NM_001160372.4:c.167_187dup

HGVS Expressions

  • NG_016478.3:g.12373_12393dup
  • NM_001160372.4:c.167_187dup
  • NP_001153844.1:p.Arg56_Pro62dup
  • NC_000008.11:g.140451188_140451208dup
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Duplication

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
613192.1Egypt2Uncertain SignificanceIntellectual Developmental Disorder, Autosomal Recessive 13Reuter et al. 2017 Authors classified the CLMN gene variant...
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