RGD:405134803 Rat Genome Database

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Variant: RGD:405134803 -  Homo sapiens

RGD ID: 405134803
ClinVar ID: CV2899133
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HMOX1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 22 35,779,224
GRCh38 22 35,383,231
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+5G>C
NG_023030.1:g.7165G>C
NC_000022.11:g.35383231G>C
NC_000022.10:g.35779224G>C
 10/15/2023 intron variant uncertain significance none provided

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

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003560325 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HMOX1 CLINVAR
OMIM 141250 CLINVAR