NM_182919.4:c.421C>T

HGVS Expressions

  • NG_031998.1:g.18786C>T
  • NM_182919.4:c.421C>T
  • NP_891549.1:p.Arg141Ter
  • NC_000019.10:g.4817957G>A
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Clinvar Clinical Significance

Risk factor

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

37265

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
614850.1.1Saudi Arabia2PathogenicHerpes Simplex Encephalitis, Susceptibility to, 4Sancho-Shimizu et al. 2011
614850.1.G.1Saudi Arabia5Sancho-Shimizu et al. 2011 Father, mother, 2 sisters and a brother ...
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