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11 records found for search term Rplp2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405738409CV3320181single nucleotide variantNM_001004.4(RPLP2):c.14C>T (p.Ala5Val)not specified [RCV004452002]uncertain significance11810248810248Humanname
156176553CV2258104single nucleotide variantNM_001004.4(RPLP2):c.62A>G (p.Lys21Arg)not specified [RCV004121497]uncertain significance11810296810296Humanname
597785792CV3594256single nucleotide variantNM_001004.4(RPLP2):c.85A>T (p.Ser29Cys)not specified [RCV004854844]uncertain significance11810319810319Humanname
156367029CV2269812single nucleotide variantNM_001004.4(RPLP2):c.184C>T (p.Leu62Phe)not specified [RCV004127053]uncertain significance11812546812546Humanname
156262098CV2282453single nucleotide variantNM_001004.4(RPLP2):c.260C>T (p.Ala87Val)not specified [RCV004133259]uncertain significance11812622812622Humanname
156180534CV2298463single nucleotide variantNM_001004.4(RPLP2):c.176T>C (p.Ile59Thr)not specified [RCV004162131]uncertain significance11812538812538Humanname
329364400CV2447422single nucleotide variantNM_001004.4(RPLP2):c.295A>G (p.Lys99Glu)not specified [RCV004262696]uncertain significance11812783812783Humanname
329382680CV2465320single nucleotide variantNM_001004.4(RPLP2):c.161T>C (p.Val54Ala)not specified [RCV004281109]uncertain significance11811634811634Humanname
407513742CV3476138single nucleotide variantNM_001004.4(RPLP2):c.277G>A (p.Glu93Lys)not specified [RCV004674230]uncertain significance11812765812765Humanname
598219885CV3902947single nucleotide variantNM_001004.4(RPLP2):c.208G>A (p.Ala70Thr)not specified [RCV005272386]uncertain significance11812570812570Humanname
598219890CV3902948single nucleotide variantNM_001004.4(RPLP2):c.316G>A (p.Asp106Asn)not specified [RCV005272387]uncertain significance11812804812804Humanname