Variant #0000046858 (NC_000022.10:g.36962409C>G, NM_006078.3:c.427G>C (CACNG2))

Chromosome 22
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.36962409C>G
DNA change (hg38) g.36566362C>G
Published as -
ISCN -
DB-ID CACNG2_000001 See all 2 reported entries
Variant remarks expression cloning in HEK293 cells using coIP shows decreased stargazin binding to GluR1/R2 AMPAR subunits; decreased miniEPSC amplitude
and frequency in transfected hippocampal neurons; reduced cell GluR1 surface expression in transfected hippocampal neurons and HEK293 cells
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 19:43:27 +01:00 (CET)
Date last edited 2020-07-17 12:29:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNG2 NM_006078.3 +/. 3 c.427G>C r.(?) p.Val143Leu


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