Variant #0001051586 (NC_000003.11:g.180349289_180349296del, NM_181426.1:c.1966_1973del (CCDC39))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.180349289_180349296del
DNA change (hg38) -
Published as CCDC39(NM_181426.2):c.1966_1973del (p.(Glu656Asnfs*21))
ISCN -
DB-ID CCDC39_000090
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC39 NM_181426.1 +?/. - c.1966_1973del r.(?) p.(Glu656Asnfs*21)


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