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38 records found for search term Letmd1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156295745CV2297499single nucleotide variantNM_015416.5(LETMD1):c.17T>C (p.Val6Ala)not specified [RCV004153427]uncertain significance125104837351048373Humanname
405817779CV3280282single nucleotide variantNM_015416.5(LETMD1):c.10T>A (p.Ser4Thr)not specified [RCV004412789]uncertain significance125104836651048366Humanname
597641026CV3696060single nucleotide variantNM_015416.5(LETMD1):c.11C>T (p.Ser4Phe)not specified [RCV004941644]uncertain significance125104836751048367Humanname
407492014CV3452729single nucleotide variantNM_015416.5(LETMD1):c.32C>T (p.Ser11Leu)not specified [RCV004642368]likely benign125104838851048388Humanname
598260129CV3984433single nucleotide variantNM_015416.5(LETMD1):c.71T>G (p.Val24Gly)not specified [RCV005347564]uncertain significance125104842751048427Humanname
156028623CV2195843single nucleotide variantNM_015416.5(LETMD1):c.230G>A (p.Arg77His)not specified [RCV004076184]uncertain significance125104914151049141Humanname
155975510CV2231359single nucleotide variantNM_015416.5(LETMD1):c.226G>C (p.Gly76Arg)not specified [RCV004096452]uncertain significance125104913751049137Humanname
156359224CV2328166single nucleotide variantNM_015416.5(LETMD1):c.253C>A (p.Leu85Met)not specified [RCV004173264]uncertain significance125104916451049164Humanname
156336179CV2333637single nucleotide variantNM_015416.5(LETMD1):c.172T>G (p.Ser58Ala)not specified [RCV004192478]uncertain significance125104908351049083Humanname
156134285CV2361995single nucleotide variantNM_015416.5(LETMD1):c.238C>T (p.Pro80Ser)not specified [RCV004207761]uncertain significance125104914951049149Humanname
156065346CV2376077single nucleotide variantNM_015416.5(LETMD1):c.133C>G (p.Leu45Val)not specified [RCV004220313]uncertain significance125104904451049044Humanname
405817780CV3280283single nucleotide variantNM_015416.5(LETMD1):c.175T>C (p.Tyr59His)not specified [RCV004412790]uncertain significance125104908651049086Humanname
405817781CV3280284single nucleotide variantNM_015416.5(LETMD1):c.179T>C (p.Val60Ala)not specified [RCV004412791]uncertain significance125104909051049090Humanname
597641021CV3696059single nucleotide variantNM_015416.5(LETMD1):c.145C>A (p.Pro49Thr)not specified [RCV004941643]uncertain significance125104905651049056Humanname
156254026CV2209610single nucleotide variantNM_015416.5(LETMD1):c.634T>C (p.Trp212Arg)not specified [RCV004093704]uncertain significance125105599551055995Humanname
156155423CV2266141single nucleotide variantNM_015416.5(LETMD1):c.601G>T (p.Val201Phe)not specified [RCV004128729]uncertain significance125105596251055962Humanname
155941185CV2294212single nucleotide variantNM_015416.5(LETMD1):c.760G>A (p.Val254Met)not specified [RCV004149568]likely benign125105624351056243Humanname
155980977CV2336983single nucleotide variantNM_015416.5(LETMD1):c.668G>A (p.Arg223His)not specified [RCV004192754]likely benign125105615151056151Humanname
156291482CV2342915single nucleotide variantNM_015416.5(LETMD1):c.415C>T (p.Leu139Phe)not specified [RCV004189947]uncertain significance125105380251053802Humanname
156170880CV2354914single nucleotide variantNM_015416.5(LETMD1):c.682G>A (p.Ala228Thr)not specified [RCV004191409]uncertain significance125105616551056165Humanname
155904580CV2385543single nucleotide variantNM_015416.5(LETMD1):c.638G>A (p.Arg213His)not specified [RCV004233184]likely benign125105599951055999Humanname
329376616CV2428483single nucleotide variantNM_015416.5(LETMD1):c.967C>G (p.Arg323Gly)not specified [RCV004253271]uncertain significance125105808351058083Humanname
329363602CV2442337single nucleotide variantNM_015416.5(LETMD1):c.483T>A (p.Phe161Leu)not specified [RCV004266599]uncertain significance125105584451055844Humanname
401769884CV2693114single nucleotide variantNM_015416.5(LETMD1):c.671G>T (p.Gly224Val)not specified [RCV004308649]uncertain significance125105615451056154Humanname
401754466CV2722707single nucleotide variantNM_015416.5(LETMD1):c.949A>G (p.Ile317Val)not specified [RCV004325145]uncertain significance125105806551058065Humanname
401870968CV2762909single nucleotide variantNM_015416.5(LETMD1):c.637C>T (p.Arg213Cys)not specified [RCV004342660]uncertain significance125105599851055998Humanname
405817863CV3280286single nucleotide variantNM_015416.5(LETMD1):c.548A>G (p.Tyr183Cys)not specified [RCV004412793]uncertain significance125105590951055909Humanname
405817784CV3280287single nucleotide variantNM_015416.5(LETMD1):c.554C>G (p.Ala185Gly)not specified [RCV004412794]uncertain significance125105591551055915Humanname
405817785CV3280288single nucleotide variantNM_015416.5(LETMD1):c.559C>T (p.Arg187Trp)not specified [RCV004412795]uncertain significance125105592051055920Humanname
405817786CV3280289single nucleotide variantNM_015416.5(LETMD1):c.880G>A (p.Gly294Arg)not specified [RCV004412796]uncertain significance125105646751056467Humanname
407492018CV3452730single nucleotide variantNM_015416.5(LETMD1):c.608C>T (p.Pro203Leu)not specified [RCV004642369]uncertain significance125105596951055969Humanname
597641015CV3696058single nucleotide variantNM_015416.5(LETMD1):c.655A>G (p.Thr219Ala)not specified [RCV004941642]uncertain significance125105601651056016Humanname
597641032CV3696061single nucleotide variantNM_015416.5(LETMD1):c.622G>A (p.Ala208Thr)not specified [RCV004941645]uncertain significance125105598351055983Humanname
597795700CV3696062single nucleotide variantNM_015416.5(LETMD1):c.701C>T (p.Ala234Val)not specified [RCV004934939]uncertain significance125105618451056184Humanname
597795703CV3696063single nucleotide variantNM_015416.5(LETMD1):c.521A>G (p.Lys174Arg)not specified [RCV004934940]uncertain significance125105588251055882Humanname
597641036CV3696064single nucleotide variantNM_015416.5(LETMD1):c.661A>T (p.Ile221Leu)not specified [RCV004941646]uncertain significance125105614451056144Humanname
597641044CV3696065single nucleotide variantNM_015416.5(LETMD1):c.406A>G (p.Thr136Ala)not specified [RCV004941647]uncertain significance125105379351053793Humanname
156215410CV2347860single nucleotide variantNM_015416.5(LETMD1):c.1078C>T (p.Arg360Cys)not specified [RCV004195511]uncertain significance125105942651059426Humanname