Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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