CDAN1 c.681A>G ;(p.Q227=)

Variant ID: 15-43028165-T-C

NM_138477.2(CDAN1):c.681A>G;(p.Q227=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosis.

Plos One
PatiƱo, Liliana Catherine LC; Battu, Rajani R; Ortega-Recalde, Oscar O; Nallathambi, Jeyabalan J; Anandula, Venkata Ramana VR; Renukaradhya, Umashankar U; Laissue, Paul P
Publication Date: 2014

Variant appearance in text: CDAN1: Q227Q
PubMed Link: 25333361
Variant Present in the following documents:
  • pone.0109576.s003.xls, sheet 3
View BVdb publication page