Variant #0000860051 (NC_000006.11:g.102134167C>G, NM_021956.4:c.890C>G (GRIK2))

Chromosome 6
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.102134167C>G
DNA change (hg38) -
Published as GRIK2(NM_001166247.1):c.890C>G (p.S297W), GRIK2(NM_021956.4):c.890C>G (p.S297W), GRIK2(NM_021956.5):c.890C>G (p.S297W)
ISCN -
DB-ID GRIK2_000027 See all 4 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) 0.00082 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 2022-05-09 15:51:19 +02:00 (CEST)
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     
GRIK2 NM_021956.4 ?/. - c.890C>G r.(?) p.(Ser297Trp)


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