PTEN c.473T>C ;(p.V158A)

Variant ID: 10-89692989-T-C

NM_000314.4(PTEN):c.473T>C;(p.V158A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: PTEN: V158A
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



HPV E6 and MAGUK protein interactions: determination of the molecular basis for specific protein recognition and degradation.

Oncogene
Thomas, M M; Glaunsinger, B B; Pim, D D; Javier, R R; Banks, L L
Publication Date: 2001-09-06

Variant appearance in text: PTEN: V158A
PubMed Link: 11571640
Variant Present in the following documents:
  • Main text
View BVdb publication page