MSH2 c.2738del ;(p.A913Vfs*3)

Variant ID: 2-47710021-GC-G

NM_000251.2(MSH2):c.2738del;(p.A913Vfs*3)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Deep sequencing of the X chromosome reveals the proliferation history of colorectal adenomas.

Genome Biology
De Grassi, Anna A; Iannelli, Fabio F; Cereda, Matteo M; Volorio, Sara S; Melocchi, Valentina V; Viel, Alessandra A; Basso, Gianluca G; Laghi, Luigi L; Caselle, Michele M; Ciccarelli, Francesca D FD
Publication Date: 2014-08-30

Variant appearance in text: MSH2: 2738delC
PubMed Link: 25175524
Variant Present in the following documents:
  • Main text
  • 13059_2014_Article_437.pdf
View BVdb publication page