Variant #0001018230 (NC_000023.10:g.148564536T>A, NM_000202.5:c.1394A>T (IDS))
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
likely pathogenic (recessive) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.148564536T>A |
DNA change (hg38) |
g.149483005T>A |
Published as |
- |
ISCN |
- |
DB-ID |
IDS_000187 See all 2 reported entries |
Variant remarks |
Reported in cis with c.1403G>A and reported in HGMD 2022.3 as a unique delins (CX149681) |
Reference |
PubMed: Zanetti 2024 |
ClinVar ID |
SCV005089545 |
dbSNP ID |
rs113993951 |
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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