Variant #0000259743 (NC_000017.10:g.19566648C>T, NM_000382.2:c.943C>T (ALDH3A2))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.19566648C>T
DNA change (hg38) g.19663335C>T
Published as ALDH3A2(NM_000382.3):c.943C>T (p.P315S), ALDH3A2(NM_001031806.1):c.943C>T (p.P315S), ALDH3A2(NM_001031806.2):c.943C>T (p.P315S)
ISCN -
DB-ID ALDH3A2_000012 See all 38 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) 0.00011 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.943C>T r.(?) p.(Pro315Ser)


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