Variant #0000665706 (NC_000019.9:g.[NC_000008.10:(119038109-119106577)_qter]delins(35762292_35940346)_qter)
| Individual ID |
00133225 |
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.[NC_000008.10:(119038109-119106577)_qter]delins(35762292_35940346)_qter |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
t(8;19)(q24.11;q13.13) |
| DB-ID |
chr19_000000 See all 2 reported entries |
| Variant remarks |
BAC clone RP11-111F21 gives split signal |
| 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 |
Ivy Jennes |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 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
|