RGD:153303403 Rat Genome Database

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Variant: RGD:153303403 -  Homo sapiens

RGD ID: 153303403
RS ID: rs9282701
ClinVar ID: CV1686211
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HMOX1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 35,777,154
GRCh38 22 35,381,161
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002133.3:c.-13C>T
NG_023030.1:g.5095C>T
NC_000022.11:g.35381161C>T
NC_000022.10:g.35777154C>T
More... 		07/09/2021 5 prime utr variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:HMOX1
Accession:NM_002133
Location:5UTRS;EXON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002261644 CLINVAR
dbSNP (RS) rs9282701 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HMOX1 CLINVAR
OMIM 141250 CLINVAR