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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.
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: 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