RGD:597763486 Rat Genome Database

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Variant: RGD:597763486 -  Homo sapiens

RGD ID: 597763486
ClinVar ID: CV3683304
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IFNA21  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 21,166,502
GRCh38 9 21,166,503
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_002175.2:c.110C>T
NG_030029.1:g.5158C>T
NC_000009.12:g.21166503G>A
NC_000009.11:g.21166502G>A
More... 		08/20/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004926346 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene IFNA21 CLINVAR
OMIM 147584 CLINVAR