HP c.322_323delinsTT ;(p.R108F)

Variant ID: 16-72092209-CG-TT

NM_005143.3(HP):c.322_323delinsTT;(p.R108F)

This variant was identified in 1 publication

View GRCh38 version.



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

Publications:

CYP2C9 amino acid residues influencing phenytoin turnover and metabolite regio- and stereochemistry.

The Journal Of Pharmacology And Experimental Therapeutics
Mosher, Carrie M CM; Tai, Guoying G; Rettie, Allan E AE
Publication Date: 2009-06

Variant appearance in text: HP: R108F
PubMed Link: 19258521
Variant Present in the following documents:
  • Main text
View BVdb publication page