Variant #0000037986 (NC_000012.11:g.14019026G>A, NM_000834.3:c.117C>T (GRIN2B))

Chromosome 12
Allele Maternal (confirmed)
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.14019026G>A
DNA change (hg38) g.13866092G>A
Published as -
ISCN -
DB-ID GRIN2B_000006
Variant remarks -
Reference PubMed: Endele 2010
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation no
Frequency 1/306 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 22:41:42 +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.117C>T r.(=) p.(=)


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