RGD:407484130 Rat Genome Database

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Variant: RGD:407484130 -  Homo sapiens

RGD ID: 407484130
ClinVar ID: CV3418369
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CCDC158  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 77,278,529
GRCh38 4 76,357,376
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.2171A>G
NM_001394954.1:c.2171A>G
NC_000004.12:g.76357376T>C
NC_000004.11:g.77278529T>C
More... 		04/23/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004602957 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CCDC158 CLINVAR