NM_001048174.2:c.1174C>A

HGVS Expressions

  • NG_008189.1:g.13986C>A
  • NM_001048174.2:c.1174C>A
  • NP_001041639.1:p.Leu392Met

Associated Genes

MutY DNA Glycosylase
Back to search Result
Genomic Location

chr1:45331485

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

41752

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.32LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B26' from family 7 in the publi...
© CAGS 2024. All rights reserved.