rs1245516372 Rat Genome Database

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Variant: rs1245516372 -  Homo sapiens

RGD ID: 151852388
RS ID: rs1245516372
ClinVar ID: CV1458980
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A24  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 108,679,460
GRCh38 1 108,136,838
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_013386.5:c.1250-1G>A
NG_032752.1:g.68521G>A
NC_000001.11:g.108136838C>T
NC_000001.10:g.108679460C>T
More...
12/06/2022 splice acceptor variant uncertain significance none provided

Gene Symbol:SLC25A24
Accession:NM_013386
Location:INTRON

Gene Symbol:SLC25A24
Accession:NM_213651
Location:INTRON

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PMID:9536098   PMID:17576681   PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002016763 CLINVAR
dbSNP (RS) rs1245516372 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC25A24 CLINVAR
OMIM 608744 CLINVAR