RGD:150419255 Rat Genome Database

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Variant: RGD:150419255 -  Homo sapiens

RGD ID: 150419255
RS ID: rs112799921
ClinVar ID: CV1179305
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LEPR  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 66,062,105
GRCh38 1 65,596,422
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_283t1:c.704-26A>G
LRG_283t2:c.704-26A>G
LRG_283t4:c.704-26A>G
NM_001003679.3:c.704-26A>G
More... 		02/29/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LEPR
Accession:NM_001003680
Location:INTRON

Gene Symbol:LEPR
Accession:NM_001198688
Location:INTRON

Gene Symbol:LEPR
Accession:NM_001198689
Location:INTRON

Gene Symbol:LEPR
Accession:NM_002303
Location:INTRON

Gene Symbol:LEPR
Accession:NM_001003679
Location:INTRON

Gene Symbol:LEPR
Accession:NM_001198687
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001550963 CLINVAR
dbSNP (RS) rs112799921 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LEPR CLINVAR
OMIM 601007 CLINVAR