Variant #0001034578 (NC_000004.11:g.55139771T>C, NM_006206.4:c.1432T>C (PDGFRA))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55139771T>C
DNA change (hg38) -
Published as PDGFRA(NM_006206.4):c.1432T>C (p.S478P), PDGFRA(NM_006206.6):c.1432T>C (p.(Ser478Pro), p.S478P)
ISCN -
DB-ID PDGFRA_000033 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.15383 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDGFRA NM_006206.4 -/. - c.1432T>C r.(?) p.(Ser478Pro)


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