Variant #0000975651 (NC_000003.11:g.167414819_167414820del, NM_007217.3:c.245_246del (PDCD10))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.167414819_167414820del
DNA change (hg38) -
Published as PDCD10(NM_007217.4):c.245_246delGT (p.R82Hfs*4)
ISCN -
DB-ID PDCD10_000040
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDCD10 NM_007217.3 +/. - c.245_246del r.(?) p.(Arg82Hisfs*4)


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