RGD:15161105 Rat Genome Database

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Variant: RGD:15161105 -  Homo sapiens

RGD ID: 15161105
RS ID: rs144760068
ClinVar ID: CV724614
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FOSL1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 65,660,600
GRCh38 11 65,893,129
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NR_125339.2:n.431C>A
NM_005438.5:c.573C>A
NG_047103.1:g.411C>A
NC_000011.10:g.65893129G>T
More... 		12/11/2018 3 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FOSL1
Accession:NM_001300855
Location:3UTRS;EXON

Gene Symbol:FOSL1
Accession:NM_001300856
Location:EXON
Amino Acid Prediction: S to R (nonsynonymous)
Amino Acid Position: 125
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MFRDFGEPGPSSGNGGGYGGPAQPPAAAQAAQQISPEEEERRRVRRERNKLAAAKCRNRRKELTDFLQAETDKLEDEKSG
LQREIEELQKQKERLELVLEAHRPICKIPEGAKEGDTGSTSGTSRPPAPCRPVPCISLSPGPVLEPEALHTPTLMTTPSL
TPFTPSLVFTYPSTPEPCASAHRKSSSSSGDPSSDPLGSPTLLAL*

Gene Symbol:FOSL1
Accession:NM_005438
Location:EXON
Amino Acid Prediction: S to R (nonsynonymous)
Amino Acid Position: 191
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MFRDFGEPGPSSGNGGGYGGPAQPPAAAQAAQQKFHLVPSINTMSGSQELQWMVQPHFLGPSSYPRPLTYPQYSPPQPRP
GVIRALGPPPGVRRRPCEQISPEEEERRRVRRERNKLAAAKCRNRRKELTDFLQAETDKLEDEKSGLQREIEELQKQKER
LELVLEAHRPICKIPEGAKEGDTGSTSGTSRPPAPCRPVPCISLSPGPVLEPEALHTPTLMTTPSLTPFTPSLVFTYPST
PEPCASAHRKSSSSSGDPSSDPLGSPTLLAL*

Gene Symbol:FOSL1
Accession:NM_001300844
Location:EXON
Amino Acid Prediction: S to R (nonsynonymous)
Amino Acid Position: 155
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MFRDFGEPGPSSGNGGGYGGPAQPPAAAQAAQQKFHLVPSINTMSGSQELQWMVQPHFLGPSSYPRPLTYPQYSPPQPRP
GVIRALGPPPGVRRRPCEQETDKLEDEKSGLQREIEELQKQKERLELVLEAHRPICKIPEGAKEGDTGSTSGTSRPPAPC
RPVPCISLSPGPVLEPEALHTPTLMTTPSLTPFTPSLVFTYPSTPEPCASAHRKSSSSSGDPSSDPLGSPTLLAL*

Gene Symbol:FOSL1
Accession:NM_001300857
Location:EXON
Amino Acid Prediction: S to R (nonsynonymous)
Amino Acid Position: 89
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MFRDFGEPGPSSGNGGGYGGPAQPPAAAQAAQQETDKLEDEKSGLQREIEELQKQKERLELVLEAHRPICKIPEGAKEGD
TGSTSGTSRPPAPCRPVPCISLSPGPVLEPEALHTPTLMTTPSLTPFTPSLVFTYPSTPEPCASAHRKSSSSSGDPSSDP
LGSPTLLAL*

Gene Symbol:FOSL1
Accession:NR_125339
Location:EXON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000881510 CLINVAR
dbSNP (RS) rs144760068 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FOSL1 CLINVAR
OMIM 136515 CLINVAR