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Variants search result for Homo sapiens
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28 records found for search term Elmod1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401905721CV2809834single nucleotide variantNM_018712.4(ELMOD1):c.54A>G (p.Lys18=)not provided [RCV003396065]likely benign11107630453107630453Humanname
156299832CV2244807single nucleotide variantNM_018712.4(ELMOD1):c.20T>C (p.Met7Thr)not specified [RCV004102784]uncertain significance11107630419107630419Humanname
156147338CV2265196single nucleotide variantNM_018712.4(ELMOD1):c.31G>C (p.Val11Leu)not specified [RCV004126316]uncertain significance11107630430107630430Humanname
407506690CV3438313single nucleotide variantNM_018712.4(ELMOD1):c.49T>G (p.Cys17Gly)not specified [RCV004624783]uncertain significance11107630448107630448Humanname
597666544CV3670990single nucleotide variantNM_018712.4(ELMOD1):c.79G>A (p.Val27Ile)not specified [RCV004912567]uncertain significance11107630478107630478Humanname
156168777CV2197716single nucleotide variantNM_018712.4(ELMOD1):c.223G>A (p.Asp75Asn)not specified [RCV004074921]uncertain significance11107631610107631610Humanname
156201485CV2256167single nucleotide variantNM_018712.4(ELMOD1):c.226G>A (p.Ala76Thr)not specified [RCV004116438]uncertain significance11107631613107631613Humanname
329382733CV2424537single nucleotide variantNM_018712.4(ELMOD1):c.280G>A (p.Val94Ile)not specified [RCV004254038]likely benign11107631667107631667Humanname
401726016CV2699028single nucleotide variantNM_018712.4(ELMOD1):c.102A>T (p.Arg34Ser)not specified [RCV004303550]uncertain significance11107630501107630501Humanname
401764823CV2728094single nucleotide variantNM_018712.4(ELMOD1):c.212G>A (p.Ser71Asn)not specified [RCV004324193]uncertain significance11107631599107631599Humanname
407506692CV3438314single nucleotide variantNM_018712.4(ELMOD1):c.115C>T (p.Arg39Trp)not specified [RCV004624784]uncertain significance11107630514107630514Humanname
407506695CV3438315single nucleotide variantNM_018712.4(ELMOD1):c.178G>A (p.Asp60Asn)not specified [RCV004624785]uncertain significance11107630714107630714Humanname
156383599CV2220123single nucleotide variantNM_018712.4(ELMOD1):c.785A>G (p.Asn262Ser)not specified [RCV004093978]uncertain significance11107656019107656019Humanname
156044815CV2308032single nucleotide variantNM_018712.4(ELMOD1):c.748C>A (p.Leu250Ile)not specified [RCV004170460]uncertain significance11107655982107655982Humanname
156103279CV2313725single nucleotide variantNM_018712.4(ELMOD1):c.846T>G (p.His282Gln)not specified [RCV004157639]uncertain significance11107665038107665038Humanname
155968972CV2337899single nucleotide variantNM_018712.4(ELMOD1):c.902G>A (p.Arg301His)not specified [RCV004183907]uncertain significance11107665094107665094Humanname
329381419CV2437480single nucleotide variantNM_018712.4(ELMOD1):c.614C>T (p.Pro205Leu)not specified [RCV004258771]uncertain significance11107650394107650394Humanname
329362714CV2439129single nucleotide variantNM_018712.4(ELMOD1):c.338G>C (p.Arg113Thr)not specified [RCV004266416]uncertain significance11107635683107635683Humanname
401765431CV2712718single nucleotide variantNM_018712.4(ELMOD1):c.854A>G (p.His285Arg)not specified [RCV004308025]uncertain significance11107665046107665046Humanname
401743507CV2715498single nucleotide variantNM_018712.4(ELMOD1):c.662C>T (p.Ala221Val)not specified [RCV004326592]uncertain significance11107654186107654186Humanname
405738918CV3248550single nucleotide variantNM_018712.4(ELMOD1):c.563C>T (p.Ala188Val)not specified [RCV004380253]uncertain significance11107650343107650343Humanname
405738925CV3248551single nucleotide variantNM_018712.4(ELMOD1):c.607C>T (p.Leu203Phe)not specified [RCV004380254]uncertain significance11107650387107650387Humanname
405738933CV3248552single nucleotide variantNM_018712.4(ELMOD1):c.845A>G (p.His282Arg)not specified [RCV004380255]uncertain significance11107665037107665037Humanname
405738940CV3248553single nucleotide variantNM_018712.4(ELMOD1):c.941T>G (p.Leu314Arg)not specified [RCV004380256]uncertain significance11107665133107665133Humanname
405738946CV3248554single nucleotide variantNM_018712.4(ELMOD1):c.976G>A (p.Ala326Thr)not specified [RCV004380257]uncertain significance11107665168107665168Humanname
407506688CV3438312single nucleotide variantNM_018712.4(ELMOD1):c.920G>T (p.Arg307Leu)not specified [RCV004624782]uncertain significance11107665112107665112Humanname
597746988CV3670991single nucleotide variantNM_018712.4(ELMOD1):c.349G>A (p.Ala117Thr)not specified [RCV004922811]uncertain significance11107635694107635694Humanname
598191184CV3957782single nucleotide variantNM_018712.4(ELMOD1):c.674A>C (p.Lys225Thr)not specified [RCV005334801]uncertain significance11107654198107654198Humanname