Variant #0001035641 (NC_000006.11:g.24502833G>A, NM_001080.3:c.437G>A (ALDH5A1))

Chromosome 6
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.24502833G>A
DNA change (hg38) -
Published as ALDH5A1(NM_001080.3):c.437G>A (p.(Ser146Asn))
ISCN -
DB-ID ALDH5A1_006184
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH5A1 NM_001080.3 ?/. - c.437G>A r.(?) p.(Ser146Asn)
ALDH5A1 NM_170740.1 ?/. - c.437G>A r.(?) p.(Ser146Asn)


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