rs17021096 Rat Genome Database

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Variant: rs17021096 -  Homo sapiens

RGD ID: 150460880
RS ID: rs17021096
ClinVar ID: CV1231404
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A24  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 108,679,151
GRCh38 1 108,136,529
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000001.11:g.108136529A>G
NC_000001.10:g.108679151A>G
NM_013386.5:c.*124T>C
NM_213651.3:c.*124T>C
More...
05/16/2021 3 prime utr variant benign none provided

Gene Symbol:SLC25A24
Accession:NM_013386
Location:3UTRS;EXON

Gene Symbol:SLC25A24
Accession:NM_213651
Location:3UTRS;EXON

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PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001640969 CLINVAR
dbSNP (RS) rs17021096 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC25A24 CLINVAR
OMIM 608744 CLINVAR