NM_020166.5:c.1267+3A>C

HGVS Expressions

  • NG_008100.1:g.63014A>C
  • NM_020166.5:c.1267+3A>C
  • NC_000003.12:g.183041564T>G
Back to search Result
CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
210200.G.3JordanNANALikely Pathogenic3-Methylcrotonyl-CoA Carboxylase 1 DeficiencyAl-Jasmi at al. 2016 UAE resident(s) of Jordanian origin. Num...
© CAGS 2024. All rights reserved.