Variant #0000330829 (NC_000006.11:g.24447087G>A, ALDH5A1(NM_001080.3):c.-48138G>A)

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.24447087G>A
DNA change (hg38) g.24446859G>A
Published as GPLD1(NM_001503.3):c.1799C>T (p.(Pro600Leu))
ISCN -
DB-ID GPLD1_000002
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) 1.0E-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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH5A1 NM_001080.3 ?/. - c.-48138G>A r.(?) p.(=)
GPLD1 NM_001503.3 ?/. - c.1799C>T r.(?) p.(Pro600Leu)
ALDH5A1 NM_170740.1 ?/. - c.-48138G>A r.(?) p.(=)