RGD:405010969 Rat Genome Database

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Variant: RGD:405010969 -  Homo sapiens

RGD ID: 405010969
ClinVar ID: CV3128042
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLCO2A1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 133,673,800
GRCh38 3 133,954,956
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_841t1:c.625+10C>T
NM_005630.3:c.625+10C>T
LRG_841:g.102229C>T
NG_031964.3:g.102229C>T
More... 		11/27/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLCO2A1
Accession:NM_005630
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003828922 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLCO2A1 CLINVAR
OMIM 601460 CLINVAR