MSH2 c.112_114del ;(p.D38del)

Variant ID: 2-47630440-TCGA-T

NM_000251.2(MSH2):c.112_114del;(p.D38del)

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:

Prognostic Significance of Oxidation Pathway Mutations in Recurrent Laryngeal Squamous Cell Carcinoma.

Cancers
Heft Neal, Molly E ME; Bhangale, Apurva D AD; Birkeland, Andrew C AC; McHugh, Jonathan B JB; Shuman, Andrew G AG; Rosko, Andrew J AJ; Swiecicki, Paul L PL; Spector, Matthew E ME; Brenner, J Chad JC
Publication Date: 2020-10-22

Variant appearance in text: MSH2: D38del
PubMed Link: 33105726
Variant Present in the following documents:
  • cancers-12-03081.pdf
View BVdb publication page