NM_000017.4:c.625G>A

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  2. NM_000017.4:c.625G>A

HGVS Expressions

  • NG_007991.1:g.17513G>A
  • NM_000017.4:c.625G>A
  • NP_000008.1:p.Gly209Ser
  • NC_000012.12:g.120738280G>A

Associated Genes

Acyl-CoA Dehydrogenase, Short-Chain
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Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1799958

Clinvar

3831

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
178500.2.1United Arab Emirates1BenignAlsamri et al. 2020; Alsamri et al. 2021
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Contributors

  • Pratibha Nair: 24.02.2022

Edit History

  • Sami Bizzari: 24.01.2024
  • Pratibha Nair: 24.02.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.