Variant #0000886177 (NC_000004.11:g.15602873C>T, NM_001080522.2:c.4688C>T (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.15602873C>T |
| DNA change (hg38) |
- |
| Published as |
CC2D2A(NM_001080522.2):c.4688C>T (p.(Pro1563Leu), p.P1563L) |
| ISCN |
- |
| DB-ID |
CC2D2A_000160 See all 2 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 |
2022-11-01 13:01:21 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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