Variant ID: 2-21246416-A-G

NM_000384.2(APOB):c.2585T>C;(p.Val862Ala)

This variant was identified in 1 publication




Publications:


Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction.

European Journal Of Human Genetics : Ejhg
I Brænne, M Kleinecke, B Reiz, E Graf, T Strom, T Wieland, M Fischer, T Kessler, C Hengstenberg, T Meitinger, J Erdmann, H Schunkert
Publication Date: 2016-02

Variant appearance in text: APOB: 2585T>C; V862A
PubMed Link: 26036859
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000233242.1 c.2585T>C p.Val862Ala missense_variant 17/29 -
NM_000384.3 c.2585T>C p.Val862Ala missense_variant 17/29 -