RGD:156350776 Rat Genome Database

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Variant: RGD:156350776 -  Homo sapiens

RGD ID: 156350776
ClinVar ID: CV1965405
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A24  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 108,742,571
GRCh38 1 108,199,949
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_013386.5:c.183+7C>T
NC_000001.10:g.108742571G>A
NG_032752.1:g.5410C>T
NC_000001.11:g.108199949G>A
More... 		02/18/2022 intron variant benign|likely benign none provided; SLC25A24-related condition
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV1965405HumanCongenital Progeroid Syndrome, Petty Type  IAGP 8554872ClinVar Annotator: match by term: SLC25A24-related conditionClinVarPMID:28492532
Gene Symbol:SLC25A24
Accession:NM_013386
Location:INTRON

Gene Symbol:SLC25A24
Accession:NM_213651
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002581045 CLINVAR
  RCV003916492 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC25A24 CLINVAR
OMIM 608744 CLINVAR