Variant #0000947217 (NC_000001.10:g.32672713C>T, NM_024296.3:c.*1864C>T (CCDC28B))

Chromosome 1
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.32672713C>T
DNA change (hg38) -
Published as IQCC(NM_001160042.1):c.790C>T (p.(Arg264Cys))
ISCN -
DB-ID CCDC28B_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) 0.00061 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 2023-11-27 17:35:39 +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     
DCDC2B NM_001099434.1 -?/. - c.-1982C>T r.(?) p.(=)
IQCC NM_018134.2 -?/. - c.550C>T r.(?) p.(Arg184Cys)
CCDC28B NM_024296.3 -?/. - c.*1864C>T r.(=) p.(=)


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