Variant #0000038002 (NC_000012.11:g.13828688C>T, NM_000834.3:c.1116G>A (GRIN2B))

Chromosome 12
Allele Unknown
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.13828688C>T
DNA change (hg38) g.13675754C>T
Published as 1116A>G
ISCN -
DB-ID GRIN2B_000021
Variant remarks variant reported erroneously or reference sequence is rare allele
Reference PubMed: Endele 2010
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency 1/630 cases
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 2014-07-01 23:23:20 +02:00 (CEST)
Date last edited 2014-07-01 23:23:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIN2B NM_000834.3 -?/. 13 c.1116G>A r.(=) p.(=)


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