SIRPG c.987C>A ;(p.C329*)

Variant ID: 20-1616007-G-T

NM_018556.3(SIRPG):c.987C>A;(p.C329*)

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:

Association of protein function-altering variants with cardiometabolic traits: the strong heart study.

Scientific Reports
Shan, Yue Y; Cole, Shelley A SA; Haack, Karin K; Melton, Phillip E PE; Best, Lyle G LG; Bizon, Christopher C; Kobes, Sayuko S; Köroğlu, Çiğdem Ç; Baier, Leslie J LJ; Hanson, Robert L RL; Sanna, Serena S; Li, Yun Y; Franceschini, Nora N
Publication Date: 2022-06-04

Variant appearance in text: SIRPG: C329X; rs757606654
PubMed Link: 35665752
Variant Present in the following documents:
  • 41598_2022_12866_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page