Variant #0000948329 (NC_000004.11:g.55147769C>T, NC_000004.11(NM_006206.4):c.2323+1120C>T (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.55147769C>T
DNA change (hg38) -
Published as PDGFRA(NM_001347827.2):c.2345C>T (p.(Thr782Met)), PDGFRA(NM_006206.4):c.2323+1120C>T
ISCN -
DB-ID PDGFRA_000026 See all 4 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDGFRA NM_006206.4 -/. - c.2323+1120C>T r.(=) p.(=)


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