PTPN22 c.2083C>G ;(p.P695A)

Variant ID: 1-114372622-G-C

NM_015967.5(PTPN22):c.2083C>G;(p.P695A)

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:

The autoimmunity risk variant LYP-W620 cooperates with CSK in the regulation of TCR signaling.

Plos One
de la Puerta, María Luisa ML; Trinidad, Antonio G AG; Rodríguez, María del Carmen Mdel C; de Pereda, José María JM; Sánchez Crespo, Mariano M; Bayón, Yolanda Y; Alonso, Andrés A
Publication Date: 2013

Variant appearance in text: PTPN22: P695A
PubMed Link: 23359562
Variant Present in the following documents:
  • Main text
  • pone.0054569.pdf
View BVdb publication page