RGD:597640123 Rat Genome Database

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Variant: RGD:597640123 -  Homo sapiens

RGD ID: 597640123
ClinVar ID: CV3692384
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLHL25  LOC127830537  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 86,311,678
GRCh38 15 85,768,447
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_022480.4:c.1364A>G
NG_132017.1:g.762T>C
NC_000015.10:g.85768447T>C
NC_000015.9:g.86311678T>C
More... 		06/28/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004941472 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene KLHL25 CLINVAR
OMIM 619893 CLINVAR