Variant #0000443412 (NC_000016.9:g.17564778_17564779insN[238], NM_022166.3:c.-126_-125insN[238] (XYLT1))

Chromosome 16
Allele Both (homozygous)
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.17564778_17564779insN[238]
DNA change (hg38) -
Published as -
ISCN -
DB-ID XYLT1_000034
Variant remarks error in reference sequence, missing 238 nucleotides (CGCCGCGCGGGCCAGGCGCCCGCCCCTCCCTGCGCGCCCCGTCCCCGAGCGCGCGCCCGGCGCCCCCCTCCGCGGCCTCCCCGCTCCCGCCTCCCGCCTTCTCCTCCTCCTGGTGACGTCCGGGTCCCTGCCCGTCTGAAAACTCCGCGCCGCGGCGGTGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGAGGAGGAGCAGCGGCGAGCCGAGGCGGCG)
Reference PubMed: Faust 2014
ClinVar ID -
dbSNP ID -
Origin Germline
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 13:26:53 +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[238] GCG[8]GCA[1]GCG[6] - -


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