Variant #0000806708 (NC_000015.9:g.45402716C>T, NM_014080.4:c.950G>A (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.45402716C>T
DNA change (hg38) -
Published as DUOX2(NM_001363711.1):c.950G>A (p.R317H)
ISCN -
DB-ID DUOX2_000120
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) 7.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.950G>A r.(?) p.(Arg317His)
DUOXA2 NM_207581.3 -?/. - c.-4088C>T r.(?) p.(=)


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