Variant #0001043082 (NC_000019.9:g.48945583C>G, NM_000836.2:c.2617C>G (GRIN2D))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48945583C>G
DNA change (hg38) -
Published as GRIN2D(NM_000836.4):c.2617C>G (p.L873V)
ISCN -
DB-ID GRIN2D_000031
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIN2D NM_000836.2 ?/. - c.2617C>G r.(?) p.(Leu873Val)
GRWD1 NM_031485.3 ?/. - c.-3680C>G r.(?) p.(=)


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