Variant #0000265748 (NC_000015.9:g.45407998G>A, NM_014080.4:c.-1842C>T (DUOX2))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45407998G>A
DNA change (hg38) g.45115800G>A
Published as DUOXA2(NM_207581.4):c.149G>A (p.R50H)
ISCN -
DB-ID DUOXA2_000008
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) 2.0E-5 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.-1842C>T r.(?) p.(=)
DUOXA1 NM_144565.2 ?/. - c.*1715C>T r.(=) p.(=)
DUOXA2 NM_207581.3 ?/. - c.149G>A r.(?) p.(Arg50His)


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