RGD:11631349 Rat Genome Database

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Variant: RGD:11631349 -  Homo sapiens

RGD ID: 11631349
RS ID: rs78189695
ClinVar ID: CV351090
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC2A10  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 45,363,813
GRCh38 20 46,735,174
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NG_016284.1:g.30535G>A
NC_000020.11:g.46735174G>A
NC_000020.10:g.45363813G>A
NM_030777.4:c.*1340G>A
More... 		01/12/2018 3 prime utr variant likely benign|uncertain significance childhood <1 / 1 000 000
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SLC2A10
Accession:XM_011529061
Location:3UTRS;EXON

Gene Symbol:SLC2A10
Accession:XM_011529062
Location:3UTRS;EXON

Gene Symbol:SLC2A10
Accession:XM_011529060
Location:3UTRS;EXON

Gene Symbol:SLC2A10
Accession:XM_017028087
Location:3UTRS;EXON

Gene Symbol:SLC2A10
Accession:XM_047440529
Location:3UTRS;EXON

Gene Symbol:SLC2A10
Accession:XM_011529065
Location:3UTRS;EXON

Gene Symbol:SLC2A10
Accession:NM_030777
Location:3UTRS;EXON

Gene Symbol:SLC2A10
Accession:XM_011529064
Location:INTRON

Gene Symbol:SLC2A10
Accession:XM_047440528
Location:INTRON

Gene Symbol:SLC2A10
Accession:XM_011529063
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000375694 CLINVAR
dbSNP (RS) rs78189695 CLINVAR
MedGen C1859726 CLINVAR
NCBI Gene SLC2A10 CLINVAR
OMIM 208050 CLINVAR
  606145 CLINVAR