Variant #0000259019 (NC_000006.11:g.24495234T>G, ALDH5A1(NM_001080.3):c.10T>G)

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.24495234T>G
DNA change (hg38) g.24495006T>G
Published as ALDH5A1(NM_170740.1):c.10T>G (p.C4G)
ISCN -
DB-ID ALDH5A1_000117
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) 0.00773 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH5A1 NM_001080.3 -/. - c.10T>G r.(?) p.(Cys4Gly)
GPLD1 NM_001503.3 -/. - c.-5495A>C r.(?) p.(=)
ALDH5A1 NM_170740.1 -/. - c.10T>G r.(?) p.(Cys4Gly)