rs201697323 Rat Genome Database

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Variant: rs201697323 -  Homo sapiens

RGD ID: 152134892
RS ID: rs201697323
ClinVar ID: CV1638463
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CACNA1B  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 140,904,539
GRCh38 9 138,010,087
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000718.4:c.2160+10G>A
NM_001243812.2:c.2160+10G>A
NG_042271.1:g.137299G>A
NC_000009.12:g.138010087G>A
More... 		01/29/2024 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CACNA1B
Accession:NM_000718
Location:INTRON

Gene Symbol:CACNA1B
Accession:NM_001243812
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002083370 CLINVAR
dbSNP (RS) rs201697323 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CACNA1B CLINVAR
OMIM 601012 CLINVAR