Variant #0000837546 (NC_000023.10:g.(?_22050443)_(22117270_22129584)del, PHEX(NM_000444.4):c.-681_(1079+1_1080-1){0})

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_22050443)_(22117270_22129584)del
DNA change (hg38) g.(?_22032325)_(22099152_22111466)del
Published as -
ISCN -
DB-ID PHEX_000684 See all 2 reported entries
Variant remarks -
Reference PubMed: Sarafrazi 2022
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHEX NM_000444.4 +?/. _1_9i c.-681_(1079+1_1080-1){0} r.? p.0?