Variant #0001037372 (NC_000009.11:g.140062280A>G, NM_007327.3:c.*301A>G (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.140062280A>G
DNA change (hg38) -
Published as GRIN1(NM_000832.7):c.2644A>G (p.(Ser882Gly))
ISCN -
DB-ID GRIN1_000108
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
LRRC26 NM_001013653.2 ?/. - c.*1026T>C r.(=) p.(=)
GRIN1 NM_007327.3 ?/. - c.*301A>G r.(=) p.(=)
TMEM210 XM_003846333.2 ?/. - c.*3147T>C r.(=) p.(=)


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