APC c.1490dup ;(p.R498Kfs*39)

Variant ID: 5-112162885-C-CT

NM_000038.5(APC):c.1490dup;(p.R498Kfs*39)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients.

The Journal Of Molecular Diagnostics : Jmd
Dymerska, Dagmara D; Serrano-Fernández, Pablo P; Suchy, Janina J; Pławski, Andrzej A; Słomski, Ryszard R; Kaklewski, Krzysztof K; Scott, Rodney J RJ; Gronwald, Jacek J; Kładny, Józef J; Byrski, Tomasz T; Huzarski, Tomasz T; Lubiński, Jan J; Kurzawski, Grzegorz G
Publication Date: 2010-01

Variant appearance in text: APC: 1490_1491insT
PubMed Link: 20007843
Variant Present in the following documents:
  • Main text
View BVdb publication page