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APC c.1155A>T ;(p.A385=)
Variant ID: 5-112154884-A-T
NM_000038.5(
APC
):c.1155A>T;(p.A385=)
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:
Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes.
Hereditary Cancer In Clinical Practice
Henn, Jonas J; Spier, Isabel I; Adam, Ronja S RS; Holzapfel, Stefanie S; Uhlhaas, Siegfried S; Kayser, Katrin K; Plotz, Guido G; Peters, Sophia S; Aretz, Stefan S
Publication Date: 2019
Variant appearance in text: APC: 1155A>T
PubMed Link:
30680046
Variant Present in the following documents:
Main text
View BVdb publication page