RGD:150427491 Rat Genome Database

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Variant: RGD:150427491 -  Homo sapiens

RGD ID: 150427491
RS ID: rs17058879
ClinVar ID: CV1186655
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLNB  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 58,117,931
GRCh38 3 58,132,204
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.4391-604C>T
NM_001164319.2:c.4391-604C>T
NM_001457.4:c.4391-604C>T
NM_001164317.2:c.4483+185C>T
More... 		08/14/2018 intron variant likely benign none provided

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 RCV001560996 CLINVAR
dbSNP (RS) rs17058879 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FLNB CLINVAR
OMIM 603381 CLINVAR