rs2148601089 Rat Genome Database

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Variant: rs2148601089 -  Homo sapiens

RGD ID: 150555626
RS ID: rs2148601089
ClinVar ID: CV1304778
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DYRK1A  LOC105372797  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 21 38,858,915
GRCh38 21 37,486,613
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001347723.2:c.549A>G
NM_001347721.2:c.636A>G
NM_001347722.2:c.636A>G
NM_130436.2:c.636A>G
More... 		04/07/2021 missense variant uncertain significance none provided

Gene Symbol:DYRK1A
Accession:NM_101395
Location:EXON

Gene Symbol:DYRK1A
Accession:NM_130436
Location:EXON

Gene Symbol:DYRK1A
Accession:NM_130438
Location:EXON

Gene Symbol:DYRK1A
Accession:NM_001396
Location:EXON

Gene Symbol:DYRK1A
Accession:NM_001347722
Location:EXON

Gene Symbol:DYRK1A
Accession:NM_001347721
Location:EXON

Gene Symbol:DYRK1A
Accession:NM_001347723
Location:EXON

Gene Symbol:LOC105372797
Accession:XR_001755034
Location:INTRON;NON-CODING

Gene Symbol:LOC105372797
Accession:XR_002958655
Location:INTRON;NON-CODING

Gene Symbol:LOC105372797
Accession:XR_002958654
Location:INTRON;NON-CODING

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Database
Acc Id
Source(s)
ClinVar RCV001773026 CLINVAR
dbSNP (RS) rs2148601089 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DYRK1A CLINVAR
OMIM 600855 CLINVAR