NM_000305.3:c.932C>G

  1. Home
  2. NM_000305.3:c.932C>G

HGVS Expressions

  • NG_008725.1:g.34610C>G
  • NM_000305.3:c.932C>G
  • NP_000296.2:p.Ser311Cys
  • NC_000007.14:g.95405463G>C

Associated Genes

Paraoxonase 2
Back to search Result
Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

7493

Clinvar

7084

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
602447.G.1United Arab Emirates1760.41BenignObineche et al. 2001 Study with 98 Left Ventricular Hypertrop...
Download Table

Contributors

  • Sayeeda Hana: 25.08.2022

Edit History

  • Sayeeda Hana: 02.09.2022
  • Sayeeda Hana: 27.08.2022
  • Sayeeda Hana: 25.08.2022
Back to search Result
© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.