NM_000059.4:c.6842G>A

HGVS Expressions

  • NG_012772.3:g.34079G>A
  • NM_000059.4:c.6842G>A
  • NP_000050.3:p.Gly2281Glu
  • NC_000013.11:g.32344558G>A

Associated Genes

BRCA2 Gene
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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

926077

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.112United Arab EmiratesNANAUncertain SignificanceBreast CancerDeuitch et al. 2020 Patient was also identified with a 'like...
612555.12United Arab EmiratesUncertain SignificanceBreast-Ovarian Cancer, Familial, Susceptibility To, 2Al-Ali et al. 2023
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