Variant #0000443420 (NC_000016.9:g.17564778_17564779insN[244], NM_022166.3:c.-126_-125insN[244] (XYLT1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.17564778_17564779insN[244]
DNA change (hg38) -
Published as +6bp
ISCN -
DB-ID XYLT1_000038
Variant remarks -
Reference PubMed: Faust 2014
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 1/45
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 14:38:45 +01:00 (CET)
Date last edited 2021-12-15 22:04:31 +01:00 (CET)
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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.-126_-125insN[244] GCG[10]GCA[1]GCG[6] - -


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