rs3729783 Rat Genome Database

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Variant: rs3729783 -  Homo sapiens

RGD ID: 14730678
RS ID: rs3729783
ClinVar ID: CV667833
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CALM1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 14 90,866,280
GRCh38 14 90,399,936
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_006888.6:c.4-129A>G
NG_013338.1:g.7954A>G
NC_000014.9:g.90399936A>G
NC_000014.8:g.90866280A>G
More... 		06/14/2018 intron variant benign none provided

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

Gene Symbol:CALM1
Accession:NM_006888
Location:INTRON

Gene Symbol:CALM1
Accession:NM_001363670
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV000835789 CLINVAR
dbSNP (RS) rs3729783 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CALM1 CLINVAR
OMIM 114180 CLINVAR