APC c.895_896delinsCG ;(p.S299R)

Variant ID: 5-112151252-TC-CG

NM_000038.5(APC):c.895_896delinsCG;(p.S299R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.

Bmc Medical Genetics
Stekrova, Jitka J; Sulova, Martina M; Kebrdlova, Vera V; Zidkova, Katerina K; Kotlas, Jaroslav J; Ilencikova, Denisa D; Vesela, Kamila K; Kohoutova, Milada M
Publication Date: 2007-04-05

Variant appearance in text: APC: S299R
PubMed Link: 17411426
Variant Present in the following documents:
  • Main text
  • 1471-2350-8-16.pdf
View BVdb publication page