Variant #0000997722 (NC_000009.11:g.140069452C>T, NM_007327.3:c.*7473C>T (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.140069452C>T
DNA change (hg38) -
Published as ANAPC2(NM_013366.3):c.2411G>A (p.(Arg804Gln))
ISCN -
DB-ID ANAPC2_000007
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) 3.0E-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 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.-5057G>A r.(?) p.(=)
SSNA1 NM_003731.2 ?/. - c.-13727C>T r.(?) p.(=)
GRIN1 NM_007327.3 ?/. - c.*7473C>T r.(=) p.(=)
ANAPC2 NM_013366.3 ?/. - c.2411G>A r.(?) p.(Arg804Gln)
TMEM210 XM_003846333.2 ?/. - c.-2973G>A r.(?) p.(=)


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