NM_000059.4:c.7558C>T

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HGVS Expressions

  • NG_012772.3:g.46071C>T
  • NM_000059.4:c.7558C>T
  • NP_000050.3:p.Arg2520Ter
  • NC_000013.11:g.32356550C>T

Associated Genes

BRCA2 Gene
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Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

dbSNP

80358981

Clinvar

52353

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
612555.7United Arab EmiratesLikely PathogenicProstate CancerAl-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.