PDE11A c.1222A>T ;(p.K408*)

Variant ID: 2-178762865-T-A

NM_016953.3(PDE11A):c.1222A>T;(p.K408*)

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:

Genetic screening for monogenic hypertension in hypertensive individuals in a clinical setting.

Journal Of Medical Genetics
Bao, Minghui M; Li, Ping P; Li, Qifu Q; Chen, Hui H; Zhong, Ying Y; Li, Shuangyue S; Jin, Ling L; Wang, Wenjie W; Chen, Zhenzhen Z; Zhong, Jiuchang J; Geng, Bin B; Fan, Yuxin Y; Yang, Xinchun X; Cai, Jun J
Publication Date: 2020-08

Variant appearance in text: PDE11A: 1222A>T; Lys408*
PubMed Link: 32561571
Variant Present in the following documents:
  • jmedgenet-2019-106145supp001.pdf
View BVdb publication page