CETP c.1316T>C ;(p.M439T)

CETP c.1316T>C ;(p.M439T)

Variant ID: 16-57016144-T-C

NM_000078.2(CETP):c.1316T>C;(p.M439T)

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:

Genetics of atrial fibrillation.

Heart Failure Clinics

Lubitz, Steven A SA; Yi, B Alexander BA; Ellinor, Patrick T PT

Publication Date: 2010-04

Variant appearance in text: CETP: Met439Thr

PubMed Link: 20347792

Variant Present in the following documents:

Main text

View BVdb publication page

Genetics of atrial fibrillation.

Cardiology Clinics

Lubitz, Steven A SA; Yi, B Alexander BA; Ellinor, Patrick T PT

Publication Date: 2009-02

Variant appearance in text: CETP: Met439Thr

PubMed Link: 19111761

Variant Present in the following documents:

Main text

View BVdb publication page