KCNH2 c.455C>T ;(p.T152I)

Variant ID: 7-150656677-G-A

NM_000238.3(KCNH2):c.455C>T;(p.T152I)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole-exome sequencing.

Journal Of Arrhythmia
Fazelifar, Amir Farjam AF; Pourirahim, Maryam M; Masoumi, Tannaz T; Biglari, Alireza A; Maleki, Majid M; Kalayinia, Samira S
Publication Date: 2023-06

Variant appearance in text: KCNH2: 455C>T
PubMed Link: 37324772
Variant Present in the following documents:
  • Main text
  • JOA3-39-430.pdf
View BVdb publication page



Genetic variants in African-American and Hispanic patients with breast cancer.

Oncology Letters
Dutta, Pranabananda P; Keung, Man Y MY; Wu, Yanyuan Y; Vadgama, Jaydutt V JV
Publication Date: 2023-02

Variant appearance in text: KCNH2: 455C>T
PubMed Link: 36644153
Variant Present in the following documents:
  • Supplementary_Data5.xlsx, sheet 1
View BVdb publication page



Brugada syndrome: a fatal disease with complex genetic etiologies - still a long way to go.

Forensic Sciences Research
Wu, Yeda Y; Ai, Mei M; Bardeesi, Adham Sameer A ASA; Xu, Lunwu L; Zheng, Jingjing J; Zheng, Da D; Yin, Kun K; Wu, Qiuping Q; Zhang, Liyong L; Huang, Lei L; Cheng, Jianding J
Publication Date: 2017

Variant appearance in text: KCNH2: T152I
PubMed Link: 30483629
Variant Present in the following documents:
  • Main text
  • tfsr-2-1333203.pdf
View BVdb publication page



Genetics of Brugada syndrome.

Journal Of Arrhythmia
Juang, Jyh-Ming Jimmy JJ; Horie, Minoru M
Publication Date: 2016-10

Variant appearance in text: KCNH2: T152I
PubMed Link: 27761167
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page