RGD:597763490 Rat Genome Database

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Variant: RGD:597763490 -  Homo sapiens

RGD ID: 597763490
ClinVar ID: CV3683305
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IFNA21  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 21,166,550
GRCh38 9 21,166,551
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_002175.2:c.62C>A
NG_030029.1:g.5110C>A
NC_000009.12:g.21166551G>T
NC_000009.11:g.21166550G>T
More... 		10/08/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004926347 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene IFNA21 CLINVAR
OMIM 147584 CLINVAR