TNNT2 c.422G>C ;(p.R141P)

Variant ID: 1-201333493-C-G

NM_001276345.1(TNNT2):c.422G>C;(p.R141P)

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:

The pathogenicity of genetic variants previously associated with left ventricular non-compaction.

Molecular Genetics & Genomic Medicine
Abbasi, Yeganeh Y; Jabbari, Javad J; Jabbari, Reza R; Yang, Ren-Qiang RQ; Risgaard, Bjarke B; Køber, Lars L; Haunsø, Stig S; Tfelt-Hansen, Jacob J
Publication Date: 2016-03

Variant appearance in text: TNNT2: R141P; rs397516464
PubMed Link: 27066506
Variant Present in the following documents:
  • MGG3-4-135-s001.xlsx, sheet 1
View BVdb publication page