NM_004304.5:c.4211T>C

HGVS Expressions

  • NG_009445.1:g.732691T>C
  • NM_004304.5:c.4211T>C
  • NP_004295.2:p.Leu1404Pro
Back to search Result
Genomic Location

chr2:29193876

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

645717

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.36LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B32' from family 36 in the publ...
© CAGS 2024. All rights reserved.