Variant #0000537546 (NC_000009.11:g.140056492G>A, NM_007327.3:c.1584G>A (GRIN1))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140056492G>A
DNA change (hg38) g.137162040G>A
Published as GRIN1(NM_007327.3):c.1584G>A (p.E528=)
ISCN -
DB-ID GRIN1_000038
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) 0.00088 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-26 13:03:57 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC26 NM_001013653.2 -/. - c.*6814C>T r.(=) p.(=)
GRIN1 NM_007327.3 -/. - c.1584G>A r.(?) p.(Glu528=)


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