Variant #0000933925 (NC_000006.11:g.24505099G>A, NM_001080.3:c.612G>A (ALDH5A1))

Chromosome 6
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.24505099G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ALDH5A1_006039 See all 46 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs118203982
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-10-09 17:24:01 +02:00 (CEST)
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.612G>A r.(?) p.(Trp204Ter)


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