Variant #0001052279 (NC_000006.11:g.24495310G>C, NM_001080.3:c.86G>C (ALDH5A1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.24495310G>C
DNA change (hg38) -
Published as ALDH5A1(NM_001080.3):c.86G>C (p.(Gly29Ala))
ISCN -
DB-ID ALDH5A1_006185
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
ALDH5A1 NM_001080.3 -?/. - c.86G>C r.(?) p.(Gly29Ala)
GPLD1 NM_001503.3 -?/. - c.-5571C>G r.(?) p.(=)
ALDH5A1 NM_170740.1 -?/. - c.86G>C r.(?) p.(Gly29Ala)


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