RGD:151811686 Rat Genome Database

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Variant: RGD:151811686 -  Homo sapiens

RGD ID: 151811686
RS ID: rs2107058611
ClinVar ID: CV1349406
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLNB  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 58,083,714
GRCh38 3 58,097,987
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.1147+10C>G
NM_001164318.2:c.1147+10C>G
NM_001164319.2:c.1147+10C>G
NM_001457.4:c.1147+10C>G
More... 		02/08/2023 intron variant likely benign|uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:FLNB
Accession:NM_001164317
Location:INTRON

Gene Symbol:FLNB
Accession:NM_001457
Location:INTRON

Gene Symbol:FLNB
Accession:NM_001164319
Location:INTRON

Gene Symbol:FLNB
Accession:NM_001164318
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001974837 CLINVAR
dbSNP (RS) rs2107058611 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FLNB CLINVAR
OMIM 603381 CLINVAR