APC c.871G>A ;(p.V291I)

Variant ID: 5-112151228-G-A

NM_000038.5(APC):c.871G>A;(p.V291I)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update.

European Journal Of Human Genetics : Ejhg
McGuigan, Anthony A; Whitworth, James J; Andreou, Avgi A; Hearn, Timothy T; , ; Tischkowitz, Marc M; Maher, Eamonn R ER
Publication Date: 2022-03

Variant appearance in text: APC: 871G>A
PubMed Link: 34983940
Variant Present in the following documents:
  • 41431_2021_1013_MOESM1_ESM.pdf
View BVdb publication page



Correlation between early dynamics in circulating tumour DNA and outcome from FOLFIRI treatment in metastatic colorectal cancer.

Scientific Reports
Lyskjær, Iben I; Kronborg, Camilla Skovhus CS; Rasmussen, Mads Heilskov MH; Sørensen, Boe Sandahl BS; Demuth, Christina C; Rosenkilde, Mona M; Johansen, Amanda Frydendahl Boll AFB; Knudsen, Michael M; Vang, Søren S; Krag, Søren Rasmus Palmelund SRP; Spindler, Karen-Lise Garm KG; Andersen, Claus Lindbjerg CL
Publication Date: 2019-08-08

Variant appearance in text: APC: Val291Ile
PubMed Link: 31395942
Variant Present in the following documents:
  • 41598_2019_47708_MOESM2_ESM.xlsx, sheet 6
View BVdb publication page