Variant #0000188649 (NC_000016.9:g.[chr16:(88700000_qter)delinschr11:(pter_12700000)inv])
| Individual ID |
00117219 |
| Chromosome |
16 |
| Allele |
Maternal (confirmed) |
| 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.[chr16:(88700000_qter)delinschr11:(pter_12700000)inv] |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
46,XX,der(16)t(11;16)(p15.3;q24.3)mat |
| DB-ID |
chr16_000467 See all 2 reported entries |
| Variant remarks |
unbalanced translocation |
| Reference |
PubMed: Nakashima 2015, for EUCID-SRS consortium |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Zeynep Tümer |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2017-08-15 16:52:29 +02:00 (CEST) |
| Date last edited |
2020-10-01 16:53:33 +02:00 (CEST) |
Variant on transcripts
Screenings
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