NM_024576.5:c.75del

HGVS Expressions

  • NM_024576.5:c.75del
  • NP_078852.3:p.Asp26ThrfsTer93
  • NC_000006.12:g.71289011del
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CTGA Clinical Significance

Likely Pathogenic

Variant Type

Deletion

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
118400.1.1Syria2Likely PathogenicCherubism
118400.1.2Syria2Likely PathogenicCherubism Brother of 118400.1.1
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