Variant #0000913131 (NC_000009.11:g.140051473G>C, NM_007327.3:c.952G>C (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.140051473G>C
DNA change (hg38) -
Published as GRIN1(NM_007327.3):c.952G>C (p.(Gly318Arg)), GRIN1(NM_007327.4):c.952G>C (p.G318R)
ISCN -
DB-ID GRIN1_000095 See all 2 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC26 NM_001013653.2 ?/. - c.*11833C>G r.(=) p.(=)
GRIN1 NM_007327.3 ?/. - c.952G>C r.(?) p.(Gly318Arg)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.