NM_016316.4:c.-10-115_-10-114insACTTG

HGVS Expressions

  • NM_016316.4:c.-10-115_-10-114insACTTG
  • NP_057400.1:p.?
  • NC_000002.12:g.99465099_99465100insCAAGT
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Variant Type

Insertion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605977.G.1United Arab Emirates0.487Almheiri et al. 2019 500 healthy Emiratis (254 females)
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