rs10103739 Rat Genome Database

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Variant: rs10103739 -  Homo sapiens

RGD ID: 150440931
RS ID: rs10103739
ClinVar ID: CV1233462
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A32  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 104,412,830
GRCh38 8 103,400,602
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_030780.5:c.813-56G>A
NG_047200.1:g.19734G>A
NC_000008.11:g.103400602C>T
NC_000008.10:g.104412830C>T
 07/31/2018 intron variant benign none provided

Gene Symbol:SLC25A32
Accession:NM_030780
Location:INTRON

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

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

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001645150 CLINVAR
dbSNP (RS) rs10103739 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC25A32 CLINVAR
OMIM 138480 CLINVAR