MSH2 c.196del ;(p.Y66Tfs*18)

Variant ID: 2-47630526-GT-G

NM_000251.2(MSH2):c.196del;(p.Y66Tfs*18)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Assessment of mismatch repair deficiency in ovarian cancer.

Journal Of Medical Genetics
Crosbie, Emma J EJ; Ryan, Neil A J NAJ; McVey, Rhona J RJ; Lalloo, Fiona F; Bowers, Naomi N; Green, Kate K; Woodward, Emma R ER; Clancy, Tara T; Bolton, James J; Wallace, Andrew J AJ; McMahon, Raymond F RF; Evans, D Gareth DG
Publication Date: 2021-10

Variant appearance in text: MSH2: 196delT
PubMed Link: 32917768
Variant Present in the following documents:
  • Main text
  • jmedgenet-2020-107270.pdf
View BVdb publication page