NM_004035.7:c.1165A>G

HGVS Expressions

  • NG_008190.1:g.33457A>G
  • NM_004035.7:c.1165A>G
  • NP_004026.2:p.Ile389Val
  • NC_000017.11:g.75950907T>C
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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
610217.1United Arab Emirates2Al-Shamsi et al. 2016 Reported with a variant in PLA2G6: UC003...
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