RGD:156026461 Rat Genome Database

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Variant: RGD:156026461 -  Homo sapiens

RGD ID: 156026461
ClinVar ID: CV2055855
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARIH1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 15 72,810,399
GRCh38 15 72,518,058
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005744.5:c.376-9C>G
NC_000015.10:g.72518058C>G
NC_000015.9:g.72810399C>G
 06/12/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ARIH1
Accession:NM_005744
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002820869 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARIH1 CLINVAR
OMIM 605624 CLINVAR