Variant #0000827651 (NC_000023.10:g.(22108616_22112100)_(22132705_22151639)del, PHEX(NM_000444.4):c.(732+1_733-1)_(1302+1_1303-1)del)

Individual ID 00394834
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(22108616_22112100)_(22132705_22151639)del
DNA change (hg38) g.(22090498_22093982)_(22114587_22133522)del
Published as del ex7-11
ISCN -
DB-ID PHEX_000690
Variant remarks -
Reference PubMed: Zheng 2020
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHEX NM_000444.4 +/. 6i_11i c.(732+1_733-1)_(1302+1_1303-1)del r.? p.?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000396081 DNA SEQ - - PHEX 1 Johan den Dunnen