KCNH2 c.3437C>G ;(p.T1146S)

Variant ID: 7-150642496-G-C

NM_000238.3(KCNH2):c.3437C>G;(p.T1146S)

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:

Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.

Mayo Clinic Proceedings
Tester, David J DJ; Medeiros-Domingo, Argelia A; Will, Melissa L ML; Haglund, Carla M CM; Ackerman, Michael J MJ
Publication Date: 2012-06

Variant appearance in text: KCNH2: T1146S
PubMed Link: 22677073
Variant Present in the following documents:
  • Main text
View BVdb publication page