MSH6 c.3984dup ;(p.S1329Vfs*12)

Variant ID: 2-48033772-A-AG

NM_000179.2(MSH6):c.3984dup;(p.S1329Vfs*12)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


GREM1 germline mutation screening in Ashkenazi Jewish patients with familial colorectal cancer.

Genetics Research
Laitman, Yael Y; Jaeger, Emma E; Katz, Lior L; Tomlinson, Ian I; Friedman, Eitan E
Publication Date: 2015-05-20

Variant appearance in text: MSH6: 3984dup
PubMed Link: 25992589
Variant Present in the following documents:
  • Main text
View BVdb publication page