KCNH2 c.2684_2685insCC ;(p.D896Rfs*79)

Variant ID: 7-150645539-C-CGG

NM_000238.3(KCNH2):c.2684_2685insCC;(p.D896Rfs*79)

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:

A Novel Frameshift Mutation, KCNH2 [p.Asp896ArgfsX79], Leading to Malignant Ventricular Arrhythmia, Identified After Treatment of Gastrointestinal Bleeding.

Cjc Open
Kim, Wan Cheol WC; Lemire, Edmond E; Nosib, Siddarth S; Nosib, Shravankumar S
Publication Date: 2021-11

Variant appearance in text: KCNH2: 2684_2685insCC
PubMed Link: 34901807
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page