NM_000059.4:c.9152del

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HGVS Expressions

  • NG_012772.3:g.69562del
  • NM_000059.4:c.9152del
  • NP_000050.3:p.Pro3051HisfsTer11
  • NC_000013.11:g.32380041del

Associated Genes

BRCA2 Gene
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Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Indel

dbSNP

587779349

Clinvar

127241

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
613029.1Saudi Arabia2PathogenicGlioma Susceptibility 3Alazami et al. 2015; Shaheen et al. 2019
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Contributors

  • Sayeeda Hana: 08.01.2022

Edit History

  • Sayeeda Hana: 19.01.2022
  • Sayeeda Hana: 08.01.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.