RGD:597788286 Rat Genome Database

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Variant: RGD:597788286 -  Homo sapiens

RGD ID: 597788286
ClinVar ID: CV3678069
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GLYCTK  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 52,327,108
GRCh38 3 52,293,092
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001144951.2:c.*657T>C
NM_145262.4:c.1538T>C
NG_023246.1:g.10273T>C
NC_000003.12:g.52293092T>C
More... 		08/26/2024 3 prime utr variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004932681 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene GLYCTK CLINVAR
OMIM 610516 CLINVAR