RGD:597755247 Rat Genome Database

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Variant: RGD:597755247 -  Homo sapiens

RGD ID: 597755247
ClinVar ID: CV3590452
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNF26  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 119,206,119
GRCh38 11 119,335,409
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_032015.5:c.287G>T
NC_000011.10:g.119335409G>T
NC_000011.9:g.119206119G>T
NM_032015.3:c.287G>T
More... 		08/14/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004847570 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene RNF26 CLINVAR
OMIM 606130 CLINVAR