Variant #0000047995 (NC_000017.10:g.(10700001_16000000)_(16000001_22200000)del)
| Individual ID |
00025123 |
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(10700001_16000000)_(16000001_22200000)del |
| DNA change (hg38) |
- |
| Published as |
del17p12-p11.2 |
| ISCN |
- |
| DB-ID |
chr17_001476 |
| Variant remarks |
cells from patient had significantly reduced levels of the two GPI anchor markers, CD59 and a GPI-binding toxin, aerolysin (FLAER) |
| Reference |
PubMed: Ng 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Philippe Campeau |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Philippe Campeau |
| Date created |
2014-12-04 23:33:42 +01:00 (CET) |
| Date last edited |
2019-03-03 17:42:23 +01:00 (CET) |

Variant on transcripts
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