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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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