rs146777169 Rat Genome Database

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Variant: rs146777169 -  Homo sapiens

RGD ID: 150534779
RS ID: rs146777169
ClinVar ID: CV1311610
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IFNA21  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 21,166,236
GRCh38 9 21,166,237
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000009.12:g.21166237C>A
NC_000009.11:g.21166236C>A
NP_002166.2:p.Glu126Ter
NG_030029.1:g.5424G>T
More... 		11/14/2021 nonsense risk factor
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV1311610Humanmultisystem inflammatory syndrome in children  IAGP 8554872ClinVar Annotator: match by term: Multisystem inflammatory syndrome in childrenClinVar 
Gene Symbol:IFNA21
Accession:NM_002175
Location:EXON
Amino Acid Prediction: E to * (nonsynonymous)
Amino Acid Position: 126
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MALSFSLLMAVLVLSYKSICSLGCDLPQTHSLGNRRALILLAQMGRISPFSCLKDRHDFGFPQEEFDGNQFQKAQAISVL
HEMIQQTFNLFSTKDSSATWEQSLLEKFSTELNQQLNDLEACVIQ*VGVEETPLMNVDSILAVKKYFQRITLYLTEKKYS
PCAWEVVRAEIMRSFSLSKIFQERLRRKE*
.


Database
Acc Id
Source(s)
ClinVar RCV001779420 CLINVAR
dbSNP (RS) rs146777169 CLINVAR
MedGen C5391534 CLINVAR
NCBI Gene IFNA21 CLINVAR
OMIM 147584 CLINVAR