Variant #0000837544 (NC_000023.10:g.(?_22050443)_(22129679_22132575)del, NM_000444.4:c.-681_(1173+1_1174-1){0} (PHEX))
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_22050443)_(22129679_22132575)del |
DNA change (hg38) |
g.(?_22032325)_(22111561_22114457)del |
Published as |
- |
ISCN |
- |
DB-ID |
PHEX_000708 See all 2 reported entries |
Variant remarks |
- |
Reference |
PubMed: Sarafrazi 2022 |
ClinVar ID |
- |
dbSNP ID |
- |
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 |
2022-02-02 15:39:05 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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