MUC16 c.2363C>T ;(p.A788V)

Variant ID: 19-9089452-G-A

NM_024690.2(MUC16):c.2363C>T;(p.A788V)

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:

Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance.

Scientific Reports
Fransson, Susanne S; Martinez-Monleon, Angela A; Johansson, Mathias M; Sjöberg, Rose-Marie RM; Björklund, Caroline C; Ljungman, Gustaf G; Ek, Torben T; Kogner, Per P; Martinsson, Tommy T
Publication Date: 2020-12-31

Variant appearance in text: MUC16: A788V
PubMed Link: 33384420
Variant Present in the following documents:
  • Main text
  • 41598_2020_Article_78370.pdf
View BVdb publication page