RGD:15160497 Rat Genome Database

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Variant: RGD:15160497 -  Homo sapiens

RGD ID: 15160497
RS ID: rs149102313
ClinVar ID: CV714244
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FOS  LOC127828010  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 14 75,747,683
GRCh38 14 75,280,980
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005252.4:c.699G>A
NG_029673.1:g.7203G>A
NC_000014.9:g.75280980G>A
NC_000014.8:g.75747683G>A
More... 		05/01/2022 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FOS
Accession:NM_005252
Location:EXON
Amino Acid Prediction: P to P (synonymous)
Amino Acid Position: 233
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MMFSGFNADYEASSSRCSSASPAGDSLSYYHSPADSFSSMGSPVNAQDFCTDLAVSSANFIPTVTAISTSPDLQWLVQPA
LVSSVAPSQTRAPHPFGVPAPSAGAYSRAGVVKTMTGGRAQSIGRRGKVEQLSPEEEEKRRIRRERNKMAAAKCRNRRRE
LTDTLQAETDQLEDEKSALQTEIANLLKEKEKLEFILAAHRPACKIPDDLGFPEEMSVASLDLTGGLPEVATPESEEAFT
LPLLNDPEPKPSVEPVKSISSMELKTEPFDDFLFPASSRPSGSETARSVPDMDLSGSFYAADWEPLHSGSLGMGPMATEL
EPLCTPVVTCTPSCTAYTSSFVFTYPEADSFPSCAAAHRKGSSSNEPSSDSLSSPTLLAL*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000969914 CLINVAR
dbSNP (RS) rs149102313 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FOS CLINVAR
OMIM 164810 CLINVAR