Variant #0000894048 (NC_000017.10:g.54912215G>A, NM_003647.2:c.59G>A (DGKE))

Chromosome 17
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.54912215G>A
DNA change (hg38) -
Published as DGKE(NM_003647.3):c.59G>A (p.(Gly20Glu), p.G20E)
ISCN -
DB-ID C17orf67_000003 See all 3 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) 0.00329 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C17orf67 NM_001085430.2 -?/. - c.-2238C>T r.(?) p.(=)
DGKE NM_003647.2 -?/. - c.59G>A r.(?) p.(Gly20Glu)


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