NM_004612.4:c.52_54GCG[6]

HGVS Expressions

  • NG_007461.1:g.5128_5130GCG[6]
  • NM_004612.4:c.52_54GCG[6]
  • NP_004603.1:p.Ala24_Ala26del
  • NC_000009.12:g.99105257_99105259GCG[6]
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Clinvar Clinical Significance

Benign, Likely Benign

Variant Type

Microsatellite

Clinvar

165381

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114500.G.1.1Lebanon180.09Colorectal CancerIbrahim et al. 2014 Study with 96 colorectal cancer patients...
114500.G.1.2Lebanon170.09Ibrahim et al. 2014 Group consisting of 97 control subjects
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