RGD:9691246 Rat Genome Database

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Variant: RGD:9691246 -  Homo sapiens

RGD ID: 9691246
RS ID: rs267607279
ClinVar ID: CV171782
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CALM1  LOC126862021  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 14 90,870,874
GRCh38 14 90,404,530
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_013338.1:g.12548C>G
NC_000014.9:g.90404530C>G
NC_000014.8:g.90870874C>G
NM_001363669.2:c.313+16C>G
More... 		07/23/2012 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CALM1
Accession:NM_006888
Location:INTRON

Gene Symbol:CALM1
Accession:NM_001363670
Location:INTRON

Gene Symbol:CALM1
Accession:NM_001363669
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:23040497  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000149484 CLINVAR
dbSNP (RS) rs267607279 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene CALM1 CLINVAR
  LOC126862021 CLINVAR
OMIM 114180 CLINVAR