RGD:150438280 Rat Genome Database

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Variant: RGD:150438280 -  Homo sapiens

RGD ID: 150438280
RS ID: rs5093
ClinVar ID: CV1238001
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: APOA4  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 116,693,354
GRCh38 11 116,822,638
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000482.4:c.176+21C>T
NG_012044.1:g.5658C>T
NC_000011.10:g.116822638G>A
NC_000011.9:g.116693354G>A
 05/11/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:APOA4
Accession:NM_000482
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001644499 CLINVAR
dbSNP (RS) rs5093 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene APOA4 CLINVAR
OMIM 107690 CLINVAR