Variant #0000827805 (NC_000023.10:g.22239729G>C, NC_000023.10(NM_000444.4):c.1769-1G>C (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.22239729G>C
DNA change (hg38) g.22221612G>C
Published as -
ISCN -
DB-ID PHEX_000468 See all 3 reported entries
Variant remarks variant analysed in mini-gene expression construct
Reference PubMed: BinEssa 2019
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
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 2021-12-03 11:30:59 +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 +/. 17i c.1769-1G>C r.[1701_1773del,=,1701_1899del] p.[Ser567_Arg591del,=,Leu569Argfs*27]


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