TNNT2 c.331G>T ;(p.E111*)

Variant ID: 1-201334399-C-A

NM_001276345.1(TNNT2):c.331G>T;(p.E111*)

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:

Finding the candidate sequence variants for diagnosis of hypertrophic cardiomyopathy in East Slovak patients.

Journal Of Clinical Laboratory Analysis
Zigova, Michaela M; Bernasovska, Jarmila J; Boronova, Iveta I; Mydlarova Blascakova, Marta M; Kmec, Jan J
Publication Date: 2018-03

Variant appearance in text: TNNT2: E111*
PubMed Link: 28815794
Variant Present in the following documents:
  • Main text
View BVdb publication page