MSH6 c.3604dup ;(p.M1202Nfs*13)

Variant ID: 2-48032803-C-CA

NM_000179.2(MSH6):c.3604dup;(p.M1202Nfs*13)

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:

Targeted deep-intronic sequencing in a cohort of unexplained cases of suspected Lynch syndrome.

European Journal Of Human Genetics : Ejhg
Arnold, Anke Marie AM; Morak, Monika M; Benet-Pagès, Anna A; Laner, Andreas A; Frishman, Dimitrij D; Holinski-Feder, Elke E
Publication Date: 2020-05

Variant appearance in text: MSH6: 3604dup; Met1202Asnfs*13
PubMed Link: 31822864
Variant Present in the following documents:
  • Main text
View BVdb publication page