Variant #0000554448 (NC_000015.9:g.45386442C>G, NM_014080.4:c.4553G>C (DUOX2))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45386442C>G
DNA change (hg38) g.45094244C>G
Published as DUOX2(NM_014080.5):c.4553G>C (p.G1518A)
ISCN -
DB-ID DUOX2_000036
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 2019-07-18 18:22:55 +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.4553G>C r.(?) p.(Gly1518Ala)
DUOXA2 NM_207581.3 +?/. - c.-20362C>G r.(?) p.(=)


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