APOB c.10373del ;(p.M3458Rfs*64)

Variant ID: 2-21229367-CA-C

NM_000384.2(APOB):c.10373del;(p.M3458Rfs*64)

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:

Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes.

Neural Development
Zou, Jizhen J; Wang, Fang F; Yang, Xueyan X; Wang, Hongyan H; Niswander, Lee L; Zhang, Ting T; Li, Huili H
Publication Date: 2020-07-10

Variant appearance in text: APOB: 10373delT; M3458fs
PubMed Link: 32650820
Variant Present in the following documents:
  • Main text
  • 13064_2020_Article_145.pdf
View BVdb publication page