RGD:150337560 Rat Genome Database

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Variant: RGD:150337560 -  Homo sapiens

RGD ID: 150337560
RS ID: rs2070666
ClinVar ID: CV1172191
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: APOC3  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 116,701,674
GRCh38 11 116,830,958
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000040.3:c.179+62T>A
NG_008949.1:g.6051T>A
NC_000011.10:g.116830958T>A
NC_000011.9:g.116701674T>A
 04/08/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:APOC3
Accession:NM_000040
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001541727 CLINVAR
dbSNP (RS) rs2070666 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene APOC3 CLINVAR
OMIM 107720 CLINVAR