Variant #0000623569 (NC_000016.9:g.88873714A>C, NM_000485.2:c.*2392T>G (APRT))
| Chromosome |
16 |
| 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.88873714A>C |
| DNA change (hg38) |
g.88807306A>C |
| Published as |
CDT1(NM_030928.3):c.1301A>C (p.Q434P, p.(Gln434Pro)) |
| ISCN |
- |
| DB-ID |
CDT1_000015 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) |
0.0002 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-12-06 12:43:26 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
|