Variant #0000815709 (NC_000008.10:g.42693306_42693313del, NM_018105.2:c.436_443del (THAP1))
| Chromosome |
8 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42693306_42693313del |
| DNA change (hg38) |
g.42838163_42838170del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
THAP1_000033 |
| Variant remarks |
variant introduced in induced pluripotent stem cell, characterisation incl. transcript profiling |
| Reference |
Journal: Domingo 2021 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2021-10-21 13:59:46 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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