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Variants search result for Homo sapiens
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18 records found for search term Maf1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598183731CV3992270single nucleotide variantNM_032272.5(MAF1):c.84G>A (p.Arg28=)not specified [RCV005372977]likely benign8144105869144105869Humanname
155927707CV2285228single nucleotide variantNM_032272.5(MAF1):c.25T>C (p.Phe9Leu)not specified [RCV004145429]uncertain significance8144105708144105708Humanname
598164627CV3992272single nucleotide variantNM_032272.5(MAF1):c.61G>A (p.Gly21Arg)not specified [RCV005369036]uncertain significance8144105744144105744Humanname
155928918CV2224460single nucleotide variantNM_032272.5(MAF1):c.233G>C (p.Gly78Ala)not specified [RCV004098058]uncertain significance8144106096144106096Humanname
155973253CV2271623single nucleotide variantNM_032272.5(MAF1):c.240G>C (p.Glu80Asp)not specified [RCV004130487]likely benign8144106103144106103Humanname
156239206CV2285952single nucleotide variantNM_032272.5(MAF1):c.190A>C (p.Thr64Pro)not specified [RCV004143870]uncertain significance8144105975144105975Humanname
407468726CV3449536single nucleotide variantNM_032272.5(MAF1):c.206C>T (p.Pro69Leu)not specified [RCV004636386]uncertain significance8144105991144105991Humanname
407468729CV3449538single nucleotide variantNM_032272.5(MAF1):c.244G>A (p.Gly82Ser)not specified [RCV004636387]uncertain significance8144106107144106107Humanname
156057299CV2239068single nucleotide variantNM_032272.5(MAF1):c.674G>A (p.Gly225Glu)not specified [RCV004112074]uncertain significance8144106888144106888Humanname
155923883CV2347577single nucleotide variantNM_032272.5(MAF1):c.709G>A (p.Gly237Ser)not specified [RCV004200515]uncertain significance8144106923144106923Humanname
156148800CV2358115single nucleotide variantNM_032272.5(MAF1):c.736A>G (p.Met246Val)not specified [RCV004211924]uncertain significance8144106950144106950Humanname
401769840CV2693069single nucleotide variantNM_032272.5(MAF1):c.679G>A (p.Glu227Lys)not specified [RCV004308613]uncertain significance8144106893144106893Humanname
405651050CV3281304single nucleotide variantNM_032272.5(MAF1):c.340C>G (p.Arg114Gly)not specified [RCV004413428]uncertain significance8144106203144106203Humanname
405651052CV3281305single nucleotide variantNM_032272.5(MAF1):c.686T>A (p.Val229Glu)not specified [RCV004413429]likely benign8144106900144106900Humanname
407484099CV3449537single nucleotide variantNM_032272.5(MAF1):c.705C>G (p.Ser235Arg)not specified [RCV004640471]uncertain significance8144106919144106919Humanname
597646862CV3693988single nucleotide variantNM_032272.5(MAF1):c.721G>A (p.Glu241Lys)not specified [RCV004942552]uncertain significance8144106935144106935Humanname
597646868CV3693989single nucleotide variantNM_032272.5(MAF1):c.638C>T (p.Pro213Leu)not specified [RCV004942553]uncertain significance8144106852144106852Humanname
598183738CV3992271single nucleotide variantNM_032272.5(MAF1):c.723G>T (p.Glu241Asp)not specified [RCV005372978]uncertain significance8144106937144106937Humanname