RGD:150457929 Rat Genome Database

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Variant: RGD:150457929 -  Homo sapiens

RGD ID: 150457929
RS ID: rs546349031
ClinVar ID: CV1278696
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HNRNPU  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 245,026,720
GRCh38 1 244,863,418
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004501.3:c.634+256T>C
NM_031844.3:c.691+199T>C
NG_042184.1:g.6108T>C
NC_000001.11:g.244863418A>G
More... 		08/06/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HNRNPU
Accession:NM_031844
Location:INTRON

Gene Symbol:HNRNPU
Accession:NM_004501
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001709312 CLINVAR
dbSNP (RS) rs546349031 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HNRNPU CLINVAR
  LOC129932913 CLINVAR
OMIM 602869 CLINVAR