Variant #0000528099 (NC_000006.11:g.24495330G>C, ALDH5A1(NM_001080.3):c.106G>C)

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.24495330G>C
DNA change (hg38) g.24495102G>C
Published as ALDH5A1(NM_001080.3):c.106G>C (p.(Gly36Arg))
ISCN -
DB-ID ALDH5A1_006130 See all 3 reported entries
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) 0.04071 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.106G>C r.(?) p.(Gly36Arg)
GPLD1 NM_001503.3 -?/. - c.-5591C>G r.(?) p.(=)
ALDH5A1 NM_170740.1 -?/. - c.106G>C r.(?) p.(Gly36Arg)