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22 records found for search term Mrpl55
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407525216CV3450392single nucleotide variantNM_181463.3(MRPL55):c.27-123C>Gnot specified [RCV004631664]uncertain significance1228107992228107992Humanname
407474680CV3450395single nucleotide variantNM_181463.3(MRPL55):c.26+176G>Anot specified [RCV004638214]uncertain significance1228108059228108059Humanname
597634056CV3557336single nucleotide variantNM_181463.3(MRPL55):c.27-181G>Anot specified [RCV004830925]uncertain significance1228108050228108050Humanname
597634090CV3557342single nucleotide variantNM_181463.3(MRPL55):c.19C>A (p.Leu7Met)not specified [RCV004830931]uncertain significance1228108242228108242Humanname
15195267CV696528single nucleotide variantNM_181463.3(MRPL55):c.228G>A (p.Ala76=)not provided [RCV000955875]benign1228107668228107668Humanname
405759144CV3364118single nucleotide variantNM_181463.3(MRPL55):c.28C>T (p.Arg10Trp)not specified [RCV004500319]uncertain significance1228107868228107868Humanname
407474668CV3450391single nucleotide variantNM_181463.3(MRPL55):c.64G>A (p.Ala22Thr)not specified [RCV004638211]uncertain significance1228107832228107832Humanname
597634072CV3557339single nucleotide variantNM_181463.3(MRPL55):c.58G>A (p.Gly20Arg)not specified [RCV004830928]uncertain significance1228107838228107838Humanname
156077535CV2248422single nucleotide variantNM_181463.3(MRPL55):c.151C>T (p.Leu51Phe)not specified [RCV004119562]uncertain significance1228107745228107745Humanname
156219404CV2393587single nucleotide variantNM_181463.3(MRPL55):c.130C>T (p.His44Tyr)not specified [RCV004231402]uncertain significance1228107766228107766Humanname
401774224CV2727773single nucleotide variantNM_181463.3(MRPL55):c.127G>A (p.Val43Met)not specified [RCV004323803]uncertain significance1228107769228107769Humanname
405759232CV3364134single nucleotide variantNM_181463.3(MRPL55):c.241C>A (p.Leu81Met)not specified [RCV004500335]uncertain significance1228106906228106906Humanname
407474677CV3450394single nucleotide variantNM_181463.3(MRPL55):c.287G>A (p.Arg96His)not specified [RCV004638213]uncertain significance1228106860228106860Humanname
597638002CV3557335single nucleotide variantNM_181463.3(MRPL55):c.214C>T (p.Arg72Trp)not specified [RCV004824841]uncertain significance1228107682228107682Humanname
597634061CV3557337single nucleotide variantNM_181463.3(MRPL55):c.200G>A (p.Arg67His)not specified [RCV004830926]uncertain significance1228107696228107696Humanname
597634067CV3557338single nucleotide variantNM_181463.3(MRPL55):c.268C>T (p.Arg90Trp)not specified [RCV004830927]uncertain significance1228106879228106879Humanname
597634085CV3557341single nucleotide variantNM_181463.3(MRPL55):c.103A>G (p.Ser35Gly)not specified [RCV004830930]uncertain significance1228107793228107793Humanname
597634100CV3557344single nucleotide variantNM_181463.3(MRPL55):c.218G>T (p.Arg73Leu)not specified [RCV004830933]uncertain significance1228107678228107678Humanname
156270097CV2195136single nucleotide variantNM_181463.3(MRPL55):c.319G>A (p.Glu107Lys)not specified [RCV004078041]uncertain significance1228106828228106828Humanname
407474672CV3450393single nucleotide variantNM_181463.3(MRPL55):c.320A>G (p.Glu107Gly)not specified [RCV004638212]uncertain significance1228106827228106827Humanname
597634078CV3557340single nucleotide variantNM_181463.3(MRPL55):c.346G>T (p.Val116Leu)not specified [RCV004830929]uncertain significance1228106801228106801Humanname
598179069CV3993460single nucleotide variantNM_181463.3(MRPL55):c.352C>T (p.Arg118Cys)not specified [RCV005371869]uncertain significance1228106795228106795Humanname