GRIN2A c.2459T>G ;(p.V820G)

Variant ID: 16-9862844-A-C

NM_001134407.1(GRIN2A):c.2459T>G;(p.V820G)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Impact of copy neutral loss of heterozygosity and total genome aberrations on survival in myelodysplastic syndrome.

Modern Pathology : An Official Journal Of The United States And Canadian Academy Of Pathology, Inc
Yeung, Cecilia C S CCS; McElhone, Scott S; Chen, Xue Yan XY; Ng, David D; Storer, Barry E BE; Deeg, H Joachim HJ; Fang, Min M
Publication Date: 2018-04

Variant appearance in text: GRIN2A: 2459T>G; V820G
PubMed Link: 29243741
Variant Present in the following documents:
  • Main text
  • nihms911889.pdf
View BVdb publication page



Jumping translocations in myelodysplastic syndromes.

Cancer Genetics
Yeung, Cecilia C S CCS; Deeg, H Joachim HJ; Pritchard, Colin C; Wu, David D; Fang, Min M
Publication Date: 2016-09

Variant appearance in text: GRIN2A: 2459T>G; V820G
PubMed Link: 27751357
Variant Present in the following documents:
  • Main text
View BVdb publication page