RGD:150421776 Rat Genome Database

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Variant: RGD:150421776 -  Homo sapiens

RGD ID: 150421776
RS ID: rs76993887
ClinVar ID: CV1197341
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PDGFRB  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 149,495,624
GRCh38 5 150,116,061
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.2655-115C>T
NM_001355016.2:c.2946-115C>T
NM_002609.4:c.3138-115C>T
NG_012303.2:g.2312C>T
More... 		03/24/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PDGFRB
Accession:NM_001355017
Location:INTRON

Gene Symbol:PDGFRB
Accession:NM_001355016
Location:INTRON

Gene Symbol:PDGFRB
Accession:NM_002609
Location:INTRON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001578176 CLINVAR
dbSNP (RS) rs76993887 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PDGFRB CLINVAR
OMIM 173410 CLINVAR