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MSH6 c.675dup ;(p.E226*)
Variant ID: 2-48025795-A-AT
NM_000179.2(
MSH6
):c.675dup;(p.E226*)
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:
Mutation accumulation in cancer genes relates to nonoptimal outcome in chronic myeloid leukemia.
Blood Advances
Adnan Awad, Shady S; Kankainen, Matti M; Ojala, Teija T; Koskenvesa, Perttu P; Eldfors, Samuli S; Ghimire, Bishwa B; Kumar, Ashwini A; Kytölä, Soili S; Kamel, Mahmoud M MM; Heckman, Caroline A CA; Porkka, Kimmo K; Mustjoki, Satu S
Publication Date: 2020-02-11
Variant appearance in text: N/A
PubMed Link:
32045476
Variant Present in the following documents:
View BVdb publication page