Variant #0000329914 (NC_000004.11:g.15560833del, NM_001080522.2:c.2875del (CC2D2A))
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.15560833del |
DNA change (hg38) |
g.15559210del |
Published as |
CC2D2A(NM_001080522.2):c.2874delG (p.(Glu959AsnfsTer3)), CC2D2A(NM_001080522.2):c.2875delG (p.E959Nfs*3) |
ISCN |
- |
DB-ID |
CC2D2A_000029 See all 5 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) |
Retrieve |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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