Bibliome.ai browser hg19
Search
About
Stats
FAQ
MSH6 c.1192del ;(p.V398Cfs*13)
Variant ID: 2-48026314-TG-T
NM_000179.2(
MSH6
):c.1192del;(p.V398Cfs*13)
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 spectrum of germline cancer susceptibility genes among unselected Chinese colorectal cancer patients.
Cancer Management And Research
Gong, Rui R; He, Yuan Y; Liu, Xiao-Yun XY; Wang, Hai-Yun HY; Sun, Li-Yue LY; Yang, Xin-Hua XH; Li, Bin B; Cao, Xin-Kai XK; Ye, Zu-Lu ZL; Kong, Ling-Heng LH; Zhang, Da-Dong DD; Li, Yu-Hong YH; Xu, Rui-Hua RH; Shao, Jian-Yong JY
Publication Date: 2019
Variant appearance in text: MSH6: 1192del; V398Cfs*13
PubMed Link:
31118792
Variant Present in the following documents:
Main text
cmar-11-3721.pdf
View BVdb publication page