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 International |
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) |

Variant on transcripts
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