NM_004004.5:c.-22-12C>T

HGVS Expressions

  • NG_008358.1:g.8361C>T
  • NM_004004.5:c.-22-12C>T
  • NP_003995.2:p.?
  • NC_000013.11:g.20189615G>A
Back to search Result
Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

9578260

Clinvar

44717

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
220290.10United Arab Emirates1BenignTlili et al. 2017
© CAGS 2024. All rights reserved.