RGD:405153983 Rat Genome Database

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Variant: RGD:405153983 -  Homo sapiens

RGD ID: 405153983
ClinVar ID: CV2883998
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: F11  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 187,206,978
GRCh38 4 186,285,824
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.1480+11T>C
LRG_583:g.24861T>C
NG_008051.1:g.24861T>C
NC_000004.12:g.186285824T>C
More... 		11/29/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:F11
Accession:XM_017007886
Location:INTRON

Gene Symbol:F11
Accession:XM_006714137
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:NM_001354804
Location:INTRON

Gene Symbol:F11
Accession:XM_047449814
Location:INTRON

Gene Symbol:F11
Accession:XM_017007884
Location:INTRON

Gene Symbol:F11
Accession:NM_000128
Location:INTRON

Gene Symbol:F11
Accession:XM_047449811
Location:INTRON

Gene Symbol:F11
Accession:XM_047449816
Location:INTRON

Gene Symbol:F11
Accession:XM_017007885
Location:INTRON

Gene Symbol:F11
Accession:XM_047449812
Location:INTRON

Gene Symbol:F11
Accession:XM_047449813
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 RCV003561847 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene F11 CLINVAR
OMIM 264900 CLINVAR