NM_007294.4:c.5260G>C

HGVS Expressions

  • NG_005905.2:g.160915G>C
  • NM_007294.4:c.5260G>C
  • NP_009225.1:p.Glu1754Gln
  • NC_000017.11:g.43057069C>G

Associated Genes

Breast Cancer 1 Gene
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Clinvar Clinical Significance

Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

462666

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
604370.8United Arab EmiratesUncertain SignificanceBreast-Ovarian Cancer, Familial, Susceptibility to, 1Al-Ali et al. 2023
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