Variant #0001018235 (NC_000023.10:g.148564527C>T, NM_000202.5:c.1403G>A (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.148564527C>T |
| DNA change (hg38) |
g.149482996C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
IDS_000014 See all 93 reported entries |
| Variant remarks |
Three patients are siblings (Parkinson et al,.,2004) and two are female (Dvorakova et al., 2017; Sukegawa et al., 1997). In one patient the variant is described in cis with c.1394A>T (Amartino et al., 2014) and is reported in HGMD 2022.3 as a unique delins (CX149681) |
| Reference |
PubMed: Zanetti 2024 |
| ClinVar ID |
SCV000929887.1 |
| dbSNP ID |
rs113993946 |
| 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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