NM_138450.6:c.571G>A

HGVS Expressions

  • NG_021342.1:g.7720G>A
  • NM_138450.6:c.571G>A
  • NP_612459.1:p.Gly191Arg
Back to search Result
Genomic Location

chr13:49631018

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.39LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B35' from family 12 in the publ...
© CAGS 2024. All rights reserved.