Variant #0000222798 (NC_000023.10:g.148606691_148608805ins[148569718_148585611])
| Individual ID |
00114374 |
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.148606691_148608805ins[148569718_148585611] |
| DNA change (hg38) |
- |
| Published as |
KT724868:g.261_2375 |
| ISCN |
- |
| DB-ID |
chrX_002904 |
| Variant remarks |
copy inserted in IDS gene Variant Error [ESYNTAX]: This genomic variant has an error (char 37: Syntax error). Please fix this entry and then remove this message. |
| Reference |
PubMed: Alcántara-Ortigoza 2016 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
DUPLICATE record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2017-11-03 16:38:15 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
Screenings
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