TG c.1900_1922del ;(p.G634Lfs*22)

Variant ID: 8-133899515-CCGGAGAGTGCTGGTGTGTGAATT-C

NM_003235.4(TG):c.1900_1922del;(p.G634Lfs*22)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


A sex-informed approach to improve the personalised decision making process in myelodysplastic syndromes: a multicentre, observational cohort study.

The Lancet. Haematology
,
Publication Date: 2022-11-24

Variant appearance in text: TG: 1900_1922del
PubMed Link: 36436542
Variant Present in the following documents:
  • mmc2.xlsx, sheet 1
View BVdb publication page



Pathophysiologic and clinical implications of molecular profiles resultant from deletion 5q.

Ebiomedicine
Adema, Vera V; Palomo, Laura L; Walter, Wencke W; Mallo, Mar M; Hutter, Stephan S; La Framboise, Thomas T; Arenillas, Leonor L; Meggendorfer, Manja M; Radivoyevitch, Tomas T; Xicoy, Blanca B; Pellagatti, Andrea A; Haferlach, Claudia C; Boultwood, Jacqueline J; Kern, Wolfgang W; Visconte, Valeria V; Sekeres, Mikkael M; Barnard, John J; Haferlach, Torsten T; Solé, Francesc F; Maciejewski, Jaroslaw P JP
Publication Date: 2022-06

Variant appearance in text: TG: 1900_1922del
PubMed Link: 35617825
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



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: 1900_1922del
PubMed Link: 34782715
Variant Present in the following documents:
  • 41375_2021_1469_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page