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TG c.3781_3782insTG ;(p.P1261Lfs*3)
Variant ID: 8-133919079-C-CTG
NM_003235.4(
TG
):c.3781_3782insTG;(p.P1261Lfs*3)
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:
Modeling clonal hematopoiesis in umbilical cord blood cells by CRISPR/Cas9.
Leukemia
Christen, Friederike F; Hablesreiter, Raphael R; Hoyer, Kaja K; Hennch, Cornelius C; Maluck-Böttcher, Antje A; Segler, Angela A; Madadi, Annett A; Frick, Mareike M; Bullinger, Lars L; Briest, Franziska F; Damm, Frederik F
Publication Date: 2022-04
Variant appearance in text: TG: 3781_3782insTG
PubMed Link:
34782715
Variant Present in the following documents:
41375_2021_1469_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page