APOB c.2915del ;(p.G972Afs*2)

Variant ID: 2-21242678-GC-G

NM_000384.2(APOB):c.2915del;(p.G972Afs*2)

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:

Implementing genomic screening in diverse populations.

Genome Medicine
Abul-Husn, Noura S NS; Soper, Emily R ER; Braganza, Giovanna T GT; Rodriguez, Jessica E JE; Zeid, Natasha N; Cullina, Sinead S; Bobo, Dean D; Moscati, Arden A; Merkelson, Amanda A; Loos, Ruth J F RJF; Cho, Judy H JH; Belbin, Gillian M GM; Suckiel, Sabrina A SA; Kenny, Eimear E EE
Publication Date: 2021-02-05

Variant appearance in text: APOB: 2915delG; Gly972fs
PubMed Link: 33546753
Variant Present in the following documents:
  • 13073_2021_832_MOESM1_ESM.pdf
View BVdb publication page