RGD:597687836 Rat Genome Database

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Variant: RGD:597687836 -  Homo sapiens

RGD ID: 597687836
ClinVar ID: CV3590448
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNF26  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 119,205,977
GRCh38 11 119,335,267
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_032015.5:c.145A>G
NC_000011.10:g.119335267A>G
NC_000011.9:g.119205977A>G
NM_032015.3:c.145A>G
More... 		09/18/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004858537 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene RNF26 CLINVAR
OMIM 606130 CLINVAR