Variant #0000999656 (NC_000012.11:g.113602036C>T, NM_001144872.1:c.*5542C>T (CCDC42B))

Chromosome 12
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.113602036C>T
DNA change (hg38) -
Published as DDX54(NM_024072.3):c.1774G>A (p.(Ala592Thr))
ISCN -
DB-ID CCDC42B_000011
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) 0.00016 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC42B NM_001144872.1 -?/. - c.*5542C>T r.(=) p.(=)
DDX54 NM_024072.3 -?/. - c.1774G>A r.(?) p.(Ala592Thr)


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