RGD:402485162 Rat Genome Database

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Variant: RGD:402485162 -  Homo sapiens

RGD ID: 402485162
ClinVar ID: CV2931562
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HMOX1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 35,779,220
GRCh38 22 35,383,227
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.144+1G>A
NG_023030.1:g.7161G>A
NC_000022.11:g.35383227G>A
NC_000022.10:g.35779220G>A
 09/29/2023 splice donor variant likely pathogenic none provided

Variant Details
Variant Transcripts
Gene Symbol:HMOX1
Accession:NM_002133
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:9884342   PMID:16199547   PMID:21088618   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003572457 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HMOX1 CLINVAR
OMIM 141250 CLINVAR