Variant #0000012027 (NC_000004.11:-, PDGFRA(NM_006206.4):c.2609A>G)

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type direct sequencing of the samples expressing

PDGFRA revealed a PDGFRA N870S mutation in a 13-y
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID PDGFRA_00015
Frequency -
Variant remarks Exon
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDGFRA NM_006206.4 ./. 19 c.2609A>G - p.Asn870Ser