NM_000059.4:c.9613_9614delinsCT

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HGVS Expressions

  • NG_012772.3:g.86530_86531delinsCT
  • NM_000059.4:c.9613_9614delinsCT
  • NP_000050.2:p.Ala3205Leu
  • NC_000013.11:g.32397009_32397010delinsCT

Associated Genes

BRCA2 Gene
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Clinvar Clinical Significance

Likely Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Indel

dbSNP

276174926

Clinvar

52875

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.110Lebanon0.2Uncertain SignificanceBreast CancerEl Saghir et al. 2015 Patient with stage III ductal carcinoma
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Contributors

  • Asha Deepthi: 17.01.2021

Edit History

  • Asha Deepthi: 17.01.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.