RGD:150505330 Rat Genome Database

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Variant: RGD:150505330 -  Homo sapiens

RGD ID: 150505330
RS ID: rs6673324
ClinVar ID: CV1222865
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LEPR  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 66,031,063
GRCh38 1 65,565,380
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_283t1:c.-20-166G>A
LRG_283t2:c.-20-166G>A
LRG_283t4:c.-20-166G>A
NM_001003679.3:c.-20-166G>A
More... 		08/09/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LEPR
Accession:NM_001198688
Location:5UTRS;INTRON

Gene Symbol:LEPR
Accession:NM_001003680
Location:5UTRS;INTRON

Gene Symbol:LEPR
Accession:NM_001198687
Location:5UTRS;INTRON

Gene Symbol:LEPR
Accession:NM_001003679
Location:5UTRS;INTRON

Gene Symbol:LEPR
Accession:NM_002303
Location:5UTRS;INTRON

Gene Symbol:LEPR
Accession:NM_001198689
Location:5UTRS;INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001621799 CLINVAR
dbSNP (RS) rs6673324 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LEPR CLINVAR
OMIM 601007 CLINVAR