rs12886342 Rat Genome Database

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Variant: rs12886342 -  Homo sapiens

RGD ID: 14726584
RS ID: rs12886342
ClinVar ID: CV656269
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CALM1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 14 90,863,489
GRCh38 14 90,397,145
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_006888.6:c.-86G>A
NG_056700.1:g.421G>A
NG_013338.1:g.5163G>A
NC_000014.9:g.90397145G>A
More... 		07/14/2021 5 prime utr variant benign none provided
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV656269Humancatecholaminergic polymorphic ventricular tachycardia 4  IAGP 8554872ClinVar Annotator: match by term: Ventricular tachycardia, catecholaminergic polymorphic, 4ClinVarPMID:25741868
Gene Symbol:CALM1
Accession:NM_006888
Location:5UTRS;EXON

Gene Symbol:CALM1
Accession:NM_001363669
Location:5UTRS;INTRON

Gene Symbol:CALM1
Accession:NM_001363670
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV000833933 CLINVAR
  RCV001554674 CLINVAR
dbSNP (RS) rs12886342 CLINVAR
MedGen C3554047 CLINVAR
  C3661900 CLINVAR
NCBI Gene CALM1 CLINVAR
OMIM 114180 CLINVAR
  614916 CLINVAR