APOB c.1189T>G ;(p.W397G)

Variant ID: 2-21255389-A-C

NM_000384.2(APOB):c.1189T>G;(p.W397G)

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:

Whole-Exome Sequencing of Germline Variants in Non-BRCA Families with Hereditary Breast Cancer.

Biomedicines
Liu, Yaxuan Y; Helgadottir, Hafdis T HT; Kharaziha, Pedram P; Choi, Jungmin J; López-Giráldez, Francesc F; Mane, Shrikant M SM; Höiom, Veronica V; Juhlin, Carl Christofer CC; Larsson, Catharina C; Bajalica-Lagercrantz, Svetlana S
Publication Date: 2022-04-26

Variant appearance in text: APOB: 1189T>G
PubMed Link: 35625741
Variant Present in the following documents:
  • biomedicines-10-01004.pdf
View BVdb publication page