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21 records found for search term Epdr1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405772364CV3242273single nucleotide variantNM_017549.5(EPDR1):c.13G>T (p.Ala5Ser)not specified [RCV004385347]uncertain significance73792095237920952Humanname
329355523CV2445522single nucleotide variantNM_017549.5(EPDR1):c.56T>C (p.Leu19Pro)not specified [RCV004257576]uncertain significance73792099537920995Humanname
156064959CV2229073single nucleotide variantNM_017549.5(EPDR1):c.179G>C (p.Gly60Ala)not specified [RCV004098845]uncertain significance73792111837921118Humanname
156098378CV2253261single nucleotide variantNM_017549.5(EPDR1):c.116C>A (p.Pro39Gln)not specified [RCV004122800]uncertain significance73792105537921055Humanname
401741475CV2677368single nucleotide variantNM_017549.5(EPDR1):c.139C>A (p.Gln47Lys)not specified [RCV004289450]uncertain significance73792107837921078Humanname
407491225CV3431588single nucleotide variantNM_017549.5(EPDR1):c.219C>G (p.Asn73Lys)not specified [RCV004620458]uncertain significance73792115837921158Humanname
407491239CV3431591single nucleotide variantNM_017549.5(EPDR1):c.223C>A (p.Arg75Ser)not specified [RCV004620461]uncertain significance73792116237921162Humanname
598168212CV3965195single nucleotide variantNM_017549.5(EPDR1):c.210C>G (p.Asp70Glu)not specified [RCV005330202]uncertain significance73792114937921149Humanname
156061362CV2239983single nucleotide variantNM_017549.5(EPDR1):c.527A>C (p.Gln176Pro)not specified [RCV004110775]uncertain significance73795024837950248Humanname
156064754CV2240249single nucleotide variantNM_017549.5(EPDR1):c.320A>G (p.Asp107Gly)not specified [RCV004112815]uncertain significance73794889037948890Humanname
156317914CV2251111single nucleotide variantNM_017549.5(EPDR1):c.361C>A (p.Pro121Thr)not specified [RCV004123651]uncertain significance73794893137948931Humanname
156327284CV2332082single nucleotide variantNM_017549.5(EPDR1):c.362C>T (p.Pro121Leu)not specified [RCV004189128]uncertain significance73794893237948932Humanname
401885662CV2778218single nucleotide variantNM_017549.5(EPDR1):c.416T>C (p.Ile139Thr)not specified [RCV004349938]uncertain significance73794898637948986Humanname
405772370CV3242274single nucleotide variantNM_017549.5(EPDR1):c.518A>G (p.Tyr173Cys)not specified [RCV004385348]uncertain significance73795023937950239Humanname
405772375CV3242275single nucleotide variantNM_017549.5(EPDR1):c.568C>T (p.Arg190Trp)not specified [RCV004385349]uncertain significance73795028937950289Humanname
407491229CV3431589single nucleotide variantNM_017549.5(EPDR1):c.455C>T (p.Ser152Leu)not specified [RCV004620459]uncertain significance73794902537949025Humanname
597803432CV3674778single nucleotide variantNM_017549.5(EPDR1):c.406C>G (p.Gln136Glu)not specified [RCV004907217]uncertain significance73794897637948976Humanname
597747642CV3674779single nucleotide variantNM_017549.5(EPDR1):c.433C>A (p.Gln145Lys)not specified [RCV004922972]uncertain significance73794900337949003Humanname
597747647CV3674780single nucleotide variantNM_017549.5(EPDR1):c.569G>A (p.Arg190Gln)not specified [RCV004922973]uncertain significance73795029037950290Humanname
598168218CV3965196single nucleotide variantNM_017549.5(EPDR1):c.605C>T (p.Ser202Leu)not specified [RCV005330203]uncertain significance73795032637950326Humanname
598168222CV3965197single nucleotide variantNM_017549.5(EPDR1):c.421G>T (p.Gly141Trp)not specified [RCV005330204]uncertain significance73794899137948991Humanname