Bibliome.ai browser hg19
Search
About
Stats
FAQ
APOB c.2T>C ;(p.M1?)
Variant ID: 2-21266816-A-G
NM_000384.2(
APOB
):c.2T>C;(p.M1?)
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:
Four novel candidate causal variants for deficient homozygous haplotypes in Holstein cattle.
Scientific Reports
Häfliger, Irene M IM; Spengeler, Mirjam M; Seefried, Franz R FR; Drögemüller, Cord C
Publication Date: 2022-03-31
Variant appearance in text: APOB: 2T>C
PubMed Link:
35361830
Variant Present in the following documents:
41598_2022_Article_9403.pdf
View BVdb publication page