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Variants search result for Homo sapiens
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34 records found for search term Gimap4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155948394CV2272127single nucleotide variantNM_018326.3(GIMAP4):c.20G>A (p.Ser7Asn)not specified [RCV004124909]uncertain significance7150569921150569921Humanname
155919031CV2254788single nucleotide variantNM_018326.3(GIMAP4):c.98T>C (p.Ile33Thr)not specified [RCV004115255]uncertain significance7150572168150572168Humanname
156267017CV2304966single nucleotide variantNM_018326.3(GIMAP4):c.33C>A (p.Asn11Lys)not specified [RCV004168864]uncertain significance7150569934150569934Humanname
401863292CV2765707single nucleotide variantNM_018326.3(GIMAP4):c.34C>G (p.Pro12Ala)not specified [RCV004335713]uncertain significance7150569935150569935Humanname
405736225CV3254820single nucleotide variantNM_018326.3(GIMAP4):c.34C>T (p.Pro12Ser)not specified [RCV004390638]uncertain significance7150569935150569935Humanname
156153332CV2265983single nucleotide variantNM_018326.3(GIMAP4):c.157C>T (p.Arg53Trp)not specified [RCV004126814]uncertain significance7150572227150572227Humanname
156165273CV2348581single nucleotide variantNM_018326.3(GIMAP4):c.218G>T (p.Ser73Ile)not specified [RCV004195810]uncertain significance7150572288150572288Humanname
155932267CV2364365single nucleotide variantNM_018326.3(GIMAP4):c.217A>G (p.Ser73Gly)not specified [RCV004223583]uncertain significance7150572287150572287Humanname
401867165CV2759116single nucleotide variantNM_018326.3(GIMAP4):c.158G>A (p.Arg53Gln)not specified [RCV004342415]likely benign7150572228150572228Humanname
405736187CV3254815single nucleotide variantNM_018326.3(GIMAP4):c.104T>C (p.Leu35Ser)not specified [RCV004390633]uncertain significance7150572174150572174Humanname
405736192CV3254816single nucleotide variantNM_018326.3(GIMAP4):c.187A>C (p.Lys63Gln)not specified [RCV004390634]uncertain significance7150572257150572257Humanname
405736208CV3254818single nucleotide variantNM_018326.3(GIMAP4):c.193A>G (p.Ile65Val)not specified [RCV004390636]uncertain significance7150572263150572263Humanname
405736217CV3254819single nucleotide variantNM_018326.3(GIMAP4):c.263G>A (p.Gly88Asp)not specified [RCV004390637]uncertain significance7150572333150572333Humanname
407513184CV3443194single nucleotide variantNM_018326.3(GIMAP4):c.124G>A (p.Gly42Arg)not specified [RCV004627067]uncertain significance7150572194150572194Humanname
597759340CV3684463single nucleotide variantNM_018326.3(GIMAP4):c.118G>A (p.Gly40Arg)not specified [RCV004925483]uncertain significance7150572188150572188Humanname
156077601CV2198242single nucleotide variantNM_018326.3(GIMAP4):c.352C>T (p.Leu118Phe)not specified [RCV004079820]uncertain significance7150572422150572422Humanname
156033006CV2259725single nucleotide variantNM_018326.3(GIMAP4):c.451C>T (p.Leu151Phe)not specified [RCV004116737]uncertain significance7150572521150572521Humanname
156362605CV2265568single nucleotide variantNM_018326.3(GIMAP4):c.763A>G (p.Ile255Val)not specified [RCV004124308]uncertain significance7150572833150572833Humanname
156368841CV2267096single nucleotide variantNM_018326.3(GIMAP4):c.866A>G (p.His289Arg)not specified [RCV004131719]uncertain significance7150572936150572936Humanname
155925975CV2365675single nucleotide variantNM_018326.3(GIMAP4):c.683G>A (p.Arg228Lys)not specified [RCV004214229]likely benign7150572753150572753Humanname
156392173CV2378347single nucleotide variantNM_018326.3(GIMAP4):c.841A>G (p.Lys281Glu)not specified [RCV004226373]uncertain significance7150572911150572911Humanname
329356874CV2460597single nucleotide variantNM_018326.3(GIMAP4):c.415A>C (p.Lys139Gln)not specified [RCV004268871]uncertain significance7150572485150572485Humanname
405736234CV3254821single nucleotide variantNM_018326.3(GIMAP4):c.632G>A (p.Arg211His)not specified [RCV004390639]uncertain significance7150572702150572702Humanname
405736241CV3254822single nucleotide variantNM_018326.3(GIMAP4):c.760C>T (p.Arg254Trp)not specified [RCV004390640]uncertain significance7150572830150572830Humanname
405736247CV3254823single nucleotide variantNM_018326.3(GIMAP4):c.883C>G (p.Gln295Glu)not specified [RCV004390641]uncertain significance7150572953150572953Humanname
407513182CV3443193single nucleotide variantNM_018326.3(GIMAP4):c.456A>G (p.Ile152Met)not specified [RCV004627066]uncertain significance7150572526150572526Humanname
407513187CV3443196single nucleotide variantNM_018326.3(GIMAP4):c.524T>G (p.Ile175Ser)not specified [RCV004627069]uncertain significance7150572594150572594Humanname
407513189CV3443197single nucleotide variantNM_018326.3(GIMAP4):c.863C>T (p.Ala288Val)not specified [RCV004627070]uncertain significance7150572933150572933Humanname
597759335CV3684461single nucleotide variantNM_018326.3(GIMAP4):c.506G>C (p.Arg169Thr)not specified [RCV004925482]uncertain significance7150572576150572576Humanname
597706649CV3684462single nucleotide variantNM_018326.3(GIMAP4):c.547G>C (p.Gly183Arg)not specified [RCV004917010]uncertain significance7150572617150572617Humanname
597759345CV3684464single nucleotide variantNM_018326.3(GIMAP4):c.947A>C (p.Gln316Pro)not specified [RCV004925484]uncertain significance7150573017150573017Humanname
597706657CV3684465single nucleotide variantNM_018326.3(GIMAP4):c.827A>G (p.Lys276Arg)not specified [RCV004917011]uncertain significance7150572897150572897Humanname
598251485CV3967282single nucleotide variantNM_018326.3(GIMAP4):c.855A>T (p.Glu285Asp)not specified [RCV005345904]uncertain significance7150572925150572925Humanname
598251491CV3967283single nucleotide variantNM_018326.3(GIMAP4):c.373C>T (p.Arg125Cys)not specified [RCV005345905]uncertain significance7150572443150572443Humanname