Variant #0001068019 (NC_000022.10:g.24919586G>A, NC_000022.10(NM_016327.2):c.917-1G>A (UPB1))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.24919586G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID UPB1_000004 See all 10 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs143493067
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00177 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-02 11:24:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UPB1 NM_016327.2 +/. - c.917-1G>A r.(?) p.(?)


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