PRRT2 c.806T>C ;(p.I269T)

Variant ID: 16-29825181-T-C

NM_145239.2(PRRT2):c.806T>C;(p.I269T)

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:

From purines to purinergic signalling: molecular functions and human diseases.

Signal Transduction And Targeted Therapy
Huang, Zhao Z; Xie, Na N; Illes, Peter P; Di Virgilio, Francesco F; Ulrich, Henning H; Semyanov, Alexey A; Verkhratsky, Alexei A; Sperlagh, Beata B; Yu, Shu-Guang SG; Huang, Canhua C; Tang, Yong Y
Publication Date: 2021-04-28

Variant appearance in text: PKC: I269T
PubMed Link: 33907179
Variant Present in the following documents:
  • Main text
View BVdb publication page