Variant #0001018347 (NC_000023.10:g.148564603G>A, NM_000202.5:c.1327C>T (IDS))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.148564603G>A |
| DNA change (hg38) |
g.149483072G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
IDS_000011 See all 60 reported entries |
| Variant remarks |
Two patients are siblings (Narayanan et al., 2016) and two are female (Sohn et al., 2010; PiƱa-Aguilar et al., 2013) |
| Reference |
PubMed: Zanetti 2024 |
| ClinVar ID |
SCV005089526 |
| dbSNP ID |
rs199422227 |
| Origin |
SUMMARY 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-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-12-06 15:50:52 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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