NM_000180.4:c.1401dup

HGVS Expressions

  • NG_009092.1:g.9413dup
  • NM_000180.4:c.1401dup
  • NP_000171.1:p.Leu468SerfsTer89
  • NC_000017.11:g.8007082dup
Back to search Result
Clinvar Clinical Significance

Likely Pathogenic

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Duplication

Clinvar

3067973

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
204000.10Saudi Arabia2Likely PathogenicLeber Congenital Amaurosis 1Khan et al. 2014
204000.12Saudi Arabia2Likely PathogenicLeber Congenital Amaurosis 1Khan et al. 2014
© CAGS 2024. All rights reserved.