CETP c.992G>A ;(p.G331D)

Variant ID: 16-57012013-G-A

NM_000078.2(CETP):c.992G>A;(p.G331D)

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: CETP: 992G>A
PubMed Link: 24109560
Variant Present in the following documents:
  • peerj-01-177-s011.xlsx, sheet 1
View BVdb publication page