RGD:150485877 Rat Genome Database

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Variant: RGD:150485877 -  Homo sapiens

RGD ID: 150485877
RS ID: rs12718464
ClinVar ID: CV1273947
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: APOA1  APOA1-AS  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 116,707,401
GRCh38 11 116,836,685
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001318021.1:c.-127-274C>T
NM_000039.3:c.201-274C>T
NM_001318017.2:c.201-274C>T
NM_001318018.2:c.201-274C>T
More...
08/30/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:APOA1
Accession:NM_001318021
Location:5UTRS;INTRON

Gene Symbol:APOA1
Accession:NM_000039
Location:INTRON

Gene Symbol:APOA1
Accession:NM_001318018
Location:INTRON

Gene Symbol:APOA1
Accession:NM_001318017
Location:INTRON

Gene Symbol:APOA1
Accession:XM_047426866
Location:INTRON

Gene Symbol:APOA1-AS
Accession:NR_126362
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001698825 CLINVAR
dbSNP (RS) rs12718464 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene APOA1 CLINVAR
  APOA1-AS CLINVAR
OMIM 107680 CLINVAR
  620112 CLINVAR