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30 records found for search term Alkbh7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405787465CV3264780single nucleotide variantNM_032306.4(ALKBH7):c.11C>T (p.Thr4Ile)not specified [RCV004398799]uncertain significance1963728316372831Humanname
155921890CV2284215single nucleotide variantNM_032306.4(ALKBH7):c.51G>T (p.Trp17Cys)not specified [RCV004146585]uncertain significance1963728716372871Humanname
401877163CV2769358single nucleotide variantNM_032306.4(ALKBH7):c.59G>A (p.Gly20Asp)not specified [RCV004357351]uncertain significance1963728796372879Humanname
405787608CV3264811single nucleotide variantNM_032306.4(ALKBH7):c.44C>A (p.Pro15His)not specified [RCV004398830]uncertain significance1963728646372864Humanname
597791440CV3682863single nucleotide variantNM_032306.4(ALKBH7):c.32C>A (p.Thr11Lys)not specified [RCV004933508]uncertain significance1963728526372852Humanname
156033000CV2214569single nucleotide variantNM_032306.4(ALKBH7):c.239G>A (p.Arg80His)not specified [RCV004088616]uncertain significance1963742376374237Humanname
156137423CV2239892single nucleotide variantNM_032306.4(ALKBH7):c.178C>T (p.Arg60Cys)not specified [RCV004110448]uncertain significance1963729986372998Humanname
155976587CV2324769single nucleotide variantNM_032306.4(ALKBH7):c.229G>A (p.Glu77Lys)not specified [RCV004173003]uncertain significance1963742276374227Humanname
156262041CV2395673single nucleotide variantNM_032306.4(ALKBH7):c.281C>T (p.Ala94Val)not specified [RCV004241512]uncertain significance1963742796374279Humanname
407459338CV3451825single nucleotide variantNM_032306.4(ALKBH7):c.260C>A (p.Ala87Asp)not specified [RCV004633571]uncertain significance1963742586374258Humanname
597791407CV3682852single nucleotide variantNM_032306.4(ALKBH7):c.265C>G (p.Leu89Val)not specified [RCV004933497]uncertain significance1963742636374263Humanname
598254891CV3971256single nucleotide variantNM_032306.4(ALKBH7):c.226A>G (p.Thr76Ala)not specified [RCV005346470]uncertain significance1963742246374224Humanname
155966208CV2304716single nucleotide variantNM_032306.4(ALKBH7):c.298G>C (p.Gly100Arg)not specified [RCV004166873]uncertain significance1963742966374296Humanname
329362492CV2442078single nucleotide variantNM_032306.4(ALKBH7):c.482C>G (p.Pro161Arg)not specified [RCV004264280]uncertain significance1963745686374568Humanname
329389402CV2445026single nucleotide variantNM_032306.4(ALKBH7):c.512C>G (p.Ala171Gly)not specified [RCV004261639]uncertain significance1963748196374819Humanname
329388181CV2468728single nucleotide variantNM_032306.4(ALKBH7):c.368A>T (p.Asp123Val)not specified [RCV004280054]uncertain significance1963743666374366Humanname
401760291CV2718787single nucleotide variantNM_032306.4(ALKBH7):c.571C>T (p.Arg191Trp)not specified [RCV004328533]uncertain significance1963748786374878Humanname
401863663CV2770783single nucleotide variantNM_032306.4(ALKBH7):c.608G>A (p.Arg203His)not specified [RCV004349819]uncertain significance1963749156374915Humanname
401865760CV2779088single nucleotide variantNM_032306.4(ALKBH7):c.404T>C (p.Leu135Pro)not specified [RCV004348721]uncertain significance1963744906374490Humanname
401894452CV2788057single nucleotide variantNM_032306.4(ALKBH7):c.431G>A (p.Arg144Gln)not specified [RCV004359003]uncertain significance1963745176374517Humanname
405787656CV3264820single nucleotide variantNM_032306.4(ALKBH7):c.511G>A (p.Ala171Thr)not specified [RCV004398839]uncertain significance1963748186374818Humanname
405794596CV3264835single nucleotide variantNM_032306.4(ALKBH7):c.607C>T (p.Arg203Cys)not specified [RCV004400922]uncertain significance1963749146374914Humanname
407459265CV3451806single nucleotide variantNM_032306.4(ALKBH7):c.494A>G (p.Tyr165Cys)not specified [RCV004633552]uncertain significance1963745806374580Humanname
407459301CV3451816single nucleotide variantNM_032306.4(ALKBH7):c.409C>G (p.Leu137Val)not specified [RCV004633562]uncertain significance1963744956374495Humanname
597791467CV3679374single nucleotide variantNM_032306.4(ALKBH7):c.397G>A (p.Ala133Thr)not specified [RCV004933517]uncertain significance1963744836374483Humanname
597791340CV3682830single nucleotide variantNM_032306.4(ALKBH7):c.320T>A (p.Val107Glu)not specified [RCV004933475]uncertain significance1963743186374318Humanname
597791373CV3682841single nucleotide variantNM_032306.4(ALKBH7):c.598G>A (p.Val200Met)not specified [RCV004933486]uncertain significance1963749056374905Humanname
598254970CV3971265single nucleotide variantNM_032306.4(ALKBH7):c.340G>A (p.Ala114Thr)not specified [RCV005346479]uncertain significance1963743386374338Humanname
598255030CV3971274single nucleotide variantNM_032306.4(ALKBH7):c.341C>A (p.Ala114Asp)not specified [RCV005346487]uncertain significance1963743396374339Humanname
598255079CV3971284single nucleotide variantNM_032306.4(ALKBH7):c.482C>T (p.Pro161Leu)not specified [RCV005346495]uncertain significance1963745686374568Humanname