rs4876928 Rat Genome Database

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Variant: rs4876928 -  Homo sapiens

RGD ID: 150446441
RS ID: rs4876928
ClinVar ID: CV1278315
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CACNA1B  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 141,009,015
GRCh38 9 138,114,563
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.241775C>T
NC_000009.12:g.138114563C>T
NC_000009.11:g.141009015C>T
NM_001243812.2:c.5649+73C>T
More... 		07/31/2024 intron variant benign AllHighlyPenetrant; 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:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001707458 CLINVAR
  RCV004598122 CLINVAR
dbSNP (RS) rs4876928 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene CACNA1B CLINVAR
OMIM 601012 CLINVAR