RGD:405117665 Rat Genome Database

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Variant: RGD:405117665 -  Homo sapiens

RGD ID: 405117665
ClinVar ID: CV2992909
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CNGB3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 87,655,990
GRCh38 8 86,643,762
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_019098.5:c.1167G>A
NG_016980.1:g.104914G>A
NC_000008.11:g.86643762C>T
NC_000008.10:g.87655990C>T
More... 		02/21/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003723468 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CNGB3 CLINVAR
OMIM 605080 CLINVAR