RGD:156300148 Rat Genome Database

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Variant: RGD:156300148 -  Homo sapiens

RGD ID: 156300148
ClinVar ID: CV2002020
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLNB  FLNB-AS1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 58,155,313
GRCh38 3 58,169,586
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001164319.2:c.7346-4T>G
NM_001164318.2:c.7385-4T>G
NM_001457.4:c.7418-4T>G
NM_001164317.2:c.7511-4T>G
More... 		01/02/2024 intron variant likely benign|uncertain significance none provided

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

Gene Symbol:FLNB
Accession:NM_001164318
Location:INTRON

Gene Symbol:FLNB
Accession:NM_001457
Location:INTRON

Gene Symbol:FLNB
Accession:NM_001164317
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON;NON-CODING

Gene Symbol:FLNB-AS1
Accession:NR_135534
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002671123 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FLNB CLINVAR
  FLNB-AS1 CLINVAR
OMIM 603381 CLINVAR