RGD:150424495 Rat Genome Database

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Variant: RGD:150424495 -  Homo sapiens

RGD ID: 150424495
RS ID: rs73887733
ClinVar ID: CV1185693
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACO2  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 41,911,621
GRCh38 22 41,515,617
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001098.3:c.684+82A>T
NG_032143.1:g.51493A>T
NC_000022.11:g.41515617A>T
NC_000022.10:g.41911621A>T
 06/26/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ACO2
Accession:NM_001098
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001556733 CLINVAR
dbSNP (RS) rs73887733 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACO2 CLINVAR
OMIM 100850 CLINVAR