NM_000059.4:c.8775G>C

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HGVS Expressions

  • NG_012772.3:g.68858G>C
  • NM_000059.4:c.8775G>C
  • NP_000050.3:p.Gln2925His

Associated Genes

BRCA2 Gene
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Genomic Location

chr13:32379337

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

80359136

Clinvar

52678

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.30LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B24' from family 5 in the publi...
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Contributors

  • Asha Deepthi: 31.08.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 30.09.2020
  • Asha Deepthi: 31.08.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.