RGD:15167860 Rat Genome Database

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Variant: RGD:15167860 -  Homo sapiens

RGD ID: 15167860
RS ID: rs1367367619
ClinVar ID: CV749347
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PDGFRB  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 149,512,504
GRCh38 5 150,132,941
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001355017.2:c.453G>A
NM_001355016.2:c.744G>A
NM_002609.4:c.936G>A
NG_023367.1:g.27919G>A
More... 		05/31/2018 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PDGFRB
Accession:NM_002609
Location:EXON

Gene Symbol:PDGFRB
Accession:NM_001355016
Location:EXON

Gene Symbol:PDGFRB
Accession:NM_001355017
Location:EXON

Gene Symbol:PDGFRB
Accession:NR_149150
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000927175 CLINVAR
dbSNP (RS) rs1367367619 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene PDGFRB CLINVAR
OMIM 173410 CLINVAR