RGD:15143484 Rat Genome Database

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Variant: RGD:15143484 -  Homo sapiens

RGD ID: 15143484
RS ID: rs143352256
ClinVar ID: CV744280
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HLA-DPA1  HLA-DPB1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 33,043,926
GRCh38 6 33,076,149
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001242525.2:c.-23-2556G>A
NM_001242524.2:c.-99-2480G>A
NM_002121.6:c.100+8C>T
NG_033242.1:g.5224C>T
More...
07/31/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HLA-DPA1
Accession:NM_001242525
Location:5UTRS;INTRON

Gene Symbol:HLA-DPA1
Accession:NM_001242524
Location:5UTRS;INTRON

Gene Symbol:HLA-DPB1
Accession:NM_002121
Location:INTRON

Gene Symbol:HLA-DPA1
Accession:NM_033554
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:HLA-DPA1
Accession:NM_001405020
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000899845 CLINVAR
dbSNP (RS) rs143352256 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HLA-DPA1 CLINVAR
  HLA-DPB1 CLINVAR
OMIM 142858 CLINVAR
  142880 CLINVAR