RGD:150468927 Rat Genome Database

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Variant: RGD:150468927 -  Homo sapiens

RGD ID: 150468927
RS ID: rs4821874
ClinVar ID: CV1218988
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PDGFB  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 22 39,626,375
GRCh38 22 39,230,370
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_033016.3:c.412-142T>G
NM_002608.4:c.457-142T>G
NG_012111.1:g.19583T>G
NC_000022.11:g.39230370A>C
More... 		07/05/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PDGFB
Accession:XM_047441394
Location:INTRON

Gene Symbol:PDGFB
Accession:NM_002608
Location:INTRON

Gene Symbol:PDGFB
Accession:XM_047441393
Location:INTRON

Gene Symbol:PDGFB
Accession:NM_033016
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001614740 CLINVAR
dbSNP (RS) rs4821874 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PDGFB CLINVAR
OMIM 190040 CLINVAR