Variant #0001078518 (NC_000023.10:g.123007657G>A, NC_000023.10(NM_001167.3):c.-32-11824G>A (XIAP))

Chromosome X
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.123007657G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID -
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs895958879
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-06-17 16:49:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
XIAP NM_001167.3 ?/. - c.-32-11824G>A r.(?) p.(?)


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