Variant #0000554486 (NC_000015.9:g.45403967A>G, NM_014080.4:c.512T>C (DUOX2))

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.45403967A>G
DNA change (hg38) g.45111769A>G
Published as DUOX2(NM_001363711.2):c.512T>C (p.L171P)
ISCN -
DB-ID DUOX2_000071
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) 0.0028 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DUOX2 NM_014080.4 -?/. - c.512T>C r.(?) p.(Leu171Pro)
DUOXA2 NM_207581.3 -?/. - c.-2837A>G r.(?) p.(=)


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