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Variants search result for Homo sapiens
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14 records found for search term Prkab2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156110133CV2387597single nucleotide variantNM_005399.5(PRKAB2):c.83C>G (p.Ala28Gly)not specified [RCV004234148]uncertain significance1147172062147172062Humanname
401887941CV2768878single nucleotide variantNM_005399.5(PRKAB2):c.82G>T (p.Ala28Ser)not specified [RCV004346987]uncertain significance1147172063147172063Humanname
405671014CV3378157single nucleotide variantNM_005399.5(PRKAB2):c.66G>C (p.Glu22Asp)not specified [RCV004515082]uncertain significance1147172079147172079Humanname
8624672CV79786single nucleotide variantNM_005399.4(PRKAB2):c.678C>T (p.Asp226=)Malignant melanoma [RCV000059862]not provided1147161775147161775Humanname
156282012CV2295162single nucleotide variantNM_005399.5(PRKAB2):c.293A>G (p.Asn98Ser)not specified [RCV004158259]uncertain significance1147167797147167797Humanname
598180536CV3904416single nucleotide variantNM_005399.5(PRKAB2):c.229C>T (p.Arg77Trp)not specified [RCV005265037]uncertain significance1147167861147167861Humanname
155975177CV2211252single nucleotide variantNM_005399.5(PRKAB2):c.782A>G (p.Lys261Arg)not specified [RCV004090188]uncertain significance1147159602147159602Humanname
155955072CV2302359single nucleotide variantNM_005399.5(PRKAB2):c.500A>G (p.Lys167Arg)not specified [RCV004161111]uncertain significance1147166536147166536Humanname
401734905CV2706578single nucleotide variantNM_005399.5(PRKAB2):c.541C>G (p.Leu181Val)not specified [RCV004319163]uncertain significance1147162571147162571Humanname
401781790CV2722275single nucleotide variantNM_005399.5(PRKAB2):c.590G>A (p.Arg197Gln)not specified [RCV004328830]uncertain significance1147162522147162522Humanname
401893935CV2770127single nucleotide variantNM_005399.5(PRKAB2):c.533G>T (p.Cys178Phe)not specified [RCV004356028]uncertain significance1147166503147166503Humanname
597749166CV3581443single nucleotide variantNM_005399.5(PRKAB2):c.326A>G (p.His109Arg)not specified [RCV004846170]uncertain significance1147166937147166937Humanname
597749171CV3581444single nucleotide variantNM_005399.5(PRKAB2):c.409C>T (p.Pro137Ser)not specified [RCV004846171]uncertain significance1147166854147166854Humanname
598180529CV3904415single nucleotide variantNM_005399.5(PRKAB2):c.799C>G (p.Leu267Val)not specified [RCV005265036]uncertain significance1147159585147159585Humanname