Variant #0000689689 (NC_000006.11:g.24437397C>T, ALDH5A1(NM_001080.3):c.-57828C>T)

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.24437397C>T
DNA change (hg38) -
Published as GPLD1(NM_001503.3):c.2141G>A (p.R714H)
ISCN -
DB-ID ALDH5A1_006169
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) Retrieve
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.-57828C>T r.(?) p.(=)
GPLD1 NM_001503.3 ?/. - c.2141G>A r.(?) p.(Arg714His)
ALDH5A1 NM_170740.1 ?/. - c.-57828C>T r.(?) p.(=)