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15 records found for search term Reg4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401884010CV2761221single nucleotide variantNM_032044.4(REG4):c.19C>T (p.Arg7Trp)not specified [RCV004341099]likely benign1119808751119808751Humanname
407532304CV3465289single nucleotide variantNM_032044.4(REG4):c.20G>A (p.Arg7Gln)not specified [RCV004658072]uncertain significance1119808750119808750Humanname
597730651CV3583243single nucleotide variantNM_032044.4(REG4):c.10A>G (p.Arg4Gly)not specified [RCV004863052]uncertain significance1119808760119808760Humanname
405683238CV3315647single nucleotide variantNM_032044.4(REG4):c.76A>G (p.Met26Val)not specified [RCV004443804]uncertain significance1119803157119803157Humanname
401726553CV2695719single nucleotide variantNM_032044.4(REG4):c.107A>G (p.Tyr36Cys)not specified [RCV004299521]uncertain significance1119803126119803126Humanname
405683233CV3315645single nucleotide variantNM_032044.4(REG4):c.272C>T (p.Pro91Leu)not specified [RCV004443802]uncertain significance1119799756119799756Humanname
597730663CV3583245single nucleotide variantNM_032044.4(REG4):c.197A>G (p.His66Arg)not specified [RCV004863053]uncertain significance1119799831119799831Humanname
155929993CV2354054single nucleotide variantNM_032044.4(REG4):c.446G>A (p.Arg149His)not specified [RCV004204480]uncertain significance1119794649119794649Humanname
329370924CV2461884single nucleotide variantNM_032044.4(REG4):c.404A>G (p.Asn135Ser)not specified [RCV004271794]uncertain significance1119798502119798502Humanname
401735406CV2699260single nucleotide variantNM_032044.4(REG4):c.371G>T (p.Gly124Val)not specified [RCV004305531]uncertain significance1119798535119798535Humanname
401750045CV2719490single nucleotide variantNM_032044.4(REG4):c.441C>G (p.Asn147Lys)not specified [RCV004326886]uncertain significance1119794654119794654Humanname
407532307CV3465290single nucleotide variantNM_032044.4(REG4):c.326A>G (p.Asp109Gly)not specified [RCV004658073]uncertain significance1119798580119798580Humanname
597765059CV3583242single nucleotide variantNM_032044.4(REG4):c.445C>T (p.Arg149Cys)not specified [RCV004849936]uncertain significance1119794650119794650Humanname
598204199CV3909293single nucleotide variantNM_032044.4(REG4):c.370G>A (p.Gly124Ser)not specified [RCV005269501]uncertain significance1119798536119798536Humanname
15193009CV696030single nucleotide variantNM_032044.4(REG4):c.403A>C (p.Asn135His)not provided [RCV000955244]benign1119798503119798503Humanname