Variant #0000528094 (NC_000006.11:g.24447166C>T, ALDH5A1(NM_001080.3):c.-48059C>T)

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.24447166C>T
DNA change (hg38) g.24446938C>T
Published as GPLD1(NM_001503.3):c.1720G>A (p.E574K)
ISCN -
DB-ID ALDH5A1_006132
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) 0.00036 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH5A1 NM_001080.3 -?/. - c.-48059C>T r.(?) p.(=)
GPLD1 NM_001503.3 -?/. - c.1720G>A r.(?) p.(Glu574Lys)
ALDH5A1 NM_170740.1 -?/. - c.-48059C>T r.(?) p.(=)