Variant #0000328966 (NC_000022.10:g.29196499_29196501dup, NM_005080.3:c.12_14dup (XBP1))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.29196499_29196501dup
DNA change (hg38) g.28800511_28800513dup
Published as XBP1(NM_001079539.1):c.14_15insGGC (p.?), XBP1(NM_005080.4):c.12_14dupGGC (p.A7dup)
ISCN -
DB-ID XBP1_000003 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
XBP1 NM_005080.3 ?/. - c.12_14dup r.(?) p.(Ala7dup)


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