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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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