Variant #0001066493 (NC_000016.9:g.50818346G>A, NM_001042355.1:c.1924G>A (CYLD))

Chromosome 16
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.50818346G>A
DNA change (hg38) -
Published as CYLD(NM_001378743.1):c.1933G>A (p.(Val645Ile))
ISCN -
DB-ID CYLD_000068
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CYLD NM_001042355.1 -?/. - c.1924G>A r.(?) p.(Val642Ile)
CYLD NM_001378743.1 -?/. - c.1933G>A r.(?) p.(Val645Ile)


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