RGD:15183806 Rat Genome Database

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Variant: RGD:15183806 -  Homo sapiens

RGD ID: 15183806
RS ID: rs73122541
ClinVar ID: CV778971
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL5RA  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 3,139,546
GRCh38 3 3,097,862
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000564.5:c.709+8C>T
NM_001243099.2:c.709+8C>T
NM_175725.3:c.709+8C>T
NM_175726.4:c.709+8C>T
More... 		07/16/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:IL5RA
Accession:NM_175726
Location:INTRON

Gene Symbol:IL5RA
Accession:NM_000564
Location:INTRON

Gene Symbol:IL5RA
Accession:NM_175728
Location:INTRON

Gene Symbol:IL5RA
Accession:NM_175725
Location:INTRON

Gene Symbol:IL5RA
Accession:NM_175727
Location:INTRON

Gene Symbol:IL5RA
Accession:NM_175724
Location:INTRON

Gene Symbol:IL5RA
Accession:NM_001243099
Location:INTRON

Gene Symbol:IL5RA
Accession:XM_011533677
Location:INTRON

Gene Symbol:IL5RA
Accession:XM_011533678
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000974961 CLINVAR
dbSNP (RS) rs73122541 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene IL5RA CLINVAR
OMIM 147851 CLINVAR