APC c.1841C>G ;(p.A614G)

Variant ID: 5-112170745-C-G

NM_000038.5(APC):c.1841C>G;(p.A614G)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria.

American Journal Of Human Genetics
Pejaver, Vikas V; Byrne, Alicia B AB; Feng, Bing-Jian BJ; Pagel, Kymberleigh A KA; Mooney, Sean D SD; Karchin, Rachel R; O'Donnell-Luria, Anne A; Harrison, Steven M SM; Tavtigian, Sean V SV; Greenblatt, Marc S MS; Biesecker, Leslie G LG; Radivojac, Predrag P; Brenner, Steven E SE; ,
Publication Date: 2022-12-01

Variant appearance in text: APC: A614G; rs1161113466
PubMed Link: 36413997
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



Genetic and epigenetic characteristics of gastric cancers with JC virus T-antigen.

World Journal Of Gastroenterology
Yamaoka, Satoshi S; Yamamoto, Hiroyuki H; Nosho, Katsuhiko K; Taniguchi, Hiroaki H; Adachi, Yasushi Y; Sasaki, Shigeru S; Arimura, Yoshiaki Y; Imai, Kohzoh K; Shinomura, Yasuhisa Y
Publication Date: 2009-11-28

Variant appearance in text: APC: A614G
PubMed Link: 19938198
Variant Present in the following documents:
  • Main text
View BVdb publication page