Variant #0000657586 (NC_000015.9:g.45392382T>C, NM_014080.4:c.3050A>G (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.45392382T>C
DNA change (hg38) g.45100184T>C
Published as DUOX2(NM_001363711.1):c.3050A>G (p.E1017G), DUOX2(NM_014080.5):c.3050A>G (p.E1017G)
ISCN -
DB-ID DUOX2_000010 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) 0.00819 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 2020-03-23 16:13:27 +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.3050A>G r.(?) p.(Glu1017Gly)
DUOXA2 NM_207581.3 -/. - c.-14422T>C r.(?) p.(=)


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