Variant #0000997718 (NC_000009.11:g.140051128G>C, NM_007327.3:c.679G>C (GRIN1))

Chromosome 9
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.140051128G>C
DNA change (hg38) -
Published as GRIN1(NM_007327.3):c.679G>C (p.(Asp227His))
ISCN -
DB-ID GRIN1_000014 See all 5 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
LRRC26 NM_001013653.2 ?/. - c.*12178C>G r.(=) p.(=)
GRIN1 NM_007327.3 ?/. - c.679G>C r.(?) p.(Asp227His)


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