rs138013864 Rat Genome Database

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Variant: rs138013864 -  Homo sapiens

RGD ID: 150487375
RS ID: rs138013864
ClinVar ID: CV1251513
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: DYRK1A  
Reference Nucleotide: -
Variant Nucleotide: TAAG
Position
Assembly Chr Position
GRCh37 21 38,792,453
GRCh38 21 37,420,151
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_130436.2:c.-223_-220dup
NM_001347721.2:c.-76-147_-76-144dup
NM_001347723.2:c.-78+52524_-78+52527dup
NG_009366.1:g.57596_57599dup
More... 		07/05/2018 5 prime utr variant benign none provided

Gene Symbol:DYRK1A
Accession:NM_130436
Location:5UTRS;EXON

Gene Symbol:DYRK1A
Accession:NM_101395
Location:5UTRS;INTRON

Gene Symbol:DYRK1A
Accession:NM_001396
Location:5UTRS;INTRON

Gene Symbol:DYRK1A
Accession:NM_001347722
Location:5UTRS;INTRON

Gene Symbol:DYRK1A
Accession:NM_001347721
Location:5UTRS;INTRON

Gene Symbol:DYRK1A
Accession:NM_001347723
Location:5UTRS;INTRON

Gene Symbol:DYRK1A
Accession:NM_130438
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001674184 CLINVAR
dbSNP (RS) rs138013864 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DYRK1A CLINVAR
OMIM 600855 CLINVAR