Variant #0000665689 (NC_000023.10:g.[NC_000012.11:(67700000_71500000)_qter]delins(67518939_67652708)_qter)
| Individual ID |
00052131 |
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.[NC_000012.11:(67700000_71500000)_qter]delins(67518939_67652708)_qter |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
t(X;12)(q11;q15) |
| DB-ID |
chrX_000000 See all 9 reported entries |
| Variant remarks |
t(X;12) balanced translocation |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
DUPLICATE record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2020-05-13 12:08:02 +02:00 (CEST) |
| Date last edited |
N/A |
Variant on transcripts
Screenings
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