NM_000059.4:c.8851G>A

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HGVS Expressions

  • NG_012772.3:g.68934G>A
  • NM_000059.4:c.8851G>A
  • NP_000050.3:p.Ala2951Thr

Associated Genes

BRCA2 Gene
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Genomic Location

chr13:32379413

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

11571769

Clinvar

41570

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.16LebanonBenignBreast CancerJalkh et al, 2012
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Contributors

  • Asha Deepthi: 10.06.2020

Edit History

  • Asha Deepthi: 11.06.2020
  • Asha Deepthi: 10.06.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.