MUC16 c.18119C>T ;(p.P6040L)

Variant ID: 19-9069327-G-A

NM_024690.2(MUC16):c.18119C>T;(p.P6040L)

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:

Identification of Key Genes Mutations Associated With the Radiosensitivity by Whole Exome Sequencing in Pancreatic Cancer.

Frontiers In Oncology
Hu, Bin B; Ma, Xiumei X; Huang, Renhua R; Wu, Zheng Z; Lu, Jun J; Guo, Yuntao Y; Tang, Jianmin J; Ma, Chunhui C; Ma, Jun J; Zhang, Lei L; Bai, Yongrui Y
Publication Date: 2021

Variant appearance in text: MUC16: 18119C>T; Pro6040Leu
PubMed Link: 34434896
Variant Present in the following documents:
  • DataSheet_5.xlsx, sheet 1
View BVdb publication page