rs560665141 Rat Genome Database

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Variant: rs560665141 -  Homo sapiens

RGD ID: 150535743
RS ID: rs560665141
ClinVar ID: CV1307043
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CACNA1B  LOC127816945  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 140,901,145
GRCh38 9 138,006,693
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.133905C>A
NC_000009.12:g.138006693C>A
NC_000009.11:g.140901145C>A
NM_000718.4:c.1975-74C>A
More... 		05/01/2021 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 RCV001759098 CLINVAR
dbSNP (RS) rs560665141 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CACNA1B CLINVAR
OMIM 601012 CLINVAR