NM_001089.2:c.4675C>T

HGVS Expressions

  • NG_011790.1:g.67416C>T
  • NM_001089.2:c.4675C>T
  • NP_001080.2:p.Arg1559Ter
  • NC_000016.10:g.2278331G>A
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Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
610921.3United Arab Emirates1Alsamri et al. 2021 Article does not list phenotype. Patient...
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