RGD:14714771 Rat Genome Database

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Variant: RGD:14714771 -  Homo sapiens

RGD ID: 14714771
RS ID: rs115788075
ClinVar ID: CV667119
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CALM1  LOC112272566  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 14 90,863,185
GRCh38 14 90,396,841
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006888.4:c.-390C>T
NC_000014.8:g.90863185C>T
NG_056700.1:g.117C>T
NM_001363669.2:c.-106+183C>T
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CALM1
Accession:NM_001363669
Location:5UTRS;INTRON

Gene Symbol:CALM1
Accession:NM_001363670
Location:INTRON

Gene Symbol:CALM1
Accession:NM_006888
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000829147 CLINVAR
dbSNP (RS) rs115788075 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CALM1 CLINVAR
  LOC112272566 CLINVAR
OMIM 114180 CLINVAR