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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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