Variant #0000615345 (NC_000015.9:g.45393428_45393431del, NM_014080.4:c.2895_2898del (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.45393428_45393431del
DNA change (hg38) g.45101230_45101233del
Published as DUOX2(NM_001363711.2):c.2895_2898delGTTC (p.F966Sfs*29), DUOX2(NM_014080.5):c.2895_2898delGTTC (p.F966Sfs*29)
ISCN -
DB-ID DUOX2_000054 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) 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 2019-12-04 15:24:38 +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.2895_2898del r.(?) p.(Phe966SerfsTer29)
DUOXA2 NM_207581.3 +/. - c.-13376_-13373del r.(?) p.(=)


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