MSH2 c.2370_2375del ;(p.L790_N792delinsF)

Variant ID: 2-47705570-TGGCCAA-T

NM_000251.2(MSH2):c.2370_2375del;(p.L790_N792delinsF)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of Novel Pathogenic Sequence Variants of the Mismatch Repair Genes During Screening for Lynch Syndrome in a Single Centre of Eastern Hungary.

Journal Of Gastrointestinal Cancer
Kóder, Gergely G; Olasz, Judit J; Tanyi, Janos L JL; George, Erin E; Tóth, László L; Antal-Szalmás, Péter P; Nagy, Béla B; Bubán, Tamás T; András, Csilla C; Urbancsek, Hilda H; Laczik, Miklós M; Csuka, Orsolya O; Damjanovich, László L; Tanyi, Miklós M
Publication Date: 2020-09

Variant appearance in text: MSH2: 2370_2375del
PubMed Link: 31939059
Variant Present in the following documents:
  • Main text
  • 12029_2020_Article_359.pdf
View BVdb publication page