Variant #0000566863 (NC_000019.9:g.33882228G>A, NM_000285.3:c.1125C>T (PEPD))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33882228G>A
DNA change (hg38) g.33391322G>A
Published as PEPD(NM_000285.3):c.1125C>T (p.D375=), PEPD(NM_000285.4):c.1125C>T (p.D375=)
ISCN -
DB-ID PEPD_000021 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) 0.00014 View details
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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEPD NM_000285.3 -?/. - c.1125C>T r.(?) p.(Asp375=)


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