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PTEN c.886_887delinsGC ;(p.C296A)
Variant ID: 10-89720735-TG-GC
NM_000314.4(
PTEN
):c.886_887delinsGC;(p.C296A)
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:
NO signaling and S-nitrosylation regulate PTEN inhibition in neurodegeneration.
Molecular Neurodegeneration
Kwak, Young-Don YD; Ma, Tao T; Diao, Shiyong S; Zhang, Xue X; Chen, Yaomin Y; Hsu, Janet J; Lipton, Stuart A SA; Masliah, Eliezer E; Xu, Huaxi H; Liao, Francesca-Fang FF
Publication Date: 2010-11-10
Variant appearance in text: PTEN: C296A
PubMed Link:
21067594
Variant Present in the following documents:
Main text
1750-1326-5-49.pdf
View BVdb publication page