RGD:150497337 Rat Genome Database

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Variant: RGD:150497337 -  Homo sapiens

RGD ID: 150497337
RS ID: rs756177494
ClinVar ID: CV1208739
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CALM2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 47,387,986
GRCh38 2 47,160,847
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001305625.2:c.314-43C>T
NM_001305626.1:c.314-43C>T
NM_001743.6:c.422-43C>T
NM_001305624.1:c.566-43C>T
More... 		11/20/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CALM2
Accession:NM_001305624
Location:INTRON

Gene Symbol:CALM2
Accession:NM_001743
Location:INTRON

Gene Symbol:CALM2
Accession:NM_001305625
Location:INTRON

Gene Symbol:CALM2
Accession:NM_001305626
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001593955 CLINVAR
dbSNP (RS) rs756177494 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CALM2 CLINVAR
OMIM 114182 CLINVAR