Variant #0000129144 (NC_000017.10:g.(70900001_qter)delins[NC_000001.10:(185800001_198700000)_qter])
| Individual ID |
00080105 |
| Chromosome |
17 |
| 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.(70900001_qter)delins[NC_000001.10:(185800001_198700000)_qter] |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
46,XY,t(1;17)(q31;q25)dn |
| DB-ID |
chr17_001702 |
| Variant remarks |
translocation |
| Reference |
PubMed: Midro 1993, PubMed: Fokstuen 2013, for EUCID-SRS consortium |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
n/a |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Zeynep Tümer |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2016-09-01 17:30:25 +02:00 (CEST) |
| Date last edited |
2020-10-01 16:53:33 +02:00 (CEST) |
Variant on transcripts
Screenings
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|