Variant #0000265756 (NC_000015.9:g.45409472C>T, NM_014080.4:c.-3316G>A (DUOX2))

Chromosome 15
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.45409472C>T
DNA change (hg38) g.45117274C>T
Published as DUOXA2(NM_207581.4):c.738C>T (p.Y246=)
ISCN -
DB-ID DUOXA2_000005
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) 0.01681 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DUOX2 NM_014080.4 -/. - c.-3316G>A r.(?) p.(=)
DUOXA1 NM_144565.2 -/. - c.*241G>A r.(=) p.(=)
DUOXA2 NM_207581.3 -/. - c.738C>T r.(?) p.(Tyr246=)


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