RGD:156161325 Rat Genome Database

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Variant: RGD:156161325 -  Homo sapiens

RGD ID: 156161325
ClinVar ID: CV2056407
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CNGB3  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 87,683,326
GRCh38 8 86,671,098
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.339C>A
NG_016980.1:g.77578C>A
NC_000008.11:g.86671098G>T
NC_000008.10:g.87683326G>T
More... 		05/18/2022 missense variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:CNGB3
Accession:XM_011517138
Location:5UTRS;INTRON

Gene Symbol:CNGB3
Accession:NM_019098
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002801641 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CNGB3 CLINVAR
OMIM 605080 CLINVAR