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14 records found for search term Mrpl42
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597634386CV3561193single nucleotide variantNM_014050.4(MRPL42):c.11C>T (p.Ala4Val)not specified [RCV004830899]uncertain significance129346929693469296Humanname
156162460CV2272687single nucleotide variantNM_014050.4(MRPL42):c.71A>G (p.Asn24Ser)not specified [RCV004135347]uncertain significance129347695493476954Humanname
597634391CV3561191single nucleotide variantNM_014050.4(MRPL42):c.62C>T (p.Pro21Leu)not specified [RCV004830898]uncertain significance129346934793469347Humanname
598178958CV3993418single nucleotide variantNM_014050.4(MRPL42):c.98A>T (p.Lys33Ile)not specified [RCV005371851]uncertain significance129347698193476981Humanname
155926231CV2287857single nucleotide variantNM_014050.4(MRPL42):c.241G>A (p.Val81Met)not specified [RCV004143296]uncertain significance129348751893487518Humanname
156214875CV2385950single nucleotide variantNM_014050.4(MRPL42):c.160G>C (p.Asp54His)not specified [RCV004229028]uncertain significance129347941393479413Humanname
401731244CV2693690single nucleotide variantNM_014050.4(MRPL42):c.245A>G (p.His82Arg)not specified [RCV004298021]uncertain significance129348752293487522Humanname
401890298CV2755709single nucleotide variantNM_014050.4(MRPL42):c.104C>T (p.Thr35Met)not specified [RCV004342091]uncertain significance129347698793476987Humanname
405740841CV3367466single nucleotide variantNM_014050.4(MRPL42):c.139G>A (p.Val47Ile)not specified [RCV004497715]uncertain significance129347939293479392Humanname
405740906CV3367475single nucleotide variantNM_014050.4(MRPL42):c.164G>A (p.Gly55Asp)not specified [RCV004497724]uncertain significance129347941793479417Humanname
598213017CV3993419single nucleotide variantNM_014050.4(MRPL42):c.202C>G (p.Pro68Ala)not specified [RCV005378269]uncertain significance129347945593479455Humanname
156119695CV2228990single nucleotide variantNM_014050.4(MRPL42):c.397C>T (p.Arg133Cys)not specified [RCV004098777]uncertain significance129350118993501189Humanname
156043119CV2261514single nucleotide variantNM_014050.4(MRPL42):c.404A>T (p.Asn135Ile)not specified [RCV004130131]uncertain significance129350119693501196Humanname
401891795CV2780798single nucleotide variantNM_014050.4(MRPL42):c.418A>G (p.Lys140Glu)not specified [RCV004352118]uncertain significance129350121093501210Humanname