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Variants search result for Homo sapiens
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35 records found for search term Cnih
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8575688CV110036single nucleotide variantNM_152495.1(CNIH3):c.198+22367C>TLung cancer [RCV000090561]uncertain significance1224707210224707210Humanname
8575687CV110035single nucleotide variantNM_001277197.1(CNIH4):c.251+3578A>CLung cancer [RCV000090560]uncertain significance1224369569224369569Humanname
15166575CV701910single nucleotide variantNM_182553.3(CNIH2):c.21G>A (p.Ala7=)not provided [RCV000948867]benign116627847766278477Humanname
156018528CV2302871single nucleotide variantNM_014184.4(CNIH4):c.8C>G (p.Ala3Gly)not specified [RCV004162767]uncertain significance1224356932224356932Humanname
597798877CV3653868single nucleotide variantNM_014184.4(CNIH4):c.7G>T (p.Ala3Ser)not specified [RCV004904919]uncertain significance1224356931224356931Humanname
155901765CV2237777single nucleotide variantNM_152495.2(CNIH3):c.16G>A (p.Ala6Thr)not specified [RCV004109026]uncertain significance1224617190224617190Humanname
155907577CV2276472single nucleotide variantNM_014184.4(CNIH4):c.19G>C (p.Val7Leu)not specified [RCV004144192]uncertain significance1224356943224356943Humanname
405663994CV3305335single nucleotide variantNM_182553.3(CNIH2):c.25T>C (p.Cys9Arg)not specified [RCV004439857]uncertain significance116627848166278481Humanname
598257418CV3941212single nucleotide variantNM_152495.2(CNIH3):c.15C>A (p.Phe5Leu)not specified [RCV005324412]uncertain significance1224617189224617189Humanname
598264682CV3941213single nucleotide variantNM_014184.4(CNIH4):c.14T>A (p.Val5Glu)not specified [RCV005326182]uncertain significance1224356938224356938Humanname
155901743CV2274568single nucleotide variantNM_014184.4(CNIH4):c.59C>T (p.Ser20Leu)not specified [RCV004138966]uncertain significance1224356983224356983Humanname
156005439CV2393999single nucleotide variantNM_152495.2(CNIH3):c.68T>G (p.Phe23Cys)not specified [RCV004236222]uncertain significance1224617242224617242Humanname
597798875CV3653867single nucleotide variantNM_014184.4(CNIH4):c.28C>T (p.Leu10Phe)not specified [RCV004904918]uncertain significance1224356952224356952Humanname
156079685CV2226565single nucleotide variantNM_152495.2(CNIH3):c.149C>A (p.Ala50Glu)not specified [RCV004101821]uncertain significance1224681025224681025Humanname
156185362CV2251671single nucleotide variantNM_152495.2(CNIH3):c.142G>A (p.Val48Ile)not specified [RCV004119688]uncertain significance1224681018224681018Humanname
401736782CV2679148single nucleotide variantNM_152495.2(CNIH3):c.176G>A (p.Arg59His)not specified [RCV004283880]uncertain significance1224684821224684821Humanname
401733215CV2685460single nucleotide variantNM_152495.2(CNIH3):c.104G>C (p.Arg35Thr)not specified [RCV004294486]uncertain significance1224680980224680980Humanname
401720656CV2702024single nucleotide variantNM_005776.3(CNIH1):c.244T>G (p.Leu82Val)not specified [RCV004320609]uncertain significance145443212754432127Humanname
401721139CV2702282single nucleotide variantNM_182553.3(CNIH2):c.133G>A (p.Gly45Arg)not specified [RCV004314613]uncertain significance116628231066282310Humanname
401763769CV2725291single nucleotide variantNM_152495.2(CNIH3):c.162G>C (p.Leu54Phe)not specified [RCV004319956]uncertain significance1224684807224684807Humanname
405663986CV3305334single nucleotide variantNM_182553.3(CNIH2):c.175C>G (p.Arg59Gly)not specified [RCV004439856]uncertain significance116628275766282757Humanname
405664000CV3305336single nucleotide variantNM_152495.2(CNIH3):c.116A>G (p.Lys39Arg)not specified [RCV004439858]uncertain significance1224680992224680992Humanname
407470275CV3429570single nucleotide variantNM_005776.3(CNIH1):c.281T>C (p.Val94Ala)not specified [RCV004615402]uncertain significance145443038754430387Humanname
597798868CV3653863single nucleotide variantNM_005776.3(CNIH1):c.172A>G (p.Ile58Val)not specified [RCV004904914]uncertain significance145443219954432199Humanname
597798871CV3653865single nucleotide variantNM_152495.2(CNIH3):c.218C>G (p.Ser73Cys)not specified [RCV004904916]uncertain significance1224730481224730481Humanname
155925540CV2230455single nucleotide variantNM_014184.4(CNIH4):c.400T>G (p.Leu134Val)not specified [RCV004097433]uncertain significance1224375802224375802Humanname
329375034CV2431111single nucleotide variantNM_014184.4(CNIH4):c.415G>T (p.Asp139Tyr)not specified [RCV004250471]uncertain significance1224375817224375817Humanname
329362660CV2439015single nucleotide variantNM_152495.2(CNIH3):c.376G>A (p.Asp126Asn)not specified [RCV004264522]uncertain significance1224734627224734627Humanname
405663980CV3305333single nucleotide variantNM_005776.3(CNIH1):c.409A>T (p.Met137Leu)not specified [RCV004439855]uncertain significance145442784054427840Humanname
407470281CV3429571single nucleotide variantNM_005776.3(CNIH1):c.409A>G (p.Met137Val)not specified [RCV004615403]uncertain significance145442784054427840Humanname
407470289CV3429573single nucleotide variantNM_014184.4(CNIH4):c.381G>C (p.Met127Ile)not specified [RCV004615405]uncertain significance1224371412224371412Humanname
597798866CV3653862single nucleotide variantNM_005776.3(CNIH1):c.415T>C (p.Tyr139His)not specified [RCV004904913]uncertain significance145442783454427834Humanname
597798869CV3653864single nucleotide variantNM_182553.3(CNIH2):c.343G>A (p.Val115Ile)not specified [RCV004904915]uncertain significance116628327966283279Humanname
597798873CV3653866single nucleotide variantNM_014184.4(CNIH4):c.348C>G (p.Ile116Met)not specified [RCV004904917]uncertain significance1224371379224371379Humanname
598257414CV3941211single nucleotide variantNM_005776.3(CNIH1):c.302A>G (p.Tyr101Cys)not specified [RCV005324411]uncertain significance145443036654430366Humanname