rs74934875 Rat Genome Database

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Variant: rs74934875 -  Homo sapiens

RGD ID: 150539270
RS ID: rs74934875
ClinVar ID: CV1308583
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A32  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 104,412,635
GRCh38 8 103,400,407
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000008.11:g.103400407G>A
NM_030780.5:c.*4C>T
NG_047200.1:g.19929C>T
NR_102338.2:n.1231C>T
More... 		01/28/2021 3 prime utr variant benign|likely benign none provided; SLC25A32-related condition
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV1308583HumanExercise Intolerance  IAGP 8554872ClinVar Annotator: match by term: SLC25A32-related conditionClinVarPMID:25741868
Gene Symbol:SLC25A32
Accession:NM_030780
Location:3UTRS;EXON

Gene Symbol:SLC25A32
Accession:NR_102337
Location:EXON;NON-CODING

Gene Symbol:SLC25A32
Accession:NR_102338
Location:EXON;NON-CODING

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001766087 CLINVAR
  RCV003976163 CLINVAR
dbSNP (RS) rs74934875 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC25A32 CLINVAR
OMIM 138480 CLINVAR