RGD:597687225 Rat Genome Database

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Variant: RGD:597687225 -  Homo sapiens

RGD ID: 597687225
ClinVar ID: CV3590316
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNF186  RNF186-AS1  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 20,141,044
GRCh38 1 19,814,551
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_019062.2:c.551T>A
NC_000001.11:g.19814551A>T
NC_000001.10:g.20141044A>T
NR_186008.1:n.143A>T
More... 		12/06/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004858470 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene RNF186 CLINVAR
  RNF186-AS1 CLINVAR
OMIM 617163 CLINVAR