RGD:597683604 Rat Genome Database

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Variant: RGD:597683604 -  Homo sapiens

RGD ID: 597683604
ClinVar ID: CV3622630
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: UBR3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 170,917,590
GRCh38 2 170,061,080
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_172070.4:c.4787G>A
NC_000002.12:g.170061080G>A
NC_000002.11:g.170917590G>A
NM_172070.3:c.4787G>A
More... 		08/27/2024 missense variant likely benign AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004883880 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene UBR3 CLINVAR
OMIM 613831 CLINVAR