RGD:150438285 Rat Genome Database

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Variant: RGD:150438285 -  Homo sapiens

RGD ID: 150438285
RS ID: rs7521667
ClinVar ID: CV1264802
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: REN  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 204,130,127
GRCh38 1 204,160,999
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012122.1:g.10339C>A
NC_000001.11:g.204160999G>T
NM_000537.4:c.373+293C>A
NC_000001.10:g.204130127G>T
 06/21/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:REN
Accession:NM_000537
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001678795 CLINVAR
dbSNP (RS) rs7521667 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene REN CLINVAR
OMIM 179820 CLINVAR