RGD:150336556 Rat Genome Database

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Variant: RGD:150336556 -  Homo sapiens

RGD ID: 150336556
RS ID: rs12555306
ClinVar ID: CV1164997
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CACNA1B  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 140,900,951
GRCh38 9 138,006,499
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.11:g.140900951G>A
NM_000718.4:c.1975-268G>A
NM_001243812.2:c.1975-268G>A
NG_042271.1:g.133711G>A
More... 		03/26/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CACNA1B
Accession:NM_001243812
Location:INTRON

Gene Symbol:CACNA1B
Accession:NM_000718
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001530897 CLINVAR
dbSNP (RS) rs12555306 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CACNA1B CLINVAR
OMIM 601012 CLINVAR