rs41278472 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: rs41278472 -  Homo sapiens

RGD ID: 150480292
RS ID: rs41278472
ClinVar ID: CV1239547
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A24  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 108,735,383
GRCh38 1 108,192,761
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_213651.3:c.-140G>A
NM_013386.5:c.184-6807G>A
NG_032752.1:g.12598G>A
NC_000001.11:g.108192761C>T
More...
05/16/2021 5 prime utr variant benign none provided

Gene Symbol:SLC25A24
Accession:NM_213651
Location:5UTRS;EXON

Gene Symbol:SLC25A24
Accession:NM_013386
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001652710 CLINVAR
dbSNP (RS) rs41278472 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC25A24 CLINVAR
OMIM 608744 CLINVAR