NM_000059.4:c.9104A>C

  1. Home
  2. 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
Back to search Result
Clinvar Clinical Significance

Benign, Likely Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

80359165

Clinvar

38211

Epidemiology in the Arab World

View Map
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
Download Table

Contributors

  • Pratibha Nair: 25.01.2024

Edit History

  • Pratibha Nair: 25.01.2024
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.