CDAN1 c.466T>G ;(p.S156A)

Variant ID: 15-43028603-A-C

NM_138477.2(CDAN1):c.466T>G;(p.S156A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Reanalysing genomic data by normalized coverage values uncovers CNVs in bone marrow failure gene panels.

Npj Genomic Medicine
Lauhasurayotin, Supanun S; Cuvelier, Geoff D GD; Klaassen, Robert J RJ; Fernandez, Conrad V CV; Pastore, Yves D YD; Abish, Sharon S; Rayar, Meera M; Steele, MacGregor M; Jardine, Lawrence L; Breakey, Vicky R VR; Brossard, Josee J; Sinha, Roona R; Silva, Mariana M; Goodyear, Lisa L; Lipton, Jeffrey H JH; Michon, Bruno B; Corriveau-Bourque, Catherine C; Sung, Lillian L; Shabanova, Iren I; Li, Hongbing H; Zlateska, Bozana B; Dhanraj, Santhosh S; Cada, Michaela M; Scherer, Stephen W SW; Dror, Yigal Y
Publication Date: 2019

Variant appearance in text: CDAN1: 466T>G
PubMed Link: 31839986
Variant Present in the following documents:
  • 41525_2019_Article_104.pdf
View BVdb publication page