Variant #0000412123 (NC_000006.11:g.24505099G>A, NM_001080.3:c.612G>A (ALDH5A1))

Chromosome 6
Allele Parent #2
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.24505099G>A
DNA change (hg38) g.24504871G>A
Published as -
ISCN -
DB-ID ALDH5A1_006039 See all 46 reported entries
Variant remarks -
Reference PubMed: Akaboshi 2003
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner Gajja Salomons
Database submission license No license selected
Created by Gajja Salomons
Date created 2016-01-05 14:32:36 +01:00 (CET)
Date last edited 2018-11-01 10:08:05 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH5A1 NM_001080.3 +/+ 4 c.612G>A r.(?) p.(Trp204*)
ALDH5A1 NM_170740.1 ./. - c.612G>A r.(?) p.(Trp204*)



Screenings

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