Variant #0000518441 (NC_000003.11:g.167437916_167437917insAA, NM_007217.3:c.30_31insTT (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.167437916_167437917insAA
DNA change (hg38) g.167720128_167720129insAA
Published as PDCD10(NM_007217.3):c.30_31insTT (p.E11Lfs*24)
ISCN -
DB-ID PDCD10_000029
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-15 16:53:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDCD10 NM_007217.3 +/. - c.30_31insTT r.(?) p.(Glu11LeufsTer24)


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