rs201723751 Rat Genome Database

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Variant: rs201723751 -  Homo sapiens

RGD ID: 150499498
RS ID: rs201723751
ClinVar ID: CV1224600
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: CALM1  
Reference Nucleotide: -
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 14 90,867,999
GRCh38 14 90,401,655
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_006888.6:c.178+269dup
NM_001363670.2:c.181+269dup
NM_001363669.2:c.70+269dup
NG_013338.1:g.9689dup
More... 		08/10/2019 intron variant 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 RCV001620431 CLINVAR
dbSNP (RS) rs201723751 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CALM1 CLINVAR
OMIM 114180 CLINVAR