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MSH6 c.3260_3261del ;(p.P1087Lfs*5)
Variant ID: 2-48030639-ACC-A
NM_000179.2(
MSH6
):c.3260_3261del;(p.P1087Lfs*5)
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:
DNA mismatch repair deficiency and hereditary syndromes in Latino patients with colorectal cancer.
Cancer
Ricker, Charité N CN; Hanna, Diana L DL; Peng, Cheng C; Nguyen, Nathalie T NT; Stern, Mariana C MC; Schmit, Stephanie L SL; Idos, Greg E GE; Patel, Ravi R; Tsai, Steven S; Ramirez, Veronica V; Lin, Sonia S; Shamasunadara, Vinay V; Barzi, Afsaneh A; Lenz, Heinz-Josef HJ; Figueiredo, Jane C JC
Publication Date: 2017-10-01
Variant appearance in text: MSH6: 3255_3256del
PubMed Link:
28640387
Variant Present in the following documents:
Main text
CNCR-123-3732.pdf
View BVdb publication page