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31 records found for search term Nkg7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15128396CV780022single nucleotide variantNM_005601.4(NKG7):c.158-4T>Anot provided [RCV000964077]benign195137231151372311Humanname
597650702CV3556245single nucleotide variantNM_005601.4(NKG7):c.14G>A (p.Arg5Gln)not specified [RCV004826804]uncertain significance195137252251372522Humanname
598239132CV3994596single nucleotide variantNM_005601.4(NKG7):c.13C>T (p.Arg5Trp)not specified [RCV005382868]uncertain significance195137252351372523Humanname
156232755CV2196312single nucleotide variantNM_005601.4(NKG7):c.63T>G (p.Ile21Met)not specified [RCV004072490]uncertain significance195137247351372473Humanname
156070811CV2232513single nucleotide variantNM_005601.4(NKG7):c.34G>A (p.Gly12Ser)not specified [RCV004099116]uncertain significance195137250251372502Humanname
407497425CV3458597single nucleotide variantNM_005601.4(NKG7):c.51G>A (p.Met17Ile)not specified [RCV004643745]likely benign195137248551372485Humanname
597650720CV3556247single nucleotide variantNM_005601.4(NKG7):c.76G>A (p.Asp26Asn)not specified [RCV004826806]likely benign195137246051372460Humanname
597650738CV3556249single nucleotide variantNM_005601.4(NKG7):c.56G>C (p.Cys19Ser)not specified [RCV004826808]uncertain significance195137248051372480Humanname
8636959CV92184single nucleotide variantNM_005601.3(NKG7):c.432C>T (p.Leu144=)Malignant melanoma [RCV000072282]not provided195137194751371947Humanname
155918838CV2360085single nucleotide variantNM_005601.4(NKG7):c.188T>A (p.Ile63Asn)not specified [RCV004215366]uncertain significance195137227751372277Humanname
156088049CV2366447single nucleotide variantNM_005601.4(NKG7):c.149T>C (p.Ile50Thr)not specified [RCV004212490]uncertain significance195137238751372387Humanname
329354737CV2448947single nucleotide variantNM_005601.4(NKG7):c.289G>A (p.Ala97Thr)not specified [RCV004264032]likely benign195137217651372176Humanname
401740531CV2684380single nucleotide variantNM_005601.4(NKG7):c.259C>G (p.Pro87Ala)not specified [RCV004289023]uncertain significance195137220651372206Humanname
405706461CV3362205single nucleotide variantNM_005601.4(NKG7):c.173C>T (p.Thr58Met)not specified [RCV004493193]uncertain significance195137229251372292Humanname
405706467CV3362206single nucleotide variantNM_005601.4(NKG7):c.217G>A (p.Val73Met)not specified [RCV004493194]uncertain significance195137224851372248Humanname
407508803CV3458598single nucleotide variantNM_005601.4(NKG7):c.209T>C (p.Leu70Pro)not specified [RCV004647235]uncertain significance195137225651372256Humanname
597650710CV3556246single nucleotide variantNM_005601.4(NKG7):c.217G>C (p.Val73Leu)not specified [RCV004826805]uncertain significance195137224851372248Humanname
597650728CV3556248single nucleotide variantNM_005601.4(NKG7):c.112G>A (p.Ala38Thr)not specified [RCV004826807]uncertain significance195137242451372424Humanname
156140774CV2212226single nucleotide variantNM_005601.4(NKG7):c.316G>C (p.Val106Leu)not specified [RCV004089110]uncertain significance195137206351372063Humanname
156305371CV2252607single nucleotide variantNM_005601.4(NKG7):c.475C>G (p.Arg159Gly)not specified [RCV004118483]uncertain significance195137180051371800Humanname
156040550CV2261306single nucleotide variantNM_005601.4(NKG7):c.454G>T (p.Gly152Cys)not specified [RCV004128168]uncertain significance195137182151371821Humanname
156147683CV2307287single nucleotide variantNM_005601.4(NKG7):c.398T>C (p.Phe133Ser)not specified [RCV004165982]uncertain significance195137198151371981Humanname
156225333CV2399626single nucleotide variantNM_005601.4(NKG7):c.316G>T (p.Val106Leu)not specified [RCV004244144]uncertain significance195137206351372063Humanname
401780231CV2725943single nucleotide variantNM_005601.4(NKG7):c.451C>A (p.Leu151Met)not specified [RCV004324314]uncertain significance195137182451371824Humanname
405706479CV3362208single nucleotide variantNM_005601.4(NKG7):c.371A>G (p.Gln124Arg)not specified [RCV004493196]uncertain significance195137200851372008Humanname
405706486CV3362209single nucleotide variantNM_005601.4(NKG7):c.491C>T (p.Thr164Ile)not specified [RCV004493197]uncertain significance195137178451371784Humanname
598193635CV3994593single nucleotide variantNM_005601.4(NKG7):c.476G>A (p.Arg159His)not specified [RCV005374581]uncertain significance195137179951371799Humanname
598239120CV3994594single nucleotide variantNM_005601.4(NKG7):c.424C>T (p.Leu142Phe)not specified [RCV005382866]likely benign195137195551371955Humanname
598239127CV3994595single nucleotide variantNM_005601.4(NKG7):c.458C>G (p.Ala153Gly)not specified [RCV005382867]uncertain significance195137181751371817Humanname
15163082CV705207single nucleotide variantNM_005601.4(NKG7):c.337A>G (p.Thr113Ala)not provided [RCV000947999]benign195137204251372042Humanname
8636958CV92183single nucleotide variantNM_005601.3(NKG7):c.479C>T (p.Pro160Leu)Malignant melanoma [RCV000072281]not provided195137179651371796Humanname