Variant #0000556396 (NC_000016.9:g.10032004T>C, NM_000833.3:c.819A>G (GRIN2A))

Chromosome 16
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.10032004T>C
DNA change (hg38) g.9938147T>C
Published as GRIN2A(NM_000833.5):c.819A>G (p.P273=), GRIN2A(NM_001134407.3):c.819A>G (p.P273=)
ISCN -
DB-ID GRIN2A_000111 See all 2 reported entries
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) 0.00019 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +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.819A>G r.(?) p.(Pro273=)
GRIN2A NM_001134407.2 -?/. - c.819A>G r.(?) p.(Pro273=)


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