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MSH6 c.3589dup ;(p.T1197Nfs*18)
Variant ID: 2-48032786-G-GA
NM_000179.2(
MSH6
):c.3589dup;(p.T1197Nfs*18)
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:
Co-occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome.
Cancer Communications (London, England)
Ferrer-Avargues, Rosario R; Castillejo, María Isabel MI; Dámaso, Estela E; Díez-Obrero, Virginia V; Garrigos, Noemí N; Molina, Tatiana T; Codoñer-Alejos, Alan A; Segura, Ángel Á; Sánchez-Heras, Ana Beatriz AB; Castillejo, Adela A; Soto, José Luis JL
Publication Date: 2021-03
Variant appearance in text: MSH6: 3588_3589insA
PubMed Link:
33630411
Variant Present in the following documents:
CAC2-41-218-s001.xlsx, sheet 3
CAC2-41-218-s001.xlsx, sheet 1
View BVdb publication page