MSH6 c.3296_3297del ;(p.I1099Nfs*8)

Variant ID: 2-48030682-ATT-A

NM_000179.2(MSH6):c.3296_3297del;(p.I1099Nfs*8)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

International Journal Of Molecular Sciences
Liccardo, Raffaella R; De Rosa, Marina M; Rossi, Giovanni Battista GB; Carlomagno, Nicola N; Izzo, Paola P; Duraturo, Francesca F
Publication Date: 2017-05-06

Variant appearance in text: MSH6: 3296_3297delTT
PubMed Link: 28481244
Variant Present in the following documents:
  • Main text
  • ijms-18-00999.pdf
View BVdb publication page