Variant #0000572081 (NC_000022.10:g.39631768G>T, NC_000022.10(NM_002608.2):c.160+15C>A (PDGFB))

Chromosome 22
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.39631768G>T
DNA change (hg38) g.39235763G>T
Published as PDGFB(NM_002608.3):c.160+15C>A, PDGFB(NM_002608.4):c.160+15C>A
ISCN -
DB-ID PDGFB_000023 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) 0.03654 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDGFB NM_002608.2 -/. - c.160+15C>A r.(=) p.(=)


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