rs80276264 Rat Genome Database

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Variant: rs80276264 -  Homo sapiens

RGD ID: 150535689
RS ID: rs80276264
ClinVar ID: CV1306988
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CACNA1B  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 140,951,935
GRCh38 9 138,057,483
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.12:g.138057483C>T
NC_000009.11:g.140951935C>T
NM_000718.4:c.3969-249C>T
NM_001243812.2:c.3969-249C>T
More... 		04/29/2021 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 Information

Database Acc Id Source(s)
ClinVar RCV001759042 CLINVAR
dbSNP (RS) rs80276264 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CACNA1B CLINVAR
OMIM 601012 CLINVAR