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31 records found for search term Cbr3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405753067CV3292082single nucleotide variantNM_001236.4(CBR3):c.5C>G (p.Ser2Trp)not specified [RCV004432411]uncertain significance213613519736135197Humanname
156251641CV2394325single nucleotide variantNM_001236.4(CBR3):c.52G>A (p.Gly18Ser)not specified [RCV004238546]uncertain significance213613524436135244Humanname
405753043CV3292079single nucleotide variantNM_001236.4(CBR3):c.50T>C (p.Ile17Thr)not specified [RCV004432408]uncertain significance213613524236135242Humanname
597785740CV3641265single nucleotide variantNM_001236.4(CBR3):c.77G>A (p.Cys26Tyr)not specified [RCV004900803]uncertain significance213613526936135269Humanname
156080255CV2258209single nucleotide variantNM_001236.4(CBR3):c.118G>A (p.Val40Met)not specified [RCV004121585]uncertain significance213613531036135310Humanname
156242269CV2262038single nucleotide variantNM_001236.4(CBR3):c.153G>C (p.Gln51His)not specified [RCV004126518]uncertain significance213613534536135345Humanname
401759057CV2694407single nucleotide variantNM_001236.4(CBR3):c.188A>G (p.Asp63Gly)not specified [RCV004304588]uncertain significance213613538036135380Humanname
401886937CV2777033single nucleotide variantNM_001236.4(CBR3):c.270C>A (p.Asn90Lys)not specified [RCV004351830]uncertain significance213613546236135462Humanname
405753025CV3292076single nucleotide variantNM_001236.4(CBR3):c.106A>C (p.Thr36Pro)not specified [RCV004432405]uncertain significance213613529836135298Humanname
405753031CV3292077single nucleotide variantNM_001236.4(CBR3):c.161G>A (p.Gly54Asp)not specified [RCV004432406]uncertain significance213613535336135353Humanname
407482464CV3421986single nucleotide variantNM_001236.4(CBR3):c.256G>A (p.Val86Ile)not specified [RCV004602684]uncertain significance213613544836135448Humanname
597785747CV3641268single nucleotide variantNM_001236.4(CBR3):c.169C>T (p.Pro57Ser)not specified [RCV004900805]uncertain significance213613536136135361Humanname
156032933CV2214555single nucleotide variantNM_001236.4(CBR3):c.614C>G (p.Ser205Trp)not specified [RCV004088603]uncertain significance213614629236146292Humanname
155901785CV2237783single nucleotide variantNM_001236.4(CBR3):c.784A>G (p.Thr262Ala)not specified [RCV004109028]uncertain significance213614646236146462Humanname
155964735CV2261677single nucleotide variantNM_001236.4(CBR3):c.362T>C (p.Met121Thr)not specified [RCV004125989]uncertain significance213613789736137897Humanname
156365602CV2272141single nucleotide variantNM_001236.4(CBR3):c.448T>C (p.Cys150Arg)not specified [RCV004124919]uncertain significance213614612636146126Humanname
156022914CV2273706single nucleotide variantNM_001236.4(CBR3):c.674C>T (p.Ala225Val)not specified [RCV004132358]uncertain significance213614635236146352Humanname
11087715CV227809single nucleotide variantNM_001236.4(CBR3):c.730G>A (p.Val244Met)anthracyclines and related substances response - Toxicity/ADR [RCV000211217]drug response213614640836146408Humanname
156038898CV2278971single nucleotide variantNM_001236.4(CBR3):c.596T>G (p.Leu199Trp)not specified [RCV004145662]uncertain significance213614627436146274Humanname
156307236CV2369646single nucleotide variantNM_001236.4(CBR3):c.605C>A (p.Thr202Lys)not specified [RCV004215050]uncertain significance213614628336146283Humanname
329358909CV2425438single nucleotide variantNM_001236.4(CBR3):c.324G>T (p.Glu108Asp)not specified [RCV004251093]uncertain significance213613785936137859Humanname
401742617CV2673829single nucleotide variantNM_001236.4(CBR3):c.380C>T (p.Pro127Leu)not specified [RCV004293212]uncertain significance213613791536137915Humanname
405753038CV3292078single nucleotide variantNM_001236.4(CBR3):c.364T>A (p.Cys122Ser)not specified [RCV004432407]uncertain significance213613789936137899Humanname
405753049CV3292080single nucleotide variantNM_001236.4(CBR3):c.541A>C (p.Asn181His)not specified [RCV004432409]uncertain significance213614621936146219Humanname
405753059CV3292081single nucleotide variantNM_001236.4(CBR3):c.547G>A (p.Val183Met)not specified [RCV004432410]uncertain significance213614622536146225Humanname
405753074CV3292083single nucleotide variantNM_001236.4(CBR3):c.631C>T (p.Arg211Cys)not specified [RCV004432412]uncertain significance213614630936146309Humanname
405753080CV3292084single nucleotide variantNM_001236.4(CBR3):c.815A>G (p.Lys272Arg)not specified [RCV004432413]uncertain significance213614649336146493Humanname
405753087CV3292085single nucleotide variantNM_001236.4(CBR3):c.820G>A (p.Val274Met)not specified [RCV004432414]uncertain significance213614649836146498Humanname
597785742CV3641267single nucleotide variantNM_001236.4(CBR3):c.353C>T (p.Thr118Ile)not specified [RCV004900804]uncertain significance213613788836137888Humanname
598176224CV3950436single nucleotide variantNM_001236.4(CBR3):c.632G>A (p.Arg211His)not specified [RCV005309992]likely benign213614631036146310Humanname
15184759CV705673single nucleotide variantNM_001236.4(CBR3):c.370G>A (p.Glu124Lys)not provided [RCV000952787]benign213613790536137905Humanname