Variant #0000827797 (NC_000023.10:g.22196499T>C, NC_000023.10(NM_000444.4):c.1586+6T>C (PHEX))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.22196499T>C
DNA change (hg38) g.22178382T>C
Published as -
ISCN -
DB-ID PHEX_000028 See all 32 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 +?/. 14i c.1586+6T>C r.[1483_1586del,=] p.[Ile495Valfs*52,=]


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