NM_020937.4:c.5224A>G

HGVS Expressions

  • NG_007417.1:g.58314A>G
  • NM_020937.4:c.5224A>G
  • NP_065988.1:p.Ile1742Val

Associated Genes

FANCM Gene
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Genomic Location

chr14:45189246

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

241324

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.48LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B44' from family 21 in the publ...
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