Variant #0000837887 (NC_000023.10:g.(22231076_22237152)_(22269427_?)del, NM_000444.4:c.(1700+1_1701-1)_*3357{0} (PHEX))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(22231076_22237152)_(22269427_?)del
DNA change (hg38) g.(22212959_22219035)_(22251310_?)del
Published as -
ISCN -
DB-ID PHEX_000521 See all 5 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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-02-02 15:39:05 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHEX NM_000444.4 +/? 16i_22_ c.(1700+1_1701-1)_*3357{0} r.? p.?


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