Variant #0000816546 (NC_000011.9:g.105769062T>G, NM_000829.3:c.794T>G (GRIA4))

Chromosome 11
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.105769062T>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID GRIA4_000015
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs759332963
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-10-26 14:51:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIA4 NM_000829.3 ?/. - c.794T>G r.(?) p.(Val265Gly)


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