CLIP4 c.1316G>A ;(p.S439N)

Variant ID: 2-29380130-G-A

NM_024692.4(CLIP4):c.1316G>A;(p.S439N)

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:

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

Plos One
Patiño, 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: CLIP4: Ser439Asn
PubMed Link: 25333361
Variant Present in the following documents:
  • pone.0109576.s001.xls, sheet 4
  • pone.0109576.s003.xls, sheet 4
View BVdb publication page