RGD:150416907 Rat Genome Database

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Variant: RGD:150416907 -  Homo sapiens

RGD ID: 150416907
RS ID: rs180869185
ClinVar ID: CV1182011
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACO2  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 41,916,335
GRCh38 22 41,520,331
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.1138+55C>A
NG_032143.1:g.56207C>A
NC_000022.11:g.41520331C>A
NC_000022.10:g.41916335C>A
 09/04/2020 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 RCV001549880 CLINVAR
dbSNP (RS) rs180869185 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACO2 CLINVAR
OMIM 100850 CLINVAR