NM_015158.5:c.1079G>A

HGVS Expressions

  • NG_016331.2:g.246552G>A
  • NM_015158.5:c.1079G>A
  • NP_055973.2:p.Ser360Asn
  • NC_000009.12:g.711845G>A
Back to search Result
CTGA Clinical Significance

Benign

Variant Type

Substitution

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608776.1United Arab Emirates2BenignAl-Shamsi et al. 2016
© CAGS 2024. All rights reserved.