RGD:597788305 Rat Genome Database

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Variant: RGD:597788305 -  Homo sapiens

RGD ID: 597788305
ClinVar ID: CV3678074
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GLYCTK  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 52,325,045
GRCh38 3 52,291,029
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001144951.2:c.447C>T
NM_145262.4:c.447C>T
NG_023246.1:g.8210C>T
NC_000003.12:g.52291029C>T
More... 		12/03/2024 non-coding transcript variant likely benign AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004932685 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene GLYCTK CLINVAR
OMIM 610516 CLINVAR