KCNH2 c.1801G>T ;(p.G601C)

Variant ID: 7-150648680-C-A

NM_000238.3(KCNH2):c.1801G>T;(p.G601C)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Evolutionary coupling analysis guides identification of mistrafficking-sensitive variants in cardiac K+ channels: Validation with hERG.

Frontiers In Pharmacology
Zhang, Yihong Y; Grimwood, Amy L AL; Hancox, Jules C JC; Harmer, Stephen C SC; Dempsey, Christopher E CE
Publication Date: 2022

Variant appearance in text: KCNH2: G601C
PubMed Link: 36339618
Variant Present in the following documents:
  • fphar-13-1010119.pdf
View BVdb publication page



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: rs199472936
PubMed Link: 32123669
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page