PDE11A c.263C>T ;(p.P88L)

Variant ID: 2-178936902-G-A

NM_016953.3(PDE11A):c.263C>T;(p.P88L)

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:

ARMC5 Alterations in Patients With Sporadic Neuroendocrine Tumors and Multiple Endocrine Neoplasia Type 1 (MEN1).

The Journal Of Clinical Endocrinology And Metabolism
Damjanovic, Svetozar S SS; Antic, Jadranka A JA; Elezovic-Kovacevic, Valentina I VI; Dundjerovic, Dusko M DM; Milicevic, Ivana T IT; Beleslin-Cokic, Bojana B BB; Ilic, Bojana B BB; Rodic, Gordana S GS; Berthon, Annabel A; Maria, Andrea Gutierrez AG; Faucz, Fabio R FR; Stratakis, Constantine A CA
Publication Date: 2020-12-01

Variant appearance in text: PDE11A: P88L
PubMed Link: 32901291
Variant Present in the following documents:
  • Main text
View BVdb publication page