Variant #0000575307 (NC_000023.10:g.23019241T>A, NM_182699.3:c.1067T>A (DDX53))

Chromosome X
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.23019241T>A
DNA change (hg38) g.23001124T>A
Published as DDX53(NM_182699.3):c.1067T>A (p.L356Q)
ISCN -
DB-ID DDX53_000015
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF645 NM_152577.3 ?/. - c.*726855T>A r.(=) p.(=)
DDX53 NM_182699.3 ?/. - c.1067T>A r.(?) p.(Leu356Gln)


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