PAH c.907T>G ;(p.S303A)

Variant ID: 12-103245470-A-C

NM_000277.1(PAH):c.907T>G;(p.S303A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


An Updated PAH Mutational Spectrum of Phenylketonuria in Mexican Patients Attending a Single Center: Biochemical, Clinical-Genotyping Correlations.

Genes
Vela-Amieva, Marcela M; Alcántara-Ortigoza, Miguel Angel MA; Ibarra-González, Isabel I; González-Del Angel, Ariadna A; Fernández-Hernández, Liliana L; Guillén-López, Sara S; López-Mejía, Lizbeth L; Carrillo-Nieto, Rosa Itzel RI; Belmont-Martínez, Leticia L; Fernández-Lainez, Cynthia C
Publication Date: 2021-10-23

Variant appearance in text: PAH: Ser303Ala
PubMed Link: 34828281
Variant Present in the following documents:
  • Main text
  • genes-12-01676.pdf
View BVdb publication page



Predicted effects of missense mutations on native-state stability account for phenotypic outcome in phenylketonuria, a paradigm of misfolding diseases.

American Journal Of Human Genetics
Pey, Angel L AL; Stricher, Francois F; Serrano, Luis L; Martinez, Aurora A
Publication Date: 2007-11

Variant appearance in text: PAH: S303A
PubMed Link: 17924342
Variant Present in the following documents:
  • Main text
View BVdb publication page