NM_000170.3:c.(?_1927)_(2052_?)del

HGVS Expressions

  • NM_000170.3:c.(?_1927)_(2052_?)del
  • NC_000009.12:g.(?_6558559)_(6558684_?)del

Associated Genes

Glycine Decarboxylase
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CTGA Clinical Significance

Likely Pathogenic

Variant Type

Deletion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
605899.5United Arab Emirates2Likely PathogenicGlycine EncephalopathyElabd et al. 2021
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