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11 records found for search term Defa6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156090048CV2241513single nucleotide variantNM_001926.4(DEFA6):c.64C>T (p.Leu22Phe)not specified [RCV004104414]uncertain significance869259726925972Humanname
155911158CV2303760single nucleotide variantNM_001926.4(DEFA6):c.181C>G (p.Leu61Val)not specified [RCV004163610]uncertain significance869258556925855Humanname
156075384CV2321781single nucleotide variantNM_001926.4(DEFA6):c.244G>C (p.Glu82Gln)not specified [RCV004179771]uncertain significance869248776924877Humanname
405668635CV3240139single nucleotide variantNM_001926.4(DEFA6):c.120G>T (p.Glu40Asp)not specified [RCV004368191]uncertain significance869259166925916Humanname
405668640CV3240140single nucleotide variantNM_001926.4(DEFA6):c.151G>A (p.Val51Ile)not specified [RCV004368192]likely benign869258856925885Humanname
405668644CV3240141single nucleotide variantNM_001926.4(DEFA6):c.169G>A (p.Ala57Thr)not specified [RCV004368193]uncertain significance869258676925867Humanname
405668647CV3240142single nucleotide variantNM_001926.4(DEFA6):c.251C>A (p.Ser84Tyr)not specified [RCV004368194]uncertain significance869248706924870Humanname
407465670CV3426746single nucleotide variantNM_001926.4(DEFA6):c.127G>A (p.Gly43Arg)not specified [RCV004613767]uncertain significance869259096925909Humanname
597640722CV3658528single nucleotide variantNM_001926.4(DEFA6):c.196T>A (p.Ser66Thr)not specified [RCV004908975]uncertain significance869249256924925Humanname
598223656CV3956517single nucleotide variantNM_001926.4(DEFA6):c.187G>C (p.Ala63Pro)not specified [RCV005318108]uncertain significance869258496925849Humanname
15197765CV700640single nucleotide variantNM_001926.4(DEFA6):c.105G>C (p.Glu35Asp)not provided [RCV000956557]benign869259316925931Humanname