NM_033084.6:c.1348A>G

HGVS Expressions

  • NG_007311.1:g.26558A>G
  • NM_033084.6:c.1348A>G
  • NP_149075.2:p.Ile450Val

Associated Genes

FANCD2 Gene
Back to search Result
Genomic Location

chr3:10047986

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

456344

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.52LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B48' from family 38 in the publ...
© CAGS 2024. All rights reserved.