NM_033028.5:c.262del

HGVS Expressions

  • NG_009416.3:g.34127del
  • NM_033028.5:c.262del
  • NP_149017.2:p.Glu88AsnfsTer54
  • NC_000015.10:g.72715332del

Associated Genes

BBS4 Gene
Back to search Result
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
268000.G.8Saudi Arabia2+Likely PathogenicRetinitis PigmentosaPatel et al. 2016 Family with unknown number of affected m...
© CAGS 2024. All rights reserved.