Variant #0001056618 (NC_000019.9:g.38796103del, NM_033520.1:c.*499del (C19orf33))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.38796103del
DNA change (hg38) -
Published as YIF1B(NM_001039672.3):c.838del (p.(Val280Serfs*14))
ISCN -
DB-ID C19orf33_000009
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C19orf33 NM_033520.1 ?/. - c.*499del r.(?) p.(=)
YIF1B NM_033557.3 ?/. - c.745del r.(?) p.(Val249Serfs*14)


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