TTN c.97084G>T ;(p.A32362S)

Variant ID: 2-179407497-C-A

NM_001267550.1(TTN):c.97084G>T;(p.A32362S)

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:

Rare coding TTN variants are associated with electrocardiographic QT interval in the general population.

Scientific Reports
Kapoor, Ashish A; Bakshy, Kiranmayee K; Xu, Linda L; Nandakumar, Priyanka P; Lee, Dongwon D; Boerwinkle, Eric E; Grove, Megan L ML; Arking, Dan E DE; Chakravarti, Aravinda A
Publication Date: 2016-06-20

Variant appearance in text: TTN: A32362S
PubMed Link: 27321809
Variant Present in the following documents:
  • Main text
  • srep28356.pdf
  • srep28356-s1.pdf
View BVdb publication page