Variant #0000859450 (NC_000004.11:g.55133783C>T, NM_006206.4:c.996C>T (PDGFRA))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55133783C>T
DNA change (hg38) -
Published as PDGFRA(NM_001347827.1):c.996C>T (p.(Val332=)), PDGFRA(NM_001347830.1):c.1035C>T (p.V345=), PDGFRA(NM_006206.6):c.996C>T (p.V332=)
ISCN -
DB-ID PDGFRA_000011 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) 0.0019 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDGFRA NM_006206.4 -?/. - c.996C>T r.(?) p.(Val332=)


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