SYNJ1 c.1775T>C ;(p.M592T)

Variant ID: 21-34042634-A-G

NM_203446.2(SYNJ1):c.1775T>C;(p.M592T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.

Nature Neuroscience
Genovese, Giulio G; Fromer, Menachem M; Stahl, Eli A EA; Ruderfer, Douglas M DM; Chambert, Kimberly K; Landén, Mikael M; Moran, Jennifer L JL; Purcell, Shaun M SM; Sklar, Pamela P; Sullivan, Patrick F PF; Hultman, Christina M CM; McCarroll, Steven A SA
Publication Date: 2016-11

Variant appearance in text: SYNJ1: 1892T>C; Met631Thr
PubMed Link: 27694994
Variant Present in the following documents:
  • NIHMS815183-supplement-supp_table3.xlsx, sheet 1
View BVdb publication page