APC c.5162G>C ;(p.G1721A)

Variant ID: 5-112176453-G-C

NM_000038.5(APC):c.5162G>C;(p.G1721A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Comprehensive analysis of common mitochondrial DNA variants and colorectal cancer risk.

British Journal Of Cancer
Webb, E E; Broderick, P P; Chandler, I I; Lubbe, S S; Penegar, S S; Tomlinson, I P M IP; Houlston, R S RS
Publication Date: 2008-12-16

Variant appearance in text: APC: G1721A
PubMed Link: 19050702
Variant Present in the following documents:
  • Main text
  • 6604805a.pdf
View BVdb publication page



Minor lesion mutational spectrum of the entire NF1 gene does not explain its high mutability but points to a functional domain upstream of the GAP-related domain.

American Journal Of Human Genetics
Fahsold, R R; Hoffmeyer, S S; Mischung, C C; Gille, C C; Ehlers, C C; Kücükceylan, N N; Abdel-Nour, M M; Gewies, A A; Peters, H H; Kaufmann, D D; Buske, A A; Tinschert, S S; Nürnberg, P P
Publication Date: 2000-03

Variant appearance in text: APC: G1721A
PubMed Link: 10712197
Variant Present in the following documents:
  • Main text
View BVdb publication page