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MSH2 c.882dup ;(p.D295*)
Variant ID: 2-47641493-C-CT
NM_000251.2(
MSH2
):c.882dup;(p.D295*)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Mismatch Repair Universal Screening of Endometrial Cancers (MUSE) in a Canadian Cohort.
Current Oncology (Toronto, Ont.)
Lawrence, Jessica J; Richer, Lara L; Arseneau, Jocelyne J; Zeng, Xing X; Chong, George G; Weber, Evan E; Foulkes, William W; Palma, Laura L
Publication Date: 2021-01-15
Variant appearance in text: MSH2: 882dupT
PubMed Link:
33467402
Variant Present in the following documents:
Main text
curroncol-28-00052-s001.pdf
curroncol-28-00052.pdf
View BVdb publication page
Deep single-cell RNA sequencing data of individual T cells from treatment-naïve colorectal cancer patients.
Scientific Data
Zhang, Yuanyuan Y; Zheng, Liangtao L; Zhang, Lei L; Hu, Xueda X; Ren, Xianwen X; Zhang, Zemin Z
Publication Date: 2019-07-24
Variant appearance in text: N/A
PubMed Link:
31341169
Variant Present in the following documents:
View BVdb publication page