rs116807296 Rat Genome Database

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Variant: rs116807296 -  Homo sapiens

RGD ID: 150416480
RS ID: rs116807296
ClinVar ID: CV1181200
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CALM1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 14 90,870,582
GRCh38 14 90,404,238
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001363669.2:c.178-141A>C
NM_006888.6:c.286-141A>C
NM_001363670.2:c.289-141A>C
NG_013338.1:g.12256A>C
More... 		09/22/2018 intron variant likely benign none provided

Gene Symbol:CALM1
Accession:NM_006888
Location:INTRON

Gene Symbol:CALM1
Accession:NM_001363669
Location:INTRON

Gene Symbol:CALM1
Accession:NM_001363670
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001549661 CLINVAR
dbSNP (RS) rs116807296 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CALM1 CLINVAR
OMIM 114180 CLINVAR