RGD:15137548 Rat Genome Database

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Variant: RGD:15137548 -  Homo sapiens

RGD ID: 15137548
RS ID: rs374117160
ClinVar ID: CV768301
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLI1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 128,651,917
GRCh38 11 128,782,022
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001167681.3:c.555A>G
LRG_646p2:p.Glu152=
LRG_646p1:p.Glu185=
LRG_646p3:p.Glu25=
More... 		07/20/2018 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FLI1
Accession:NM_001167681
Location:EXON

Gene Symbol:FLI1
Accession:XM_011542701
Location:EXON

Gene Symbol:FLI1
Accession:XM_017017405
Location:EXON

Gene Symbol:FLI1
Accession:XM_011542702
Location:EXON

Gene Symbol:FLI1
Accession:XM_017017406
Location:EXON

Gene Symbol:FLI1
Accession:XM_047426630
Location:EXON

Gene Symbol:FLI1
Accession:NM_002017
Location:EXON

Gene Symbol:FLI1
Accession:NM_001271012
Location:EXON

Gene Symbol:FLI1
Accession:NM_001271010
Location:EXON

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000943257 CLINVAR
  RCV003970634 CLINVAR
dbSNP (RS) rs374117160 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FLI1 CLINVAR
OMIM 193067 CLINVAR