Bibliome.ai browser hg19
Search
About
Stats
FAQ
PTEN c.394_396delinsTGA ;(p.G132*)
Variant ID: 10-89692910-GGT-TGA
NM_000314.4(
PTEN
):c.394_396delinsTGA;(p.G132*)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Hidden association of Cowden syndrome, PTEN mutation and meningioma frequency.
Oncoscience
Yakubov, Eduard E; Ghoochani, Ali A; Buslei, Rolf R; Buchfelder, Michael M; EyĆ¼poglu, Ilker Y IY; Savaskan, Nicolai N
Publication Date: 2016
Variant appearance in text: PTEN: Gly132Ter
PubMed Link:
27489861
Variant Present in the following documents:
oncoscience-03-149-s001.pdf
View BVdb publication page