NM_000059.4:c.8782G>T

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  2. NM_000059.4:c.8782G>T

HGVS Expressions

  • NG_012772.3:g.68865G>T
  • NM_000059.4:c.8782G>T
  • NP_000050.3:p.Ala2928Ser
  • NC_000013.11:g.32379344G>T

Associated Genes

BRCA2 Gene
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Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

587781762

Clinvar

141459

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
612555.11AlgeriaUncertain SignificanceBreast-Ovarian Cancer, Familial, Susceptibility To, 2Al-Ali et al. 2023
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Contributors

  • Pratibha Nair: 24.01.2024

Edit History

  • Pratibha Nair: 24.01.2024
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.