PCSK9 c.1823G>T ;(p.C608F)

Variant ID: 1-55527189-G-T

NM_174936.3(PCSK9):c.1823G>T;(p.C608F)

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:

Patterns and tempo of PCSK9 pseudogenizations suggest an ancient divergence in mammalian cholesterol homeostasis mechanisms.

Genetica
van Asch, Barbara B; Teixeira da Costa, Luís Filipe LF
Publication Date: 2021-02

Variant appearance in text: PCSK9: C608F
PubMed Link: 33515402
Variant Present in the following documents:
  • Main text
  • 10709_2021_Article_113.pdf
View BVdb publication page