Bibliome.ai browser hg19
Search
About
Stats
FAQ
CEP152 c.4093+1099G>A
Variant ID: 15-49032699-C-T
NM_001194998.1(
CEP152
):c.4093+1099G>A
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:
RNA editing of BFP, a point mutant of GFP, using artificial APOBEC1 deaminase to restore the genetic code.
Scientific Reports
Bhakta, Sonali S; Sakari, Matomo M; Tsukahara, Toshifumi T
Publication Date: 2020-10-14
Variant appearance in text: CEP152: 4093+1099G>A
PubMed Link:
33057101
Variant Present in the following documents:
41598_2020_74374_MOESM3_ESM.xlsx, sheet 2
41598_2020_74374_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page