MSH2 c.14del ;(p.P5Rfs*59)

Variant ID: 2-47630342-GC-G

NM_000251.2(MSH2):c.14del;(p.P5Rfs*59)

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:

DNA mismatch repair deficiency and hereditary syndromes in Latino patients with colorectal cancer.

Cancer
Ricker, Charité N CN; Hanna, Diana L DL; Peng, Cheng C; Nguyen, Nathalie T NT; Stern, Mariana C MC; Schmit, Stephanie L SL; Idos, Greg E GE; Patel, Ravi R; Tsai, Steven S; Ramirez, Veronica V; Lin, Sonia S; Shamasunadara, Vinay V; Barzi, Afsaneh A; Lenz, Heinz-Josef HJ; Figueiredo, Jane C JC
Publication Date: 2017-10-01

Variant appearance in text: MSH2: 14del
PubMed Link: 28640387
Variant Present in the following documents:
  • Main text
  • CNCR-123-3732.pdf
View BVdb publication page