KCNH2 c.1058C>G ;(p.T353S)

Variant ID: 7-150654449-G-C

NM_000238.3(KCNH2):c.1058C>G;(p.T353S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies.

Cancer Gene Therapy
Denisova, Evgeniya E; Westphal, Dana D; Surowy, Harald M HM; Meier, Friedegund F; Hutter, Barbara B; Reifenberger, Julia J; Rütten, Arno A; Schulz, Alexander A; Sergon, Mildred M; Ziemer, Mirjana M; Brors, Benedikt B; Betz, Regina C RC; Redler, Silke S
Publication Date: 2022-06

Variant appearance in text: KCNH2: T353S
PubMed Link: 34045664
Variant Present in the following documents:
  • 41417_2021_347_MOESM4_ESM.xls, sheet 1
View BVdb publication page



Genetic variants in post myocardial infarction patients presenting with electrical storm of unstable ventricular tachycardia.

Indian Pacing And Electrophysiology Journal
Rangaraju, Advithi A; Krishnan, Shuba S; Aparna, G G; Sankaran, Satish S; Mannan, Ashraf U AU; Rao, B Hygriv BH
Publication Date: 2018

Variant appearance in text: KCNH2: Thr353Ser
PubMed Link: 29396286
Variant Present in the following documents:
  • Main text
View BVdb publication page