RGD:14726708 Rat Genome Database

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Variant: RGD:14726708 -  Homo sapiens

RGD ID: 14726708
RS ID: rs8030980
ClinVar ID: CV667723
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EIF2AK4  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 40,278,192
GRCh38 15 39,985,991
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000015.9:g.40278192T>C
NM_001013703.3:c.2403+103T>C
NM_001013703.4:c.2403+103T>C
NG_034053.1:g.56868T>C
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:EIF2AK4
Accession:NM_001013703
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000833985 CLINVAR
dbSNP (RS) rs8030980 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene EIF2AK4 CLINVAR
OMIM 609280 CLINVAR