RGD:156062670 Rat Genome Database

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Variant: RGD:156062670 -  Homo sapiens

RGD ID: 156062670
ClinVar ID: CV2316596
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: URB1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 21 33,734,329
GRCh38 21 32,362,020
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014825.3:c.1511T>G
NC_000021.9:g.32362020A>C
NC_000021.8:g.33734329A>C
NM_014825.2:c.1511T>G
More... 		11/18/2022 missense variant uncertain significance AllHighlyPenetrant

Gene Symbol:URB1
Accession:NM_014825
Location:EXON

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Database
Acc Id
Source(s)
ClinVar RCV004171844 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene URB1 CLINVAR
OMIM 608865 CLINVAR