NM_014974.3:c.3283C>T

HGVS Expressions

  • NM_014974.3:c.3283C>T
  • NP_055789.1:p.Arg1095Trp
  • NC_000010.11:g.345059G>A
Back to search Result
CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
611380.1.1Saudi Arabia2NAUncertain SignificanceMaddirevula et al. 2018
611380.1.2Saudi Arabia2NAUncertain SignificanceMaddirevula et al. 2018 Relative of 611380.1.1
© CAGS 2024. All rights reserved.