RGD:14730756 Rat Genome Database

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Variant: RGD:14730756 -  Homo sapiens

RGD ID: 14730756
RS ID: rs113249258
ClinVar ID: CV669154
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC2A10  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 45,362,334
GRCh38 20 46,733,695
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_030777.4:c.1548-61C>G
NG_016284.1:g.29056C>G
NC_000020.11:g.46733695C>G
NC_000020.10:g.45362334C>G
More... 		06/16/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC2A10
Accession:XM_011529062
Location:INTRON

Gene Symbol:SLC2A10
Accession:XM_047440528
Location:INTRON

Gene Symbol:SLC2A10
Accession:XM_011529060
Location:INTRON

Gene Symbol:SLC2A10
Accession:NM_030777
Location:INTRON

Gene Symbol:SLC2A10
Accession:XM_011529064
Location:INTRON

Gene Symbol:SLC2A10
Accession:XM_011529065
Location:INTRON

Gene Symbol:SLC2A10
Accession:XM_011529061
Location:INTRON

Gene Symbol:SLC2A10
Accession:XM_017028087
Location:INTRON

Gene Symbol:SLC2A10
Accession:XM_011529063
Location:INTRON

Gene Symbol:SLC2A10
Accession:XM_047440529
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000835822 CLINVAR
dbSNP (RS) rs113249258 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC2A10 CLINVAR
OMIM 606145 CLINVAR