Variant #0000046864 (NC_000020.10:g.34810239C>T, NM_012156.2:c.2560C>T (EPB41L1))

Chromosome 20
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.34810239C>T
DNA change (hg38) g.36222317C>T
Published as -
ISCN -
DB-ID EPB41L1_000001 See all 2 reported entries
Variant remarks expression cloning in HEK293 cells shows disruption of 4.1N binding to GluR1 (0.5) by coIP, insertion of AMPAR subunit GluR1 at synaptic membranesignificantly decreased in transfected hippocampal neurons
Reference PubMed: Hamdan 2011
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-11-14 21:58:23 +01:00 (CET)
Date last edited 2020-07-16 17:10:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPB41L1 NM_012156.2 +/. - c.2560C>T r.(?) p.Pro854Ser


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.