Variant #0000972007 (NC_000023.10:g.22095778T>A, NM_000444.4:c.621T>A (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.22095778T>A
DNA change (hg38) g.22077660T>A
Published as -
ISCN -
DB-ID PHEX_000228 See all 4 reported entries
Variant remarks in vitro mini-gene splicing assay
Reference Fengjiao Pan 2024, submitted
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Fengjiao Pan
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Fengjiao Pan
Date created 2024-03-15 17:03:45 +01:00 (CET)
Date last edited 2024-03-18 22:29:32 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHEX NM_000444.4 +/. 5 c.621T>A r.[621u>a,618_663del] p.[Tyr207Ter,Leu216PhefsTer11]


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.