RGD:155960748 Rat Genome Database

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Variant: RGD:155960748 -  Homo sapiens

RGD ID: 155960748
ClinVar ID: CV2314060
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IFNA21  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 21,166,218
GRCh38 9 21,166,219
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_002175.2:c.394A>T
NG_030029.1:g.5442A>T
NC_000009.12:g.21166219T>A
NC_000009.11:g.21166218T>A
More... 		10/26/2022 missense variant uncertain significance AllHighlyPenetrant

Gene Symbol:IFNA21
Accession:NM_002175
Location:EXON
Amino Acid Prediction: T to S (nonsynonymous)
Amino Acid Position: 132
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MALSFSLLMAVLVLSYKSICSLGCDLPQTHSLGNRRALILLAQMGRISPFSCLKDRHDFGFPQEEFDGNQFQKAQAISVL
HEMIQQTFNLFSTKDSSATWEQSLLEKFSTELNQQLNDLEACVIQEVGVEESPLMNVDSILAVKKYFQRITLYLTEKKYS
PCAWEVVRAEIMRSFSLSKIFQERLRRKE*
.


Database
Acc Id
Source(s)
ClinVar RCV004164338 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene IFNA21 CLINVAR
OMIM 147584 CLINVAR