APC c.2663C>T ;(p.A888V)

Variant ID: 5-112173954-C-T

NM_000038.5(APC):c.2663C>T;(p.A888V)

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:

Lynch syndrome-associated ultra-hypermutated pediatric glioblastoma mimicking a constitutional mismatch repair deficiency syndrome.

Cold Spring Harbor Molecular Case Studies
Yang, Chen C; Austin, Frances F; Richard, Hope H; Idowu, Michael M; Williamson, Vernell V; Sabato, Fernanda F; Ferreira-Gonzalez, Andrea A; Turner, Scott A SA
Publication Date: 2019-10

Variant appearance in text: APC: 2663C>T; Ala888Val
PubMed Link: 31604779
Variant Present in the following documents:
  • Main text
  • MCS003863Yan.pdf
View BVdb publication page