Variant #0000443417 (NC_000016.9:g.17565503G>T, NM_022166.3:c.-850C>A (XYLT1))

Chromosome 16
Allele Both (homozygous)
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.17565503G>T
DNA change (hg38) g.17471646G>T
Published as -1088C>A
ISCN -
DB-ID XYLT1_000036 See all 3 reported entries
Variant remarks expression cloning luciferase promoter activity shows 0.5 reduced activity; serum XT activity unchanged
Reference PubMed: Faust 2014
ClinVar ID -
dbSNP ID rs59423557
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 2018-12-29 14:15:08 +01:00 (CET)
Date last edited 2022-04-07 15:58:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
XYLT1 NM_022166.3 +/. _1 c.-850C>A - r.=|[0.5] p.(=)


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