NM_001098668.3:c.73G>A

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  2. NM_001098668.3:c.73G>A

HGVS Expressions

  • NG_013046.1:g.5997G>A
  • NM_001098668.3:c.73G>A
  • NP_001092138.1:p.Val25Ile
  • NC_000010.11:g.79559411C>T

Associated Genes

Surfactant, Pulmonary-Associated Protein A2
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CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

dbSNP

753973926

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
178642.1.1United Arab Emirates1Likely BenignAlsamri et al. 2021 Variant classified as likely benign.
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Contributors

  • Sami Bizzari: 14.06.2022

Edit History

  • Sami Bizzari: 18.07.2022
  • Sami Bizzari: 14.06.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.