RGD:150490893 Rat Genome Database

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Variant: RGD:150490893 -  Homo sapiens

RGD ID: 150490893
RS ID: rs78742257
ClinVar ID: CV1280023
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CNGB3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 87,590,850
GRCh38 8 86,578,622
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.2103+67C>T
NG_016980.1:g.170054C>T
NC_000008.11:g.86578622G>A
NC_000008.10:g.87590850G>A
 02/10/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CNGB3
Accession:NM_019098
Location:INTRON

Gene Symbol:CNGB3
Accession:XM_011517138
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001716551 CLINVAR
dbSNP (RS) rs78742257 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CNGB3 CLINVAR
OMIM 605080 CLINVAR