MSH2 c.1222_1223insTC ;(p.Y408Ffs*5)

Variant ID: 2-47657026-T-TTC

NM_000251.2(MSH2):c.1222_1223insTC;(p.Y408Ffs*5)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Concordance analysis of microsatellite instability status between polymerase chain reaction based testing and next generation sequencing for solid tumors.

Scientific Reports
Shimozaki, Keitaro K; Hayashi, Hideyuki H; Tanishima, Shigeki S; Horie, Sara S; Chida, Akihiko A; Tsugaru, Kai K; Togasaki, Kazuhiro K; Kawasaki, Kenta K; Aimono, Eriko E; Hirata, Kenro K; Nishihara, Hiroshi H; Kanai, Takanori T; Hamamoto, Yasuo Y
Publication Date: 2021-10-08

Variant appearance in text: MSH2: Y408Ffs*5
PubMed Link: 34625576
Variant Present in the following documents:
  • Main text
  • 41598_2021_Article_99364.pdf
View BVdb publication page


Concordance analysis of microsatellite instability status between polymerase chain reaction based testing and next generation sequencing for solid tumors.

Scientific Reports
Shimozaki, Keitaro K; Hayashi, Hideyuki H; Tanishima, Shigeki S; Horie, Sara S; Chida, Akihiko A; Tsugaru, Kai K; Togasaki, Kazuhiro K; Kawasaki, Kenta K; Aimono, Eriko E; Hirata, Kenro K; Nishihara, Hiroshi H; Kanai, Takanori T; Hamamoto, Yasuo Y
Publication Date: 2021-10-08

Variant appearance in text: MSH2: Y408Ffs*5
PubMed Link: 34625576
Variant Present in the following documents:
  • Main text
  • 41598_2021_Article_99364.pdf
View BVdb publication page