NM_000251.3:c.1787A>G

  1. Home
  2. NM_000251.3:c.1787A>G

HGVS Expressions

  • NG_007110.2:g.76929A>G
  • NM_000251.3:c.1787A>G
  • NP_000242.1:p.Asn596Ser

Associated Genes

Muts Homolog 2
Back to search Result
Genomic Location

chr2:47475052

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

41295288

Clinvar

41646

Epidemiology in the Arab World

View Map
Download Table

Contributors

  • Asha Deepthi: 15.09.2020

Edit History

  • Asha Deepthi: 26.01.2021
  • Asha Deepthi: 05.10.2020
  • Asha Deepthi: 15.09.2020
Back to search Result
© CAGS 2025. All rights reserved.
© CAGS 2025. All rights reserved.