APC c.1385A>G ;(p.H462R)

Variant ID: 5-112157665-A-G

NM_000038.5(APC):c.1385A>G;(p.H462R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Rare germline variants in DNA repair-related genes are accountable for papillary thyroid cancer susceptibility.

Endocrine
Mio, Catia C; Verrienti, Antonella A; Pecce, Valeria V; Sponziello, Marialuisa M; Damante, Giuseppe G
Publication Date: 2021-09

Variant appearance in text: APC: 1385A>G
PubMed Link: 33821390
Variant Present in the following documents:
  • 12020_2021_Article_2705.pdf
View BVdb publication page