NM_018725.4:c.529G>A

HGVS Expressions

  • NM_018725.4:c.529G>A
  • NP_061195.2:p.Gly177Arg
  • NC_000003.12:g.53855341G>A
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

2232337

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
249100.28Lebanon1Uncertain SignificanceFamilial Mediterranean FeverUmar et al, 2020
249100.34Lebanon1Uncertain SignificanceFamilial Mediterranean FeverUmar et al, 2020
249100.40Lebanon1Uncertain SignificanceFamilial Mediterranean FeverUmar et al, 2020
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