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36 records found for search term Gnl1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8581852CV116298single nucleotide variantNM_005275.3(GNL1):c.529-24C>TLung cancer [RCV000096821]uncertain significance63055467030554670Humanname
329356530CV2460387single nucleotide variantNM_005275.5(GNL1):c.61G>C (p.Glu21Gln)not specified [RCV004268701]uncertain significance63055614330556143Humanname
156264924CV2198613single nucleotide variantNM_005275.5(GNL1):c.221G>C (p.Arg74Pro)not specified [RCV004075631]uncertain significance63055557330555573Humanname
329375056CV2431119single nucleotide variantNM_005275.5(GNL1):c.284G>A (p.Arg95Lys)not specified [RCV004250477]uncertain significance63055514730555147Humanname
405768473CV3262112single nucleotide variantNM_005275.5(GNL1):c.110G>A (p.Arg37His)not specified [RCV004395502]uncertain significance63055568430555684Humanname
405768492CV3262115single nucleotide variantNM_005275.5(GNL1):c.217C>G (p.Pro73Ala)not specified [RCV004395505]uncertain significance63055557730555577Humanname
156239198CV2193698single nucleotide variantNM_005275.5(GNL1):c.367C>A (p.Pro123Thr)not specified [RCV004074292]uncertain significance63055506430555064Humanname
155971713CV2227922single nucleotide variantNM_005275.5(GNL1):c.857G>C (p.Gly286Ala)not specified [RCV004096180]uncertain significance63055313130553131Humanname
155995351CV2374957single nucleotide variantNM_005275.5(GNL1):c.847C>T (p.Arg283Trp)not specified [RCV004227974]uncertain significance63055314130553141Humanname
156090836CV2389385single nucleotide variantNM_005275.5(GNL1):c.938G>A (p.Arg313Gln)not specified [RCV004238121]uncertain significance63055262830552628Humanname
156188758CV2395500single nucleotide variantNM_005275.5(GNL1):c.448C>T (p.Arg150Trp)not specified [RCV004241366]uncertain significance63055484430554844Humanname
401877491CV2761151single nucleotide variantNM_005275.5(GNL1):c.728A>G (p.His243Arg)not specified [RCV004341037]uncertain significance63055343030553430Humanname
405768498CV3262116single nucleotide variantNM_005275.5(GNL1):c.466C>T (p.Leu156Phe)not specified [RCV004395506]uncertain significance63055482630554826Humanname
407520030CV3443592single nucleotide variantNM_005275.5(GNL1):c.754G>A (p.Val252Ile)not specified [RCV004629901]uncertain significance63055340430553404Humanname
407520034CV3443594single nucleotide variantNM_005275.5(GNL1):c.830G>T (p.Arg277Leu)not specified [RCV004629903]uncertain significance63055315830553158Humanname
407520038CV3443596single nucleotide variantNM_005275.5(GNL1):c.842G>T (p.Trp281Leu)not specified [RCV004629905]uncertain significance63055314630553146Humanname
597788475CV3678253single nucleotide variantNM_005275.5(GNL1):c.829C>T (p.Arg277Trp)not specified [RCV004932751]uncertain significance63055315930553159Humanname
597730476CV3678254single nucleotide variantNM_005275.5(GNL1):c.830G>C (p.Arg277Pro)not specified [RCV004919825]uncertain significance63055315830553158Humanname
597788478CV3678255single nucleotide variantNM_005275.5(GNL1):c.505A>C (p.Ser169Arg)not specified [RCV004932752]uncertain significance63055478730554787Humanname
598264193CV3974389single nucleotide variantNM_005275.5(GNL1):c.678G>T (p.Lys226Asn)not specified [RCV005348799]uncertain significance63055348030553480Humanname
156149423CV2200930single nucleotide variantNM_005275.5(GNL1):c.1654G>A (p.Glu552Lys)not specified [RCV004081543]uncertain significance63054624230546242Humanname
156258204CV2383715single nucleotide variantNM_005275.5(GNL1):c.1520G>A (p.Arg507Gln)not specified [RCV004231601]uncertain significance63054675830546758Humanname
156268422CV2398435single nucleotide variantNM_005275.5(GNL1):c.1537C>T (p.Arg513Cys)not specified [RCV004237763]uncertain significance63054674130546741Humanname
329401227CV2442215single nucleotide variantNM_005275.5(GNL1):c.1309A>C (p.Ile437Leu)not specified [RCV004264707]uncertain significance63054724430547244Humanname
329387291CV2463521single nucleotide variantNM_005275.5(GNL1):c.1624T>G (p.Leu542Val)not specified [RCV004277335]uncertain significance63054627230546272Humanname
401761801CV2699417single nucleotide variantNM_005275.5(GNL1):c.1237C>G (p.Pro413Ala)not specified [RCV004305992]uncertain significance63054739330547393Humanname
401776682CV2703317single nucleotide variantNM_005275.5(GNL1):c.1818G>T (p.Glu606Asp)not specified [RCV004315670]uncertain significance63054607830546078Humanname
401738203CV2711675single nucleotide variantNM_005275.5(GNL1):c.1561C>G (p.Pro521Ala)not specified [RCV004309351]uncertain significance63054671730546717Humanname
401766455CV2725555single nucleotide variantNM_005275.5(GNL1):c.1135G>A (p.Gly379Arg)not specified [RCV004320164]uncertain significance63054749530547495Humanname
401896075CV2777425single nucleotide variantNM_005275.5(GNL1):c.1413C>A (p.His471Gln)not specified [RCV004356207]uncertain significance63054714030547140Humanname
405768479CV3262113single nucleotide variantNM_005275.5(GNL1):c.1357G>A (p.Val453Met)not specified [RCV004395503]uncertain significance63054719630547196Humanname
405768485CV3262114single nucleotide variantNM_005275.5(GNL1):c.1772C>G (p.Ser591Cys)not specified [RCV004395504]uncertain significance63054612430546124Humanname
407520032CV3443593single nucleotide variantNM_005275.5(GNL1):c.1432A>G (p.Ile478Val)not specified [RCV004629902]uncertain significance63054712130547121Humanname
407520036CV3443595single nucleotide variantNM_005275.5(GNL1):c.1064G>A (p.Arg355His)not specified [RCV004629904]uncertain significance63055250230552502Humanname
407520040CV3443597single nucleotide variantNM_005275.5(GNL1):c.1064G>T (p.Arg355Leu)not specified [RCV004629906]uncertain significance63055250230552502Humanname
598264189CV3974388single nucleotide variantNM_005275.5(GNL1):c.1628A>C (p.Gln543Pro)not specified [RCV005348798]uncertain significance63054626830546268Humanname