MSH2 c.2007_2008insA ;(p.P670Tfs*6)

Variant ID: 2-47703507-C-CA

NM_000251.2(MSH2):c.2007_2008insA;(p.P670Tfs*6)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Determining the frequency of de novo germline mutations in DNA mismatch repair genes.

Journal Of Medical Genetics
Win, Aung Ko AK; Jenkins, Mark A MA; Buchanan, Daniel D DD; Clendenning, Mark M; Young, Joanne P JP; Giles, Graham G GG; Goldblatt, Jack J; Leggett, Barbara A BA; Hopper, John L JL; Thibodeau, Stephen N SN; Lindor, Noralane M NM
Publication Date: 2011-08

Variant appearance in text: MSH2: Pro670fs
PubMed Link: 21636617
Variant Present in the following documents:
  • Main text
View BVdb publication page