NM_003072.5:c.1098C>G

HGVS Expressions

  • NG_011556.2:g.31983C>G
  • NM_003072.5:c.1098C>G
  • NP_003063.2:p.Ile366Met
Back to search Result
Genomic Location

chr19:10987904

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

484848

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.45LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B41' from family 18 in the publ...
© CAGS 2024. All rights reserved.