Variant #0001049367 (NC_000009.11:g.104189780G>T, NM_000035.3:c.524C>A (ALDOB))

Chromosome 9
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.104189780G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ALDOB_000009 See all 41 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs76917243
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00035 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-15 06:40:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDOB NM_000035.3 +/. - c.524C>A r.(?) p.(Ala175Asp)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.