RGD:407454751 Rat Genome Database

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Variant: RGD:407454751 -  Homo sapiens

RGD ID: 407454751
ClinVar ID: CV3425232
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CDCA8  LOC127268764  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 38,158,586
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001256875.2:c.104G>A
NM_018101.4:c.104G>A
NG_090625.1:g.226G>A
NC_000001.11:g.37692914G>A
More... 		06/04/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004609974 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CDCA8 CLINVAR
OMIM 609977 CLINVAR