ADA c.1069G>A ;(p.A357T)

Variant ID: 20-43248949-C-T

NM_000022.2(ADA):c.1069G>A;(p.A357T)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Systematic Review of Cerebral Phenotypes Associated With Monogenic Cerebral Small-Vessel Disease.

Journal Of The American Heart Association
Whittaker, Ed E; Thrippleton, Sophie S; Chong, Liza Y W LYW; Collins, Victoria G VG; Ferguson, Amy C AC; Henshall, David E DE; Lancastle, Emily E; Wilkinson, Tim T; Wilson, Blair B; Wilson, Kirsty K; Sudlow, Cathie C; Wardlaw, Joanna J; Rannikmäe, Kristiina K
Publication Date: 2022-06-21

Variant appearance in text: ADA: 1069G>A; A357T
PubMed Link: 35699195
Variant Present in the following documents:
  • JAH3-11-e025629-s001.pdf
  • JAH3-11-e025629.pdf
View BVdb publication page



Epigenomic and genomic analysis of transcriptome modulation in skin cutaneous melanoma.

Aging
Chen, Wuzhen W; Cheng, Pu P; Jiang, Jingxin J; Ren, Yunqing Y; Wu, Dang D; Xue, Dan D
Publication Date: 2020-07-07

Variant appearance in text: ADA: 1069G>A
PubMed Link: 32639949
Variant Present in the following documents:
  • aging-12-103115-s013..xlsx, sheet 1
View BVdb publication page