rs907854023 Rat Genome Database

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Variant: rs907854023 -  Homo sapiens

RGD ID: 150422213
RS ID: rs907854023
ClinVar ID: CV1194887
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CALM1  LOC130056273  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 14 90,863,908
GRCh38 14 90,397,564
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001363669.2:c.-106+906C>A
NM_006888.6:c.3+331C>A
NG_013338.1:g.5582C>A
NC_000014.9:g.90397564C>A
More... 		10/31/2018 intron variant likely 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

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Database
Acc Id
Source(s)
ClinVar RCV001570915 CLINVAR
dbSNP (RS) rs907854023 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CALM1 CLINVAR
  LOC130056273 CLINVAR
OMIM 114180 CLINVAR