Variant #0001038051 (NC_000010.10:g.82102041del, NM_138812.3:c.327del (DYDC1))

Chromosome 10
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.82102041del
DNA change (hg38) -
Published as DYDC1(NM_001269053.2):c.327del (p.(Glu110Asnfs*3))
ISCN -
DB-ID DYDC1_000002
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYDC2 NM_032372.5 ?/. - c.-14703del r.(?) p.(=)
DYDC1 NM_138812.3 ?/. - c.327del r.(?) p.(Glu110Asnfs*3)


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