rs115002974 Rat Genome Database

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Variant: rs115002974 -  Homo sapiens

RGD ID: 153348071
RS ID: rs115002974
ClinVar ID: CV1695120
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CACNA1B  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 140,972,514
GRCh38 9 138,078,062
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_042271.1:g.205274C>T
NC_000009.12:g.138078062C>T
NC_000009.11:g.140972514C>T
NM_000718.4:c.4950-52C>T
More... 		09/16/2021 intron variant likely 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 RCV002279051 CLINVAR
dbSNP (RS) rs115002974 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CACNA1B CLINVAR
OMIM 601012 CLINVAR