Variant #0000078729 (NC_000008.10:g.(139900001_146364022)_qterdelins[NC_000023.10:pter_(32533500_32633500)inv])
| Individual ID |
00049892 |
| Chromosome |
8 |
| 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.(139900001_146364022)_qterdelins[NC_000023.10:pter_(32533500_32633500)inv] |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
t(X;8)(p21.1;q24.3) |
| DB-ID |
chr8_000000 See all 5 reported entries |
| Variant remarks |
translocation |
| Reference |
PubMed: Meitinger 1988, Journal: Meitinger 1988 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline/De novo (untested) |
| 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 |
2015-09-14 15:44:41 +02:00 (CEST) |
| Date last edited |
2020-05-12 19:21:26 +02:00 (CEST) |
Variant on transcripts
Screenings
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