Variant #0000443418 (NC_000016.9:g.17564818G>A, NM_022166.3:c.-165C>T (XYLT1))

Chromosome 16
Allele Both (homozygous)
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.17564818G>A
DNA change (hg38) g.17470961G>A
Published as -403C>T
ISCN -
DB-ID XYLT1_000035 See all 3 reported entries
Variant remarks expression cloning luciferase promoter activity unchanged
Reference PubMed: Faust 2014
ClinVar ID -
dbSNP ID rs118030014
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 14:17:42 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
XYLT1 NM_022166.3 -/. _1 c.-165C>T - r.= p.=


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