NM_024110.4:c.239G>A

HGVS Expressions

  • NG_032778.1:g.17689G>A
  • NM_024110.4:c.239G>A
  • NP_077015.2:p.Arg80Gln
  • NC_000017.11:g.80182680G>A
Back to search Result
Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

1516066

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
249100.10Lebanon1Uncertain SignificanceUmar et al, 2020
© CAGS 2024. All rights reserved.