Variant #0000837753 (NC_000023.10:g.(22117270_22129584)_(22129679_22132575)del, NC_000023.10(NM_000444.4):c.(1079+1_1080-1)_(1173+1_1174-1)del (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.(22117270_22129584)_(22129679_22132575)del |
| DNA change (hg38) |
g.(22099152_22111466)_(22111561_22114457)del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PHEX_000537 See all 3 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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