TTC28 c.166_168delinsCAA ;(p.A56Q)

Variant ID: 22-29025753-AGC-TTG

NM_001145418.1(TTC28):c.166_168delinsCAA;(p.A56Q)

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:

Genetic fusions favor tumorigenesis through degron loss in oncogenes.

Nature Communications
Liu, Jing J; Tokheim, Collin C; Lee, Jonathan D JD; Gan, Wenjian W; North, Brian J BJ; Liu, X Shirley XS; Pandolfi, Pier Paolo PP; Wei, Wenyi W
Publication Date: 2021-11-18

Variant appearance in text: TTC28: A56Q
PubMed Link: 34795215
Variant Present in the following documents:
  • 41467_2021_26871_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page