TTN c.84306G>T ;(p.W28102C)

Variant ID: 2-179426553-C-A

NM_001267550.1(TTN):c.84306G>T;(p.W28102C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Molecular investigation by whole exome sequencing revealed a high proportion of pathogenic variants among Thai victims of sudden unexpected death syndrome.

Plos One
Suktitipat, Bhoom B; Sathirareuangchai, Sakda S; Roothumnong, Ekkapong E; Thongnoppakhun, Wanna W; Wangkiratikant, Purin P; Vorasan, Nutchavadee N; Krittayaphong, Rungroj R; Pithukpakorn, Manop M; Boonyapisit, Warangkna W
Publication Date: 2017

Variant appearance in text: TTN: Trp28102Cys
PubMed Link: 28704380
Variant Present in the following documents:
  • Main text
  • pone.0180056.pdf
View BVdb publication page