NM_000059.4:c.5612G>A

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  2. NM_000059.4:c.5612G>A

HGVS Expressions

  • NG_012772.3:g.29488G>A
  • NM_000059.4:c.5612G>A
  • NP_000050.2:p.Ser1871Asn
  • NC_000013.11:g.32339967G>A

Associated Genes

BRCA2 Gene
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Clinvar Clinical Significance

Likely Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

80358782

Clinvar

51891

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.96Lebanon0.2Uncertain SignificanceBreast CancerEl Saghir et al. 2015 Patient with stage II ductal carcinoma
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Contributors

  • Asha Deepthi: 14.01.2021

Edit History

  • Asha Deepthi: 17.01.2021
  • Asha Deepthi: 14.01.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.