RGD:150431570 Rat Genome Database

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Variant: RGD:150431570 -  Homo sapiens

RGD ID: 150431570
RS ID: rs150846056
ClinVar ID: CV1206393
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC35A2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 48,763,604
GRCh38 X 48,906,327
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001042498.3:c.426+65A>G
NM_001282647.2:c.426+65A>G
NM_005660.3:c.426+65A>G
NM_001282650.2:c.465+65A>G
More... 		05/09/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC35A2
Accession:NM_005660
Location:INTRON

Gene Symbol:SLC35A2
Accession:NM_001042498
Location:INTRON

Gene Symbol:SLC35A2
Accession:NM_001032289
Location:INTRON

Gene Symbol:SLC35A2
Accession:NM_001282647
Location:INTRON

Gene Symbol:SLC35A2
Accession:NM_001282648
Location:INTRON

Gene Symbol:SLC35A2
Accession:NM_001282649
Location:INTRON

Gene Symbol:SLC35A2
Accession:NM_001282651
Location:INTRON

Gene Symbol:SLC35A2
Accession:NM_001282650
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001581042 CLINVAR
dbSNP (RS) rs150846056 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC35A2 CLINVAR
OMIM 314375 CLINVAR