Variant #0000926864 (NC_000019.9:g.33878269G>A, NM_000285.3:c.1463C>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.33878269G>A
DNA change (hg38) -
Published as PEPD(NM_000285.4):c.1463C>T (p.P488L)
ISCN -
DB-ID CEBPG_000003
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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     
PEPD NM_000285.3 -?/. - c.1463C>T r.(?) p.(Pro488Leu)
CEBPG NM_001806.3 -?/. - c.*7671G>A r.(=) p.(=)


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