DNMT3A c.2597G>T ;(p.R866M)

Variant ID: 2-25458576-C-A

NM_022552.4(DNMT3A):c.2597G>T;(p.R866M)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


appreci8: a pipeline for precise variant calling integrating 8 tools.

Bioinformatics (Oxford, England)
Sandmann, Sarah S; Karimi, Mohsen M; de Graaf, Aniek O AO; Rohde, Christian C; Göllner, Stefanie S; Varghese, Julian J; Ernsting, Jan J; Walldin, Gunilla G; van der Reijden, Bert A BA; Müller-Tidow, Carsten C; Malcovati, Luca L; Hellström-Lindberg, Eva E; Jansen, Joop H JH; Dugas, Martin M
Publication Date: 2018-12-15

Variant appearance in text: DNMT3A: 2597G>T; Arg866Met
PubMed Link: 29945233
Variant Present in the following documents:
  • bty518_supplementary_data_s4.xlsx, sheet 9
View BVdb publication page



Ultra-sensitive Sequencing Identifies High Prevalence of Clonal Hematopoiesis-Associated Mutations throughout Adult Life.

American Journal Of Human Genetics
Acuna-Hidalgo, Rocio R; Sengul, Hilal H; Steehouwer, Marloes M; van de Vorst, Maartje M; Vermeulen, Sita H SH; Kiemeney, Lambertus A L M LALM; Veltman, Joris A JA; Gilissen, Christian C; Hoischen, Alexander A
Publication Date: 2017-07-06

Variant appearance in text: DNMT3A: Arg866Met
PubMed Link: 28669404
Variant Present in the following documents:
  • Main text
View BVdb publication page