Variant #0000274926 (NC_000023.10:g.23019368C>T, NM_182699.3:c.1194C>T (DDX53))

Chromosome X
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.23019368C>T
DNA change (hg38) g.23001251C>T
Published as DDX53(NM_182699.3):c.1194C>T (p.R398=)
ISCN -
DB-ID DDX53_000005
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-17 21:15:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF645 NM_152577.3 -?/. - c.*726982C>T r.(=) p.(=)
DDX53 NM_182699.3 -?/. - c.1194C>T r.(?) p.(Arg398=)


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