER2):c.82A>G (p.Ser28Gly)not specified [RCV004180867]uncertain significance145231463052314630Humanname
407532079CV3468272single nucleotide variantNM_000956.4(PTGER2):c.65G>A (p.Gly22Asp)not specified [RCV004657957]uncertain significance145231461352314613Humanname
597751396CV3588697single nucleotide variantNM_000956.4(PTGER2):c.98C>T (p.Ser33Leu)not specified [RCV004846671]uncertain significance145231464652314646Humanname
155983010CV2239941single nucleotide variantNM_000956.4(PTGER2):c.232G>C (p.Asp78His)not specified [RCV004110742]uncertain significance145231478052314780Humanname
156145556CV2292503single nucleotide variantNM_000956.4(PTGER2):c.260C>T (p.Pro87Leu)not specified [RCV004150284]uncertain significance145231480852314808Humanname
405673104CV3377744single nucleotide variantNM_000956.4(PTGER2):c.125C>T (p.Ala42Val)not specified [RCV004515604]uncertain significance145231467352314673Humanname
405673107CV3377745single nucleotide variantNM_000956.4(PTGER2):c.205G>A (p.Val69Met)not specified [RCV004515605]uncertain significance145231475352314753Humanname
597751607CV3588694single nucleotide variantNM_000956.4(PTGER2):c.212T>G (p.Val71Gly)not specified [RCV004846668]uncertain significance145231476052314760Humanname
597751408CV3588700single nucleotide variantNM_000956.4(PTGER2):c.217G>A (p.Glu73Lys)not specified [RCV004846674]uncertain significance145231476552314765Humanname
597751413CV3588701single nucleotide variantNM_000956.4(PTGER2):c.179G>A (p.Arg60His)not specified [RCV004846675]uncertain significance145231472752314727Humanname
15165674CV725687single nucleotide variantNM_000956.4(PTGER2):c.247T>G (p.Cys83Gly)not provided [RCV000882465]benign|likely benign145231479552314795Humanname
155974128CV2211133single nucleotide variantNM_000956.4(PTGER2):c.311C>T (p.Pro104Leu)not specified [RCV004088304]uncertain significance145231485952314859Humanname
155970355CV2213467single nucleotide variantNM_000956.4(PTGER2):c.540G>C (p.Gln180His)not specified [RCV004087438]uncertain significance145231508852315088Humanname
155976890CV2266352single nucleotide variantNM_000956.4(PTGER2):c.377T>C (p.Met126Thr)not specified [RCV004129166]uncertain significance145231492552314925Humanname
329384725CV2435184single nucleotide variantNM_000956.4(PTGER2):c.724C>T (p.Arg242Trp)not specified [RCV004252821]uncertain significance145231527252315272Humanname
329369665CV2461178single nucleotide variantNM_000956.4(PTGER2):c.728G>T (p.Gly243Val)not specified [RCV004267379]uncertain significance145231527652315276Humanname
401876590CV2767644single nucleotide variantNM_000956.4(PTGER2):c.647T>G (p.Phe216Cys)not specified [RCV004343784]uncertain significance145231519552315195Humanname
401866650CV2782905single nucleotide variantNM_000956.4(PTGER2):c.347T>G (p.Met116Arg)not specified [RCV004361707]uncertain significance145231489552314895Humanname
405673110CV3377746single nucleotide variantNM_000956.4(PTGER2):c.439C>T (p.Arg147Cys)not specified [RCV004515606]uncertain significance145231498752314987Humanname
405673114CV3377747single nucleotide variantNM_000956.4(PTGER2):c.482A>T (p.Tyr161Phe)not specified [RCV004515607]uncertain significance145231503052315030Humanname
405673118CV3377748single nucleotide variantNM_000956.4(PTGER2):c.747G>T (p.Arg249Ser)not specified [RCV004515608]uncertain significance145231529552315295Humanname
405673121CV3377749single nucleotide variantNM_000956.4(PTGER2):c.856A>G (p.Met286Val)not specified [RCV004515609]uncertain significance145232723352327233Humanname
407532071CV3468268single nucleotide variantNM_000956.4(PTGER2):c.791T>C (p.Ile264Thr)not specified [RCV004657953]uncertain significance145231533952315339Humanname
407532073CV3468269single nucleotide variantNM_000956.4(PTGER2):c.313G>A (p.Glu105Lys)not specified [RCV004657954]uncertain significance145231486152314861Humanname
407532075CV3468270single nucleotide variantNM_000956.4(PTGER2):c.935C>T (p.Pro312Leu)not specified [RCV004657955]uncertain significance145232731252327312Humanname
407532077CV3468271single nucleotide variantNM_000956.4(PTGER2):c.370A>G (p.Met124Val)not specified [RCV004657956]uncertain significance145231491852314918Humanname
597751602CV3588695single nucleotide variantNM_000956.4(PTGER2):c.466G>C (p.Val156Leu)not specified [RCV004846669]uncertain significance145231501452315014Humanname
597751431CV3588696single nucleotide variantNM_000956.4(PTGER2):c.916A>G (p.Ile306Val)not specified [RCV004846670]uncertain significance145232729352327293Humanname
597751404CV3588699single nucleotide variantNM_000956.4(PTGER2):c.809C>G (p.Thr270Ser)not specified [RCV004846673]uncertain significance145231535752315357Humanname
598172493CV3908528single nucleotide variantNM_000956.4(PTGER2):c.842C>T (p.Thr281Met)not specified [RCV005263554]uncertain significance145231539052315390Humanname
598172500CV3908529single nucleotide variantNM_000956.4(PTGER2):c.998G>A (p.Arg333Gln)not specified [RCV005263555]uncertain significance145232737552327375Humanname
15102440CV725688single nucleotide variantNM_000956.4(PTGER2):c.854A>G (p.Tyr285Cys)not provided [RCV000892480]likely benign145232723152327231Humanname
597751612CV3588693single nucleotide variantNM_000956.4(PTGER2):c.1071C>A (p.Asp357Glu)not specified [RCV004846667]uncertain significance145232744852327448Humanname