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23 records found for search term Mrps11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156388131CV2380127single nucleotide variantNM_022839.5(MRPS11):c.20C>T (p.Ala7Val)not specified [RCV004224504]likely benign158846773788467737Humanname
405772087CV3364280single nucleotide variantNM_022839.5(MRPS11):c.44G>T (p.Trp15Leu)not specified [RCV004502465]uncertain significance158846776188467761Humanname
407474693CV3450402single nucleotide variantNM_022839.5(MRPS11):c.58A>G (p.Thr20Ala)not specified [RCV004638218]uncertain significance158846777588467775Humanname
597634171CV3557362single nucleotide variantNM_022839.5(MRPS11):c.47C>T (p.Thr16Ile)not specified [RCV004830947]uncertain significance158846776488467764Humanname
156087930CV2290631single nucleotide variantNM_022839.5(MRPS11):c.191C>T (p.Pro64Leu)not specified [RCV004149167]uncertain significance158847263588472635Humanname
407474697CV3450403single nucleotide variantNM_022839.5(MRPS11):c.133G>A (p.Ala45Thr)not specified [RCV004638219]uncertain significance158846797588467975Humanname
597634180CV3557365single nucleotide variantNM_022839.5(MRPS11):c.156C>G (p.Asn52Lys)not specified [RCV004830949]likely benign158846799888467998Humanname
598213176CV3993476single nucleotide variantNM_022839.5(MRPS11):c.289A>G (p.Ile97Val)not specified [RCV005378299]uncertain significance158847511788475117Humanname
156379598CV2211455single nucleotide variantNM_022839.5(MRPS11):c.403G>A (p.Ala135Thr)not specified [RCV004090682]uncertain significance158847523188475231Humanname
156391716CV2382517single nucleotide variantNM_022839.5(MRPS11):c.560G>A (p.Arg187His)not specified [RCV004232852]uncertain significance158847795488477954Humanname
401752346CV2682788single nucleotide variantNM_022839.5(MRPS11):c.353G>A (p.Arg118Gln)not specified [RCV004281761]uncertain significance158847518188475181Humanname
401856350CV2754631single nucleotide variantNM_022839.5(MRPS11):c.490G>A (p.Gly164Arg)not specified [RCV004339304]uncertain significance158847788488477884Humanname
405772106CV3364283single nucleotide variantNM_022839.5(MRPS11):c.482C>T (p.Ala161Val)not specified [RCV004502468]uncertain significance158847787688477876Humanname
405772146CV3364290single nucleotide variantNM_022839.5(MRPS11):c.523A>G (p.Ile175Val)not specified [RCV004502475]uncertain significance158847791788477917Humanname
405772165CV3364293single nucleotide variantNM_022839.5(MRPS11):c.559C>T (p.Arg187Cys)not specified [RCV004502478]uncertain significance158847795388477953Humanname
597634160CV3557359single nucleotide variantNM_022839.5(MRPS11):c.407C>T (p.Ala136Val)not specified [RCV004830945]uncertain significance158847523588475235Humanname
597634166CV3557360single nucleotide variantNM_022839.5(MRPS11):c.430G>A (p.Val144Met)not specified [RCV004830946]uncertain significance158847700788477007Humanname
597638025CV3557361single nucleotide variantNM_022839.5(MRPS11):c.436C>T (p.His146Tyr)not specified [RCV004824845]uncertain significance158847701388477013Humanname
597638029CV3557363single nucleotide variantNM_022839.5(MRPS11):c.513A>T (p.Glu171Asp)not specified [RCV004824846]uncertain significance158847790788477907Humanname
598179117CV3993473single nucleotide variantNM_022839.5(MRPS11):c.352C>T (p.Arg118Trp)not specified [RCV005371877]uncertain significance158847518088475180Humanname
598213171CV3993474single nucleotide variantNM_022839.5(MRPS11):c.541A>G (p.Ile181Val)not specified [RCV005378298]uncertain significance158847793588477935Humanname
598179123CV3993475single nucleotide variantNM_022839.5(MRPS11):c.410C>T (p.Ala137Val)not specified [RCV005371878]uncertain significance158847523888475238Humanname
598179129CV3993477single nucleotide variantNM_022839.5(MRPS11):c.575G>C (p.Arg192Pro)not specified [RCV005371879]uncertain significance158847796988477969Humanname