Variant #0000037988 (NC_000012.11:g.14018915G>A, NM_000834.3:c.228C>T (GRIN2B))

Chromosome 12
Allele Parent #1
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.14018915G>A
DNA change (hg38) g.13865981G>A
Published as -
ISCN -
DB-ID GRIN2B_000008 See all 3 reported entries
Variant remarks -
Reference PubMed: Endele 2010
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation no
Frequency 2/936 cases
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00079 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-07-01 22:45:08 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIN2B NM_000834.3 -?/. 2 c.228C>T r.(=) p.(=)


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