RGD:156252830 Rat Genome Database

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Variant: RGD:156252830 -  Homo sapiens

RGD ID: 156252830
ClinVar ID: CV2390088
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IFNA4  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 21,187,329
GRCh38 9 21,187,330
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021068.4:c.202G>A
NC_000009.12:g.21187330C>T
NC_000009.11:g.21187329C>T
NM_021068.2:c.202G>A
More... 		04/25/2022 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:IFNA4
Accession:NM_021068
Location:EXON
Amino Acid Prediction: G to S (nonsynonymous)
Amino Acid Position: 68
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MALSFSLLMAVLVLSYKSICSLGCDLPQTHSLGNRRALILLAQMGRISHFSCLKDRHDFGFPEEEFDSHQFQKAQAISVL
HEMIQQTFNLFSTEDSSAAWEQSLLEKFSTELYQQLNDLEACVIQEVGVEETPLMNEDSILAVRKYFQRITLYLTEKKYS
PCAWEVVRAEIMRSLSFSTNLQKRLRRKD*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002768975 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene IFNA4 CLINVAR
OMIM 147564 CLINVAR