Variant #0000972007 (NC_000023.10:g.22095778T>A, NM_000444.4:c.621T>A (PHEX))
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.22095778T>A |
DNA change (hg38) |
g.22077660T>A |
Published as |
- |
ISCN |
- |
DB-ID |
PHEX_000228 See all 4 reported entries |
Variant remarks |
in vitro mini-gene splicing assay |
Reference |
Fengjiao Pan 2024, submitted |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Fengjiao Pan |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Fengjiao Pan |
Date created |
2024-03-15 17:03:45 +01:00 (CET) |
Date last edited |
2024-03-18 22:29:32 +01:00 (CET) |

Variant on transcripts
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