Variant #0000000372 (NC_000004.11:g.55161348T>A, PDGFRA(NM_006206.4):c.3179T>A)

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.55161348T>A
Reference -
DB-ID PDGFRA_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDGFRA NM_006206.4 ?/? - c.3179T>A r.(?) p.(Ile1060Asn)