Variant #0001029995 (NC_000012.11:g.14019050dup, NM_000834.3:c.99dup (GRIN2B))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.14019050dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID GRIN2B_000177 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs398122823
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-03-19 15:54:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIN2B NM_000834.3 +/. - c.99dup r.(?) p.(Ser34GlnfsTer25)


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