Variant #0000615346 (NC_000015.9:g.45396354C>G, NM_014080.4:c.2544G>C (DUOX2))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45396354C>G
DNA change (hg38) g.45104156C>G
Published as DUOX2(NM_001363711.1):c.2544G>C (p.L848=), DUOX2(NM_001363711.2):c.2544G>C (p.L848=)
ISCN -
DB-ID DUOX2_000089 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) 0.00236 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.2544G>C r.(?) p.(Leu848=)
DUOXA2 NM_207581.3 -?/. - c.-10450C>G r.(?) p.(=)


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