Variant #0000838055 (NC_000023.10:g.(22239861_22244559)_(22269427_?)dup, PHEX(NM_000444.4):c.(1899+1_1900-1)_*3357{2})
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(22239861_22244559)_(22269427_?)dup |
DNA change (hg38) |
g.(22221744_22226442)_(22251310_?)dup |
Published as |
- |
ISCN |
- |
DB-ID |
USP9X_000005 See all 207 reported entries |
Variant remarks |
- |
Reference |
PubMed: Sarafrazi 2022 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |

Variant on transcripts
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