RGD:405134962 Rat Genome Database

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Variant: RGD:405134962 -  Homo sapiens

RGD ID: 405134962
ClinVar ID: CV2957983
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLNB  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 58,111,348
GRCh38 3 58,125,621
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.3939C>A
NM_001164318.2:c.3939C>A
NM_001164319.2:c.3939C>A
NM_001457.4:c.3939C>A
More... 		10/19/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003672734 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FLNB CLINVAR
OMIM 603381 CLINVAR