PPP1R9A c.2935G>A ;(p.D979N)

Variant ID: 7-94898630-G-A

NM_001166160.1(PPP1R9A):c.2935G>A;(p.D979N)

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:

Cronkhite-Canada syndrome complicated with three malignant tumors: a case report and whole exome sequencing analysis.

Chinese Medical Journal
Liu, Shuang S; You, Yan Y; Chen, Dan D; Qian, Jia-Ming JM; Li, Ji J
Publication Date: 2019-12-20

Variant appearance in text: PPP1R9A: D979N
PubMed Link: 31764169
Variant Present in the following documents:
  • cm9-132-3001-s001.xlsx, sheet 1
View BVdb publication page