NM_000492.3:c.1993A>T

HGVS Expressions

  • NG_016465.4:g.131377A>T
  • NM_000492.3:c.1993A>T
  • NP_000483.3:p.Thr665Ser
  • NC_000007.14:g.117592160A>T
Back to search Result
Clinvar Clinical Significance

Likely Pathogenic

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Clinvar

993031

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
219700.47Tunisia1NALikely PathogenicCystic FibrosisMessaoud et al. 2005
© CAGS 2024. All rights reserved.