PTPN22 c.1196C>T ;(p.T399I)

Variant ID: 1-114380826-G-A

NM_015967.5(PTPN22):c.1196C>T;(p.T399I)

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:

Genetic susceptibility to delayed graft function following kidney transplantation: a systematic review of the literature.

Clinical Kidney Journal
Huart, Justine J; Krzesinski, Jean-Marie JM; Jouret, François F
Publication Date: 2018-08

Variant appearance in text: PTPN22: T399I
PubMed Link: 30090630
Variant Present in the following documents:
  • Main text
View BVdb publication page