NM_000329.3:c.310G>C

HGVS Expressions

  • NG_008472.2:g.10141G>C
  • NM_000329.3:c.310G>C
  • NP_000320.1:p.Gly104Arg
  • NC_000001.11:g.68444819C>G
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Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

978980

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
204100.G.2Saudi Arabia4+PathogenicLeber Congenital Amaurosis 2Patel et al. 2016 Family with unknown number of affected m...
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