Variant #0000339422 (NC_000009.11:g.140051238A>G, NM_007327.3:c.789A>G (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.140051238A>G
DNA change (hg38) g.137156786A>G
Published as -
ISCN -
DB-ID GRIN1_000012 See all 3 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) 0.26314 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-26 13:02:49 +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.*12068T>C r.(=) p.(=)
GRIN1 NM_007327.3 -/. - c.789A>G r.(?) p.(Pro263=)


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