RGD:13831819 Rat Genome Database

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Variant: RGD:13831819 -  Homo sapiens

RGD ID: 13831819
RS ID: rs1447625985
ClinVar ID: CV582316
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC2A9  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 9,892,336
GRCh38 4 9,890,712
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000004.12:g.9890712C>G
NG_011540.1:g.154537G>C
NC_000004.11:g.9892336C>G
NG_011540.2:g.154558G>C
More... 		09/16/2018 splice acceptor variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC2A9
Accession:XM_017008460
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_047415978
Location:INTRON

Gene Symbol:SLC2A9
Accession:NM_001001290
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_011513865
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_047415977
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_011513867
Location:INTRON

Gene Symbol:SLC2A9
Accession:NM_020041
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_011513856
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_047415973
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_047415980
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_011513858
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_011513859
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_024454151
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_011513861
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_011513866
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_047415979
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_047415974
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_017008457
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_011513860
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_017008458
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_024454153
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_047415975
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_011513864
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_006713968
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_017008459
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_024454152
Location:INTRON

Gene Symbol:SLC2A9
Accession:XM_047415976
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000722502 CLINVAR
dbSNP (RS) rs1447625985 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene SLC2A9 CLINVAR
OMIM 606142 CLINVAR