Variant #0000692245 (NC_000016.9:g.9943738del, NM_000833.3:c.1204del (GRIN2A))

Chromosome 16
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.9943738del
DNA change (hg38) -
Published as GRIN2A(NM_000833.5):c.1204delG (p.D402Mfs*21)
ISCN -
DB-ID GRIN2A_000207
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIN2A NM_000833.3 +/. - c.1204del r.(?) p.(Asp402MetfsTer21)
GRIN2A NM_001134407.2 +/. - c.1204del r.(?) p.(Asp402MetfsTer21)


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