DSG2 c.2194T>G ;(p.F732V)

Variant ID: 18-29122675-T-G

NM_001943.3(DSG2):c.2194T>G;(p.F732V)

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:

Targeted next generation sequencing in a young population with suspected inherited malignant cardiac arrhythmias.

European Journal Of Human Genetics : Ejhg
Broendberg, Anders Krogh AK; Christiansen, Morten Krogh MK; Nielsen, Jens Cosedis JC; Pedersen, Lisbeth Noerum LN; Jensen, Henrik Kjaerulf HK
Publication Date: 2018-03

Variant appearance in text: DSG2: 2194T>G
PubMed Link: 29343803
Variant Present in the following documents:
  • 41431_2017_Article_60.pdf
View BVdb publication page