Variant #0000806710 (NC_000015.9:g.45408787C>G, NM_014080.4:c.-2631G>C (DUOX2))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45408787C>G
DNA change (hg38) -
Published as DUOXA2(NM_207581.4):c.414C>G (p.Y138*)
ISCN -
DB-ID DUOX2_000122
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.-2631G>C r.(?) p.(=)
DUOXA1 NM_144565.2 +/. - c.*926G>C r.(=) p.(=)
DUOXA2 NM_207581.3 +/. - c.414C>G r.(?) p.(Tyr138*)


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