RGD:14718200 Rat Genome Database

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Variant: RGD:14718200 -  Homo sapiens

RGD ID: 14718200
RS ID: rs10663545
ClinVar ID: CV660019
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: FLNB  
Reference Nucleotide: -
Variant Nucleotide: AT
Position
Assembly Chr Position
GRCh37 3 58,131,376
GRCh38 3 58,145,649
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.58131376_58131377insAT
NM_001457.3:c.5426-272_5426-271insAT
NM_001164317.2:c.5519-272_5519-271insAT
NM_001164319.2:c.5354-272_5354-271insAT
More... 		06/14/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FLNB
Accession:NM_001164317
Location:INTRON

Gene Symbol:FLNB
Accession:NM_001164319
Location:INTRON

Gene Symbol:FLNB
Accession:NM_001164318
Location:INTRON

Gene Symbol:FLNB
Accession:NM_001457
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000830316 CLINVAR
dbSNP (RS) rs10663545 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FLNB CLINVAR
OMIM 603381 CLINVAR