Variant #0000537542 (NC_000009.11:g.140051247G>A, NC_000009.11(NM_007327.3):c.793+5G>A (GRIN1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140051247G>A
DNA change (hg38) g.137156795G>A
Published as GRIN1(NM_000832.6):c.793+5G>A (p.?)
ISCN -
DB-ID GRIN1_000034
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-26 13:02:56 +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.*12059C>T r.(=) p.(=)
GRIN1 NM_007327.3 -?/. - c.793+5G>A r.spl? p.?


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