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MUC16 c.4966T>C ;(p.S1656P)
Variant ID: 19-9086849-A-G
NM_024690.2(
MUC16
):c.4966T>C;(p.S1656P)
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:
Genomic clonal evolution correlated with phenotype and prognosis in gastric cancer.
Clinical And Translational Medicine
Ge, Jie J; Li, Xuan X; Deng, Zhenghao Z; Gao, Xuan X; Liu, Yaoyao Y; Xiong, Xingui X; Zhao, Xianhui X; Peng, Huan H; Yi, Xin X; Xia, Xuefeng X; Chen, Zihua Z; Li, Lifeng L; Zhou, Haiyan H; Liu, Heli H
Publication Date: 2022-04
Variant appearance in text: MUC16: 4966T>C; S1656P
PubMed Link:
35384329
Variant Present in the following documents:
CTM2-12-e799-s006.xlsx, sheet 2
View BVdb publication page
Splicing mutation analysis reveals previously unrecognized pathways in lymph node-invasive breast cancer.
Scientific Reports
Dorman, Stephanie N SN; Viner, Coby C; Rogan, Peter K PK
Publication Date: 2014-11-14
Variant appearance in text: MUC16: S1656P; rs76004345
PubMed Link:
25394353
Variant Present in the following documents:
srep07063-s2.xls, sheet 2
View BVdb publication page