KCNH2 c.809_812delinsAAAAGC ;(p.T270Kfs*91)

Variant ID: 7-150655250-GCGCG-GGCTTTT

NM_000238.3(KCNH2):c.809_812delinsAAAAGC;(p.T270Kfs*91)

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:

PHARMIP: An insilico method to predict genetics that underpin adverse drug reactions.

Methodsx
Zidan, Ahmad M AM; Saad, Eman A EA; Ibrahim, Nasser E NE; Mahmoud, Amal A; Hashem, Medhat H MH; Hemeida, Alaa A AA
Publication Date: 2020

Variant appearance in text: rs794728426
PubMed Link: 32123669
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page