RGD:14734902 Rat Genome Database

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Variant: RGD:14734902 -  Homo sapiens

RGD ID: 14734902
RS ID: rs188358034
ClinVar ID: CV657288
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CACNA1S  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 201,054,863
GRCh38 1 201,085,735
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000069.3:c.1005-154C>T
NG_009816.2:g.31832C>T
NC_000001.11:g.201085735G>A
NC_000001.10:g.201054863G>A
More... 		06/16/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CACNA1S
Accession:XM_005245478
Location:INTRON

Gene Symbol:CACNA1S
Accession:NM_000069
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000837766 CLINVAR
dbSNP (RS) rs188358034 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CACNA1S CLINVAR
OMIM 114208 CLINVAR