NM_000455.5:c.1211C>T

HGVS Expressions

  • NG_007460.2:g.42150C>T
  • NM_000455.5:c.1211C>T
  • NP_000446.1:p.Ser404Phe
Back to search Result
Genomic Location

chr19:1226556

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

127700

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.40LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B36' from family 13 in the publ...
© CAGS 2024. All rights reserved.