Variant #0000831663 (NC_000022.10:g.(?_21714498)_(24953112_?)dup)
| Individual ID |
00398062 |
| Chromosome |
22 |
| Allele |
Parent #1 |
| 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.(?_21714498)_(24953112_?)dup |
| DNA change (hg38) |
g.(?_21360209)_(24598823_?)dup |
| Published as |
hg18 18640301-21928915dup |
| ISCN |
- |
| DB-ID |
chr22_003024 |
| Variant remarks |
3.2 Mb interstitial duplication |
| Reference |
PubMed: Hilhorst-Hofstee 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2021-12-31 11:08:47 +01:00 (CET) |
| Date last edited |
2021-12-31 11:09:48 +01:00 (CET) |

Variant on transcripts
Screenings
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