RGD:15178488 Rat Genome Database

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Variant: RGD:15178488 -  Homo sapiens

RGD ID: 15178488
RS ID: rs757543142
ClinVar ID: CV775785
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLI1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 128,638,174
GRCh38 11 128,768,279
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002017.5:c.385+7C>T
NG_032912.1:g.86745C>T
NC_000011.10:g.128768279C>T
NC_000011.9:g.128638174C>T
More... 		09/19/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FLI1
Accession:NM_001271012
Location:INTRON

Gene Symbol:FLI1
Accession:NM_002017
Location:INTRON

Gene Symbol:FLI1
Accession:XM_047426630
Location:INTRON

Gene Symbol:FLI1
Accession:XM_011542701
Location:INTRON

Gene Symbol:FLI1
Accession:XM_017017405
Location:INTRON

Gene Symbol:FLI1
Accession:XM_017017406
Location:INTRON

Gene Symbol:FLI1
Accession:NM_001271010
Location:INTRON

Gene Symbol:FLI1
Accession:XM_011542702
Location:INTRON

Gene Symbol:FLI1
Accession:NM_001167681
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000929409 CLINVAR
dbSNP (RS) rs757543142 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene FLI1 CLINVAR
OMIM 193067 CLINVAR