Variant #0000554457 (NC_000015.9:g.45389524C>T, NM_014080.4:c.3759G>A (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.45389524C>T
DNA change (hg38) g.45097326C>T
Published as DUOX2(NM_001363711.2):c.3759G>A (p.(Pro1253=)), DUOX2(NM_014080.5):c.3759G>A (p.P1253=)
ISCN -
DB-ID DUOX2_000045 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) 0.00587 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.3759G>A r.(?) p.(Pro1253=)
DUOXA2 NM_207581.3 -/. - c.-17280C>T r.(?) p.(=)


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