KCNH2 c.46del ;(p.D16Tfs*44)

Variant ID: 7-150674955-TC-T

NM_000238.3(KCNH2):c.46del;(p.D16Tfs*44)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Network expansion of genetic associations defines a pleiotropy map of human cell biology.

Nature Genetics
Barrio-Hernandez, Inigo I; Schwartzentruber, Jeremy J; Shrivastava, Anjali A; Del-Toro, Noemi N; Gonzalez, Asier A; Zhang, Qian Q; Mountjoy, Edward E; Suveges, Daniel D; Ochoa, David D; Ghoussaini, Maya M; Bradley, Glyn G; Hermjakob, Henning H; Orchard, Sandra S; Dunham, Ian I; Anderson, Carl A CA; Porras, Pablo P; Beltrao, Pedro P
Publication Date: 2023-02-23

Variant appearance in text: KCNH2: 46del; Asp16fs
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



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: 46delG
PubMed Link: 34901807
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page