CGN c.2091T>A ;(p.C697*)

Variant ID: 1-151502020-T-A

NM_020770.2(CGN):c.2091T>A;(p.C697*)

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:

Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) in the Brain and Relevance for Neuropsychiatric Disorders.

Frontiers In Neuroscience
O'Connell, Emma M EM; Lohoff, Falk W FW
Publication Date: 2020

Variant appearance in text: CGN: C697X
PubMed Link: 32595449
Variant Present in the following documents:
  • Main text
  • fnins-14-00609.pdf
View BVdb publication page