RGD:150503787 Rat Genome Database

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Variant: RGD:150503787 -  Homo sapiens

RGD ID: 150503787
RS ID: rs35965249
ClinVar ID: CV1223820
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HNRNPD  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 83,279,722
GRCh38 4 82,358,569
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001003810.2:c.564+90A>G
NM_031369.3:c.564+90A>G
NM_002138.4:c.621+90A>G
NM_031370.3:c.621+90A>G
More... 		06/19/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HNRNPD
Accession:NM_001003810
Location:INTRON

Gene Symbol:HNRNPD
Accession:NM_031370
Location:INTRON

Gene Symbol:HNRNPD
Accession:NM_002138
Location:INTRON

Gene Symbol:HNRNPD
Accession:NM_031369
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001621469 CLINVAR
dbSNP (RS) rs35965249 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HNRNPD CLINVAR
OMIM 601324 CLINVAR