RGD:407484166 Rat Genome Database

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Variant: RGD:407484166 -  Homo sapiens

RGD ID: 407484166
ClinVar ID: CV3418375
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CCDC158  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 77,317,481
GRCh38 4 76,396,328
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001042784.1:c.229G>C
NM_001394954.1:c.229G>C
NC_000004.12:g.76396328C>G
NC_000004.11:g.77317481C>G
More... 		03/26/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004602963 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CCDC158 CLINVAR