Variant #0000619413 (NC_000023.10:g.23018781A>G, NM_182699.3:c.607A>G (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.23018781A>G
DNA change (hg38) g.23000664A>G
Published as DDX53(NM_182699.3):c.607A>G (p.I203V)
ISCN -
DB-ID DDX53_000018
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_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 2025-02-07 18:57:27 +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.*726395A>G r.(=) p.(=)
DDX53 NM_182699.3 -?/. - c.607A>G r.(?) p.(Ile203Val)


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