RGD:156388355 Rat Genome Database

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Variant: RGD:156388355 -  Homo sapiens

RGD ID: 156388355
ClinVar ID: CV1989874
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PDE6C  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 95,418,846
GRCh38 10 93,659,089
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.2145-15T>C
NG_016752.1:g.51502T>C
NC_000010.11:g.93659089T>C
NC_000010.10:g.95418846T>C
 07/24/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PDE6C
Accession:NM_006204
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002604453 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PDE6C CLINVAR
OMIM 600827 CLINVAR