RGD:28871569 Rat Genome Database

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Variant: RGD:28871569 -  Homo sapiens

RGD ID: 28871569
RS ID: rs781073886
ClinVar ID: CV891695
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLNB  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 58,106,963
GRCh38 3 58,121,236
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001164318.2:c.2864-5T>A
NM_001164319.2:c.2864-5T>A
NM_001164317.2:c.2864-5T>A
NM_001457.4:c.2864-5T>A
More... 		04/28/2017 intron variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FLNB
Accession:NM_001164319
Location:INTRON

Gene Symbol:FLNB
Accession:NM_001457
Location:INTRON

Gene Symbol:FLNB
Accession:NM_001164318
Location:INTRON

Gene Symbol:FLNB
Accession:NM_001164317
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001145917 CLINVAR
dbSNP (RS) rs781073886 CLINVAR
MedGen CN239400 CLINVAR
NCBI Gene FLNB CLINVAR
OMIM 603381 CLINVAR