RGD:28880035 Rat Genome Database

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Variant: RGD:28880035 -  Homo sapiens

RGD ID: 28880035
RS ID: rs193215681
ClinVar ID: CV889533
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLNB  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 58,156,960
GRCh38 3 58,171,233
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000003.11:g.58156960G>A
NM_001457.3:c.*471G>A
NM_001164318.2:c.*471G>A
NM_001164319.2:c.*471G>A
More... 		01/12/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FLNB
Accession:NM_001457
Location:3UTRS;EXON

Gene Symbol:FLNB
Accession:NM_001164318
Location:3UTRS;EXON

Gene Symbol:FLNB
Accession:NM_001164317
Location:3UTRS;EXON

Gene Symbol:FLNB
Accession:NM_001164319
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001149178 CLINVAR
dbSNP (RS) rs193215681 CLINVAR
MedGen CN239400 CLINVAR
NCBI Gene FLNB CLINVAR
OMIM 603381 CLINVAR