APOB c.3778G>T ;(p.E1260*)

Variant ID: 2-21237384-C-A

NM_000384.2(APOB):c.3778G>T;(p.E1260*)

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:

Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders.

Nature Communications
Oetjens, M T MT; Kelly, M A MA; Sturm, A C AC; Martin, C L CL; Ledbetter, D H DH
Publication Date: 2019-10-25

Variant appearance in text: APOB: 3778G>T
PubMed Link: 31653860
Variant Present in the following documents:
  • 41467_2019_12869_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page