Variant #0000809637 (NC_000022.10:g.39621843_39621852dup, NM_002608.2:c.607_616dup (PDGFB))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.39621843_39621852dup
DNA change (hg38) -
Published as PDGFB(NM_002608.3):c.607_616dupACGCCCCAAA (p.T206Nfs*29)
ISCN -
DB-ID PDGFB_000032
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDGFB NM_002608.2 ?/. - c.607_616dup r.(?) p.(Thr206Asnfs*29)


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