NM_000542.3:c.1039-6C>G

HGVS Expressions

  • NM_000542.3:c.1039-6C>G
  • NP_000533.3:p.?
  • NC_000002.12:g.85662115G>C
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
265120.2United Arab Emirates1Uncertain SignificanceSurfactant Metabolism Dysfunction, Pulmonary, 1Alsamri et al. 2021 No clinical significance prediction is p...
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