RGD:405196132 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: RGD:405196132 -  Homo sapiens

RGD ID: 405196132
ClinVar ID: CV3128756
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLNB  FLNB-AS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 58,155,322
GRCh38 3 58,169,595
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.7351C>T
NM_001164318.2:c.7390C>T
NM_001457.4:c.7423C>T
NM_001164317.2:c.7516C>T
More...
12/28/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003821494 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FLNB CLINVAR
  FLNB-AS1 CLINVAR
OMIM 603381 CLINVAR