NM_000159.4:c.242C>T

HGVS Expressions

  • NG_009292.1:g.5786C>T
  • NM_000159.4:c.242C>T
  • NP_000150.1:p.Pro81Leu
  • NC_000019.10:g.12891945C>T
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CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
231670.1United Arab Emirates2Likely PathogenicGlutaric Acidemia IAl-Shamsi et al. 2014
231670.G.1United Arab Emirates2Likely PathogenicGlutaric Acidemia IAl-Jasmi at al. 2016; Saleh et al. 2021 Mutations identified in two Emirati pati...
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