RGD:405147291 Rat Genome Database

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Variant: RGD:405147291 -  Homo sapiens

RGD ID: 405147291
ClinVar ID: CV3141860
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLNB  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 58,135,639
GRCh38 3 58,149,912
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001164317.2:c.6247C>G
NG_012801.1:g.146513C>G
NC_000003.12:g.58149912C>G
NC_000003.11:g.58135639C>G
More... 		08/05/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532   PMID:34491919  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003839782 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FLNB CLINVAR
OMIM 603381 CLINVAR