Variant #0000608269 (NC_000003.11:g.123674953_123674954del, NM_022757.4:c.313_314del (CCDC14))
| Chromosome |
3 |
| 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.123674953_123674954del |
| DNA change (hg38) |
g.123956106_123956107del |
| Published as |
CCDC14(NM_022757.5):c.169_170delGT (p.V57Tfs*4) |
| ISCN |
- |
| DB-ID |
CCDC14_000005 |
| 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-12-04 14:54:23 +01:00 (CET) |
| Date last edited |
2020-06-15 13:03:39 +02:00 (CEST) |

Variant on transcripts
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