Variant #0000046862 (NC_000009.11:g.140056670_140056672dup, NM_007327.3:c.1679_1681dup (GRIN1))

Chromosome 9
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.140056670_140056672dup
DNA change (hg38) g.137162218_137162220dup
Published as -
ISCN -
DB-ID GRIN1_000002 See all 2 reported entries
Variant remarks electrophysiology of Xenopus oocyte coinjection with NR2B shows almost blocked activity of the receptor
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 21:47:21 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIN1 NM_007327.3 +/. 12 c.1679_1681dup r.(?) p.Ser560dup


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