Variant #0000298847 (NC_000005.9:g.149515397T>A, NM_002609.3:c.85A>T (PDGFRB))

Chromosome 5
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.149515397T>A
DNA change (hg38) g.150135834T>A
Published as PDGFRB(NM_002609.3):c.85A>T (p.(Ile29Phe)), PDGFRB(NM_002609.4):c.85A>T (p.I29F)
ISCN -
DB-ID PDGFRB_000049 See all 2 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) 0.03773 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDGFRB NM_002609.3 -/. - c.85A>T r.(?) p.(Ile29Phe)


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