All variants in the GRIA2 gene

Information The variants shown are described using the NM_000826.3 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
+/. - c.967C>T r.(?) p.(Arg323*) - pathogenic g.158254055C>T g.157332903C>T - - GRIA2_000020 - - - - De novo - - - 0 - Stephanie Efthymiou
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