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.




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