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31 records found for search term Lair1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156338089CV2271218single nucleotide variantNM_002287.6(LAIR1):c.50A>G (p.Gln17Arg)not specified [RCV004136366]uncertain significance195436431554364315Humanname
405808704CV3287037single nucleotide variantNM_002287.6(LAIR1):c.98C>T (p.Ala33Val)not specified [RCV004407187]uncertain significance195436118254361182Humanname
156239265CV2235904single nucleotide variantNM_002287.6(LAIR1):c.259C>T (p.Arg87Cys)not specified [RCV004113796]uncertain significance195436102154361021Humanname
155960596CV2249442single nucleotide variantNM_002287.6(LAIR1):c.118C>A (p.Pro40Thr)not specified [RCV004120499]uncertain significance195436116254361162Humanname
401747961CV2699968single nucleotide variantNM_002287.6(LAIR1):c.124G>A (p.Gly42Arg)not specified [RCV004310403]uncertain significance195436115654361156Humanname
598196931CV3991493single nucleotide variantNM_002287.6(LAIR1):c.149G>A (p.Arg50Gln)not specified [RCV005355261]uncertain significance195436113154361131Humanname
598196937CV3991495single nucleotide variantNM_002287.6(LAIR1):c.101A>C (p.Glu34Ala)not specified [RCV005355262]uncertain significance195436117954361179Humanname
598196943CV3991496single nucleotide variantNM_002287.6(LAIR1):c.289G>A (p.Gly97Arg)not specified [RCV005355263]uncertain significance195436099154360991Humanname
156058959CV2239285single nucleotide variantNM_002287.6(LAIR1):c.490C>A (p.Leu164Met)not specified [RCV004112247]uncertain significance195435658454356584Humanname
156140821CV2260390single nucleotide variantNM_002287.6(LAIR1):c.814A>G (p.Thr272Ala)not specified [RCV004123201]uncertain significance195435531854355318Humanname
155906679CV2279370single nucleotide variantNM_002287.6(LAIR1):c.697G>A (p.Asp233Asn)not specified [RCV004141924]uncertain significance195435597454355974Humanname
405808694CV3287032single nucleotide variantNM_002287.6(LAIR1):c.299G>C (p.Arg100Pro)not specified [RCV004407182]uncertain significance195436098154360981Humanname
405808696CV3287033single nucleotide variantNM_002287.6(LAIR1):c.545T>C (p.Val182Ala)not specified [RCV004407183]uncertain significance195435652954356529Humanname
405808698CV3287034single nucleotide variantNM_002287.6(LAIR1):c.563G>A (p.Arg188His)not specified [RCV004407184]uncertain significance195435651154356511Humanname
405808700CV3287035single nucleotide variantNM_002287.6(LAIR1):c.641T>C (p.Val214Ala)not specified [RCV004407185]uncertain significance195435625354356253Humanname
405808702CV3287036single nucleotide variantNM_002287.6(LAIR1):c.650T>C (p.Leu217Pro)not specified [RCV004407186]uncertain significance195435624454356244Humanname
407480967CV3456031single nucleotide variantNM_002287.6(LAIR1):c.403G>A (p.Gly135Ser)not specified [RCV004639833]uncertain significance195436003454360034Humanname
407480973CV3456032single nucleotide variantNM_002287.6(LAIR1):c.656G>A (p.Arg219Lys)not specified [RCV004639834]uncertain significance195435623854356238Humanname
407480979CV3456033single nucleotide variantNM_002287.6(LAIR1):c.788C>T (p.Thr263Ile)not specified [RCV004639835]uncertain significance195435534454355344Humanname
597631059CV3692785single nucleotide variantNM_002287.6(LAIR1):c.447C>A (p.His149Gln)not specified [RCV004939617]uncertain significance195435693554356935Humanname
597631063CV3692786single nucleotide variantNM_002287.6(LAIR1):c.709G>C (p.Asp237His)not specified [RCV004939618]uncertain significance195435596254355962Humanname
597631069CV3692788single nucleotide variantNM_002287.6(LAIR1):c.707C>T (p.Thr236Met)not specified [RCV004939620]uncertain significance195435596454355964Humanname
597631073CV3692789single nucleotide variantNM_002287.6(LAIR1):c.791C>A (p.Ala264Asp)not specified [RCV004939621]uncertain significance195435534154355341Humanname
598196924CV3991491single nucleotide variantNM_002287.6(LAIR1):c.386C>T (p.Ser129Phe)not specified [RCV005355260]uncertain significance195436005154360051Humanname
598173702CV3991492single nucleotide variantNM_002287.6(LAIR1):c.382G>T (p.Asp128Tyr)not specified [RCV005370972]uncertain significance195436005554360055Humanname
598222549CV3991494single nucleotide variantNM_002287.6(LAIR1):c.302G>A (p.Cys101Tyr)not specified [RCV005361004]uncertain significance195436097854360978Humanname
598196950CV3991497single nucleotide variantNM_002287.6(LAIR1):c.299G>A (p.Arg100His)not specified [RCV005355264]uncertain significance195436098154360981Humanname
598222558CV3991498single nucleotide variantNM_002287.6(LAIR1):c.661G>A (p.Ala221Thr)not specified [RCV005361005]uncertain significance195435623354356233Humanname
598173709CV3991499single nucleotide variantNM_002287.6(LAIR1):c.848C>A (p.Ala283Asp)not specified [RCV005370973]uncertain significance195435528454355284Humanname
598196956CV3991500single nucleotide variantNM_002287.6(LAIR1):c.615G>T (p.Lys205Asn)not specified [RCV005355265]uncertain significance195435636754356367Humanname
598196963CV3991501single nucleotide variantNM_002287.6(LAIR1):c.727G>T (p.Ala243Ser)not specified [RCV005355266]uncertain significance195435540554355405Humanname