RGD:15190451 Rat Genome Database

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Variant: RGD:15190451 -  Homo sapiens

RGD ID: 15190451
RS ID: rs60211209
ClinVar ID: CV730329
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL3  LOC105379174  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 131,398,103
GRCh38 5 132,062,410
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000588.4:c.294+9A>T
NC_000005.10:g.132062410A>T
NC_000005.9:g.131398103A>T
NM_000588.3:c.294+9A>T
 07/06/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:IL3
Accession:NM_000588
Location:INTRON

Gene Symbol:LOC105379174
Accession:XR_948785
Location:INTRON;NON-CODING

Gene Symbol:LOC105379174
Accession:XR_948784
Location:INTRON;NON-CODING

Gene Symbol:LOC105379174
Accession:XR_001742531
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000888102 CLINVAR
dbSNP (RS) rs60211209 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene IL3 CLINVAR
OMIM 147740 CLINVAR