Variant #0000837564 (NC_000023.10:g.(22051242_22056586)_(22056656_22065167)del, NC_000023.10(NM_000444.4):c.(118+1_119-1)_(187+1_188-1)del (PHEX))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(22051242_22056586)_(22056656_22065167)del
DNA change (hg38) g.(22033124_22038468)_(22038538_22047049)del
Published as -
ISCN -
DB-ID PHEX_000526 See all 2 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 +?/. 1i_2i c.(118+1_119-1)_(187+1_188-1)del r.? p.?


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