Variant #0000553561 (NC_000015.9:g.101420155A>G, NM_000693.2:c.43A>G (ALDH1A3))

Chromosome 15
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.101420155A>G
DNA change (hg38) g.100879950A>G
Published as ALDH1A3(NM_000693.2):c.43A>G (p.(Arg15Gly)), ALDH1A3(NM_000693.3):c.43A>G (p.R15G)
ISCN -
DB-ID ALDH1A3_000007 See all 2 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) 0.00462 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALDH1A3 NM_000693.2 -?/. - c.43A>G r.(?) p.(Arg15Gly)


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