RGD:405191052 Rat Genome Database

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Variant: RGD:405191052 -  Homo sapiens

RGD ID: 405191052
ClinVar ID: CV2988065
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PDE6C  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 95,422,841
GRCh38 10 93,663,084
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006204.4:c.2424C>T
NG_016752.1:g.55497C>T
NC_000010.11:g.93663084C>T
NC_000010.10:g.95422841C>T
More... 		12/09/2022 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003706420 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PDE6C CLINVAR
OMIM 600827 CLINVAR