Variant #0000930383 (NC_000015.9:g.45401069G>A, NM_014080.4:c.1316C>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.45401069G>A
DNA change (hg38) -
Published as DUOX2(NM_001363711.2):c.1316C>T (p.P439L)
ISCN -
DB-ID DUOX2_000142
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 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DUOX2 NM_014080.4 ?/. - c.1316C>T r.(?) p.(Pro439Leu)
DUOXA2 NM_207581.3 ?/. - c.-5735G>A r.(?) p.(=)


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