NM_000256.3:c.776delinsTT

HGVS Expressions

  • NG_007667.1:g.9801delinsTT
  • NM_000256.3:c.776delinsTT
  • NP_000247.2:p.Ala259ValfsTer27
  • NC_000011.10:g.47347902delinsAA
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CTGA Clinical Significance

Likely Pathogenic

Variant Type

Indel

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615396.1United Arab Emirates1Likely PathogenicLeft Ventricular Noncompaction 10Al-Shamsi et al. 2016
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