Variant #0000554495 (NC_000015.9:g.45408874C>G, NM_014080.4:c.-2718G>C (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.45408874C>G
DNA change (hg38) g.45116676C>G
Published as DUOXA2(NM_207581.4):c.501C>G (p.C167W)
ISCN -
DB-ID DUOX2_000079
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) 1.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DUOX2 NM_014080.4 ?/. - c.-2718G>C r.(?) p.(=)
DUOXA1 NM_144565.2 ?/. - c.*839G>C r.(=) p.(=)
DUOXA2 NM_207581.3 ?/. - c.501C>G r.(?) p.(Cys167Trp)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.