MSH6 c.142_144delinsTGT ;(p.A48C)

Variant ID: 2-48010514-GCG-TGT

NM_000179.2(MSH6):c.142_144delinsTGT;(p.A48C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Extreme intratumour heterogeneity and driver evolution in mismatch repair deficient gastro-oesophageal cancer.

Nature Communications
von Loga, Katharina K; Woolston, Andrew A; Punta, Marco M; Barber, Louise J LJ; Griffiths, Beatrice B; Semiannikova, Maria M; Spain, Georgia G; Challoner, Benjamin B; Fenwick, Kerry K; Simon, Ronald R; Marx, Andreas A; Sauter, Guido G; Lise, Stefano S; Matthews, Nik N; Gerlinger, Marco M
Publication Date: 2020-01-16

Variant appearance in text: MSH6: A48C
PubMed Link: 31949146
Variant Present in the following documents:
  • Main text
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