RGD:15148718 Rat Genome Database

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Variant: RGD:15148718 -  Homo sapiens

RGD ID: 15148718
RS ID: rs781825586
ClinVar ID: CV745357
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HIRA  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 19,343,274
GRCh38 22 19,355,751
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003325.4:c.2561+9G>A
NG_009231.2:g.80946G>A
NC_000022.11:g.19355751C>T
NC_000022.10:g.19343274C>T
More... 		06/18/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HIRA
Accession:NM_003325
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000900779 CLINVAR
  RCV003958137 CLINVAR
dbSNP (RS) rs781825586 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HIRA CLINVAR
OMIM 600237 CLINVAR