RGD:15125327 Rat Genome Database

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Variant: RGD:15125327 -  Homo sapiens

RGD ID: 15125327
RS ID: rs370991682
ClinVar ID: CV774895
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: F11  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 187,196,931
GRCh38 4 186,275,777
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000128.4:c.486-10T>A
NG_008051.1:g.14814T>A
NC_000004.12:g.186275777T>A
NC_000004.11:g.187196931T>A
More...
01/24/2020 intron variant likely benign|uncertain significance none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:F11
Accession:NM_000128
Location:INTRON

Gene Symbol:F11
Accession:XM_005262821
Location:INTRON

Gene Symbol:F11
Accession:XM_005262822
Location:INTRON

Gene Symbol:F11
Accession:XM_005262823
Location:INTRON

Gene Symbol:F11
Accession:XM_006714137
Location:INTRON

Gene Symbol:F11
Accession:XM_017007884
Location:INTRON

Gene Symbol:F11
Accession:XM_017007885
Location:INTRON

Gene Symbol:F11
Accession:XM_017007886
Location:INTRON

Gene Symbol:F11
Accession:NM_001354804
Location:INTRON

Gene Symbol:F11
Accession:XM_047449812
Location:INTRON

Gene Symbol:F11
Accession:XM_047449811
Location:INTRON

Gene Symbol:F11
Accession:XM_047449813
Location:INTRON

Gene Symbol:F11
Accession:XM_047449814
Location:INTRON

Gene Symbol:F11
Accession:XM_047449816
Location:INTRON

Gene Symbol:F11
Accession:XM_047449815
Location:INTRON

Gene Symbol:F11
Accession:XM_047449817
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000941186 CLINVAR
  RCV001275725 CLINVAR
dbSNP (RS) rs370991682 CLINVAR
MedGen C3661900 CLINVAR
  CN517202 CLINVAR
NCBI Gene F11 CLINVAR
OMIM 264900 CLINVAR