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APOB c.11230C>G ;(p.L3744V)
Variant ID: 2-21228510-G-C
NM_000384.2(
APOB
):c.11230C>G;(p.L3744V)
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: 11230C>G; L3744V
PubMed Link:
32650820
Variant Present in the following documents:
Main text
13064_2020_Article_145.pdf
View BVdb publication page