rs141007341 Rat Genome Database

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Variant: rs141007341 -  Homo sapiens

RGD ID: 150471541
RS ID: rs141007341
ClinVar ID: CV1209568
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CALM1  LOC112272566  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 14 90,863,414
GRCh38 14 90,397,070
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001363669.2:c.-106+412C>T
NM_006888.6:c.-161C>T
NG_056700.1:g.346C>T
NG_013338.1:g.5088C>T
More... 		07/15/2018 5 prime utr variant likely benign none provided

Gene Symbol:CALM1
Accession:NM_006888
Location:5UTRS;EXON

Gene Symbol:CALM1
Accession:NM_001363669
Location:5UTRS;INTRON

Gene Symbol:CALM1
Accession:NM_001363670
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001588679 CLINVAR
dbSNP (RS) rs141007341 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CALM1 CLINVAR
  LOC112272566 CLINVAR
OMIM 114180 CLINVAR