Variant #0000892079 (NC_000015.9:g.45399615G>T, NM_014080.4:c.1621C>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.45399615G>T
DNA change (hg38) -
Published as DUOX2(NM_001363711.2):c.1621C>A (p.R541=)
ISCN -
DB-ID DUOX2_000136
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) 0.00102 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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DUOX2 NM_014080.4 -/. - c.1621C>A r.(?) p.(Arg541=)
DUOXA2 NM_207581.3 -/. - c.-7189G>T r.(?) p.(=)


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