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.




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
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