CYP2C9 c.778C>T ;(p.P260S)

Variant ID: 10-96709000-C-T

NM_000771.3(CYP2C9):c.778C>T;(p.P260S)

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:

Integrating precision medicine in the study and clinical treatment of a severely mentally ill person.

Peerj
O'Rawe, Jason A JA; Fang, Han H; Rynearson, Shawn S; Robison, Reid R; Kiruluta, Edward S ES; Higgins, Gerald G; Eilbeck, Karen K; Reese, Martin G MG; Lyon, Gholson J GJ
Publication Date: 2013

Variant appearance in text: CYP2C9: 778C>T
PubMed Link: 24109560
Variant Present in the following documents:
  • peerj-01-177-s012.xlsx, sheet 1
View BVdb publication page