RGD:13540956 Rat Genome Database

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Variant: RGD:13540956 -  Homo sapiens

RGD ID: 13540956
RS ID: rs1555982713
ClinVar ID: CV507529
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DYRK1A  LOC105372797  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 21 38,858,924
GRCh38 21 37,486,622
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009366.1:g.124066A>C
NC_000021.9:g.37486622A>C
NC_000021.8:g.38858924A>C
NM_001396.3:c.664+8A>C
More... 		02/23/2017 intron variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_001347721
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_130438
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_130436
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_001347722
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_101395
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_001396
Location:INTRON

Gene Symbol:DYRK1A
Accession:NM_001347723
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000615456 CLINVAR
dbSNP (RS) rs1555982713 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene DYRK1A CLINVAR
OMIM 600855 CLINVAR