NM_000059.4:c.65C>T

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HGVS Expressions

  • NG_012772.3:g.6046C>T
  • NM_000059.4:c.65C>T
  • NP_000050.3:p.Ala22Val

Associated Genes

BRCA2 Gene
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Genomic Location

chr13:32316525

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.26LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B19' from family 1 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.