NM_000492.4:c.80G>T

HGVS Expressions

  • NG_016465.4:g.43496G>T
  • NM_000492.4:c.80G>T
  • NP_000483.3:p.Gly27Val
  • NC_000007.14:g.117504279G>T
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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Clinvar

495958

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
219700.79.1United Arab Emirates2Likely PathogenicCystic FibrosisHafiz et al. 2023 Patient died at 27 years of age due to r...
219700.79.2United Arab Emirates2Likely PathogenicCystic FibrosisHafiz et al. 2023 Sister of 219700.79.1
219700.G.14.4United Arab EmiratesLikely PathogenicCystic FibrosisShafiq et al.2021 This variant was reported in 5% of patie...
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