NM_000059.4:c.6841+80_6841+83delTTAA

HGVS Expressions

  • NG_012772.3:g.30797_30800del
  • NM_000059.4:c.6841+80_6841+83delTTAA

Associated Genes

BRCA2 Gene
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Genomic Location

chr13:32341276-32341279

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Deletion

Clinvar

126122

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.1.36LebanonBenignBreast CancerJalkh et al, 2012 10 unrelated patients with breast cancer
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