MSH6 c.3355G>A ;(p.E1119K)

Variant ID: 2-48030741-G-A

NM_000179.2(MSH6):c.3355G>A;(p.E1119K)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12

Variant appearance in text: MSH6: 3355G>A; Glu1119Lys
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page