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Variants search result for Homo sapiens
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41 records found for search term Mrps35
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156222310CV2399716single nucleotide variantNM_021821.4(MRPS35):c.23C>T (p.Ala8Val)not specified [RCV004245534]uncertain significance122771086627710866Humanname
329354615CV2444559single nucleotide variantNM_021821.4(MRPS35):c.20C>T (p.Pro7Leu)not specified [RCV004256782]uncertain significance122771086327710863Humanname
597634628CV3557455single nucleotide variantNM_021821.4(MRPS35):c.14C>T (p.Ala5Val)not specified [RCV004831008]uncertain significance122771085727710857Humanname
15138987CV713491single nucleotide variantNM_021821.4(MRPS35):c.16C>A (p.Leu6Ile)not provided [RCV000965886]benign122771085927710859Humanname
401877434CV2764639single nucleotide variantNM_021821.4(MRPS35):c.71C>T (p.Thr24Ile)not specified [RCV004341014]uncertain significance122771091427710914Humanname
401865691CV2786095single nucleotide variantNM_021821.4(MRPS35):c.59G>A (p.Arg20His)not specified [RCV004359907]uncertain significance122771090227710902Humanname
405742328CV3371824single nucleotide variantNM_021821.4(MRPS35):c.29T>A (p.Leu10Gln)not specified [RCV004497897]uncertain significance122771087227710872Humanname
405742166CV3371858single nucleotide variantNM_021821.4(MRPS35):c.675A>T (p.Leu225=)not specified [RCV004497931]likely benign122773758127737581Humanname
407525227CV3450455single nucleotide variantNM_021821.4(MRPS35):c.669G>A (p.Val223=)not specified [RCV004631678]likely benign122773757527737575Humanname
597634644CV3557458single nucleotide variantNM_021821.4(MRPS35):c.91C>G (p.Pro31Ala)not specified [RCV004831011]uncertain significance122771093427710934Humanname
597634654CV3557460single nucleotide variantNM_021821.4(MRPS35):c.53C>A (p.Thr18Asn)not specified [RCV004831013]uncertain significance122771089627710896Humanname
597634660CV3557461single nucleotide variantNM_021821.4(MRPS35):c.663T>C (p.Tyr221=)not specified [RCV004831014]likely benign122773756927737569Humanname
598213503CV3993576single nucleotide variantNM_021821.4(MRPS35):c.53C>T (p.Thr18Ile)not specified [RCV005378360]uncertain significance122771089627710896Humanname
15166659CV702284single nucleotide variantNM_021821.4(MRPS35):c.83C>T (p.Ser28Leu)not provided [RCV000948886]benign122771092627710926Humanname
15138993CV713492single nucleotide variantNM_021821.4(MRPS35):c.957A>G (p.Leu319=)not provided [RCV000965887]benign122775543527755435Humanname
150501441CV1238398single nucleotide variantNM_021821.4(MRPS35):c.127G>A (p.Gly43Arg)not provided [RCV001656828]benign122771479427714794Human2name
156331316CV2339619single nucleotide variantNM_021821.4(MRPS35):c.131A>G (p.Asn44Ser)not specified [RCV004196328]likely benign122771479827714798Humanname
401753450CV2674896single nucleotide variantNM_021821.4(MRPS35):c.229A>G (p.Lys77Glu)not specified [RCV004294164]uncertain significance122771636627716366Humanname
597634623CV3557454single nucleotide variantNM_021821.4(MRPS35):c.289A>G (p.Met97Val)not specified [RCV004831007]uncertain significance122771642627716426Humanname
597634650CV3557459single nucleotide variantNM_021821.4(MRPS35):c.283G>A (p.Val95Met)not specified [RCV004831012]uncertain significance122771642027716420Humanname
598213516CV3993578single nucleotide variantNM_021821.4(MRPS35):c.182C>A (p.Ala61Asp)not specified [RCV005378362]uncertain significance122771631927716319Humanname
156332642CV2220718single nucleotide variantNM_021821.4(MRPS35):c.314T>G (p.Leu105Arg)not specified [RCV004097888]uncertain significance122771645127716451Humanname
156149689CV2234885single nucleotide variantNM_021821.4(MRPS35):c.590G>A (p.Arg197Gln)not specified [RCV004113095]uncertain significance122773551427735514Humanname
156155890CV2388820single nucleotide variantNM_021821.4(MRPS35):c.658G>A (p.Asp220Asn)not specified [RCV004239671]uncertain significance122773756427737564Humanname
329361779CV2437912single nucleotide variantNM_021821.4(MRPS35):c.347C>G (p.Pro116Arg)not specified [RCV004263246]uncertain significance122771983327719833Humanname
329391735CV2444980single nucleotide variantNM_021821.4(MRPS35):c.415A>G (p.Ser139Gly)not specified [RCV004261600]uncertain significance122772407927724079Humanname
329398339CV2464462single nucleotide variantNM_021821.4(MRPS35):c.407C>T (p.Ala136Val)not specified [RCV004276384]uncertain significance122772407127724071Humanname
401752606CV2682876single nucleotide variantNM_021821.4(MRPS35):c.889G>T (p.Val297Phe)not specified [RCV004283675]uncertain significance122775536727755367Humanname
401889937CV2763551single nucleotide variantNM_021821.4(MRPS35):c.437A>G (p.His146Arg)not specified [RCV004343070]uncertain significance122772410127724101Humanname
404980354CV2850482microsatelliteNM_021821.4(MRPS35):c.34_35del (p.Leu12fs)not provided [RCV003488041]uncertain significance122771087427710875Humanname
405742032CV3371839single nucleotide variantNM_021821.4(MRPS35):c.490C>T (p.Arg164Trp)not specified [RCV004497912]uncertain significance122772415427724154Humanname
405742050CV3371842single nucleotide variantNM_021821.4(MRPS35):c.502G>C (p.Ala168Pro)not specified [RCV004497915]uncertain significance122772416627724166Humanname
405742073CV3371845single nucleotide variantNM_021821.4(MRPS35):c.551A>C (p.Asp184Ala)not specified [RCV004497918]uncertain significance122773547527735475Humanname
405742179CV3371860single nucleotide variantNM_021821.4(MRPS35):c.680C>A (p.Thr227Lys)not specified [RCV004497933]uncertain significance122773758627737586Humanname
405742230CV3371868single nucleotide variantNM_021821.4(MRPS35):c.754A>G (p.Ile252Val)not specified [RCV004497941]likely benign122775523227755232Humanname
407474836CV3450454single nucleotide variantNM_021821.4(MRPS35):c.886G>A (p.Val296Ile)not specified [RCV004638261]uncertain significance122775536427755364Humanname
407474841CV3450456single nucleotide variantNM_021821.4(MRPS35):c.329A>T (p.Asn110Ile)not specified [RCV004638262]uncertain significance122771981527719815Humanname
407474845CV3450457single nucleotide variantNM_021821.4(MRPS35):c.905A>G (p.Glu302Gly)not specified [RCV004638263]uncertain significance122775538327755383Humanname
597634639CV3557457single nucleotide variantNM_021821.4(MRPS35):c.760G>C (p.Glu254Gln)not specified [RCV004831010]uncertain significance122775523827755238Humanname
598179359CV3993575single nucleotide variantNM_021821.4(MRPS35):c.701G>C (p.Trp234Ser)not specified [RCV005371917]uncertain significance122773760727737607Humanname
598213510CV3993577single nucleotide variantNM_021821.4(MRPS35):c.491G>A (p.Arg164Gln)not specified [RCV005378361]uncertain significance122772415527724155Humanname