Variant #0000670908 (NC_000006.11:g.24495578G>C, ALDH5A1(NM_001080.3):c.354G>C)

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.24495578G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID ALDH5A1_006149
Variant remarks overexpression in HEK293 cells showed normal SSADH activity. This variant may affect splicing.
Reference PubMed: Popp 2020, Journal: Pop 2020
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Gajja Salomons
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH5A1 NM_001080.3 ?/. 1 c.354G>C - p.Lys118Asn