Variant #0000717429 (NC_000001.10:g.32669645C>T, NM_024296.3:c.330C>T (CCDC28B))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32669645C>T
DNA change (hg38) -
Published as CCDC28B(NM_001301011.2):c.330C>T (p.F110=), CCDC28B(NM_024296.4):c.330C>T (p.F110=), CCDC28B(NM_024296.5):c.330C>T (p.(Phe110=))
ISCN -
DB-ID CCDC28B_000004 See all 11 reported entries
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) 0.0115 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IQCC NM_018134.2 -/. - c.-1638C>T r.(?) p.(=)
CCDC28B NM_024296.3 -/. - c.330C>T r.(?) p.(Phe110=)


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