Variant #0000248690 (NC_000017.10:g.19578873A>T, NM_000382.2:c.1446A>T (ALDH3A2))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19578873A>T
DNA change (hg38) g.19675560A>T
Published as ALDH3A2(NM_000382.3):c.1446A>T (p.A482=)
ISCN -
DB-ID ALDH3A2_000055 See all 7 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) 0.61886 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH3A2 NM_000382.2 -/. - c.1446A>T r.(?) p.(Ala482=)
SLC47A2 NM_152908.3 -/. - c.*3126T>A r.(=) p.(=)


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