GLA c.691G>T ;(p.D231Y)

Variant ID: X-100653883-C-A

NM_000169.2(GLA):c.691G>T;(p.D231Y)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Detection of novel Fabry disease-associated pathogenic variants in Japanese patients by newborn and high-risk screening.

Molecular Genetics & Genomic Medicine
Sawada, Takaaki T; Kido, Jun J; Sugawara, Keishin K; Matsumoto, Shirou S; Takada, Fumio F; Tsuboi, Kazuya K; Ohtake, Akira A; Endo, Fumio F; Nakamura, Kimitoshi K
Publication Date: 2020-11

Variant appearance in text: GLA: D231Y
PubMed Link: 33016649
Variant Present in the following documents:
  • Main text
  • MGG3-8-e1502.pdf
View BVdb publication page



Fabry disease screening in high-risk populations in Japan: a nationwide study.

Orphanet Journal Of Rare Diseases
Yoshida, Shinichiro S; Kido, Jun J; Sawada, Takaaki T; Momosaki, Ken K; Sugawara, Keishin K; Matsumoto, Shirou S; Endo, Fumio F; Nakamura, Kimitoshi K
Publication Date: 2020-08-26

Variant appearance in text: GLA: D231Y
PubMed Link: 32843101
Variant Present in the following documents:
  • Main text
  • 13023_2020_Article_1494.pdf
View BVdb publication page



Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: GLA: D231Y
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page