Variant #0000528096 (NC_000006.11:g.24454292_24454312del, ALDH5A1(NM_001080.3):c.-40933_-40913del)

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.24454292_24454312del
DNA change (hg38) g.24454064_24454084del
Published as GPLD1(NM_001503.3):c.1274_1294delGCCTGCCACCTGTTGACCTGG (p.G425_L431del)
ISCN -
DB-ID ALDH5A1_006134
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.-40933_-40913del r.(?) p.(=)
GPLD1 NM_001503.3 -?/. - c.1274_1294del r.(?) p.(Gly425_Leu431del)
ALDH5A1 NM_170740.1 -?/. - c.-40933_-40913del r.(?) p.(=)