RGD:155927971 Rat Genome Database

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Variant: RGD:155927971 -  Homo sapiens

RGD ID: 155927971
ClinVar ID: CV2227424
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FOS  LOC127828010  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 14 75,747,843
GRCh38 14 75,281,140
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005252.4:c.859C>T
NG_129509.1:g.543C>T
NG_029673.1:g.7363C>T
NC_000014.9:g.75281140C>T
More... 		08/16/2021 missense variant uncertain significance AllHighlyPenetrant

Gene Symbol:FOS
Accession:NM_005252
Location:EXON
Amino Acid Prediction: R to C (nonsynonymous)
Amino Acid Position: 287
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MMFSGFNADYEASSSRCSSASPAGDSLSYYHSPADSFSSMGSPVNAQDFCTDLAVSSANFIPTVTAISTSPDLQWLVQPA
LVSSVAPSQTRAPHPFGVPAPSAGAYSRAGVVKTMTGGRAQSIGRRGKVEQLSPEEEEKRRIRRERNKMAAAKCRNRRRE
LTDTLQAETDQLEDEKSALQTEIANLLKEKEKLEFILAAHRPACKIPDDLGFPEEMSVASLDLTGGLPEVATPESEEAFT
LPLLNDPEPKPSVEPVKSISSMELKTEPFDDFLFPASSRPSGSETACSVPDMDLSGSFYAADWEPLHSGSLGMGPMATEL
EPLCTPVVTCTPSCTAYTSSFVFTYPEADSFPSCAAAHRKGSSSNEPSSDSLSSPTLLAL*
.


Database
Acc Id
Source(s)
ClinVar RCV004092088 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene FOS CLINVAR
OMIM 164810 CLINVAR