APC c.856_875del ;(p.H286Efs*3)

Variant ID: 5-112151213-CCATGAAACAGCCAGTGTTTT-C

NM_000038.5(APC):c.856_875del;(p.H286Efs*3)

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:

panelcn.MOPS: Copy-number detection in targeted NGS panel data for clinical diagnostics.

Human Mutation
Povysil, Gundula G; Tzika, Antigoni A; Vogt, Julia J; Haunschmid, Verena V; Messiaen, Ludwine L; Zschocke, Johannes J; Klambauer, Günter G; Hochreiter, Sepp S; Wimmer, Katharina K
Publication Date: 2017-07

Variant appearance in text: APC: 856_875del
PubMed Link: 28449315
Variant Present in the following documents:
  • Main text
  • HUMU-38-889.pdf
View BVdb publication page