NM_000059.4:c.9104A>C

HGVS Expressions

  • NG_012772.3:g.69421A>C
  • NM_000059.4:c.9104A>C
  • NP_000050.3:p.Tyr3035Ser
  • NC_000013.11:g.32379900A>C

Associated Genes

BRCA2 Gene
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Clinvar Clinical Significance

Benign, Likely Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

38211

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
612555.13United Arab EmiratesUncertain SignificanceBreast-Ovarian Cancer, Familial, Susceptibility To, 2Al-Ali et al. 2023
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