Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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