rs150348065 Rat Genome Database

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Variant: rs150348065 -  Homo sapiens

RGD ID: 28882365
RS ID: rs150348065
ClinVar ID: CV889477
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLNB  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 57,994,195
GRCh38 3 58,008,468
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001164318.2:c.-97C>T
NM_001164319.2:c.-97C>T
NM_001457.4:c.-97C>T
NG_012801.1:g.5069C>T
More... 		01/12/2018 5 prime utr variant likely benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FLNB
Accession:NM_001164317
Location:5UTRS;EXON

Gene Symbol:FLNB
Accession:NM_001457
Location:5UTRS;EXON

Gene Symbol:FLNB
Accession:NM_001164318
Location:5UTRS;EXON

Gene Symbol:FLNB
Accession:NM_001164319
Location:5UTRS;EXON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001149923 CLINVAR
  RCV004711551 CLINVAR
dbSNP (RS) rs150348065 CLINVAR
MedGen C3661900 CLINVAR
  CN239400 CLINVAR
NCBI Gene FLNB CLINVAR
OMIM 603381 CLINVAR