PTEN c.394_395delinsTT ;(p.G132F)

Variant ID: 10-89692910-GG-TT

NM_000314.4(PTEN):c.394_395delinsTT;(p.G132F)

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: G132F
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Hidden association of Cowden syndrome, PTEN mutation and meningioma frequency.

Oncoscience
Yakubov, Eduard E; Ghoochani, Ali A; Buslei, Rolf R; Buchfelder, Michael M; Eyüpoglu, Ilker Y IY; Savaskan, Nicolai N
Publication Date: 2016

Variant appearance in text: PTEN: G132F
PubMed Link: 27489861
Variant Present in the following documents:
  • Main text
  • oncoscience-03-149-s001.pdf
  • oncoscience-03-149.pdf
View BVdb publication page