MSH6 c.3438+16del

Variant ID: 2-48030837-TA-T

NM_000179.2(MSH6):c.3438+16del

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes.

Molecular Genetics & Genomic Medicine
Hansen, Maren F MF; Neckmann, Ulrike U; Lavik, Liss A S LA; Vold, Trine T; Gilde, Bodil B; Toft, Ragnhild K RK; Sjursen, Wenche W
Publication Date: 2014-03

Variant appearance in text: MSH6: 3438+14del
PubMed Link: 24689082
Variant Present in the following documents:
  • Main text
  • mgg30002-0186.pdf
View BVdb publication page