Variant #0000728364 (NC_000023.10:g.118985712_118985727dup, NC_000023.10(NM_080632.2):c.263+3_263+18dup (UPF3B))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.118985712_118985727dup |
| DNA change (hg38) |
- |
| Published as |
UPF3B(NM_080632.2):c.263+3_263+18dupAAAAAAAAAAAAAAAA |
| ISCN |
- |
| DB-ID |
UPF3B_000030 |
| 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_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2021-02-08 18:36:18 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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