PPP1R9A c.2619G>T ;(p.E873D)

Variant ID: 7-94881396-G-T

NM_001166160.1(PPP1R9A):c.2619G>T;(p.E873D)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia.

Bmc Medical Genomics
Lin, Dafeng D; Wang, Dianpeng D; Li, Peimao P; Deng, Lihua L; Zhang, Zhimin Z; Zhang, Yanfang Y; Zhang, Ming M; Zhang, Naixing N
Publication Date: 2023-01-26

Variant appearance in text: PPP1R9A: 2619G>T; Glu873Asp
PubMed Link: 36703207
Variant Present in the following documents:
  • 12920_2023_1442_MOESM3_ESM.xlsx, sheet 1
  • 12920_2023_1442_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page