Bibliome.ai browser hg19
Search
About
Stats
FAQ
PCSK9 c.853_855delinsATC ;(p.V285I)
Variant ID: 1-55521719-GTG-ATC
NM_174936.3(
PCSK9
):c.853_855delinsATC;(p.V285I)
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:
Human GPR17 missense variants identified in metabolic disease patients have distinct downstream signaling profiles.
The Journal Of Biological Chemistry
Conley, Jason M JM; Sun, Hongmao H; Ayers, Kristin L KL; Zhu, Hu H; Chen, Rong R; Shen, Min M; Hall, Matthew D MD; Ren, Hongxia H
Publication Date: 2021-07
Variant appearance in text: PCSK9: V285I
PubMed Link:
34144038
Variant Present in the following documents:
Main text
main.pdf
View BVdb publication page