NM_001558.3:c.475A>G

HGVS Expressions

  • NG_016275.1:g.11958A>G
  • NM_001558.3:c.475A>G
  • NP_001549.2:p.Ser159Gly
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Genomic Location

chr11:117993348

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

3135932

Clinvar

197197

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
266600.G.2.1Lebanon19.083BenignInflammatory Bowel Disease 1Ghaith et al. 2010 Study of a group of 228 patients with IB...
266600.G.2.2Lebanon21.092BenignGhaith et al. 2010 Study of a group of 228 controls
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