RGD:405115913 Rat Genome Database

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Variant: RGD:405115913 -  Homo sapiens

RGD ID: 405115913
ClinVar ID: CV2996495
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ADIPOR1  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 202,917,567
GRCh38 1 202,948,439
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001290553.2:c.142-19T>A
NM_001290557.1:c.142-19T>A
NM_001290629.1:c.142-19T>A
NM_015999.6:c.142-19T>A
More... 		02/20/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ADIPOR1
Accession:XM_047421959
Location:INTRON

Gene Symbol:ADIPOR1
Accession:NM_001290553
Location:INTRON

Gene Symbol:ADIPOR1
Accession:NM_001290557
Location:INTRON

Gene Symbol:ADIPOR1
Accession:NM_015999
Location:INTRON

Gene Symbol:ADIPOR1
Accession:XM_024447427
Location:INTRON

Gene Symbol:ADIPOR1
Accession:NM_001290629
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003723354 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ADIPOR1 CLINVAR
OMIM 607945 CLINVAR