DNMT3A c.2617C>A ;(p.H873N)

Variant ID: 2-25457270-G-T

NM_022552.4(DNMT3A):c.2617C>A;(p.H873N)

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: DNMT3A: 2617C>A; H873N
PubMed Link: 36436542
Variant Present in the following documents:
  • mmc2.xlsx, sheet 1
View BVdb publication page



Comprehensive germline and somatic genomic profiles of Chinese patients with biliary tract cancer.

Frontiers In Oncology
Yu, Haipeng H; Xu, Yan Y; Gao, Wei W; Li, Mei M; He, Ji'an J; Deng, Xiaoqian X; Xing, Wenge W
Publication Date: 2022

Variant appearance in text: DNMT3A: H873N
PubMed Link: 36072793
Variant Present in the following documents:
  • Table_3.xlsx, sheet 1
View BVdb publication page



In a multi-institutional cohort of myeloid sarcomas, NFE2 mutation prevalence is lower than previously reported.

Blood Advances
Anekpuritanang, Tauangtham T; Klairmont, Matthew M MM; Gradowski, Joel J; Hagiwara, Kohei K; Bailey, Nathanael G NG; Chandra, Pranil P; Liu, Yiwei Y; Mulder, Heather L HL; Easton, John J; Zhang, Jinghui J; Martin, Michael G MG; Owczarczyk, Anna B AB; Dunlap, Jennifer B JB; Fan, Guang G; Press, Richard D RD; Raess, Philipp W PW
Publication Date: 2021-12-14

Variant appearance in text: DNMT3A: H873N
PubMed Link: 34559205
Variant Present in the following documents:
  • advancesADV2021004983-suppl1.pdf
View BVdb publication page